WO2007033083A2 - Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same - Google Patents

Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same Download PDF

Info

Publication number
WO2007033083A2
WO2007033083A2 PCT/US2006/035321 US2006035321W WO2007033083A2 WO 2007033083 A2 WO2007033083 A2 WO 2007033083A2 US 2006035321 W US2006035321 W US 2006035321W WO 2007033083 A2 WO2007033083 A2 WO 2007033083A2
Authority
WO
WIPO (PCT)
Prior art keywords
dmso
dimethyl sulfoxide
resin
adsorbent
related compounds
Prior art date
Application number
PCT/US2006/035321
Other languages
French (fr)
Other versions
WO2007033083A3 (en
Inventor
Harvey L. Claussen
Colette Cozean
Original Assignee
Abela Pharmaceuticals, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to JP2008530021A priority Critical patent/JP5399072B2/en
Priority to CA2622204A priority patent/CA2622204C/en
Priority to AU2006291134A priority patent/AU2006291134C1/en
Priority to US12/066,485 priority patent/US7955418B2/en
Priority to EP06814457.5A priority patent/EP1966229B1/en
Application filed by Abela Pharmaceuticals, Inc. filed Critical Abela Pharmaceuticals, Inc.
Publication of WO2007033083A2 publication Critical patent/WO2007033083A2/en
Publication of WO2007033083A3 publication Critical patent/WO2007033083A3/en
Priority to US13/099,120 priority patent/US8480797B2/en
Priority to US13/099,098 priority patent/US8298320B2/en
Priority to US13/098,941 priority patent/US8673061B2/en
Priority to US13/659,797 priority patent/US8440001B2/en
Priority to US13/892,190 priority patent/US9186472B2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0087Environmental safety or protection means, e.g. preventing explosion
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D13/00Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches
    • A41D13/05Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches protecting only a particular body part
    • A41D13/11Protective face masks, e.g. for surgical use, or for use in foul atmospheres
    • A41D13/1107Protective face masks, e.g. for surgical use, or for use in foul atmospheres characterised by their shape
    • A41D13/1115Protective face masks, e.g. for surgical use, or for use in foul atmospheres characterised by their shape with a horizontal pleated pocket
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D13/00Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches
    • A41D13/05Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches protecting only a particular body part
    • A41D13/11Protective face masks, e.g. for surgical use, or for use in foul atmospheres
    • A41D13/1107Protective face masks, e.g. for surgical use, or for use in foul atmospheres characterised by their shape
    • A41D13/1123Protective face masks, e.g. for surgical use, or for use in foul atmospheres characterised by their shape with a duckbill configuration
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D13/00Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches
    • A41D13/05Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches protecting only a particular body part
    • A41D13/11Protective face masks, e.g. for surgical use, or for use in foul atmospheres
    • A41D13/1192Protective face masks, e.g. for surgical use, or for use in foul atmospheres with antimicrobial agent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/01Deodorant compositions
    • A61L9/014Deodorant compositions containing sorbent material, e.g. activated carbon
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0087Environmental safety or protection means, e.g. preventing explosion
    • A61M16/009Removing used or expired gases or anaesthetic vapours
    • A61M16/0093Removing used or expired gases or anaesthetic vapours by adsorption, absorption or filtration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/06Respiratory or anaesthetic masks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/105Filters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/105Filters
    • A61M16/106Filters in a path
    • A61M16/1065Filters in a path in the expiratory path
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62BDEVICES, APPARATUS OR METHODS FOR LIFE-SAVING
    • A62B23/00Filters for breathing-protection purposes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • B01D53/508Sulfur oxides by treating the gases with solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28054Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J20/28078Pore diameter
    • B01J20/28085Pore diameter being more than 50 nm, i.e. macropores
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/105Filters
    • A61M16/1055Filters bacterial
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/1075Preparation of respiratory gases or vapours by influencing the temperature
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/20Valves specially adapted to medical respiratory devices
    • A61M16/208Non-controlled one-way valves, e.g. exhalation, check, pop-off non-rebreathing valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/75General characteristics of the apparatus with filters
    • A61M2205/7527General characteristics of the apparatus with filters liquophilic, hydrophilic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/20Organic adsorbents
    • B01D2253/202Polymeric adsorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/30Physical properties of adsorbents
    • B01D2253/302Dimensions
    • B01D2253/311Porosity, e.g. pore volume
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/30Sulfur compounds
    • B01D2257/306Organic sulfur compounds, e.g. mercaptans
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/90Odorous compounds not provided for in groups B01D2257/00 - B01D2257/708
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/91Bacteria; Microorganisms
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/45Gas separation or purification devices adapted for specific applications
    • B01D2259/4533Gas separation or purification devices adapted for specific applications for medical purposes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/45Gas separation or purification devices adapted for specific applications
    • B01D2259/4541Gas separation or purification devices adapted for specific applications for portable use, e.g. gas masks

Definitions

  • the present invention relates generally to materials for facilitating the administration of DMSO and associated compounds.
  • these materials comprises adsorbents for the removal of the odors and compounds resulting from the metabolism or degradation of DMSO and associated compounds.
  • these materials comprise clean air members and fabrics that absorb odors or compounds.
  • these materials comprise a clean air supply assembly for removing odors and compounds.
  • these materials comprises indicators to reveal the presence or absence of DMSO and associated compounds.
  • Odors and chemicals resulting from the treatment of patients with DMSO and related compounds can be so oppressive as to diminish the effectiveness and receptiveness of the medical staff. Such odors may be likened to the smell of rotten eggs. New procedures are emerging which require the treatment of seriously ill persons by using far larger volumes of DMSO than at present. The resulting highly oppressive odors may emanate from any part of the patient's body. The capture of these odors can be crucial to the success of the new medical procedures.
  • DMSO associated compounds methylsulfonylmethane (MSM or DMSO 2 ) and dimethyl sulfide or methylthiomethane (DMS).
  • MSM methylsulfonylmethane
  • DMS dimethyl sulfide or methylthiomethane
  • Several embodiments of present invention relate to materials and methods for the removal of odors and chemicals resulting from the treatment of patients with DMSO and other compounds and chemicals. Also provided are modified polyamines, odor capturing fabrics which comprise these modified polyamines, items manufactured from these fabrics and methods of manufacture and use of the fabrics.
  • the invention comprises an indicator for DMSO associated compounds, its method of manufacture, and an apparatus including the indicating material.
  • the invention comprises a device to purify the air at a DMSO delivery or metabolism site.
  • a clean air device that removes DMSO metabolites and/or DMSO odors may be well-suited for hospital rooms where a patient is receiving DMSO or in a room where a patient is recovering after receiving DMSO therapy.
  • the clean air device comprises a portable, collapsible, adjustably directable clean air delivery supply assembly and enclosure for use in DMSO treated medical patient environments to provide localized clean air free of the odors, DMS 5 and/or compounds resulting from the metabolism of DMSO and DMSO associated compounds, including, but not limited to, hydrogen sulfide and potentially methyl mercaptan.
  • the invention comprises visual color indicators to detect the presence or absence of DMSO metabolites such as DMS.
  • the invention comprises core particles that adsorb DMSO or related compounds, or the odors associated with said compounds.
  • the invention comprises an adsorbent for adsorbing DMSO or related compounds, or the odors associated with said compounds.
  • the adsorbent comprises an inner layer, an intermediate layer, and an outer layer.
  • the inner layer comprises adsorbing core particles that adsorb DMSO or related compounds, or the odors associated with said compounds.
  • the intermediate layer which is optional, contacts the inner layer and the outer layer.
  • the outer layer comprises a porous coating.
  • the adsorbent may reduce undesired pathogens and odors that are unrelated to DMSO
  • the adsorbent comprises at least one indicator for indicating the presence of DMSO or related compounds.
  • the indicator comprises permanganate in one embodiment.
  • the indicator is colored, and is adapted to decrease in color or intensity as DMSO or related compounds are removed.
  • color intensity can be correlated to the concentration of undesired compounds or odors.
  • different colors indicate different levels of undesired odors or compounds.
  • the adsorbing core particles are selected from the group consisting of one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, an ion exchange resin, and a chemical deodorizer.
  • the intermediate layer comprises a metal compound and a water-soluble organic material disposed between the core particles and the porous coating.
  • the outer layer consists only of a porous coating.
  • a porous coating is applied directly to the intermediate layer or to the core particles.
  • the outer layer comprises a layer of material which is additionally coated with a porous coating.
  • the outer layer comprises a polymer selected from the group consisting of one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefin resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer or derivative thereof.
  • a fluororesin a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefin resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer or derivative thereof.
  • the polymer may also be selected from the group consisting of one or more of the following: polytetrafluoroethylene, polyhexafiuoropropylene, polydifluoroethylene, polyvinylidene fluoride, polyvinyl fluoride, and a copolymer or derivative thereof.
  • the porous coating has a thickness of about 0.01 ⁇ m to about 1,000 ⁇ m, an average pore diameter of about 0.01 ⁇ m to about 500 ⁇ m, and/or a porosity of about 3% to about 90%.
  • the invention comprises a method for removing DMSO metabolites, comprising contacting said metabolites with an adsorbent according to any one of the embodiments described herein.
  • the DMSO metabolites may be produced by an individual receiving DMSO treatment.
  • the DMSO metabolites may be degradation products caused by the exposure of DMSO to the environment (e.g., the air or a fluid).
  • the invention comprises a method for removing odors associated with DMSO or related compounds, comprising exposing said odors to an adsorbent according to any one of the embodiments described herein.
  • the invention comprises a clean air member for removal of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising adsorbent according to any one of the embodiments described herein.
  • the invention comprises a clean air supply assembly for removal of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising adsorbent according to any one of the embodiments described herein.
  • the invention comprises an apparatus for removing DMSO or related compounds, or the odors associated with said DMSO or related compounds from the exhaust outlet of a medical respiratory ventilator, wherein said apparatus comprises a gas scavenging device comprising the adsorbent of according to any one of the embodiments described herein.
  • the gas scavenging device is optionally connected to said exhaust outlet.
  • the invention comprises a face mask for reducing exposure of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising an adsorbent of according to any one of the preceding claims.
  • the face mask filters out undesired odors that are unrelated to DMSO.
  • the face mask may also filter airborne pathogens, including viruses and bacteria.
  • the filtering of these other compounds may be in addition to or instead of the filtering of DMSO and associated compounds.
  • the face mask may be a duckbill-type mask, and may comprise an exhale valve.
  • the invention comprises a face mask comprising an outer shield layer comprising a synthetic fiber; a copper layer comprising a fiber and powdered copper; a carbon layer comprising a fiber and activated carbon; a chemical layer comprising a fiber and one or more, odor absorbing chemicals; and a facial layer comprising a synthetic fiber.
  • the face mask may contain less than the layers described herein, or may comprise additional layers.
  • the multi-layered face mask may protect a user from pathogens and/or DMSO compounds.
  • Figure 1 shows an adsorbent according to one embodiment of the invention.
  • Figure 2 is a schematic diagram of a rollably positioned, adjustably directable clean air delivery supply assembly and enclosure according to one embodiment.
  • Figure 3 shows a front view of a "duckbill" type odor-absorbing mask according to one embodiment.
  • Figure 4 shows a front view of a "duckbill" type mask according to one embodiment, showing the mask partially open.
  • Figure 5 shows a surgical mask according to one embodiment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • these materials comprises adsorbents for the removal of the odors and compounds resulting from the metabolism or degradation of DMSO and associated compounds.
  • these materials comprise clean air members and fabrics that absorb odors or compounds.
  • these materials comprise a clean air supply assembly for removing odors and compounds.
  • these materials comprises indicators to reveal the presence of these compounds.
  • the invention comprises an adsorbent adapted for the partial or complete removal of the metabolites of DMSO and other compounds, and/or related odors.
  • the adsorbent material comprises three layers: an inner layer; an intermediate layer, and an outer layer.
  • the adsorbent material may comprise one, two, or three of the layers described above.
  • additional layers are provided. Layers can be fixed or otherwise coupled to one another or to other materials (using, for example, adhesives, sealants, stitches, etc).
  • the inner layer comprises core particles containing at least one adsorbing material.
  • the intermediate layer comprises at least one porous coating layer including a polymer material that coats the core particles.
  • the intermediate layer may comprise a metal compound and a water-soluble organic material disposed between the core particles and a porous coating layer.
  • the water-soluble organic material is selected from the group consisting of one or more of the following: polymers of sugar, cellulose derivatives, alginic acid, methacrylic acid, acrylic acid, vinylpyrrolidone, vinyl alcohol, oxyolefins, and organic sulfur oxides such as DMSO 2 (dimethyl sulfone).
  • the outer layer comprises a coating, such as a porous coating layer
  • the coating layer may be formed by spraying and applying a suspension or a solution containing a polymer material over the adsorbing material, or by immersing the adsorbing material into the suspension or the solution.
  • an adsorbent according to any one of the embodiments described herein preferentially absorbs DMS is provided. In another embodiment, the adsorbent preferentially adsorbs MSM. In other embodiments, the adsorbent adsorbs all odor causing compounds related to DMSO.
  • a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an inner layer.
  • Figure 1 shows the adsorbent material according to one embodiment of the invention.
  • the inner layer 1 comprises core particles.
  • the core particles may or may not represent the entire adsorbent material and may comprise one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, a modified compound thereof, an ion exchange resin, a chemical deodorizer, silica gel, alumina gel, zeolite, a molecular sieve, diatomaceous earth, inorganic oxide (e.g., copper oxide, iron oxide), chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid or a derivative thereof. Combinations of two or more of these compounds are used in some embodiments.
  • activated carbon an inorganic oxide
  • a compound having ion exchange capacity e.g., a modified compound thereof, an ion exchange resin
  • a chemical deodorizer e.g., silica gel, alumina gel, zeolite, a molecular sieve
  • the compound having ion exchange capacity is selected from the group consisting of one or more of the following: chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid and a derivative thereof.
  • the inner layer is an adsorbent that comprises core particles, which adsorb odors or compounds by physically trapping, enclosing, or isolating said odors and compounds.
  • the inner layer is an adsorbent that comprises core particles, which adsorb odors or compounds by chemically oxidizing or reducing said odors and compounds.
  • undesired odors and compounds are reduced or eliminated because the core particles chemically react with said odors and compounds to render them inert or inactive.
  • the core particles have an average particle size of about 0.01 mm to about 100 mm.
  • the inner layer has a thickness of about 0.1 ⁇ m to 1,000 ⁇ m. In certain embodiments relating to use of the core particles as an indicator, greater size may provide greater absorbency but lesser sensitivity, and lower size may give inadequate visual indication.
  • the core particles are formed by a tableting process.
  • the inner layer comprises core particles that are coated. This coating can be the same or different than the outer layer.
  • the core particles have a porous coating layer having an average pore size of 0.001 ⁇ m to 50 ⁇ m.
  • the core particles are fixed on or otherwise coupled to a member having a one-dimensional structure or a two-dimensional structure.
  • the core particles are fixed onto the member having the two- dimensional structure at a density of about 0.1 to about 100,000 particles per 1 cm 2 of a surface of said member having the two-dimensional structure.
  • the particles having said porous coating layer formed thereon are fixed on one surface of said member having the two-dimensional structure, and an adhesive is applied on another surface of said member having the two- dimensional structure.
  • the particles having said porous coating layer formed thereon are fixed on a member having a three-dimensional structure.
  • the core particles are fixed onto said three-dimensional structure at a density of about 1 to about 1 ,000,000 particles per 1 cm 3 of a volume of said member having the three-dimensional structure.
  • the core particles having said porous coating layer formed thereon are fixed to a member in a state of a layer having a thickness of a single particle to about 1,000 particles.
  • greater density may provide greater adsorbency but lesser sensitivity, and lower density may give inadequate visual indication at some point.
  • the core particles having said porous coating layer formed thereon are fixed to the member with an adhesive.
  • the adhesive may comprise an organic solvent type adhesive, a water type adhesive, a hot melt type adhesive, or combinations thereof.
  • the member may comprise a portion covered by an air permeable sheet.
  • the member may be entirely wrapped with an air permeable sheet.
  • the member may be contained in an air permeable container.
  • the air permeable container may comprise an unwoven cloth, a woven cloth, a mesh, a net, or combinations thereof.
  • the core particles having said porous coating layer formed thereon are wrapped with an air permeable sheet, m one embodiment, the core particles having said porous coating layer formed thereon are contained in the air permeable sheet in a number of about 1 to about 100,000,000. In certain embodiments, greater density may provide greater adsorbency but lesser sensitivity, and lower density may give inadequate visual indication.
  • greater size may provide greater adsorbency but lesser sensitivity, and smaller size may give inadequate visual indication at some point.
  • a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an intermediate layer.
  • Figure 1 reference numeral 2 shows the intermediate layer according to one embodiment of the invention.
  • the intermediate layer of the adsorbent may comprise one or more of the following: the oxide, hydroxide, carbonate, sulfates, phosphate, metasilicate, borate, oxalate, tungstate, molybdate, vanadate, chromate, selenate, and manganate of a metal or the metal itself.
  • the metal may also include titanium, zirconium, silicon, zinc, iron, manganese, aluminum, magnesium, nickel, copper, silver, barium, calcium, scandium, bismuth, molybdenum, niobium, neodymium, antimony, selenium, stannum, strontium, terbium, tellurium, thorium, and yttrium.
  • the metal compound has a particulate shape having an average particle size of about 0.001 ⁇ m to about 50 ⁇ m Other shapes and sizes may be used.
  • the intermediate layer has a thickness of about 1 ⁇ m to about 10,000 ⁇ m.
  • too thin a coating may result in poor indication due to lack of color, and too thick a coating may result in too much adsorption and loss of sensitivity.
  • a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an outer layer.
  • Figure 1, reference numeral 3 shows the outer layer (e.g., porous material) according to one embodiment of the invention.
  • the outer lay may comprises a porous coating layer.
  • the outer layer may comprise one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefin resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer thereof, and a derivative thereof or polytetrafluoroethylene, polyhexafluoropropylene, polydifluoroethylene, polyvinyliden fluoride, polyvinyl fluoride, and a copolymer or derivative thereof. Combinations of two or more of these materials are used in some embodiments.
  • the porous coating layer has a thickness of about 0.01 ⁇ m to about 1,000 ⁇ m. In one embodiment, the greater number lending toward more adsorbency but less efficiency of coating use while the lower number contributes to high efficiency of coating use but lower volumetric adsorbency.
  • the porous coating layer has an average pore diameter of about 0.01 ⁇ m to about 500 ⁇ m and/or has a porosity of about 3% to about 90%. In one embodiment, the porous coating layer is colored.
  • a method for producing the adsorbent, or indicating adsorbent comprises forming the coating layer by applying a liquid containing said polymer material onto a surface of said core particles.
  • the coating layer may be formed by spraying said liquid over said core particles and/or immersing said core particles into said liquid.
  • the liquid comprises a suspension of said polymer material and/or a solution of said polymer material.
  • At least one of a step of heating and a step of decreasing a pressure is carried out to draw said porous coating layer.
  • a heating process is carried out so that said coating layer partially shrinks and partially expands.
  • the core particles in said step of forming the coating layer are in a water-containing state, in an oil-containing state, or in a frozen state thereof.
  • the liquid comprises a pore-forming agent.
  • the pore-forming agent may comprise a water-soluble polymer or oligomer.
  • the water- soluble polymer or oligomer may be selected from the group consisting of one or more of the following: cellulose, poly(oxyolefm), polyvinylpyrrolidone, polyvinyl alcohol, a saponification compound of polyvinyl acetate, polyacrylic acid, polymethacrylic acid, and derivatives thereof.
  • the water-soluble polymer or oligomer is selected from the group consisting of one or more of the following: methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, polyvinylpyrrolidone, polyvinyl alcohol, polyethylene glycol, polypropylene glycol, and derivative thereof.
  • the pore-forming agent comprises an oil soluble polymer or oligomer.
  • the oil soluble polymer may comprise liquid paraffin.
  • the pore-forming agent is removed during or after the step of forming said coating layer. In another embodiment, the pore-forming agent is removed by one or more of the following processes: extraction, evaporation, sublimation or combustion.
  • the invention comprises a packed bed containing the adsorbent of one embodiment of the present invention.
  • the packed bed in some embodiments, functions as a holder for the adsorbent material.
  • the packed bed of adsorbent may be incorporated into a cartridge for containment of the adsorbent material.
  • the cartridge may be in the form of a rectangular, cylindrical or otherwise shaped vessel.
  • the cartridge may be provided in conjunction with a device for introducing air into said rectangular, cylindrical or otherwise shaped vessel, wherein the adsorbent is partially or completely contacted when the air is introduced therein.
  • Clean Air Member One of skill in the art will understand that other shapes may also be used according to alternative embodiments of the invention. Clean Air Member
  • a device and method for cleaning air comprising contacting air with an indoor ambient air cleaning member (such as a cartridge or filter).
  • the clean air member comprises the adsorbent material described above.
  • the clean air member adsorbs DMSO and/or DMSO related compounds, and/or odors associated with same.
  • the clean air member additionally removes one or more undesired compounds from the air that are unrelated to DMSO (e.g., toxic fumes or gases).
  • the clean air member (such as a cartridge or filter) comprises an inner layer, an intermediate layer, and an outer layer, as described above.
  • the clean air member may be contained in a rectangular, cylindrical or otherwise shaped vessel, and said indoor ambient air cleaning member is freely convected when the air is introduced therein.
  • the vessel may be tilted.
  • the clean air member according to any one of the embodiments described herein is an ambience odor or sulfur chemical regulating member.
  • the clean air member (such as a cartridge or filter) comprises core particles comprising at least one odor or sulfur chemical regulating material of an acid or acid salt, and a porous coating layer including a polymer material that coats the core particles.
  • the acid is selected from the group consisting of one or more of the following: lactic acid, malic acid, tartaric acid, oxalic acid, chromic acid, dichromic acid, manganic acid, permanganic acid, thiocyanic acid, cyanic acid, carbonic acid, hydrochloric acid, perchloric acid, chloric acid, chlorous acid, hypochlorous acid, hydriodic acid, periodic acid, iodic acid, iodous acid, hypoiodous acid, sulfuric acid, sulfurous acid, nitric acid, nitrous acid, and phosphoric acid.
  • the clean air member comprises an odor or sulfur chemical regulating material selected from the group consisting of one or more of the following: sodium sulfate, an alkali metal salt of phosphoric acid, an alkali metal salt of hydrogenphosphate, an ammonium salt of phosphoric acid, and an ammonium salt of hydrogen phosphate.
  • the clean air member comprises core particles that comprises a hydrophilic polymer compound.
  • the hydrophilic polymer compound may be selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
  • the clean air member comprises core particles that have an average particle size of about 0.01 mm to about 100 mm.
  • the clean air member comprises core particles comprising at least one odor or sulfur chemical regulating material of an acid salt, and a porous coating layer comprising a polymer material that coats said core particles is provided.
  • the acid salt may be selected from the group consisting of one or more of the following: an alkali metal salt, an alkaline earth metal salt, and an ammonium salt.
  • the core particles further comprises a hydrophilic polymer compound.
  • the hydrophilic polymer compound may be selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
  • the clean air member comprises a porous coating layer having a thickness of about 0.1 ⁇ m to about 1,000 ⁇ m and/or average pore size of about 0.001 ⁇ m to about 50 ⁇ m.
  • the porous coating layer of the clean air member may comprise a silver deposit layer.
  • the clean air member comprises a porous coating layer that comprises material selected from the group consisting of one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefm resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin, copolymers thereof, and derivative thereof.
  • the porous coating layer may be colored.
  • an adsorbent for removal of respiratory exhalation from a patient treated with DMSO is provided.
  • an adsorbent for removal of DMSO metabolites from a respiratory ventilator or an isolation room ventilator is provided. The adsorbent may be part of the clean air member.
  • the clean air member comprises an oxidizing agent.
  • the oxidizing agent is selected from the group consisting of one or more of the following: a mixture of ascorbic acid and an iron-containing compound, permanganates, manganese dioxide, chromates, dichromates, osmium tetraoxide, ruthenium tetraoxide, silver oxide and palladium chloride.
  • the iron-containing compound is selected from the group consisting of one or more of the following: iron chloride, iron bromide, iron iodide, iron oxide, iron perchlorate, iron thiocyanate, iron sulfate, iron sulfide, iron acetate, iron oxalate, Mohr's salt, di-iron monophosphide and tri-iron monophosphide. Fabrics
  • a fabric that reduces or eliminates the odor of DMSO and associated compounds comprises odor adsorbing woven or non-woven fabric suitable for the manufacture of clothing, bedding and other protective items capable of the partial or complete capture of the metabolites of DMSO and others.
  • Adsorption may include chemical oxidation, reduction, physical entrapment in fissures, or other means.
  • the adsorbent fabric may include adsorbent fibers or fibers coated with an adsorbent or it may be layered with adsorbent material between the layers.
  • the fabric may incorporate any or all of these modes of odor capture simultaneously.
  • the fabric comprises a three dimensional web.
  • the basic fiber support structure of the three dimensional web comprises woven or non-woven web of the fibers of polyethylene, polypropylene, polyvinyl chloride, polyurethane, polyamide, nylon, polyacrilan, rayon, silk, ramey, cellulosic material and any other suitable fibrous material or material which may be made fibrous.
  • Intermediate layers may comprise knit or randomly formed copper, aluminum, iron, glass, carbon, or other inorganic fibers. Each layer may be formed on a knitting, weaving, moving web, fluid dispersion, or other device. Layers may be combined following the forming of each or one or more layers may be formed as they are layered. Layers may be adhered together by crosslinking, hot melt stitching, sewing, gluing, or other methods well known in the art.
  • the odor adsorbing fibers of the fabric may comprise a modified polyamine which comprises a hybrid inorganic/organic material comprising a polyamine and an inorganic oxide.
  • the polyamine may comprise one or more of the following: amine-containing polysaccharides, amine-containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylamine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups, poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine, amine-containing polysaccharides, amine-containing polypeptid
  • MSM methyl sulfonyl methane
  • adsorbents may also be included as coatings, admixtures of the above or alone.
  • MSM is both a metabolite of DMSO and used as an adsorbent, hi this embodiment, the MSM used as the adsorbent is substantially odorless and can adsorb odorous DMS (which can be obtained from DMSO through reduction, potentially in an anaerobic metabolic environment), and other odorous compounds that result from DMSO metabolism.
  • exogenous MSM can be used as an adsorbent alone or in combination with other adsorbents.
  • MSM may also be used to adsorb sulfur contain compounds that are related or unrelated to DMSO.
  • the odor adsorbing coatings of the fibers, the cross linking members or the intermediate layers of a multilayer fabric may comprise one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, a modified compound thereof, an ion exchange resin, a chemical deodorizer, silica gel, alumina gel, zeolite, a molecular sieve, diatomaceous earth, copper oxide, iron oxide, chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid or a derivative thereof.
  • these odor adsorbing coatings may comprise a fiuororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefm resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer thereof, and a derivative thereof or polytetrafluoroethylene, polyhexafluoropropylene, polydifluoroethylene, polyvinyliden fluoride, polyvinyl fluoride, and a copolymer thereof.
  • MSM adsorbents may also be included as coatings, admixtures of the above or alone.
  • the invention comprises a modified polyamine comprising: a hybrid inorganic/organic material comprising a polyamine and an inorganic material having one or more characteristics selected from the group consisting of: amorphous structures, high surface areas, large pore volumes, and nanocrystalline structures.
  • the inorganic material is an inorganic oxide material.
  • the invention comprises a modified polyamine comprising a polyamine impregnated into or attached to a porous inorganic or organic microbead.
  • the polyamine is coupled to one or more microbeads.
  • the invention comprises a modified polyamine which comprises a polyamine having inorganic molecules or organic molecules, or both, chemically attached to it.
  • the invention comprises a modified polyamine which comprises a bio-compatible copolymer of a polyamine and a dermatologically compatible aqueous-soluble and/or oil-soluble polymer.
  • the invention comprises a nanostructured polyamine which comprises a polyamine reacted with one or more crosslinkers.
  • the polyamine is selected from the group consisting of one or more of the following: amine-containing polysaccharides, amine- containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylar ⁇ ine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups.
  • the polyamine is selected from the group consisting of one or more of the following: poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine.
  • the invention comprises an article comprising: a liquid pervious topsheet; a backsheet; and an absorbent core intermediate between said backsheet and said topsheet.
  • the absorbent core comprises from about 0.5 g/m 2 to about 500 g/m 2 of a cationic polysaccharide comprising an aminopolysaccharide selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof; and from about 0.1 g/m 2 to about 250 g/m 2 of an acidic pH buffering means having a pH in the range of from about 3.5 to about 6.5 and comprises a weak acid having its pKa or at least one of its pKas in the range from about 3.5 to about 6.5 and its conjugate base; and from about 5 g/m 2 to about 250 g/m 2 of absorbent gelling material.
  • the cationic polysaccharide is selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof having a degree of deacetylation of more than about 75%.
  • the chitosan salt is selected from the group consisting of one or more of the following: citric acid, formic acid, acetic acid, N- acetylglycine, acetylsalicylic acid, tlimaric acid, glycolic acid, iminodiacetic acid, itaconic acid, lactic acid, maleic acid, inalic acid, nicotinic acid, salicylic acid, succinamic acid, succinic acid, ascorbic acid, aspartic acid, glutamic acid, glutaric acid, malonic acid, pyruvic acid, sulfonyldiacetic acid, benzoic acid, epoxysuccinic acid, adipic acid, thiodiacetic acid, thioglycolic acid, alanine, valine, leucine, isoleucine, prolinephenylalanine, tryptophan, methionine, glycine, serine, cysteine, tyrosine
  • the pH buffering means is selected from the group consisting of one or more of the following: citric acid/sodium hydroxide, citric acid/sodium citrate, citric acid/potassium citrate, oxalic acid/sodium oxalate, tartaric acid/potassium hydrogen tartarate, oxalic acid/potassium tetra oxalate dihydrate, phthalic acid/potassium phthalate, phthalic acid/sodium phthalate acetic acid/sodium acetate, benzoic acid/sodium benzoate, glutaric acid/sodium glutarate, adipic acid/sodium adipate, carbonic acid/sodium carbonate and mixture thereof and most preferably is citric acid/sodium citrate, citric acid/sodium hydroxide and/or citric acid/potassium citrate.
  • the invention comprises an additional odor control agent selected from the group consisting of one or more of the following: zeolites, silicates, activated carbons, diatomaceous earth, cyclodextrine, clay, chelating agents, ion exchange resins, perfumes and mixture thereof.
  • the level of the additional odor control agent or a mixture thereof is from about 0.5 g/m 2 to about 600 g/m 2 .
  • the invention comprises a method of controlling odor associated with DMSO and related odorous metabolites wherein said bodily fluids are contacted with an odor control system comprising a cationic polysaccharide, selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof, and an acid pH buffering means typically having a pH in the range of about 3.5 to 6.5.
  • an odor control system comprising a cationic polysaccharide, selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof, and an acid pH buffering means typically having a pH in the range of about 3.5 to 6.5.
  • the invention comprises an odor eliminating fiber structure having an indicator comprising a fiber substrate containing odor eliminating fibers, a surface thereof being visibly determined for change of odor eliminating power with a difference between a color of the fiber substrate discoloring through adsorption of a smelling gas and a color of a standard color display part.
  • the color of the standard color display part provided on the surface of the fiber substrate becomes difficult to be distinguished by discoloration of the fiber substrate through adsorption of a smelling gas.
  • the color difference between the color of the fiber substrate upon losing the odor eliminating power and the color of the standard color display part provided on the surface of the fiber substrate is 4 or more grades upon evaluation with gray scale for assessing change in color.
  • the odor eliminating fibers contain at least one odor eliminating component selected from silver, copper and a metallic compound thereof, and a content of silver and/or copper is 0.1% by weight or more of the total fiber substrate.
  • the odor eliminating fibers comprises an odor eliminating component-containing crosslinked acrylate fibers containing at least one odor eliminating component selected from silver, copper and a metallic compound thereof, and content of a silver and/or copper is 0.1% by weight or more of the total acrylate fibers.
  • one surface of the fiber substrate has an easy- sticking and easy-releasing function.
  • the odor-absorbing fabric may be used in the manufacture of a disposable absorbent article selected from the group consisting of one or more of the following: a patient bedcover, patient gown, caregiver scrubs, gowns, masks, or any other required item to be worn or used to protect the patient or staff or visitors.
  • the patient bedding may comprise one or more of the following: suitably large sheets of odor absorbing material which may be coated partially or fully with slightly adhering material to prevent slippage. They may be assembled using methods well known in the art of clothing manufacture, including thermal, ultrasonic or electronic sealing, hot melt, adhesives, sewing, multineedle sewing, serging, basting, binding, or other joining methods. Seams may be folded, lapped, flat felled, straight stitched, trenched, overcast, enclosed, bound, hemmed, reinforced, top stitched, or other suitable seaming method. This bedding can be used at all times while the patient is undergoing treatment using DMSO and related compounds.
  • the clothing and mask items for the patient and for the caregivers may be shaped and formed to provide the maximum freedom of movement and access. These items may be constructed of cut sheets of odor absorbing material and may include ties, belts, snaps, or other fasteners to maintain the position of the article. These items may be assembled using thermal, ultrasonic or electronic sealing, hot melt, adhesives, sewing, multineedle sewing, serging, basting, binding, or other joining methods. Seams may be folded, lapped, flat felled, straight stitched, trenched, overcast, enclosed, bound, hemmed, reinforced, top stitched, or other suitable seaming method. These items can be used at all times while the patient is undergoing treatment using DMSO and related compounds.
  • the clothing and mask items described herein may comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
  • the invention comprises a method of providing disposable, strong, absorbent DMSO and related odorous metabolite capturing health care bedding which comprises providing DMSO and related odorous metabolite capturing fabric plus a non- woven fabric comprised of randomly entangled mixtures of natural and synthetic fibers interconnected so that the individual fibers are held in place to form a coherent, stable, strong fabric having a high absorbency capacity; cutting the fabric to the desired length in the cross direction; and converting said fabric to a desired size and shape.
  • Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
  • the natural fiber is cellulosic wood pulp.
  • the synthetic fiber is selected from the group consisting of one or more of the following: a polyester, a nylon, a rayon, a polypropylene and mixtures thereof. In one embodiment, the synthetic fiber is polyester.
  • the invention comprises a method of providing disposable strong, absorbent DMSO and related odorous metabolite capturing health care bedding which comprises employing as the bedding material DMSO and related odorous metabolite capturing fabric principally composed of polyester fibers combined with cellulosic wood pulp fibers, said fibers locked into place by a three-dimensional fiber entanglement wherein the individual fibers are intertwined, tangled and interconnected to each other so as to be virtually inseparable, said fabric having an absorptive capacity of at least that of woven fabric made of natural fibers, cutting the fabric to a desired length in the cross direction, and converting said cut fabric to a desired size and shape.
  • Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein. '
  • the fabric has a weight of about 0.5 to about 10 ounces per square yard.
  • a strip of elastic is attached along the edges to provide a close fit to a platform it is to cover.
  • the platform may be a six-sided gurney.
  • the invention comprises a method of providing disposable, strong, moisture absorbent DMSO and related odorous metabolite capturing health care bed and gurney coverings comprising: employing as the bedding material DMSO and related odorous metabolite capturing fabric principally composed of polyester fibers combined with cellulosic wood pulp fibers, said fibers interlocked by a three- dimensional fiber entanglement, wherein the individual fibers are intertwined, tangled and interconnected to each other so as to be virtually inseparable, and wherein said fabric has an absorptive capacity higher than that of conventional bedding made from cotton- polyester blends.
  • the method further comprises cutting across the fabric and converting said bedding material to a desired shape suitable for a gurney covering, so that its strongest direction is along the cut direction of the covering.
  • Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
  • a breathable DMSO and related odorous metabolite capturing composite having hydrostatic head according to 1ST 80.4-92 of at least about 4 inches comprising a laminate of at least one fibrous, nonwoven web layer and at least one thermoplastic film layer, the laminate being stretched no more than about 5% in a lengthwise and widthwise direction, and wherein the film layer comprises at least one thermoplastic resin, a finely divided particulate material capable of promoting breathability, and a plurality of point-like deformations which provide breathability of the composite, wherein the breathable composite has a breathability of at least about 500 g/m 2 /day.
  • Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
  • the composite has a MVTR of at least about 500 g/m 2 /day, wherein the laminate can be stretched to less than about 5% lengthwise or widthwise stretching.
  • the fibrous nonwoven web layer comprises filaments comprising at least one polyolefin resin.
  • thermoplastic film layer comprises at least one polyolefin resin.
  • thermoplastic film layer comprises at least one polyolefin resin and the nonwoven web layer comprises filaments comprising at least one polyolefin resin.
  • the nonwoven web layer has substantial segments of filaments unadhered to the film layer whereby a cloth texture suitable for diaper and apparel uses is provided on at least one surface of the composite.
  • the composite has a hydrostatic head of at least about 7 inches.
  • the polyolefin resin of the thermoplastic film layer comprises at least one polyethylene resin.
  • the polyolefin resin of the thermoplastic, breathable film layer comprises at least one polypropylene resin.
  • the polyolefin resin of the filaments comprises at least one polyethylene or polypropylene resin. In one embodiment, the polyolefin resin of the filaments comprises at least one polyethylene resin.
  • the invention comprises a breathable composite DMSO and related odorous metabolite capturing material comprising a laminate comprising at least one film layer and at least one nonwoven web layer, the laminate being no more than insignificantly stretched in a lengthwise and widthwise direction, and wherein the nonwoven web layer comprises filaments of at least one polyolefin resin, and the film layer comprises a polyolefin resin, a finely divided particulate material capable of promoting breathability, and a plurality of embossed, point-like deformations, such deformations providing breathability of the composite by occupying about 8 to about 40% of the area of a surface of the composite and being present on such surface at a density of about 100 to 500 points per square inch.
  • Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
  • the polyolefin resin of the film layer comprises at least one polyethylene resin.
  • the nonwoven web layer comprises a web of substantially continuous filaments.
  • the filaments comprise at least one polypropylene resin. In one embodiment, the filaments of the web of substantially continuous filaments provide a cloth texture to said nonwoven web layer on at least one surface of the composite. In one embodiment, the filaments comprise at least one polyethylene resin. In one embodiment, the filaments of the web of substantially continuous filaments provide a cloth texture to said nonwoven web layer on at least one surface of the composite.
  • the nonwoven web layer comprises a web of staple fibers.
  • the staple fibers comprise at least one polypropylene resin. In one embodiment, the staple fibers of the web of staple fibers provide a cloth texture to said nonwoven web layer on at least one surface of the composite. In one embodiment, the staple fibers comprise at least one polyethylene resin, hi one embodiment, the staple fibers of the web of staple fibers provide a cloth texture to said nonwoven web layer on at least one surface of the composite.
  • the polyolefin resin of the film layer comprises at least one polypropylene resin.
  • the nonwoven web layer comprises a web of substantially continuous filaments comprising at least one polypropylene resin. In one embodiment, the nonwoven web layer comprises staple fibers comprising at least one polypropylene resin. In one embodiment, the nonwoven web layer comprises a web of substantially continuous filaments comprising at least one polyethylene resin. In one embodiment, the nonwoven web layer comprises staple fibers comprising at least one polyethylene resin.
  • the adsorbent materials/fibers described herein are incorporated into one or more portions of a disposable gown for DMSO treated medical patients, such as the gown described in U.S. Patent No. 4,819,275, the entire contents of which are incorporated herein by reference.
  • This patent describes a disposable, double-breasted gown for medical patients formed, without sewing, of non- woven synthetic plastic fabric sheeting which is soft and ultrasonically sealable, said gown comprising: a body formed from a rectangular blank having a straight upper long edge that is die cut to form chamfered corners on either side, an off-center arcuate neck indentation and isosceles triangular arm hole indentations on the left and right sides of the arcuate indentation, the resultant straight edge shoulder segments formed between the corners and the indentations all having the same length and a common line, the peaks of the triangular indentations being aligned with parallel left and right transverse fold lines that define between the lines a rear gown section on one side of which is a relatively narrow left-front section and on the other side of which is a broad right-front section, the left-front section being folded over the rear section and the right-front section being folded over the folded left-front section to overlap this section, the straight edge segments of the left and right front sections being
  • the adsorbent materials/fibers described herein are incorporated into one or more portions of a surgical gown or scrubs for caregivers of DMSO treated patients, such as the type described in U.S. Patent No. 4,171,542, the entire contents of which are incorporated herein by reference.
  • the gown described in US 4,171,542 has sleeves, a front portion having a chest area covering the chest of the user and side portions which close and overlap at the back of the user, a bib affixed about its periphery to the inside surface of the surgical gown at the chest area with a portion of the bib inwardly of the periphery remaining unsecured to the gown, the chest area having a pair of spaced, substantially vertical slits formed therein within the confines of the peripheral portions of the bib, the slits communicating with the unsecured portion of the bib and being of a length to allow passage of the user's hands therethrough whereby the bib provides a sterile hand support pocket maintaining the user's hands in the aseptic zone bounded by the user's neck, shoulders and waist line.
  • the adsorbent materials/fibers described herein are incorporated into one or more portions of a disposable face mask for caregivers of DMSO treated patients.
  • Exemplary masks include those described in U.S. Patent Nos. 6,055,982; 5,765,556 and 5,322,061, herein incorporated by reference.
  • the masks described in these patents comprise a filter body having an opening sized to cover the nose and mouth of a wearer, the body having top and bottom edges with the top edge arranged to extend across the nose of the wearer and the bottom edge arranged to extend under the chin of the wearer; the top edge having ends opposite from each other and the bottom edge having ends opposite from each other; first securing means attached to the filter body adjacent to each end of the top edge and arranged to extend generally about the back of the head of the wearer in an approximate linear continuation from the top edge, the first securing means for urging the top edge into tight engagement with the wearer to prevent fluid flow between the top edge and the wearer; second securing means attached to the filter body adjacent to each end of the bottom edge and arranged to extend generally over the top of the head of the wearer in an approximate linear continuation from the bottom edge, the second securing means for urging the bottom edge into tight engagement with the wearer to prevent fluid flow between the bottom edge and the wearer; the filter body comprising an upper portion of generally trap
  • color changes indicate adsorption. Color changes upon adsorbing odors may be tested as follows based on several methods, including but not limited to that described in US Patent Publication No. 20030190266, herein incorporated by reference:
  • Example 1 Hg ;ht beige light umber 1 1 2 3 4 —
  • Example 5 very light beige beige 3 3 2 2 1 4-5
  • the invention comprises a mask that is designed to reduce, eliminate or shield the user from odors associated with DIvISO and related compounds.
  • Embodiments described above that relate to the fabric may be used to construct some embodiments of the mask.
  • the mask comprises one or more layers.
  • the face mask may be a "duckbill" type mask (Figs. 3-4), or surgical mask (Fig. 5).
  • an exhale valve comprising two flat strips of elastomer is installed in place of the entire seam at the bottom of the duckbill mask which has a large cross-sectional area when open.
  • the surgical masks may also comprise one or more odor-masking "scratch and sniff patches which release one or more pleasant odors when abraded. Such odors include lemon, perfume, peppermint, vanilla and the like. These patches may be square, circular rectangular or any other desired shape.
  • the layers include from outer (distal to the face) to inner (proximal to the face): 1) outer shield; 2) copper layer; 3) carbon layer; 4) chemical layer; and 5) facial layer.
  • the mask comprises one or more of these layers. The layers need not be present in the order identified above.
  • the outer shield may provide N95 or N99 filtration.
  • the mask filters at least about 75%, 80%, 85%, 90%, 95%, 97%, 99%, 99.9%, or 100% of airborne particles.
  • the outer shield layer may comprise 100% synthetic fiber. Examples of synthetic fibers include those described herein, and other synthetic fibers well known in the art (e.g., polyester, rayon, acrylic, nylon, dacron).
  • the copper layer may act as a catalytic converter.
  • the copper layer may comprise one or more fibers and powdered copper.
  • the fiber comprises about 40% wood pulp and about 60% synthetic fiber.
  • the powdered copper may be present on the fiber in an amount ranging from about 100% w/w to about 500% w/w, preferably from about 200% w/w to about 400% w/w, and more preferably about 250% w/w.
  • the carbon layer may comprise activated charcoal and acts as an odor adsorber.
  • the carbon layer comprises two sub-layers: activate charcoal adsorber I and activated charcoal adsorber II.
  • the carbon layer may comprise one or more fibers and activated carbon.
  • the fiber comprises about 40% wood pulp and about 60% synthetic fiber.
  • the activated carbon may be present on the fiber in an amount ranging from about 100% w/w to about 500% w/w, preferably from about 200% w/w to about 400% w/w, and more preferably about 250% w/w.
  • One or more types of activated carbon may be incorporated into the carbon layer.
  • the following Chemsorb activated carbon compositions are used: 1202-70 G12 (for. acid gases), 620-70 G12 (for ammonia and amines), 1505-70 G12 (for aldehydes) and 1000-70 (for organic vapors).
  • the chemical layer may allow breath-activated odor removal.
  • the chemical layer comprises one or more fibers and one or more odor-removing chemicals, which may be breath-activated, such as citric acid, chitosan, MSM and other compounds.
  • the chitosan, citric acid and MSM may be present on the fiber in " amounts of about 50% w/w, about 40% w/w and about 30% w/w, with the remainder being one or more other compounds.
  • the facial layer may provide soft facial protection.
  • the facial layer may comprise 100% synthetic fiber.
  • natural fibers are used, alone or in combination with synthetic fibers.
  • the mask is made by placing the coatings on separate layers prior to forming the masks on the same multi-sheet airlay machine. Clean Air Supply Assembly
  • the present invention comprises a system for removing odors and chemicals resulting from the treatment of patients with DMSO and related compounds.
  • this system is a clean air supply assembly.
  • the invention comprises a rollably positioned, adjustably directable clean air supply assembly and enclosure for use in DMSO treated medical patient environments.
  • the clean air supply assembly provides, in some embodiments, localized clean air free of the odors, DMS (dimethyl sulfide) and compounds resulting from the metabolism of DMSO and DMSO associated compounds including, but not limited to, hydrogen sulfide and methyl mercaptan.
  • the clean air supply assembly comprises a fully portable device providing for the effective capture and movement of room air through an adsorbent material suitable for the complete removal of the metabolites of DMSO and other related compounds.
  • This device may have battery power for backup or for use while moving a patient.
  • the device is capable of turning any hospital room into a virtual clean room.
  • a portable curtaining containment system which may encompass the patient's upper torso or the entire patient bed area with provisions for caregiver access is provided.
  • the invention comprises a rollably positioned, passable through doorways, adjustably directable clean air supply assembly which provides air free of the metabolites of DMSO and others for use in an area where a patient is being treated using DMSO and associated compounds.
  • the clean air supply assembly may comprise one or more of a base module, a powered air moving assembly and a filtration system.
  • the clean air supply assembly 4 is shown schematically in Figure 2 and comprises a rollable support assembly 19 having wheels 21. Attached to the platform are a power supply unit 5 powering an electronics package 7 providing either DC or AC power depending on the motor selected.
  • the power supply unit 5 comprises a battery with a charger.
  • An internal or external chemical and/or odor filter and adsorbent cartridge 9 containing an adsorbent is mounted on platform 19 adjacent power supply unit 5 and electronics package 7.
  • the adsorbent cartridge 9 follows the air moving assembly and is capable of removing metabolites of DMSO and other related compounds, and may incorporate visual indication of depletion of such metabolites.
  • the adsorbent may be augmented or replaced by ultraviolet lamps and/or ozone (e.g., ozone injection) to further or fully remove odors, DMS, methyl mercaptan and/or hydrogen sulfide and other chemicals.
  • clean air supply assembly 4 directs a controlled amount of clean grade air through an adjustably oriented top hood assembly 11 which contains a pre-filter 13 and a sealed final filter 15 (e.g., high efficiency particle arrestor (HEPA) filter) which may be mounted within the lower portion of the base 14 or within the top final filter hood assembly 11.
  • This final filter 15 filters the air and allows the discharge of the air at minimal-eddy creating air velocities for improved air quality levels, which creates certifiable cleanrooms, clean zones, improved recirculated air quality within an given area, where a patient is being treated with DMSO.
  • the clean air supply assembly 4 is shown optionally attached to a patient isolation unit 17.
  • the clean air supply assembly is a modification of the clean air supply assembly shown in Figure 2 of US Patent No. 6,099,607, the entire contents of which are incorporated herein by reference.
  • the rollable support assembly in US 6,099,607 is extended in a direction opposite the hood top assembly 328, and the battery/power module/adsorbent cartridge assembly shown in Figure 2 of the present application is placed on, or attached to, the rollable support assembly.
  • This device may be attached to a wheelchair or gurney via a wheelchair/gurney attachment, and filters odors and chemicals resulting from DMSO treatment of a patient.
  • the clean air supply assembly may also be attached to a patient isolation unit comprising a frame body foldable and/or capable of being disassembled; and a flexible envelope adapted to be detachably attached to the frame body as assembled as described in US Patent No. 6,099,607.
  • the patient isolation unit may also comprise a collapsible framework constructed of rods pi vo tally joined at their ends to hubs to form a self-standing unit when expanded and to fold into a small set of nearly parallel rods when folded as described in US Patent Nos. 4,986,016 and 5,125,205, the entire contents of which are incorporated herein by reference.
  • the exhauster device 5 shown in Figure 1 of US Patent No. 6,966,937, herein incorporated by reference is modified by extending the reliable support assembly in a direction opposite exhaust duct 4 and the battery/power module/adsorbent cartridge assembly shown in Figure 2 of the present application is placed on, or attached to, the reliable support assembly ⁇
  • the device may then be attached to a patient isolation unit to filter odors and chemicals resulting from DMSO treatment of a patient.
  • the patient isolation unit may include an integral patient isolation curtain rod, or a separate foldable frame body, and a flexible envelope made of a natural or polymeric porous or nonporous film, knit, woven or non-woven sheet which can be attached to the assembled frame body, which may or may not include a bottom.
  • the patient isolation assembly includes a low cost disposable curtain to be affixed to the patient privacy curtain, or to an inexpensive plastic frame.
  • Indicator
  • the present invention also provides a visual color indicator, particularly a metal permanganate visual color indicator material suitable for the detection of DMS and other metabolites of DMSO.
  • a visual color indicator particularly a metal permanganate visual color indicator material suitable for the detection of DMS and other metabolites of DMSO.
  • sulfides such as DMS are oxidized by potassium permanganate to produce sulfone with the resulting reduction of the permanganate ion eliminating its characteristically intense purple color.
  • the indicator may be included in any one of the layers of the adsorbant described herein, or in an additional layer on a base layer having one, two, or three parts.
  • an indicator for DMS and the metabolites of DMSO and other related compounds includes core particles containing an adsorbing material as described herein in which the intermediate layer comprises one or more indicators and a metal or other compound, and is disposed between the core particles and the porous coating layer.
  • the intermediate layer comprises one or more indicators and a metal or other compound, and is disposed between the core particles and the porous coating layer.
  • the structure and components of the core particles are described in detail above.
  • Visual indicators other than color may also be used.
  • One or more indicators may be included within a layer, on the inner surface of a layer, on an outer surface of a layer, or integral with one of the layers. ⁇
  • the present invention comprises a system which includes a transparent container with a packed bed containing the detecting indicator of the present invention.
  • the packed bed functions as a holder for the indicator material and may be separate from, or included in, an indicating adsorbent bed utilized for the removal of DMS and other DMSO metabolites.
  • the indicator as the indicator is exposed to DMS, methyl mercaptan and related materials, it becomes progressively lighter and the lightening progresses through the bed.
  • the present invention includes a personal monitor comprising one or more detecting indicators to sample airborne contaminants by the process of diffusion. Exposure levels may then be compared to permissible exposure limits published in health and safety standards. In one embodiment, the lighter the personal monitoring patch, the greater exposure is indicated.
  • the present invention includes a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator.
  • a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator.
  • the invention comprises a functional ambience odor or sulfur chemical or DMS indicating and/or regulating member comprising the ambience odor or sulfur chemical regulating member .
  • the invention comprises an ambience odor or sulfur chemical or DMS indicating and/or regulating member, comprising core particles containing at least one odor or sulfur chemical regulating material of an acid salt, and a porous coating layer including a polymer material that coats said core particles, wherein the acid salt is at least one of an alkali metal salt, an alkaline earth metal salt, and an ammonium salt.
  • the odor or sulfur chemical regulating material is selected from the group consisting of one or more of the following: sodium sulfate, an alkali metal salt of phosphoric acid, an alkali metal salt of hydrogen phosphate, an ammonium salt of phosphoric acid, and an ammonium salt of hydrogen phosphate.
  • the core particles further contains a hydrophilic polymer compound .
  • the hydrophilic polymer compound is selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
  • the invention comprises any or all of the above indicting absorbents incorporated into a personal monitor sampling, detecting, and indicating airborne DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds by the process of diffusion.
  • the invention comprises any or all of the above indicting absorbents incorporated into a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator for indicating airborne DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds.
  • a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds directly from the patient's exhaled respiratory air is provided.
  • the device e.g., the adsorbent
  • the device is directly connected to the patient's mask. In one embodiment, this may require treating the highest concentration of odor bearing material.
  • an apparatus to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the exhaust outlet of a medical respiratory ventilator is provided.
  • the device is connected to the ventilator's exhaust outlet through a gas scavenging device.
  • the apparatus comprises a gas scavenging device comprising the adsorbent described herein, wherein the gas scavenging device is connected to the exhaust outlet.
  • a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the recirculated or vented stream a room sized HVAC or clean room system is provided.
  • the device e.g., the adsorbent
  • the device is connected to the system's ductwork.
  • an adsorbent to be adhered to or sandwiched between three dimensional fiber material as in fabric, cloth, felt, nonwoven or other flexible material to become part of clothing, bedding, masks and other items used by the patient or the medical staff is provided.
  • An article of patient clothing to capture the odors and compounds emanating from the dermal areas of the patient's body and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is also provided.
  • An article of caregiver clothing to capture the odors and compounds emanating from all areas of the patient including respiration and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is provided.
  • a caregiver mask to reduce and/or prevent the breathing by the caregiver of the odors and compounds emanating all areas of the patient including respiration and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is provided.
  • a device to remove the odors, DMS, methyl mercaptan and/or hydrogen sulfide and compounds resulting from the metabolism of DMSO and associated compounds directly from the area around a patient e.g., the patient's upper torso
  • the flexible patient isolation assembly may or may not be connected to the clean air delivery assembly's top final filter hood assembly.
  • a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the entire patient bed area with or without enough space for caregiver occupancy of the patient isolation assembly is provided.
  • the clean air delivery assembly device may be connected to the patient isolation assembly sized to enclose only the bed or to provide caregiver access.
  • a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the entire patient room is provided.
  • the clean air delivery assembly may positioned with the top final filter hood assembly over the patient or preferably within the room should the patient be served by another unit.
  • a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds directly from the area around the patient's wheelchair or gurney is provided.
  • the portable clean air delivery assembly device may be connected to the wheelchair or gurney by means of clamps, straps or other suitable means.
  • the flexible patient isolation assembly may or may not be connected to the clean air delivery assembly's top final filter hood assembly.
  • a device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds directly from the patient's exhaled respiratory air is provided. Such compounds may be detected in concentrations of about 1 to about 10,000 parts per million.
  • the device may be directly connected to the patient's mask.
  • a device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds from the exhaust of a medical respiratory ventilator is provided. Such compounds may be detected in concentrations of about 1 to about 1 ,000 parts per million.
  • the device may be integral to or connected to an adsorber located on the ventilator's discharge or directly on the ventilator's discharge through a gas scavenging device.
  • a device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds from the recirculated or vented stream from a room sized HVAC or clean room system is provided. Such compounds may be detected in concentrations of about 1 to about 10 parts per million.
  • the device may be connected to the system's ductwork.
  • An indicating adsorbent included in a personal monitor containing the detecting indicator and sampling airborne contaminants by the process of diffusion is provided. Such compounds may be detected in concentrations of about 1 to about 1 ,000 parts per million.
  • such personal monitor may be pinned, clipped, or otherwise affixed to the clothing or person of the staff, visitors or patients in the medical facility.
  • An indicating adsorbent included in a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator is provided.
  • Such compounds may be detected in concentrations of about 1 to about 10,000 parts per million.
  • Such sampling may be from the patient's bed area, the room, the respiratory ventilator, the room's HVAC system, or other location.

Abstract

Preferred embodiments of the invention relate to systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same. The systems include adsorbents, odor adsorbing fabrics, masks, clean air members and clean air supply assemblies.

Description

SYSTEMS FOR REMOVING DIMETHYL SULFOXIDE (DMSO) OR RELATED COMPOUNDS, OR ODORS ASSOCIATED WITH SAME
Related applications
This application claims priority to United States Provisional Application Serial Nos. 60/716,271; 60/716,336; 60/716,278; and 60/716,369, all of which were filed September 12, 2005, and are herein incorporated by reference.
BACKGROUND OF THE INVENTION Field of the Invention
[0001] The present invention relates generally to materials for facilitating the administration of DMSO and associated compounds. In some embodiments, these materials comprises adsorbents for the removal of the odors and compounds resulting from the metabolism or degradation of DMSO and associated compounds. In other embodiments, these materials comprise clean air members and fabrics that absorb odors or compounds. In further embodiments, these materials comprise a clean air supply assembly for removing odors and compounds. In yet other embodiments, these materials comprises indicators to reveal the presence or absence of DMSO and associated compounds. Description of the Related Art
[0002] Odors and chemicals resulting from the treatment of patients with DMSO and related compounds can be so oppressive as to diminish the effectiveness and receptiveness of the medical staff. Such odors may be likened to the smell of rotten eggs. New procedures are emerging which require the treatment of seriously ill persons by using far larger volumes of DMSO than at present. The resulting highly oppressive odors may emanate from any part of the patient's body. The capture of these odors can be crucial to the success of the new medical procedures.
[0003] At present, Applicant believes that there is no known effective method practiced for the removal of these noxious odors. Previous odor collecting disposables containing activated carbon for other applications have been directed toward specific bodily areas and fluids, but not for removal of metabolites of DMSO. In addition, the need for compact, easily positioned air cleaning devices has not been fully addressed. Currently, the intravenous administration of DMSO has been limited by side effects associated with the noxious odors. As DMSO becomes a much more routine drug of choice for the treatment of seriously ill or injured patients, the success of these treatment methods may well rest on the availability of highly effective air cleaning devices for the protection of the medical staff and visitors. In addition, at present, the only method known to Applicant for detection of these odorous compounds is human olfaction which can be undependable.
SUMMARY OF THE INVENTION
[0004] There is a need for compositions, devices, and methods for the removal of DMSO metabolites and related compounds which will remove these chemicals and/or their noxious odors, as well as indicators to determine the presence of these compounds.
[0005] The phrases "DMSO associated compounds", "associated compounds", or "related compounds" as used herein shall be given their ordinary meaning and shall include degradation compounds, derivatives, precursors, and metabolites of DMSO, such as methylsulfonylmethane (MSM or DMSO2) and dimethyl sulfide or methylthiomethane (DMS).
[0006] Several embodiments of present invention relate to materials and methods for the removal of odors and chemicals resulting from the treatment of patients with DMSO and other compounds and chemicals. Also provided are modified polyamines, odor capturing fabrics which comprise these modified polyamines, items manufactured from these fabrics and methods of manufacture and use of the fabrics.
[0007] In one embodiment, the invention comprises an indicator for DMSO associated compounds, its method of manufacture, and an apparatus including the indicating material.
[0008] In another embodiment, the invention comprises a device to purify the air at a DMSO delivery or metabolism site. For example, a clean air device that removes DMSO metabolites and/or DMSO odors may be well-suited for hospital rooms where a patient is receiving DMSO or in a room where a patient is recovering after receiving DMSO therapy. In one embodiment, the clean air device comprises a portable, collapsible, adjustably directable clean air delivery supply assembly and enclosure for use in DMSO treated medical patient environments to provide localized clean air free of the odors, DMS5 and/or compounds resulting from the metabolism of DMSO and DMSO associated compounds, including, but not limited to, hydrogen sulfide and potentially methyl mercaptan.
[0009] In one embodiment, it may be desirable to detect the presence of DMSO and associated compounds. Accordingly, in one embodiment, the invention comprises visual color indicators to detect the presence or absence of DMSO metabolites such as DMS.
[0010] In one embodiment, the invention comprises core particles that adsorb DMSO or related compounds, or the odors associated with said compounds.
[0011] In another embodiment, the invention comprises an adsorbent for adsorbing DMSO or related compounds, or the odors associated with said compounds. The adsorbent comprises an inner layer, an intermediate layer, and an outer layer. The inner layer comprises adsorbing core particles that adsorb DMSO or related compounds, or the odors associated with said compounds. The intermediate layer, which is optional, contacts the inner layer and the outer layer. The outer layer comprises a porous coating. In some embodiments, the adsorbent may reduce undesired pathogens and odors that are unrelated to DMSO
[0012] In a further embodiment, the adsorbent comprises at least one indicator for indicating the presence of DMSO or related compounds. The indicator comprises permanganate in one embodiment. In one embodiment, the indicator is colored, and is adapted to decrease in color or intensity as DMSO or related compounds are removed. Thus, in one embodiment, color intensity can be correlated to the concentration of undesired compounds or odors. In other embodiments, different colors indicate different levels of undesired odors or compounds.
[0013] In one embodiment, the adsorbing core particles are selected from the group consisting of one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, an ion exchange resin, and a chemical deodorizer.
[0014] In one embodiment, the intermediate layer comprises a metal compound and a water-soluble organic material disposed between the core particles and the porous coating.
[0015] In one embodiment, the outer layer consists only of a porous coating. In other words, a porous coating is applied directly to the intermediate layer or to the core particles. In other embodiments, the outer layer comprises a layer of material which is additionally coated with a porous coating.
[0016] In another embodiment, the outer layer comprises a polymer selected from the group consisting of one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefin resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer or derivative thereof. The polymer may also be selected from the group consisting of one or more of the following: polytetrafluoroethylene, polyhexafiuoropropylene, polydifluoroethylene, polyvinylidene fluoride, polyvinyl fluoride, and a copolymer or derivative thereof.
[0017] In one embodiment, the porous coating has a thickness of about 0.01 μm to about 1,000 μm, an average pore diameter of about 0.01 μm to about 500 μm, and/or a porosity of about 3% to about 90%.
[0018] In a further embodiment, the invention comprises a method for removing DMSO metabolites, comprising contacting said metabolites with an adsorbent according to any one of the embodiments described herein. The DMSO metabolites may be produced by an individual receiving DMSO treatment. Alternatively, the DMSO metabolites may be degradation products caused by the exposure of DMSO to the environment (e.g., the air or a fluid).
[0019] In another embodiment, the invention comprises a method for removing odors associated with DMSO or related compounds, comprising exposing said odors to an adsorbent according to any one of the embodiments described herein.
[0020] In yet another embodiment, the invention comprises a clean air member for removal of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising adsorbent according to any one of the embodiments described herein.
[0021] In another embodiment, the invention comprises a clean air supply assembly for removal of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising adsorbent according to any one of the embodiments described herein.
[0022] In one embodiment, the invention comprises an apparatus for removing DMSO or related compounds, or the odors associated with said DMSO or related compounds from the exhaust outlet of a medical respiratory ventilator, wherein said apparatus comprises a gas scavenging device comprising the adsorbent of according to any one of the embodiments described herein. The gas scavenging device is optionally connected to said exhaust outlet.
[0023] In another embodiment, the invention comprises a face mask for reducing exposure of DMSO or related compounds, or the odors associated with said DMSO or related compounds comprising an adsorbent of according to any one of the preceding claims.
[0024] In another embodiment, the face mask filters out undesired odors that are unrelated to DMSO. The face mask may also filter airborne pathogens, including viruses and bacteria. The filtering of these other compounds may be in addition to or instead of the filtering of DMSO and associated compounds. The face mask may be a duckbill-type mask, and may comprise an exhale valve.
[0025] In one embodiment, the invention comprises a face mask comprising an outer shield layer comprising a synthetic fiber; a copper layer comprising a fiber and powdered copper; a carbon layer comprising a fiber and activated carbon; a chemical layer comprising a fiber and one or more, odor absorbing chemicals; and a facial layer comprising a synthetic fiber. The face mask may contain less than the layers described herein, or may comprise additional layers. The multi-layered face mask may protect a user from pathogens and/or DMSO compounds.
BRIEF DESCRIPTION OF THE DRAWINGS
[0026] Figure 1 shows an adsorbent according to one embodiment of the invention.
[0027] Figure 2 is a schematic diagram of a rollably positioned, adjustably directable clean air delivery supply assembly and enclosure according to one embodiment.
[0028] Figure 3 shows a front view of a "duckbill" type odor-absorbing mask according to one embodiment.
[0029] Figure 4 shows a front view of a "duckbill" type mask according to one embodiment, showing the mask partially open.
[0030] Figure 5 shows a surgical mask according to one embodiment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0031] Several embodiments of the present invention relates generally to materials for facilitating the administration of DMSO and associated compounds. In some embodiments, these materials comprises adsorbents for the removal of the odors and compounds resulting from the metabolism or degradation of DMSO and associated compounds. In other embodiments, these materials comprise clean air members and fabrics that absorb odors or compounds. In further embodiments, these materials comprise a clean air supply assembly for removing odors and compounds. In yet other embodiments, these materials comprises indicators to reveal the presence of these compounds. Adsorbents
[0032] In one embodiment, the invention comprises an adsorbent adapted for the partial or complete removal of the metabolites of DMSO and other compounds, and/or related odors.
[0033] hi one embodiment, the adsorbent material comprises three layers: an inner layer; an intermediate layer, and an outer layer. In another embodiment, the adsorbent material may comprise one, two, or three of the layers described above. In other embodiments, additional layers are provided. Layers can be fixed or otherwise coupled to one another or to other materials (using, for example, adhesives, sealants, stitches, etc).
[0034] In one embodiment, the inner layer comprises core particles containing at least one adsorbing material.
[0035] In one embodiment, the intermediate layer comprises at least one porous coating layer including a polymer material that coats the core particles. The intermediate layer may comprise a metal compound and a water-soluble organic material disposed between the core particles and a porous coating layer. The water-soluble organic material is selected from the group consisting of one or more of the following: polymers of sugar, cellulose derivatives, alginic acid, methacrylic acid, acrylic acid, vinylpyrrolidone, vinyl alcohol, oxyolefins, and organic sulfur oxides such as DMSO2 (dimethyl sulfone).
[0036] In one embodiment, the outer layer comprises a coating, such as a porous coating layer, hi one embodiment, the coating layer may be formed by spraying and applying a suspension or a solution containing a polymer material over the adsorbing material, or by immersing the adsorbing material into the suspension or the solution.
[0037] In one embodiment, an adsorbent according to any one of the embodiments described herein preferentially absorbs DMS is provided. In another embodiment, the adsorbent preferentially adsorbs MSM. In other embodiments, the adsorbent adsorbs all odor causing compounds related to DMSO.
[0038] The layers, according to some embodiments of the invention, are described below. The Inner Layer Of The Adsorbent
[0039] In one embodiment, a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an inner layer. Figure 1 shows the adsorbent material according to one embodiment of the invention. In one embodiment, the inner layer 1 comprises core particles. The core particles may or may not represent the entire adsorbent material and may comprise one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, a modified compound thereof, an ion exchange resin, a chemical deodorizer, silica gel, alumina gel, zeolite, a molecular sieve, diatomaceous earth, inorganic oxide (e.g., copper oxide, iron oxide), chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid or a derivative thereof. Combinations of two or more of these compounds are used in some embodiments.
[0040] In one embodiment, the compound having ion exchange capacity is selected from the group consisting of one or more of the following: chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid and a derivative thereof.
[0041] Mechanisms of adsorption include chemical oxidation or reduction and/or mechanical entrapment. Thus, in one embodiment, the inner layer is an adsorbent that comprises core particles, which adsorb odors or compounds by physically trapping, enclosing, or isolating said odors and compounds. In another embodiment, the inner layer is an adsorbent that comprises core particles, which adsorb odors or compounds by chemically oxidizing or reducing said odors and compounds. In yet another embodiment, undesired odors and compounds are reduced or eliminated because the core particles chemically react with said odors and compounds to render them inert or inactive.
[0042] In one embodiment, the core particles have an average particle size of about 0.01 mm to about 100 mm. In one embodiment, the inner layer has a thickness of about 0.1 μm to 1,000 μm. In certain embodiments relating to use of the core particles as an indicator, greater size may provide greater absorbency but lesser sensitivity, and lower size may give inadequate visual indication. [0043] In one embodiment, the core particles are formed by a tableting process.
[0044] In one embodiment, the inner layer comprises core particles that are coated. This coating can be the same or different than the outer layer. In one embodiment, the core particles have a porous coating layer having an average pore size of 0.001 μm to 50 μm.
[0045] In another embodiment, the core particles are fixed on or otherwise coupled to a member having a one-dimensional structure or a two-dimensional structure. In one embodiment, the core particles are fixed onto the member having the two- dimensional structure at a density of about 0.1 to about 100,000 particles per 1 cm2 of a surface of said member having the two-dimensional structure.
[0046] In one embodiment, the particles having said porous coating layer formed thereon are fixed on one surface of said member having the two-dimensional structure, and an adhesive is applied on another surface of said member having the two- dimensional structure.
[0047] In one embodiment, the particles having said porous coating layer formed thereon are fixed on a member having a three-dimensional structure. In a preferred embodiment, the core particles are fixed onto said three-dimensional structure at a density of about 1 to about 1 ,000,000 particles per 1 cm3 of a volume of said member having the three-dimensional structure.
[0048] In one embodiment, the core particles having said porous coating layer formed thereon are fixed to a member in a state of a layer having a thickness of a single particle to about 1,000 particles. In certain embodiments relating to use as a visual indicator, greater density may provide greater adsorbency but lesser sensitivity, and lower density may give inadequate visual indication at some point.
[0049] In one embodiment, the core particles having said porous coating layer formed thereon are fixed to the member with an adhesive. The adhesive may comprise an organic solvent type adhesive, a water type adhesive, a hot melt type adhesive, or combinations thereof. The member may comprise a portion covered by an air permeable sheet. The member may be entirely wrapped with an air permeable sheet. The member may be contained in an air permeable container. The air permeable container may comprise an unwoven cloth, a woven cloth, a mesh, a net, or combinations thereof. [0050] In one embodiment, the core particles having said porous coating layer formed thereon are wrapped with an air permeable sheet, m one embodiment, the core particles having said porous coating layer formed thereon are contained in the air permeable sheet in a number of about 1 to about 100,000,000. In certain embodiments, greater density may provide greater adsorbency but lesser sensitivity, and lower density may give inadequate visual indication.
[0051] In certain embodiments relating to use of the core particles as an indicator, greater size may provide greater adsorbency but lesser sensitivity, and smaller size may give inadequate visual indication at some point. The Intermediate Layer Of The Adsorbent
[0052] In one embodiment, a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an intermediate layer. Figure 1 , reference numeral 2 shows the intermediate layer according to one embodiment of the invention. The intermediate layer of the adsorbent may comprise one or more of the following: the oxide, hydroxide, carbonate, sulfates, phosphate, metasilicate, borate, oxalate, tungstate, molybdate, vanadate, chromate, selenate, and manganate of a metal or the metal itself. The metal may also include titanium, zirconium, silicon, zinc, iron, manganese, aluminum, magnesium, nickel, copper, silver, barium, calcium, scandium, bismuth, molybdenum, niobium, neodymium, antimony, selenium, stannum, strontium, terbium, tellurium, thorium, and yttrium.
[0053] In another embodiment, the metal compound has a particulate shape having an average particle size of about 0.001 μm to about 50 μm Other shapes and sizes may be used.
[0054] In one embodiment, the intermediate layer has a thickness of about 1 μm to about 10,000 μm. In one embodiment, the greater number lending toward more adsorbency but less efficiency of coating use while the lower number contributes to high efficiency of coating use but lower volumetric adsorbency. In certain embodiments, too thin a coating may result in poor indication due to lack of color, and too thick a coating may result in too much adsorption and loss of sensitivity. The Outer Layer Of The Adsorbent
[0055] In one embodiment, a material for adsorbing DMSO and associated compounds, and/or the odors related to same comprises an outer layer. Figure 1, reference numeral 3 shows the outer layer (e.g., porous material) according to one embodiment of the invention. The outer lay may comprises a porous coating layer. The outer layer may comprise one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefin resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer thereof, and a derivative thereof or polytetrafluoroethylene, polyhexafluoropropylene, polydifluoroethylene, polyvinyliden fluoride, polyvinyl fluoride, and a copolymer or derivative thereof. Combinations of two or more of these materials are used in some embodiments.
[0056] In one embodiment, the porous coating layer has a thickness of about 0.01 μm to about 1,000 μm. In one embodiment, the greater number lending toward more adsorbency but less efficiency of coating use while the lower number contributes to high efficiency of coating use but lower volumetric adsorbency.
[0057] In one embodiment, the porous coating layer has an average pore diameter of about 0.01 μm to about 500 μm and/or has a porosity of about 3% to about 90%. In one embodiment, the porous coating layer is colored.
[0058] In one embodiment, a method for producing the adsorbent, or indicating adsorbent, is provided. In a preferred embodiment, the method comprises forming the coating layer by applying a liquid containing said polymer material onto a surface of said core particles. The coating layer may be formed by spraying said liquid over said core particles and/or immersing said core particles into said liquid. In one embodiment, the liquid comprises a suspension of said polymer material and/or a solution of said polymer material.
[0059] In one embodiment, during said step of forming the coating layer or after said step of forming the coating layer, at least one of a step of heating and a step of decreasing a pressure is carried out to draw said porous coating layer.
[0060] In one embodiment, during said step of forming the coating layer or after said step of forming the coating layer, a heating process is carried out so that said coating layer partially shrinks and partially expands.
[0061] In one embodiment, the core particles in said step of forming the coating layer are in a water-containing state, in an oil-containing state, or in a frozen state thereof.
[0062] In one embodiment, the liquid comprises a pore-forming agent. The pore-forming agent may comprise a water-soluble polymer or oligomer. The water- soluble polymer or oligomer may be selected from the group consisting of one or more of the following: cellulose, poly(oxyolefm), polyvinylpyrrolidone, polyvinyl alcohol, a saponification compound of polyvinyl acetate, polyacrylic acid, polymethacrylic acid, and derivatives thereof. In another embodiment, the water-soluble polymer or oligomer is selected from the group consisting of one or more of the following: methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, polyvinylpyrrolidone, polyvinyl alcohol, polyethylene glycol, polypropylene glycol, and derivative thereof.
[0063] In one embodiment, the pore-forming agent comprises an oil soluble polymer or oligomer. The oil soluble polymer may comprise liquid paraffin.
[0064] In one embodiment, the pore-forming agent is removed during or after the step of forming said coating layer. In another embodiment, the pore-forming agent is removed by one or more of the following processes: extraction, evaporation, sublimation or combustion.
[0065] In an alternative embodiment, the invention comprises a packed bed containing the adsorbent of one embodiment of the present invention. The packed bed, in some embodiments, functions as a holder for the adsorbent material. The packed bed of adsorbent may be incorporated into a cartridge for containment of the adsorbent material. The cartridge may be in the form of a rectangular, cylindrical or otherwise shaped vessel. The cartridge may be provided in conjunction with a device for introducing air into said rectangular, cylindrical or otherwise shaped vessel, wherein the adsorbent is partially or completely contacted when the air is introduced therein. One of skill in the art will understand that other shapes may also be used according to alternative embodiments of the invention. Clean Air Member
[0066] In one embodiment of the invention, a device and method for cleaning air comprising contacting air with an indoor ambient air cleaning member (such as a cartridge or filter). In one embodiment, the clean air member comprises the adsorbent material described above. In one embodiment, the clean air member adsorbs DMSO and/or DMSO related compounds, and/or odors associated with same. In some embodiments, the clean air member additionally removes one or more undesired compounds from the air that are unrelated to DMSO (e.g., toxic fumes or gases). [0067] In one embodiment, the clean air member (such as a cartridge or filter) comprises an inner layer, an intermediate layer, and an outer layer, as described above.
[0068] The clean air member may be contained in a rectangular, cylindrical or otherwise shaped vessel, and said indoor ambient air cleaning member is freely convected when the air is introduced therein. The vessel may be tilted.
[0069] In several embodiments of the invention, the clean air member according to any one of the embodiments described herein is an ambiance odor or sulfur chemical regulating member.
[0070] In one embodiment, the clean air member (such as a cartridge or filter) comprises core particles comprising at least one odor or sulfur chemical regulating material of an acid or acid salt, and a porous coating layer including a polymer material that coats the core particles. In one embodiment, the acid is selected from the group consisting of one or more of the following: lactic acid, malic acid, tartaric acid, oxalic acid, chromic acid, dichromic acid, manganic acid, permanganic acid, thiocyanic acid, cyanic acid, carbonic acid, hydrochloric acid, perchloric acid, chloric acid, chlorous acid, hypochlorous acid, hydriodic acid, periodic acid, iodic acid, iodous acid, hypoiodous acid, sulfuric acid, sulfurous acid, nitric acid, nitrous acid, and phosphoric acid.
[0071] In one embodiment, the clean air member comprises an odor or sulfur chemical regulating material selected from the group consisting of one or more of the following: sodium sulfate, an alkali metal salt of phosphoric acid, an alkali metal salt of hydrogenphosphate, an ammonium salt of phosphoric acid, and an ammonium salt of hydrogen phosphate.
[0072] In one embodiment, the clean air member comprises core particles that comprises a hydrophilic polymer compound. The hydrophilic polymer compound may be selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
[0073] In one embodiment, the clean air member comprises core particles that have an average particle size of about 0.01 mm to about 100 mm.
[0074] In one embodiment, the clean air member comprises core particles comprising at least one odor or sulfur chemical regulating material of an acid salt, and a porous coating layer comprising a polymer material that coats said core particles is provided. The acid salt may be selected from the group consisting of one or more of the following: an alkali metal salt, an alkaline earth metal salt, and an ammonium salt.
[0075] In one embodiment, the core particles further comprises a hydrophilic polymer compound. The hydrophilic polymer compound may be selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
[0076] In one embodiment, the clean air member comprises a porous coating layer having a thickness of about 0.1 μm to about 1,000 μm and/or average pore size of about 0.001 μm to about 50 μm. The porous coating layer of the clean air member may comprise a silver deposit layer.
[0077] In one embodiment, the clean air member comprises a porous coating layer that comprises material selected from the group consisting of one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefm resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin, copolymers thereof, and derivative thereof. The porous coating layer may be colored.
[0078] In a further embodiment, an adsorbent for removal of respiratory exhalation from a patient treated with DMSO is provided. In yet another embodiment, an adsorbent for removal of DMSO metabolites from a respiratory ventilator or an isolation room ventilator is provided. The adsorbent may be part of the clean air member.
[0079] In one embodiment, the clean air member comprises an oxidizing agent. The oxidizing agent is selected from the group consisting of one or more of the following: a mixture of ascorbic acid and an iron-containing compound, permanganates, manganese dioxide, chromates, dichromates, osmium tetraoxide, ruthenium tetraoxide, silver oxide and palladium chloride. In one embodiment, the iron-containing compound is selected from the group consisting of one or more of the following: iron chloride, iron bromide, iron iodide, iron oxide, iron perchlorate, iron thiocyanate, iron sulfate, iron sulfide, iron acetate, iron oxalate, Mohr's salt, di-iron monophosphide and tri-iron monophosphide. Fabrics
[0080] In several embodiments of the present invention, a fabric that reduces or eliminates the odor of DMSO and associated compounds is provided. In one embodiment, the fabric comprises odor adsorbing woven or non-woven fabric suitable for the manufacture of clothing, bedding and other protective items capable of the partial or complete capture of the metabolites of DMSO and others. Adsorption may include chemical oxidation, reduction, physical entrapment in fissures, or other means. The adsorbent fabric may include adsorbent fibers or fibers coated with an adsorbent or it may be layered with adsorbent material between the layers. Finally, the fabric may incorporate any or all of these modes of odor capture simultaneously.
[0081] In one embodiment, the fabric comprises a three dimensional web. In one embodiment, the basic fiber support structure of the three dimensional web comprises woven or non-woven web of the fibers of polyethylene, polypropylene, polyvinyl chloride, polyurethane, polyamide, nylon, polyacrilan, rayon, silk, ramey, cellulosic material and any other suitable fibrous material or material which may be made fibrous. Intermediate layers may comprise knit or randomly formed copper, aluminum, iron, glass, carbon, or other inorganic fibers. Each layer may be formed on a knitting, weaving, moving web, fluid dispersion, or other device. Layers may be combined following the forming of each or one or more layers may be formed as they are layered. Layers may be adhered together by crosslinking, hot melt stitching, sewing, gluing, or other methods well known in the art.
[0082] In one embodiment, the odor adsorbing fibers of the fabric may comprise a modified polyamine which comprises a hybrid inorganic/organic material comprising a polyamine and an inorganic oxide. The polyamine may comprise one or more of the following: amine-containing polysaccharides, amine-containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylamine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups, poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine, amine-containing polysaccharides, amine-containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylamine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups, poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine, amine-containing polysaccharides, amine-containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), ρoly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylamine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups., poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine, amine-containing polysaccharides, amine-containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylamine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine or a nanostructured polyamine which comprises a polyamine reacted with one or more crosslinkers. MSM (methyl sulfonyl methane) adsorbents may also be included as coatings, admixtures of the above or alone. In one embodiment, MSM is both a metabolite of DMSO and used as an adsorbent, hi this embodiment, the MSM used as the adsorbent is substantially odorless and can adsorb odorous DMS (which can be obtained from DMSO through reduction, potentially in an anaerobic metabolic environment), and other odorous compounds that result from DMSO metabolism. In embodiments where the two main metabolites of DMSO are DMS and MSM, exogenous MSM can be used as an adsorbent alone or in combination with other adsorbents. MSM may also be used to adsorb sulfur contain compounds that are related or unrelated to DMSO.
[0083] In one embodiment, the odor adsorbing coatings of the fibers, the cross linking members or the intermediate layers of a multilayer fabric may comprise one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, a modified compound thereof, an ion exchange resin, a chemical deodorizer, silica gel, alumina gel, zeolite, a molecular sieve, diatomaceous earth, copper oxide, iron oxide, chitosan, dextran sulfate, polyallylamine, sulfonated polystyrene resins, polyacrylic acid, polymethacrylic acid or a derivative thereof. Further, these odor adsorbing coatings may comprise a fiuororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefm resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer thereof, and a derivative thereof or polytetrafluoroethylene, polyhexafluoropropylene, polydifluoroethylene, polyvinyliden fluoride, polyvinyl fluoride, and a copolymer thereof. They may also consist partially or fully of the oxide, hydroxide, carbonate, sulfates, phosphate, metasilicate, borate, oxalate, tungstate, molybdate, vanadate, cliromate, selenate, and manganate of a metal or the metal itself selected from the group consisting of: titanium, zirconium, silicon, zinc, iron, manganese, aluminum, magnesium, nickel, copper, silver, barium, calcium, scandium, bismuth, molybdenum, niobium, neodymium, antimony, selenium, stannum, strontium, terbium, tellurium, thorium, yttrium, and combinations thereof. MSM adsorbents may also be included as coatings, admixtures of the above or alone.
[0084] In one embodiment, the invention comprises a modified polyamine comprising: a hybrid inorganic/organic material comprising a polyamine and an inorganic material having one or more characteristics selected from the group consisting of: amorphous structures, high surface areas, large pore volumes, and nanocrystalline structures. In one embodiment, the inorganic material is an inorganic oxide material.
[0085] In one embodiment, the invention comprises a modified polyamine comprising a polyamine impregnated into or attached to a porous inorganic or organic microbead. In one embodiment, the polyamine is coupled to one or more microbeads.
[0086] In one embodiment, the invention comprises a modified polyamine which comprises a polyamine having inorganic molecules or organic molecules, or both, chemically attached to it.
[0087] In one embodiment, the invention comprises a modified polyamine which comprises a bio-compatible copolymer of a polyamine and a dermatologically compatible aqueous-soluble and/or oil-soluble polymer.
[0088] In one embodiment, the invention comprises a nanostructured polyamine which comprises a polyamine reacted with one or more crosslinkers.
[0089] In one embodiment, the polyamine is selected from the group consisting of one or more of the following: amine-containing polysaccharides, amine- containing polypeptides, polyethylenimine, polyethylenimine derivatives, poly(vinylamine), poly(diallylamine), poly(allylamine), copolymers of diallylamine and allylamine, copolymers containing diallylarαine or allylamine, copolymers containing diallylamine and allylamine, and condensation polymers formed from polyamine monomers and monomers with two or more amine-reactive groups.
[0090] In another embodiment, the polyamine is selected from the group consisting of one or more of the following: poly(lysine), polyethylenimine, polyethylenimine derivatives, poly(vinylamine), polymers containing diallylamine, and polymers containing allylamine.
[0091] In one embodiment, the invention comprises an article comprising: a liquid pervious topsheet; a backsheet; and an absorbent core intermediate between said backsheet and said topsheet. In one embodiment, the absorbent core comprises from about 0.5 g/m2 to about 500 g/m2 of a cationic polysaccharide comprising an aminopolysaccharide selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof; and from about 0.1 g/m2 to about 250 g/m2 of an acidic pH buffering means having a pH in the range of from about 3.5 to about 6.5 and comprises a weak acid having its pKa or at least one of its pKas in the range from about 3.5 to about 6.5 and its conjugate base; and from about 5 g/m2 to about 250 g/m2 of absorbent gelling material.
[0092] In one embodiment, the cationic polysaccharide is selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof having a degree of deacetylation of more than about 75%.
[0093] In one embodiment, the chitosan salt is selected from the group consisting of one or more of the following: citric acid, formic acid, acetic acid, N- acetylglycine, acetylsalicylic acid, tlimaric acid, glycolic acid, iminodiacetic acid, itaconic acid, lactic acid, maleic acid, inalic acid, nicotinic acid, salicylic acid, succinamic acid, succinic acid, ascorbic acid, aspartic acid, glutamic acid, glutaric acid, malonic acid, pyruvic acid, sulfonyldiacetic acid, benzoic acid, epoxysuccinic acid, adipic acid, thiodiacetic acid, thioglycolic acid, alanine, valine, leucine, isoleucine, prolinephenylalanine, tryptophan, methionine, glycine, serine, cysteine, tyrosine, asparagine, glutamine, lysine, arginine, hydroxyproline, pyrrolidone carboxylic acid, chitosonium pyrrolidone carboxylate and mixtures thereof.
[0094] In one embodiment, the pH buffering means is selected from the group consisting of one or more of the following: citric acid/sodium hydroxide, citric acid/sodium citrate, citric acid/potassium citrate, oxalic acid/sodium oxalate, tartaric acid/potassium hydrogen tartarate, oxalic acid/potassium tetra oxalate dihydrate, phthalic acid/potassium phthalate, phthalic acid/sodium phthalate acetic acid/sodium acetate, benzoic acid/sodium benzoate, glutaric acid/sodium glutarate, adipic acid/sodium adipate, carbonic acid/sodium carbonate and mixture thereof and most preferably is citric acid/sodium citrate, citric acid/sodium hydroxide and/or citric acid/potassium citrate.
[0095] In one embodiment, the invention comprises an additional odor control agent selected from the group consisting of one or more of the following: zeolites, silicates, activated carbons, diatomaceous earth, cyclodextrine, clay, chelating agents, ion exchange resins, perfumes and mixture thereof. In one embodiment, the level of the additional odor control agent or a mixture thereof is from about 0.5 g/m2 to about 600 g/m2.
[0096] hi one embodiment, the invention comprises a method of controlling odor associated with DMSO and related odorous metabolites wherein said bodily fluids are contacted with an odor control system comprising a cationic polysaccharide, selected from the group consisting of one or more of the following: chitosan, chitosan salt, crosslinked chitosan and a mixture thereof, and an acid pH buffering means typically having a pH in the range of about 3.5 to 6.5.
[0097] In one embodiment, the invention comprises an odor eliminating fiber structure having an indicator comprising a fiber substrate containing odor eliminating fibers, a surface thereof being visibly determined for change of odor eliminating power with a difference between a color of the fiber substrate discoloring through adsorption of a smelling gas and a color of a standard color display part.
[0098] In one embodiment, the color of the standard color display part provided on the surface of the fiber substrate becomes difficult to be distinguished by discoloration of the fiber substrate through adsorption of a smelling gas.
[0099] In one embodiment, the color difference between the color of the fiber substrate upon losing the odor eliminating power and the color of the standard color display part provided on the surface of the fiber substrate is 4 or more grades upon evaluation with gray scale for assessing change in color.
[0100] In one embodiment, the odor eliminating fibers contain at least one odor eliminating component selected from silver, copper and a metallic compound thereof, and a content of silver and/or copper is 0.1% by weight or more of the total fiber substrate. [0101] In one embodiment, the odor eliminating fibers comprises an odor eliminating component-containing crosslinked acrylate fibers containing at least one odor eliminating component selected from silver, copper and a metallic compound thereof, and content of a silver and/or copper is 0.1% by weight or more of the total acrylate fibers.
[0102] In one embodiment, one surface of the fiber substrate has an easy- sticking and easy-releasing function.
[0103] The odor-absorbing fabric may be used in the manufacture of a disposable absorbent article selected from the group consisting of one or more of the following: a patient bedcover, patient gown, caregiver scrubs, gowns, masks, or any other required item to be worn or used to protect the patient or staff or visitors.
[0104] The patient bedding may comprise one or more of the following: suitably large sheets of odor absorbing material which may be coated partially or fully with slightly adhering material to prevent slippage. They may be assembled using methods well known in the art of clothing manufacture, including thermal, ultrasonic or electronic sealing, hot melt, adhesives, sewing, multineedle sewing, serging, basting, binding, or other joining methods. Seams may be folded, lapped, flat felled, straight stitched, trenched, overcast, enclosed, bound, hemmed, reinforced, top stitched, or other suitable seaming method. This bedding can be used at all times while the patient is undergoing treatment using DMSO and related compounds.
[0105] The clothing and mask items for the patient and for the caregivers may be shaped and formed to provide the maximum freedom of movement and access. These items may be constructed of cut sheets of odor absorbing material and may include ties, belts, snaps, or other fasteners to maintain the position of the article. These items may be assembled using thermal, ultrasonic or electronic sealing, hot melt, adhesives, sewing, multineedle sewing, serging, basting, binding, or other joining methods. Seams may be folded, lapped, flat felled, straight stitched, trenched, overcast, enclosed, bound, hemmed, reinforced, top stitched, or other suitable seaming method. These items can be used at all times while the patient is undergoing treatment using DMSO and related compounds. The clothing and mask items described herein may comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
[0106] In one embodiment, the invention comprises a method of providing disposable, strong, absorbent DMSO and related odorous metabolite capturing health care bedding which comprises providing DMSO and related odorous metabolite capturing fabric plus a non- woven fabric comprised of randomly entangled mixtures of natural and synthetic fibers interconnected so that the individual fibers are held in place to form a coherent, stable, strong fabric having a high absorbency capacity; cutting the fabric to the desired length in the cross direction; and converting said fabric to a desired size and shape. Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
[0107] In one embodiment, the natural fiber is cellulosic wood pulp. In one embodiment, the synthetic fiber is selected from the group consisting of one or more of the following: a polyester, a nylon, a rayon, a polypropylene and mixtures thereof. In one embodiment, the synthetic fiber is polyester.
[0108] In one embodiment, the invention comprises a method of providing disposable strong, absorbent DMSO and related odorous metabolite capturing health care bedding which comprises employing as the bedding material DMSO and related odorous metabolite capturing fabric principally composed of polyester fibers combined with cellulosic wood pulp fibers, said fibers locked into place by a three-dimensional fiber entanglement wherein the individual fibers are intertwined, tangled and interconnected to each other so as to be virtually inseparable, said fabric having an absorptive capacity of at least that of woven fabric made of natural fibers, cutting the fabric to a desired length in the cross direction, and converting said cut fabric to a desired size and shape. Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein. '
[0109] In one embodiment, the fabric has a weight of about 0.5 to about 10 ounces per square yard.
[0110] In one embodiment, after cutting said bedding material in the cross (CD) direction, a strip of elastic is attached along the edges to provide a close fit to a platform it is to cover. The platform may be a six-sided gurney.
[0111] In one embodiment, the invention comprises a method of providing disposable, strong, moisture absorbent DMSO and related odorous metabolite capturing health care bed and gurney coverings comprising: employing as the bedding material DMSO and related odorous metabolite capturing fabric principally composed of polyester fibers combined with cellulosic wood pulp fibers, said fibers interlocked by a three- dimensional fiber entanglement, wherein the individual fibers are intertwined, tangled and interconnected to each other so as to be virtually inseparable, and wherein said fabric has an absorptive capacity higher than that of conventional bedding made from cotton- polyester blends. In another embodiment, the method further comprises cutting across the fabric and converting said bedding material to a desired shape suitable for a gurney covering, so that its strongest direction is along the cut direction of the covering. Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
[0112] A breathable DMSO and related odorous metabolite capturing composite having hydrostatic head according to 1ST 80.4-92 of at least about 4 inches comprising a laminate of at least one fibrous, nonwoven web layer and at least one thermoplastic film layer, the laminate being stretched no more than about 5% in a lengthwise and widthwise direction, and wherein the film layer comprises at least one thermoplastic resin, a finely divided particulate material capable of promoting breathability, and a plurality of point-like deformations which provide breathability of the composite, wherein the breathable composite has a breathability of at least about 500 g/m2/day. Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
[0113] In one embodiment, the composite has a MVTR of at least about 500 g/m2/day, wherein the laminate can be stretched to less than about 5% lengthwise or widthwise stretching.
[0114] In one embodiment, the fibrous nonwoven web layer comprises filaments comprising at least one polyolefin resin.
[0115] In one embodiment, the thermoplastic film layer comprises at least one polyolefin resin.
[0116] In one embodiment, the thermoplastic film layer comprises at least one polyolefin resin and the nonwoven web layer comprises filaments comprising at least one polyolefin resin.
[0117] In one embodiment, the nonwoven web layer has substantial segments of filaments unadhered to the film layer whereby a cloth texture suitable for diaper and apparel uses is provided on at least one surface of the composite.
[0118] In one embodiment, the composite has a hydrostatic head of at least about 7 inches. [0119] In one embodiment, the polyolefin resin of the thermoplastic film layer comprises at least one polyethylene resin. In one embodiment, the polyolefin resin of the thermoplastic, breathable film layer comprises at least one polypropylene resin.
[0120] In one embodiment, the polyolefin resin of the filaments comprises at least one polyethylene or polypropylene resin. In one embodiment, the polyolefin resin of the filaments comprises at least one polyethylene resin.
[0121] In one embodiment, the invention comprises a breathable composite DMSO and related odorous metabolite capturing material comprising a laminate comprising at least one film layer and at least one nonwoven web layer, the laminate being no more than insignificantly stretched in a lengthwise and widthwise direction, and wherein the nonwoven web layer comprises filaments of at least one polyolefin resin, and the film layer comprises a polyolefin resin, a finely divided particulate material capable of promoting breathability, and a plurality of embossed, point-like deformations, such deformations providing breathability of the composite by occupying about 8 to about 40% of the area of a surface of the composite and being present on such surface at a density of about 100 to 500 points per square inch. Such material may also comprise any or all of the DMSO and related odorous metabolite capturing capabilities and features of embodiments described herein.
[0122] In one embodiment, the polyolefin resin of the film layer comprises at least one polyethylene resin.
[0123] In one embodiment, the nonwoven web layer comprises a web of substantially continuous filaments.
[0124] In one embodiment, the filaments comprise at least one polypropylene resin. In one embodiment, the filaments of the web of substantially continuous filaments provide a cloth texture to said nonwoven web layer on at least one surface of the composite. In one embodiment, the filaments comprise at least one polyethylene resin. In one embodiment, the filaments of the web of substantially continuous filaments provide a cloth texture to said nonwoven web layer on at least one surface of the composite.
[0125] In one embodiment, the nonwoven web layer comprises a web of staple fibers.
[0126] In one embodiment, the staple fibers comprise at least one polypropylene resin. In one embodiment, the staple fibers of the web of staple fibers provide a cloth texture to said nonwoven web layer on at least one surface of the composite. In one embodiment, the staple fibers comprise at least one polyethylene resin, hi one embodiment, the staple fibers of the web of staple fibers provide a cloth texture to said nonwoven web layer on at least one surface of the composite.
[0127] In one embodiment, the polyolefin resin of the film layer comprises at least one polypropylene resin.
[0128] In one embodiment, the nonwoven web layer comprises a web of substantially continuous filaments comprising at least one polypropylene resin. In one embodiment, the nonwoven web layer comprises staple fibers comprising at least one polypropylene resin. In one embodiment, the nonwoven web layer comprises a web of substantially continuous filaments comprising at least one polyethylene resin. In one embodiment, the nonwoven web layer comprises staple fibers comprising at least one polyethylene resin.
[0129] In another embodiment, the adsorbent materials/fibers described herein are incorporated into one or more portions of a disposable gown for DMSO treated medical patients, such as the gown described in U.S. Patent No. 4,819,275, the entire contents of which are incorporated herein by reference. This patent describes a disposable, double-breasted gown for medical patients formed, without sewing, of non- woven synthetic plastic fabric sheeting which is soft and ultrasonically sealable, said gown comprising: a body formed from a rectangular blank having a straight upper long edge that is die cut to form chamfered corners on either side, an off-center arcuate neck indentation and isosceles triangular arm hole indentations on the left and right sides of the arcuate indentation, the resultant straight edge shoulder segments formed between the corners and the indentations all having the same length and a common line, the peaks of the triangular indentations being aligned with parallel left and right transverse fold lines that define between the lines a rear gown section on one side of which is a relatively narrow left-front section and on the other side of which is a broad right-front section, the left-front section being folded over the rear section and the right-front section being folded over the folded left-front section to overlap this section, the straight edge segments of the left and right front sections being ultrasonically seamed to the corresponding segments of the rear section to define left and right arm holes; and a pair of sleeves whose inlets are ultrasonically seamed to the arm holes of the body, each sleeve being formed of a relatively small rectangular blank having at its upper edge an isosceles triangular indentation whose peak is aligned with a center transverse fold line, and having a straight lower edge, such that when this blank is folded in half, and the folded over lower straight edge is ultrasonically seamed, this creates a tubular sleeve having an inlet which is ultrasonically seamed to the arm holes of the body of the gown.
[0130] In one embodiment, the adsorbent materials/fibers described herein are incorporated into one or more portions of a surgical gown or scrubs for caregivers of DMSO treated patients, such as the type described in U.S. Patent No. 4,171,542, the entire contents of which are incorporated herein by reference.
[0131] The gown described in US 4,171,542 has sleeves, a front portion having a chest area covering the chest of the user and side portions which close and overlap at the back of the user, a bib affixed about its periphery to the inside surface of the surgical gown at the chest area with a portion of the bib inwardly of the periphery remaining unsecured to the gown, the chest area having a pair of spaced, substantially vertical slits formed therein within the confines of the peripheral portions of the bib, the slits communicating with the unsecured portion of the bib and being of a length to allow passage of the user's hands therethrough whereby the bib provides a sterile hand support pocket maintaining the user's hands in the aseptic zone bounded by the user's neck, shoulders and waist line.
[0132] In another embodiment, the adsorbent materials/fibers described herein are incorporated into one or more portions of a disposable face mask for caregivers of DMSO treated patients. Exemplary masks include those described in U.S. Patent Nos. 6,055,982; 5,765,556 and 5,322,061, herein incorporated by reference. In general, the masks described in these patents comprise a filter body having an opening sized to cover the nose and mouth of a wearer, the body having top and bottom edges with the top edge arranged to extend across the nose of the wearer and the bottom edge arranged to extend under the chin of the wearer; the top edge having ends opposite from each other and the bottom edge having ends opposite from each other; first securing means attached to the filter body adjacent to each end of the top edge and arranged to extend generally about the back of the head of the wearer in an approximate linear continuation from the top edge, the first securing means for urging the top edge into tight engagement with the wearer to prevent fluid flow between the top edge and the wearer; second securing means attached to the filter body adjacent to each end of the bottom edge and arranged to extend generally over the top of the head of the wearer in an approximate linear continuation from the bottom edge, the second securing means for urging the bottom edge into tight engagement with the wearer to prevent fluid flow between the bottom edge and the wearer; the filter body comprising an upper portion of generally trapezoidal configuration having a longer side forming the top edge and a lower portion of generally trapezoidal configuration having a longer side forming the bottom edge; the upper and lower portions being joined along all remaining sides; a plurality of radii formed on opposite sides of the filter body extending from the opening; a first strip of sealing material disposed within the filter body adjacent to the opening and extending along the top edge; a second strip of sealing material disposed within the filter body adjacent to the opening and extending along the bottom edge; and the first sealing strip and the second sealing strip cooperating with each other to form a fluid barrier between the opening of the filter body and the face of the wearer.
[0133] In one embodiment, color changes indicate adsorption. Color changes upon adsorbing odors may be tested as follows based on several methods, including but not limited to that described in US Patent Publication No. 20030190266, herein incorporated by reference:
Color of fiber substrate Visibility of display part Color difference on
Odor eliminating power [0Zo) Odor eliminating power (%) saturated adsorption
100 0 100 75 50 30 0 (grade)
Example 1 Hg ;ht beige light umber 1 1 2 3 4 —
Comparative — white no odor eliminating power —
Example 1
Example 2 lip ;ht beige light umber 4 3 3 2 1 4-5
Example 3 light dark green brown 4 3 2 2 1 4-5
Example 4 Beige umber 4 2 2-1 1 4-5
Example 5 very light beige beige 3 3 2 2 1 4-5
Mask
[0134] In one embodiment, the invention comprises a mask that is designed to reduce, eliminate or shield the user from odors associated with DIvISO and related compounds. Embodiments described above that relate to the fabric may be used to construct some embodiments of the mask.
[0135] In one embodiment, the mask comprises one or more layers. The face mask may be a "duckbill" type mask (Figs. 3-4), or surgical mask (Fig. 5). In one embodiment, an exhale valve comprising two flat strips of elastomer is installed in place of the entire seam at the bottom of the duckbill mask which has a large cross-sectional area when open. The surgical masks may also comprise one or more odor-masking "scratch and sniff patches which release one or more pleasant odors when abraded. Such odors include lemon, perfume, peppermint, vanilla and the like. These patches may be square, circular rectangular or any other desired shape.
[0136] In one embodiment, the layers include from outer (distal to the face) to inner (proximal to the face): 1) outer shield; 2) copper layer; 3) carbon layer; 4) chemical layer; and 5) facial layer. In another embodiment, the mask comprises one or more of these layers. The layers need not be present in the order identified above.
[0137] The outer shield may provide N95 or N99 filtration. In one embodiment, the mask filters at least about 75%, 80%, 85%, 90%, 95%, 97%, 99%, 99.9%, or 100% of airborne particles. The outer shield layer may comprise 100% synthetic fiber. Examples of synthetic fibers include those described herein, and other synthetic fibers well known in the art (e.g., polyester, rayon, acrylic, nylon, dacron).
[0138] The copper layer may act as a catalytic converter. The copper layer may comprise one or more fibers and powdered copper. In one embodiment, the fiber comprises about 40% wood pulp and about 60% synthetic fiber. The powdered copper may be present on the fiber in an amount ranging from about 100% w/w to about 500% w/w, preferably from about 200% w/w to about 400% w/w, and more preferably about 250% w/w.
[0139] The carbon layer may comprise activated charcoal and acts as an odor adsorber. In one embodiment, the carbon layer comprises two sub-layers: activate charcoal adsorber I and activated charcoal adsorber II. The carbon layer may comprise one or more fibers and activated carbon. In one embodiment, the fiber comprises about 40% wood pulp and about 60% synthetic fiber. The activated carbon may be present on the fiber in an amount ranging from about 100% w/w to about 500% w/w, preferably from about 200% w/w to about 400% w/w, and more preferably about 250% w/w. One or more types of activated carbon may be incorporated into the carbon layer. In one embodiment, the following Chemsorb activated carbon compositions are used: 1202-70 G12 (for. acid gases), 620-70 G12 (for ammonia and amines), 1505-70 G12 (for aldehydes) and 1000-70 (for organic vapors).
[0140] The chemical layer may allow breath-activated odor removal. The chemical layer comprises one or more fibers and one or more odor-removing chemicals, which may be breath-activated, such as citric acid, chitosan, MSM and other compounds. In one embodiment, the chitosan, citric acid and MSM may be present on the fiber in " amounts of about 50% w/w, about 40% w/w and about 30% w/w, with the remainder being one or more other compounds.
[0141] The facial layer may provide soft facial protection. The facial layer may comprise 100% synthetic fiber. In one embodiment, natural fibers are used, alone or in combination with synthetic fibers.
[0142] In one embodiment, the mask is made by placing the coatings on separate layers prior to forming the masks on the same multi-sheet airlay machine. Clean Air Supply Assembly
[0143] hi one embodiment, the present invention comprises a system for removing odors and chemicals resulting from the treatment of patients with DMSO and related compounds. In one embodiment, this system is a clean air supply assembly.
[0144] In one embodiment, the invention comprises a rollably positioned, adjustably directable clean air supply assembly and enclosure for use in DMSO treated medical patient environments. The clean air supply assembly provides, in some embodiments, localized clean air free of the odors, DMS (dimethyl sulfide) and compounds resulting from the metabolism of DMSO and DMSO associated compounds including, but not limited to, hydrogen sulfide and methyl mercaptan.
[0145] In one embodiment, the clean air supply assembly comprises a fully portable device providing for the effective capture and movement of room air through an adsorbent material suitable for the complete removal of the metabolites of DMSO and other related compounds. This device may have battery power for backup or for use while moving a patient. In one embodiment, the device is capable of turning any hospital room into a virtual clean room.
[0146] In another embodiment of the present invention, a portable curtaining containment system which may encompass the patient's upper torso or the entire patient bed area with provisions for caregiver access is provided.
[0147] In one embodiment, the invention comprises a rollably positioned, passable through doorways, adjustably directable clean air supply assembly which provides air free of the metabolites of DMSO and others for use in an area where a patient is being treated using DMSO and associated compounds. The clean air supply assembly may comprise one or more of a base module, a powered air moving assembly and a filtration system.
[0148] The clean air supply assembly 4 is shown schematically in Figure 2 and comprises a rollable support assembly 19 having wheels 21. Attached to the platform are a power supply unit 5 powering an electronics package 7 providing either DC or AC power depending on the motor selected. In one embodiment, the power supply unit 5 comprises a battery with a charger. An internal or external chemical and/or odor filter and adsorbent cartridge 9 containing an adsorbent is mounted on platform 19 adjacent power supply unit 5 and electronics package 7.
[0149] In one embodiment, the adsorbent cartridge 9 follows the air moving assembly and is capable of removing metabolites of DMSO and other related compounds, and may incorporate visual indication of depletion of such metabolites. The adsorbent may be augmented or replaced by ultraviolet lamps and/or ozone (e.g., ozone injection) to further or fully remove odors, DMS, methyl mercaptan and/or hydrogen sulfide and other chemicals.
[0150] In one embodiment, clean air supply assembly 4 directs a controlled amount of clean grade air through an adjustably oriented top hood assembly 11 which contains a pre-filter 13 and a sealed final filter 15 (e.g., high efficiency particle arrestor (HEPA) filter) which may be mounted within the lower portion of the base 14 or within the top final filter hood assembly 11. This final filter 15 filters the air and allows the discharge of the air at minimal-eddy creating air velocities for improved air quality levels, which creates certifiable cleanrooms, clean zones, improved recirculated air quality within an given area, where a patient is being treated with DMSO. The clean air supply assembly 4 is shown optionally attached to a patient isolation unit 17.
[0151] In one embodiment, the clean air supply assembly is a modification of the clean air supply assembly shown in Figure 2 of US Patent No. 6,099,607, the entire contents of which are incorporated herein by reference. In this device, the rollable support assembly in US 6,099,607 is extended in a direction opposite the hood top assembly 328, and the battery/power module/adsorbent cartridge assembly shown in Figure 2 of the present application is placed on, or attached to, the rollable support assembly. This device may be attached to a wheelchair or gurney via a wheelchair/gurney attachment, and filters odors and chemicals resulting from DMSO treatment of a patient. [0152] The clean air supply assembly according to one embodiment of the present invention may also be attached to a patient isolation unit comprising a frame body foldable and/or capable of being disassembled; and a flexible envelope adapted to be detachably attached to the frame body as assembled as described in US Patent No. 6,099,607. The patient isolation unit may also comprise a collapsible framework constructed of rods pi vo tally joined at their ends to hubs to form a self-standing unit when expanded and to fold into a small set of nearly parallel rods when folded as described in US Patent Nos. 4,986,016 and 5,125,205, the entire contents of which are incorporated herein by reference.
[0153] In another embodiment, the exhauster device 5 shown in Figure 1 of US Patent No. 6,966,937, herein incorporated by reference, is modified by extending the reliable support assembly in a direction opposite exhaust duct 4 and the battery/power module/adsorbent cartridge assembly shown in Figure 2 of the present application is placed on, or attached to, the reliable support assembly ^ The device may then be attached to a patient isolation unit to filter odors and chemicals resulting from DMSO treatment of a patient.
[0154] The patient isolation unit may include an integral patient isolation curtain rod, or a separate foldable frame body, and a flexible envelope made of a natural or polymeric porous or nonporous film, knit, woven or non-woven sheet which can be attached to the assembled frame body, which may or may not include a bottom.
[0155] In one embodiment, the patient isolation assembly includes a low cost disposable curtain to be affixed to the patient privacy curtain, or to an inexpensive plastic frame. Indicator
[0156] The present invention also provides a visual color indicator, particularly a metal permanganate visual color indicator material suitable for the detection of DMS and other metabolites of DMSO. In one embodiment, sulfides such as DMS are oxidized by potassium permanganate to produce sulfone with the resulting reduction of the permanganate ion eliminating its characteristically intense purple color. The indicator may be included in any one of the layers of the adsorbant described herein, or in an additional layer on a base layer having one, two, or three parts. In one embodiment, an indicator for DMS and the metabolites of DMSO and other related compounds includes core particles containing an adsorbing material as described herein in which the intermediate layer comprises one or more indicators and a metal or other compound, and is disposed between the core particles and the porous coating layer. The structure and components of the core particles are described in detail above. Visual indicators other than color may also be used. One or more indicators may be included within a layer, on the inner surface of a layer, on an outer surface of a layer, or integral with one of the layers. <
[0157] In another embodiment, the present invention comprises a system which includes a transparent container with a packed bed containing the detecting indicator of the present invention. In one embodiment, the packed bed functions as a holder for the indicator material and may be separate from, or included in, an indicating adsorbent bed utilized for the removal of DMS and other DMSO metabolites. In one embodiment, as the indicator is exposed to DMS, methyl mercaptan and related materials, it becomes progressively lighter and the lightening progresses through the bed.
[0158] In a further embodiment, the present invention includes a personal monitor comprising one or more detecting indicators to sample airborne contaminants by the process of diffusion. Exposure levels may then be compared to permissible exposure limits published in health and safety standards. In one embodiment, the lighter the personal monitoring patch, the greater exposure is indicated.
[0159] In yet another embodiment, the present invention includes a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator. In one embodiment, the longer the lightened area, the more DMS, methyl mercaptan or other sulfide detected.
[0160] In one embodiment, the invention comprises a functional ambiance odor or sulfur chemical or DMS indicating and/or regulating member comprising the ambiance odor or sulfur chemical regulating member .
[0161] In one embodiment, the invention comprises an ambiance odor or sulfur chemical or DMS indicating and/or regulating member, comprising core particles containing at least one odor or sulfur chemical regulating material of an acid salt, and a porous coating layer including a polymer material that coats said core particles, wherein the acid salt is at least one of an alkali metal salt, an alkaline earth metal salt, and an ammonium salt.
[0162] In one embodiment, the odor or sulfur chemical regulating material is selected from the group consisting of one or more of the following: sodium sulfate, an alkali metal salt of phosphoric acid, an alkali metal salt of hydrogen phosphate, an ammonium salt of phosphoric acid, and an ammonium salt of hydrogen phosphate.
[0163] In one embodiment, the core particles further contains a hydrophilic polymer compound . In one embodiment, the hydrophilic polymer compound is selected from the group consisting of one or more of the following: vinyl alcohol, vinylpyrrolidone, acrylic acid, methacrylic acid, a saponification compound of vinyl acetate, a cellulose ester, an oxyolefin, and a sugar.
[0164] In one embodiment, the invention comprises any or all of the above indicting absorbents incorporated into a personal monitor sampling, detecting, and indicating airborne DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds by the process of diffusion.
[0165] In one embodiment, the invention comprises any or all of the above indicting absorbents incorporated into a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator for indicating airborne DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds.
EXAMPLES
[0166] The following examples describe non-limiting uses of the compositions, methods and apparatus described herein.
[0167] In one embodiment, a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds directly from the patient's exhaled respiratory air is provided. In a preferred embodiment, the device (e.g., the adsorbent) is directly connected to the patient's mask. In one embodiment, this may require treating the highest concentration of odor bearing material.
[0168] In one embodiment, an apparatus to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the exhaust outlet of a medical respiratory ventilator is provided. In another embodiment, the device is connected to the ventilator's exhaust outlet through a gas scavenging device. In one embodiment, the apparatus comprises a gas scavenging device comprising the adsorbent described herein, wherein the gas scavenging device is connected to the exhaust outlet. Thus, the DMSO metabolite-containing exhaust leaving the ventilator passes through the adsorbent which filters out the metabolites and odors, resulting in air that does not contain the odors associated with the metabolites. [0169] In one embodiment, a device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the recirculated or vented stream a room sized HVAC or clean room system is provided. In one embodiment, the device (e.g., the adsorbent) is connected to the system's ductwork.
[0170] In one embodiment, an adsorbent to be adhered to or sandwiched between three dimensional fiber material as in fabric, cloth, felt, nonwoven or other flexible material to become part of clothing, bedding, masks and other items used by the patient or the medical staff is provided.
[0171] , An article of patient bed covering to capture the odors and compounds emanating from the dermal areas of the patient and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is provided.
[0172] An article of patient clothing to capture the odors and compounds emanating from the dermal areas of the patient's body and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is also provided.
[0173] An article of caregiver clothing to capture the odors and compounds emanating from all areas of the patient including respiration and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is provided.
[0174] A caregiver mask to reduce and/or prevent the breathing by the caregiver of the odors and compounds emanating all areas of the patient including respiration and resulting from the metabolism of DMSO (dimethyl sulfoxide) and associated compounds is provided.
[0175] A device to remove the odors, DMS, methyl mercaptan and/or hydrogen sulfide and compounds resulting from the metabolism of DMSO and associated compounds directly from the area around a patient (e.g., the patient's upper torso) is provided. The flexible patient isolation assembly may or may not be connected to the clean air delivery assembly's top final filter hood assembly.
[0176] A device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the entire patient bed area with or without enough space for caregiver occupancy of the patient isolation assembly is provided. The clean air delivery assembly device may be connected to the patient isolation assembly sized to enclose only the bed or to provide caregiver access.
[0177] A device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds from the entire patient room is provided. The clean air delivery assembly may positioned with the top final filter hood assembly over the patient or preferably within the room should the patient be served by another unit.
[0178] A device to remove the odors and compounds resulting from the metabolism of DMSO and associated compounds directly from the area around the patient's wheelchair or gurney is provided. The portable clean air delivery assembly device may be connected to the wheelchair or gurney by means of clamps, straps or other suitable means. The flexible patient isolation assembly may or may not be connected to the clean air delivery assembly's top final filter hood assembly.
[0179] A device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds directly from the patient's exhaled respiratory air is provided. Such compounds may be detected in concentrations of about 1 to about 10,000 parts per million. The device may be directly connected to the patient's mask.
[0180] A device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds from the exhaust of a medical respiratory ventilator is provided. Such compounds may be detected in concentrations of about 1 to about 1 ,000 parts per million. The device may be integral to or connected to an adsorber located on the ventilator's discharge or directly on the ventilator's discharge through a gas scavenging device.
[0181] A device to indicate the presence of DMS and other odorous compounds resulting from the metabolism of DMSO and associated compounds from the recirculated or vented stream from a room sized HVAC or clean room system is provided. Such compounds may be detected in concentrations of about 1 to about 10 parts per million. The device may be connected to the system's ductwork.
[0182] An indicating adsorbent included in a personal monitor containing the detecting indicator and sampling airborne contaminants by the process of diffusion is provided. Such compounds may be detected in concentrations of about 1 to about 1 ,000 parts per million. In some embodiments, such personal monitor may be pinned, clipped, or otherwise affixed to the clothing or person of the staff, visitors or patients in the medical facility.
[0183] An indicating adsorbent included in a standard format ambient air sampling tube for a standard air sampling pump such tube containing the detecting indicator is provided. Such compounds may be detected in concentrations of about 1 to about 10,000 parts per million. Such sampling may be from the patient's bed area, the room, the respiratory ventilator, the room's HVAC system, or other location.
[0184] It will be understood by those of skill in the art that numerous and various modifications can be made without departing from the spirit of the present invention. Therefore, it should be clearly understood that the forms of the present invention are illustrative only and are not intended to limit the scope of the present invention.

Claims

WHAT IS CLAIMED IS:
1. An adsorbent for adsorbing dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said compounds, comprising: an inner layer, an intermediate layer, and an outer layer, wherein said inner layer comprises adsorbing core particles; wherein said adsorbing core particles adsorb dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said compounds. wherein said intermediate layer contacts said inner layer and said outer layer; and wherein said outer layer comprises a porous coating.
2. An adsorbent according to any one of the preceding claims, further comprising an indicator for indicating the presence of dimethyl sulfoxide (DMSO) or related compounds.
3. The adsorbent of Claim 2, wherein said indicator comprises permanganate.
4. The adsorbent of Claim 2, wherein said indicator is colored, and is adapted to decrease in color or intensity as dimethyl sulfoxide (DMSO) or related compounds are removed.
5. An adsorbent according to any one of the preceding claims, wherein said adsorbing core particles are selected from the group consisting of one or more of the following: activated carbon, an inorganic oxide, a compound having ion exchange capacity, an ion exchange resin, and a chemical deodorizer.
6. An adsorbent according to any one of the preceding claims, wherein said intermediate layer comprises a metal compound and a water-soluble organic material disposed between the core particles and the porous coating.
7. An adsorbent according to any one of the preceding claims, wherein said outer layer consists only of a porous coating.
8. An adsorbent according to any one of the preceding claims, wherein said outer layer comprises a polymer selected from the group consisting of one or more of the following: a fluororesin, a polyamide resin, a polyimide resin, a polyester resin, a polystyrene resin, a polyolefm resin, a polycarbonate resin, a polysulfone resin, an acrylic resin, a cellulose resin, a vinyl chloride resin, a polyacetal resin, a polyurethane resin and a copolymer or derivative thereof.
9. An adsorbent according to any one of the preceding claims, wherein said outer layer comprises a polymer selected from the group consisting of one or more of the following: polytetrafluoroethylene, polyhexafluoropropylene, polydifluoroethylene, polyvinylidene fluoride, polyvinyl fluoride, and a copolymer or derivative thereof.
10. An adsorbent according to any one of the preceding claims, wherein said porous coating has a thickness of about 0.01 μm to about 1,000 μm.
11. An adsorbent according to any one of the preceding claims, wherein said porous coating has an average pore diameter of about 0.01 μm to about 500 μm.
12. An adsorbent according to any one of the preceding claims, wherein said porous coating has a porosity of about 3% to about 90%.
13. A method for removing dimethyl sulfoxide (DMSO) metabolites, comprising contacting said metabolites with an adsorbent according to any one of the preceding claims.
14. The method of Claim 13, wherein said dimethyl sulfoxide (DMSO) metabolites are produced by an individual receiving dimethyl sulfoxide (DMSO) treatment.
15. A method for removing odors associated with dimethyl sulfoxide (DMSO) or related compounds, comprising exposing said odors to an adsorbent according to any one of the preceding claims.
16. A clean air member for removal of dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said dimethyl sulfoxide (DMSO) or related compounds comprising adsorbent according to any one of the preceding claims.
17. A clean air supply assembly for removal of dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said dimethyl sulfoxide (DMSO) or related compounds comprising adsorbent according to any one of the preceding claims.
18. An apparatus for removing dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said dimethyl sulfoxide (DMSO) or related compounds from the exhaust outlet of a medical respiratory ventilator, wherein said apparatus comprises a gas scavenging device comprising the adsorbent of according to any one of the preceding claims, and wherein said gas scavenging device is connected to said exhaust outlet.
19. A face mask for reducing exposure of dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said dimethyl sulfoxide (DMSO) or related compounds comprising an adsorbent of according to any one of the preceding claims.
20. A face mask for reducing exposure of dimethyl sulfoxide (DMSO) or related compounds, or the odors associated with said dimethyl sulfoxide (DMSO) or related compounds comprising: an outer shield layer comprising a synthetic fiber; a copper layer comprising a fiber and powdered copper; a carbon layer comprising a fiber and activated carbon; a chemical layer comprising a fiber and one or more, odor absorbing chemicals; and a facial layer comprising a synthetic fiber.
21. The face mask according to any of Claims 19-20, wherein said face mask comprises an exhale valve.
22. The face mask according to any of Claims 19-21, wherein said face mask is a duckbill mask.
PCT/US2006/035321 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same WO2007033083A2 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP2008530021A JP5399072B2 (en) 2005-09-12 2006-09-11 System for removing dimethyl sulfoxide (DMSO) or related compounds or odors associated therewith
CA2622204A CA2622204C (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same
AU2006291134A AU2006291134C1 (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
US12/066,485 US7955418B2 (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (DMSO) or related compounds or odors associated with same
EP06814457.5A EP1966229B1 (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same
US13/099,120 US8480797B2 (en) 2005-09-12 2011-05-02 Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors
US13/098,941 US8673061B2 (en) 2005-09-12 2011-05-02 Methods for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors
US13/099,098 US8298320B2 (en) 2005-09-12 2011-05-02 Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
US13/659,797 US8440001B2 (en) 2005-09-12 2012-10-24 Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
US13/892,190 US9186472B2 (en) 2005-09-12 2013-05-10 Devices for removal of dimethyl sulfoxide (DMSO) or related compounds or associated odors and methods of using same

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US71636905P 2005-09-12 2005-09-12
US71627105P 2005-09-12 2005-09-12
US71627805P 2005-09-12 2005-09-12
US71633605P 2005-09-12 2005-09-12
US60/716,336 2005-09-12
US60/716,369 2005-09-12
US60/716,278 2005-09-12
US60/716,271 2005-09-12

Related Child Applications (4)

Application Number Title Priority Date Filing Date
US12/066,485 A-371-Of-International US7955418B2 (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (DMSO) or related compounds or odors associated with same
US11087508P Continuation-In-Part 2005-09-12 2008-11-03
PCT/US2009/063006 Continuation-In-Part WO2010062721A1 (en) 2005-09-12 2009-11-02 Activated carbon systems for facilitating use or treatment with dimethyl sulfoxide (dmso)
US13/099,098 Continuation US8298320B2 (en) 2005-09-12 2011-05-02 Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same

Publications (2)

Publication Number Publication Date
WO2007033083A2 true WO2007033083A2 (en) 2007-03-22
WO2007033083A3 WO2007033083A3 (en) 2007-09-27

Family

ID=37865488

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/035321 WO2007033083A2 (en) 2005-09-12 2006-09-11 Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same

Country Status (6)

Country Link
US (4) US7955418B2 (en)
EP (1) EP1966229B1 (en)
JP (1) JP5399072B2 (en)
AU (1) AU2006291134C1 (en)
CA (1) CA2622204C (en)
WO (1) WO2007033083A2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008040966A1 (en) 2006-10-02 2008-04-10 M-I Drilling Fluids Uk Limited Method of forming an agent and its use in desulphurisation
EP2134447A2 (en) * 2007-03-22 2009-12-23 Mvp Textiles&Apparel, Inc. Antimicrobial filtration article
CN102421310A (en) * 2009-02-26 2012-04-18 奥特勒洁净室技术有限公司 Clean room, clean room suit and arrangement therefor
US9427419B2 (en) 2005-09-12 2016-08-30 Abela Pharmaceuticals, Inc. Compositions comprising dimethyl sulfoxide (DMSO)
US9839609B2 (en) 2009-10-30 2017-12-12 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (DMSO) and methylsulfonylmethane (MSM) formulations to treat osteoarthritis
US20210093822A1 (en) * 2019-09-27 2021-04-01 Koninklijke Philips N.V. Selectively altering deformation characteristics of a synthetic fabric material
AT17149U1 (en) * 2020-04-17 2021-07-15 Omnignostica Forschungs Gmbh & Co Kg Respirator
WO2022148796A1 (en) * 2021-01-06 2022-07-14 Insu Pharma Ag Protective mask comprising a conductor fabric
WO2023287630A1 (en) * 2021-07-12 2023-01-19 Decarbontek LLC Modular adsorbent devices and applications

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007033180A1 (en) 2005-09-12 2007-03-22 Abela Pharmaceuticals, Inc. Materials for facilitating administration of dimethyl sulfoxide (dmso) and related compounds
US8480797B2 (en) 2005-09-12 2013-07-09 Abela Pharmaceuticals, Inc. Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors
AU2006291134C1 (en) 2005-09-12 2013-08-15 Abela Pharmaceuticals, Inc. Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
US8182568B2 (en) * 2006-04-26 2012-05-22 Volo Giovanni D Two-stage air filter and mask incorporating the same
EP2162223B1 (en) * 2007-06-26 2019-11-20 Innonix Technologies, Incorporated Devices for decreasing human pathogen transmission
US20090114228A1 (en) * 2007-11-01 2009-05-07 Garry William Kirschner Disposable outdoors mask and method of use
US20090211581A1 (en) * 2008-02-26 2009-08-27 Vishal Bansal Respiratory mask with microporous membrane and activated carbon
CN101679892A (en) * 2008-02-26 2010-03-24 松下电器产业株式会社 Desulfurizer, hydrogen generation apparatus, fuel cell power generating system, and desulfurizing agent cartridge
BRPI0921494A2 (en) * 2008-11-03 2018-10-30 Prad Reasearch And Development Ltd method of planning a underground forming sampling operation, method of controlling a underground forming sampling operation, method of controlling a drilling operation for an underground formation, and method of sampling during the drilling operation.
US20130209312A1 (en) * 2012-02-13 2013-08-15 Morgan Adhesives Company Film With Absorbing Coating
US11059024B2 (en) * 2012-10-25 2021-07-13 Georgia Tech Research Corporation Supported poly(allyl)amine and derivatives for CO2 capture from flue gas or ultra-dilute gas streams such as ambient air or admixtures thereof
EP2916880B1 (en) * 2012-11-12 2017-10-25 SCA Hygiene Products AB Odor control material prepared by extrusion comprising particles encapsulated in a polymeric matrix
JP6417717B2 (en) * 2013-05-31 2018-11-07 大日本印刷株式会社 PTP blister sheet and PTP blister package comprising the same
WO2015002324A1 (en) 2013-07-05 2015-01-08 Nitto Denko Corporation Filter element for decomposing contaminants, system for decomposing contaminants and method using the system
DE102013224431B4 (en) * 2013-11-28 2015-06-18 4A Engineering Gmbh Setting aid for setting a catheter for diabetics
EP3082704A4 (en) 2013-12-20 2017-08-23 SCA Hygiene Products AB Absorbent product comprising an odor control material
EP3082703B8 (en) 2013-12-20 2018-09-12 Essity Hygiene and Health Aktiebolag Absorbent product comprising odor control material
US20160327491A1 (en) * 2014-01-06 2016-11-10 3M Innovative Properties Company Colorimetric indicator responsive to air flow
JP6226383B2 (en) * 2014-03-25 2017-11-08 株式会社セフテック Air purification device
US10792194B2 (en) 2014-08-26 2020-10-06 Curt G. Joa, Inc. Apparatus and methods for securing elastic to a carrier web
US10953188B2 (en) * 2015-01-09 2021-03-23 Fisher & Paykel Healthcare Limited Gas therapy system
CN104799450B (en) * 2015-04-08 2016-08-17 广西师范大学 A kind of haze-proof mask and preparation method thereof
JP6555933B2 (en) * 2015-06-04 2019-08-07 共同印刷株式会社 Laminate for sulfide gas adsorption
US20180214817A1 (en) * 2015-07-23 2018-08-02 Linde Aktiengesellschaft Adsorbent for a temperature swing adsorption method
US20170055597A1 (en) * 2015-08-29 2017-03-02 Diane Villarreal Lekven Hepa Hoodie
JP6834128B2 (en) * 2016-01-07 2021-02-24 昭和電工マテリアルズ株式会社 Separator and column
JP6848203B2 (en) * 2016-04-20 2021-03-24 昭和電工マテリアルズ株式会社 Separator and column
JP2017213118A (en) * 2016-05-31 2017-12-07 住江織物株式会社 Deodorizing filter
US20180153230A1 (en) * 2016-12-05 2018-06-07 Marolina Outdoor Inc. Ozone garment system and methods thereof
CN107569969B (en) * 2017-08-31 2020-09-25 昆明理工大学 High-efficient purifying material of high toxicity gaseous pollutant and operative installations
WO2019098100A1 (en) 2017-11-18 2019-05-23 株式会社クリエイティブテクノロジー Headgear cleaner and headgear stand
EP3746021B1 (en) 2018-01-29 2024-01-31 Curt G. Joa, Inc. Apparatus and method of manufacturing an elastic composite structure for an absorbent sanitary product
JP2022505269A (en) * 2018-10-19 2022-01-14 ゴッチャル クラウス Materials and methods to remove contaminants
US11925538B2 (en) 2019-01-07 2024-03-12 Curt G. Joa, Inc. Apparatus and method of manufacturing an elastic composite structure for an absorbent sanitary product
US11173072B2 (en) 2019-09-05 2021-11-16 Curt G. Joa, Inc. Curved elastic with entrapment
US11578413B2 (en) 2020-01-13 2023-02-14 Hamilton Sundstrand Corporation Sabatier reactor apparatus
KR102413878B1 (en) * 2020-04-08 2022-07-06 주식회사 지와이씨가양 Mask
CN111389381B (en) * 2020-04-14 2021-01-05 广西大学 Near-infrared low-temperature desorption type intelligent adsorption material and preparation method and application thereof
CN111408357B (en) * 2020-04-14 2021-01-29 广西大学 Biomass intelligent fiber-based amphoteric multifunctional adsorption material and preparation method and application thereof
KR102361230B1 (en) * 2020-04-14 2022-02-10 신하랑 Manufacturing method of mask and bag fabric with antibacterial, odor and dehumidification functions and Antibacterial masks and antiseptic bags manufactured by the method
IT202000010285A1 (en) * 2020-05-07 2021-11-07 Pietro Galliani S P A PERSONAL PROTECTIVE EQUIPMENT
WO2021247720A1 (en) * 2020-06-02 2021-12-09 University Of Kentucky Research Foundation Antiviral mask and antiviral filter made from a breathable microporous polymeric membrane
US10980296B1 (en) * 2020-06-12 2021-04-20 Tracy Hosac Facemask sustenance access port assembly
DE102020207985A1 (en) 2020-06-28 2021-12-30 Innomotion AG Sterile device for covering human skin and method of making a sterile device
US11123584B1 (en) 2020-10-05 2021-09-21 Iowa State University Research Foundation, Inc. Personal protective anti-viral face mask

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4171542A (en) 1978-06-05 1979-10-23 Buckeye Cellulose Corporation Disposable surgical gown with a bib forming a hand support
US4819275A (en) 1987-11-18 1989-04-11 Lunt Audrey T Disposable gown for medical patients
US4986016A (en) 1986-12-10 1991-01-22 Wichman William J Folding display frame with offset hub configuration
US5125205A (en) 1986-12-10 1992-06-30 William John Wichman Display frame with folding display attachment devices
US5322061A (en) 1992-12-16 1994-06-21 Tecnol Medical Products, Inc. Disposable aerosol mask
US5765556A (en) 1992-12-16 1998-06-16 Tecnol Medical Products, Inc. Disposable aerosol mask with face shield
US6055982A (en) 1993-12-15 2000-05-02 Kimberly-Clark Worldwide, Inc. Disposable face mask with enhanced fluid barrier
US6099607A (en) 1998-07-22 2000-08-08 Haslebacher; William J. Rollably positioned, adjustably directable clean air delivery supply assembly, for use in weather protected environments to provide localized clean air, where activities require clean air quality per strict specifications
US20030190266A1 (en) 2002-04-05 2003-10-09 Hideyuki Tsurumi Odor eliminating fiber structure having indicator
US6966937B2 (en) 2002-10-22 2005-11-22 Sanki Engineering Co., Ltd. Patient isolation unit

Family Cites Families (497)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2638179A (en) * 1950-01-06 1953-05-12 Edward M Yard Drying capsule
US3549770A (en) 1963-12-09 1970-12-22 Crown Zellerbach Corp Therapeutic administration of effective amounts of dimethyl sulfoxide to human and animal subjects
US4177267A (en) 1963-12-09 1979-12-04 Crown Zellerbach Enhancing tissue penetration of physiologically active steroidal agents with DMSC
US3549771A (en) 1964-02-10 1970-12-22 Crown Zellerbach Corp Retarding the growth of microorganisms with dimethyl sulfoxide
US3334012A (en) 1964-02-10 1967-08-01 Crown Zellerbach Corp Dimethyl sulfoxide inhibition and control of plant virus diseases
DE1211169B (en) 1964-03-26 1966-02-24 Hoechst Ag Process for the production of pure dimethyl sulfoxide
CH401363A (en) 1964-05-13 1965-10-31 Vifor Sa Apparatus for infusing liquids into a body
US3527863A (en) 1964-11-25 1970-09-08 Brunswick Corp Tissue infiltrant
US3393080A (en) 1965-10-20 1968-07-16 Fmc Corp Microcrystalline colloidal collagen dispersions in dispersing media containing dimethyl sulfoxide and water-miscible organic solvents
US3361555A (en) 1966-04-13 1968-01-02 Crown Zellerbach Corp Method of stimulating plant growth
US3558434A (en) 1966-04-13 1971-01-26 Crown Zellerbach Corp Stimulation of the growth of microorganisms
US3573214A (en) 1966-09-12 1971-03-30 Merck & Co Inc Process for preparing stable dimethyl sulfoxide-hydrogen fluoride mixture
US3790682A (en) * 1967-11-28 1974-02-05 Crown Zellerbach Corp Ataractic use of dimethyl sulfoxide
US3740420A (en) 1967-11-28 1973-06-19 Crown Zellerbach Corp Pharmaceutical compositions with dimethyl sulfoxide
US3551554A (en) 1968-08-16 1970-12-29 Crown Zellerbach Corp Enhancing tissue penetration of physiologically active agents with dmso
US3592936A (en) 1969-04-25 1971-07-13 Merck & Co Inc Method of treatment using pharmaceutical composition containing dimethyl sulfoxide
US3675654A (en) 1970-04-01 1972-07-11 Procter & Gamble Disposable article with mositure-actuated indicating agent
US3690808A (en) 1970-08-28 1972-09-12 Univ Ohio Method and apparatus for sulfur dioxide emission control in combustion systems
US3711606A (en) 1970-09-02 1973-01-16 Crown Zellerbach Corp Enhancing tissue penetration of physiologically active steroidal agents with dmso
US3654165A (en) 1970-09-10 1972-04-04 Stanley Charles Bryant Telephone cleaner-sanitizer
PL74243B1 (en) 1971-03-01 1974-10-31
US3757495A (en) * 1971-12-30 1973-09-11 W Sievers Portable air purifier
IT1044231B (en) 1972-03-16 1980-03-20 Hoffmann La Roche COMBINATION OF ACTIVE SUBSTANCES USEFUL TO FIGHT BACTERIA INFECTIONS GRAM POSITIVE AND GRAN NEGATIVE
US3852408A (en) 1972-09-21 1974-12-03 Lone Star Steel Co Process for the removal of sulfur dioxide from carrier gases
US3823676A (en) 1972-10-10 1974-07-16 Warren Cook Chem Inc Method of reducing sulphur dioxide emissions from coal
US3948617A (en) 1972-10-11 1976-04-06 Benjamin Withorn Method of reducing sulphur dioxide emissions from combustible materials
US3861894A (en) 1972-10-13 1975-01-21 Bio Dynamics Inc Portable clean-air generator
US3972962A (en) 1973-10-23 1976-08-03 Emery Industries, Inc. Non-migrating polymeric plasticizers for polyvinyl chloride
FR2277080A1 (en) 1974-07-04 1976-01-30 Ugine Kuhlmann DIMETHYLSULFOXIDE MANUFACTURING PROCESS
US4333922A (en) 1974-09-12 1982-06-08 Herschler R J Method for the treatment of water-living animals with health modifying agents
US4015025A (en) 1974-09-24 1977-03-29 General Foods Corporation Hydrocolloids as potentiators of dimethyl sulfide flavor
US3988129A (en) 1974-12-16 1976-10-26 Union Carbide Corporation Process for removing sulfur dioxide from gas streams
US3976747A (en) 1975-06-06 1976-08-24 The United States Of America As Represented By The United States Energy Research And Development Administration Modified dry limestone process for control of sulfur dioxide emissions
US4719105A (en) 1975-11-05 1988-01-12 Bush Boake Allen, Inc. Method, compositions and compounds useful in room fresheners employing cyclohexyl alcohol and ester derivatives
US4622221A (en) 1975-11-05 1986-11-11 Bush Boake Allen Inc. Method, compositions and compounds, useful in room fresheners employing cyclohexyl alcohol and ester derivatives
US4125589A (en) 1976-01-16 1978-11-14 Quad Corporation Odor control system
US4129122A (en) 1977-04-27 1978-12-12 Sterilaire Medical, Inc. Patient isolation room with laminar flow feature
US4169550A (en) 1977-05-12 1979-10-02 Emergency Medical Equipment Incorporated Emergency medical kit
US4316795A (en) 1978-03-24 1982-02-23 Atlantic Richfield Company Hydrocarbon conversion process with reduced sulfur oxide emissions
DE2826237C2 (en) * 1978-06-15 1981-11-19 Riensch & Held, 2000 Hamburg Grease filters, in particular for extractor hoods
US4202676A (en) 1978-07-31 1980-05-13 Raymond Fink Safety enclosure
US4252054A (en) 1978-08-30 1981-02-24 Marinus Bakels Dental clean air device
US4194628A (en) 1978-09-18 1980-03-25 Campos Juan M Medical case
JPS5551422A (en) 1978-10-11 1980-04-15 Takeda Chem Ind Ltd Deodorization
US4225381A (en) 1978-12-12 1980-09-30 Oji Paper Co., Ltd. Method for removing odor from fluid
US4493930A (en) 1979-01-04 1985-01-15 The United States Of America As Represented By The Secretary Of The Army Medicinal 2-acetyl- and 2-propionylpyridine thiosemicarbazones and preparation thereof
US4212392A (en) 1979-02-09 1980-07-15 Bristol-Myers Company Medical emergency treatment kit
US4277450A (en) 1979-03-16 1981-07-07 Allis-Chalmers Corporation Removal of sulfur dioxide from gas
JPS55142523A (en) 1979-04-23 1980-11-07 Osaka Oxgen Ind Ltd Deodorizing waste gas containing malodorous component
US4296104A (en) 1979-08-30 1981-10-20 Herschler R J Therapeutic dimethyl sulfoxide composition and methods of use
DE2934156A1 (en) 1979-08-23 1981-03-12 Hans Elstner, Festartikel- Und Chenille-Fabrik, 8867 Oettingen CONTAINER FOR THE PROTECTED STORAGE OF TICKPENS.
US4568547A (en) 1979-08-30 1986-02-04 Herschler R J Solid pharmaceutical compositions comprising MSM and their production
US4296130A (en) 1979-08-30 1981-10-20 Herschler R J Methylsulfonylmethane and methods of use
US4559329A (en) 1982-09-14 1985-12-17 Herschler R J Dietary and pharmaceutical uses of methyl-sulfonylmethane and compositions comprising it
US4973605A (en) 1979-08-30 1990-11-27 Herschler R J Use of methylsulfonylmethane to relieve pain and relieve pain and nocturnal cramps and to reduce stress-induced deaths in animals
US4914135A (en) 1979-08-30 1990-04-03 Herschler R J Use of Methylsulfonylmethane to treat parasitic infections
US5071878A (en) 1979-08-30 1991-12-10 Herschler R J Use of methylsulfonylmethane to enhance diet of an animal
US4477469A (en) 1979-08-30 1984-10-16 Herschler R J Preparations containing methylsulfonylmethane and methods of use and purification
US4616039A (en) 1979-08-30 1986-10-07 Herschler R J Methylsulfonylmethane in dietary products
US4514421A (en) 1979-08-30 1985-04-30 Herschler R J Dietary and pharmaceutical uses of methylsulfonylmethane and compositions comprising it
US4863748A (en) 1979-08-30 1989-09-05 Herschler R J Dietary products and uses comprising methylsulfonylmethane
FR2475457A1 (en) 1980-02-08 1981-08-14 Charbonnages Ste Chimique SEED FILMS OBTAINED FROM ETHYLENE-PROPYLENE COPOLYMERS, PROCESS FOR THE PRODUCTION THEREOF AND INSTALLATION FOR CARRYING OUT SAID METHOD
US4357288A (en) 1980-02-25 1982-11-02 Deacon Machinery, Inc. Method of making clear transparent polypropylene containers
JPS5915143B2 (en) 1980-04-08 1984-04-07 ト−レ・シリコ−ン株式会社 Compounded rubber composition
FR2483430B1 (en) 1980-05-28 1985-06-07 Charbonnages Ste Chimique ETHYLENE COPOLYMERS CAPABLE OF MOLDING AND / OR INJECTED AND A PROCESS FOR THE PRODUCTION THEREOF
US4335148A (en) 1980-06-04 1982-06-15 Pennwalt Corporation Methods of preventing grain sprouting after harvest through the application of sulfur dioxide, nitrogen and ammonia gases
US4309393A (en) 1980-10-14 1982-01-05 Domtar Inc. Fluidized bed sulfur dioxide removal
FR2498083B1 (en) 1981-01-19 1986-05-23 Charbonnages De France
US4497824A (en) 1981-06-23 1985-02-05 Schulte Thomas L Method of chemically debriding ulcerated necrotic tissue
US4626530A (en) 1981-06-23 1986-12-02 Schulte Thomas L Treatment of eye inflammation with biphenamine
US4469702A (en) 1981-06-23 1984-09-04 Schulte Thomas L Analgesic composition and use thereof to ameliorate deep and intractable pain
US4369190A (en) 1981-06-23 1983-01-18 Schulte Thomas L Analgesic composition and use thereof to ameliorate intractable pain
US4372915A (en) 1981-06-26 1983-02-08 Beckman Instruments, Inc. Fluorescent sulfur dioxide analyzer having an improved sulfur dioxide generator
DE3224619A1 (en) 1981-07-14 1983-05-19 Freund Industrial Co., Ltd., Tokyo Oral pharmaceutical composition
JPS5849488A (en) 1981-09-18 1983-03-23 Kao Corp Composition for deodorant
US4902558A (en) 1982-03-12 1990-02-20 Henriksen Henning R Method for protecting skin from hazardous chemicals
EP0102992B2 (en) 1982-03-12 1993-05-05 HENRIKSEN, Henning Risvig Protective garment
JPS5936116A (en) 1982-08-24 1984-02-28 Chisso Corp Expanding ethylene-propylene copolymer and manufacture of the same
US4512245A (en) 1982-09-24 1985-04-23 Adsorbent Products Inc. Portable point source adsorber
US4505708A (en) 1982-09-27 1985-03-19 Baxter Travenol Laboratories, Inc. Blood component storage container and method utilizing a polyvinyl chloride plastic formulation free or essentially free of leachable materials
US4491563A (en) 1982-12-10 1985-01-01 Phillips Petroleum Company Process for deodorizing a paraffinic hydrocarbon feedstock
US4616064A (en) 1983-04-26 1986-10-07 Raychem Corporation Polymeric compositions suitable for use in the medical field and comprising a thermoplastic olefin, a siloxane polymer, and an elastomer
US4507287A (en) 1983-06-20 1985-03-26 Dixon Glen J Preparation and method for the treatment of acne
US4747845A (en) 1983-10-17 1988-05-31 Enquay Pharmaceutical Associates Synthetic resin matrix system for the extended delivery of drugs
US4507114A (en) 1983-10-21 1985-03-26 Baxter Travenol Laboratories, Inc. Multiple chamber container having leak detection compartment
JPS60122567A (en) 1983-12-08 1985-07-01 高砂香料工業株式会社 Odor masking deodorant
US4686124A (en) 1983-12-12 1987-08-11 Sumitomo Bakelite Company Ltd. Thermoplastic resin-silicone rubber composite shaped article
US4545414A (en) 1984-02-21 1985-10-08 Baum Frank M Belt-supported camera bag
US4803047A (en) 1984-03-14 1989-02-07 Pluim Jr Arthur W Method for neutralizing offensive chemicals
CA1236029A (en) 1984-05-14 1988-05-03 Edmund Sandborn Pharmaceutical solutions comprising dimethyl sulfoxide
JPS6125837A (en) 1984-07-16 1986-02-04 日本石油化学株式会社 Novel multilayer structure
US4911691A (en) 1984-09-21 1990-03-27 Menlo Care, Inc. Assembly for adminstering IV solution
US4600002A (en) 1984-10-24 1986-07-15 American Optical Corporation Disposable respirator
DE3445639A1 (en) * 1984-12-14 1986-06-26 Drägerwerk AG, 2400 Lübeck COLORIMETRIC INDICATOR TO INDICATE THE EXHAUST OF GAS FILTERS
US4595102A (en) 1984-12-18 1986-06-17 The Kendall Company Kit for performing a medical procedure
WO1986007369A1 (en) 1985-06-11 1986-12-18 Products Research And Chemical Corporation Method of producing mercaptan terminated polymers with increased reactivity and reduced odor
US5070597A (en) 1985-07-19 1991-12-10 Raychem Corporation Tubular article
JPS6221034A (en) 1985-07-19 1987-01-29 Junkosha Co Ltd Liquid leak detection sensor
US4686204A (en) 1985-09-30 1987-08-11 Union Oil Company Of California Sorbent for reducing sulfur oxide emissions from catalytic cracking units and process for producing the sorbent
US4642177A (en) 1985-09-30 1987-02-10 Union Oil Company Of California Process for reducing sulfur oxide emissions from catalytic cracking units
GB8525047D0 (en) 1985-10-10 1985-11-13 Interox Chemicals Ltd Waste treatment
US4830718A (en) 1985-10-21 1989-05-16 John Stauffer Removal of sulfur dioxide (SO2) from waste gases and recovery as sulfuric acid
US4655148A (en) 1985-10-29 1987-04-07 Combustion Engineering, Inc. Method of introducing dry sulfur oxide absorbent material into a furnace
US4778697A (en) 1985-11-29 1988-10-18 American National Can Company Polymeric films
US5071686A (en) 1985-11-29 1991-12-10 Genske Roger P Films of polypropylene blends and polyethylene blends and articles made therewith
US5032613A (en) 1986-02-12 1991-07-16 W. Keith R. Watson Method and composition for treating arthritis
US4737173A (en) 1986-07-03 1988-04-12 Amway Corporation Room air treatment system
JPS6341408A (en) 1986-08-07 1988-02-22 Nippon Zeon Co Ltd Copper-containing composition
US4721813A (en) 1986-08-25 1988-01-26 Phillips Petroleum Company Method for the oxidation of mercaptoalkanols to dithiodiglycols
JPS6354937A (en) 1986-08-26 1988-03-09 Nippon Zeon Co Ltd Copper containing composition
US4784909A (en) 1986-09-16 1988-11-15 Teijin Limited Anti-fungus, deodorant fiber material
US4863687A (en) 1986-09-26 1989-09-05 Solarchem Enterprises Inc. Method for removing malodorous or toxic gases from an air stream
US4796790A (en) 1986-10-09 1989-01-10 Hamilton Olivia B Medical supply case
JPS63111869A (en) 1986-10-29 1988-05-17 株式会社 青木建設 Drain sterilizing autoclave apparatus
US4725290A (en) 1986-11-14 1988-02-16 Kernforschungszentrum Karlsruhe Gmbh Method for the purification of air or gas streams by a multi-path adsorption principle and moving-bed filtering apparatus for performing the method
CN1016429B (en) 1986-11-18 1992-04-29 昭和电工株式会社 Mfg. process
US4940658A (en) 1986-11-20 1990-07-10 University Patents, Inc. Assay for sulfhydryl amino acids and methods for detecting and distinguishing cobalamin and folic acid deficency
US5218036A (en) 1987-01-19 1993-06-08 Tonen Sekiyukagaku K.K. Shrinkable film from ethylene-vinyl acetate polymer talc and ethylene-propylene copolymers blend
ES2033838T3 (en) 1987-01-21 1993-04-01 Nippon Shokubai Co., Ltd. A METHOD AND A CATALYST FOR GAS PURIFICATION.
JPH0352503Y2 (en) 1987-02-21 1991-11-14
JPS63230171A (en) 1987-03-20 1988-09-26 東海興業株式会社 Deodorizing apparatus
JPS63274435A (en) 1987-05-07 1988-11-11 Sankyo Kogyo Kk Method for purifying treatment of malodorous gas
US5679399A (en) 1987-07-17 1997-10-21 Bio Barrier, Inc. Method of forming a membrane, especially a latex or polymer membrane, including multiple discrete layers
US20010018095A1 (en) 1987-07-17 2001-08-30 Shlenker Robin Renee Thill Method of forming a membrant, especially a latex or polymer membrane, including multiple discrete layers
US4919925A (en) 1987-07-17 1990-04-24 Nippon Zeon Co., Ltd. Deodorant, deodorizing composite material, deodorizing resin composition, deodorizing resin articles and deodorizing foam
US4941991A (en) 1987-10-22 1990-07-17 Rajamannan A H J Composition and process for use in neutralizing malodorous gases
US4931276A (en) 1987-10-30 1990-06-05 Franco Robert S Method for introducing desired agents into red blood cells
US5091180A (en) 1987-11-20 1992-02-25 Administrators Of The Tulane Educational Fund Protection against rhabdomyolysis-induced nephrotoxicity
US4910803A (en) 1987-12-02 1990-03-27 Cukier Daniel S Apparel having a breach indicator
GB2213057A (en) 1987-12-08 1989-08-09 I Pascuchi Josep Maria Vich Anti-viral agent
JP2583084B2 (en) 1987-12-17 1997-02-19 日本合成化学工業株式会社 Waste container
US4887751A (en) 1987-12-30 1989-12-19 Michael Lehman Traveler's organizer bag luggage
US5135904A (en) 1988-02-05 1992-08-04 Tayca Corporation Adsorbent composition for malodorous gases
US4937115A (en) 1988-03-18 1990-06-26 Ppg Industries, Inc. Bacteria impermeable, gas permeable package
AU632048B2 (en) 1988-06-23 1992-12-17 Kohjin Co. Ltd. Deodorant material and process for its production
DE3823848A1 (en) 1988-07-14 1990-01-18 Sueddeutsche Kalkstickstoff METHOD FOR REDUCING SO (ARROW DOWN) 2 (ARROW DOWN) AND / OR NO (ARROW DOWN) X (ARROW DOWN) EMISSIONS IN COMBUSTION PROCESSES
US4980045A (en) 1988-08-02 1990-12-25 Chevron Research Company Heavy oil pretreatment process with reduced sulfur oxide emissions
US5143831A (en) 1988-08-30 1992-09-01 G. D. Searle & Co. Fructose 1,6-diphosphate aldolase catalyzed steroselective synthesis of sugars
JPH02174932A (en) 1988-09-16 1990-07-06 Nissan Chem Ind Ltd Deodorant
US4904520A (en) 1988-10-17 1990-02-27 Hercules Incorporated Gas-permeable, liquid-impermeable nonwoven material
US4891221A (en) 1988-11-23 1990-01-02 Edward Shanborm Whole blood antiviral process and composition
US5626820A (en) 1988-12-12 1997-05-06 Kinkead; Devon A. Clean room air filtering
US5582865A (en) * 1988-12-12 1996-12-10 Extraction Systems, Inc. Non-woven filter composite
US5480860A (en) 1988-12-23 1996-01-02 Petrolite Corporation Methods for reducing sulfides in sewage gas
CN1019403B (en) 1988-12-28 1992-12-09 中国矿业大学北京研究生部型煤研究设计所 Technology for lowering so2 content in flue gas of boiler
US4948787A (en) 1989-01-04 1990-08-14 Imperial Chemical Industries Plc Inhibition of mercaptan odor in organothiophosphate biocides
US4948643A (en) 1989-01-23 1990-08-14 W. R. Grace & Co.-Conn. Flexible medical solution tubing
US4940405A (en) 1989-02-23 1990-07-10 Kelly John T Pulse combustion driven in-furnace NOx and SO2 control system for furnaces and boilers
CA1332265C (en) 1989-03-14 1994-10-11 Walter Berndt Mueller Impact modified medical film
US5007999A (en) 1989-04-13 1991-04-16 Mobil Oil Corporation Method for reducing sulfur oxide emission during an FCC operation
US5055279A (en) 1989-05-20 1991-10-08 Skw Trostberg Aktiengesellschaft Process for the reduction of emissions of sulphur dioxide and/or oxides of nitrogen in the case of combustion processes
US5006510A (en) 1989-06-20 1991-04-09 Ellis Wladislaw V Method for relieving chronic pain with a somatostatin analog composition
US5160707A (en) 1989-08-25 1992-11-03 Washington Suburban Sanitary Commission Methods of and apparatus for removing odors from process airstreams
US4994245A (en) 1989-08-25 1991-02-19 Washington Suburban Sanitary Commission Methods for removing odors from process airstreams
US5071622A (en) 1989-09-15 1991-12-10 E. I. Du Pont De Nemours And Company Process for odor control
GB2236681B (en) * 1989-10-12 1992-04-22 Harry Cole Respiratory protection device
FR2653661A1 (en) 1989-10-26 1991-05-03 Faure Jean Marie PACKAGING FOR THE ADMINISTRATION OF STERILE LIQUIDS, ESPECIALLY PHARMACEUTICAL LIQUIDS.
US5139831A (en) 1990-03-02 1992-08-18 W. R. Grace & Co.-Conn. Impact modified medical film with ph control
US5182016A (en) * 1990-03-22 1993-01-26 Regents Of The University Of Minnesota Polymer-coated carbon-clad inorganic oxide particles
US5133788A (en) 1990-04-10 1992-07-28 Backus Alan L Air filtering device
JP3029841B2 (en) 1990-04-16 2000-04-10 株式会社豊田中央研究所 Composite adsorbent and method for producing the same
GB2244126B (en) 1990-05-15 1994-03-02 Univ Bath Localised clean air system
CA2047148C (en) 1990-07-25 2000-07-04 Walter B. Mueller High melt flow polypropylene medical film
US5460625A (en) 1990-07-31 1995-10-24 Baxter International Inc. Cryogenic resistant coextruded tubing
JP3033995B2 (en) 1990-08-03 2000-04-17 オキツモ株式会社 Deodorizer and products using it
US5650329A (en) 1990-08-23 1997-07-22 Awc. Inc. Acid indicators
US5083558A (en) 1990-11-06 1992-01-28 Thomas William R Mobile surgical compartment with micro filtered laminar air flow
US5149576A (en) 1990-11-26 1992-09-22 Kimberly-Clark Corporation Multilayer nonwoven laminiferous structure
US5086804A (en) 1991-01-23 1992-02-11 Solkatronic Chemicals, Inc. Emergency security device for head of a leaking gas cylinder
US5152814A (en) 1991-02-01 1992-10-06 Component Systems, Inc. Apparatus for isolating contagious respiratory hospital patients
US5169217A (en) 1991-04-10 1992-12-08 International Portland Corporation Controlled environment chamber apparatus
US5344529A (en) 1991-06-17 1994-09-06 Stauffer John E Bipolar process for removal of sulfur dioxide from waste gases
US5207303A (en) 1991-07-15 1993-05-04 Oswalt Brenda K Medical emergency carrying case
US5199263A (en) 1991-08-12 1993-04-06 Texas Utilities Electric Co. Combustion system with reduced sulfur oxide emissions
JPH0817671B2 (en) 1991-09-18 1996-02-28 功 境 Garlic / green onion odor treatment method
US5190640A (en) 1991-09-18 1993-03-02 Baker Hughes Incorporated Treatment of oils using aminocarbinols
US5192498A (en) 1991-10-11 1993-03-09 Imperial Chemical Industries Plc Elimination of sulfide odor in thiocarbamate herbicides
US5117821A (en) 1991-10-18 1992-06-02 White George M Hunting mask with breath odor control system
US5335373A (en) 1991-11-29 1994-08-09 Dresdner Jr Karl P Protective medical gloves and methods for their use
US5177050A (en) * 1991-12-16 1993-01-05 Phillips Petroleum Company Sulfur absorbents
US5213680A (en) 1991-12-20 1993-05-25 Baker Hughes Incorporated Sweetening of oils using hexamethylenetetramine
US6149997A (en) 1992-01-30 2000-11-21 Baxter International Inc. Multilayer coextruded material for medical grade products and products made therefrom
US5218147A (en) 1992-02-10 1993-06-08 Phillips Petroleum Company Stable polysulfides and process therefor
US6007520A (en) 1992-02-12 1999-12-28 Daikyo Gomu Seiko, Ltd. Medical instrument
ZA931680B (en) 1992-03-30 1993-10-05 Grace W R & Co Medical solution tubing
US5458861A (en) 1992-04-15 1995-10-17 Mobil Oil Corporation Desulfurizing a gas stream
US5192342A (en) 1992-04-15 1993-03-09 Baron Robert A Apparatus for enhancing the environmental quality of work spaces
US5356709A (en) 1992-05-14 1994-10-18 Baxter International, Inc. Non-PVC coextruded medical grade port tubing
US5439454A (en) 1992-05-14 1995-08-08 Baxter International Inc. Coextruded medical grade port tubing
US5269294A (en) 1992-05-26 1993-12-14 Wallace J. Rogozinski Face mask impregnated with odor reducing molecular sieve material
US5200092A (en) 1992-06-23 1993-04-06 Carus Corporation Composition and method for sulfide control
US5240478A (en) 1992-06-26 1993-08-31 Messina Gary D Self-contained, portable room air treatment apparatus and method therefore
US5620760A (en) 1992-06-30 1997-04-15 Montell Technology Company Bv Shaped articles for biomedical use
US5419812A (en) 1992-09-03 1995-05-30 The Foxboro Company Method for regulating sulfur dioxide emissions from a recovery furnace
WO1994005272A1 (en) 1992-09-04 1994-03-17 Aws Shakir Mustafa Salim Skin treatment compositions containing dimethylsulphone and dimethylsulphoxide
AU4975093A (en) 1992-09-04 1994-03-29 Aws Shakir Mustafa Salim Gastrointestinal compositions containing dimethylsulfone and dimethylsulfoxide
US5792505A (en) 1992-09-22 1998-08-11 Mccormick & Company, Inc. Flavor encapsulation
FR2701220B1 (en) 1993-02-08 1995-04-14 Inst Francais Du Petrole Process for catalytic deodorization and reduction of the nitrogen content of slurry tank effluents.
US5584986A (en) 1993-03-19 1996-12-17 Bar-Co Processes Joint Venture Fluidized process for improved stripping and/or cooling of particulate spent solids, and reduction of sulfur oxide emissions
US5358443A (en) 1993-04-14 1994-10-25 Centercore, Inc. Dual fan hepa filtration system
CA2120315C (en) 1993-04-30 2001-05-15 Joel L. Williams Medical articles and process therefor
FR2704451B1 (en) 1993-04-30 1995-06-30 Oreal Method for deodorizing a formulation containing at least one compound carrying a thiol group and deodorized formulation thus obtained.
RU2035909C1 (en) 1993-06-02 1995-05-27 Виноходов Владимир Олегович Preparation for preventing and treating avian diseases
CA2168203C (en) 1993-07-30 2009-09-15 Jack De La Torre Medicinal for protection from neurological damage
FR2708602B1 (en) 1993-08-02 1995-10-06 Oreal Process for the extraction of smelly compounds present in a formulation containing at least one compound comprising a thiol group and deodorized compositions thus obtained.
EP0712354B1 (en) 1993-08-06 1999-01-13 Minnesota Mining And Manufacturing Company Multilayered tubing
JPH09501364A (en) 1993-08-06 1997-02-10 ミネソタ マイニング アンド マニュファクチャリング カンパニー Chlorine-free multilayer film medical device assembly
US5415180A (en) 1993-11-03 1995-05-16 Devon Industries, Inc. System and kit for medical procedures
FR2709678B1 (en) 1993-09-09 1995-12-08 David Philippe Marie Process for the purification of gaseous or liquid effluents containing sulfur derivatives.
EP0643014B1 (en) 1993-09-14 1998-08-12 Kuraray Chemical Co., Ltd. Deodorant comprising metal oxide-carrying activated carbon
US5998019A (en) 1993-11-16 1999-12-07 Baxter International Inc. Multi-layered polymer structure for medical products
US5607647A (en) 1993-12-02 1997-03-04 Extraction Systems, Inc. Air filtering within clean environments
US5724964A (en) * 1993-12-15 1998-03-10 Tecnol Medical Products, Inc. Disposable face mask with enhanced fluid barrier
CA2136278A1 (en) 1993-12-17 1995-06-18 Viviano Banzi Catalyst for the preparation of elastomeric ethylene-propylene copolymers
US5441729A (en) 1994-02-14 1995-08-15 Conair Corporation Lotion for reduction of post permanent wave odors
WO1995029897A1 (en) 1994-04-29 1995-11-09 G.D. Searle & Co. METHOD OF USING (H+/K+) ATPase INHIBITORS AS ANTIVIRAL AGENTS
US5658801A (en) 1994-05-03 1997-08-19 Spectral Diagnostics Inc. Medical test kit
US5487766A (en) 1994-05-24 1996-01-30 Vannier; Mervin R. Portable air filtration apparatus
US5579723A (en) 1994-07-22 1996-12-03 International Flavors & Fragrances Inc. Process for exciting, attracting, stimulating, and/or inciting members of the penaeus genus of the class crustacea
US5849846A (en) 1994-07-25 1998-12-15 Advanced Cardiovascular Systems, Inc. Balloons for medical catheters
TW517059B (en) 1994-07-25 2003-01-11 Ciba Geigy Ag New process for the production of biologically active protein
US5554120A (en) 1994-07-25 1996-09-10 Advanced Cardiovascular Systems, Inc. Polymer blends for use in making medical devices including catheters and balloons for dilatation catheters
US6057018A (en) 1994-07-28 2000-05-02 Siecor Corporation Blend of non plasticized polyvinyl chloride and ether-based polyurethane
US5538545A (en) * 1994-11-04 1996-07-23 W. L. Gore & Associates Nonparticulating adsorbent recirculating filter
IT1271278B (en) 1994-12-15 1997-05-27 Enichem Elastomers SUPPORTED CATALYTIC SYSTEM FOR THE PRODUCTION OF ETHYLENE PROPYLENE COPOLYMERS
JP3665970B2 (en) 1994-12-27 2005-06-29 南姜エフニカ株式会社 Deodorizing composition and deodorizing resin composition containing iron (II) compound
US5569679A (en) 1994-12-30 1996-10-29 Russell A. Krueger Pharmaceuticals, Inc. Pharmacologic management of snoring
US20020131933A1 (en) 1996-01-16 2002-09-19 Yves Delmotte Biopolymer membrane and methods for its preparation
US5654061A (en) 1995-01-17 1997-08-05 E. I. Du Pont De Nemours And Company Sulfide scavenging packaging materials
US5574816A (en) 1995-01-24 1996-11-12 Alcatel Na Cable Sytems, Inc. Polypropylene-polyethylene copolymer buffer tubes for optical fiber cables and method for making the same
KR100397384B1 (en) 1995-03-23 2003-12-24 도토기키 가부시키가이샤 Deodorization method, deodorant manufacturing method and deodorizer
US5512144A (en) 1995-03-28 1996-04-30 John E. Stauffer Pulse method for sulfur dioxide electrolysis
US5521268A (en) 1995-03-29 1996-05-28 Eastman Kodak Company Odor reduction in toner polymers
DE19515254C2 (en) 1995-04-26 1998-06-04 Fresenius Ag PVC-free multilayer film, process for producing the same and its use
US5624649A (en) 1995-04-26 1997-04-29 General Electric Co. Process for reduction of sulfur dioxide emission from combustion gases combined with production of potassium sulfate
BE1009397A3 (en) 1995-05-12 1997-03-04 Solvay Tube or multi leaf.
WO1997000717A1 (en) * 1995-06-20 1997-01-09 Donaldson Company, Inc. Filter and method for making a filter
IT1275452B (en) 1995-06-30 1997-08-07 Enichem Elastomers PROCEDURE FOR THE PREPARATION OF ETHYLENE-PROPYLENE COPOLYMERS
DE19534455C1 (en) 1995-09-16 1996-12-12 Fresenius Ag Multilayer plastics tube free from PVC, for medical purposes
US5667799A (en) 1995-10-30 1997-09-16 Caldwell; Larry J. Method for treating headache pain with topical local anesthetic compositions
US5616408A (en) 1995-12-22 1997-04-01 Fiberweb North America, Inc. Meltblown polyethylene fabrics and processes of making same
US5803249A (en) 1996-06-03 1998-09-08 Harsanyi, Jr.; Steve Medical clean up kit
US5910165A (en) * 1996-07-31 1999-06-08 Parker-Hannifin Corporation Receiver/dryer and method of assembly
JPH1053521A (en) 1996-08-12 1998-02-24 Kagaku Gijutsu Shinko Jigyodan Activity suppressor and activity enhancer of intracranial glutaminic acid
GB9617305D0 (en) 1996-08-17 1996-09-25 Glaxo Wellcome Spa Heterocyclic compounds
FR2753396B1 (en) 1996-09-16 1998-10-30 Inst Francais Du Petrole METHOD AND DEVICE FOR TREATING A GAS CONTAINING SULFUR HYDROGEN AND SULFUR DIOXIDE COMPRISING A SULFUR DEPLETION STAGE OF RECYCLED SOLVENT
US5885566A (en) 1996-09-25 1999-03-23 University Of Florida Surface modified surgical instruments, medical devices, implants, contact lenses and the like
US5931303A (en) 1996-09-30 1999-08-03 Salvadori; Lawrence A. Compact, pocketed wrapping for a medical procedure kit and process for using same
JPH10108915A (en) * 1996-10-03 1998-04-28 Hitachi Chem Co Ltd Deodorizing mask
IT1284927B1 (en) 1996-10-08 1998-05-28 Enichem Elastomers PROCEDURE FOR THE PREPARATION OF ETHYLENE PROPYLENE COPOLYMERS WITH A LOW RESIDUAL CHLORINE CONTENT
US5753696A (en) 1996-12-12 1998-05-19 Cluster Technology Corp. Compositions and methods for enhancement of dehydroepiandrosterone
US6106502A (en) 1996-12-18 2000-08-22 Richmond; Frank M. IV sets with needleless fittings and valves
US6267941B1 (en) 1997-01-08 2001-07-31 Nec Corporation Catalyst system for deodorization of a mixture of sulfur compounds and compounds such as aldehydes, alcohols and/or hydrocarbons
US5967061A (en) 1997-01-14 1999-10-19 Energy And Environmental Research Corporation Method and system for reducing nitrogen oxide and sulfur oxide emissions from carbonaceous fuel combustion flue gases
JP3625976B2 (en) 1997-01-30 2005-03-02 高砂香料工業株式会社 Deodorant composition
WO1998043691A1 (en) 1997-03-31 1998-10-08 Lane Eugene Jr Iv prep kit
USRE38597E1 (en) 1997-03-31 2004-09-21 Lane Jr Eugene IV prep kit
CA2287298A1 (en) 1997-04-02 1998-10-08 Konstantin Andreevich Krasnov Tetracyclical derivatives from pyrimidine
US6045596A (en) 1997-04-07 2000-04-04 Medtek Devices, Inc. Filter system to remove a contaminant from a fluid stream
US5779679A (en) 1997-04-18 1998-07-14 Shaw; Thomas J. Winged IV set with retractable needle
DE19718543A1 (en) 1997-05-02 1998-11-05 Braun Melsungen Ag Flexible, tight multi-chamber bag
US5861096A (en) 1997-05-09 1999-01-19 Sabre Oxidation Technologies, Inc. Odor Control In Industrial Lagoons
US5891508A (en) * 1997-06-09 1999-04-06 Portland State University Mask for disguising or counteracting odors
US5935412A (en) 1997-06-17 1999-08-10 Atlantis Limited Partnership Method and apparatus for eliminating odors in sewage systems
JP3035734B2 (en) 1997-06-27 2000-04-24 東京瓦斯株式会社 DMS detector, method for preparing the same, and detector tube for DMS
AU8173898A (en) 1997-06-30 1999-01-19 Kimberly-Clark Worldwide, Inc. Medical packaging paper
US5913859A (en) 1997-07-01 1999-06-22 Shapira; Ira L. Apparatus for extracting bone marrow
US5871562A (en) 1997-07-16 1999-02-16 Culoso; Richard Air conditioning odor control apparatus and method
US5989497A (en) 1997-07-31 1999-11-23 Labonte, Jr.; Roland R. Process and apparatus for deodorizing malodorous substances with a chlorine dioxide-containing composition
EP1000093B1 (en) * 1997-08-01 2001-12-12 The Dow Chemical Company Zwitterionic catalyst activator
DE19735120A1 (en) 1997-08-13 1999-02-18 Peter Hans Prof D Hofschneider Use of thiol-compositions for inactivating virus in cell-free environments
FI105215B (en) 1997-09-05 2000-06-30 Ahlstrom Machinery Oy A method for treating odor gases in a pulp mill
US6238767B1 (en) 1997-09-15 2001-05-29 Kimberly-Clark Worldwide, Inc. Laminate having improved barrier properties
US6094549A (en) 1997-09-26 2000-07-25 Hitachi, Ltd. Electrograph apparatus enabling removal of offensive substances
US6197288B1 (en) 1997-10-16 2001-03-06 Bush Boake Allen, Inc. Malodor counteractant compositions and method for preparing and using same
JPH11123327A (en) * 1997-10-21 1999-05-11 Elf Atochem Japan Kk Adsorbing/desorbing material and its production
US6012586A (en) 1997-11-24 2000-01-11 Maxxim Medical, Inc. Medical procedure kit
US6248733B1 (en) 1998-01-09 2001-06-19 3M Innovative Properties Company Method for limiting the growth of microorganisms using metal-containing compounds
JP2002500233A (en) 1998-01-09 2002-01-08 アリゾナ ボード オブ リーゼンツ Anti-cryptococcal peptides
AR014299A1 (en) 1998-01-14 2001-02-07 Ecolab Inc A PROCEDURE FOR REMOVING A ODOR FROM AN ATMOSPHERIC EFFLUENT, A PRIOR TREATMENT OR A AFTER TREATMENT TO REMOVE A ODOR FROM AN ATMOSPHERIC EFFLUENT AND ATMOSPHERIC EFFLUENT OBTAINED WITH SUCH PROCEDURE.
US6015536A (en) 1998-01-14 2000-01-18 Ecolab Inc. Peroxyacid compound use in odor reduction
US5931304A (en) 1998-01-20 1999-08-03 Hammond; David A. First aid kit and method of replenishing
US6303200B1 (en) 1998-01-27 2001-10-16 Baxter International Inc. Low modulus and autoclavable monolayer medical tubing
US6183758B1 (en) 1998-01-29 2001-02-06 Highland Laboratories, Inc. Phytochemicals, nutrients & medication absorption &/or treatment
FR2774376B1 (en) 1998-02-03 2000-03-17 Elf Aquitaine Exploration Prod PRODUCTION OF STABILIZED AND DEODORIZED ORGANIC POLYSULFIDES
US6070578A (en) 1998-02-23 2000-06-06 Baughman; David A. Breath odor eliminator mask
US5972993A (en) 1998-03-20 1999-10-26 Avon Products, Inc. Composition and method for treating rosacea and sensitive skin with free radical scavengers
US6312713B1 (en) 1998-06-12 2001-11-06 Bernard Korol Polymer matrices for storage and sustained release of drugs and chemicals
US6042640A (en) 1998-06-29 2000-03-28 Xerox Corporation Deodorization of sulfur-containing solvents by oxidation
USD427299S (en) 1998-07-22 2000-06-27 Haslebacher William J Rollably positioned, adjustably directed, clean air supply assembly unit
US6495096B1 (en) 1998-07-30 2002-12-17 Mitsubishi Gas Chemical Company, Inc. Deodorant and process for deodorization using said deodorant
FR2781795B1 (en) 1998-07-31 2000-09-08 Atochem Elf Sa DIMETHYLDISULPHIDE COMPOSITIONS WITH MASKED ODOR
US6060152A (en) 1998-08-21 2000-05-09 Murchie; Colin C. Fabric with microencapsulated breach indication coating
US6521675B1 (en) 1998-09-03 2003-02-18 Bp Corporation North America Inc. Foamed polypropylene sheet having improved appearance and a foamable polypropylene composition therefor
US6221325B1 (en) 1998-09-08 2001-04-24 Marsulex Environmental Technologies, Llc Process for controlling ammonia slip in the reduction of sulfur dioxide emission
US20040121023A1 (en) 1998-11-02 2004-06-24 Victor Stevens Composition to alleviate pain and topical method of applying same
US6365099B1 (en) 1998-11-12 2002-04-02 Fmc Corporation In situ gas scrubbing method and system for odor and corrosion control in wastewater collection systems
US6348177B1 (en) 1999-02-10 2002-02-19 Southwest Research Institute Apparatus and method for bypassing sulfur dioxide around an aftertreatment device in an exhaust gas aftertreatment system
US6479150B1 (en) 1999-02-26 2002-11-12 Kimberly-Clark Worldwide, Inc. Layer materials treated with surfactant-modified hydrophobic odor control agents
DE19910503C1 (en) 1999-03-10 2000-07-06 Daimler Chrysler Ag Desulfating the nitrogen oxide or sulfur oxide storage unit of a catalytic converter comprises variably operating different groups of engine cylinders with different fuel/air ratios
US6203779B1 (en) 1999-03-19 2001-03-20 Charlie Ricci Methods for treating endoleaks during endovascular repair of abdominal aortic aneurysms
CA2367002A1 (en) * 1999-03-19 2000-09-28 Michael A. Moskowitz Increasing cerebral bioavailability of drugs
USD431353S (en) 1999-03-25 2000-10-03 Mellin Carl F Soft body medical instrument case
USD431902S (en) 1999-03-25 2000-10-17 Mellin Carl F Hard body medical instrument case
US6060083A (en) 1999-04-01 2000-05-09 Topical Technologies, Inc. Topical DMSO treatment for palmar-plantar erythrodysethesia
WO2000064868A1 (en) 1999-04-23 2000-11-02 Gaylord Chemical Corporation Process and apparatus for making ultra-pure dmso
EP1206287B1 (en) 1999-05-21 2008-12-17 Micro Therapeutics, Inc. High viscosity embolizing compositions
AU5331300A (en) 1999-06-11 2001-01-02 Henceforth Hibernia, Inc. Prophylactic, therapeutic and industrial antioxidant compositions enhanced with stabilized atomic hydrogen/free electrons and methods to prepare and use such compositions
JP4422819B2 (en) 1999-06-21 2010-02-24 株式会社ロッテ Deodorant, food and drink containing the same, composition for oral cavity and toiletry product
US6426112B1 (en) 1999-07-23 2002-07-30 University Of Kentucky Research Foundation Soy products having improved odor and flavor and methods related thereto
US6680194B1 (en) 1999-07-30 2004-01-20 Central Illinois Light, Co. Mercaptan deodorizing for storage tanks
US6436446B1 (en) 1999-07-30 2002-08-20 Pharmavite Llc Composition for increasing bone density
US6830794B2 (en) 1999-08-13 2004-12-14 Richard G. Cartledge Insulated intravenous administration tubing
US6403642B1 (en) 1999-08-16 2002-06-11 Pq Holding, Inc. Sulfur adsorbent for reducing onion or garlic breath odor
EP1212093B1 (en) 1999-08-26 2004-07-07 Ganeden Biotech, Inc. Use of emu oil as a carrier for antifungal, antibacterial and antiviral medications
US6737089B2 (en) 1999-08-27 2004-05-18 Morinda, Inc. Morinda citrifolia (Noni) enhanced animal food product
US6653352B2 (en) 1999-09-29 2003-11-25 Medical Merchandising, Inc. Pain reliever and method of use
US6723349B1 (en) 1999-10-12 2004-04-20 Emory University Polyoxometalate materials, metal-containing materials, and methods of use thereof
JP3766771B2 (en) * 1999-11-08 2006-04-19 日本エンバイロケミカルズ株式会社 Adsorbent
US6461631B1 (en) 1999-11-16 2002-10-08 Atrix Laboratories, Inc. Biodegradable polymer composition
US6638605B1 (en) 1999-11-16 2003-10-28 Allegiance Corporation Intermittently bonded nonwoven disposable surgical laminates
US20050035062A1 (en) 1999-11-23 2005-02-17 Hiltzik Laurence H. Coated activated carbon for contaminant removal from a fluid stream
WO2001051010A1 (en) 2000-01-11 2001-07-19 Clinical Results, Inc. Dermatological suspensions (micro-matrix)
US6418932B2 (en) 2000-02-10 2002-07-16 The United States Of America As Represented By The Secretary Of The Army Convertible patient isolation pod
JP2003521935A (en) 2000-02-11 2003-07-22 フイラデルフイア・ヘルス・アンド・エデユケーシヨン・コーポレーシヨン Differentiation of bone marrow cells into neuronal cells and uses therefor
US6969483B1 (en) 2000-03-16 2005-11-29 Baxter International Inc. Autoclavable, non-adherent, heat sealable polymer blends for fabricating monolayer and multiple layered films
AU2001255821A1 (en) 2000-03-28 2001-10-08 Cubist Pharmaceuticals, Inc. Enhanced production of secondary metabolites in the presence of organic additives
US20040048376A1 (en) 2000-04-10 2004-03-11 Benoit Chabot Methods for modulating splicing and/or alternative splicing, and for identifying alternatively spliced units in genes
US6844430B2 (en) 2000-04-25 2005-01-18 The Proctor & Gamble Company Articles comprising cationic polysaccharides and acidic pH buffering means
US6412639B1 (en) 2000-04-28 2002-07-02 Closure Medical Corporation Medical procedure kit having medical adhesive
DE10022095B4 (en) 2000-05-08 2005-07-14 Südzucker AG Mannheim/Ochsenfurt Gel of a poly-α-1,4-glucan and starch
US6454097B1 (en) 2000-05-09 2002-09-24 Juan Carlos Aceves Blanco Prioritized first aid kit
ATE361001T1 (en) 2000-05-12 2007-05-15 Vitak Bv FOODS CONTAINING VITAMIN K2
US6440391B1 (en) 2000-06-02 2002-08-27 Elstan Corporation Management of snoring by oral administration of dimethyl sulfone
ATE289335T1 (en) 2000-06-07 2005-03-15 Kraton Polymers Res Bv KINK-RESISTANT MEDICAL HOSE
AU2001274511A1 (en) 2000-06-19 2002-01-02 Bridgestone Corporation Adsorbent, process for producing the same, and applications thereof
GB0015470D0 (en) 2000-06-23 2000-08-16 Bush Boake Allen Ltd Malodor counteractants and methods for preparing and using the same
US6514489B1 (en) 2000-06-30 2003-02-04 Medicis Pharmaceutical Corp. Sulfur containing dermatological compositions and methods for reducing malodors in dermatological compositions
GB0016452D0 (en) 2000-07-04 2000-08-23 Kilgowan Limited Vitamin K and essential fatty acids
US6552231B2 (en) 2000-07-05 2003-04-22 Sloss Industries Corporation Method for making dimethyl sulfone from dimethyl sulfoxide and hydrogen peroxide
AUPQ878600A0 (en) 2000-07-13 2000-08-03 Gropep Pty Ltd Compositions and methods for the treatment of intact skin
US6923955B2 (en) 2000-08-16 2005-08-02 Newlens, Llc Presbyopia treatment by lens alteration
AU2001283413A1 (en) 2000-08-17 2002-02-25 Vase Technology Bi/multi-directional filter cartridge and filter platform for mounting the cartridge thereon
US20020043501A1 (en) 2000-08-22 2002-04-18 Irvine Robert L. Process for treating liquid streams to remove unwanted impurities
CA2420744A1 (en) 2000-09-07 2002-07-18 Solutia Inc. Compositions and methods for reducing odor
US6460539B1 (en) * 2000-09-21 2002-10-08 3M Innovative Properties Company Respirator that includes an integral filter element, an exhalation valve, and impactor element
FR2814533B1 (en) 2000-09-27 2002-10-31 Alstom Power Nv METHOD FOR SIMULTANEOUSLY REDUCING SO2 CO2 EMISSIONS IN A COMBUSTION PLANT
US6722295B2 (en) 2000-09-29 2004-04-20 Bert Zauderer Method for the combined reduction of nitrogen oxide and sulfur dioxide concentrations in the furnace region of boilers
TW546163B (en) 2000-10-05 2003-08-11 Smidth & Co As F L Method for reducing the SOx emission from a plant for manufacturing cement clinker and such plant
GB2368012A (en) 2000-10-19 2002-04-24 Nicholas John Larkins Preparation for the relief of inflammatory disease
US6599472B1 (en) 2000-11-03 2003-07-29 Surface Chemists Of Florida Inc. Oil soluble scavengers for sulfides and mercaptans
CN1469738A (en) 2000-11-09 2004-01-21 �����ʩ���عɷݹ�˾ Soft capsules comprising a starch mixture having reduced branching degree
AU2002235145A1 (en) 2000-11-27 2002-06-03 Conagra Foods, Inc. Stabilization method and composition utilizing an amphoteric polymer
WO2002048032A2 (en) 2000-12-11 2002-06-20 United States Filter Corporation Activated carbon for odor control and method for making same
AU3104102A (en) 2000-12-18 2002-07-01 Univ Texas Local regional chemotherapy and radiotherapy using in situ hydrogel
US6579444B2 (en) 2000-12-28 2003-06-17 Exxonmobil Research And Engineering Company Removal of sulfur compounds from hydrocarbon feedstreams using cobalt containing adsorbents in the substantial absence of hydrogen
US6416772B1 (en) 2001-01-12 2002-07-09 H. Wayne Van Engelen Topical dermal anaesthetic
US20050142096A1 (en) 2001-01-29 2005-06-30 Paul Wegner Product for and method of controlling odor in open waste water treatment environments
EP1227126B1 (en) 2001-01-30 2006-07-19 Daikyo Seiko, Ltd. A rubber composition used for a rubber stopper for a medicament or for a medical treatment or its crosslinked product
WO2002070399A1 (en) 2001-03-06 2002-09-12 Texas Research International, Inc. A chemically and biologically resistant hydration system
US6656723B1 (en) 2001-03-26 2003-12-02 Organic Products Co. Odor controlling composition and methods of making and using
ZA200308347B (en) 2001-03-28 2005-01-27 Sgt Technology Holdings Llc Reducing sulfur dioxide emissions from coal combustion.
US6884797B2 (en) 2001-03-30 2005-04-26 Robert F. Hofmann Targeted oxidative therapeutic formulation
WO2002085975A1 (en) 2001-04-19 2002-10-31 Diversified Chemical Technologies, Inc. Composition of acrylated urethane oligomer, epoxy resin and amine hardener
NZ531337A (en) 2001-04-27 2006-05-26 Gen Hospital Corp Ocular diagnosis of alzheimer's disease
AR050812A1 (en) 2001-06-01 2006-11-29 Stenti Haydee Alba A CHARACTERIZED PHARMACOLOGICAL SOLUTION BECAUSE IT INCLUDES DMSO (DIMETILSULFOXIDE), OXYGEN AND VEGETABLE OILS AND USES IN THE MANUFACTURE OF MEDICINES
US6689438B2 (en) 2001-06-06 2004-02-10 Cryovac, Inc. Oxygen detection system for a solid article
US6902739B2 (en) 2001-07-23 2005-06-07 Nutracea Methods for treating joint inflammation, pain, and loss of mobility
US6578715B2 (en) 2001-07-24 2003-06-17 M-I, L.L.C. Product for treating contaminated fluids and method of making and using the same
US20050176778A1 (en) 2001-08-03 2005-08-11 Vitak Bv Isoprenyl derivatives and their use in the title treatment and prevention of osteoporosis and cardiovascular calcification
IL144949A0 (en) 2001-08-16 2002-06-30 Hadasit Med Res Service Treatment of prion diseases with dmso
US20030108810A1 (en) 2001-08-22 2003-06-12 Williamson Sue Ellen Deodorizing agent for sulfur- or nitrogen-containing salt photoinitiators
US20030109495A1 (en) 2001-08-27 2003-06-12 Kretschmer Louis Frank Nutraceutical solutions comprising dimethyl sulfoxide
US6893627B2 (en) 2001-08-31 2005-05-17 Rutgers, The State University Of New Jersey Method for treating type 2 diabetes with an extract of Artemisia
US20040086888A1 (en) 2001-10-18 2004-05-06 Kornblith Paul L Method for tandem genomic/proteomic analysis of proliferating cells
JP2005519996A (en) 2001-10-18 2005-07-07 ミシガン ステイト ユニバーシティー Method for producing oxazolidinones and method for using the same
JP2005508245A (en) 2001-10-19 2005-03-31 イノベイティブ コンストラクション アンド ビルディング マテリアルズ, エルエルシー Anti-pathogenic air filtration media and air treatment device with protection against infectious airborne microorganisms
JP2003221335A (en) 2001-10-26 2003-08-05 Dey Lp Albuterol and ipratropium inhalation solution, system, kit and method for relieving symptom of chronic obstructive pulmonary disease
EP1448052B1 (en) 2001-11-21 2007-03-21 Altachem Pharma Ltd. Anti-pathogenic composition useful in blood preservation
US20030157006A1 (en) 2001-11-27 2003-08-21 Ecolab Inc. Aromatic substituted nonionic surfactants in soil prevention, reduction or removal in treatment zones
US6764566B1 (en) 2001-12-12 2004-07-20 Kimberly-Clark Worldwide, Inc. Nonwoven filled film laminate with barrier properties
US6706257B1 (en) 2001-12-18 2004-03-16 Discovery Partners, LLC Sunless tanning products and processes
US6652845B2 (en) 2001-12-18 2003-11-25 Kimberly-Clark Worldwide, Inc. Layer materials treated with durable acidic odor control/binder systems
WO2003061696A2 (en) 2002-01-23 2003-07-31 Light Sciences Corporation Systems and methods for photodynamic therapy
EP1482909B1 (en) 2002-02-13 2018-07-04 Creagri, Inc. Method and composition for treatment of inflammation
JP2003306446A (en) 2002-02-14 2003-10-28 Fancl Corp Skin ageing-preventing agent and/or pimple-improving agent kit
US6579543B1 (en) 2002-02-22 2003-06-17 Jackie H. McClung Composition for topical application to skin
US6841173B2 (en) 2002-03-26 2005-01-11 Peter L. Reynolds Compositions and methods directed towards sore muscles and joints
US6881419B2 (en) 2002-04-09 2005-04-19 William E. Lovett Vitamin formulation for enhancing bone strength
AU2003236052A1 (en) 2002-04-11 2003-10-20 Kyowa Hakko Kogyo Co., Ltd. Liquid food/drink containing fat-soluble vitamin and method of stabilizing fat-soluble vitamin
EP1501473A2 (en) 2002-04-16 2005-02-02 Cosmetica, Inc. Polymeric odor absorption ingredients for personal care products
US7578997B2 (en) 2002-04-30 2009-08-25 Kimberly-Clark Worldwide, Inc. Metal ion modified high surface area materials for odor removal and control
US20040001817A1 (en) 2002-05-14 2004-01-01 Giampapa Vincent C. Anti-aging nutritional supplement
US6663679B1 (en) 2002-05-23 2003-12-16 William P. Duncan High intensity, non-reversing humidity indicator
GB0212749D0 (en) 2002-06-01 2002-07-10 Boots Co Plc Personal care compositions
US6860924B2 (en) * 2002-06-07 2005-03-01 Nanoscale Materials, Inc. Air-stable metal oxide nanoparticles
US6723399B2 (en) 2002-06-12 2004-04-20 Ferro Corporation Medical multilayer film structure
US6797042B2 (en) * 2002-06-21 2004-09-28 Pyramid Air Solutions, Inc. Pyramid air cleaner
US6718914B2 (en) 2002-07-23 2004-04-13 Philip J. Riddles Method for neutralizing offensive chemical odors
FR2843069B1 (en) 2002-07-31 2004-10-15 Hutchinson MULTILAYERED ELASTOMERIC MATERIAL LOADED WITH ACTIVE CHEMICAL SUBSTANCE AND USES THEREOF.
US7985422B2 (en) 2002-08-05 2011-07-26 Torrent Pharmaceuticals Limited Dosage form
US8216609B2 (en) 2002-08-05 2012-07-10 Torrent Pharmaceuticals Limited Modified release composition of highly soluble drugs
US8268352B2 (en) 2002-08-05 2012-09-18 Torrent Pharmaceuticals Limited Modified release composition for highly soluble drugs
GB0220182D0 (en) 2002-08-30 2002-10-09 Cardiovascular Res Inst Maastr Organic compounds
US6783004B1 (en) 2002-09-17 2004-08-31 Pilling Weck Incorporated Kit of medical tools for removing screws
MXPA05003272A (en) 2002-09-27 2005-07-05 Nestec Sa Stabilizer-free stabilized coffee aroma.
US20040082667A1 (en) 2002-10-16 2004-04-29 Mccadden Kenneth Hangover treatment
US20040157802A1 (en) 2002-11-15 2004-08-12 Marcus Horwitz Anti-microbial agents derived from methionine sulfoximine analogues
US7368153B2 (en) 2002-12-06 2008-05-06 Cryovac, Inc. Oxygen detection system for a rigid container
US6854135B2 (en) 2002-12-06 2005-02-15 Microtek Medical Holdings, Inc. Reusable, launderable water-soluble coveralls
US20040115818A1 (en) 2002-12-16 2004-06-17 Puri Pushpinder Singh Leak detection by reactions at the leak site
US20050112177A1 (en) 2002-12-20 2005-05-26 Dopson Minter H. Nutritional supplement composition and method
US20050112176A1 (en) 2002-12-20 2005-05-26 Dopson Minter H. Nutritional supplement composition and method
US20050031651A1 (en) 2002-12-24 2005-02-10 Francine Gervais Therapeutic formulations for the treatment of beta-amyloid related diseases
DE10297842T5 (en) 2002-12-27 2005-10-27 Council Of Scientific And Industrial Research Process for the preparation of alkanesulfonic acid
US20040151826A1 (en) 2003-01-14 2004-08-05 Milligan Robert Stieper Injection molded meat-based pet products
KR100905847B1 (en) * 2003-01-17 2009-07-02 주식회사 엘지생활건강 Impregnated multilayered mesoporous and microporus core-shell carbon nanoball for deodorising
US20040265291A1 (en) 2003-01-24 2004-12-30 Flora Technology Inc. Compositions and methods for restoring bacterial flora
US20040197339A1 (en) 2003-01-29 2004-10-07 Brown Paul R. Vaccine for Lyme disease
US20040156742A1 (en) 2003-02-11 2004-08-12 Milan Jolanda Bianca Synergistically-effective cyclohexylethan-1-yl ester mixtures as malodour counteractants as measured physiologically and psychometrically and methods for using same
US8182794B2 (en) 2003-03-05 2012-05-22 Concept Laboratories Sunless tanning products and processes
US7326340B2 (en) 2003-03-05 2008-02-05 Siemens Water Technologies Holding Corp. System for controlling sulfide generation
WO2004093541A1 (en) 2003-03-21 2004-11-04 Dunphy Brian W Formaldehyde-free aqueous tissue preservation compositions
JP3720336B2 (en) 2003-04-30 2005-11-24 住江織物株式会社 Deodorant and production method thereof
US8703121B2 (en) 2003-06-27 2014-04-22 DePuy Synthes Products, LLC Postpartum-derived cells for use in treatment of disease of the heart and circulatory system
KR101110983B1 (en) 2003-07-18 2012-03-13 가부시끼가이샤 하야시바라 세이부쓰 가가꾸 겐꾸조 Accelerator for mineral absorption and use thereof
US8277762B2 (en) 2003-08-01 2012-10-02 Tioga Research, Inc. Apparatus and methods for evaluating the barrier properties of a membrane
US20050031761A1 (en) 2003-08-05 2005-02-10 Donald Brucker Methods of producing a functionalized coffee
US6826948B1 (en) 2003-10-09 2004-12-07 Delphi Technologies, Inc. Leak detection apparatus for a liquid circulation cooling system
US7678367B2 (en) 2003-10-16 2010-03-16 Kimberly-Clark Worldwide, Inc. Method for reducing odor using metal-modified particles
US7438875B2 (en) 2003-10-16 2008-10-21 Kimberly-Clark Worldwide, Inc. Method for reducing odor using metal-modified silica particles
US7754197B2 (en) 2003-10-16 2010-07-13 Kimberly-Clark Worldwide, Inc. Method for reducing odor using coordinated polydentate compounds
US7837663B2 (en) 2003-10-16 2010-11-23 Kimberly-Clark Worldwide, Inc. Odor controlling article including a visual indicating device for monitoring odor absorption
US7879350B2 (en) 2003-10-16 2011-02-01 Kimberly-Clark Worldwide, Inc. Method for reducing odor using colloidal nanoparticles
US20050136125A1 (en) 2003-10-22 2005-06-23 Roth Mark B. Methods, compositions and devices for inducing stasis in cells, tissues, organs, and organisms
AU2004285468B2 (en) 2003-10-22 2011-02-24 Fred Hutchinson Cancer Research Center Methods, compositions and devices for inducing stasis in cells, tissues, organs, and organisms
US7253002B2 (en) 2003-11-03 2007-08-07 Advanced Technology Materials, Inc. Fluid storage and dispensing vessels having colorimetrically verifiable leak-tightness, and method of making same
US20050191343A1 (en) 2003-11-26 2005-09-01 Shire Laboratories, Inc. Micellar systems useful for delivery of lipophilic or hydrophobic compounds
JP3887703B2 (en) 2003-12-01 2007-02-28 学校法人 関西大学 Gelatin fiber and method for producing the same
US7285217B2 (en) 2003-12-02 2007-10-23 Siemens Water Technologies Corp. Removing odoriferous sulfides from wastewater
US7153345B2 (en) 2004-02-04 2006-12-26 Battelle Memorial Institute Sulfur oxide adsorbents and emissions control
US20050182076A1 (en) 2004-02-13 2005-08-18 Adam A. Pachelo (Ano) Tina Weiss Transdermal penetration system and treatment for cellulite
US20050181047A1 (en) 2004-02-18 2005-08-18 Jaime Romero Compositions and methods for timed release of water-soluble nutritional supplements
US7135449B2 (en) 2004-02-20 2006-11-14 Milliken & Company Composition for removal of odors and contaminants from textiles and method
JP2005270589A (en) * 2004-03-22 2005-10-06 Sky Clean:Kk Deodorizing device for chemical smell in hospital using ozone gas
US7553612B2 (en) 2004-03-24 2009-06-30 Showa University Method for cryopreserving microencapsulated living animal cells enclosed in immunoisolation membranes, such microencapsulated living animal cells in immunoisolation membranes, and biohybrid artificial organ modules using such microencapsulated living animal cells in immunoisolation membranes
US20050215515A1 (en) 2004-03-29 2005-09-29 Claudio Bucolo Viscoelastic composition, method of use and package
US20050226827A1 (en) 2004-04-09 2005-10-13 Thienna Ho Skin lightening composition
AR051429A1 (en) 2004-04-20 2007-01-17 Stenti De Pirillo Haydee A OZONIZED PHARMACEUTICAL COMPOSITION AND METHODS TO OBTAIN IT
CN104174071A (en) 2004-04-28 2014-12-03 安希奥设备国际有限责任公司 Compositions and systems for forming crosslinked biomaterials and associated methods of preparation and use
US7351739B2 (en) 2004-04-30 2008-04-01 Wellgen, Inc. Bioactive compounds and methods of uses thereof
US7972601B2 (en) 2004-05-11 2011-07-05 The Regents Of The University Of California Method of promoting delivery of an antioxidant agent to a cell expression neuroligin
JP2005330199A (en) 2004-05-18 2005-12-02 Nippon Kenko Kagaku Kenkyu Center:Kk Joint cream
US7537794B2 (en) 2004-05-21 2009-05-26 David Baldus Animal chew
ITBS20040068A1 (en) 2004-05-24 2004-08-24 Gen Topics Srl COSMETIC AND / OR PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF ROSACEA
US20050266064A1 (en) 2004-05-29 2005-12-01 Mccarthy Kathryn J Cosmetic compositions and methods
BRPI0510938A (en) 2004-06-18 2007-11-20 Dsm Ip Assets Bv Vitamin K1 as Energizer in Cosmetic Formulations
US7255796B2 (en) 2004-07-08 2007-08-14 General Electric Company Method of preventing hydrogen sulfide odor generation in an aqueous medium
US20070241062A9 (en) 2004-07-08 2007-10-18 Simpson Gregory D Synergistic composition and method for odor control
EP1634948A1 (en) 2004-09-10 2006-03-15 Basf Aktiengesellschaft Means and methods for preventing and/or treating caries
CA2580619C (en) 2004-09-20 2013-11-12 Mount Sinai School Of Medicine Use of memantine (namenda) to treat autism, compulsivity, and impulsivity
US7534615B2 (en) 2004-12-03 2009-05-19 Cryovac, Inc. Process for detecting leaks in sealed packages
US20060143767A1 (en) 2004-12-14 2006-07-06 Kaiyuan Yang Breathable protective articles
US20060194759A1 (en) 2005-02-25 2006-08-31 Eidelson Stewart G Topical compositions and methods for treating pain and inflammation
US20060281822A1 (en) 2005-04-20 2006-12-14 Cardinal Associates, Inc. Treatment and prevention of elevated homocysteine
WO2006129149A2 (en) 2005-05-31 2006-12-07 Wockhardt Limited Novel supplements for poultry and livestock
WO2006135854A2 (en) 2005-06-10 2006-12-21 Board Of Regents, The University Of Texas System Antiseptic compositions
US7378084B2 (en) 2005-07-01 2008-05-27 Playtex Products, Inc. Sunless tanning composition and method of sunless tanning
CA2616008A1 (en) 2005-07-21 2007-01-25 Stefan Meuer Stabilized chlorite solutions in combination with fluoropyrimidines for cancer treatment.
WO2007016050A1 (en) 2005-07-28 2007-02-08 Global Cosmeceutical Innovations, Llc Composition and method for treating cellulite
US20080319092A1 (en) 2005-08-05 2008-12-25 Nuvo Research Inc. Transdermal Drug Delivery Formulation
US20070028772A1 (en) * 2005-08-08 2007-02-08 Ravi Jain Method and system for purifying a gas
US20070048386A1 (en) 2005-08-30 2007-03-01 Mallozzi Ottavio Sr Medicament for treating inflammatory and non-inflammatory arthritis
US8480797B2 (en) 2005-09-12 2013-07-09 Abela Pharmaceuticals, Inc. Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors
WO2007033082A2 (en) 2005-09-12 2007-03-22 Abela Pharmaceuticals, Inc. Compositions comprising dimethyl sulfoxide (dmso)
AU2006291134C1 (en) 2005-09-12 2013-08-15 Abela Pharmaceuticals, Inc. Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
WO2007033180A1 (en) 2005-09-12 2007-03-22 Abela Pharmaceuticals, Inc. Materials for facilitating administration of dimethyl sulfoxide (dmso) and related compounds
WO2007049262A1 (en) 2005-10-27 2007-05-03 Berand Limited Methods and compositions for the promotion of neuronal growth and the treatment of asociality and affective disorders
CN101299993A (en) 2005-11-04 2008-11-05 伊士曼化工公司 Carboxyalkylcellulose esters for administration of poorly soluble pharmaceutically active agents
US20080102107A1 (en) 2005-12-16 2008-05-01 Valex Pharmaceuticals, Llc Compositions and methods for transdermal joint pain therapy
US20090215888A1 (en) 2006-03-02 2009-08-27 Singh Jagat Topical nail formulation
KR100698452B1 (en) 2006-05-02 2007-03-23 대한민국(관리부서:농촌진흥청) Development of ruminally protected nutrients and their utilization for milk and beef enrichment
US7282224B1 (en) 2006-06-09 2007-10-16 Guthy-Renker Corporation Pain relief composition
US20070292493A1 (en) 2006-06-15 2007-12-20 Brierre Barbara T Pharmaceutical composition and method for the transdermal delivery of calcium
US20080038219A1 (en) 2006-08-07 2008-02-14 Calgenex Corporation Novel Composition for a Topical Skin Treatment Base and Medicated Applications Thereof
US20080076831A1 (en) 2006-09-22 2008-03-27 Bernard Goetz Hemorrhoid reliever and method of use
RU2463038C2 (en) 2006-10-17 2012-10-10 Нуво Рисерч Инк. Diclofenac gel
WO2008091704A2 (en) 2007-01-25 2008-07-31 Georgetown University Treatment of cushing's syndrome and autism
EP1958639A1 (en) 2007-02-14 2008-08-20 Polichem S.A. Use of chitosans for the treatment of nail inflammatory diseases
US20080260871A1 (en) 2007-04-18 2008-10-23 Fruitman Clinton O Method and composition for infusing herbal extracts and pharmaceuticals through the skin
US20080275015A1 (en) 2007-05-01 2008-11-06 Potter Jeffrey A Formulation and Method for Treating Interstitial Cystitis and Related Bladder Conditions
WO2009158013A1 (en) 2008-06-26 2009-12-30 Nano Terra Inc. Methods for reducing the sensory effects of odorous compounds
BRPI0921494A2 (en) 2008-11-03 2018-10-30 Prad Reasearch And Development Ltd method of planning a underground forming sampling operation, method of controlling a underground forming sampling operation, method of controlling a drilling operation for an underground formation, and method of sampling during the drilling operation.
US20110288123A1 (en) 2008-11-06 2011-11-24 Nuvo Research Inc. Formulations for the treatment of acute herpes zoster pain
EP2493314B1 (en) 2009-10-30 2020-04-08 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (dmso) and methylsulfonylmethane (msm) formulations to treat osteoarthritis
EP2494059B1 (en) 2009-10-30 2016-11-23 Biogenic Innovations, Llc Use of methylsulfonylmethane (msm) to modulate microbial activity
EP2552200B1 (en) 2010-03-31 2015-10-14 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (dmso) formulations for treating autism

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4171542A (en) 1978-06-05 1979-10-23 Buckeye Cellulose Corporation Disposable surgical gown with a bib forming a hand support
US4986016A (en) 1986-12-10 1991-01-22 Wichman William J Folding display frame with offset hub configuration
US5125205A (en) 1986-12-10 1992-06-30 William John Wichman Display frame with folding display attachment devices
US4819275A (en) 1987-11-18 1989-04-11 Lunt Audrey T Disposable gown for medical patients
US5322061A (en) 1992-12-16 1994-06-21 Tecnol Medical Products, Inc. Disposable aerosol mask
US5322061B1 (en) 1992-12-16 1998-06-02 Tecnol Med Prod Inc Disposable aerosol mask
US5765556A (en) 1992-12-16 1998-06-16 Tecnol Medical Products, Inc. Disposable aerosol mask with face shield
US6055982A (en) 1993-12-15 2000-05-02 Kimberly-Clark Worldwide, Inc. Disposable face mask with enhanced fluid barrier
US6099607A (en) 1998-07-22 2000-08-08 Haslebacher; William J. Rollably positioned, adjustably directable clean air delivery supply assembly, for use in weather protected environments to provide localized clean air, where activities require clean air quality per strict specifications
US20030190266A1 (en) 2002-04-05 2003-10-09 Hideyuki Tsurumi Odor eliminating fiber structure having indicator
US6966937B2 (en) 2002-10-22 2005-11-22 Sanki Engineering Co., Ltd. Patient isolation unit

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1966229A4

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9427419B2 (en) 2005-09-12 2016-08-30 Abela Pharmaceuticals, Inc. Compositions comprising dimethyl sulfoxide (DMSO)
US9987625B2 (en) 2006-10-02 2018-06-05 M-I Drilling Fluids Uk Limited Desulfurization agent
GB2443290B (en) * 2006-10-02 2010-03-17 M I Drilling Fluids Uk Ltd Separation agent
US8871675B2 (en) 2006-10-02 2014-10-28 M I Drilling Fluids Uk Ltd. Method of forming an agent and its use in desulphurisation
WO2008040966A1 (en) 2006-10-02 2008-04-10 M-I Drilling Fluids Uk Limited Method of forming an agent and its use in desulphurisation
EP2134447A4 (en) * 2007-03-22 2011-07-06 Mvp Textiles & Apparel Inc Antimicrobial filtration article
EP2134447A2 (en) * 2007-03-22 2009-12-23 Mvp Textiles&Apparel, Inc. Antimicrobial filtration article
CN102421310A (en) * 2009-02-26 2012-04-18 奥特勒洁净室技术有限公司 Clean room, clean room suit and arrangement therefor
US9855212B2 (en) 2009-10-30 2018-01-02 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (DMSO) or DMSO and methylsulfonylmethane (MSM) formulations to treat infectious diseases
US9839609B2 (en) 2009-10-30 2017-12-12 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (DMSO) and methylsulfonylmethane (MSM) formulations to treat osteoarthritis
US10596109B2 (en) 2009-10-30 2020-03-24 Abela Pharmaceuticals, Inc. Dimethyl sulfoxide (DMSO) or DMSO and methylsulfonylmethane (MSM) formulations to treat infectious diseases
US20210093822A1 (en) * 2019-09-27 2021-04-01 Koninklijke Philips N.V. Selectively altering deformation characteristics of a synthetic fabric material
AT17149U1 (en) * 2020-04-17 2021-07-15 Omnignostica Forschungs Gmbh & Co Kg Respirator
WO2022148796A1 (en) * 2021-01-06 2022-07-14 Insu Pharma Ag Protective mask comprising a conductor fabric
WO2023287630A1 (en) * 2021-07-12 2023-01-19 Decarbontek LLC Modular adsorbent devices and applications

Also Published As

Publication number Publication date
WO2007033083A3 (en) 2007-09-27
EP1966229A4 (en) 2010-01-13
US20140116444A1 (en) 2014-05-01
AU2006291134B2 (en) 2013-02-21
US20130052112A1 (en) 2013-02-28
AU2006291134A1 (en) 2007-03-22
CA2622204A1 (en) 2007-03-22
EP1966229B1 (en) 2015-10-21
EP1966229A2 (en) 2008-09-10
US8298320B2 (en) 2012-10-30
JP5399072B2 (en) 2014-01-29
US9186472B2 (en) 2015-11-17
US8440001B2 (en) 2013-05-14
JP2009509724A (en) 2009-03-12
US20080251081A1 (en) 2008-10-16
AU2006291134C1 (en) 2013-08-15
US20110203584A1 (en) 2011-08-25
US7955418B2 (en) 2011-06-07
CA2622204C (en) 2016-10-11

Similar Documents

Publication Publication Date Title
US9186472B2 (en) Devices for removal of dimethyl sulfoxide (DMSO) or related compounds or associated odors and methods of using same
US8480797B2 (en) Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors
CA2742397C (en) Activated carbon systems for facilitating use or treatment with dimethyl sulfoxide (dmso)
CN103742988B (en) Air purification medium unit, air purification device and air purification method
US9421294B2 (en) Deodorizing mask
JP5199441B2 (en) Protective enclosure
JP5155884B2 (en) Multilayer mask
WO2014042171A1 (en) Disposable mask able to collect and adsorb radioactive organic iodine
JP2006187508A (en) Mask
CN111700330A (en) Comfortable respirator feels
CN108618235A (en) catalyst mask
JPH10108915A (en) Deodorizing mask
AU2012216375A1 (en) Systems for removing dimethyl sulfoxide (DMSO) or related compounds, or odors associated with same
CN206586434U (en) Catalyst mouth mask
CN2633397Y (en) Sterilizing and purifying type air filter chip
CN105876931B (en) A kind of Mobyneb haze protective mask
CN100509087C (en) Self-cleaning type gas filter for medical respiratory instrument
CN215347164U (en) Dry and comfortable mask
CN213992532U (en) Iodine-containing compound antibacterial and antiviral daily protective mask
JP2004215693A (en) Water absorption material and diapers
JPH0856796A (en) Deodorant sheet
CN105901803A (en) Multifunctional smog protection respirator

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
ENP Entry into the national phase

Ref document number: 2622204

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2006291134

Country of ref document: AU

Ref document number: 2008530021

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 12066485

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2006291134

Country of ref document: AU

Date of ref document: 20060911

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2006814457

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2993/DELNP/2008

Country of ref document: IN