US20040193202A1 - Integrated lance and strip for analyte measurement - Google Patents

Integrated lance and strip for analyte measurement Download PDF

Info

Publication number
US20040193202A1
US20040193202A1 US10/460,030 US46003003A US2004193202A1 US 20040193202 A1 US20040193202 A1 US 20040193202A1 US 46003003 A US46003003 A US 46003003A US 2004193202 A1 US2004193202 A1 US 2004193202A1
Authority
US
United States
Prior art keywords
lance
lancing
channel
separation
separation element
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
US10/460,030
Inventor
John Allen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LifeScan Inc
Original Assignee
LifeScan 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=32853620&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20040193202(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by LifeScan Inc filed Critical LifeScan Inc
Priority to US10/460,030 priority Critical patent/US20040193202A1/en
Assigned to LIFESCAN, INC. reassignment LIFESCAN, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ALLEN, JOHN J.
Priority to IL16082704A priority patent/IL160827A0/en
Priority to KR1020040020329A priority patent/KR101065599B1/en
Priority to TW093108213A priority patent/TWI324059B/en
Priority to DE602004000825T priority patent/DE602004000825T2/en
Priority to EP06075525.3A priority patent/EP1674037B2/en
Priority to ES06075525.3T priority patent/ES2321330T5/en
Priority to DK06075525.3T priority patent/DK1674037T4/en
Priority to DE602004019952T priority patent/DE602004019952D1/en
Priority to JP2004092767A priority patent/JP4531423B2/en
Priority to AT04251803T priority patent/ATE325579T1/en
Priority to AT06075525T priority patent/ATE424763T1/en
Priority to SG200401667A priority patent/SG115655A1/en
Priority to EP04251803A priority patent/EP1464284B1/en
Priority to CA2462364A priority patent/CA2462364C/en
Priority to CNB2004100314147A priority patent/CN100393277C/en
Publication of US20040193202A1 publication Critical patent/US20040193202A1/en
Priority to HK05101576A priority patent/HK1069094A1/en
Priority to US11/231,130 priority patent/US7169117B2/en
Priority to US11/251,189 priority patent/US7473264B2/en
Priority to HK06112206.9A priority patent/HK1091707A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1486Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using enzyme electrodes, e.g. with immobilised oxidase
    • EFIXED CONSTRUCTIONS
    • E01CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
    • E01DCONSTRUCTION OF BRIDGES, ELEVATED ROADWAYS OR VIADUCTS; ASSEMBLY OF BRIDGES
    • E01D19/00Structural or constructional details of bridges
    • E01D19/08Damp-proof or other insulating layers; Drainage arrangements or devices ; Bridge deck surfacings
    • E01D19/083Waterproofing of bridge decks; Other insulations for bridges, e.g. thermal ; Bridge deck surfacings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14507Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood
    • A61B5/1451Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood for interstitial fluid
    • A61B5/14514Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue specially adapted for measuring characteristics of body fluids other than blood for interstitial fluid using means for aiding extraction of interstitial fluid, e.g. microneedles or suction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14532Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150015Source of blood
    • A61B5/150022Source of blood for capillary blood or interstitial fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150206Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
    • A61B5/150213Venting means
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150358Strips for collecting blood, e.g. absorbent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150374Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
    • A61B5/150381Design of piercing elements
    • A61B5/150442Blade-like piercing elements, e.g. blades, cutters, knives, for cutting the skin
    • A61B5/15045Blade-like piercing elements, e.g. blades, cutters, knives, for cutting the skin comprising means for capillary action
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150374Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
    • A61B5/150381Design of piercing elements
    • A61B5/150442Blade-like piercing elements, e.g. blades, cutters, knives, for cutting the skin
    • A61B5/150465Specific design of proximal end
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/150007Details
    • A61B5/150374Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
    • A61B5/150381Design of piercing elements
    • A61B5/150503Single-ended needles
    • A61B5/150511Details of construction of shaft
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/151Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/151Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
    • A61B5/15146Devices loaded with multiple lancets simultaneously, e.g. for serial firing without reloading, for example by use of stocking means.
    • A61B5/15148Constructional features of stocking means, e.g. strip, roll, disc, cartridge, belt or tube
    • A61B5/15157Geometry of stocking means or arrangement of piercing elements therein
    • A61B5/15165Piercing elements stocked in or on a strip
    • A61B5/15167Characterized by a folded strip
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/68Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A61B5/6848Needles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B10/00Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
    • A61B10/0045Devices for taking samples of body liquids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/3209Incision instruments
    • A61B17/32093Incision instruments for skin incisions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/02Details of sensors specially adapted for in-vivo measurements
    • A61B2562/0295Strip shaped analyte sensors for apparatus classified in A61B5/145 or A61B5/157
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/02028Determining haemodynamic parameters not otherwise provided for, e.g. cardiac contractility or left ventricular ejection fraction
    • A61B5/02035Determining blood viscosity
    • EFIXED CONSTRUCTIONS
    • E01CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
    • E01DCONSTRUCTION OF BRIDGES, ELEVATED ROADWAYS OR VIADUCTS; ASSEMBLY OF BRIDGES
    • E01D19/00Structural or constructional details of bridges
    • E01D19/06Arrangement, construction or bridging of expansion joints

Definitions

  • the present invention relates, in general, to lancing elements for use in drawing bodily fluids out of a patient and, more particularly, to an improved lancing element including first and second elements positioned relative to each other such that an incision formed by the first element is held open by the second element and bodily fluids are pulled up the lancing element by surface tension on the first and second lancing elements.
  • Integrated skin lancing and body fluid analysis samplers are known in the art.
  • One such system is described and illustrated in WO 02/49507.
  • the integrated system described in WO 02/49507 includes a lancing element or lance, which is attached to or integrated with a test strip adapted to measure the quantity of an analyte in bodily fluid or, alternatively, some characteristic of the bodily fluid.
  • Usable bodily fluids may include, for example, blood or interstitial fluid (ISF).
  • ISF interstitial fluid
  • the lancing element is used to make an incision in the skin and the bodily fluid is drawn up the lancing element to the test strip by, for example, capillary action.
  • Such integrated samplers may be combined with, for example, an electrochemical meter and referred to as monolithic or in-situ sampling devices.
  • Hollow needles have also been described for use in drawing fluids out of the body for testing purposes; such needles may have a pointed or beveled end to facilitate opening the incision.
  • the incision is held open by the outer diameter of the needle to facilitate the flow of bodily fluids out of the incision and the bodily fluids are drawn up the needle either by a vacuum or by capillary action or by a combination of vacuum and capillary action.
  • the lance is a flat or partially curved piece which includes an open channel for guiding fluid from the sharpened tip to the proximal end of the lance by means of, for example, surface tension and/or capillary action.
  • lacing elements are advantageous because of the ease of manufacture and the ease of integrating them into, for example, a test strip, in order to facilitate both lancing and measurement in a single element.
  • the landing element is a flat or partially flat piece which includes an open channel for guiding fluid, it is possible for the edges of the incision to close on the channel, fully or partially blocking the channel and preventing bodily fluids from flowing to the proximal end of the channel or limiting the amount of fluid which can flow.
  • the lancing element is a flat or partially curved piece including an open channel and the lancing element includes a separation element for holding the incision open when the lancing element is in the wound and preventing the edges of the incision from closing on the lancing element and partially or fully blocking the open channel. It would be advantageous to design a lancing device wherein the separation element is positioned slightly proximal to the sharpened tip of the lancing element to facilitate insertion of the lance into the skin. It would further be advantageous to design a lancing device wherein the lancing element and the separation element are formed from a single metal sheet.
  • lancing device wherein the lancing element and the separation element are positioned opposite each other such that fluid is pulled up the lancing element and into the open channel by surface tension between the fluid and the lancing element and separation element, thus facilitating the filling of the channel. It would further be advantageous to design a lancing device wherein the lancing element and the separation element are formed from a single sheet of metal rolled to position the separation element opposite the lancing element such that the proximal end of the lancing element and the separation element form an open channel. It would further be advantageous to manufacture the lancing devices described herein using, for example, a metal forming or stamping process.
  • a lance according to the present invention includes a lancing element having a first sharpened end point, a separation element having a second sharpened end point wherein the second sharpened end point is positioned proximal to the first sharpened end point, a connector connecting a proximal portion of the first lancing element to a proximal portion of the separation element, the connector forming a channel.
  • the separation element is positioned at an angle to the lancing element.
  • the lancing element, the separation element and the channel are formed from a single sheet of metal.
  • a space between the lancing element and the separation element forms a gap, the gap increasing in size proximal to the second sharpened tip.
  • least a portion of the channel is treated with a hydrophilic surface coating.
  • at least a portion of the lancing element and at least a portion of the separation element are coated with a hydrophilic surface coating.
  • a proximal end of the channel is integrated into a sensor strip.
  • the sensor strip is connected at a proximal end thereof to a plurality of additional sensor strips
  • FIG. 1 is a perspective view of a lancing element and strip according to the present invention.
  • FIG. 2 is a perspective view of the top layer of a lancing element and strip according to the present invention.
  • FIG. 3 is a perspective view of another embodiment of the invention in which multiple strips form an array of sensors for use in a cartridge format.
  • FIG. 1 is a perspective view of lance 15 and sensor strip 100 according to the present invention.
  • lance 15 is connected to sensor strip 100 .
  • Sensor strip 100 may be, for example, a glucose sensor strip which uses electrochemistry to measure the amount of glucose in a bodily fluid, such as, for example, blood or interstitial fluid.
  • sensor strip 100 may be, for example, a coagulation sensor which measures a physical characteristic of a body fluid such as viscosity, capacitance, resistance, and the like.
  • lance 15 further includes lancing element 22 and separation element 24 .
  • Sensor strip 100 further includes first electrode contact 10 , adhesive layer 11 , conductive substrate 12 , vent hole 13 , second electrode contact 17 , insulating substrate 18 , insulating layer 20 , registration hole 23 and working electrode 36 .
  • sensor strip 100 may have an approximate width of 0.22 inches and an approximate length of 0.55 inches.
  • FIG. 2 is a perspective view of lance 15 and the top layer of sensor strip 100 for use in the present invention.
  • the top layer of sensor strip 100 and lance 15 is formed from conductive substrate 12 .
  • conductive substrate 12 includes vent hole 13 and registration hole 23 .
  • lance 15 includes lancing element 22 , separation element 24 and fill channel 21 .
  • sensor strip 100 includes first electrode contact 10 , wherein first electrode contact 10 may be screen printed on an insulating substrate 18 , and a second electrode contact 17 , wherein second electrode contact 17 comprises a portion of conductive substrate 12 which is contiguous with reference electrode 37 and lance 15 .
  • first electrode contact 10 and second electrode contact 17 are arranged such that an analyte measurement meter, such as, for example, a glucose meter (not shown) can establish electrical contact with sensor strip 100 .
  • first electrode contact 10 and second electrode contact 17 are arranged on the same side of insulating substrate 18 to facilitate contact of both electrodes at the distal end of sensor strip 100 .
  • Sensor strip 100 is manufactured using adhesive layer 11 to attach insulating substrate 18 to conductive substrate 12 .
  • Adhesive layer 11 could be implemented in a number of ways, including using pressure sensitive material, heat activated material, or UV cured double sided adhesive material.
  • Conductive substrate 12 may be, for example, a sheet of electrically conductive material such as gold or plated stainless steel.
  • the geometry of conductive substrate 12 may be formed by, for example, stamping process or photo etching.
  • lance 15 may be manufactured as an integral part of conductive substrate 12 .
  • Vent hole 13 may be formed by, for example, punching through conductive substrate 12 . Vent hole 13 is used to facilitate the transport of bodily fluid up lance 15 and across working electrode 36 .
  • Registration hole 23 may be formed during the stamping process of making conductive substrate 12 .
  • an analyte sensing layer may be, for example, a glucose sensing layer, including an enzyme, a buffer, and a redox mediator.
  • An analyte sensing layer (not shown) may preferably be deposited on top of working electrode 36 . Where an analyte sensing layer is used to detect the presence and concentration of glucose in a bodily fluid, at least a portion of glucose sensing layer dissolves in the bodily fluid and is used to convert the glucose concentration into an electrically measured parameter which is proportional to the glucose concentration in the sample.
  • lance 15 has a distal and proximal end and the proximal end is integrated with reference electrode 37 and the distal end includes sharpened tip 38 at the distal end of lacing element 22 .
  • Lance 15 may be formed by the process of stamping or photo-etching a conductive metal sheet. Photo-etching lance 15 is also beneficial in facilitating the manufacture of a lancing element which has a sharp lancing element 22 and separation element 24 . In a subsequent process step, lance 15 , lancing element 22 , and separation element 24 may be bent to form a “V” or “U” shaped channel geometry as shown in FIG. 2.
  • Fill channel 21 serves as a conduit from lancing element 22 and separation element 24 to working electrode 36 and reference electrode 37 .
  • the distal end of lacing element 22 and separation tip 40 of separation element 24 are offset by about 0.005 inches to 0.020 inches.
  • lance 15 is adapted to more effectively cut skin due to a sharper leading point of lancing element 22 .
  • the extreme distal end of lance 15 comprises only sharpened tip 38 which may be a very sharp point or edge to facilitate the initial incision as lancing element 22 enters the skin.
  • the leading point of lance 15 would include both sharpened tip 38 and separation tip 40 making the combination less sharp than the embodiment illustrated in FIG. 2 and requiring more force to create the initial incision.
  • the lance 15 further includes reference electrode 37 and second electrode contact 17 .
  • Alternative embodiments may include forming all of the electrodes and electrode contacts on insulating substrate 18 .
  • lance 15 includes fill channel 21 , wherein the seamless transition between the lancing element 22 and separation element 24 ; and fill channel 21 facilitates the flow of body fluid from the wound to working electrode 36 . Additionally, the seamless transition between the lancing element 22 , separation element 24 and fill channel 21 prevents the introduction of stop junctions which can impede the capillary flow rate of liquid samples.
  • the unique geometry increases the likelihood that a liquid sample will sufficiently cover working electrode 36 and reference electrode 37 regardless of the height of the lance 15 above or below the skin wound, or even if lance 15 lies horizontally offset from the wound.
  • sample can be applied to the side of lance 15 rather than just the proximal end of lance 15 which provides a user the option of dosing sample onto sensor strip 100 after a site has been lanced separately.
  • the gap 42 between lancing element 22 and separation element 24 guides bodily fluids into fill channel 21 .
  • the increasing separation between lancing element 22 and separation element 24 as fluid moves distally towards fill channel 21 facilitates the drawing of fluid into fill channel 21 and from fill channel 21 to sensor strip 100 .
  • Gap 42 is also advantageous in that it facilitates the introduction of bodily fluids into fill channel 21 by facilitating the flow of bodily fluids positioned to the side of gap 42 , thus enhancing the ways in which sensor strip 100 may be used to gather bodily fluids.
  • Fill channel 21 may facilitate the flow of bodily fluids by, for example, wicking or capillary action.
  • fill channel 21 has an open geometry which facilitates the wicking of viscous samples and provides for simpler manufacturing techniques when compared with closed capillary channels.
  • fill channel 21 may be coated with a surfactant coating or undergo a hydrophilic surface treatment to increase the capillary force within fill channel 21 .
  • separation element 24 and lancing element 22 may be coated with a surfactant coating or undergo hydrophilic surface treatment to increase the capillary flow force within gap 42 .
  • the open geometry of fill channel 21 facilitates the wicking of sample because it prevents the formation of a vacuum block.
  • a capillary inlet can become plugged if it is positioned too close to the wound or inside the wound preventing air from facilitating the flow of sample to the capillary.
  • the open geometry of fill channel 21 With the open geometry of fill channel 21 , the proximal end of lance 15 can be positioned arbitrarily close to the source of the blood and allow for sufficient fill of sample.
  • the open geometry of fill channel 21 has the capacity to hold a larger sample volume than the minimum sample volume to cover reference electrode 37 and working electrode 36 . The open geometry of fill channel 21 thus allows excess sample to accumulate along fill channel 21 which helps leave a cleaner wound site.
  • the geometry of reference electrode 37 may be formed during the stamping process which effectively embosses the surface of conductive substrate 12 .
  • the stamping process may provide the pressure needed to create a recess in conductive substrate 12 which can help define the distance between reference electrode 37 and working electrode 36 .
  • insulating substrate 18 consists of material such as polyester or ceramic on which a conductive material can be printed onto insulating substrate 18 through silk-screening, sputtering, or electro-less deposition. Conductive material deposited on insulating substrate 18 forms first electrode contact 10 and working electrode 36 . Insulating layer 20 may be, for example, screen printed to form a boundary for first electrode contact 10 and working electrode 36 .
  • FIG. 3 is a perspective view of another embodiment of the invention in which multiple strips form an array of sensors for use in a cartridge format. Such an array may be inserted into a meter (not shown) having strips dispensed in a serial manner, one by one.
  • the format of this embodiment allows a row of strips to be folded in a manner similar to an accordion wherein several strips similar to sensor strip 100 in FIG. 1 are attached together on an arrangement which facilitates their use in a cartridge.
  • conductive substrate 12 is stamped in a progressive manner to form lance 15 such that several of them are chained together in series. The stamping process of conductive substrate 12 forms index hole 31 , neck 32 , and contact hole 33 .
  • a second electrode layer (not shown) comprising an adhesive layer and glucose sensing layer would be attached to conductive substrate 12 as illustrated in FIG. 3.
  • a contact area for a reference electrode for all of the strips within the array may be formed using a single area within conductive substrate 12 .
  • individual contacts must be made for working electrode 36 for all of the strips within the array.
  • index hole 31 is used to index the strip cartridge so that it can move a fresh strip to a test position.
  • Neck 32 is punched in between 2 adjacent strips. The purpose of neck 32 is to facilitate the strip bending at the location of neck 32 . In order for the strip to be expressed such that a user can apply blood, the strip is bent downward and neck 32 facilitates bending at a defined location.
  • Contact hole 33 on conductive substrate 12 allows electrical contact to be made with a working electrode on an insulating substrate.
  • a lance similar to the embodiments illustrated in FIGS. 1 through 3 having a lancing element 22 with a sharpened tip 38 , a separation element 24 having a separation tip 40 is positioned proximal to sharpened tip 38 .
  • the separation tip 40 may be positioned between approximately 0.005 inches and 0.020 inches proximal to sharpened tip 38 .
  • a method according to the present invention further includes the step of providing a connector connecting the proximal end of lancing element 22 to the proximal end of separation element 24 wherein the connector forms a fill channel 21 extending from the proximal end of lancing element 22 and the proximal end of separation element 24 to a working electrode 36 of sensor strip 100 .
  • the method further including the steps of inserting the lancing element into skin to form an incision, inserting the separation element 24 to further open the incision and maintaining the position of the lancing element 22 and the separation element 24 in the incision while blood or other bodily fluids are drawn into a gap 42 between the lancing element 22 and. separation element 24 .
  • the method further comprising the step of drawing the bodily fluids from gap 42 into fill channel 21 .
  • a lance 15 constructed in accordance with the present invention is beneficial due to the seamless transition between the tip section and the capillary section, and because the tip itself is a type of capillary.
  • the unique construction of this design better insures that bodily fluids enter the fill channel 21 regardless of the height of the tip above or below the skin wound, or even if the tip lies horizontally offset from the wound, where the lance acts as a conduit for the bodily fluids.
  • a sensor strip 100 constructed according to the present invention is more easily by manufactured than a closed channel sensor strip.
  • a closed channel sensor strip may be manufactured by, for example, injection molding, embossing, or chemical etching, or even simple machining. While the capillary force of an open channel may be weaker than a comparable closed channel, the weakness can be overcome with the use of, for example, hydrophilic surface treatments or surfactant coatings including: Tween-80, a product of Sigma Chemical Co., St. Louis, Mo.; Aerosol OT a product of Cytec Industries, West Paterson, N.J.; JBR-515, a product of Jeneil Biosurfactant Company of Saukville, Wis.; and Niaproof a product of Sigma Chemical Co., St. Louis, Mo.
  • a sensor strip 100 constructed according to the present invention may have improved transfer properties because the invention described herein prevents the creation of a vacuum block in fill channel 21 that would prevent fluid from moving through the fill channel 21 and onto the measurement pad.
  • the inlet With a closed channel capillary, the inlet must be positioned or designed to ensure that air is not prevented from freely entering the capillary during transfer into the measurement area. Thus, in a closed channel system, if the inlet is positioned too close to the wound or even inside it, flow may be disrupted or stopped. With the open channel of a sensor strip designed in accordance with the present invention, however, the inlet to the channel can be positioned arbitrarily close to the source of the blood.
  • a strip in accordance with the present invention including an open channel has the capacity to hold a larger volume of fluid than the minimum required to fill and initiate transfer into the measurement pad.
  • the minimum volume required to fill the lance such that the column of fluid reaches the measurement pad is approximately 230 nL.
  • lancing may produce quantities which are greater than 230 nL. Because of the open channel form in the present invention, the excess blood that is presented to the lance will continue to accumulate along the lance channel, forming a bulging drop of blood. This property is useful in that it clears away excess blood from the skin, leaving a cleaner lance wound.
  • Another advantage of the open channel design in accordance with the present invention is that a drop of fluid can be applied to the side of the lance rather than just at the tip of the lance (i.e. in a closed channel there is a distinct area where fluid must be presented to be drawn into the capillary. Manual application of blood might be required if the blood comes from a site that has been lanced separately.
  • a sensor strip designed in accordance with the present invention provides the option of ‘side’ filling increases the user's options.
  • the stamped metal of conductive substrate 12 could also serve as a working or counter electrode.
  • a unique aspect of the sheet metal design used in the present invention is the fact that it also allows the assembly to be constructed with first electrical contact 10 and second electrode contact 17 on the same side of the strip. This greatly simplifies the requirements for mating contacts on a meter because conductive substrate 12 comprises a solid conductor allowing electrical contact to be established from both the top and bottom side of conductive substrate 12 , wherein the top side of conductive substrate 12 is on the same side as second electrical contact 17 and the bottom side of conductive substrate is on the same side as reference electrode 37 .
  • sheet metal forming can be done as a progressive die stamping, in a strip designed in accordance with the present invention with individual lances chained together in series, it could be possible to construct an array of test sensors with a single, common reference thus requiring just one contact.

Abstract

The present invention relates, in general, to lancing elements for use in drawing bodily fluids out of a patient and, more particularly, to an improved lancing element including first and second elements positioned relative to each other such that an incision formed by the first element is held open by the second element and bodily fluids are pulled up the lancing element by surface tension on the first and second lancing elements.

Description

    CROSS-REFERENCE
  • This application claims priority to Provisional Application No. 60/458,242 filed Mar. 28, 2003, which is incorporated herein by reference in its entirety.[0001]
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0002]
  • The present invention relates, in general, to lancing elements for use in drawing bodily fluids out of a patient and, more particularly, to an improved lancing element including first and second elements positioned relative to each other such that an incision formed by the first element is held open by the second element and bodily fluids are pulled up the lancing element by surface tension on the first and second lancing elements. [0003]
  • 2. Description of the Related Art [0004]
  • Integrated skin lancing and body fluid analysis samplers are known in the art. One such system is described and illustrated in WO 02/49507. The integrated system described in WO 02/49507 includes a lancing element or lance, which is attached to or integrated with a test strip adapted to measure the quantity of an analyte in bodily fluid or, alternatively, some characteristic of the bodily fluid. Usable bodily fluids may include, for example, blood or interstitial fluid (ISF). The lancing element is used to make an incision in the skin and the bodily fluid is drawn up the lancing element to the test strip by, for example, capillary action. Such integrated samplers may be combined with, for example, an electrochemical meter and referred to as monolithic or in-situ sampling devices. [0005]
  • Many lancing devices have been devised to form incisions and to enable bodily fluids to be withdrawn from those incisions. Solid lancets are used to open an incision in the skin to allow bodily fluids to escape to the surface of the skin where they can be sampled by the patient or the doctor. In order to ensure that enough fluid is released from the incision, such solid lancing elements are generally larger in diameter to facilitate the flow of sufficient bodily fluids from the incision for sampling purposes. However, such solid needles generally rely on the size of the incision to ensure that enough bodily fluids are expressed and are not used to facilitate the flow of fluids to the testing apparatus. [0006]
  • Hollow needles have also been described for use in drawing fluids out of the body for testing purposes; such needles may have a pointed or beveled end to facilitate opening the incision. In such needles, the incision is held open by the outer diameter of the needle to facilitate the flow of bodily fluids out of the incision and the bodily fluids are drawn up the needle either by a vacuum or by capillary action or by a combination of vacuum and capillary action. [0007]
  • Other lancing devices have been described wherein the lance is a flat or partially curved piece which includes an open channel for guiding fluid from the sharpened tip to the proximal end of the lance by means of, for example, surface tension and/or capillary action. Such lacing elements are advantageous because of the ease of manufacture and the ease of integrating them into, for example, a test strip, in order to facilitate both lancing and measurement in a single element. Where the landing element is a flat or partially flat piece which includes an open channel for guiding fluid, it is possible for the edges of the incision to close on the channel, fully or partially blocking the channel and preventing bodily fluids from flowing to the proximal end of the channel or limiting the amount of fluid which can flow. [0008]
  • Problem to be Solved [0009]
  • It would, therefore, be advantageous to design a lancing device where the lancing element is a flat or partially curved piece including an open channel and the lancing element includes a separation element for holding the incision open when the lancing element is in the wound and preventing the edges of the incision from closing on the lancing element and partially or fully blocking the open channel. It would be advantageous to design a lancing device wherein the separation element is positioned slightly proximal to the sharpened tip of the lancing element to facilitate insertion of the lance into the skin. It would further be advantageous to design a lancing device wherein the lancing element and the separation element are formed from a single metal sheet. It would further be advantageous to design a lancing device wherein the lancing element and the separation element are positioned opposite each other such that fluid is pulled up the lancing element and into the open channel by surface tension between the fluid and the lancing element and separation element, thus facilitating the filling of the channel. It would further be advantageous to design a lancing device wherein the lancing element and the separation element are formed from a single sheet of metal rolled to position the separation element opposite the lancing element such that the proximal end of the lancing element and the separation element form an open channel. It would further be advantageous to manufacture the lancing devices described herein using, for example, a metal forming or stamping process. [0010]
  • SUMMARY OF THE INVENTION
  • A lance according to the present invention includes a lancing element having a first sharpened end point, a separation element having a second sharpened end point wherein the second sharpened end point is positioned proximal to the first sharpened end point, a connector connecting a proximal portion of the first lancing element to a proximal portion of the separation element, the connector forming a channel. In a further embodiment of the present invention, the separation element is positioned at an angle to the lancing element. In a further embodiment of the present invention the lancing element, the separation element and the channel are formed from a single sheet of metal. In a further embodiment of the present invention, a space between the lancing element and the separation element forms a gap, the gap increasing in size proximal to the second sharpened tip. In a further embodiment of the present invention, least a portion of the channel is treated with a hydrophilic surface coating. In a further embodiment of the present invention, at least a portion of the lancing element and at least a portion of the separation element are coated with a hydrophilic surface coating. In a further embodiment of the present invention, a proximal end of the channel is integrated into a sensor strip. In a further embodiment of the present invention, the sensor strip is connected at a proximal end thereof to a plurality of additional sensor strips[0011]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • While the novel features of the invention are set forth with particularity in the appended claims, a better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which: [0012]
  • FIG. 1 is a perspective view of a lancing element and strip according to the present invention. [0013]
  • FIG. 2 is a perspective view of the top layer of a lancing element and strip according to the present invention. [0014]
  • FIG. 3 is a perspective view of another embodiment of the invention in which multiple strips form an array of sensors for use in a cartridge format.[0015]
  • DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS OF THE INVENTION
  • FIG. 1 is a perspective view of [0016] lance 15 and sensor strip 100 according to the present invention. In FIG. 1, lance 15 is connected to sensor strip 100. Sensor strip 100 may be, for example, a glucose sensor strip which uses electrochemistry to measure the amount of glucose in a bodily fluid, such as, for example, blood or interstitial fluid. Additionally, sensor strip 100 may be, for example, a coagulation sensor which measures a physical characteristic of a body fluid such as viscosity, capacitance, resistance, and the like. In FIG. 1, lance 15 further includes lancing element 22 and separation element 24. Sensor strip 100 further includes first electrode contact 10, adhesive layer 11, conductive substrate 12, vent hole 13, second electrode contact 17, insulating substrate 18, insulating layer 20, registration hole 23 and working electrode 36. In an embodiment of the invention, sensor strip 100 may have an approximate width of 0.22 inches and an approximate length of 0.55 inches.
  • FIG. 2 is a perspective view of [0017] lance 15 and the top layer of sensor strip 100 for use in the present invention. In FIG. 2, the top layer of sensor strip 100 and lance 15 is formed from conductive substrate 12. In the embodiment illustrated in FIG. 2, conductive substrate 12 includes vent hole 13 and registration hole 23. In FIG. 2, lance 15 includes lancing element 22, separation element 24 and fill channel 21.
  • One embodiment of a lancing element and sensor strip suitable for use in the present invention may be described with reference to FIGS. 1 and 2. In the embodiment illustrated in FIGS. 1 and 2, [0018] sensor strip 100 includes first electrode contact 10, wherein first electrode contact 10 may be screen printed on an insulating substrate 18, and a second electrode contact 17, wherein second electrode contact 17 comprises a portion of conductive substrate 12 which is contiguous with reference electrode 37 and lance 15. In the embodiment of the lancing element and sensor strip illustrated in FIGS. 1 and 2, the orientation of first electrode contact 10 and second electrode contact 17 are arranged such that an analyte measurement meter, such as, for example, a glucose meter (not shown) can establish electrical contact with sensor strip 100. In the illustrated embodiment, first electrode contact 10 and second electrode contact 17 are arranged on the same side of insulating substrate 18 to facilitate contact of both electrodes at the distal end of sensor strip 100.
  • [0019] Sensor strip 100 is manufactured using adhesive layer 11 to attach insulating substrate 18 to conductive substrate 12. Adhesive layer 11 could be implemented in a number of ways, including using pressure sensitive material, heat activated material, or UV cured double sided adhesive material. Conductive substrate 12 may be, for example, a sheet of electrically conductive material such as gold or plated stainless steel. The geometry of conductive substrate 12 may be formed by, for example, stamping process or photo etching. In the embodiment illustrated in FIGS. 1 and 2, lance 15 may be manufactured as an integral part of conductive substrate 12. Vent hole 13, may be formed by, for example, punching through conductive substrate 12. Vent hole 13 is used to facilitate the transport of bodily fluid up lance 15 and across working electrode 36. Registration hole 23 may be formed during the stamping process of making conductive substrate 12.
  • In one embodiment of the invention, an analyte sensing layer may be, for example, a glucose sensing layer, including an enzyme, a buffer, and a redox mediator. An analyte sensing layer (not shown) may preferably be deposited on top of working [0020] electrode 36. Where an analyte sensing layer is used to detect the presence and concentration of glucose in a bodily fluid, at least a portion of glucose sensing layer dissolves in the bodily fluid and is used to convert the glucose concentration into an electrically measured parameter which is proportional to the glucose concentration in the sample.
  • In the embodiment illustrated in FIGS. 1 and 2, [0021] lance 15 has a distal and proximal end and the proximal end is integrated with reference electrode 37 and the distal end includes sharpened tip 38 at the distal end of lacing element 22. Lance 15 may be formed by the process of stamping or photo-etching a conductive metal sheet. Photo-etching lance 15 is also beneficial in facilitating the manufacture of a lancing element which has a sharp lancing element 22 and separation element 24. In a subsequent process step, lance 15, lancing element 22, and separation element 24 may be bent to form a “V” or “U” shaped channel geometry as shown in FIG. 2. Fill channel 21 serves as a conduit from lancing element 22 and separation element 24 to working electrode 36 and reference electrode 37. In one embodiment of the present invention, the distal end of lacing element 22 and separation tip 40 of separation element 24 are offset by about 0.005 inches to 0.020 inches.
  • The design of [0022] lance 15 is adapted to more effectively cut skin due to a sharper leading point of lancing element 22. As illustrated in FIG. 2, with separation tip 40 offset distally from sharpened tip 38 of element 22, the extreme distal end of lance 15 comprises only sharpened tip 38 which may be a very sharp point or edge to facilitate the initial incision as lancing element 22 enters the skin. In contrast, if lancing element 22 and separation element 24 were coincident, the leading point of lance 15 would include both sharpened tip 38 and separation tip 40 making the combination less sharp than the embodiment illustrated in FIG. 2 and requiring more force to create the initial incision. The offset of sharpened tip 38 and separation tip 40 make lance 15 more manufacturable because it reduces the inherent alignment difficulties in bringing the sharp point of lancing element 22 and separation element 24 into alignment or contact with each other. The embodiment of the invention illustrated in FIGS. 1 and 2 is further beneficial because it enhances fluid egress by helping to spread and hold open the skin wound after the initial incision is made. In the embodiment illustrated in FIGS. 1 and 2, the lance 15 further includes reference electrode 37 and second electrode contact 17. Alternative embodiments may include forming all of the electrodes and electrode contacts on insulating substrate 18.
  • In the embodiment of the invention illustrated in FIG. 2, [0023] lance 15 includes fill channel 21, wherein the seamless transition between the lancing element 22 and separation element 24; and fill channel 21 facilitates the flow of body fluid from the wound to working electrode 36. Additionally, the seamless transition between the lancing element 22, separation element 24 and fill channel 21 prevents the introduction of stop junctions which can impede the capillary flow rate of liquid samples. The unique geometry increases the likelihood that a liquid sample will sufficiently cover working electrode 36 and reference electrode 37 regardless of the height of the lance 15 above or below the skin wound, or even if lance 15 lies horizontally offset from the wound. In certain embodiments of the invention, sample can be applied to the side of lance 15 rather than just the proximal end of lance 15 which provides a user the option of dosing sample onto sensor strip 100 after a site has been lanced separately.
  • In the embodiment of the invention illustrated in FIG. 2, the [0024] gap 42 between lancing element 22 and separation element 24 guides bodily fluids into fill channel 21. The increasing separation between lancing element 22 and separation element 24 as fluid moves distally towards fill channel 21 facilitates the drawing of fluid into fill channel 21 and from fill channel 21 to sensor strip 100. As gap 42 narrows towards a distal end of separation tip 40 of separation element 24, the surface tension between the bodily fluid in gap 42 and the walls of gap 42 increases, thus bodily fluid is drawn more readily into gap 42, and up into sensor strip 100. Gap 42 is also advantageous in that it facilitates the introduction of bodily fluids into fill channel 21 by facilitating the flow of bodily fluids positioned to the side of gap 42, thus enhancing the ways in which sensor strip 100 may be used to gather bodily fluids.
  • [0025] Fill channel 21 may facilitate the flow of bodily fluids by, for example, wicking or capillary action. In the embodiment illustrated in FIGS. 1 and 2, fill channel 21 has an open geometry which facilitates the wicking of viscous samples and provides for simpler manufacturing techniques when compared with closed capillary channels. For certain embodiments of the invention, fill channel 21 may be coated with a surfactant coating or undergo a hydrophilic surface treatment to increase the capillary force within fill channel 21. For certain embodiments of the invention separation element 24 and lancing element 22 may be coated with a surfactant coating or undergo hydrophilic surface treatment to increase the capillary flow force within gap 42. Additionally, the open geometry of fill channel 21 facilitates the wicking of sample because it prevents the formation of a vacuum block. In a closed channel geometry, a capillary inlet can become plugged if it is positioned too close to the wound or inside the wound preventing air from facilitating the flow of sample to the capillary. With the open geometry of fill channel 21, the proximal end of lance 15 can be positioned arbitrarily close to the source of the blood and allow for sufficient fill of sample. In this embodiment of the invention, the open geometry of fill channel 21 has the capacity to hold a larger sample volume than the minimum sample volume to cover reference electrode 37 and working electrode 36. The open geometry of fill channel 21 thus allows excess sample to accumulate along fill channel 21 which helps leave a cleaner wound site.
  • In the illustrated embodiment as shown in FIG. 2, the geometry of [0026] reference electrode 37 may be formed during the stamping process which effectively embosses the surface of conductive substrate 12. The stamping process may provide the pressure needed to create a recess in conductive substrate 12 which can help define the distance between reference electrode 37 and working electrode 36. For certain applications of the described invention, it may be advantageous to control the distance between reference electrode 37 and working electrode 36 by embossing conductive substrate 12 instead of controlling the thickness of adhesive layer 11. For other applications of the described invention, it may also be advantageous to not emboss the conductive substrate 12 and use adhesive layer 11 to help define the geometry of reference electrode 37.
  • In the embodiment of [0027] sensor strip 100 illustrated in FIG. 1, insulating substrate 18 consists of material such as polyester or ceramic on which a conductive material can be printed onto insulating substrate 18 through silk-screening, sputtering, or electro-less deposition. Conductive material deposited on insulating substrate 18 forms first electrode contact 10 and working electrode 36. Insulating layer 20 may be, for example, screen printed to form a boundary for first electrode contact 10 and working electrode 36.
  • FIG. 3 is a perspective view of another embodiment of the invention in which multiple strips form an array of sensors for use in a cartridge format. Such an array may be inserted into a meter (not shown) having strips dispensed in a serial manner, one by one. The format of this embodiment allows a row of strips to be folded in a manner similar to an accordion wherein several strips similar to [0028] sensor strip 100 in FIG. 1 are attached together on an arrangement which facilitates their use in a cartridge. In FIG. 3, conductive substrate 12 is stamped in a progressive manner to form lance 15 such that several of them are chained together in series. The stamping process of conductive substrate 12 forms index hole 31, neck 32, and contact hole 33.
  • In a further embodiment of the invention, a second electrode layer (not shown) comprising an adhesive layer and glucose sensing layer would be attached to [0029] conductive substrate 12 as illustrated in FIG. 3. A contact area for a reference electrode for all of the strips within the array may be formed using a single area within conductive substrate 12. However, individual contacts must be made for working electrode 36 for all of the strips within the array. In the embodiment of this invention, index hole 31 is used to index the strip cartridge so that it can move a fresh strip to a test position. Neck 32 is punched in between 2 adjacent strips. The purpose of neck 32 is to facilitate the strip bending at the location of neck 32. In order for the strip to be expressed such that a user can apply blood, the strip is bent downward and neck 32 facilitates bending at a defined location. Contact hole 33 on conductive substrate 12 allows electrical contact to be made with a working electrode on an insulating substrate.
  • In a method of lancing in accordance with the present invention, a lance similar to the embodiments illustrated in FIGS. 1 through 3 is provided having a lancing [0030] element 22 with a sharpened tip 38, a separation element 24 having a separation tip 40 is positioned proximal to sharpened tip 38. In one embodiment of the invention the separation tip 40 may be positioned between approximately 0.005 inches and 0.020 inches proximal to sharpened tip 38. A method according to the present invention further includes the step of providing a connector connecting the proximal end of lancing element 22 to the proximal end of separation element 24 wherein the connector forms a fill channel 21 extending from the proximal end of lancing element 22 and the proximal end of separation element 24 to a working electrode 36 of sensor strip 100. The method further including the steps of inserting the lancing element into skin to form an incision, inserting the separation element 24 to further open the incision and maintaining the position of the lancing element 22 and the separation element 24 in the incision while blood or other bodily fluids are drawn into a gap 42 between the lancing element 22 and. separation element 24. The method further comprising the step of drawing the bodily fluids from gap 42 into fill channel 21.
  • A [0031] lance 15 constructed in accordance with the present invention is beneficial due to the seamless transition between the tip section and the capillary section, and because the tip itself is a type of capillary. The unique construction of this design better insures that bodily fluids enter the fill channel 21 regardless of the height of the tip above or below the skin wound, or even if the tip lies horizontally offset from the wound, where the lance acts as a conduit for the bodily fluids.
  • A [0032] sensor strip 100 constructed according to the present invention is more easily by manufactured than a closed channel sensor strip. Such a strip may be manufactured by, for example, injection molding, embossing, or chemical etching, or even simple machining. While the capillary force of an open channel may be weaker than a comparable closed channel, the weakness can be overcome with the use of, for example, hydrophilic surface treatments or surfactant coatings including: Tween-80, a product of Sigma Chemical Co., St. Louis, Mo.; Aerosol OT a product of Cytec Industries, West Paterson, N.J.; JBR-515, a product of Jeneil Biosurfactant Company of Saukville, Wis.; and Niaproof a product of Sigma Chemical Co., St. Louis, Mo.
  • A [0033] sensor strip 100 constructed according to the present invention may have improved transfer properties because the invention described herein prevents the creation of a vacuum block in fill channel 21 that would prevent fluid from moving through the fill channel 21 and onto the measurement pad. With a closed channel capillary, the inlet must be positioned or designed to ensure that air is not prevented from freely entering the capillary during transfer into the measurement area. Thus, in a closed channel system, if the inlet is positioned too close to the wound or even inside it, flow may be disrupted or stopped. With the open channel of a sensor strip designed in accordance with the present invention, however, the inlet to the channel can be positioned arbitrarily close to the source of the blood.
  • Another advantage of a strip in accordance with the present invention including an open channel is that such a strip has the capacity to hold a larger volume of fluid than the minimum required to fill and initiate transfer into the measurement pad. One embodiment of the present invention the minimum volume required to fill the lance such that the column of fluid reaches the measurement pad is approximately 230 nL. However, lancing may produce quantities which are greater than 230 nL. Because of the open channel form in the present invention, the excess blood that is presented to the lance will continue to accumulate along the lance channel, forming a bulging drop of blood. This property is useful in that it clears away excess blood from the skin, leaving a cleaner lance wound. [0034]
  • Another advantage of the open channel design in accordance with the present invention is that a drop of fluid can be applied to the side of the lance rather than just at the tip of the lance (i.e. in a closed channel there is a distinct area where fluid must be presented to be drawn into the capillary. Manual application of blood might be required if the blood comes from a site that has been lanced separately. Thus, using a sensor strip designed in accordance with the present invention, provides the option of ‘side’ filling increases the user's options. [0035]
  • In one embodiment of the present invention, the stamped metal of [0036] conductive substrate 12 could also serve as a working or counter electrode. A unique aspect of the sheet metal design used in the present invention is the fact that it also allows the assembly to be constructed with first electrical contact 10 and second electrode contact 17 on the same side of the strip. This greatly simplifies the requirements for mating contacts on a meter because conductive substrate 12 comprises a solid conductor allowing electrical contact to be established from both the top and bottom side of conductive substrate 12, wherein the top side of conductive substrate 12 is on the same side as second electrical contact 17 and the bottom side of conductive substrate is on the same side as reference electrode 37.
  • On a conventionally constructed electrochemical strips using a facing electrode arrangement where both working and reference electrodes are printed or applied onto an insulating substrate, the electrical contacts must be positioned on opposites sides of the strip making the meter contacts more complex. If [0037] reference electrode 37 was printed or applied onto an insulating substrate, conductive substrate 12 would be insulated on the top side preventing electrical connection to be established from the top side. It could be possible to establish electrical connection from the top side if there was a partial removal of insulation from conductive substrate 12, however, this would add additional complexity to the manufacturing of the strip.
  • Finally, because sheet metal forming can be done as a progressive die stamping, in a strip designed in accordance with the present invention with individual lances chained together in series, it could be possible to construct an array of test sensors with a single, common reference thus requiring just one contact. [0038]
  • It will be recognized that equivalent structures may be substituted for the structured illustrated and described herein and that the described embodiment of the invention is not the only structure which may be employed to implement the claimed invention. In addition, it should be understood that every structure described above has a function and such structure can be referred to as a means for performing that function. [0039]
  • While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. [0040]
  • It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby. [0041]

Claims (8)

What is claimed is:
1. A lance comprising:
a lancing element having a first sharpened end point;
a separation element having a second end point wherein said second end point is positioned proximal to said first sharpened end point;
a connector connecting a proximal portion of said lancing element to a proximal portion of said separation element, said connector forming a channel.
2. A lance according to claim 1, wherein said separation element is positioned at an angle to said lancing element.
3. A lance according to claim 1, wherein said lancing element, said separation element and said channel are formed from a single sheet of metal.
4. A lance according to claim 1, wherein a space between said lancing element and said separation element forms a gap, said gap increasing in size proximal to said second end point.
5. A lance according to claim 1, wherein at least a portion of said channel is treated with a hydrophilic surface coating.
6. A lance according to claim 5, wherein at least a portion of said lancing element and at least a portion of said separation element are coated with a hydrophilic surface coating.
7. A lance in accordance with claim 1, wherein a proximal end of said channel is integrated into a sensor strip.
8. A lance in accordance with claim 7, wherein said sensor strip is connected at a proximal end thereof to a plurality of additional sensor strips.
ELEMENTS 10 1st electrode contact 11 adhesive layer 12 Conductive substrate 13 vent hole 15 Lance 17 2nd electrode contact 18 insulating substrate 37 reference electrode 20 insulating layer 21 fill channel 22 lancing element 23 Registration hole 24 Separation element 31 Index hole 32 Neck 33 Contact hole 36 Working electrode 38 Sharpened tip 40 Separation tip 42 Gap 100 sensor strip
US10/460,030 2003-03-28 2003-06-11 Integrated lance and strip for analyte measurement Abandoned US20040193202A1 (en)

Priority Applications (20)

Application Number Priority Date Filing Date Title
US10/460,030 US20040193202A1 (en) 2003-03-28 2003-06-11 Integrated lance and strip for analyte measurement
IL16082704A IL160827A0 (en) 2003-03-28 2004-03-11 Integrated lance and strip for analyte measurement
KR1020040020329A KR101065599B1 (en) 2003-03-28 2004-03-25 Integrated lance and strip for analyte measurement
EP04251803A EP1464284B1 (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
DE602004000825T DE602004000825T2 (en) 2003-03-28 2004-03-26 Integrated lancet and test strips for analytical measurement
JP2004092767A JP4531423B2 (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
SG200401667A SG115655A1 (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
EP06075525.3A EP1674037B2 (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
ES06075525.3T ES2321330T5 (en) 2003-03-28 2004-03-26 Integrated lancet and strip for the measurement of an analyte
DK06075525.3T DK1674037T4 (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
DE602004019952T DE602004019952D1 (en) 2003-03-28 2004-03-26 Integrated lancet and test strips for analytical measurement
TW093108213A TWI324059B (en) 2003-03-28 2004-03-26 Integrated lance and strip for analyte measurement
AT04251803T ATE325579T1 (en) 2003-03-28 2004-03-26 INTEGRATED LANCET AND TEST STRIPS FOR ANALYTICAL MEASUREMENTS
AT06075525T ATE424763T1 (en) 2003-03-28 2004-03-26 INTEGRATED LANCET AND TEST STRIPS FOR ANALYTICAL MEASUREMENTS
CA2462364A CA2462364C (en) 2003-03-28 2004-03-29 Integrated lance and strip for analyte measurement
CNB2004100314147A CN100393277C (en) 2003-03-28 2004-03-29 Integrated pricking pin and braid used for analyte measurement
HK05101576A HK1069094A1 (en) 2003-03-28 2005-02-24 Integrated lance and strip for analyte measurement
US11/231,130 US7169117B2 (en) 2003-03-28 2005-09-20 Integrated lance and strip for analyte measurement
US11/251,189 US7473264B2 (en) 2003-03-28 2005-10-14 Integrated lance and strip for analyte measurement
HK06112206.9A HK1091707A1 (en) 2003-03-28 2006-11-06 Integrated lance and strip for analyte measurement

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US45824203P 2003-03-28 2003-03-28
US10/460,030 US20040193202A1 (en) 2003-03-28 2003-06-11 Integrated lance and strip for analyte measurement

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US11/231,130 Continuation US7169117B2 (en) 2003-03-28 2005-09-20 Integrated lance and strip for analyte measurement
US11/251,189 Continuation-In-Part US7473264B2 (en) 2003-03-28 2005-10-14 Integrated lance and strip for analyte measurement

Publications (1)

Publication Number Publication Date
US20040193202A1 true US20040193202A1 (en) 2004-09-30

Family

ID=32853620

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/460,030 Abandoned US20040193202A1 (en) 2003-03-28 2003-06-11 Integrated lance and strip for analyte measurement
US11/231,130 Expired - Lifetime US7169117B2 (en) 2003-03-28 2005-09-20 Integrated lance and strip for analyte measurement

Family Applications After (1)

Application Number Title Priority Date Filing Date
US11/231,130 Expired - Lifetime US7169117B2 (en) 2003-03-28 2005-09-20 Integrated lance and strip for analyte measurement

Country Status (14)

Country Link
US (2) US20040193202A1 (en)
EP (2) EP1674037B2 (en)
JP (1) JP4531423B2 (en)
KR (1) KR101065599B1 (en)
CN (1) CN100393277C (en)
AT (2) ATE424763T1 (en)
CA (1) CA2462364C (en)
DE (2) DE602004000825T2 (en)
DK (1) DK1674037T4 (en)
ES (1) ES2321330T5 (en)
HK (2) HK1069094A1 (en)
IL (1) IL160827A0 (en)
SG (1) SG115655A1 (en)
TW (1) TWI324059B (en)

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020137998A1 (en) * 2001-03-26 2002-09-26 Wilson Smart Silicon microprobe with integrated biosensor
US20030018282A1 (en) * 2001-07-20 2003-01-23 Carlo Effenhauser System for withdrawing small amounts of body fluid
US20060173478A1 (en) * 2005-01-28 2006-08-03 Stat Medical Devices, Inc. Multi-lancet unit, method and lancet device using the multi-lancet unit, and method of assembling and/or making the multi-lancet unit
US20060196031A1 (en) * 2003-04-04 2006-09-07 Joachim Hoenes Method for producing a puncturing and measuring device
US20060200045A1 (en) * 2005-03-02 2006-09-07 Roe Steven N Dynamic integrated lancing test strip with sterility cover
EP1790288A1 (en) * 2005-11-25 2007-05-30 Roche Diagnostics GmbH Bent lancet
US20070167869A1 (en) * 2005-03-02 2007-07-19 Roe Steven N System and method for breaking a sterility seal to engage a lancet
WO2008043565A2 (en) * 2006-10-13 2008-04-17 Roche Diagnostics Gmbh Tape transport lance sampler
US20080300509A1 (en) * 2007-05-29 2008-12-04 Joachim Hoenes Flexible lancet
US20090010802A1 (en) * 2002-12-27 2009-01-08 Abner David Joseph Method for manufacturing a sterilized lancet integrated biosensor
US20090099477A1 (en) * 2007-10-15 2009-04-16 Joachim Hoenes Lancet wheel
US20090137931A1 (en) * 2006-01-05 2009-05-28 Chan Frank A Lancet integrated test element tape dispenser
US20100174211A1 (en) * 2007-09-17 2010-07-08 Roche Diagnostics Operations, Inc. Body fluid lancing, acquiring, and testing cartridge design
WO2010094426A1 (en) 2009-02-19 2010-08-26 Roche Diagnostics Gmbh Method for producing an analytical magazine
US20100331729A1 (en) * 2008-03-21 2010-12-30 Nitto Denko Corporation Circuit board for body fluid collection, and biosensor
US20100331730A1 (en) * 2008-03-21 2010-12-30 Nitto Denko Corporation Circuit board for body fluid collection, method for producing the same, method for using the same, and biosensor
US20110077554A1 (en) * 2009-09-28 2011-03-31 Roe Steven N Body fluid lancing, acquiring, and testing cartridge design
US20110230905A1 (en) * 2006-10-13 2011-09-22 Roche Diagnostics Operations, Inc. Tape transport lance sampler
WO2012140027A1 (en) 2011-04-12 2012-10-18 Roche Diagnostics Gmbh Analytical aid
CN102764132A (en) * 2011-05-06 2012-11-07 霍夫曼-拉罗奇有限公司 Lancet
US8852123B2 (en) 2010-12-30 2014-10-07 Roche Diagnostics Operations, Inc. Handheld medical diagnostic devices housing with sample transfer
US9066689B2 (en) 2008-05-03 2015-06-30 Roche Diagnostics Operations, Inc. Lancet wheel and method for producing a lancet wheel
US9486164B2 (en) 2010-12-30 2016-11-08 Roche Diabetes Care, Inc. Handheld medical diagnostic device with lancet and sample transfer
WO2016209731A1 (en) * 2015-06-22 2016-12-29 Fluxergy, Llc Test card for assay and method of manufacturing same
US9717452B2 (en) 2010-12-30 2017-08-01 Roche Diabetes Care, Inc. Handheld medical diagnostic devices with lancing speed control
US9726612B2 (en) 2011-04-12 2017-08-08 Roche Diabetes Care, Inc. Analytical aid
US10519493B2 (en) 2015-06-22 2019-12-31 Fluxergy, Llc Apparatus and method for image analysis of a fluid sample undergoing a polymerase chain reaction (PCR)
US11371091B2 (en) 2015-06-22 2022-06-28 Fluxergy, Inc. Device for analyzing a fluid sample and use of test card with same

Families Citing this family (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6391005B1 (en) * 1998-03-30 2002-05-21 Agilent Technologies, Inc. Apparatus and method for penetration with shaft having a sensor for sensing penetration depth
US8641644B2 (en) 2000-11-21 2014-02-04 Sanofi-Aventis Deutschland Gmbh Blood testing apparatus having a rotatable cartridge with multiple lancing elements and testing means
US7033371B2 (en) 2001-06-12 2006-04-25 Pelikan Technologies, Inc. Electric lancet actuator
CA2448902C (en) * 2001-06-12 2010-09-07 Pelikan Technologies, Inc. Self optimizing lancing device with adaptation means to temporal variations in cutaneous properties
US9226699B2 (en) 2002-04-19 2016-01-05 Sanofi-Aventis Deutschland Gmbh Body fluid sampling module with a continuous compression tissue interface surface
US7749174B2 (en) 2001-06-12 2010-07-06 Pelikan Technologies, Inc. Method and apparatus for lancet launching device intergrated onto a blood-sampling cartridge
US7981056B2 (en) 2002-04-19 2011-07-19 Pelikan Technologies, Inc. Methods and apparatus for lancet actuation
US8337419B2 (en) 2002-04-19 2012-12-25 Sanofi-Aventis Deutschland Gmbh Tissue penetration device
US9427532B2 (en) 2001-06-12 2016-08-30 Sanofi-Aventis Deutschland Gmbh Tissue penetration device
US7041068B2 (en) * 2001-06-12 2006-05-09 Pelikan Technologies, Inc. Sampling module device and method
US7344507B2 (en) 2002-04-19 2008-03-18 Pelikan Technologies, Inc. Method and apparatus for lancet actuation
US9795747B2 (en) 2010-06-02 2017-10-24 Sanofi-Aventis Deutschland Gmbh Methods and apparatus for lancet actuation
US8372016B2 (en) * 2002-04-19 2013-02-12 Sanofi-Aventis Deutschland Gmbh Method and apparatus for body fluid sampling and analyte sensing
US7976476B2 (en) 2002-04-19 2011-07-12 Pelikan Technologies, Inc. Device and method for variable speed lancet
US7901362B2 (en) * 2002-04-19 2011-03-08 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US8702624B2 (en) 2006-09-29 2014-04-22 Sanofi-Aventis Deutschland Gmbh Analyte measurement device with a single shot actuator
US7297122B2 (en) 2002-04-19 2007-11-20 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US7892183B2 (en) 2002-04-19 2011-02-22 Pelikan Technologies, Inc. Method and apparatus for body fluid sampling and analyte sensing
US7491178B2 (en) 2002-04-19 2009-02-17 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US7648468B2 (en) * 2002-04-19 2010-01-19 Pelikon Technologies, Inc. Method and apparatus for penetrating tissue
US8267870B2 (en) 2002-04-19 2012-09-18 Sanofi-Aventis Deutschland Gmbh Method and apparatus for body fluid sampling with hybrid actuation
US7331931B2 (en) 2002-04-19 2008-02-19 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US8579831B2 (en) * 2002-04-19 2013-11-12 Sanofi-Aventis Deutschland Gmbh Method and apparatus for penetrating tissue
US9314194B2 (en) * 2002-04-19 2016-04-19 Sanofi-Aventis Deutschland Gmbh Tissue penetration device
US8784335B2 (en) 2002-04-19 2014-07-22 Sanofi-Aventis Deutschland Gmbh Body fluid sampling device with a capacitive sensor
US8221334B2 (en) 2002-04-19 2012-07-17 Sanofi-Aventis Deutschland Gmbh Method and apparatus for penetrating tissue
US7909778B2 (en) 2002-04-19 2011-03-22 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US9248267B2 (en) 2002-04-19 2016-02-02 Sanofi-Aventis Deustchland Gmbh Tissue penetration device
US7547287B2 (en) * 2002-04-19 2009-06-16 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US8360992B2 (en) 2002-04-19 2013-01-29 Sanofi-Aventis Deutschland Gmbh Method and apparatus for penetrating tissue
US7226461B2 (en) 2002-04-19 2007-06-05 Pelikan Technologies, Inc. Method and apparatus for a multi-use body fluid sampling device with sterility barrier release
US7229458B2 (en) 2002-04-19 2007-06-12 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US7232451B2 (en) 2002-04-19 2007-06-19 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US7674232B2 (en) 2002-04-19 2010-03-09 Pelikan Technologies, Inc. Method and apparatus for penetrating tissue
US9795334B2 (en) 2002-04-19 2017-10-24 Sanofi-Aventis Deutschland Gmbh Method and apparatus for penetrating tissue
US8574895B2 (en) 2002-12-30 2013-11-05 Sanofi-Aventis Deutschland Gmbh Method and apparatus using optical techniques to measure analyte levels
EP1620021A4 (en) * 2003-05-02 2008-06-18 Pelikan Technologies Inc Method and apparatus for a tissue penetrating device user interface
ES2347248T3 (en) 2003-05-30 2010-10-27 Pelikan Technologies Inc. PROCEDURE AND APPLIANCE FOR FLUID INJECTION.
WO2004107964A2 (en) 2003-06-06 2004-12-16 Pelikan Technologies, Inc. Blood harvesting device with electronic control
WO2006001797A1 (en) 2004-06-14 2006-01-05 Pelikan Technologies, Inc. Low pain penetrating
WO2005033659A2 (en) 2003-09-29 2005-04-14 Pelikan Technologies, Inc. Method and apparatus for an improved sample capture device
US9351680B2 (en) 2003-10-14 2016-05-31 Sanofi-Aventis Deutschland Gmbh Method and apparatus for a variable user interface
EP1706026B1 (en) 2003-12-31 2017-03-01 Sanofi-Aventis Deutschland GmbH Method and apparatus for improving fluidic flow and sample capture
US7822454B1 (en) 2005-01-03 2010-10-26 Pelikan Technologies, Inc. Fluid sampling device with improved analyte detecting member configuration
US8828203B2 (en) 2004-05-20 2014-09-09 Sanofi-Aventis Deutschland Gmbh Printable hydrogels for biosensors
GB2414734B (en) * 2004-06-01 2010-09-08 Rosti As Devices for retaining and presenting for use a plurality of components
US9775553B2 (en) 2004-06-03 2017-10-03 Sanofi-Aventis Deutschland Gmbh Method and apparatus for a fluid sampling device
US9820684B2 (en) 2004-06-03 2017-11-21 Sanofi-Aventis Deutschland Gmbh Method and apparatus for a fluid sampling device
EP1835848A4 (en) * 2004-12-30 2009-07-29 Pelikan Technologies Inc Method and apparatus for analyte measurement test time
US20060167382A1 (en) * 2004-12-30 2006-07-27 Ajay Deshmukh Method and apparatus for storing an analyte sampling and measurement device
US8652831B2 (en) 2004-12-30 2014-02-18 Sanofi-Aventis Deutschland Gmbh Method and apparatus for analyte measurement test time
DK2260759T3 (en) * 2005-06-17 2015-08-17 Hoffmann La Roche Feel and conditioning device and method for monitoring a connection, in particular glucose, in body tissue
JP2007282864A (en) * 2006-04-17 2007-11-01 Sumitomo Electric Ind Ltd Biosensor system
DE102007018383A1 (en) * 2007-04-17 2008-10-23 Tesa Ag Sheet-like material with hydrophilic and hydrophobic areas and their production
EP1992284A1 (en) * 2007-05-15 2008-11-19 F.Hoffmann-La Roche Ag Method for storing piecing elements and belt magazine
EP2025287A1 (en) 2007-08-16 2009-02-18 F.Hoffmann-La Roche Ag Diagnostic disposable part and method for its production
US20090050862A1 (en) * 2007-08-23 2009-02-26 Cruce Vann K Security fence spike
EP2030566B1 (en) * 2007-08-31 2016-08-24 Roche Diabetes Care GmbH Analysis system for determining an analyte in a body fluid, magazine for an analysis system and analyzing element, and method for analyzing a body fluid
US20090209883A1 (en) * 2008-01-17 2009-08-20 Michael Higgins Tissue penetrating apparatus
DE102008006225A1 (en) * 2008-01-25 2009-07-30 Tesa Ag Biosensor and its production
US20090209882A1 (en) * 2008-02-15 2009-08-20 Trinity Research Limited Integrated cap and sample applicator
WO2009126900A1 (en) * 2008-04-11 2009-10-15 Pelikan Technologies, Inc. Method and apparatus for analyte detecting device
EP2316339A4 (en) * 2008-08-01 2012-10-24 Lightnix Inc Sensor with fine needle having channel formed therein
US9375169B2 (en) 2009-01-30 2016-06-28 Sanofi-Aventis Deutschland Gmbh Cam drive for managing disposable penetrating member actions with a single motor and motor and control system
EP2248463A1 (en) * 2009-05-09 2010-11-10 F. Hoffmann-La Roche AG Test unit for use in a test device and test system
US8965476B2 (en) 2010-04-16 2015-02-24 Sanofi-Aventis Deutschland Gmbh Tissue penetration device
WO2012089660A1 (en) * 2010-12-27 2012-07-05 Roche Diagnostics Gmbh Container made from a composite of aluminium foil and polymer and used for analytical aids, and method for producing said container

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2896628A (en) * 1957-06-12 1959-07-28 Propper Mfg Company Inc Blood lancets
US5820570A (en) * 1993-10-13 1998-10-13 Integ Incorporated Interstitial fluid collection and constituent measurement
US5857983A (en) * 1996-05-17 1999-01-12 Mercury Diagnostics, Inc. Methods and apparatus for sampling body fluid
US5928207A (en) * 1997-06-30 1999-07-27 The Regents Of The University Of California Microneedle with isotropically etched tip, and method of fabricating such a device
US6171325B1 (en) * 1998-03-30 2001-01-09 Ganapati R. Mauze Apparatus and method for incising
US20020168290A1 (en) * 2002-05-09 2002-11-14 Yuzhakov Vadim V. Physiological sample collection devices and methods of using the same
US20020177761A1 (en) * 2001-04-26 2002-11-28 Phoenix Bioscience Integrated lancing and analytic device
US20030016282A1 (en) * 2001-07-17 2003-01-23 Koizumi David H. Thermochromic writing device
US6612111B1 (en) * 2000-03-27 2003-09-02 Lifescan, Inc. Method and device for sampling and analyzing interstitial fluid and whole blood samples
US20030171699A1 (en) * 2002-03-05 2003-09-11 Bayer Healthcare, Llc Fluid collection apparatus having an integrated lance and reaction area
US20040106941A1 (en) * 2002-12-03 2004-06-03 Roe Steven N. Dual blade lancing test strip

Family Cites Families (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US59306A (en) 1866-10-30 Improvement in artificial leeches
US3143793A (en) 1962-06-08 1964-08-11 Dade Reagents Inc Method of forming a lancet
US3303959A (en) 1964-11-02 1967-02-14 Dayton Reliable Tool And Mfg C Can top
CH500707A (en) 1968-07-26 1970-12-31 Micromedic Systems Inc Device for performing percutaneous and digital blood sampling
US3593060A (en) * 1969-04-09 1971-07-13 Gen Mfg Inc Fluorescent lamp apparatus including inverter circuit and reflector
US3831814A (en) 1969-07-25 1974-08-27 Cutter Lab Trocar-cannula
CH538277A (en) 1970-09-04 1973-06-30 Micromedic Systems Inc Percutaneous blood test device
US4585446A (en) 1984-03-16 1986-04-29 Joseph Kempf Dialysis needle
US4713165A (en) 1986-07-02 1987-12-15 Ilex Corporation Sensor having ion-selective electrodes
US4873993A (en) 1986-07-22 1989-10-17 Personal Diagnostics, Inc. Cuvette
US4753641A (en) * 1987-09-10 1988-06-28 Vaslow Dale F Emergency medical needle
GB8817421D0 (en) 1988-07-21 1988-08-24 Medisense Inc Bioelectrochemical electrodes
US4924879A (en) 1988-10-07 1990-05-15 Brien Walter J O Blood lancet device
GB9320850D0 (en) 1993-10-09 1993-12-01 Terwee Thomas H M Monitoring the concentration of a substance or a group of substances in a body fluid of a human or an animal
US5591139A (en) 1994-06-06 1997-01-07 The Regents Of The University Of California IC-processed microneedles
US5700695A (en) 1994-06-30 1997-12-23 Zia Yassinzadeh Sample collection and manipulation method
JP2913372B2 (en) 1994-12-16 1999-06-28 株式会社コーテックス Hollow needle for locking piece mounting machine
AUPN363995A0 (en) 1995-06-19 1995-07-13 Memtec Limited Electrochemical cell
US5711861A (en) 1995-11-22 1998-01-27 Ward; W. Kenneth Device for monitoring changes in analyte concentration
US5989917A (en) 1996-02-13 1999-11-23 Selfcare, Inc. Glucose monitor and test strip containers for use in same
US6241862B1 (en) 1996-02-14 2001-06-05 Inverness Medical Technology, Inc. Disposable test strips with integrated reagent/blood separation layer
US5708247A (en) 1996-02-14 1998-01-13 Selfcare, Inc. Disposable glucose test strips, and methods and compositions for making same
US6332871B1 (en) 1996-05-17 2001-12-25 Amira Medical Blood and interstitial fluid sampling device
US6015392A (en) 1996-05-17 2000-01-18 Mercury Diagnostics, Inc. Apparatus for sampling body fluid
DE29723400U1 (en) 1996-10-30 1998-09-10 Mercury Diagnostics Inc Synchronized analysis test system
US6071249A (en) 1996-12-06 2000-06-06 Abbott Laboratories Method and apparatus for obtaining blood for diagnostic tests
ATE227844T1 (en) 1997-02-06 2002-11-15 Therasense Inc SMALL VOLUME SENSOR FOR IN-VITRO DETERMINATION
US6046051A (en) 1997-06-27 2000-04-04 Hemosense, Inc. Method and device for measuring blood coagulation or lysis by viscosity changes
US5938679A (en) 1997-10-14 1999-08-17 Hewlett-Packard Company Apparatus and method for minimally invasive blood sampling
GB2374019B (en) 1997-12-04 2002-11-27 Agilent Technologies Inc Method for sampling blood
US6173202B1 (en) 1998-03-06 2001-01-09 Spectrx, Inc. Method and apparatus for enhancing flux rates of a fluid in a microporated biological tissue
US6086545A (en) 1998-04-28 2000-07-11 Amira Medical Methods and apparatus for suctioning and pumping body fluid from an incision
US6153085A (en) 1998-08-17 2000-11-28 Stat-Chem, Inc. Information storage and transmittal for medical diagnostic devices
DE19848112C2 (en) 1998-10-19 2001-12-13 Meinhard Knoll Minimally invasive sensor system
US6475372B1 (en) 2000-02-02 2002-11-05 Lifescan, Inc. Electrochemical methods and devices for use in the determination of hematocrit corrected analyte concentrations
US6132449A (en) 1999-03-08 2000-10-17 Agilent Technologies, Inc. Extraction and transportation of blood for analysis
US6193873B1 (en) 1999-06-15 2001-02-27 Lifescan, Inc. Sample detection to initiate timing of an electrochemical assay
CN2412527Y (en) * 2000-01-11 2001-01-03 郭宏 Once-used automatic quantitative blood taking needle
US6716577B1 (en) 2000-02-02 2004-04-06 Lifescan, Inc. Electrochemical test strip for use in analyte determination
US6706159B2 (en) 2000-03-02 2004-03-16 Diabetes Diagnostics Combined lancet and electrochemical analyte-testing apparatus
GB0005564D0 (en) 2000-03-08 2000-05-03 Inverness Medical Ltd Measurjement of substances in liquid
MXPA02009666A (en) 2000-03-28 2004-07-30 Inverness Medical Technology I Continuous process for manufacture of disposable electro-chemical sensor.
PT1269173E (en) 2000-03-28 2005-10-31 Diabetes Diagnostics Inc QUICK RESPONSE GLUCOSE SENSOR
CN2420976Y (en) * 2000-05-20 2001-02-28 朱德新 Multifunctional hemostix
US6607543B2 (en) 2000-06-13 2003-08-19 Bayer Corporation Lancing mechanism
US6444115B1 (en) 2000-07-14 2002-09-03 Lifescan, Inc. Electrochemical method for measuring chemical reaction rates
CZ2003409A3 (en) 2000-07-14 2003-10-15 Lifescan, Inc. Electrochemical measuring method of chemical reaction rate
US6620310B1 (en) 2000-12-13 2003-09-16 Lifescan, Inc. Electrochemical coagulation assay and device
GB0030929D0 (en) 2000-12-19 2001-01-31 Inverness Medical Ltd Analyte measurement
US6558528B1 (en) 2000-12-20 2003-05-06 Lifescan, Inc. Electrochemical test strip cards that include an integral dessicant
CA2435439A1 (en) 2001-01-22 2002-07-25 F. Hoffmann-La Roche Ag Lancet device having capillary action
US6591124B2 (en) 2001-05-11 2003-07-08 The Procter & Gamble Company Portable interstitial fluid monitoring system
US7041068B2 (en) 2001-06-12 2006-05-09 Pelikan Technologies, Inc. Sampling module device and method
US7699791B2 (en) * 2001-06-12 2010-04-20 Pelikan Technologies, Inc. Method and apparatus for improving success rate of blood yield from a fingerstick
DE10134650B4 (en) 2001-07-20 2009-12-03 Roche Diagnostics Gmbh System for taking small amounts of body fluid
US20030028125A1 (en) 2001-08-06 2003-02-06 Yuzhakov Vadim V. Physiological sample collection devices and methods of using the same
MXPA04006477A (en) 2002-10-30 2005-07-13 Johnson & Johnson Method of lancing skin for the extraction of blood.

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2896628A (en) * 1957-06-12 1959-07-28 Propper Mfg Company Inc Blood lancets
US5820570A (en) * 1993-10-13 1998-10-13 Integ Incorporated Interstitial fluid collection and constituent measurement
US5857983A (en) * 1996-05-17 1999-01-12 Mercury Diagnostics, Inc. Methods and apparatus for sampling body fluid
US5928207A (en) * 1997-06-30 1999-07-27 The Regents Of The University Of California Microneedle with isotropically etched tip, and method of fabricating such a device
US6171325B1 (en) * 1998-03-30 2001-01-09 Ganapati R. Mauze Apparatus and method for incising
US6612111B1 (en) * 2000-03-27 2003-09-02 Lifescan, Inc. Method and device for sampling and analyzing interstitial fluid and whole blood samples
US20020177761A1 (en) * 2001-04-26 2002-11-28 Phoenix Bioscience Integrated lancing and analytic device
US20030016282A1 (en) * 2001-07-17 2003-01-23 Koizumi David H. Thermochromic writing device
US20030171699A1 (en) * 2002-03-05 2003-09-11 Bayer Healthcare, Llc Fluid collection apparatus having an integrated lance and reaction area
US20020168290A1 (en) * 2002-05-09 2002-11-14 Yuzhakov Vadim V. Physiological sample collection devices and methods of using the same
US20030143113A2 (en) * 2002-05-09 2003-07-31 Lifescan, Inc. Physiological sample collection devices and methods of using the same
US20040106941A1 (en) * 2002-12-03 2004-06-03 Roe Steven N. Dual blade lancing test strip

Cited By (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020137998A1 (en) * 2001-03-26 2002-09-26 Wilson Smart Silicon microprobe with integrated biosensor
US7310543B2 (en) 2001-03-26 2007-12-18 Kumetrix, Inc. Silicon microprobe with integrated biosensor
US20080097171A1 (en) * 2001-03-26 2008-04-24 Wilson Smart Silicon microprobe with integrated biosensor
US20030018282A1 (en) * 2001-07-20 2003-01-23 Carlo Effenhauser System for withdrawing small amounts of body fluid
US7993284B2 (en) 2001-07-20 2011-08-09 Roche Diagnostics Operations, Inc. System for withdrawing small amounts of body fluid
US8821413B2 (en) 2001-07-20 2014-09-02 Roche Diagnostics Operations, Inc. System for withdrawing small amounts of body fluid
US20080009767A1 (en) * 2001-07-20 2008-01-10 Roche Diagnostics Operations, Inc. System for withdrawing small amounts of body fluid
US8388552B2 (en) 2001-07-20 2013-03-05 Roche Diagnostics Operations, Inc. System for withdrawing small amounts of body fluid
US7288073B2 (en) 2001-07-20 2007-10-30 Roche Diagnostics Operations, Inc. System for withdrawing small amounts of body fluid
US20090010802A1 (en) * 2002-12-27 2009-01-08 Abner David Joseph Method for manufacturing a sterilized lancet integrated biosensor
US8052926B2 (en) 2002-12-27 2011-11-08 Roche Diagnostics Operations, Inc. Method for manufacturing a sterilized lancet integrated biosensor
US8015685B2 (en) * 2003-04-04 2011-09-13 Roche Diagnostics Operations, Inc. Method for producing a puncturing and measuring device
US20060196031A1 (en) * 2003-04-04 2006-09-07 Joachim Hoenes Method for producing a puncturing and measuring device
US9289161B2 (en) 2005-01-28 2016-03-22 Stat Medical Divices, Inc. Multi-lancet unit, method and lancet device using the multi-lancet unit, and method of assembling and/or making the multi-lancet unit
US9282918B2 (en) 2005-01-28 2016-03-15 Stat Medical Devices, Inc. Multi-lancet unit, method and lancet device using the multi-lancet unit, and method of assembling and/or making the multi-lancet unit
WO2006083676A3 (en) * 2005-01-28 2007-11-22 Stat Medical Devices Inc Multi-lancet unit, method and lancet device using the multi-lancet unit, and method of assembling and/or making the multi-lancet unit
US20060173478A1 (en) * 2005-01-28 2006-08-03 Stat Medical Devices, Inc. Multi-lancet unit, method and lancet device using the multi-lancet unit, and method of assembling and/or making the multi-lancet unit
US9034250B2 (en) 2005-03-02 2015-05-19 Roche Diagnostics Operations, Inc. Dynamic integrated lancing test strip with sterility cover
US20070167869A1 (en) * 2005-03-02 2007-07-19 Roe Steven N System and method for breaking a sterility seal to engage a lancet
US20110000168A1 (en) * 2005-03-02 2011-01-06 Roe Steven N Dynamic integrated lancing test strip with sterility cover
US9445756B2 (en) 2005-03-02 2016-09-20 Roche Diabetes Care, Inc. Dynamic integrated lancing test strip with sterility cover
US20060200045A1 (en) * 2005-03-02 2006-09-07 Roe Steven N Dynamic integrated lancing test strip with sterility cover
US20110178435A1 (en) * 2005-03-02 2011-07-21 Roe Steven N System and method for breaking a sterility seal to engage a lancet
US7935063B2 (en) 2005-03-02 2011-05-03 Roche Diagnostics Operations, Inc. System and method for breaking a sterility seal to engage a lancet
US7815579B2 (en) 2005-03-02 2010-10-19 Roche Diagnostics Operations, Inc. Dynamic integrated lancing test strip with sterility cover
US20080269791A1 (en) * 2005-11-25 2008-10-30 Joachim Hoenes Kinked lancet
EP1790288A1 (en) * 2005-11-25 2007-05-30 Roche Diagnostics GmbH Bent lancet
WO2007060004A1 (en) * 2005-11-25 2007-05-31 Roche Diagnostics Gmbh Kinked lancet
US20090137931A1 (en) * 2006-01-05 2009-05-28 Chan Frank A Lancet integrated test element tape dispenser
US8621828B2 (en) 2006-01-05 2014-01-07 Roche Diagnostics Operations, Inc. Lancet integrated test element tape dispenser
US8196374B2 (en) * 2006-01-05 2012-06-12 Roche Diagnostics Operations, Inc. Lancet integrated test element tape dispenser
US20120067006A1 (en) * 2006-01-05 2012-03-22 Chan Frank A Lancet integrated test element tape dispenser
US8083992B2 (en) * 2006-01-05 2011-12-27 Roche Diagnostics Operations, Inc. Lancet integrated test element tape dispenser
CN101522103B (en) * 2006-10-13 2012-01-11 霍夫曼-拉罗奇有限公司 Tape transport lance sampler
US20110230905A1 (en) * 2006-10-13 2011-09-22 Roche Diagnostics Operations, Inc. Tape transport lance sampler
US20080103415A1 (en) * 2006-10-13 2008-05-01 Roe Steven N Tape transport lance sampler
US7955271B2 (en) 2006-10-13 2011-06-07 Roche Diagnostics Operations, Inc. Tape transport lance sampler
US8852124B2 (en) 2006-10-13 2014-10-07 Roche Diagnostics Operations, Inc. Tape transport lance sampler
WO2008043565A3 (en) * 2006-10-13 2008-07-03 Roche Diagnostics Gmbh Tape transport lance sampler
WO2008043565A2 (en) * 2006-10-13 2008-04-17 Roche Diagnostics Gmbh Tape transport lance sampler
US8328736B2 (en) 2006-10-13 2012-12-11 Roche Diagnostics Operations, Inc. Tape transport lance sampler
US9138179B2 (en) 2007-05-29 2015-09-22 Roche Diagnostics Operations, Inc. Flexible lancet
US20080300509A1 (en) * 2007-05-29 2008-12-04 Joachim Hoenes Flexible lancet
US20100174211A1 (en) * 2007-09-17 2010-07-08 Roche Diagnostics Operations, Inc. Body fluid lancing, acquiring, and testing cartridge design
US9186097B2 (en) 2007-09-17 2015-11-17 Roche Diabetes Care, Inc. Body fluid lancing, acquiring, and testing cartridge design
US20090099477A1 (en) * 2007-10-15 2009-04-16 Joachim Hoenes Lancet wheel
US8152741B2 (en) 2007-10-15 2012-04-10 Roche Diagnostics Operations, Inc. Lancet wheel
US20100331730A1 (en) * 2008-03-21 2010-12-30 Nitto Denko Corporation Circuit board for body fluid collection, method for producing the same, method for using the same, and biosensor
US20100331729A1 (en) * 2008-03-21 2010-12-30 Nitto Denko Corporation Circuit board for body fluid collection, and biosensor
US9066689B2 (en) 2008-05-03 2015-06-30 Roche Diagnostics Operations, Inc. Lancet wheel and method for producing a lancet wheel
EP2286725A1 (en) 2009-02-19 2011-02-23 Roche Diagnostics GmbH Method for producing an analytical magazine
WO2010094426A1 (en) 2009-02-19 2010-08-26 Roche Diagnostics Gmbh Method for producing an analytical magazine
EP2226008A1 (en) 2009-02-19 2010-09-08 Roche Diagnostics GmbH Method for producing an analytical magazine
US8961431B2 (en) 2009-09-28 2015-02-24 Roche Diagnostics Operations, Inc. Body fluid lancing, acquiring, and testing cartridge design
US20110077554A1 (en) * 2009-09-28 2011-03-31 Roe Steven N Body fluid lancing, acquiring, and testing cartridge design
US9717452B2 (en) 2010-12-30 2017-08-01 Roche Diabetes Care, Inc. Handheld medical diagnostic devices with lancing speed control
US8852123B2 (en) 2010-12-30 2014-10-07 Roche Diagnostics Operations, Inc. Handheld medical diagnostic devices housing with sample transfer
US9486164B2 (en) 2010-12-30 2016-11-08 Roche Diabetes Care, Inc. Handheld medical diagnostic device with lancet and sample transfer
EP2977004A1 (en) 2011-04-12 2016-01-27 Roche Diagniostics GmbH Analytical aid
US9097679B2 (en) 2011-04-12 2015-08-04 Roche Diabetes Care, Inc. Analytical aid
WO2012140027A1 (en) 2011-04-12 2012-10-18 Roche Diagnostics Gmbh Analytical aid
US9726612B2 (en) 2011-04-12 2017-08-08 Roche Diabetes Care, Inc. Analytical aid
CN102764132A (en) * 2011-05-06 2012-11-07 霍夫曼-拉罗奇有限公司 Lancet
WO2016209731A1 (en) * 2015-06-22 2016-12-29 Fluxergy, Llc Test card for assay and method of manufacturing same
US10214772B2 (en) 2015-06-22 2019-02-26 Fluxergy, Llc Test card for assay and method of manufacturing same
US10519493B2 (en) 2015-06-22 2019-12-31 Fluxergy, Llc Apparatus and method for image analysis of a fluid sample undergoing a polymerase chain reaction (PCR)
US11371091B2 (en) 2015-06-22 2022-06-28 Fluxergy, Inc. Device for analyzing a fluid sample and use of test card with same
US11413621B2 (en) * 2015-06-22 2022-08-16 Fluxergy, Inc. Test card for assay and method of manufacturing same

Also Published As

Publication number Publication date
DE602004019952D1 (en) 2009-04-23
JP4531423B2 (en) 2010-08-25
EP1674037B1 (en) 2009-03-11
US7169117B2 (en) 2007-01-30
HK1091707A1 (en) 2007-01-26
DE602004000825T2 (en) 2006-12-07
TW200427433A (en) 2004-12-16
ES2321330T3 (en) 2009-06-04
SG115655A1 (en) 2005-10-28
ATE325579T1 (en) 2006-06-15
EP1674037A1 (en) 2006-06-28
DE602004000825D1 (en) 2006-06-14
DK1674037T4 (en) 2017-11-20
EP1464284A1 (en) 2004-10-06
KR20040084822A (en) 2004-10-06
IL160827A0 (en) 2004-08-31
US20060074351A1 (en) 2006-04-06
CN1533742A (en) 2004-10-06
TWI324059B (en) 2010-05-01
ATE424763T1 (en) 2009-03-15
DK1674037T3 (en) 2009-06-02
CA2462364A1 (en) 2004-09-28
CN100393277C (en) 2008-06-11
EP1674037B2 (en) 2017-08-16
CA2462364C (en) 2012-07-24
ES2321330T5 (en) 2017-12-20
HK1069094A1 (en) 2005-05-13
EP1464284B1 (en) 2006-05-10
JP2004298628A (en) 2004-10-28
KR101065599B1 (en) 2011-09-20

Similar Documents

Publication Publication Date Title
US7169117B2 (en) Integrated lance and strip for analyte measurement
US7473264B2 (en) Integrated lance and strip for analyte measurement
EP1462053B1 (en) An improved lance with two elements
AU770595B2 (en) Hollow microneedle patch
AU2003286783B2 (en) Improved method of lancing skin for the extraction of blood
US20050049522A1 (en) Method of lancing skin for the extraction of blood

Legal Events

Date Code Title Description
AS Assignment

Owner name: LIFESCAN, INC., CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ALLEN, JOHN J.;REEL/FRAME:014371/0517

Effective date: 20030616

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION