WO2004051249A1 - 分析用具 - Google Patents
分析用具 Download PDFInfo
- Publication number
- WO2004051249A1 WO2004051249A1 PCT/JP2003/015358 JP0315358W WO2004051249A1 WO 2004051249 A1 WO2004051249 A1 WO 2004051249A1 JP 0315358 W JP0315358 W JP 0315358W WO 2004051249 A1 WO2004051249 A1 WO 2004051249A1
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- WO
- WIPO (PCT)
- Prior art keywords
- electrode
- analysis tool
- analyzer
- tool according
- disturbance noise
- 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.)
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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
Definitions
- the present invention relates to an analytical device used for analyzing a specific component in a sample, for example, an analytical device used for measuring a blood glucose level.
- a blood glucose level As a general method of measuring a blood glucose level, there is a method utilizing an oxidation-reduction reaction.
- a simple type of blood glucose measuring device that is small enough to fit in the palm of a hand is widely used so that the blood glucose can be easily measured at home or on the road.
- a blood glucose level is measured by supplying an oxygen reaction field and mounting a disposable nanosensor, and then supplying blood to the biosensor.
- a blood glucose level is measured by attaching a Pyo sensor 90 to a blood glucose level measuring device 91 (for example, see Japanese Patent Publication No. 8-10208).
- the biosensor 90 is provided with first and second comforters 93 and 94 for applying a voltage to an enzyme reaction field on an insulating substrate 92.
- the blood glucose level measuring device 91 is based on a connector 97 having first and second terminals 95 and 96 for causing the first and second electrodes 93 and 94 to insect, and based on information from the connector 97.
- a measurement circuit 98 for calculating the blood sugar level.
- the blood glucose measuring device 91 is affected by various disturbance noises, but the measured value is affected by the disturbance noise, or the electronic component force S is destroyed, and the measurement becomes impossible; In particular, small portable measuring devices are easily affected by static electricity from the human body. That is, in the blood glucose level measuring device 91, the Noo sensor 90 is usually manually attached to the blood glucose level measuring device 91. Therefore, if the human body is charged with static electricity, the static electricity is the first sensor of the biosensor 90. And the second electrode 93, 94. To the first and second terminals 95, 96 If no measures are taken, this static electricity will be input to the measurement circuit 98 via the first comfort 93 or the first terminal 95, for example, as disturbance noise.
- a method of devising the arrangement of the first and second terminals 95 and 96 of the blood glucose measuring device 91 or increasing the flffi of individual electronic components constituting the measuring circuit 98 is considered. And so on.
- a method of arranging a conductive sheet at or near the connector portion has also been considered (for example, see Japanese Utility Model Publication No. 8-2609).
- the conventional countermeasures against disturbance noise are performed by adopting a method of improving the configuration of the blood glucose level measuring device 91 by using a method. Therefore, the configuration of the blood sugar level measuring device 91 becomes complicated, the size of the device becomes large, and the manufacturing cost increases.
- the size of the biosensor 90 including the first and second electrodes 93 and 94 must be reduced.
- the resistance between the first electrode 93 and the first terminal 95 of the blood glucose level measuring device 91 is increased because the resistance of the first and second electrodes 93 and 94 increases.
- the installed bio-sensor 90 cannot measure the blood glucose level.
- the molten material of the first electrode 93 of the pyro sensor 90 adheres to the first terminal 95 of the blood glucose level measuring device 91 because the molten glucose cannot be measured. 1
- the resistance value of terminal 95 changes, which causes an error in the subsequent measurement of the response current value. Such a problem becomes more conspicuous as the thickness of the first comfort 93 is reduced. Disclosure of the invention
- the present invention can reduce the influence of disturbance noise such as static electricity even if the thickness of the electrode of the analysis tool is reduced, without increasing the size of the analysis apparatus for analyzing the sample using the analysis tool.
- the purpose is to provide an analytical tool that can be reduced in cost.
- the analysis tool according to the present invention is mounted on an analyzer having a plurality of terminals and an analysis circuit.
- An analysis tool having a plurality of ridges for removing the plurality of terminals when mounted on the analyzer, wherein at least one of the plurality of ridges is
- the disturbance noise is configured to make it easier for disturbance noise to fly than the other electrodes except the m3 ⁇ 4.
- the plurality of comforts include, for example, a first electrode for electrically connecting to the analysis circuit, and a second electrode for applying mm to a target portion together with the first comfort.
- the second electrode can be used as a disturbance noise countermeasure electrode.
- the second comforter is configured so that it is not electrically connected to the analysis circuit when the analysis tool is attached to the analyzer, for example. More specifically, the second electrode is configured to repel the duland connection terminal when the analysis tool is attached to the analyzer, for example.
- the plurality of electrodes may be configured to include, in addition to the first electrode and the second electrode, a third electrode that is not involved in applying ME to the target portion.
- the third electrode can be used as a disturbance noise countermeasure electrode.
- the third electrode is configured so as not to be electrically connected to the analysis circuit when, for example, the analysis tool is mounted on the analysis device. More specifically, the third electrode is configured to be infested with the ground connection terminal, for example, when the analysis tool is attached to the analyzer.
- both the second and third comforters may be used as disturbance noise countermeasure electrodes.
- the second and third electrodes are attached to the analyzer so that, for example, the analyzer is not electrically connected to the analysis circuit when the analyzer is mounted on the analyzer. When it does, it is configured to invert the ground connection ⁇ .
- the analysis tool of the present invention is configured to include, for example, a flow path for moving a sample, and an exhaust port for discharging gas inside the flow path. It is preferable that the disturbance noise countermeasure electrode is configured to have an input portion for inputting disturbance noise flying through an exhaust port.
- the input unit is, for example, forms that faces through at least a portion force s outlet. More specifically, the input section is provided directly below the exhaust port and covered with an insulating film having an opening. This However, a part of the input part is exposed through the S exhaust port by the opening of the thread color film.
- the analysis tool of the present invention may be configured to include a storage in which a plurality of rattans are formed, and a cover joined to the substrate and having a gusset.
- the input unit is configured as having a portion located in the periphery of the exhaust port in plan view.
- the input unit is formed so as to surround the exhaust port in plan view.
- the disturbance noise countermeasure is formed so as to surround at least one of the electrodes other than the disturbance noise countermeasure electrode out of the plurality of jigs.
- the disturbance noise countermeasure comfort may be formed along the periphery of the substrate.
- the disturbance noise countermeasure m m when the analysis tool is attached to the analysis apparatus, the disturbance noise countermeasure m m is set to a plurality of times in the analysis apparatus before the electrodes other than the disturbance noise countermeasure electrode among the plurality of electrodes. It is preferable to configure the terminal so as to insulate the corresponding terminal. More specifically, the disturbance noise countermeasure electrode is located on the board at the insertion edge of the board (in the insertion direction with respect to the analyzer in the board), compared to the electrodes other than the disturbance noise countermeasure among the plurality of comforts. Edge).
- the analysis tool of the present invention is preferably configured to have a knob used when mounting the analysis tool on the analyzer or when removing the analysis tool from the analyzer. Les ,.
- the disturbance noise countermeasure electrode be covered with an insulating film while a portion located near the knob is exposed.
- the knob is configured as a concave portion that is depressed inward, for example, in a plan view of the analysis tool.
- FIG. 1 is an overall view showing a state where the biosensor according to the first embodiment of the present invention is mounted on an analyzer.
- Fig. 2 is a plan view of the state shown in Fig. This is shown in a block diagram.
- FIG. 3 is an overall view of the biosensor shown in FIGS. 1 and 2.
- FIG. 4 is a cross-sectional view taken along the line IV-IV of FIG.
- FIG. 5 is a plan view showing a state where the biosensor shown in FIG. 3 is disassembled.
- FIG. 6 is a plan view for explaining a working electrode and a counter electrode of the biosensor.
- FIG. 7 is a schematic plan view showing a process of attaching a biosensor to an analyzer, with a plan view of the biosensor and a circuit block of the analyzer.
- FIG. 8 is a perspective plan view showing a Pyo sensor according to the second embodiment of the present invention.
- FIG. 9 is a perspective plan view showing a biosensor according to the third embodiment of the present invention.
- FIG. 10 is a perspective plan view showing a biosensor according to the fourth embodiment of the present invention.
- FIG. 11 is a schematic diagram showing a state in which the biosensor shown in FIG. 10 is mounted on the analyzer in a circuit block diagram of the analyzer and a plan view of the nanosensor.
- FIG. 12 is a schematic diagram for explaining a biosensor according to a fifth embodiment of the present invention.
- FIG. 12 is a plan view of a sensor and a circuit block of an analyzer. .
- FIG. 13 is a schematic diagram for explaining a biosensor according to the sixth embodiment of the present invention, which is a plan view of a biosensor and a circuit block of an analyzer, respectively.
- FIG. 14 is a schematic diagram for explaining a conventional simple blood sugar level measuring device and a conventional biosensor.
- the biosensor X1 shown in FIG. 1 and FIG. 2 is configured to be used and discarded, and is used by being attached to the connector section 10 of the analyzer 1.
- This biosensor XI has a plate-like form in which a cover 4 is laminated on a top surface 20 of a substrate 2 via a spacer 3 as well shown in FIGS. 3 and 4.
- the flow path 5 and the knob 6 are constructed by the elements 2 to 4.
- the spacer 3 is for defining the dimensions of the flow path 5, and has a slit 30 whose tip is open as shown in FIG.
- the width and length of the flow path 5 are defined by the slit 30.
- An open portion 31 at the tip of the slit 30 constitutes a sample introduction port 50 for introducing a sample into the flow channel 5.
- the force par 4 has an exhaust port 40 and a window 41 as shown in FIG. 3 and FIG.
- the exhaust port 40 is for exhausting the gas inside the flow path 5 to the outside, and communicates with the inside of the flow path 5.5.
- the window 41 is used to measure the force and force of the sample introduced into the inside of the flow path 5 and the state of movement of the sample in the flow path 5. Thus, it is formed between the sample introduction port 50 and the exhaust port 40.
- a window 41 is formed, for example, by forming a notch 41A in the cover 4 and disposing a transparent member 41B in the notch 41A.
- the substrate 2 is formed of an insulating material so as to be long in one direction (longitudinal direction), and the through hole 2 formed in a portion where the cover 4 is not laminated.
- the through hole 2A is for providing information on the biosensor XI, for example, mouth information to the analyzer 1 (see FIGS. 1 and 2). Lot information is read according to presence / absence, size, formation position, etc.
- the working electrode 21, the counter electrode 22, the reagent 23, and the insulating film 24 are formed on the upper surface 20 of such 2.
- the working electrode 21 is used together with the counter electrode 22 when applying mffi to the reaction field.
- the working electrode 21 extends in the longitudinal direction of the entire body 2 as a whole.
- the end 21A of the working electrode 21 is disposed near the second short edge 25A.
- the biosensor X1 is attached to the analyzer 1, the end 21A is connected to the analyzer 1 to be described later. This is the part for removing the insects from the first terminal 11 (see Fig. 2).
- 521 B of the working electrode 21 is disposed so as to extend in the short direction of the male 2 in the vicinity of the circular arc 25 B of 2.
- the counter electrode 22 functions as a disturbance noise countermeasure electrode, and includes a main line portion 22A formed in a hairpin shape along the periphery of the substrate 2, an island portion 22B protruding from the main line portion 22A, and have.
- the counter electrode 22 surrounds the entire working electrode 21 such that 53 ⁇ 43 ⁇ 421B of the working electrode 21 is located between the corner portion 22a of the main line portion 22A and the island portion 22B.
- ⁇ 3 ⁇ 4 22Aa of the main line portion 22A is located near the short edge 25A of the anti-aggression 2.
- the separation 22Aa is a portion for allowing the second terminal 12 of the analyzer 1 to be fiber-bonded when the pyrosensor X1 is attached to the analyzer 1, and the substrate 2 is located closer to the substrate 2 than the end 21A of the working electrode 21. It is located near the proximal site by the short edge 25A of the (see Fig. 2).
- the island portion 22B is formed to have a larger area in plan view than the force and the exhaust port 40 so as to be located immediately below the exhaust port 40 in a plan view of the biosensor X1.
- the reagent part 23 is formed so as to connect between the end part 21B of the working electrode 21 and the corner part 22a of the main line part 22A.
- the reagent section 23 is formed in a solid state containing, for example, a reductase and an electron transfer substance, and is configured to be dissolved when a sample is supplied.
- the type of oxidoreductase or electron mediator is selected according to the type of the fiber component to be measured. For example, to measure glucose concentration: ⁇ uses gnorecose dehydrogenase (glucose oxidase) as an oxidoreductase and uses ferricyanide-powered lime as an electron mediator.
- the insulating film 24 is formed so as to cover most of the working electrode 21 and the counter electrode 22, as is clearly shown in FIG.
- the working electrode 21 and the counter electrode 22 are exposed so that i3 ⁇ 43 ⁇ 421A, 22Aa, portions 21B, 22a where the reagent portion 23 is formed, and portions 21C, 22C near the knob 6 are not covered with the insulating film 24. I have.
- a through hole 24A is formed in a portion corresponding to the island portion 22B of the counter electrode 22, and a part of the island portion 22B is exposed without being covered by the insulating film 24.
- the flow path 5 is for moving the sample by utilizing the capillary force to create a capping reaction field.
- flow path 5 is located at the end of working electrode 21. It extends in the longitudinal direction so as to cross the corner 21a of the part 21B and the main line part 22A. Therefore, the reagent section 23 is disposed inside the flow path 5.
- the knob 6 allows the user to hold the biosensor XI when attaching the biosensor X1 to the analyzer 1 as shown in Fig. 1 or removing the biosensor XI from the analyzer 1. This is the part to use.
- the knob 6 is formed with cutouts 28, 38, and 48 having the same shape in the substrate 2, the spacer 3, and the cover 4, thereby forming an arc-shaped curved surface. It is formed as a recess having
- the analyzer 1 used for the use of the biosensor X1 is configured to analyze a sample by an electrochemical method, and is equipped with the biosensor X1 as shown in FIGS. 1 and 2. And an analysis circuit 13 for performing calculations necessary for analyzing a specific component in a sample based on information from the connector section 10.
- the connector section 10 has first and second terminals 11 and 12 as well shown in FIG.
- the first terminal 11 is for letting the end 21A of the working electrode 21 worm
- the second terminal 12 is for letting the end 22Aa of the counter electrode 22 infest.
- the first terminal 11 and the analysis circuit 13 are electrically connected via a signal H 14, and a current mffi conversion amplifier 15 is arranged in the middle of the signal spring 14.
- the current conversion amplifier 15 converts information obtained as a current value from the biosensor X1 into a flffi value and inputs the information to the analysis circuit 13.
- the second terminal 12 is connected to ground.
- Sample typically blood or urine
- the biosensor X1 is attached to the connector 10 of the analyzer 1 with the short edge 25A (see Fig. 3). It is done by importing.
- the biosensor X1 is attached to the analyzer 1, and the ends 21A and 22Aa of the working electrode 21 and the counter electrode 22 in the biosensor X1 are the first and second terminals of the analyzer 1. Removed as 11,12. Counter electrode in biosensor XI 22 22Aa is formed at a position closer to the short edge 25A of the substrate 2 than the end 21A of the working electrode 21. Therefore, in the process of attaching the biosensor XI to the analyzer 1, after the 3 ⁇ 422Aa of the counter electrode 22 is connected to the second terminal 12 as shown in FIG. The end 21 A of the pole 21 is connected to the first terminal 11.
- the sample supplied to the biosensor XI moves inside the flow path 5 toward the exhaust port 40 by capillary action as expected from FIG. 4, thereby filling the inside of the flow path 5. .
- the reagent part dissolves 23 S in the sample, and a liquid phase reaction system is constructed inside the flow path 5.
- the liquid-phase reaction system is connected to the first and second terminals 11, 12 of the analyzer 1, the working electrode 21 and the counter electrode by a direct current (not shown) of the analyzer 1, for example.
- the response current obtained at this time is subjected to ttiB conversion in a current-to-conversion amplifier 15, and is converted into a digital signal by, for example, an AD conversion (not shown) and then input to the analysis circuit 13.
- the analysis circuit 13 performs an operation necessary for analyzing a sample, for example, determining a glucose concentration in blood, based on a digital signal corresponding to the response current.
- biosensor X1 is configured as disposable. Therefore, after the calculation in the analysis circuit 13, it is necessary to extract the biosensor X1 from the analyzer 1. The extraction of the nanosensor X1 can be performed with the fingertip holding the biosensor X1 at the knob 6.
- the knob 6 of the biosensor X1 is used. That is, in the biosensor XI, a part to be picked up by the user at the time of attaching and detaching the biosensor XI is set in advance. Therefore, the biosensor X1 is easy to use and detach when attaching and detaching the biosensor X1, and the sample is not inadvertently attached to the fingertip when the biosensor X1 is extracted, which is sanitary. In fact, since the knob 6 is formed as a recess, the possibility that the fingertip slips when the biosensor XI is attached or detached is reduced. Even in this regard, it can be said that the handling and performance of the Pyosensor X1 have been improved.
- static electricity charged on the human body may fly to the working electrode 11 and the counter electrode 12 of the biosensor X1, as described above.
- static electricity flies from the exhaust port 40 to the working electrode 21 and the counter electrode 22.
- the biosensor XI responds to incoming static electricity with the counter electrode 22. That is, the counter electrode 22 is formed as having the island portion 22B located immediately below the exhaust port 40, and the static electricity that has flown through the exhaust port 40 is more positively applied to the counter electrode 22 than to the working electrode 21. To be entered.
- the static electricity input to the counter electrode 22 is dropped to the ground via the second terminal 12 and removed because the counter electrode 22 is connected to the ground via the second terminal 12 of the analyzer 1.
- the end 22Aa of the counter electrode 22 is removed before the end 21A of the working electrode 21 as shown in FIG. Therefore, the above-mentioned static electricity is removed at the moment when the end 22Aa of the counter electrode 22 contacts the second terminal 12 before the end 21A of the working electrode 21 is infested with the first terminal 11. .
- the biosensor XI is provided with a knob 6, and a part of the counter electrode 22 is exposed from the insulating film 24 in the vicinity of the knob 6. Therefore, if the biosensor X 1 is attached to the analyzer 1 by holding the knob 6, for example, even if the human body is charged with static electricity, the static electricity will positively act on the counter electrode 22. Entered. As a result, the static electricity charged on the human body is eliminated through the counter electrode 22 without being input to the working electrode 21 or the analysis circuit 13.
- the biosensor X1 if the biosensor X1 is used, the input of static electricity to the analysis circuit 13 via the working electrode 21 and the first end 11 of the analyzer 1 can be suppressed. As a result, the occurrence of measurement errors and measurement due to static electricity entering the analysis circuit 13 is suppressed, and the generation of Joule heat at the working electrode 21 due to static electricity is suppressed. Thus, it is possible to avoid melting of the portion that is in contact with the first terminal 11.
- Such an effect can be obtained by devising the form of the counter electrode 22 in the biosensor X1 without changing the configuration of the analyzer 1. Therefore, the configuration of the analyzer 1 is not neglected to take measures against disturbance noise, and the analyzer 1 is not increased in size.
- the working electrode 21 and counter electrode 22 are marked on the screen.
- ⁇ only requires changing the shape of the opening in the mask. Therefore, disturbance noise such as static electricity can be prevented only by adding a small amount of material without changing the existing production line, which is advantageous in terms of production cost.
- Biosensor XI can remove not only static electricity coming from the human body but also other disturbance noise.
- the island portion 22B at the counter electrode 22 may be omitted, and only the main line portion 22A may cope with disturbance noise.
- biosensors according to the second to sixth embodiments of the present invention will be described with reference to FIGS.
- the same elements as those of the biosensor X1 or the analyzer 1 (see FIG. 1 and FIG. 7) according to the first embodiment of the present invention are described.
- FIG. 8 is a perspective plan view showing a biosensor according to the second embodiment of the present invention.
- the biosensor X2 differs from the biosensor X1 according to the first embodiment described above (especially, see FIG. 6) in the configuration of the counter electrode 7A.
- the counter electrode 7A functions as a disturbance noise countermeasure electrode, and has a main line portion 70A and a pair of branch portions 71A.
- the pair of branch portions 71A are arranged side by side in the longitudinal direction of the substrate 2 so as to be located around the exhaust port 40 in plan view.
- the counter electrode 7 A is configured to surround the exhaust port 40 in addition to the working electrode 21 in plan view.
- one of the pair of branch portions 71A may be omitted.
- FIG. 9 is a perspective plan view showing a biosensor according to the third embodiment of the present invention. You.
- the biosensor X3 has a form similar to the biosensor X2 (see FIG. 8) according to the second embodiment of the present invention.
- the biosensor X3 is configured such that the counter electrode 7B has a main line section 70B and a loop section 71B.
- the roof 71B extends from the main line portion 70B so as to surround the exhaust port 40.
- FIGS. 10 and 11 are diagrams for explaining a biosensor according to a fourth embodiment of the present invention.
- FIG. 10 is a perspective plan view of the biosensor
- FIG. 11 is a plan view of the biosensor.
- the analysis device is shown by a circuit block.
- the biosensor X4 has a working electrode 21, a counter electrode 7C, and a mouth electrode 8C.
- the counter electrode 7C is arranged in the periphery of the exhaust port 40—formed in an F-shape with a pair of branches 70C.
- the opening electrode 8C extends along the periphery of the substrate 2 and is formed in a U-shape surrounding the working electrode 21 and the counter electrode 7C.
- the analyzer 1C has a third terminal 16C for removing the insects from the additional electrode 8C separately from the first and second terminals 11 and 12. .
- the third terminal 16 C is connected to the land separately from the second terminal 12.
- the second terminal 12 and the third terminal 16C are separately connected to the ground, but these terminals 12, 16C may be collectively connected to the ground.
- il3 ⁇ 4 ⁇ Comfort 8 C functions as a disturbance noise suppression electrode. More specifically, disturbance noise such as static electricity flying through the exhaust port 40 is exclusively dealt with at the counter electrode 7 C, and disturbance noise such as static electricity flying from the side of the biosensor X 4. It is decided to use only 8 C electrode.
- the counter electrode 7 C and the ⁇ 3 ⁇ 4 electrode 8 C are configured to be connected to the ground when the biosensor ⁇ 4 is mounted on the analyzer 1 C. Therefore, the disturbance noise is dropped to the ground via the counter electrode 7 C and the il opening electrode 8 C.
- FIG. 12 is for explaining a biosensor according to a fifth embodiment of the present invention, and is a plan view of a biosensor and a circuit block of an analyzer, respectively.
- the biosensor X5 shown in FIG. 12 has two il3 ⁇ 4P® ⁇ S80D and 81D in addition to the working electrode 21 and the counter electrode 7D.
- the working electrode 21 and the counter electrode 7D have the same configuration as the biosensor X4 described above (see FIGS. 10 and 11).
- the two openings IID 80D and 81D have a form in which the additional electrode 8C described above (see FIGS. 10 and 11) is divided at the sample liquid inlet 50 at a part. That is, each of the electrodes 80D and 81D is formed in an L-shape along the periphery of.
- the analyzer 1D has third and fourth terminals 16D and 17D for removing the two tubes 80D and 81D. These terminals 16D and 17D are collectively connected to the ground.
- FIG. 13 is a view for explaining a biosensor according to a sixth embodiment of the present invention, and is a plan view of a biosensor and a circuit block of an analyzer, respectively.
- the biosensor X6 shown in FIG. 13 has two additional electrodes 80E and 81E which are attached to working electrodes 70E and 71E having the same configuration as the conventional biosensor 90 shown in FIG. .
- the additional electrode 80E has the same form as the additional electrode 8C of the biosensor X4 described above (see FIGS. 10 and 11). That is, the additional electrode 80E is formed in a U shape along the periphery of the substrate 2.
- the recess 81E extends in the longitudinal direction of the substrate 2 from the exhaust port 40 to the short side 5A of the substrate 2.
- the analyzer 1E has third and fourth terminals 16E, 17E for removing the two additional consols 80E, 81E.
- the third and fourth terminals 16E, 17E are collectively connected to the ground.
- the present invention is not limited to the above-described first and sixth embodiments, and can be variously modified.
- the form and number of the disturbance noise suppression electrodes are the same as those described above. Is not limited and the design can be changed.
- the biosensor configured to measure a single item has been described as an example.
- the present invention provides an electrochemical sensor configured to measure a plurality of items.
- the present invention can be applied to an electrochemical sensor configured to measure the concentration of gnorecose and cholesterol in blood.
- disturbance noise such as static electricity was removed by being dropped to the ground.However, disturbance noise should be eliminated by installing electronic components and electric circuits that consume power in the analyzer. You may.
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Abstract
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004556875A JP4352152B2 (ja) | 2002-12-02 | 2003-12-01 | 分析用具 |
| AU2003284512A AU2003284512A1 (en) | 2002-12-02 | 2003-12-01 | Analysis instrument |
| EP03775991.7A EP1571442B1 (en) | 2002-12-02 | 2003-12-01 | Analyser system |
| US10/537,708 US8460523B2 (en) | 2002-12-02 | 2003-12-01 | Analysis instrument |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002-350198 | 2002-12-02 | ||
| JP2002350198 | 2002-12-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2004051249A1 true WO2004051249A1 (ja) | 2004-06-17 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2003/015358 Ceased WO2004051249A1 (ja) | 2002-12-02 | 2003-12-01 | 分析用具 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8460523B2 (ja) |
| EP (1) | EP1571442B1 (ja) |
| JP (1) | JP4352152B2 (ja) |
| CN (1) | CN100442047C (ja) |
| AU (1) | AU2003284512A1 (ja) |
| WO (1) | WO2004051249A1 (ja) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2009175118A (ja) * | 2007-12-27 | 2009-08-06 | Horiba Ltd | 被検液分析用チップ |
| JP2010535340A (ja) * | 2007-07-31 | 2010-11-18 | バイエル・ヘルスケア・エルエルシー | 試験センサ及び側面に取り付けられた計器接点 |
| EP2916126A1 (en) * | 2005-09-02 | 2015-09-09 | ARKRAY, Inc. | Analytical tool for for detecting sample supply condition |
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| MX2008014251A (es) | 2006-05-08 | 2008-11-26 | Bayer Healthcare Llc | Sensor electroquimico de prueba con volumen reducido de muestra. |
| KR20080080841A (ko) * | 2007-03-02 | 2008-09-05 | 주식회사 아이센스 | 전기화학적 바이오센서 및 이의 측정기 |
| US8021528B2 (en) * | 2007-03-07 | 2011-09-20 | Yong-Sang Jang | Biosensor |
| US7794658B2 (en) * | 2007-07-25 | 2010-09-14 | Lifescan, Inc. | Open circuit delay devices, systems, and methods for analyte measurement |
| US7943022B2 (en) | 2007-09-04 | 2011-05-17 | Lifescan, Inc. | Analyte test strip with improved reagent deposition |
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| US9658188B2 (en) | 2007-07-31 | 2017-05-23 | Ascensia Diabetes Care Holdings Ag | Electrochemical test sensor |
| JP2009175118A (ja) * | 2007-12-27 | 2009-08-06 | Horiba Ltd | 被検液分析用チップ |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003284512A1 (en) | 2004-06-23 |
| CN100442047C (zh) | 2008-12-10 |
| EP1571442A1 (en) | 2005-09-07 |
| US8460523B2 (en) | 2013-06-11 |
| JP4352152B2 (ja) | 2009-10-28 |
| US20060042943A1 (en) | 2006-03-02 |
| EP1571442B1 (en) | 2014-09-17 |
| CN1720447A (zh) | 2006-01-11 |
| JPWO2004051249A1 (ja) | 2006-04-06 |
| EP1571442A4 (en) | 2011-03-23 |
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