EP1642126A1 - Systeme et procede de codage d'informations sur une bandelette d'essai de type biocapteur - Google Patents
Systeme et procede de codage d'informations sur une bandelette d'essai de type biocapteurInfo
- Publication number
- EP1642126A1 EP1642126A1 EP04776797A EP04776797A EP1642126A1 EP 1642126 A1 EP1642126 A1 EP 1642126A1 EP 04776797 A EP04776797 A EP 04776797A EP 04776797 A EP04776797 A EP 04776797A EP 1642126 A1 EP1642126 A1 EP 1642126A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- test strip
- test
- contact pad
- meter
- contact pads
- 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.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/4875—Details of handling test elements, e.g. dispensing or storage, not specific to a particular test method
- G01N33/48771—Coding of information, e.g. calibration data, lot number
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/327—Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
- G01N27/3271—Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
- G01N27/3272—Test elements therefor, i.e. disposable laminated substrates with electrodes, reagent and channels
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/00584—Control arrangements for automatic analysers
- G01N35/00722—Communications; Identification
- G01N35/00732—Identification of carriers, materials or components in automatic analysers
Definitions
- the present invention relates to an apparatus for use in measuring concentrations of an analyte in a biological fluid.
- the invention relates more particularly to a system and method for coding information on a biosensor test strip.
- Measuring the concentration of substances in biological fluids is an important tool for the diagnosis and treatment of many medical conditions.
- the measurement of glucose in body fluids, such as blood is crucial to the effective treatment of diabetes.
- Diabetic therapy typically involves two types of insulin treatment: basal, and meal-time.
- Basal insulin refers to continuous, e.g. time-released insulin, often taken before bed.
- Meal-time insulin treatment provides additional doses of faster acting insulin to regulate fluctuations in blood glucose caused by a variety of factors, including the metabolization of sugars and carbohydrates.
- Proper regulation of blood glucose fluctuations requires accurate measurement of the concentration of glucose in the blood. Failure to do so can produce extreme complications, including blindness and loss of circulation in the extremities, which can ultimately deprive the diabetic of use of his or her fingers, hands, feet, etc.
- Optical methods generally involve spectroscopy to observe the spectrum shift in the fluid caused by concentration of the analyte, typically in conjunction with a reagent that produces a known color when combined with the analyte.
- Electrochemical methods generally rely upon the conelation between a cunent (Amperometry), a potential (Potentiometry) or accumulated charge (Coulometry) and the concentration of the analyte, typically in conjunction with a reagent that produces charge-carriers when combined with the analyte. See, for example, U.S. Patent Nos.
- the biosensor for conducting the tests is typically a disposable test strip having a reagent thereon that chemically reacts with the analyte of interest in the biological fluid.
- the test strip is mated to a nondisposable test meter such that the test meter can measure the reaction between the analyte and the reagent in order to determine and display the concentration of the analyte to the user.
- test meter/test strip systems It is common practice in such test meter/test strip systems to ensure proper identification of the test strip in order to ensure proper test results. For example, a single test meter may be able to analyze several different types of test strips, wherein each type of test strip is designed to test for the presence of a different analyte in the biological fluid. In order to properly conduct the test, the test meter must know which type of test is to be performed for the test strip cunently in use.
- lot-to-lot variations in the test strips normally require calibration information to be loaded into the test meter in order to ensure accurate test results.
- a common practice for downloading such calibration information into the test meter is the use of an electronic read-only memory key (ROM key) that is inserted into a socket of the test meter. Because this calibration data may only be accurate for a particular production lot of test strips, the user is usually asked to confirm that the lot number of the test strip cunently in use matches the lot number for which the ROM key was programmed.
- ROM key electronic read-only memory key
- the present invention provides a test strip for measuring a concentration of an analyte of interest in a biological fluid, wherein the test strip may be encoded with information that can be read by a test meter into which the test strip is inserted.
- a method for forming a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising the steps of: providing a basic test strip design comprising: a substrate having a surface and at least one measurement electrode formed thereon; a plurality of conductive contact pads formed upon the substrate surface, including at least one information contact pad and at least one measurement contact pad; and a plurality of potential conductive links conductively coupling various ones of the plurality of contact pads; wherein the at least one information contact pad is not coupled to any of the at least one measurement electrodes except by one or more of the plurality of potential conductive links, and the at least one measurement contact pad is coupled to one of the at least one measurement electrodes by a path other than one or more of the plurality of potential conductive links; defining a set of valid test strip designs; wherein each one of the set of valid test strip designs incorporates none, one or more than one of the plurality of potential conductive links; and wherein at least one of the
- a plurality of test strips for measuring a concentration of an analyte of interest in a biological fluid comprising: a substrate having a surface and at least one measurement electrode formed thereon; a plurality of conductive contact pads formed upon the substrate surface, including at least one information contact pad and at least one measurement contact pad; and a plurality of conductive links selected from the plurality of potential conductive links, wherein the plurality of conductive links conductively couple at least three contact pads together; wherein the at least one information contact pad is not coupled to any of the at least one measurement electrodes except by one or more of the plurality of potential conductive links, and the at least one measurement contact pad is coupled to one of the at least one measurement electrodes by a path other than one or more of the plurality of potential conductive links.
- a method for forming a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising the steps of: providing a basic test strip design comprising: a substrate having a surface and at least one measurement electrode formed thereon; a plurality of conductive contact pads formed upon the substrate surface, including at least one information contact pad and at least one measurement contact pad; and a plurality of potential conductive links conductively coupling various ones of the plurality of contact pads; wherein the at least one information contact pad is not coupled to any of the at least one measurement electrodes except by one or more of the plurality of potential conductive links, and the at least one measurement contact pad is coupled to one of the at least one measurement electrodes by a path other than one or more of the plurality of potential conductive links; defining a set of valid test strip designs; wherein each one of the set of valid test strip designs incorporates none, one or more than one of the plurality of potential conductive links; and wherein at least one of the
- a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising: a substrate having a surface and at least one measurement electrode formed thereon; a plurality of conductive contact pads formed upon the substrate surface, including at least one information contact pad and at least one measurement contact pad; and at least one conductive link conductively coupling at least three of the contact pads; wherein the at least one information contact pad is not coupled to any of the at least one measurement electrodes except by one or more of the at least one conductive links, and the at least one measurement contact pad is coupled to one of the at least one measurement electrodes by a path other than one or more of the at least one conductive links.
- a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising: a substrate having a surface and at least one measurement electrode formed thereon; a plurality of conductive contact pads formed upon the substrate surface, including at least one information contact pad and at least one measurement contact pad; and at least one conductive link conductively coupling at least three of the contact pads; wherein the at least one information contact pad is not coupled to any of the at least one measurement electrodes except by one or more of the at least one conductive links, and the at least one measurement contact pad is coupled to one of the at least one measurement electrodes by a path other than one or more of the at least one conductive links.
- a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising: a substrate having a top surface; a conductive layer formed on at least a portion of the substrate top surface; and at least one predetermined contact pad position defined upon the substrate top surface; wherein each of the at least one contact pad positions is touched by a respective one of the at least one connector contacts when the at least one connector contacts touch the test strip; wherein a presence of the conductive layer in a respective one of the contact pad positions is operative to indicate a first state of a binary bit to the test meter; and wherein an absence of the conductive layer in a respective one of the contact pad positions is operative to indicate a second state of a binary bit to the test meter.
- a method for measuring a concentration of an analyte of interest in a biological fluid comprising the steps of: providing a test meter having at least one connector contact that touches an inserted test strip, providing a test strip adapted to be inserted into the test meter, the test strip comprising: a substrate having a top surface; a conductive layer formed on at least a portion of the substrate top surface; and at least one predetermined contact pad position defined upon the substrate top surface; touching each of the at least one predetermined contact pad positions with a respective one of the at least one connector contacts; indicating a first state of a binary bit within the test meter in response to a presence of the conductive layer in a respective one of the contact pad positions; and indicating a second state of a binary bit within the test meter in response to an absence of the conductive layer in a respective one of the contact pad positions.
- a test strip for measuring a concentration of an analyte of interest in a biological fluid comprising a substrate having a surface; a first measurement electrode formed on the surface; a second measurement electrode formed on the surface; a third potential electrode formed on the surface; a fourth potential electrode formed on the surface; a first contact pad formed on the surface and conductively coupled to the first measurement electrode; a second contact pad formed on the surface and conductively coupled to the second measurement electrode; a third contact pad formed on the surface and conductively coupled to the third potential electrode; a fourth contact pad formed on the surface and conductively coupled to the fourth potential electrode; and a conductive link coupling one of the third and fourth potential electrodes to the first measurement electrode, whereby another one of the third and fourth potential electrodes becomes an actual electrode.
- a method of using a test meter and associated test strip for measuring a concentration of an analyte of interest in a biological fluid comprising the steps of a) providing a test strip comprising a substrate having at least a first, second and third contact pad formed thereon; b) providing a test meter comprising a connector configured to make conductive contact with the first, second and third contact pads when the test strip is inserted into the test meter; c) operating the test meter to determine if conductivity exists between the first and second contact pads; d) operating the test meter to determine if conductivity exists between the first and third contact pads; e) designating the second contact pad to have a first function and the third contact pad to have a second function if the test meter determines that conductivity exists between the first and second contact pads and that conductivity does not exist between the first and third contact pads; and f) designating the second contact pad to have the second function and the third contact pad to have the first function if the test
- a method of using a test meter and associated test strip for measuring a concentration of an analyte of interest in a biological fluid comprising the steps of a) providing a test strip comprising a substrate having at least a first, second and third contact pad formed thereon; b) providing a test meter comprising a connector configured to make conductive contact with the first, second and third contact pads when the test strip is inserted into the test meter; c) operating the test meter to determine if conductivity exists between the first and second contact pads; d) designating the second contact pad to have a first function and the third contact pad to have a second function if the test meter determines that conductivity exists between the first and second contact pads; and e) designating the second contact pad to have the second function and the third contact pad to have the first function if the test meter determines that conductivity does not exist between the first and second contact pads.
- a method of using a test meter adapted to measure a concentration of an analyte of interest in a biological fluid placed on a test strip comprising the steps of a) inserting the test strip into the test meter such that the test meter makes electrical contact with the test strip; b) operating the meter to read information encoded onto the test strip; and c) choosing a language in which the test meter displays user operating instructions based upon the information read from the test strip.
- a method of using a test meter adapted to measure a concentration of an analyte of interest in a biological fluid placed on a test strip comprising the steps of a) inserting the test strip into the test meter such that the test meter makes electrical contact with the test strip; b) operating the meter to read information encoded onto the test strip; and c) determining if the test meter and the test strip were sold in the same geographic market based upon the information read from the test strip.
- a method of using a test meter adapted to measure a concentration of an analyte of interest in a biological fluid placed on a test strip comprising the steps of a) inserting the test strip into the test meter such that the test meter makes electrical contact with the test strip; b) operating the meter to read information encoded onto the test strip; c) determining if the test strip is a subscription test strip based upon the information read from the test strip; and d) preventing use of the test strip by the meter if the test strip is a subscription test strip.
- a method of using a test meter adapted to measure a concentration of an analyte of interest in a biological fluid placed on a test strip comprising the steps of a) inserting the test strip into the test meter such that the test meter makes electrical contact with the test strip; b) operating the meter to read information encoded onto the test strip; and c) activating a latent feature of the test meter based upon the information read from the test strip.
- a method of using a test meter adapted to measure a concentration of an analyte of interest in a biological fluid placed on a test strip comprising the steps of a) inserting the test strip into the test meter such that the test meter makes electrical contact with the test strip; b) operating the meter to read information encoded onto the test strip; and c) changing the user operating instructions displayed to the user based upon the information read from the test strip.
- a test system for measuring a concentration of an analyte of interest in a biological fluid comprising a test meter comprising a connector having at least ten contacts; and a test strip adapted to be inserted into the test meter connector, the test strip comprising: a substrate having a surface; at least ten contact pads formed on the surface; wherein the at least ten contacts make contact with the respective at least ten contact pads when the test strip is inserted into the test meter connector.
- FIG. 1 is an exploded perspective view of a first typical test strip for use in measuring the concentration of an analyte of interest in a biological fluid.
- FIG. 2 is a schematic plan view of a first embodiment test strip electrode and contact pad anangement according to the present invention.
- FIG. 3 is a table showing a first embodiment coding sequence for the test strip of FIG. 2.
- FIG. 4 is a perspective view of a second typical test strip for use in measuring the concentration of an analyte of interest in a biological fluid.
- FIG. 5 illustrates a view of an ablation apparatus suitable for use with the present invention.
- FIG. 6 is a view of the laser ablation apparatus of Figure 5 showing a second mask.
- FIG. 7 is a view of an ablation apparatus suitable for use with the present invention.
- FIG. 8 is a schematic process flow diagram of a prior art process for verifying the applicability of the calibration data in the test meter to the test strip cunently inserted into the test meter.
- FIG. 9 is a schematic process flow diagram of a first embodiment process of the present invention for verifying the applicability of the calibration data in the test meter to the test strip cunently inserted into the test meter.
- FIG. 10 is a schematic plan view of a second embodiment test strip electrode and contact pad anangement according to the present invention.
- FIG. 11 is a schematic plan view of a third embodiment test strip electrode and contact pad anangement according to the present invention.
- FIG. 12 is a schematic plan view of an electrical connector-to-test strip contact pad interface illustrating worst case left tolerance stack-ups.
- FIG. 13 is a schematic plan view of the electrical connector-to-test strip contact pad interface of FIG. 12 illustrating normal case tolerance stack-ups.
- FIG. 14 is a schematic plan view of the electrical connector-to-test strip contact pad interface of FIG. 12 illustrating worst case right tolerance stack-ups.
- FIG. 15 is a schematic plan view of a fourth embodiment test strip electrode and contact pad anangement according to the present invention.
- the test strip 10 comprises a bottom substrate 12 formed from an opaque piece of 350 ⁇ m thick polyester (such as Melinex 329 available from DuPont) coated on its top surface with a 50 nm conductive (gold) layer (by sputtering or vapor deposition, for example). Electrodes, connecting traces and contact pads therefor are then patterned in the conductive layer by a laser ablation process.
- the laser ablation process is performed by means of an excimer laser which passes through a chrome-on-quartz mask.
- the mask pattern causes parts of the laser field to be reflected while allowing other parts of the field to pass through, creating a pattern on the gold which is ablated where contacted by the laser light.
- the laser ablation process is described in greater detail hereinbelow.
- working 20, counter 22, dose sufficiency working 24, and dose sufficiency counter 26 electrodes may be formed as shown and coupled, respectively, to measurement contact pads W, C, DW and DC. These contact pads provide a conductive area upon the test strip 10 to be contacted by a connector contact of the test meter once the test strip 10 is inserted into the test meter.
- the bottom substrate 12 is then coated in the area extending over the electrodes with a reagent layer 14 as a continuous, extremely thin reagent film.
- the reagent layer 14 is a stripe of approximately 6 millimeters width across the substrate 12 in the region labeled "Reagent Layer" on FIG. 1. For example, this region may be coated at a wet-coat weight of 50 grams per square meter of coated surface area.
- the reagent strip is dried conventionally with an in-line drying system where the nominal air temperature is at 110°C. The rate of processing is nominally 30-38 meters per minute and depends upon the rheology of the reagent.
- the materials are processed in continuous reels such that the electrode pattern is orthogonal to the length of the reel, in the case of the substrate 12.
- the spacers 16 are slit and placed in a reel-to-reel process onto the substrate 12.
- Two spacers 16 formed from 100 ⁇ m polyester (for example, Melinex 329 available from DuPont) coated with 25 ⁇ m PSA (hydrophobic adhesive) on both the dorsal and ventral surfaces are applied to the bottom substrate 12, such that the spacers 16 are separated by 1.5 mm and the working, counter and dose sufficiency electrodes are centered in this gap.
- the hydrophilic film is coated with a mixture of Nitel and Rhodapex surfactant at a nominal thickness of 10 microns.
- the top foil layer 18 is laminated using a reel-to-reel process. The test strips can then be produced from the resulting reels of material by means of slitting and cutting.
- test strip 10 illustrated in FIG. 1 can provide accurate measurements of blood glucose in a whole blood sample, it does not provide any means for the test meter into which it is inserted to identify anything about the test strip.
- the present invention presents several systems by which information relating to the test strip can be coded directly onto the test strip itself, such that this information can be conveyed to a test meter into which the test strip is inserted.
- information about the test strip can be coded directly onto the test strip by the addition of two or more contact pads dedicated to reading such coded information.
- a pair of additional information contact pads Bl and B2 are added to the proximal end of the test strip.
- potential conductive links between the information contact pads Bl and B2 and between them and measurement contact pads connected to test strip measurement electrodes are identified at 28, 30, 32, 34 and 36. These links are denominated as potential conductive links because they may either be present or absent in the finished test strip, depending upon the information that is to be coded onto the test strip.
- a “potential conductive link” indicates a conductive link that is found on some, but not all, of a group of otherwise substantially identical test strips.
- the phrase "information contact pad” is defined as a contact pad on the test strip that is either not conductively coupled to a measurement electrode of the test strip at all, or is so coupled only by a potential conductive link.
- the phrase “measurement contact pad” is defined as a contact pad on the test strip that is always conductively coupled to a measurement electrode of the test strip, regardless of the presence or absence of the potential conductive links.
- potential conductive link 28 couples the DC contact pad and the Bl contact pad.
- Potential conductive link 30 couples the Bl contact pad and the B2 contact pad.
- Potential conductive link 32 couples the B2 contact pad and the C contact pad.
- Potential conductive link 34 couples the DC contact pad and the B2 contact pad.
- Potential conductive link 36 couples the Bl contact pad and the C contact pad.
- the first embodiment of the present invention illustrates potential conductive links between the information contact pads Bl and B2 and the measurement contact pads DC and C by way of example only, and that the information contact pads may be conductively linked to any desired measurement contact pad(s) on the test strip.
- FIG. 3 illustrates a table showing the possible combinations for the potential conductive links 28-36 formed on any one test strip of the first embodiment.
- the first five columns of the table represent each of the potential conductive links 28-36, which are labeled C1-C5, respectively.
- Each of the nine rows of the table numbered 0-8 represent a different number that can be encoded using the potential conductive links 28-36.
- a "0" in a table position indicates that the potential conductive link is not formed when encoding the number of that row, while a "1" in a table position indicates that the potential conductive link is formed when encoding the number of that row.
- potential conductive links 34 and 36 may not be used at the same time, as they cross one another and therefore would conductively connect the DC contact pad to the C contact pad.
- potential conductive links 28, 30 and 32 may not be used at the same time.
- the last two columns of the table of FIG. 3 are labeled Bl and B2, respectively, and indicate to which of the other contact pads the labeled contact pad is coupled when the number of that row is encoded onto the test strip. For example, when the number six (6) is encoded onto the test strip (i.e. potential conductive links 28 and 32 are formed on the test strip) the Bl contact pad is conductively coupled to the DC contact pad, and the B2 contact pad is conductively coupled to the C contact pad, but Bl and B2 are not conductively coupled to any other contact pads (including to each other).
- the present invention also comprehend other methods for determining the presence or absence of potential conductive links on the test strip other than by measurement of resistance or conductivity.
- the potential conductive links can also be sensed in a non-contact fashion by inducing and sensing eddy cunents using an electromagnetic field, by capacitive means, by optical scanning techniques, or by other methods that would be apparent to one having ordinary skill in the art.
- the absence of all of the potential conductive links 28-36 is preferably not considered to be a valid state as this could be caused by a localized defect obliterating the region of the test strip containing the potential conductive links 28-36, but this state could be considered a valid state in other, non-prefened, embodiments. It should also be noted that a reading of conduction between combinations of contact pads not indicated as a valid combination in the table of FIG. 3 will be interpreted by the test meter as a defective strip with an unintended short.
- One method of preparing a test strip encoded with information as described herein is by the use of laser ablation techniques. Examples of the use of these techniques in preparing electrodes for biosensors are described in United States Patent Application Serial Number 09/866,030, "Biosensors with Laser Ablation Electrodes with a Continuous Coverlay Channel” filed May 25, 2001, and in United States Patent Application Serial Number 09/411,940, entitled “Laser Defined Features for Patterned Laminates and Electrode,” filed October 4, 1999, both disclosures incorporated herein by reference. It is desirable in the present invention to provide for the accurate placement of the electrical components relative to one another and to the overall biosensor.
- the relative placement of components is achieved, at least in part, by the use of broad field laser ablation that is performed through a mask or other device that has a precise pattern for the electrical components. This allows accurate positioning of adjacent edges, which is further enhanced by the close tolerances for the smoothness of the edges.
- Figure 4 illustrates a simple biosensor 401 useful for illustrating the laser ablation process of the present invention, including a substrate 402 having formed thereon conductive material 403 defining electrode systems comprising a first electrode set 404 and a second electrode set 405, and corresponding traces 406, 407 and contact pads 408, 409, respectively.
- the conductive material 403 may contain pure metals or alloys, or other materials, which are metallic conductors.
- the conductive material is absorptive at the wavelength of the laser used to form the electrodes and of a thickness amenable to rapid and precise processing.
- Non- limiting examples include aluminum, carbon, copper, chromium, gold, indium tin oxide (LTO), palladium, platinum, silver, tin oxide/gold, titanium, mixtures thereof, and alloys or metallic compounds of these elements.
- the conductive material includes noble metals or alloys or their oxides.
- the conductive material includes gold, palladium, aluminum, titanium, platinum, ITO and chromium.
- the conductive material ranges in thickness from about 10 nm to 80 nm, more preferably, 30 nm to 70 nm, and most preferably 50 nm. It is appreciated that the thickness of the conductive material depends upon the transmissive property of the material and other factors relating to use of the biosensor.
- the resulting patterned conductive material can be coated or plated with additional metal layers.
- the conductive material may be copper, which is then ablated with a laser into an electrode pattern; subsequently, the copper may be plated with a titanium/tungsten layer, and then a gold layer, to form the desired electrodes.
- a single layer of conductive material is used, which lies on the base 402.
- seed or ancillary layers such as chromium nickel or titanium.
- biosensor 401 has a single layer of gold, palladium, platinum or ITO.
- Biosensor 401 is illustratively manufactured using two apparatuses 10, 10', shown in Figures 4,6 and 7, respectively. It is appreciated that unless otherwise described, the apparatuses 410, 410' operate in a similar manner. Referring first to Figure 5, biosensor 401 is manufactured by feeding a roll of ribbon 420 having an 80 nm gold laminate, which is about 40 mm in width, into a custom fit broad field laser ablation apparatus 410.
- the apparatus 410 comprises a laser source 411 producing a beam of laser light 412, a chromium-plated quartz mask 414, and optics 416. It is appreciated that while the illustrated optics 416 is a single lens, optics 416 is preferably a variety of lenses that cooperate to make the light 412 in a pre-determined shape.
- a non-limiting example of a suitable ablation apparatus 410 is a customized MicrolineLaser 200-4 laser system commercially available from LPKF Laser Electronic GmbH, of Garbsen, Germany, which incorporates an LPX-400, LPX-300 or LPX-200 laser system commercially available from Lambda Physik AG, Gottingen, Germany and a chromium-plated quartz mask commercially available from International Phototool Company, Colorado Springs, Co.
- the laser source 411 is a LPX-200 KrF-UN-laser. It is appreciated, however, that higher wavelength UN lasers can be used in accordance with this disclosure.
- the laser source 411 works at 248nm, with a pulse energy of 600mJ, and a pulse repeat frequency of 50 Hz.
- the intensity of the laser beam 412 can be infinitely adjusted between 3% and 92% by a dielectric beam attenuator (not shown).
- the beam profile is 27 15mm 2 (0.62 sq. inch) and the pulse duration 25ns.
- the layout on the mask 414 is homogeneously projected by an optical elements beam expander, homogenizer, and field lens (not shown).
- the performance of the homogenizer has been determined by measuring the energy profile.
- the imaging optics 416 transfer the structures of the mask 414 onto the ribbon 420.
- the imaging ratio is 2:1 to allow a large area to be removed on the one hand, but to keep the energy density below the ablation point of the applied chromium mask on the other hand. While an imaging of 2:1 is illustrated, it is appreciated that the any number of alternative ratios are possible in accordance with this disclosure depending upon the desired design requirements.
- the ribbon 420 moves as shown by anow 425 to allow a number of layout segments to be ablated in succession.
- the positioning of the mask 414, movement of the ribbon 420, and laser energy are computer controlled. As shown in Figure 5, the laser beam 412 is projected onto the ribbon 420 to be ablated. Light 412 passing through the clear areas or windows 418 of the mask 414 ablates the metal from the ribbon 420. Chromium coated areas 424 of the mask 414 blocks the laser light 412 and prevent ablation in those areas, resulting in a metallized structure on the ribbon 420 surface.
- a complete structure of electrical components may require additional ablation steps through a second mask 414'. It is appreciated that depending upon the optics and the size of the electrical component to be ablated, that only a single ablation step or greater than two ablation steps may be necessary in accordance with this disclosure. Further, it is appreciated that instead of multiple masks, that multiple fields may be formed on the same mask in accordance with this disclosure.
- a second non-limiting example of a suitable ablation apparatus 410' is a customized laser system commercially available from LPKF Laser Electronic GmbH, of Garbsen, Germany, which incorporates a Lambda STEEL (Stable energy eximer laser) laser system commercially available from Lambda Physik AG, Gottingen, Germany and a chromium-plated quartz mask commercially available from International Phototool Company, Colorado Springs, Co.
- the laser system features up to 1000 mJ pulse energy at a wavelength of 308 nm. Further, the laser system has a frequency of 100 Hz.
- the apparatus 410' may be formed to produce biosensors with two passes as shown in Figures 5 and 6, but preferably its optics permit the formation of a 10x40 mm pattern in a 25 ns single pass.
- the laser pulse or beam 412 that passes through the mask 414, 414' , 414" is absorbed within less than 1 ⁇ m of the surface 402 on the ribbon 420.
- the photons of the beam 412 have an energy sufficient to cause photo-dissociation and the rapid breaking of chemical bonds at the metal/polymer interface. It is believed that this rapid chemical bond breaking causes a sudden pressure increase within the absorption region and forces material (metal film 403) to be ejected from the polymer base surface. Since typical pulse durations are around 20-25 nanoseconds, the interaction with the material occurs very rapidly and thermal damage to edges of the conductive material 403 and sunounding structures is minimized. The resulting edges of the electrical components have high edge quality and accurate placement as contemplated by the present invention.
- Fluence energies used to remove or ablate metals from the ribbon 420 are dependent upon the material from which the ribbon 420 is formed, adhesion of the metal film to the base material, the thickness of the metal film, and possibly the process used to place the film on the base material, i.e. supporting and vapor deposition.
- Fluence levels for gold on KALADEX ® range from about 50 to about 90 mJ/cm 2 , on polyimide about 100 to about 120 mJ/cm 2 , and on MELINEX ® about 60 to about 120 mJ/cm 2 . It is understood that fluence levels less than or greater than the above mentioned can be appropriate for other base materials in accordance with the disclosure.
- Patterning of areas of the ribbon 420 is achieved by using the masks 414, 414'.
- Each mask 414, 414' illustratively includes a mask field 422 containing a precise two-dimensional illustration of a pre-determined portion of the electrode component patterns to be formed.
- Figure 5 illustrates the mask field 422 including contact pads and a portion of traces.
- the second mask 414' contains a second conesponding portion of the traces and the electrode patterns containing fingers.
- the mask 414 can contain a complete illustration of the electrode patterns ( Figure 7), or portions of patterns different from those illustrated in Figures 5 and 6 in accordance with this disclosure.
- the entire pattern of the electrical components on the test strip are laser ablated at one time, i.e., the broad field encompasses the entire size of the test strip ( Figure 7).
- the broad field encompasses the entire size of the test strip ( Figure 7).
- mask 414 will be discussed hereafter, it is appreciated that unless indicated otherwise, the discussion will apply to masks 414', 414" as well.
- areas 424 of the mask field 422 protected by the chrome will block the projection of the laser beam 412 to the ribbon 420.
- Clear areas or windows 418 in the mask field 422 allow the laser beam 412 to pass through the mask 414 and to impact predetermined areas of the ribbon 420.
- the clear area 418 of the mask field 422 conesponds to the areas of the ribbon 420 from which the conductive material 403 is to be removed.
- the mask field 422 has a length shown by line 430 and a width as shown by line 432. Given the imaging ratio of 2: 1 of the LPX-200, it is appreciated that the length 30 of the mask is two times the length of a length 434 of the resulting pattern and the width 432 of the mask is two times the width of a width 436 of the resulting pattern on ribbon 420.
- the optics 416 reduces the size of laser beam 412 that strikes the ribbon 420. It is appreciated that the relative dimensions of the mask field 422 and the resulting pattern can vary in accordance with this disclosure.
- Mask 414' ( Figure 6) is used to complete the two-dimensional illustration of the electrical components.
- the excimer laser source 411 emits beam 412, which passes through the chrome-on- quartz mask 414.
- the mask field 422 causes parts of the laser beam 412 to be reflected while allowing other parts of the beam to pass through, creating a pattern on the gold film where impacted by the laser beam 412.
- ribbon 420 can be stationary relative to apparatus 410 or move continuously on a roll through apparatus 410. Accordingly, non-limiting rates of movement of the ribbon 420 can be from about 0 m/min to about 100 m min, more preferably about 30 m/min to about 60 m/min. It is appreciated that the rate of movement of the ribbon 420 is limited only by the apparatus 410 selected and may well exceed 100 m/min depending upon the pulse duration of the laser source 411 in accordance with the present disclosure.
- the ribbon is rewound and fed through the apparatus 410 again, with mask 414' ( Figure 6).
- masks 414, 414' large areas of the ribbon 420 can be patterned using step-and-repeat processes involving multiple mask fields 422 in the same mask area to enable the economical creation of intricate electrode patterns and other electrical components on a substrate of the base, the precise edges of the electrode components, and the removal of greater amounts of the metallic film from the base material.
- the ability to code information directly onto the test strip can dramatically increase the capabilities of the test strip and enhance its interaction with the test meter.
- ROM key read-only memory key
- the user inserts the ROM key into a port in the test meter so that the test meter may have access to this data while performing tests using the test strip.
- the quality of the measurement result can be verified by allowing the meter to electronically assess the applicability of the ROM key data to the test strip cunently inserted into the meter, without the need for an optical reader to read bar code information on the test strip as has been taught in the prior art.
- FIG. 8 illustrates a typical prior art process for verifying the match between the ROM key data and the test strip lot identification (LD) number.
- LD test strip lot identification
- the test meter displays the lot ED of the cunently loaded calibration data (step 104) in order to give the user the chance to verify that this lot LD matches the lot ED printed on the vial/package (for example) containing a plurality of test strips from the same production lot as the test strip cunently inserted into the test meter.
- the process of FIG. 8 therefore indicates an optional step for the user to compare the lot LD on the test meter display to the lot LD on the test strip vial (step 106) and to determine (step 108) if there is a match. If the two lot EDs do not match, then the user should remove the test strip (step 110) and insert the ROM key that matches the test strip vial into the test meter (step 112) so that the proper calibration code can be loaded into the test meter. The process would then start over at step 100 with the insertion of the test strip. Once it has been determined that the test meter's calibration code lot ED matches the lot ED of the test strip (step 108), then the measurement sequence can continue by applying blood to the test strip (step 114) and beginning the blood glucose measurement cycle (step 116).
- the information contact pads of the present invention allow the test meter itself to perform checks as to the applicability of the cunently loaded calibration data to the cunently inserted test strip.
- a first embodiment process of the present invention to allow the test meter to actively participate in such verification is illustrated in FIG. 9.
- the steps of the process of FIG. 9 that are identical to the conesponding steps in FIG. 8 are numbered with the same reference designators.
- the ROM key Prior to executing this process, the ROM key has been inserted into the test meter, the ROM data has been loaded into the test meter, and the test meter is turned off.
- the process begins by inserting a test strip (step 100) into the test meter, which causes the test meter to automatically turn on (step 102).
- the test meter measures the conductivity between the various information and measurement contact pads on the test strip that have been designated for encoding information onto the test strip in order to ascertain the lot or family LD of the test strip (step 200).
- the test strips usable in the test meter may be of two or more families where significant differences exist between the family test strip designs. For example, two families may use a different reagent on the test strip. In such situations, the test meter can still verify that the loaded calibration data matches the test strip family encoded onto the test strip, even if it is not possible to verify the precise production lot of the test strip. Therefore, as used herein, the phrase "lot ED" is intended to encompass any information that identifies a group to which the test strip or calibration data belongs, even if that group is not as small as a production lot of the test strip.
- the test meter compares (step 202) the lot
- the test meter displays the lot ED of the cunently loaded calibration data (step 204) and a warning in order to give the user the chance to insert a conect test strip or to insert a different ROM key into the test meter.
- the test meter may simply display an enor message to the user.
- the fact that the lot EDs do not match is flagged (step 206) in the test meter's result memory 208 so that there is a record in the memory 208 that the measurement result obtained is suspect in view of the discrepancy in the lot LDs.
- the user may be prohibited from running a test and the process may be aborted.
- the process of FIG. 9 indicates an optional step for the user to compare the lot ED on the test meter display to the lot LD on the test strip vial (step 106) and to determine (step 108) if there is a match. If the two lot IDs do not match, then the user should remove the test strip (step 110) and insert the ROM key that matches the test strip vial into the test meter (step 112) so that the proper calibration code can be loaded into the test meter. The process would then start over at step 100 with the insertion of the test strip.
- the meter may determine the multiple lot EDs of calibration data that may be stored within the test meter and automatically choose the calibration dataset that matches the test strip cunently inserted into the meter. The meter can then return to step 114. Once it has been determined that the test meter' s calibration code lot LD matches the lot ED of the test strip (step 108), then the measurement sequence can continue by applying blood to the test strip (step 114) and beginning the blood glucose measurement cycle (step 116). It will be appreciated that the process of FIG. 9 represents an improvement over the prior art process of FIG.
- the present invention allows the test strip to activate or deactivate certain features programmed into the test meter.
- a single test meter may be designed to be used in several different geographic markets, where a different language is spoken in each market.
- the encoded information can cause the test meter to display user instructions and data in a language that is appropriate for that market.
- a meter may be designed for sale in a certain geographic market and it is desired that the meter not be used with test strips obtained in a different geographic market (for example when governmental regulations require the test strips sold in one geographic market to have different features than those sold in other geographic markets).
- information coded onto the test strip may be used by the test meter to determine that the test strip did not originate in the designated geographic market and therefore may not provide the features required by regulation, in which case the test may be aborted or flagged.
- a business model may be applied for the distribution of test strips where proliferation of the test strips into other sales channels is not desired.
- users may enroll into a subscription program in which they are provided with a test meter designed for use by subscription participants, and the subscription participants may be provided with subscription test strips on a regular basis (for example by mail or any other convenient form of delivery).
- the "subscription test strips" may be encoded to indicate that they were supplied to a subscription participant.
- the manufacturer of the subscription test strips may not want the subscription test strips to be sold in other channels of trade.
- One way to prevent this is to design test meters provided to users who are not subscription participants that will not work with subscription test strips.
- the present invention may be used to provide test meters to subscription participants in the subscription business model that are programmed to accept subscription test strips encoded to indicate that they are delivered to a user on the basis of a subscription, while other test meters are programmed not to accept subscription test strips so encoded.
- the test meter can have certain functionalities (software- and/or hardware-implemented) designed into the meter that are not active when the test meter is first sold.
- the performance of the test meter can then be upgraded at a later date by including information encoded on the test strips sold at that later time that will be recognized by the meter as an instruction to activate these latent features.
- activating a latent feature of the test meter comprehends turning on a test meter functionality that previously was not active, such that the test meter functionality thereafter remains activated indefinitely (i.e. after the cunent test with the present test strip is finished).
- test strip Another example of information that can be encoded onto the test strip using the present invention is an indication of whether the test strip was sold to the hospital market or to the consumer market. Having this information may allow the test meter to take action accordingly, such as displaying user instructions in less detail for the hospital professional. It will be appreciated by those skilled in the art that a variety of types of communication between the test strip and the test meter may be facilitated by the information encoding provided by the present invention.
- a second embodiment test strip configuration that allows information to be encoded directly onto the test strip is illustrated in FIG. 10 and indicated generally at 300.
- the test strip 300 may preferably be formed generally as described above with respect to the test strips 10 and 401, with working 320, counter 322, dose sufficiency working 324, and dose sufficiency counter 326 electrodes may be formed as shown and coupled, respectively, to measurement contact pads W, C, DW and DC. These contact pads provide a conductive area upon the test strip 300 to be contacted by an electrical connector contact of the test meter once the test strip 300 is inserted into the test meter.
- the test strip may be formed with a sample inlet in the distal end of the test strip (as shown in FIG. 10), or with a sample inlet on the side of the test strip as shown in FIG. 1. The functionality of the information encoding portion thereof is not affected by the positioning of the measurement electrodes in either position.
- the area sunounding the counter electrode contact pad C is formed to provide a relatively large expanse of conductive layer, which is divided into information contact pad positions Bl - B7.
- the conductive layer may be formed during manufacture of the test strip such that the conductive layer is either present or absent within each of the contact pad positions Bl - B7, depending upon what number is to be encoded onto the test strip 300.
- the counter electrode contact pad C is always formed with the conductive layer present in this area, as this contact pad is always necessary for the making of measurements.
- Each of the contact pads C, W, DC and DW, as well as each of the contact pad positions B 1 - B7 are contacted by individual contacts of a multi-pin electrical connector located within the test meter when the test strip 300 is inserted into the test meter.
- the multi-pin electrical connector allows electrical signals to be applied from the test meter to the test strip and vice versa.
- the test meter is programmed (by means well-known in the art), to measure the conductivity between the counter electrode contact pad C and each of the contact pad positions Bl - B7.
- the contact pad C can therefore be selectively conductively coupled to each of the contact pad positions Bl - B7 depending upon whether the conductive layer is formed, respectively, in each of the contact pad positions B 1 - B7.
- the test meter By measuring the conductivity between the contact pad C and each of the contact pad positions Bl - B7, the test meter is able to determine the presence or absence of the conductive layer in each of the contact pad positions Bl - B7. By assigning, for example, a digital value of "1" when the conductive layer is present in a particular contact pad position and a digital value of "0" when the conductive layer is absent in a particular contact pad position, a digital word may be encoded onto the test strip 300.
- the second embodiment has the added advantage that, because the contact pad positions Bl - B7 can never be conductively coupled to more than one measurement electrode, there are no "forbidden” states and each of the contact pad positions Bl - B7 may be coded as a "0" or "1" in any possible seven digit digital word to be encoded onto the test strip. This provides 2 or 128 possible unique words that can be encoded onto the test strip using the contact pad positions Bl - B7.
- the number of contact pad positions that can be designated for such information encoding is only limited by the available space on the test strip surface, the resolution of the process used to define the conductive features on the test strip, the electrical connector contact spacing, and the tolerance stack-ups relevant to placing the connector contact on the contact pad position once the test strip is inserted into the test meter.
- the number of possible states in the second embodiment of the present invention can be further increased by severing the conductive path between individual pairs of the contact pad positions Bl - B7. Therefore, a connector contacting contact pad Bl (for example) can check for electrical continuity not only with contact pad C (as described hereinabove), but also for electrical continuity with any of the other contact pads B2 - B7.
- FIG. 11 a third embodiment of the present invention is illustrated in FIG. 11 and indicated generally at 500.
- the test strip 500 is similar to the test strip 300 of FIG. 10, except that the resolution of the laser ablation process allows for an even greater number of contact pads to be formed on the test strip.
- Equivalent structures in FIG. 11 are given the same reference designators as used in FIG. 10.
- a total of sixteen contact pads are formed on the test strip 500, with Bl- B10 being designated as information contact pads in addition to the measurement contact pads W, WS, C, CS, DW and DC coupled to working 520, counter 522, dose sufficiency working 524, and dose sufficiency counter 526 electrodes.
- These contact pads provide a conductive area upon the test strip 500 to be contacted by an electrical connector contact of the test meter once the test strip 500 is inserted into the test meter.
- the test strip may be formed with a sample inlet in the distal end of the test strip (as shown in FIG. 11), or with a sample inlet on the side of the test strip as shown in FIG. 1. The functionality of the information encoding portion thereof is not affected by the positioning of the measurement electrodes in either position.
- the area sunounding the counter electrode contact pad C is formed to provide a relatively large expanse of conductive layer, which is divided into information contact pad positions B 1 - B 10.
- the conductive layer may be formed during manufacture of the test strip such that the conductive layer is either present or absent within each of the contact pad positions B 1 - B 10, depending upon what number is to be encoded onto the test strip 500.
- the counter electrode contact pad C is always formed with the conductive layer present in this area, as this contact pad is always necessary for the making of measurements.
- Each of the contact pads C, CS, W, WS, DC and DW, as well as each of the contact pad positions Bl - B10 are contacted by individual contacts of a multi-pin electrical connector located within the test meter when the test strip 500 is inserted into the test meter.
- the multi-pin electrical connector allows electrical signals to be applied from the test meter to the test strip and vice versa.
- the test meter is programmed to measure the conductivity between the counter electrode contact pad C and each of the contact pad positions Bl - BIO.
- the contact pad C can therefore be selectively conductively coupled to each of the contact pad positions B 1 - B 10 depending upon whether the conductive layer is formed, respectively, in each of the contact pad positions Bl - BIO.
- the test meter By measuring the conductivity between the contact pad C and each of the contact pad positions Bl - BIO, the test meter is able to determine the presence or absence of the conductive layer in each of the contact pad positions Bl - BIO. By assigning, for example, a digital value of "1" when the conductive layer is present in a particular contact pad position and a digital value of "0" when the conductive layer is absent in a particular contact pad position, a digital word may be encoded onto the test strip 500.
- the third embodiment has the added advantage that, because the contact pad positions Bl - B10 can never be conductively coupled to more than one measurement electrode, there are no
- each of the contact pad positions B 1 - B 10 may be coded as a "0" or "1" in any possible ten digit digital word to be encoded onto the test strip. This provides 2 10 or 1,024 possible unique words that can be encoded onto the test strip using the contact pad positions Bl - B10.
- the number of possible states in the third embodiment test strip 500 of the present invention can be further increased by severing the conductive path between individual pairs of the contact pad positions Bl - B10. Therefore, a connector contacting contact pad Bl (for example) can check for electrical continuity not only with contact pad C (as described hereinabove), but also for electrical continuity with any of the other contact pads B2 - BIO. This greatly increases the number of unique digital words that can be encoded onto the test strip 500.
- contact pad densities achieved in the present invention through the use of the laser ablation process represent a significant advancement over the prior art.
- published European patent application EP 1 024 358 Al discloses a system which uses up to 35 contact pads on a single test strip; however, the density of features is so low that the inventors are forced to contact only five of those contact pads at any one time. Not only does this require much more test strip surface area than the present invention to form the same number of contact pads, but it is impossible for the test meter to make conductivity checks between each of the contact pads because the test meter is never in contact with more than five of the contact pads at any one time.
- the embodiment of FIG. 10 allows eleven contact pads to be contacted simultaneously by the test meter connector. Even greater density is achieved in the embodiment of Figure 11, where sixteen contact pads may be contacted simultaneously by the test meter connector.
- Some embodiments of the present invention therefore preferably include at least ten test strip contact pads coupled to at least ten test meter connector contacts; more preferably include at least eleven test strip contact pads coupled to at least eleven test meter connector contacts; and most preferably includes at least fifteen test strip contact pads coupled to at least fifteen test meter connector contacts.
- FIGs. 12-14 illustrate a prefened embodiment multiple-pin electrical connector mating with the third embodiment test strip 500 of FIG. 11.
- the electrical connector is housed in the test meter (not shown) and includes multiple contacts that produce contact traces 502 when mated with respective contact pads on the test strip 500 when the test strip 500 is inserted into the test meter electrical connector.
- FIG. 13 illustrates the nominal case in which each electrical connector contact is positioned approximately at the center of the respective test strip 500 contact pad when the test strip 500 is mated to the test meter.
- the tolerances of the placement of the conductive features on the test strip 500, as well as the tolerances of the placement of the electrical connector contacts with respect to the test strip mating port of the test meter are controlled such that the worst case tolerance stack-ups will still result in reliable contact between each connector contact and the respective contact pad. As can be seen in FIG.
- a fourth embodiment test strip of the present invention is schematically illustrated in FIG. 15 and designated as 600.
- the test strip 600 is similar to the test strip 300 of FIG. 10, except that the fourth embodiment uses only six contact pads on the test strip. Embodiments using fewer or more contact pads are contemplated by the present invention. Equivalent structures in FIG. 15 are given the same reference designators as used in FIG. 10.
- the test strip includes a working electrode 320, a counter electrode 322, a dose sufficiency working electrode 324, and two potential dose sufficiency counter electrodes 326 A and 326B. Each of the electrodes is coupled to at least one contact pad formed on the test strip 600.
- the working electrode 320 is coupled to both a W and a WS contact pad.
- the counter electrode 322 is coupled to a C contact pad and a CS contact pad, although which contact pad is designated as C is optional as explained hereinbelow.
- the dose sufficiency working electrode 324 is coupled to a DW contact pad.
- the dose sufficiency counter electrode 326A 326B is coupled to a DC contact pad, although which contact pad is designated as DC is optional as explained hereinbelow.
- the test strip 600 allows a single binary bit to be encoded onto the test strip 600, depending on which of the two potential conductive links 602 and 604 are formed on the test strip 600. At least one of the potential conductive links 602/604 is preferably formed on the test strip 600, and both potential conductive links
- 602/604 may not be formed at the same time without losing the second separate dose sufficiency electrode functionality.
- the contact pad 606 becomes the C contact pad (since it is coupled to the counter electrode 322 by the potential conductive link 602). Without the presence of the potential conductive link 604, electrode 326B functions as the actual dose sufficiency counter electrode and contact pad 608 becomes the DC contact pad.
- the contact pad 608 becomes the C contact pad (since it is coupled to the counter electrode 322 by the potential conductive link 604).
- electrode 326A functions as the actual dose sufficiency counter electrode and contact pad 606 becomes the DC contact pad.
- the test meter can easily determine if the potential conductive link 602 is present by checking the conductivity between the CS contact pad and the contact pad 606. Conductivity between these two contact pads indicates the presence of the potential conductive link 602. Similarly, the test meter can determine if the potential conductive link 604 is present by checking the conductivity between the CS contact pad and the contact pad 608. Conductivity between these two contact pads indicates the presence of the potential conductive link 604. Once the test meter has determined which potential conductive link 602/604 is present, it thereafter knows which contact pad to treat as the C contact pad and which to treat as the DC contact pad.
- the test meter only checks for the presence or absence of one of the potential conductive links 602/604 and assumes that the other potential conductive link 602/604 is absent or present, respectively. In another embodiment, the test meter confirms the presence or absence of both potential conductive links 602/604, which is a more robust methodology as it is more likely to detect a damaged test strip.
- the code key inserted into the test meter tells the test meter which of the two possible configurations to expect.
- the test meter then checks to see if the expected contact pad 606/608 is coupled to the CS contact pad. If the expected connection is not present, then the meter checks to see if the other contact pad 606/608 is coupled to the CS contact pad. If the wrong contact pad 606/608 is coupled to the CS contact pad, then the meter indicates a code key enor (i.e. a code key has been inserted into the test meter that does not match the test strip inserted into the test meter). If neither contact pad 606/608 is coupled to the CS contact pad, then the test meter indicates a strip error (i.e. the test strip is defective and cannot be used).
- the test meter has been supplied with one bit of information from the test strip 600.
- This single bit of information can convey important information to the test meter, such as whether the test strip is designed to test for a first analyte or a second analyte, where the test meter should look for calibration information relating to the test strip, etc. Therefore, supplying a single bit of information by simply reassigning the functions of some of the contact pads on the test strip can easily provide important information to the test meter about the test strip that has been inserted therein.
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Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP17196182.4A EP3361249B1 (fr) | 2003-06-20 | 2004-06-18 | Procede d'utilisation d'un instrument de mesure et d'une bandelette d'essai associee pour mesurer la concentration d'un analyte dans un fluide biologique |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US48019903P | 2003-06-20 | 2003-06-20 | |
PCT/US2004/019653 WO2004113914A1 (fr) | 2003-06-20 | 2004-06-18 | Systeme et procede de codage d'informations sur une bandelette d'essai de type biocapteur |
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Application Number | Title | Priority Date | Filing Date |
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EP17196182.4A Division EP3361249B1 (fr) | 2003-06-20 | 2004-06-18 | Procede d'utilisation d'un instrument de mesure et d'une bandelette d'essai associee pour mesurer la concentration d'un analyte dans un fluide biologique |
Publications (1)
Publication Number | Publication Date |
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EP1642126A1 true EP1642126A1 (fr) | 2006-04-05 |
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Application Number | Title | Priority Date | Filing Date |
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EP17196182.4A Expired - Lifetime EP3361249B1 (fr) | 2003-06-20 | 2004-06-18 | Procede d'utilisation d'un instrument de mesure et d'une bandelette d'essai associee pour mesurer la concentration d'un analyte dans un fluide biologique |
EP04776797A Withdrawn EP1642126A1 (fr) | 2003-06-20 | 2004-06-18 | Systeme et procede de codage d'informations sur une bandelette d'essai de type biocapteur |
EP04755694A Withdrawn EP1639366A1 (fr) | 2003-06-20 | 2004-06-18 | Systeme et procede pour coder des informations sur une bande diagnostique utilisee comme biodetecteur |
EP17196179.0A Pending EP3336542A1 (fr) | 2003-06-20 | 2004-06-18 | Procédés d`utilisation d'une bande d'essai de biocapteur selon un programme de suscription |
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EP17196182.4A Expired - Lifetime EP3361249B1 (fr) | 2003-06-20 | 2004-06-18 | Procede d'utilisation d'un instrument de mesure et d'une bandelette d'essai associee pour mesurer la concentration d'un analyte dans un fluide biologique |
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EP04755694A Withdrawn EP1639366A1 (fr) | 2003-06-20 | 2004-06-18 | Systeme et procede pour coder des informations sur une bande diagnostique utilisee comme biodetecteur |
EP17196179.0A Pending EP3336542A1 (fr) | 2003-06-20 | 2004-06-18 | Procédés d`utilisation d'une bande d'essai de biocapteur selon un programme de suscription |
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JP (2) | JP4916309B2 (fr) |
CN (2) | CN1839314B (fr) |
CA (2) | CA2529301C (fr) |
HK (2) | HK1094035A1 (fr) |
WO (6) | WO2005001474A1 (fr) |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8419650B2 (en) | 1999-04-16 | 2013-04-16 | Cariocom, LLC | Downloadable datasets for a patient monitoring system |
US6290646B1 (en) | 1999-04-16 | 2001-09-18 | Cardiocom | Apparatus and method for monitoring and communicating wellness parameters of ambulatory patients |
US20050103624A1 (en) | 1999-10-04 | 2005-05-19 | Bhullar Raghbir S. | Biosensor and method of making |
US7073246B2 (en) * | 1999-10-04 | 2006-07-11 | Roche Diagnostics Operations, Inc. | Method of making a biosensor |
US8148164B2 (en) * | 2003-06-20 | 2012-04-03 | Roche Diagnostics Operations, Inc. | System and method for determining the concentration of an analyte in a sample fluid |
CN1846131B (zh) | 2003-06-20 | 2012-01-18 | 霍夫曼-拉罗奇有限公司 | 制备窄的均匀试剂条的方法和试剂 |
US7776559B2 (en) * | 2004-01-22 | 2010-08-17 | Hewlett-Packard Development Company, L.P. | Disposable blood test device |
US7601299B2 (en) * | 2004-06-18 | 2009-10-13 | Roche Diagnostics Operations, Inc. | System and method for coding information on a biosensor test strip |
WO2006113840A2 (fr) * | 2005-04-19 | 2006-10-26 | Bayer Healthcare Llc | Procede de formation d'une etiquette d'auto-etalonnage au moyen d'un laser |
US7875240B2 (en) | 2005-04-19 | 2011-01-25 | Bayer Healthcare Llc | Auto-calibration label and method of forming the same |
WO2006113721A2 (fr) | 2005-04-19 | 2006-10-26 | Bayer Healthcare Llc | Etiquette d'auto-etalonnage et procede permettant de former cette derniere |
JP4903783B2 (ja) * | 2005-05-17 | 2012-03-28 | エフ.ホフマン−ラ ロシュ アーゲー | 測定プロセスにおいて消耗試薬を使用する測定装置に較正情報および試薬情報を提供するホスト装置および方法 |
WO2006127635A1 (fr) * | 2005-05-24 | 2006-11-30 | Bayer Healthcare Llc | Boitier de capteur pourvu d'un circuit d'auto-etalonnage intermediaire |
US8101415B2 (en) | 2005-07-05 | 2012-01-24 | Bayer Healthcare Llc | Calibration system for use with lateral flow assay test strips |
EP2138843B1 (fr) * | 2005-08-05 | 2011-10-26 | Bayer HealthCare, LLC | Procédé pour la détection des informations d'étallonage de capteurs électrochimiques |
GB0518527D0 (en) * | 2005-09-10 | 2005-10-19 | Oxford Biosensors Ltd | Scaling factor for an output of an electrochemical cell |
KR100680267B1 (ko) * | 2005-09-16 | 2007-02-08 | 주식회사 인포피아 | 식별정보를 포함하는 바이오 센서 및 바이오 센서의식별정보 판독장치 |
EP1813937A1 (fr) * | 2006-01-25 | 2007-08-01 | Roche Diagnostics GmbH | Système d'analysè biocapteur électrochimique |
US7887682B2 (en) | 2006-03-29 | 2011-02-15 | Abbott Diabetes Care Inc. | Analyte sensors and methods of use |
US20070231209A1 (en) * | 2006-04-03 | 2007-10-04 | Cosentino Daniel L | Test strip calibration system for a glucose meter, and method |
EP2008087B1 (fr) * | 2006-04-11 | 2020-06-03 | Nipro Diagnostics, Inc. | Procédé de fabrication d'un biocapteur |
EP2005137B1 (fr) * | 2006-04-11 | 2017-08-30 | Leica Biosystems Melbourne Pty Ltd | Dispositif et procédé d'établissement de références croisées |
US7918121B2 (en) | 2006-08-14 | 2011-04-05 | Bayer Healthcare, Llc | Meter system designed to run singulated test sensors |
US8029735B2 (en) | 2006-08-14 | 2011-10-04 | Bayer Healthcare, Llc | System and method for transferring calibration data |
DE102006062053A1 (de) * | 2006-12-29 | 2008-07-03 | Robert Bosch Gmbh | Verfahren zur Herstellung eines Sensorelements für Gasgemische |
US9029157B2 (en) | 2007-04-12 | 2015-05-12 | Nipro Diagnostics, Inc. | Error detection and rejection for a diagnostic testing system |
JP2009008574A (ja) * | 2007-06-29 | 2009-01-15 | Sumitomo Electric Ind Ltd | センサチップ及びバイオセンサカートリッジ並びにバイオセンサ装置 |
US8206564B2 (en) * | 2007-07-23 | 2012-06-26 | Bayer Healthcare Llc | Biosensor calibration system |
US7875461B2 (en) * | 2007-07-24 | 2011-01-25 | Lifescan Scotland Limited | Test strip and connector |
CN101815941A (zh) | 2007-07-31 | 2010-08-25 | 拜尔健康护理有限责任公司 | 检测传感器和使用侧装式测量计接触件的方法 |
US7943022B2 (en) * | 2007-09-04 | 2011-05-17 | Lifescan, Inc. | Analyte test strip with improved reagent deposition |
TW200918896A (en) * | 2007-10-19 | 2009-05-01 | Hmd Biomedical Inc | Test stripe with identification function and testing device thereof |
US7809512B2 (en) | 2007-11-11 | 2010-10-05 | Bayer Healthcare Llc | Biosensor coding system |
EP2232251B1 (fr) | 2007-12-10 | 2014-03-19 | Bayer HealthCare LLC | Capteur d'essai à auto-calibrage et son procédé de fabrication |
US8124014B2 (en) | 2008-06-09 | 2012-02-28 | Bayer Healthcare Llc | Auto-calibration circuit or label and method of forming the same |
US8032321B2 (en) | 2008-07-15 | 2011-10-04 | Bayer Healthcare Llc | Multi-layered biosensor encoding systems |
EP2344863A2 (fr) | 2008-10-21 | 2011-07-20 | Bayer HealthCare LLC | Procédé d'auto-étalonnage optique |
CN103180725B (zh) * | 2010-10-19 | 2015-01-14 | 松下健康医疗器械株式会社 | 生物试样测定装置及使用于该生物试样测定装置的生物试样测定传感器 |
JP5978868B2 (ja) * | 2012-09-06 | 2016-08-24 | オムロンヘルスケア株式会社 | 生体成分測定用の試験片、測定装置本体、およびそれらを含む生体成分測定装置 |
KR101413618B1 (ko) | 2012-09-24 | 2014-07-04 | (주) 더바이오 | 디지털 코드를 이용한 코드프리 센서 스트립 |
JPWO2014064978A1 (ja) * | 2012-10-22 | 2016-09-08 | 株式会社村田製作所 | バイオセンサおよびその製造方法 |
US9395234B2 (en) | 2012-12-05 | 2016-07-19 | Cardiocom, Llc | Stabilizing base for scale |
JP6048109B2 (ja) | 2012-12-14 | 2016-12-21 | オムロンヘルスケア株式会社 | 生体成分測定用の試験片およびその製造方法 |
US9474474B2 (en) * | 2013-03-14 | 2016-10-25 | Masimo Corporation | Patient monitor as a minimally invasive glucometer |
US10168313B2 (en) * | 2013-03-15 | 2019-01-01 | Agamatrix, Inc. | Analyte detection meter and associated method of use |
TW201819637A (zh) | 2016-08-26 | 2018-06-01 | 美商翠維迪亞健康股份有限公司 | 電容式自動編碼技術 |
PL239378B1 (pl) * | 2018-02-07 | 2021-11-29 | Sensdx Spolka Z Ograniczona Odpowiedzialnoscia | Czujnik do pomiarów impedancyjnych próbki czynnika biologicznego lub chemicznego oraz sposób wykrywania czynnika biologicznego lub chemicznego w próbce za pomocą takiego czujnika |
CN112485301B (zh) * | 2020-11-25 | 2023-07-14 | 三诺生物传感股份有限公司 | 一种电化学测试装置的测试方法、系统、设备及介质 |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4008448A (en) | 1975-10-03 | 1977-02-15 | Polaroid Corporation | Solenoid with selectively arrestible plunger movement |
US4233029A (en) | 1978-10-25 | 1980-11-11 | Eastman Kodak Company | Liquid transport device and method |
US4225410A (en) | 1978-12-04 | 1980-09-30 | Technicon Instruments Corporation | Integrated array of electrochemical sensors |
US4323536A (en) | 1980-02-06 | 1982-04-06 | Eastman Kodak Company | Multi-analyte test device |
DE3228542A1 (de) | 1982-07-30 | 1984-02-02 | Siemens AG, 1000 Berlin und 8000 München | Verfahren zur bestimmung der konzentration elektrochemisch umsetzbarer stoffe |
US5682884A (en) | 1983-05-05 | 1997-11-04 | Medisense, Inc. | Strip electrode with screen printing |
US5509410A (en) | 1983-06-06 | 1996-04-23 | Medisense, Inc. | Strip electrode including screen printing of a single layer |
SE8305704D0 (sv) | 1983-10-18 | 1983-10-18 | Leo Ab | Cuvette |
US5108564A (en) | 1988-03-15 | 1992-04-28 | Tall Oak Ventures | Method and apparatus for amperometric diagnostic analysis |
US5128015A (en) | 1988-03-15 | 1992-07-07 | Tall Oak Ventures | Method and apparatus for amperometric diagnostic analysis |
DE68924026T3 (de) | 1988-03-31 | 2008-01-10 | Matsushita Electric Industrial Co., Ltd., Kadoma | Biosensor und dessen herstellung. |
US5288636A (en) | 1989-12-15 | 1994-02-22 | Boehringer Mannheim Corporation | Enzyme electrode system |
US5243516A (en) | 1989-12-15 | 1993-09-07 | Boehringer Mannheim Corporation | Biosensing instrument and method |
JPH0820412B2 (ja) * | 1990-07-20 | 1996-03-04 | 松下電器産業株式会社 | 使い捨てセンサを用いた定量分析方法、及び装置 |
US5264103A (en) * | 1991-10-18 | 1993-11-23 | Matsushita Electric Industrial Co., Ltd. | Biosensor and a method for measuring a concentration of a substrate in a sample |
EP0622119B1 (fr) * | 1993-04-23 | 1999-11-03 | Roche Diagnostics GmbH | Système pour l'approvisionnement et pour la distribution d'élements de test |
US5366609A (en) * | 1993-06-08 | 1994-11-22 | Boehringer Mannheim Corporation | Biosensing meter with pluggable memory key |
US5437999A (en) | 1994-02-22 | 1995-08-01 | Boehringer Mannheim Corporation | Electrochemical sensor |
US6335203B1 (en) * | 1994-09-08 | 2002-01-01 | Lifescan, Inc. | Optically readable strip for analyte detection having on-strip orientation index |
US5628890A (en) | 1995-09-27 | 1997-05-13 | Medisense, Inc. | Electrochemical sensor |
JP3365184B2 (ja) | 1996-01-10 | 2003-01-08 | 松下電器産業株式会社 | バイオセンサ |
US5856195A (en) * | 1996-10-30 | 1999-01-05 | Bayer Corporation | Method and apparatus for calibrating a sensor element |
JP3702582B2 (ja) * | 1997-06-03 | 2005-10-05 | Nok株式会社 | バイオセンサを用いた測定方法 |
EP2056108A1 (fr) * | 1997-07-22 | 2009-05-06 | ARKRAY, Inc. | Appareil de mesure de concentration, bande de test pour l'appareil de mesure de concentration, système de biocapteur, et procédé de formation d'un terminal sur la bande de test |
US6054039A (en) | 1997-08-18 | 2000-04-25 | Shieh; Paul | Determination of glycoprotein and glycosylated hemoglobin in blood |
US5997817A (en) | 1997-12-05 | 1999-12-07 | Roche Diagnostics Corporation | Electrochemical biosensor test strip |
JP2000019147A (ja) * | 1998-07-01 | 2000-01-21 | Nok Corp | 反応生成物測定装置 |
DE29814997U1 (de) * | 1998-08-20 | 1998-12-03 | LRE Technology Partner GmbH, 80807 München | Teststreifenmeßsystem |
DE69941366D1 (fr) * | 1998-11-30 | 2009-10-15 | Abbott Lab | |
JP3455799B2 (ja) | 1999-06-14 | 2003-10-14 | 杉山建設株式会社 | 緑化コンクリートブロック及びコンクリート二次製品 |
JP4226756B2 (ja) * | 1999-11-15 | 2009-02-18 | パナソニック株式会社 | バイオセンサ、それを用いた定量方法及び定量装置 |
KR100445489B1 (ko) * | 1999-11-15 | 2004-08-21 | 마츠시타 덴끼 산교 가부시키가이샤 | 바이오 센서, 박막 전극 형성 방법, 정량 장치, 및 정량방법 |
JP4184573B2 (ja) * | 2000-04-28 | 2008-11-19 | 松下電器産業株式会社 | バイオセンサ |
US6413213B1 (en) * | 2000-04-18 | 2002-07-02 | Roche Diagnostics Corporation | Subscription based monitoring system and method |
JP2002156358A (ja) * | 2000-11-20 | 2002-05-31 | Matsushita Electric Ind Co Ltd | バイオセンサ、通知装置、及び測定装置 |
CN100346158C (zh) * | 2000-11-30 | 2007-10-31 | 松下电器产业株式会社 | 基质的定量方法 |
US6814844B2 (en) * | 2001-08-29 | 2004-11-09 | Roche Diagnostics Corporation | Biosensor with code pattern |
EP1431758B1 (fr) * | 2001-09-28 | 2013-11-13 | ARKRAY, Inc. | Instrument de mesure et appareil de mesure de concentration |
-
2004
- 2004-06-18 CN CN2004800237971A patent/CN1839314B/zh not_active Expired - Lifetime
- 2004-06-18 WO PCT/US2004/019454 patent/WO2005001474A1/fr active Application Filing
- 2004-06-18 WO PCT/US2004/019581 patent/WO2004113911A1/fr active Application Filing
- 2004-06-18 JP JP2006517451A patent/JP4916309B2/ja not_active Expired - Lifetime
- 2004-06-18 WO PCT/US2004/019653 patent/WO2004113914A1/fr active Search and Examination
- 2004-06-18 WO PCT/US2004/019686 patent/WO2004113915A1/fr active Search and Examination
- 2004-06-18 EP EP17196182.4A patent/EP3361249B1/fr not_active Expired - Lifetime
- 2004-06-18 JP JP2006517461A patent/JP4874099B2/ja not_active Expired - Lifetime
- 2004-06-18 WO PCT/US2004/019480 patent/WO2004113909A1/fr active Application Filing
- 2004-06-18 WO PCT/US2004/019639 patent/WO2005003751A1/fr active Application Filing
- 2004-06-18 CA CA2529301A patent/CA2529301C/fr not_active Expired - Lifetime
- 2004-06-18 EP EP04776797A patent/EP1642126A1/fr not_active Withdrawn
- 2004-06-18 CN CN2004800238298A patent/CN1839315B/zh not_active Expired - Lifetime
- 2004-06-18 EP EP04755694A patent/EP1639366A1/fr not_active Withdrawn
- 2004-06-18 EP EP17196179.0A patent/EP3336542A1/fr active Pending
- 2004-06-18 CA CA2529302A patent/CA2529302C/fr not_active Expired - Lifetime
-
2007
- 2007-01-09 HK HK07100297.3A patent/HK1094035A1/xx not_active IP Right Cessation
- 2007-01-09 HK HK07100296.4A patent/HK1094034A1/xx not_active IP Right Cessation
Non-Patent Citations (2)
Title |
---|
None * |
See also references of WO2004113914A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2005003751A1 (fr) | 2005-01-13 |
EP3361249A1 (fr) | 2018-08-15 |
JP2007524823A (ja) | 2007-08-30 |
WO2005001474A1 (fr) | 2005-01-06 |
WO2004113911A1 (fr) | 2004-12-29 |
EP1639366A1 (fr) | 2006-03-29 |
CA2529302A1 (fr) | 2004-12-29 |
WO2004113909A8 (fr) | 2005-03-17 |
CA2529301A1 (fr) | 2004-12-29 |
CN1839314A (zh) | 2006-09-27 |
CN1839315A (zh) | 2006-09-27 |
WO2004113914A8 (fr) | 2006-02-23 |
HK1094035A1 (en) | 2007-03-16 |
WO2004113915A1 (fr) | 2004-12-29 |
CA2529301C (fr) | 2011-08-02 |
HK1094034A1 (en) | 2007-03-16 |
CN1839314B (zh) | 2012-02-08 |
JP4916309B2 (ja) | 2012-04-11 |
JP4874099B2 (ja) | 2012-02-08 |
WO2004113909A1 (fr) | 2004-12-29 |
JP2007524819A (ja) | 2007-08-30 |
EP3361249B1 (fr) | 2023-08-02 |
CA2529302C (fr) | 2011-09-20 |
WO2004113914A1 (fr) | 2004-12-29 |
CN1839315B (zh) | 2012-03-21 |
EP3336542A1 (fr) | 2018-06-20 |
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