CA2285942C - Material for purification of physiological liquids of organism, and method of producing the material - Google Patents

Material for purification of physiological liquids of organism, and method of producing the material Download PDF

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CA2285942C
CA2285942C CA002285942A CA2285942A CA2285942C CA 2285942 C CA2285942 C CA 2285942C CA 002285942 A CA002285942 A CA 002285942A CA 2285942 A CA2285942 A CA 2285942A CA 2285942 C CA2285942 C CA 2285942C
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groups
vinyl groups
surface exposed
hydrophilic
molecular
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CA2285942A1 (en
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Vadim Davankov
Maria Tsyurupa
Ludmila Pavlova
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Cytosorbents Corp
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Medasorb Technologies Inc
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/40Introducing phosphorus atoms or phosphorus-containing groups
    • 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3679Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits by absorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D15/00Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • 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
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26Synthetic macromolecular compounds
    • B01J20/261Synthetic macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds
    • 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
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26Synthetic macromolecular compounds
    • B01J20/264Synthetic macromolecular compounds derived from different types of monomers, e.g. linear or branched copolymers, block copolymers, graft copolymers
    • 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
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26Synthetic macromolecular compounds
    • B01J20/265Synthetic macromolecular compounds modified or post-treated polymers
    • 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
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3202Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the carrier, support or substrate used for impregnation or coating
    • B01J20/3206Organic carriers, supports or substrates
    • B01J20/3208Polymeric carriers, supports or substrates
    • B01J20/321Polymeric carriers, supports or substrates consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds
    • 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
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3214Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the method for obtaining this coating or impregnating
    • B01J20/3217Resulting in a chemical bond between the coating or impregnating layer and the carrier, support or substrate, e.g. a covalent bond
    • 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
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3242Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
    • 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
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3242Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
    • B01J20/3268Macromolecular compounds
    • B01J20/3272Polymers obtained by reactions otherwise than involving only carbon to carbon unsaturated bonds
    • 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
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3242Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
    • B01J20/3268Macromolecular compounds
    • B01J20/3278Polymers being grafted on the carrier
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3627Degassing devices; Buffer reservoirs; Drip chambers; Blood filters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2800/00Copolymer characterised by the proportions of the comonomers expressed
    • C08F2800/20Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2810/00Chemical modification of a polymer
    • C08F2810/20Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249987With nonvoid component of specified composition

Abstract

Purification of physiological liquids of organism is performed by passing a physiological liquid with toxicants removed from a patient through a material which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and which is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups with a greater hydrophilicity and greater biocompatibility than those of the vinyl groups.

Description

NtA."I'ERIAL FOR PURIFICATION OF PHYSIOLOGICAL LIQUIDS OF
ORGA.NISM, AND METHOD OF PRODUCING THE MATERIAL
TECHNICAL FIELD
The present invention relates to a material for purification of physiological liqu.ids of organisms, and method of producing the material.

BACKGROUND ART
It is well known that physiological liquids of organisms such as blood, plasma, peritoneal liquid etc., accumulate and transport various toxicants in the case of poisoning the organism as well as in the case of diseases, in particular diseases of liver and kidneys. It is therefore advisable to remove the toxicants from the physiological liquids to significantly improve the situation of the patient. A plurality of methods have been invented and have been utilized for removing toxicants from blood, plasma and other physiological liquids. One of the most efficient methods is hemodialysis. This method, however, is generally restricted to removing small toxic molecules, whereas toxins belonging to the so-called middle-size molecules (between 500 and 30000 Dalton niolecular weight) are eliminated too slowiy, even with modern "high flux"
dialyser membranes. It is believed to be advisable to further improve the existing methods so as to provide an efficient purification of the physiological liquid of organisms, especially with respect to above toxicants having larger molecular sizes, for the purpose of preventing propagation of diseases or curing the disease.
SUMMARY OF INVENTION

In accordance with the present invention, it is proposed to remove a wider spectrum of toxic compouttds from blood or other physiological fluids by supplementing a conventional hemodialysis procedure with an adsorption procedure. The latter should be responsible for removing larger toxins which diffuse through the,membrane of the dialyser too slowly.
Preferably, the adsorbing material should both exhibit high adsorption capacity toward toxins in the middle range of molecular weights and display sufficient compatibility with blood or the corresponding phys-ological fluid. Designing suitable polymeric adsorbing material is one of the aims of the present invention.

Macroporous styrene-divinylbenzene copolymers represent the most popular type of polymeric adsorbing materials. Many companies manufacture adsorbents of this category, AIVIEERLITE T"' XAD-4 (by Rohm and Haas) being probably the best known one. Equally interesting, are macroporous adsorbing materiala wumufacturod by copolymerization of divinylbenzene (DVB) with other monomers, e_g., butyl methacrylate, acrylo nitrile and others, In order to maintain the porous arciiitecture and nearly constant volume of polymenc particles under various conditions of usage, the three-dimensional network of these polyniers has to be sufficiently rigid, i.e., it must contain a high proportion of cirosslinking divinylbenzene. The latter product, when in pure state, is rather expensive.
The more available technical product contains up to 30-40% of ethylvinyl styrene, so that commercially available macroporous adsorbents should be better referred to as copolymers of DVB, ethylvinyl styrene and styrene_ Usually, this monomer mixture is provided with organic solvents serving as the diluents which cause a micro phase separation during the polymerization procedure and thus result in the macroporous structure of the fnal material.

It has been shown repeatedly that the radical polymerization procedure never consumes all the vinyl groups of DVB introduced into copolymerization. On the average, about 30% of DVB species fail to serve as crosslinking bridges and remain involved in the network with only one of its two vinyl groups. The presence of a relatively high amount of pendamt vinyl groups is therefore a characteristic feature afthe macroporous adsorbents. It can be expected that these free vinyl groups are preferably exposed to the surface of the polymer beads and their macropores and should be readily available to chernical modification.
The chemical modification of the surface of macroporous DVB-copolymers relies on chemical rea.ctions of the surface-exposed pendant vinyl groups and aims at converting these groups into more hydrophilic functional groups. This conversion provides the initial hydrophobic adsorbing material with the property of hemocompatibility, since the hydropliilic surfaces adsorb less blood cells and plasma proteins and do not activate the clotting cascades as rapidly as does the initial hydrophobic surface.

Accordingly, it is an object of present invention to provide a material for puri$cation of physiological liquids of organism, which is a further modification in the above specified field.

In accordance with a~trst aspect of the present invention, a material for purification of physiological liquid of an organism, has a size, a shape, and a structure selected so as to remove toxic compounds in the molecu)ar range of 300 to 30000 Dalton from the physiological liquid and is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups which are hydrophilic and biocompatible.
According to a second aspect of the invention, a method of producing a material for purification of a physiological liquid of an organism, comprises the steps of providing a porous hydrophobic divinylbenzene copolymer which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30,000 Dalton from a physiological liquid and which initially has surface exposed vinyl groups; and thereafter chemically modifying the vinyl groups so as to form different surface exposed functional groups which are hydrophilic and biocompatible.

According to a third aspect of the invention, a material for purification of a physiological Fiquid of an organism, has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which tbereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups which are hydrophilic and biocompatible by one of the following procedures:
-grafting hydrophilic polymer chains by a radial polymerization of 2-hydroxyethylmethacrylate, N-vinylpyrroGdone, N-vinylcaprolactame, or other water soluble monomers, -oxidation of the vinyl groups to epoxy groups with a subsequent reaction of the epoxy groups with water, ethylene glycol, aniines or 2-amonoetbanol molecules, and -depositing high-molecular-weight hemocompatible polymer, in particular poly(tritluorethyoxy) phosphazene onto a surface of polymeric beads.

According to a fourth aspect of the invention, a method of producing a material for purification of a physiological liquid of an organism, comprising the steps of providing a porous hydrophobic divinylbenzene copolymer which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30,000 Dalton from a physiological liquid and which initially has surface exposed vinyl groups; and thereafter chemically modifying the vinyl groups so as to form dit%rent surface exposed functional groups which are hydrophilic and biocompatible by one of the following procedures;
-grafting hydrophilic polymer chains by a radial polymerization of 2-hydroxyethylmethacrylate, N-vinylpyrrolidone, N-vinylcaprolactame, or other water soluble monomers, -oxidation of the vinyl groups to epoxy groups with a subsequent reaction of the epoxy groups with water, ethylene glycol, amines or 2-annonoethanol molecules, and -depositing high-molecular-weight hemocompatible polymer, in particular poly(trifluorethyoxy) phosphazene onto a surface of polymeric beads.

~

When the materials for purification of physiological liquids of organisms and tlxe methods of producing the material are provided in accordance with the applicant's invention, they provide for highly advantageous results.

BEST MODE OF CAitItYIlNG (aUT 7HE IIWENTTON

Embodiments of the present invention which provide a purification of physiological liquids of organisms by removing toxicants will now be described. A patient's blood is withdrawn from an axterial blood circulatory access point, passed through a material embodying the present invention which removes toxicants, and re-enters the patient through a venous access point. The material has a size, a shape, and a stnr.cture selected so as to remove the toxic compounds in the molecular range of 300 to 30,000 Dalton from the physiological liquid.

Material embodying the present invention which is produced in accordance with the inventive production method, is a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which therea#ter the vinyl groups are chemically modified so as to form different surface exposed functional groups which are hydrophilic and bioconapatible, 'preferably with a greater hydrophilicity and greater biocompatibility than those of the viinyl groups.

Preferably, the modification of the surface vinyl groups is taade in aqueous or aqueous organic media by one of the following three principal directions;

- graiting hydrophilic polymer chains by a radial polymerization of 2-hydroxyethyl metha.crylate, N-vinylpyrrolidone, N-vinylcaprolactwne, or other water soluble monomers, - oxidation of the vinyl groups to epoxy groups with the subsequent reaction of the epoxy groups with water, ethylene glycol, aznines or 2-amonoethanol molecules, and - depositing high-molecular-weight hemocompatible polymer, in particular poly(trifluorethyoxy) phosphazene onto the surface of the polymeric beads.

In any case the hydrophilic nature of thus naodified surfaces could be visualized by the easy wetting of dried modiflcation material with water, whereas the initial dry unmodified adsorbent cannot be wetted by an immediate contact with water.

In the following examples, a mesoporous divinylbenzerae-etrylstyrene-styrene copolymer, a typical polystyrene-type adsorbing material and a copolymer of DVB
with buthyl methactylate with surface exposed double bonds were taken for the modification.

The surface-modified materials were shown to exhibit good hemocompatibility, i.e_, they did not change noticeably the coagulation time of blood, caused no hemolysis and showed no cytotoxicity effects. When contacted with plasma or whole blood, the materials effectively removed the pool of middle-sized molecules, as could be easily followed by conventional spectrophotometric measurements.

Preparation of mesoporous divinylbenzerie copolymers Example 1 A solution of 130 g p-ethylstyrene, 132 g divinylbenzene (a mixture of para and metha-isomers of about 1:1) and 2.62 g benzoyl peroxide in a mixture of 150 mi toluene and 100 ml iso-amyl alcohol was suspended in 4 liters of pure water containing 1% cellulose stabilizer. After 39 min stirring at room temperature, the mixture was heated at 40 C for I
hours, 60 C for 2 hours, 80 C for 5 hours and 90 C for 2 hours. After cooling the mixture to'room temperature, the beads of the material obtained were filtered and washed with hot water, methanol and water. The polymer was dried in an oven at 80 C within one day.

Example 2 A solution of 75 g buthyl acrylate, 51 g divinylbenzene (a mixture of para and metha-isomers of about 1:1) and 1 g benzoyl in 250 ml of toluene was suspended in 2.4 liters of pure water containing 15 g of cellulose stabilizer at room temperature. After 30 min stirring, the mixture was heated stepwise at 60, 80 and 95 C vvithin 3 hours for each temperature.
After cooling to room temperature, the beads obtained were filtered, washed with hot water, methanol and water. Ttie beads were dried in oven for 7 hours at 80 C.

SUBSTITUTE SHEET (RULE 26) Grafting hydrophilic polymeric chains to the surface exposed vinyl groups Example 3 The polymer prepared in Example 1 was washed with ethanol and then rinsed with water, which results in a material fully wetted by water with all its pores filled with water. The material contains 40% polymer and 60% water. To 1 g of the polymer thus wetted with water, 1 ml of 3%
aqueous solution of 2-hydroxyethyl methacrylate (HEMA) and 0.1 mi of 10%
aqueous ammonium persulfate were added, and, under constant stirring of the mixture with a magnetic stirrer, provided with an aqueous solution of sodium sulfite (2 moles per mole of persulfate). The mixture was slowly mixed at a temperature of 40 C for 2 hours or at a temperature of 10 C for 10 h. The polymer was filtered, washed with water and dried at a temperature below 80 C.

Example 4 To 1 g of dry polymer prepared in Example 1, 3, 5 mi of ethanol and then 1.6 ml of 6% aqueous solution of HEMA, 0.3 ml of 10% aqueous solution of ammonium persulfate, and finally 0.3 ml of 1 M aqueous solution of sodium sulfite (or 0.3 mi of 0.5 M solution of ascorbinic acid) were added.
The mixture was stirred for 10 h at a temperature of 10 C. The polymer was filtered, washed with water and dried at 'ir0 C.

The copolymer of divinylbenzene with buthyl methacrylate prepared in Example 2 was grafted with E-IEMA in exactly the same manner.
SU8STITUTE SHEET (RULE 26) Example 5 To I g of the wetted with water polymer prepared in Example 1, 1.0 mf of 6% aqueous solution of N-vinylpyrrolidone, and 0.2 mi of 10%
aqueous solution of ammonium persulfate were added, and the mixture was S stirred for 2 h at a temperature of 40 C. The polymer was filtered, washed with water and dried.

Example 6 To 1 g of the polymer wetted with water and prepared in Example 1 2.0 mi of 3% N-vinylpyrrolidone, 0.3 ml of aqueous 10% solution of sodium persulfate and 0.3 mi of sodium sulfite solution were added and the mixture was stirred at 25 C for 2 h. The polymer was filtered and treated as above.

Polymer analogous reactions on the surface exposed double bonds Example 7 To 1 g of the polymer wetteci with water and prepared in Example 2, 2.0 mi of 3% N-acryiamide, 0.3 ml of aqueous 10% solution of sodium persulfate and 0.3 ml of 1 M aqueous solution of sodium sulfite were added and the mixture was stirred at 25 C for 2 h. The polymer was filtered t0 and treated as above.

Example 8 SUBSTITUTE SHEET (RULE 26) *rB

To 6 g of dry polymer prepared in Example 1, 25 ml of acetic anhydride were added, the mixture was cooled to 0 C, slowly provided with 2 mi of aqueous 40% solution of hydrogen peroxide, and stirred at 10-15 C
for 8 h. The polymer was filtered, washed with glacial acetic acid to result in epoxy groups containing material.

2 g of the above epoxy modified polymer, swollen with glacial acetic acid, were provided with 10-15 ml water and 2 drops of concentrated sulfuric acid and heated under stirring 50-70 C for 3-5 h, thus converting epoxy groups into diol groups. The polyrner was filtered, carefully washed with water and dried.

Example 9 To 2 g of the epoxy modified (according to Example 7) polymer, swollen with glacial acetic acid, I ml of ethylene glycol in 5 ml glacial acetic acid (or 5 ml dry ethyl acetate) were added, provided with 2 drops of concentrated sulfuric acid and heated under stirring for 5-8 h at 50-70 C.
This procedure results in the addition of ethylene glycol to the epoxy functional group. The polymer is filtered, washed with water, ethanol and again with water, and dried.

Example 10 2 g of the epoxy modified (according to Example 7) polymer, swollen with glacial acetic acid) were carefully washed with dry ethyl acetate and provided with 1 ml of 2-hydroxyethyl amine in 4 ml ethyl acetate. The mixture was stirred at 40 C for 5h, which results in the addition of the SUBSTITUTE SHEET (RULE 26) WO 99/39823 PC1'/US98/27739 hydroxyethylamino group to the epoxy group. The polymer was filtered, washed with water, 1 NHCI and again water to neutral pH.

In a separate experiment, diethylamine was taken, instead of 2-hydroxyethyl amine. The product was washed with water 1 N HCI and water as described above.

Depositing poly(trifluoroethoxy) phosphazene onto the surface of the polymer (molecular weight 20.106 IDalton) Example 11 The product obtained in Example 9 was dried in vacuum. A
soiution of 0.3 mg poly(trifluoroethoxy) phosphazene (molecular weight 20 106) in 10 ml ethyl acetate were added quickly to 3 g of the dried polymer and agitated until the whole of the solvent was totally absorbed by beads of the polymer. The material was then dried under reduced pressure and washed with ethanol.

Example 12 3 g of dry unmodified polymer prepared in Example 2 were quickly provided with a solution of I mg poly(trifluoroethoxy) phosphazene in 10 ml ethyi acetate and then dried from the solvent as described in Example 10.

SU9STITUTE SHEET (RULE 26) It will be understood that each of the elements described above, or two or more together, may also find a useful application in other types of methods and products differing from the types described above.
While the invention has been illustrated and described as embodied in method of and material for purification of physiological liquids of organism, and method of producing the material it is not intended to be limited to the details shown, since various modifications and structural changes may be made without departirig in any way from the spirit of the present invention.

Without further analysis, the foregoing will so fully reveal the gist of the present invention that others can, by applying current knowledge, readily adapt it for various applications without omitting features that, from the standpoint of prior art, fairly constitute essential characteristics of the generic or specific aspects of this invention.

What is claimed as new and desired to be protected by Letters Patent is set forth in the appended clairris.

SUBSTITUTE SHEET (RULE 26)

Claims (13)

1. A material for purification of a physiological liquid of an organism, which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups which are hydrophilic and biocompatible.
2. A material as defined in claim 1, wherein said porous hydrophobic divinylbenzene copolymer comprises a copolymer of divinylbeazene with comonomers selected from the group consisting of styrene, ethylstyrene, acrylo nitrile, and buthyl methacrylate.
3. A material as defined in claim 1, wherein said surface exposed functional groups which are hydrophilic and biocompatible are grafted hydrophilic polymeric chains selected from the group consisting of polymers of 2-hydroxyethyl methacrylate, N-vinylpyrrolidone, N-vinylcaprolactame, and N-acrylamide.
4. A material as defined in claim 1, wherein said exposed functional groups which are hydrophilic and biocompatible are products of oxidation of said vinyl groups to epoxy groups and subsequent addition of polar compounds selected from the group consisting of water, ethylene glycole, small primary or secondary amines, and hydroxyethyl-amine.
5. A material as defined in claim 4, wherein said surface exposed functional groups which are hydrophilic and biocompatible are products of oxidation of said vinyl groups to epoxy groups and subsequent addition-of small primary or secondary amines or 2-hydroxyethyl-amine and depositing high-molecular-weight poly(trifluoroethoxy) phosphazene.
6. A method of producing a material for purification of a physiological liquid of an organism, comprising the steps of providing a porous hydrophobic divinylbenzene copolymer which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30,000 Dalton from a physiological liquid and which initially has surface exposed vinyl groups; and thereafter chemically modifying the vinyl groups so as to form different surface exposed functional groups which are hydrophilic and biocompatible.
7. A method of producing the material as defined in claim 6, wherein said chemical modification of vinyl groups comprises the step of graft polymerization in an aqueous or aqueous organic media of water soluble monomers selected from the group consisting of 2-hydroxyethyl methacrylate, N-vinylpyrrolidons, N-vinylcaprolactame, and N-acrylamide.
8. A method of producing the material as defined in claim 6, wherein said chemical modification of vinyl groups includes oxidation of said vinyl groups to epoxy groups followed by addition to the epoxy group of polar compounds selected from the group consisting of water, ethylene glycole, small primary or secondary amines, and 2-hydroxyethyl-amine.
9. A method as defined in claim 8, wherein said oxidation of said vinyl groups to epoxy groups is followed by addition to the epoxy groups of small primary or secondary amines or 2-hydroxyethyl-amine and then depositing high-moIecular-weight poly(trifluoroethoxy) phosphazene from its solution in an organic solvent via complexing the above polyphosphazene with the surface exposed amino groups,
10. A material for purification of a physiological liquid of an organism, having a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and being composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups which are hydrophilic and biocompatible by one of the following procedures:
-grafting hydrophilic polymer chains by a radial polymerization of 2-hydroxyethylmethacrylate, N-vinylpyrrolidone, N-vinylcaprolactame, or other water soluble monomers, -oxidation of the vinyl groups to epoxy groups with a subsequent reaction of the epoxy groups with water, ethylene glycol, amines or 2-amonoethanol molecules, and -depositing a high-molecular-weight hemocompatible polymer onto a surface of polymeric beads,
11. A material as defined in claim 10, wherein the high-molecular-weight hemocompatible polymer comprises poly(trifluorethyoxy) phosphazene.
12. A method of producing a material for puzification of a physiological liquid of an organism, comprising the steps of providing a porous hydrophobic divinylbenzene copolymer which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30,000 Dalton from a physiological liquid and which initially has surface exposed vinyl groups; and thereafter chemically modifying the vinyl groups so as to form different surface exposed functional groups which are hydrophilic and biocompatible by one of the following procedures:
-grafting hydrophilic polymer chains by a radial polymerization of 2-hydroxyethylmethacrylate, N-vinylpyrrolidone, N-vinylcaprolactame, or other water soluble monomers, -oxidation of the vinyl groups to epoxy groups with a subsequent reaction of the epoxy groups with water, ethylene glycol, amines or 2-amonoethanol molecules, and -depositing high-molecular-weight hemocompatible polymer onto a surface of polymeric beads.
13, A method as defined in claim 12, wherein the high-molecular-weight hemocompatible polymer comprises poly(trifluorethoxy) phosphazene.
CA002285942A 1998-02-06 1998-12-30 Material for purification of physiological liquids of organism, and method of producing the material Expired - Lifetime CA2285942C (en)

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US6114466A (en) 2000-09-05
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JP2001524878A (en) 2001-12-04
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US6087300A (en) 2000-07-11
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US6133393A (en) 2000-10-17
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