WO2010116624A1 - センサチップとこれを用いる測定器及び血液検査装置 - Google Patents
センサチップとこれを用いる測定器及び血液検査装置 Download PDFInfo
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- WO2010116624A1 WO2010116624A1 PCT/JP2010/001909 JP2010001909W WO2010116624A1 WO 2010116624 A1 WO2010116624 A1 WO 2010116624A1 JP 2010001909 W JP2010001909 W JP 2010001909W WO 2010116624 A1 WO2010116624 A1 WO 2010116624A1
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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
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- G01N27/307—Disposable laminated or multilayered electrodes
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- A61B5/14—Devices for taking samples of blood ; Measuring characteristics of blood in vivo, e.g. gas concentration within the blood, pH-value of blood
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- A61B5/1411—Devices for taking blood samples by percutaneous method, e.g. by lancet
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- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
- A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
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- A61B5/1486—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using enzyme electrodes, e.g. with immobilised oxidase
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- A61B5/150053—Details for enhanced collection of blood or interstitial fluid at the sample site, e.g. by applying compression, heat, vibration, ultrasound, suction or vacuum to tissue; for reduction of pain or discomfort; Skin piercing elements, e.g. blades, needles, lancets or canulas, with adjustable piercing speed
- A61B5/150061—Means for enhancing collection
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- A61B5/15134—Bladeless capillary blood sampling devices, i.e. devices for perforating the skin in order to obtain a blood sample but not using a blade, needle, canula, or lancet, e.g. by laser perforation, suction or pressurized fluids
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- A61B5/15136—Bladeless capillary blood sampling devices, i.e. devices for perforating the skin in order to obtain a blood sample but not using a blade, needle, canula, or lancet, e.g. by laser perforation, suction or pressurized fluids by use of radiation, e.g. laser
- A61B5/15138—Bladeless capillary blood sampling devices, i.e. devices for perforating the skin in order to obtain a blood sample but not using a blade, needle, canula, or lancet, e.g. by laser perforation, suction or pressurized fluids by use of radiation, e.g. laser provided with means to ensure the protection of the user, e.g. to avoid laser light entering the eyes of a user
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- 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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- 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
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- G01N2035/1027—General features of the devices
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- G01N2035/1062—General features of the devices using the transfer device for another function for testing the liquid while it is in the transfer device
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- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1009—Characterised by arrangements for controlling the aspiration or dispense of liquids
- G01N35/1016—Control of the volume dispensed or introduced
Definitions
- the present invention relates to a sensor chip for measuring a blood sugar level and the like, a measuring instrument using the sensor chip, and a blood test apparatus.
- Diabetes patients need to regularly measure blood sugar levels, inject insulin based on the blood sugar levels, and keep the blood sugar levels normal. Therefore, a patient collects a small amount of blood from a fingertip or the like, and detects a blood glucose level from the collected blood. In order to detect this blood glucose level, the sensor chip 1 (see FIG. 43) is required.
- the sensor chip 1 includes a base body 2, an inlet 4, a supply path (not shown), a detection electrode 4b provided in the supply path 4a, and an air hole 4c provided at the end of the supply path 4a.
- the substrate 2 has a substantially rectangular shape and a plate shape.
- the inflow port 4 is provided on one short side of the base 2 and the blood 3 for measurement flows in.
- the supply path 4 a communicates with the inflow port 4.
- the detection electrode 4b is provided in the supply path 4a.
- the air hole 4c is provided at the end of the supply path 4a.
- the puncture device 5 is brought into contact with the skin 6 such as the finger 6a as shown in FIG.
- the puncture button 5a of the puncture device 5 is pressed.
- the finger 6a (skin 6) is punctured by pressing the puncture button 5a.
- pressure is applied around the punctured finger 6a (skin 6) to exude the blood 3.
- the blood glucose level is measured using the measuring instrument 7 to which the sensor chip 1 is attached. That is, the inlet 4 of the sensor chip 1 is brought into contact with the exuded blood 3.
- the blood 3 is guided to the detection electrode 4b through the supply path 4a.
- the blood glucose level of the blood 3 guided to the detection electrode 4b is measured, and the result is displayed on the display unit 7a. Then, an amount of insulin determined based on this blood glucose level is injected.
- Patent Document 1 is known as prior art document information related to the invention of this application.
- an object of the present invention is to provide a sensor chip that can easily process excess blood.
- a sensor chip of the present invention is a sensor chip for analyzing a component of a biological sample, which is a plate-shaped substrate, an inlet, a supply path, a detection electrode, and excess blood reservoir. And a section.
- the inflow port is provided at one end of the substrate and a biological sample for analysis flows in.
- the supply path communicates with the inflow port and a biological sample is introduced.
- the detection electrode is provided in the supply path and detects a signal for analysis.
- the surplus blood reservoir is provided on the base and sucks and stores surplus blood, which is an extra biological sample that has not been used for analysis.
- the measuring instrument of the present invention is a measuring instrument that uses the sensor chip, and includes a housing, a sensor insertion part, a connector, a measurement circuit part, and a display part.
- the sensor insertion portion is provided at the first end portion of the housing in which the sensor chip is inserted.
- the connector is provided in the sensor insertion part.
- the measurement circuit unit is connected to the connector.
- the display unit is connected to the output of the measurement circuit unit, and displays the measurement result of the analysis data of the biological sample introduced into the sensor chip measured in the measurement circuit unit.
- the blood test apparatus is an apparatus that uses the sensor chip, and includes a housing, a sensor insertion part, a puncturing means, a connector, an electric circuit part, and a display part.
- the sensor insertion part is provided in a part of the housing, into which the sensor chip is inserted.
- the puncturing means is provided at a position facing or close to the sensor insertion portion, and punctures the skin.
- the connector is provided in the sensor insertion part.
- the electric circuit unit is connected to the connector and analyzes the biological sample.
- the display unit is connected to the output of the electric circuit unit.
- FIG. 1 is a plan view of a sensor chip according to Embodiment 1 of the present invention.
- FIG. 2 is a cross-sectional view taken along line AA in FIG. 1.
- BB sectional drawing of FIG. FIG. 2 is an exploded plan view of the sensor chip in FIG. 1.
- A) is a top view of a cover.
- B) is a top view of a spacer.
- C) is a top view of a board
- the disassembled perspective view of the sensor chip of FIG. The block diagram of the measuring device using the sensor chip of FIG.
- FIG. 9 is an exploded plan view of the sensor chip of FIG. 8.
- A is a top view of the cover for excess blood suction.
- B is a top view of the spacer for excess blood suction.
- C is a top view of a cover.
- D is a top view of a spacer.
- E is a top view of a board
- the exploded plan view which shows the structure of the surplus blood storage part provided in the sensor chip concerning Embodiment 3 of this invention.
- A) is a top view of the cover for excess blood suction.
- B is a top view of the spacer for excess blood suction.
- the top view which shows the excess blood storage part of the sensor chip of FIG. FIG.
- FIG. 13 is an exploded plan view of a blood measurement unit of the sensor chip in FIG. 12.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the blood measurement part which comprises the sensor chip of FIG.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip concerning Embodiment 6 of the present invention.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip concerning Embodiment 7 of the present invention.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip concerning Embodiment 8 of the present invention.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip which concerns on Embodiment 9 of this invention.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip based on Embodiment 10 of this invention.
- (A) is a top view of a cover.
- FIG. 20 is a component layout diagram of a blood test apparatus according to Embodiment 11 of the present invention.
- FIG. 32 is an essential part cross-sectional view of the blood test apparatus of FIG.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- (A) is a top view of a cover.
- FIG. 36 is a plan view of the sensor chip of FIG. 35.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- the top view of the sensor chip of FIG. The exploded plan view of the sensor chip based on Embodiment 15 of this invention.
- (A) is a top view of a cover.
- (B) is a top view of a spacer.
- (C) is a top view of a board
- FIG. 42 is a plan view of the sensor chip of FIG. 41.
- the external view of the conventional sensor chip The figure which shows the puncture state by the conventional puncture device. The figure which shows a mode that the blood is squeezed out after puncturing using the conventional puncture device. The figure which shows a mode that the blood which exuded on the sensor chip with which the conventional measuring device was mounted
- the perspective view which shows the mode of the post-process after the conventional puncture.
- FIG. 1 is a plan view of the sensor chip 11 according to the first embodiment.
- 2 is a cross-sectional view taken along the line AA in FIG. 1
- FIG. 3 is a cross-sectional view taken along the line BB in FIG. 1, 2, and 3
- the sensor chip 11 has a plate shape.
- the sensor chip 11 includes three layers including a substrate 12, a spacer 13 bonded to the upper side of the substrate 12, and a cover 14 bonded to the upper side of the spacer 13. It has a structure. That is, the plate-like substrate 12, the spacer 13, and the cover 14 form the base body 15.
- the sensor chip 11 has a substantially rectangular shape, and one short side 16a side is semicircular.
- Detection electrodes 17, 18, and 19 are laid on the substrate 12.
- the detection electrodes 17, 18, and 19 are formed so as to extend toward the other short side 16b of the sensor chip 11, and are connected to connection terminals 17a, 18a, and 19a, respectively.
- an inlet 20 through which blood 3 for measurement (see FIGS. 30, 43 and 44) flows is provided.
- a supply path (capillary) 21 for blood 3 for measurement is provided from the inlet 20 toward the other short side 16b.
- An air hole 22 is provided at the end of the supply path 21.
- detection electrodes 17, 18, 19 constituting the detection unit 23 are arranged on the supply path 21.
- a reagent 24 (see FIG. 5) is placed on the detection unit 23.
- Reagent 24 is 0.01 to 2.0 wt% CMC aqueous solution with PQQ-GDH 0.1 to 5.0 U / sensor, potassium ferricyanide 10 to 200 mM, maltitol 1 to 50 mM, taurine 20 to 200 mM Then, the reagent solution is prepared by being melted and dropped onto the detection electrodes 17, 18, and 19 constituting the detection unit 23 and dried.
- the excess blood reservoir 25 (see FIGS. 1 and 3) is provided on one long side 16c side (upward in FIG. 1) and the other long side 16d side (downward in FIG. 1) of the sensor chip 11, respectively. ) Is provided.
- the surplus blood storage unit 25 stores the surplus blood remaining on the skin surface without being used for blood glucose level measurement, out of the blood flowing out to the skin surface by puncture. And the surplus blood storage part 25 has the surplus blood inflow port 25a which flows in the surplus blood 3a. The surplus blood inlet 25 a communicates with a space as the surplus blood reservoir 25.
- the surplus blood reservoir 25 forms a minute gap in the same manner as the supply channel 21 described above, and allows blood 3 as a biological sample for analysis to flow in by capillary action.
- the volume of the excess blood reservoir 25 is three times or more the volume of the supply path 21. For this reason, even when surplus blood 3a more than the blood used for measurement / analysis remains, all surplus can be easily obtained by simply contacting surplus blood 3a with surplus blood inlet 25a on the side surface of sensor chip 11. The blood 3a can be reliably introduced into the surplus blood reservoir 25 and stored.
- the inlet 20 and the excess blood inlet 25a are separately provided at different positions. That is, the inflow port 20 is provided on the short side 16a (left side in FIG. 1) side of the sensor chip 11. On the other hand, the surplus blood inlet 25a is provided on the long sides 16c and 16d (vertical direction in FIG. 1) side of the sensor chip 11. Therefore, when the measurement blood 3 flows into the inlet 20, the measurement blood 3 does not flow into the surplus blood inlet 25a. Therefore, even if the sensor chip 11 is provided with the surplus blood inlet 25a, an appropriate amount of blood 3 can flow into the detection unit 23.
- the sensor chip 11 in the present embodiment includes the surplus blood reservoir 25.
- the user flows blood 3 from the inflow port 20 and measures the blood sugar level, and then the surplus blood 3a is removed via the surplus blood inflow port 25a formed on the long side 16c or the long side 16d of the sensor chip 11. It can be stored in the excess blood storage unit 25. Therefore, the user does not have to carry the tissue 8a, the cleaning cotton 8b, etc. as in the conventional case. Furthermore, the user can discard the sensor chip 11 contaminated by sucking the excess blood 3a as it is. Therefore, the excess blood 3a is also stored in the sensor chip 11 together with the measurement blood 3 flowing into the sensor chip 11, so that the excess blood 3a can be easily discarded.
- the surplus blood inlet 25a is provided on both of the long sides 16c and 16d of the sensor chip 11 (a plurality). For this reason, the excess blood 3a can be made to flow in from either side of the long side of the sensor chip 11.
- the excess blood inlet 25 a is formed in the layer of the spacer 13 disposed in the middle of the three layers constituting the base body 15. As a result, even if the user touches the substrate 12 and the cover 14 disposed on the uppermost surface and the lowermost surface of the sensor chip 11, the extra blood 3a once taken in leaks to the outside or adheres to a finger or the like. There is no contamination.
- the inner surface of the excess blood reservoir 25 is subjected to a hydrophilic treatment or is formed of a hydrophilic material.
- the periphery of the excess blood storage part 25 is water-repellent or formed of a water-repellent material.
- the surplus blood storage part 25 has sufficient volume in order to store the surplus blood 3a. Thereby, it is possible to prevent excess blood 3a once taken in by capillary action from flowing out from the side surface of the sensor chip 11. Therefore, the used sensor chip 11 storing the excess blood 3a does not need to be wrapped with the tissue 8a or the like and can be discarded as it is.
- FIG. 4C is a plan view of the substrate 12 constituting the sensor chip 11.
- the sensor chip 11 has a short side 16a (left side in FIG. 4C), a short side 16b (right side in FIG. 4C) of about 6 mm, and long sides 16c and 16d of about 20 mm. It is rectangular (however, the short side 16a may be semicircular).
- the material of the substrate 12 is a resin material such as polyethylene terephthalate (PET).
- PET polyethylene terephthalate
- the substrate 12 has a thickness of 0.188 mm (in the range of 0.075 mm to 0.250 mm).
- a conductive layer is formed on the upper surface of the substrate 12 by sputtering or vapor deposition. Then, the conductive layers are laser processed to integrally form detection electrodes 17 to 19 and connection terminals 17a to 19a derived from these detection electrodes 17 to 19, respectively.
- FIG. 4B is a plan view of the spacer 13 constituting the sensor chip 11.
- the spacer 13 has a substantially rectangular shape with short sides 16e and 16f having dimensions of about 6 mm and long sides 16g and 16h of about 15 mm (however, the short side 16e may be semicircular). Therefore, when the spacer 13 is affixed on the substrate 12, the connection terminals 17a to 19a having a width of about 5 mm are exposed on the surface.
- a slit 13a having a width of 0.6 mm and a length of 2.4 mm is formed from the tip of the short side 16e of the spacer 13 toward the short side 16f.
- the slit 13 a forms a supply path 21 for the sensor chip 11.
- the volume of the supply path 21 is 0.14 ⁇ L, which enables blood sugar level measurement with a small blood volume. Therefore, since a lot of blood is not required for blood glucose level measurement, the burden on the patient can be reduced.
- rectangular cuts 13b are respectively provided on both long sides 16g and 16h of the spacer 13 (upper side and lower side in FIG. 4B). Then, by laminating the substrate 12 and a cover 14 which will be described later, the excess blood reservoir 25 having a rectangular shape is formed on both sides of the sensor chip 11, i.e., symmetrically with respect to the center line in the longitudinal direction of the substrate 15. 1) is formed.
- the material of the spacer 13 is polyethylene terephthalate, and a thickness of 0.100 mm (in the range of 0.050 mm to 0.125 mm) can be used.
- FIG. 4A is a plan view of the cover 14 constituting the sensor chip 11.
- the cover 14 has dimensions of short sides 16j and 16k (left side and right side in FIG. 4A) of about 6 mm, and long sides 16m and 16n (upper side and bottom side in FIG. 4A) of about 15 mm.
- the short side 16j may be semicircular). Therefore, when this cover 14 is affixed onto the spacer 13, the connection terminals 17a to 19a having a width of about 5 mm are exposed on the surface on the short side 16k side.
- the cover 14 has an air hole 22 having a diameter of 0.05 mm at a position corresponding to the end portion of the slit 13 a formed in the spacer 13.
- the cover 14 is made of polyethylene terephthalate, and a thickness of 0.075 mm (in the range of 0.050 mm to 0.125 mm) can be used.
- At least the back surface of the cover 14 corresponding to the ceiling of the supply path 21 and the excess blood reservoir 25 is preferably subjected to hydrophilic treatment. This is because the blood 3 flowing into the detection unit 23 due to the capillary phenomenon flows smoothly. Moreover, it is for flowing the surplus blood 3a smoothly also about the surplus blood storage part 25 similarly.
- the cover 14 is formed using a transparent member, it is possible to visually confirm the state of the surplus blood 3a flowing into the surplus blood reservoir 25. Furthermore, before and after use of the sensor chip 11 can be easily confirmed by the presence or absence of the excess blood 3a in the excess blood reservoir 25.
- FIG. 5 shows an exploded perspective view of the sensor chip 11 described above.
- the substrate 12, the spacer 13, and the cover 14 constitute a base 15 of the sensor chip 11.
- a supply path 21 (see FIG. 1 or FIG. 6) is formed by the slit 13a of the spacer 13. Further, a surplus blood reservoir 25 is formed by the notch 13 b of the spacer 13.
- FIG. 6 is a block diagram showing a configuration of a measuring instrument 31 that is loaded with the sensor chip 11 and measures a blood glucose level.
- a sensor insertion portion 33 into which the sensor chip 11 is inserted is provided at one end portion of the housing 32.
- a connector 34 (respective connectors 34a to 34c) to which connection terminals 17a to 19a formed on the sensor chip 11 are connected is attached to the back of the sensor insertion portion 33.
- the sensor chip except for the sensor chips 111 and 141) described in the later-described embodiment can be inserted.
- 34a is a connector to which the connection terminal 17a is connected, and 34b is a connector to be connected to the connection terminal 19a.
- Reference numeral 34c denotes a connector to which the connection terminal 18a is connected.
- Each connector 34a, 34b, 34c is connected to a switching circuit 35a and can be switched according to the measurement contents.
- the connector 34a is connected to the connection terminal 17a and is input to the current / voltage converter 35b via the switching circuit 35a.
- the output is connected to the arithmetic unit 35d via an analog / digital converter (hereinafter referred to as A / D converter) 35c.
- a / D converter analog / digital converter
- the calculation unit 35d not only receives the output of the A / D converter 35c but also has a control function for the measuring instrument 31 as a whole.
- the calculation unit 35d is connected to an A / D converter 35c, a control terminal of a reference voltage source 35e that applies a voltage to the sensor chip 11, a switching circuit 35a, a display unit 36, and a communication unit 37 that communicates with the outside. .
- FIG. 7 is an external perspective view showing a state where the sensor chip 11 is inserted into the sensor insertion portion 33 of the measuring instrument 31.
- the sensor chip 11 is inserted into the sensor insertion portion 33 of the measuring device 31. Whether or not the sensor chip 11 is in the inserted state can be detected by a change in the resistance value between the connector 34b and the connector 34c. That is, when the sensor chip 11 is not inserted, the resistance value is usually infinite because the connector 34b and the connector 34c are open. On the other hand, when the sensor chip 11 is inserted, a predetermined resistance value is indicated. Thereby, it can be easily detected that the sensor chip 11 is inserted into the sensor insertion portion 33. When the sensor chip 11 is inserted into the sensor insertion portion 33 of the measuring instrument 31, the connection terminals 17a, 19a, and 18a of the sensor chip 11 are connected to the connectors 34a, 34b, and 34c of the measurement circuit portion 35, respectively.
- the blood 3 for measurement is spotted on the inlet 20 of the sensor chip 11 in a state where the sensor chip 11 is mounted on the sensor insertion portion 33 (see FIG. 7)
- the blood 3 flows into the inlet by capillary action.
- the light is guided to the detection electrode 19 disposed on the most downstream side through a supply path 21 communicating with 20.
- the calculation unit 35d controls the switching circuit 35a to connect the detection electrode 18 to the ground. Thereafter, control is performed so that no voltage is supplied from the current / voltage converter 35b to the detection electrode 17 for a certain period of time. During this time, the reaction between the detection electrode 18 and the reagent 24 placed on the detection electrode 17 and the blood 3 proceeds. After a predetermined time (2 to 5 seconds), a constant voltage is applied between the detection electrode 17 and the detection electrode 18 of the sensor chip 11 by the reference voltage source 35e via the switching circuit 35a and the connector 34. At this time, a current proportional to the blood glucose level concentration in the blood 3 is generated between the detection electrode 17 and the detection electrode 18.
- This current is input to the current / voltage converter 35b via the connector 34 and the switching circuit 35a and converted into a voltage.
- the voltage is converted into digital data by the A / D converter 35c.
- the converted digital data is taken into the calculation unit 35d.
- the computing unit 35d calculates a blood glucose level from the digital data and displays it on the display unit 36.
- the sensor chip 41 according to the second embodiment has the above-described embodiment in that the surplus blood storage section 42 (corresponding to the surplus blood storage section 25 according to the first embodiment) is formed in a layer different from the supply path 21. 1 and different.
- the same reference numerals are given to the same components as those in the first embodiment, and the description is simplified. This also applies to the following embodiments.
- FIG. 8 is a plan view of the sensor chip 41 according to the second embodiment. 9 is a cross-sectional view taken along the line CC in FIG. 8, and FIG. 10 is a cross-sectional view taken along the line DD in FIG.
- the sensor chip 41 includes a substrate 43 (corresponding to the substrate 12 in the first embodiment) and a spacer 44 bonded to the upper surface of the substrate 43 (on the spacer 13 in the first embodiment).
- a cover 45 bonded to the upper surface of the spacer 44 (corresponding to the cover 14 in the first embodiment)
- a surplus blood suction spacer 46 bonded to the upper surface of the cover 45
- the surplus blood suction It has a five-layer structure with a surplus blood suction cover 47 bonded to the upper surface of the spacer 46.
- the substrate 43, the spacer 44, the cover 45, the surplus blood suction spacer 46, and the surplus blood suction cover 47 form a plate-like base body 48.
- the sensor chip 41 has the same outer shape as the sensor chip 11 in the first embodiment except for the thickness, and the same material is used.
- the outer shape and material of the surplus blood suction spacer 46 are the same as those of the spacer 13 of the first embodiment, and the outer shape and material of the surplus blood suction cover 47 are the same as those of the cover 14 of the first embodiment. It is common.
- FIG. 11E is a plan view of the substrate 43 constituting the sensor chip 41, and has the same configuration as the substrate 12 of the sensor chip 11 in the first embodiment described above.
- FIG. 11D is a plan view of the spacer 44 constituting the sensor chip 41, and is provided with a slit 13a that forms the supply path 21 (see FIG. 8 or FIG. 10).
- spacer 44 is different from the spacer 13 in the first embodiment described above in that the rectangular cut 25a that forms the excess blood reservoir 25 is not formed.
- FIG. 11C is a plan view of the cover 45 constituting the sensor chip 41, and has the same configuration as the cover 14 in the first embodiment described above. Note that it is not necessary to use a transparent member for the material of the cover 45.
- FIG. 11B is a plan view of the surplus blood suction spacer 46 that constitutes the sensor chip 41.
- the surplus blood suction spacer 46 has rectangular cuts 46a forming the surplus blood reservoir 42 (see FIGS. 8 and 9) at both sides of the long side at symmetrical positions with respect to the center line in the longitudinal direction of the base 48. Each surface is formed.
- the surplus blood suction spacer 46 has a through hole 46 b having a diameter larger than that of the air hole 22 at a position corresponding to the air hole 22 of the cover 45.
- FIG. 11A is a plan view of the surplus blood suction cover 47 constituting the sensor chip 41.
- the surplus blood suction cover 47 is formed with a through hole 47 a at a position corresponding to the through hole 46 b of the surplus blood suction spacer 46.
- the surplus blood suction cover 47 is preferably formed using a transparent member. The reason is the same as in the first embodiment.
- the sensor chip 41 according to the second embodiment can increase the volume of the excess blood reservoir 42 as compared with the sensor chip 11 according to the first embodiment described above. Specifically, a maximum volume of about two-thirds of the volume of the base 48 of the sensor chip 41 can be secured. Other features are the same as those of the sensor chip 11 of the first embodiment described above.
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- the sensor chip 51 in the third embodiment (corresponding to the sensor chip 41 in the second embodiment) has a configuration of the surplus blood reservoir 52 as compared with the sensor chip 41 in the second embodiment described above. Only the difference. That is, in order to increase the thickness strength of the surplus blood reservoir 52, a plurality of protrusions 52b are provided in the surplus blood reservoir 52 in the third embodiment. Thereby, even when the sensor chip 51 is pressed in the thickness direction, the thickness dimension can be kept substantially constant. Even when a pressing force is applied from the outside in the thickness direction of the surplus blood reservoir 52, the sensor chip 51 hardly bends in the thickness direction due to the pressing force, so that surplus blood 3a flows out of the surplus blood inlet 52a. Can be prevented.
- a convex 52b is arranged on the upper surface of the surplus blood suction spacer 53 having a rectangular shape.
- the height of the projection 52b is about 0.1 mm (in the range of 0.050 mm to 0.125 mm). That is, it is the same as the spacer 13 in the first embodiment in that a capillary phenomenon is caused by the minute gap defined by the height dimension.
- a plurality of protrusions 52b are formed uniformly in the surplus blood reservoir 52.
- the smaller the number of protrusions 52b in the surplus blood reservoir 52 the greater the volume of the surplus blood reservoir 52 increases.
- the number of the protrusions 52b increases, the substantial volume of the excess blood reservoir 52 decreases, but the strength in the thickness direction of the excess blood reservoir 52 improves. Therefore, in the present embodiment, 23 protrusions 52b are provided in consideration of these balances.
- the number of the protrusions 52b may be increased or decreased appropriately according to the area of the excess blood storage part of the sensor chip 51.
- the volume of the surplus blood storage section 52 can be increased as in the case of the second embodiment described above, and can be expanded to about two thirds of the volume of the base body of the sensor chip 51. It is.
- a surplus blood suction cover 54 is attached to the upper surface of the surplus blood suction spacer 53.
- the surplus blood suction cover 54 has the same dimensions as the surplus blood suction spacer 53.
- FIG. 13 is a plan view of the surplus blood storage portion 52 formed by bonding the surplus blood suction spacer 53 and the surplus blood suction cover 54 together.
- FIG. 15 is a plan view of the blood measurement unit 55.
- the blood measurement unit 55 includes a substrate 43 (see FIG. 14C), a spacer 44 (see FIG. 14B) bonded to the upper surface of the substrate 43, and a cover 45 (see FIG. 14) bonded to the upper surface of the spacer 44. 14 (a)).
- the surplus blood storage part 52 shown in FIG. 13 is affixed on the upper surface of the blood measurement part 55, and the sensor chip 51 shown in FIG. 16 is completed.
- a paste that has been applied with a paste and bonded to the back surface of the surplus blood suction cover 54 may be used.
- a hot-melt material etc. can be used for a paste material.
- the protrusion 52b may be formed by embossing the surplus blood suction cover 54 protruding to the back surface side.
- the user does not need to carry around tissue or washing cotton for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 18 is a plan view of sensor chip 61 (corresponding to sensor chip 11 in the first embodiment) in the fourth embodiment.
- the surplus blood reservoir 62 includes a detection electrode 63 (corresponding to the detection electrode 17 in the first embodiment) and a detection electrode 64 (corresponding to the detection electrode 18 in the first embodiment). This is different from the first embodiment described above in that it is not in contact with the first embodiment. With this configuration, the excess blood reservoir 62 does not affect the detection electrodes 63 and 64.
- FIG. 17 (a) to 17 (c) are exploded plan views of the sensor chip 61.
- FIG. FIG. 17C is a plan view of substrate 65 (corresponding to substrate 12 in the first embodiment).
- the widths of the detection electrodes 63 and 64 are narrower than the widths of the detection electrodes 17 and 18 of the substrate 12 in the sensor chip 11 of the first embodiment described above.
- FIG. 17B is a plan view of the spacer 66 (corresponding to the spacer 13 in the first embodiment).
- the notch 66a forming the surplus blood reservoir 62 is thin so as not to contact the detection electrodes 63 and 64.
- FIG. 17A shows the cover 14 attached to the upper surface of the spacer 66.
- the sensor chip 61 is configured by combining these members (the substrate 65, the spacer 66, and the cover 14).
- the user does not have to carry around tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 20 is a plan view of sensor chip 71 in the fifth embodiment (corresponding to sensor chip 61 in the fourth embodiment).
- the sensor chip 71 in the present embodiment is different from the above-described fourth embodiment in that a detection electrode 72 (Hct pole) is provided between the inlet 20 and the detection electrode 63. Due to this difference, the measurement value can be corrected in the blood test, and the measurement accuracy is improved.
- a detection electrode 72 Hct pole
- FIGS. 19A to 19C are exploded plan views of the sensor chip 71 of FIG.
- FIG. 19C is a plan view of the substrate 73 (corresponding to the substrate 65 in the fourth embodiment).
- a detection electrode 72 is provided on the substrate 73 between the detection electrode 63 and the inlet 20.
- FIG. 19B is a plan view of the spacer 66. The spacer 66 is attached to the upper surface of the substrate 73.
- FIG. 19A is a plan view of the cover 14 attached to the upper surface of the spacer 66.
- the sensor chip 71 is configured by combining these members (the substrate 73, the spacer 66, and the cover 14).
- the user does not need to carry around tissue or washing cotton for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 22 is a plan view of sensor chip 81 in the sixth embodiment (corresponding to sensor chip 11 in the first embodiment).
- the sensor chip 81 according to the present embodiment is different from the sensor chip 11 according to the first embodiment described above in that the inflow of blood 3 into the excess blood reservoir 25 can be electrically detected.
- FIG. 21C is a plan view of substrate 82 (corresponding to substrate 12 in the first embodiment).
- the substrate 82 is divided into two portions in the longitudinal direction corresponding to the detection electrode 17 (see FIG. 4C) of the sensor chip 11 in the first embodiment, and the detection electrode 83 (working electrode) and excess blood detection.
- the electrode 85 is formed.
- a portion corresponding to the detection electrode 18 (see FIG. 4C) of the sensor chip 11 in the first embodiment is divided into two in the longitudinal direction, and the detection electrode 84 (counter electrode), the excess blood detection electrode 86, and Is forming.
- FIG. 21B is a plan view of the spacer 13.
- the spacer 13 is attached to the upper surface of the substrate 82.
- the notches 13b formed in the spacer 13 are provided at symmetrical positions with respect to the center line in the longitudinal direction of the base 82.
- the notch 13b has such a dimensional relationship as to straddle the detection electrode 83, the excess blood detection electrode 85, the detection electrode 84, and the excess blood detection electrode 86. This is to electrically detect the inflow of blood 3 into the surplus blood reservoir 25.
- the slit 13a and the notch 13b are provided at positions separated from each other. That is, the supply path 21 and the surplus blood storage unit 25 are arranged at positions independent of each other, and the blood 3 and the surplus blood 3a that flow into each other and store do not affect each other.
- FIG. 21A shows a cover 14 to be attached to the upper surface of the spacer 13. Since the sensor chip 81 of the present embodiment is configured as described above, a voltage is applied between the detection electrode 83 and the excess blood detection electrode 85, the detection electrode 84, and the excess blood detection electrode 86, By measuring the electrical resistance, it is possible to detect the inflow of blood 3 or surplus blood 3a into surplus blood reservoir 25.
- the display unit 36 displays information that prompts the introduction of the blood 3 into the supply channel 21. (See FIG. 6) to notify the user.
- the inflow of blood 3 into the supply path 21 is detected by applying a voltage between the detection electrode 84 and the detection electrode 19 and measuring its electrical resistance.
- the surplus blood detection electrodes 85 and 86 shown in the present embodiment can also be applied to the sensor chip 71 having the detection electrode 72 (Hct pole) shown in the fifth embodiment.
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 24 is a plan view of sensor chip 91 according to the seventh embodiment (corresponding to sensor chip 11 according to the first embodiment).
- the surplus blood inlet 92a communicating with the surplus blood reservoir 92 has an upper side (first end side) above the short side 93a of the substantially rectangular sensor chip 91 and a long side 93c.
- the sensor chip 11 is different from the sensor chip 11 of the first embodiment described above in that it is formed on the lower side (second end side) of the short side 93a and the long side 93d. Therefore, the surplus blood 3a can be introduced into the surplus blood storage part 92 provided on the short side 93a side by moving the sensor chip 91 a little after flowing the blood 3 for measurement into the inflow port 20. .
- FIG. 23 (a) to 23 (c) are exploded plan views of the sensor chip 91.
- FIG. FIG. 23C is a plan view of the substrate 12.
- a spacer 94 (corresponding to the spacer 13 in the first embodiment) shown in FIG. 23B is attached to the upper surface of the substrate 12.
- the spacer 94 is provided with a notch 94b in a portion from the upper side of the short side 93a to the long side 93c of the substantially rectangular spacer 94 and a portion from the lower side of the short side 93a to the long side 93d. Yes.
- An excess blood reservoir 92 and an excess blood inlet 92a are formed by the notch 94b.
- the notch 94b is provided at a position separated from the slit 13a forming the inflow port 20.
- a cover 14 shown in FIG. 23A is attached to the upper surface of the spacer 94.
- the sensor chip 91 is configured by combining these members (the substrate 12, the spacer 94, and the cover 14).
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 26 is a plan view of sensor chip 101 according to the eighth embodiment (corresponding to sensor chip 11 according to the first embodiment).
- the sensor chip 101 according to the eighth embodiment forms a large surplus blood reservoir 102 while having a three-layer structure. Further, a plurality of protrusions 102b are provided inside the surplus blood reservoir 102 to improve the strength.
- FIG. 25 (a) to 25 (c) are exploded plan views of the sensor chip 101.
- FIG. FIG. 25C is a plan view of the substrate 12.
- a spacer 103 (corresponding to the spacer 13 in the first embodiment) shown in FIG. 25B is attached to the upper surface of the substrate 12.
- the spacer 103 has a slit 13a formed in the substantially rectangular spacer 103 and a plurality of protrusions 102b formed on the entire back side of the slit 13a.
- the protrusion 102b is formed in the same manner as the protrusion 52b (see FIGS. 12 and 16) in the third embodiment described above.
- the sensor chip 101 is configured by combining these members (the substrate 12, the spacer 103, and the cover 14).
- the user does not need to carry tissue or washing cotton for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 28 is a plan view of sensor chip 111 (corresponding to sensor chip 11 in the first embodiment) in the ninth embodiment.
- the sensor chip 111 is provided with an excess blood reservoir 113 on one side surface of a substantially rectangular sensor chip 111 and an inlet 112 for blood 3 at a substantially center in plan view. .
- the sensor chip 111 is used in a blood test apparatus 151 (one step) (see FIG. 31) that measures the properties of blood 3 simultaneously with puncturing.
- a reservoir 114 for blood 3 is formed in the center of the sensor chip 111 in plan view.
- the reservoir 114 has a circular shape with a diameter of about 2 mm, and an inlet 112 into which the blood 3 for measurement flows is provided on the side of the reservoir 114.
- a supply path 115 (corresponding to the supply path 21 in the first embodiment) is formed in communication with the inflow port 112.
- An air hole 116 is provided at the end of the supply path 115.
- the electrodes constituting the detection unit 121 (detection electrode 117 (Hct electrode), detection electrode 118 (counter electrode), detection electrode 119 (working electrode), detection electrode) are arranged in order from the storage unit 114. 120).
- a reagent 24 (see FIG. 2) is placed on the detection unit 121.
- the detection electrodes 117, 118, 119, 120 are led out to the end along the longitudinal direction of the sensor chip 111, and are connected to the connection terminals 117a, 118a, 119a, 120a.
- FIGS. 27A to 27C are exploded plan views of the sensor chip 111.
- FIG. 27A to 27C are exploded plan views of the sensor chip 111.
- FIG. 27C is a plan view of a substantially rectangular substrate 125 (corresponding to the substrate 12 in the first embodiment).
- the substrate 125 is formed with a hole 126 formed at a position corresponding to the storage portion 114, detection electrodes 117, 118, 119, and 120, and connection terminals 117a, 118a, 119a, and 120a respectively derived therefrom. ing.
- a spacer 127 (corresponding to the spacer 13 in the first embodiment) shown in FIG. 27B is attached to the upper surface of the substrate 125.
- the spacer 127 has a hole 128 corresponding to the reservoir 114, a slit 129 communicating with the hole 128 at a position corresponding to the supply path 115, and a notch 130 at a position corresponding to the excess blood reservoir 113. It has been.
- a cover 131 shown in FIG. 27A is attached to the upper surface of the spacer 127.
- the cover 131 is provided with a hole 132 and an air hole 116 at a position corresponding to the storage part 114.
- the storage portion 114 is configured by the hole 126 provided in the substrate 125, the hole 128 provided in the spacer 127, and the hole 132 provided in the cover 131.
- the sensor chip 111 is configured by combining these members (the substrate 125, the spacer 127, and the cover 131).
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 30 is a plan view of sensor chip 141 in the tenth embodiment (corresponding to sensor chip 111 in the ninth embodiment).
- the sensor chip 141 includes a surplus blood reservoir 142 on one entire side surface of the substantially rectangular sensor chip 141.
- a plurality of protrusions 142 a are provided inside the surplus blood storage unit 142. Therefore, as in the above-described eighth embodiment, the strength of the excess blood reservoir 142 can be improved.
- the surplus blood inlet 142b of the surplus blood reservoir 142 is provided on the short side 143a side of the substantially rectangular sensor chip 141 and the long sides 143c and 143d on both sides. Surplus blood 3a can be sucked even from the direction.
- FIG. 29 (a) to 29 (c) are exploded plan views of the sensor chip 141.
- FIG. FIG. 29C is a plan view of the substrate 125.
- a spacer 144 (corresponding to the spacer 127 in the ninth embodiment) shown in FIG. 29B is attached to the upper surface of the substrate 125.
- the spacer 144 has a plurality of protrusions 142a on one side of a substantially rectangular shape.
- a cover 131 shown in FIG. 29A is attached to the upper surface of the spacer 144.
- the sensor chip 141 is configured by combining these members (the substrate 125, the spacer 144, and the cover 131).
- the user does not have to carry around tissue or washing cotton for wiping off excess blood as in the prior art, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 31 is a component layout diagram of blood test apparatus 151 that performs blood sugar level measurement and the like using sensor chips 111 and 141 shown in the ninth and tenth embodiments.
- Blood test apparatus 151 punctures the skin of a diabetic patient or the like, and inspects blood 3 exuded by this puncture. Therefore, there is no need to prepare and use a puncture device for exuding blood 3 and a measuring instrument for measuring blood 3 as in the prior art. In addition, a series of operations (one-step operation) of skin puncture, blood sampling, measurement / inspection can be performed with a single operation.
- the casing 152 has a rectangular parallelepiped shape. And the cover part 152c is connected with the edge part of the main-body part 152a which comprises the housing
- the puncture portion 153 is provided at a corner below the main body portion 152a, and is configured to sandwich the sensor chip 111 or the sensor chip 141 described above between the upper holder 153a and the lower holder 153b. In this embodiment, the case where the sensor chip 111 is used will be described.
- a laser puncture unit 154 as a puncture means is mounted facing the puncture unit 153.
- a needle puncturing unit may be used instead of the laser puncturing unit 154.
- a sensor unit 155 is disposed at a position adjacent to the laser puncture unit 154.
- the sensor unit 155 has a sensor chamber 155a and a drying chamber 155b.
- the sensor chip 111 is stacked and stored in the sensor chamber 155a. The stacked sensor chip 111 is pressed downward by a push plate 155d by a spring 155c.
- the desiccant 155e is accommodated in the drying chamber 155b.
- An outlet 155f through which the sensor chip 111 is carried out is formed at the lower corner of the sensor chamber 155a.
- the sensor chip 111 unloaded from the outlet 155f is unloaded by the transfer means 155g.
- the transport means 155g has a transport plate 155h and a spring 155j that biases the transport plate 155h to its original state.
- a high voltage generation circuit 156 that supplies a high voltage to the laser puncture unit 154 is disposed above the laser puncture unit 154.
- An electric circuit unit 157 is disposed above the high voltage generation circuit 156.
- a negative pressure means 158 is provided above the sensor unit 155. The negative pressure means 158 supplies negative pressure to the negative pressure chamber 153d (see FIG. 32) of the puncture unit 153 via the negative pressure path 158a.
- a puncture button 154b for emitting laser light 154a from the laser puncture unit 154 is provided on the upper side surface of the main body 152a.
- the puncture button 154b By pressing the puncture button 154b, the laser beam 154a is emitted from the laser puncture unit 154.
- the opening angle of the lid 152c is regulated at a certain angle. Therefore, the laser beam 154a does not leak to the outside, and safety can be ensured.
- FIG. 32 is a cross-sectional view of the main part in the vicinity of puncture unit 153 in blood test apparatus 151.
- the puncture unit 153 has an upper holder 153a and a lower holder 153b.
- the lower holder 153b is urged toward the upper holder 153a by a leaf spring 153e.
- the connector 159 is connected to connection terminals 117a, 118a, 119a, and 120a (see FIG. 28) of the sensor chip 111 sandwiched between the upper holder 153a and the lower holder 153b, and transmits a signal to the electric circuit unit 157.
- a transparent member 153f is detachably provided on the upper surface of the upper holder 153a.
- a hole 153g is provided below the transparent member 153f. Therefore, the laser beam 154a emitted from the laser puncture unit 154 penetrates the skin 6 through the transparent member 153f, the hole 153g, the storage portion 114 of the sensor chip 111, and the negative pressure chamber 153d in a straight line. . Thereby, a puncture wound is formed in the skin 6 and the blood 3 exudes.
- the blood 3 exuding from the skin 6 is taken in from the storage part 114 of the sensor chip 111 shown in FIG. Then, it introduce
- FIG. 1
- the result of this chemical reaction is transmitted to the electric circuit unit 157 via the connector 159, the blood glucose level is measured, and displayed on a display unit (not shown) provided on the surface of the housing 152.
- the electric circuit unit 157 includes a measurement circuit similar to the measurement circuit unit 35 described in the first embodiment and a circuit that generates a control signal for controlling the high voltage generation circuit 156 by a pressing signal of the puncture button 154b. Are included.
- the user causes the excess blood 3a in the vicinity of the puncture wound formed by laser puncture to flow into the excess blood reservoir 113 of the sensor chip 111 described above.
- the user takes out the sensor chip 111 from the blood test apparatus 151, and the opening portion of the minute gap formed on the side surface on the long side of the sensor chip 111 is placed on the skin surface where the excess blood 3a is left. Touch it against the surface. Thereby, the surplus blood 3a left on the skin is taken into the surplus blood reservoir 113 from the minute gap and held by the capillary phenomenon. Therefore, the user can use the used sensor chip 111 as a substitute for absorbent cotton or the like for wiping off the excess blood 3a.
- the sensor chip attached to blood test apparatus 151 is not limited to sensor chip 111 shown in FIG. 28, and the above-described sensor chips and sensor chips described below may be used. Of course it is possible.
- FIG. 34 is a plan view of sensor chip 161 in the twelfth embodiment (corresponding to sensor chip 11 in the first embodiment).
- a surplus blood reservoir 162 is provided on one entire side surface of the substantially rectangular sensor chip 161, and the supply path 163 penetrating between both side surfaces is provided on the other side surface (supply in the first embodiment). Corresponding to the path 21). Therefore, the excess blood 3a can be sucked in the entire one side surface of the sensor chip 161, and the blood 3 for measurement can be flowed into the predetermined detection electrode from either side surface of the sensor chip 161.
- FIG. 33C is a plan view of the substrate 165.
- a detection electrode 166 counter electrode
- a detection electrode 167 working electrode
- a detection electrode 168 detection electrode
- the detection electrode 168 serves as an electrode for detecting the inflow of the blood 3.
- the detection electrode 166 serves as an electrode that detects the inflow of blood 3.
- a spacer 169 (corresponding to the spacer 13 in the first embodiment) shown in FIG. 33B is attached to the upper surface of the substrate 165.
- the spacer 169 has a concave surface 169b that forms a surplus blood reservoir 162 on one short side 169a of a substantially rectangular shape. On the other short side 169c, a groove 169d forming the supply path 163 is provided so as to penetrate between the side surfaces.
- a cover 170 shown in FIG. 33A is attached to the upper surface of the spacer 169.
- Air holes are not formed in the cover 170.
- the sensor chip 161 is configured by combining these members (the substrate 165, the spacer 169, and the cover 170).
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the prior art, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 36 is a plan view of sensor chip 171 (corresponding to sensor chip 161 in Embodiment 12) in the thirteenth embodiment.
- the above-described implementation is provided in that the surplus blood reservoir 172 having the surplus blood inlet 172a is provided only on one short side of the substantially rectangular sensor chip 171. Different from Form 12. Therefore, the excess blood 3a can be sucked only from one short side of the sensor chip 171. Further, similarly to the above-described twelfth embodiment, the blood 3 for measurement can be introduced from either side of the sensor chip 171.
- FIG. 35C is a plan view of the substrate 165.
- a spacer 174 (corresponding to the spacer 169 in Embodiment Mode 12) shown in FIG. 35B is attached to the upper surface of the substrate 165.
- a concave surface 174b that forms the surplus blood reservoir 172 is formed in a portion excluding both end portions of one short side 174a of a substantially rectangular shape.
- a groove 169d that forms the supply path 163 is provided on the long side 174c of the spacer 174 so as to penetrate between both side surfaces.
- a cover 175 shown in FIG. 33A is attached to the upper surface of the spacer 174.
- a slit-like air hole 176 is formed in the cover 175 at a position corresponding to the deep part of the excess blood reservoir 172.
- the sensor chip 171 is configured by combining these members (the substrate 165, the spacer 174, and the cover 175).
- the user does not have to carry around tissue or washing cotton for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 38 is a plan view of sensor chip 181 in the fourteenth embodiment (corresponding to sensor chip 171 in the thirteenth embodiment).
- the sensor chip 181 in the present embodiment is different from the sensor chip 171 only in the shape of the air hole 182 formed in the upper surface of the excess blood reservoir 172.
- FIG. 37 (a) to 37 (c) are exploded plan views of the sensor chip 181.
- FIG. FIG. 37C is a plan view of the substrate 165.
- a spacer 174 shown in FIG. 37B is attached to the upper surface of the substrate 165.
- a cover 183 shown in FIG. 37A is attached to the upper surface of the spacer 174.
- a plurality of air holes 182 are formed in the cover 183 over the entire position corresponding to the excess blood reservoir 172.
- the sensor chip 181 is configured by combining these members (the substrate 165, the spacer 174, and the cover 183).
- the user does not need to carry tissue or washing cotton for wiping off excess blood as in the conventional case, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 40 is a plan view of sensor chip 191 in the fifteenth embodiment (corresponding to sensor chip 11 in the first embodiment).
- the sensor chip 191 in the present embodiment has an inlet 192 for blood 3 for measurement (corresponding to the inlet 20 in the first embodiment) on one side (upper side) of the substantially rectangular long side, and this inlet.
- a supply path 193 communicating with 192 (corresponding to the supply path 21 in the first embodiment) is provided.
- a surplus blood inlet 194a formed over substantially the entire long side, and a surplus blood reservoir 194 communicating with the surplus blood inlet 194a. It has been.
- blood 3 for measurement can be introduced from one long side of the sensor chip 191. Moreover, since the surplus blood inlet 194a is provided over the other long side, the opening which takes in the surplus blood 3a can be ensured widely, and it can flow in easily.
- FIG. 39C is a plan view of the substrate 195.
- a detection electrode 196 (C pole), a detection electrode 197 (W pole), and a detection electrode 198 are laid in parallel with each other on the substantially rectangular substrate 195 in order from one long side toward the center along the long side direction. Has been.
- the detection electrodes 196, 197, and 198 are laid between one long side and the center.
- a spacer 199 shown in FIG. 39B is attached to the upper surface of the substrate 195.
- the spacer 199 is provided with a slit 199a that forms a supply path 193 from one long side toward the center.
- the spacer 199 is provided with a cut 199b that forms a surplus blood reservoir 194 between the other long side and the center.
- the slit 199a and the notch 199b are independently formed at spaced positions.
- a cover 200 shown in FIG. 39A is attached to the upper surface of the spacer 199.
- the cover 200 is provided with an air hole 200 a at a position corresponding to the inner portion of the supply path 193.
- the sensor chip 191 is configured by combining these members (the substrate 195, the spacer 199, and the cover 200).
- the user does not need to carry tissue or washing cotton for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- FIG. 42 is a plan view of sensor chip 201 in the sixteenth embodiment (corresponding to sensor chip 51 in the third embodiment).
- the sensor chip 201 in the present embodiment is different from the above-described embodiments in that a surplus blood suction member 202 as a surplus blood reservoir is attached to an upper surface or a lower surface. Therefore, surplus blood 3a can be sucked and stored in the sensor chip 201 by bringing the upper surface or the lower surface of the sensor chip 201 into contact with the surplus blood 3a.
- FIG. 41 (a) and 41 (b) are exploded plan views of the sensor chip 201.
- FIG. FIG. 41 (a) shows blood measurement unit 55 (see FIG. 15) in the third embodiment described above.
- Blood measurement unit 55 includes substrate 43 shown in FIG. 14, spacer 44 attached to the upper surface of substrate 43, and cover 45 attached to the upper surface of spacer 44.
- a surplus blood suction member (used as an example of a surplus blood reservoir) 202 shown in FIG. 41B is attached to the upper surface or the lower surface of the blood measuring unit 55 configured as described above.
- the surplus blood suction member 202 has a rectangular shape and is attached to a position where the air hole 22 is not covered (so that the air hole 22 is exposed).
- the surplus blood suction member 202 can be a porous member such as filter paper.
- the sensor chip 201 is configured by combining these members (blood measurement unit 55, surplus blood suction member 202).
- the user does not need to carry tissue or washing cotton etc. for wiping off excess blood as in the past, and the measurement is finished and the excess blood is aspirated.
- the entire sensor chip can be discarded.
- the sensor chip of the present invention is a sensor chip for analyzing a component of a biological sample such as blood, and includes a plate-shaped substrate, an inlet, a supply path, and a detection electrode.
- An inflow port is provided at one end of the substrate and a biological sample for analysis flows in.
- the supply path communicates with the inflow port and a biological sample is introduced.
- a detection electrode is provided in this supply path, and detects a signal for analysis.
- the substrate has a surplus blood reservoir that aspirates surplus blood, which is an extra biological sample that has not been used for analysis, and stores the aspirated surplus blood.
- a sensor chip in which a base member is provided with an absorbing member that absorbs excess blood, which is an extra biological sample that has not been used for analysis.
- the measuring instrument of the present invention is a measuring instrument using the sensor chip, and includes a housing, a sensor insertion part, a connector, a measurement circuit part, and a display part.
- the sensor insertion portion is provided on one side of the housing and a sensor chip is inserted.
- the connector is provided in this sensor insertion part.
- the measurement circuit unit is connected to this connector.
- the display unit is connected to the output of the measurement circuit unit.
- the measurement circuit unit measures the analysis data of the biological sample introduced into the sensor chip and displays the result on the display unit.
- the measuring instrument of the present invention includes a housing, a sensor insertion part, a connector, a measurement circuit part, and a display part.
- the sensor insertion part is provided on one side of the housing while the sensor chip is inserted.
- the connector is provided in the sensor insertion part.
- the measurement circuit unit is connected to the connector.
- the display unit is connected to the output of the measurement circuit unit.
- the connector has a terminal for an extra blood detection electrode that detects that extra blood has been sucked into the sensor chip.
- the blood test apparatus of the present invention includes a housing, a sensor insertion portion, a puncturing means, a connector, an electric circuit portion, and a display portion.
- the sensor insertion portion is provided in a part of the casing, and the above-described sensor chip for analysis (including a case where an excess blood detection electrode is included) is attached.
- the puncturing means is provided at a position facing or close to the sensor insertion portion, and is provided for puncturing the skin.
- the connector is provided in the sensor insertion part.
- the electric circuit unit is connected to the connector and analyzes a biological sample such as a body fluid.
- the display unit is connected to the output of the electric circuit unit.
- the inside of the excess blood reservoir is formed of a hydrophilic treatment or a hydrophilic material
- the periphery of the excess blood reservoir is formed of a water repellent treatment or a water repellent material
- the excess blood reservoir is formed.
- the part has a sufficient volume. For this reason, the blood, which is a biological sample once stored in the sensor chip, is safe without leaking or adhering to the outside from the sensor chip.
- the sensor chip according to the present invention can easily process surplus blood, it can be widely applied to blood tests in measuring instruments, blood test apparatuses, and the like.
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Abstract
Description
即ち、余剰血液3aを拭き取るために、ユーザはティシュ8aや洗浄綿8b等を持ち歩かなければならない。更に、ユーザは拭き取った後の余剰血液3aが付着したティシュ8aや洗浄綿8b等を持ち歩かなければならない。このように、余剰血液3aを拭き取るためにティシュ8aや洗浄綿8b等を持ち歩くことは、ユーザにとっては衛生上且つ安全上好ましくなく、かつその処理は煩わしいものであった。
図1は、実施の形態1におけるセンサチップ11の平面図である。図2は、図1のA―A断面図であり、図3は、図1のB-B断面図である。図1、図2、図3において、センサチップ11は、板体状をしている。そして、図2、図3に示すように、センサチップ11は、基板12と、この基板12の上方に貼り合わされたスペーサ13と、このスペーサ13の上方に貼り合わされたカバー14とを含む3層構造になっている。つまり、板体状の基板12とスペーサ13とカバー14とが、基体15を形成している。
基板12、スペーサ13およびカバー14によってセンサチップ11の基体15が構成される。スペーサ13のスリット13aによって供給路21(図1または図6参照)が形成される。また、スペーサ13の切り込み13bによって余剰血液貯留部25が形成される。
図7は、センサチップ11が測定器31のセンサ挿入部33に挿入された状態を示した外観斜視図である。
次に、図8~図11を用いて、実施の形態2におけるセンサチップ41(実施の形態1におけるセンサチップ11に対応)について説明する。
図11(e)は、センサチップ41を構成する基板43の平面図であり、上述した実施の形態1におけるセンサチップ11の基板12と同様の構成である。
本実施の形態3におけるセンサチップ51(実施の形態2におけるセンサチップ41に対応)は、図16に示すように、上述した実施の形態2におけるセンサチップ41と比べて余剰血液貯留部52の構成のみが異なる。すなわち、余剰血液貯留部52の厚み強度を増すため、本実施の形態3では、余剰血液貯留部52内に複数個の凸52bを設けている。これにより、センサチップ51が厚み方向に押圧された場合でも、厚み寸法を略一定に保つことができる。そして、余剰血液貯留部52の厚み方向へ外部から押圧力が加わった場合でも、センサチップ51が押圧力により厚み方向に撓むことはほとんど無いため、余剰血液3aが余剰血液流入口52aから流出することを防止できる。
図18は、本実施の形態4におけるセンサチップ61(実施の形態1におけるセンサチップ11に対応)の平面図である。
図20は、本実施の形態5におけるセンサチップ71(実施の形態4におけるセンサチップ61に対応)の平面図である。
図22は、実施の形態6におけるセンサチップ81(実施の形態1におけるセンサチップ11に対応)の平面図である。
図21(c)は、基板82(実施の形態1における基板12に対応)の平面図である。基板82は、上述の実施の形態1におけるセンサチップ11の検出電極17(図4(c)参照)に対応する部分を、長手方向に2分割して検出電極83(作用極)と余剰血液検知電極85とを形成している。また、上述の実施の形態1におけるセンサチップ11の検出電極18(図4(c)参照)に対応する部分を、長手方向に2分割して検出電極84(対極)と余剰血液検知電極86とを形成している。
本実施の形態のセンサチップ81は、以上のように構成されているので、検出電極83と余剰血液検知電極85、検出電極84、および余剰血液検知電極86の間に電圧を印加して、その間の電気抵抗を測定することにより、余剰血液貯留部25への血液3あるいは余剰血液3aの流入を検知することができる。
図24は、本実施の形態7におけるセンサチップ91(実施の形態1におけるセンサチップ11に対応)の平面図である。
図23(c)は、基板12の平面図である。基板12の上面には、図23(b)に示すスペーサ94(実施の形態1におけるスペーサ13に対応)が貼り付けられる。
図26は、本実施の形態8におけるセンサチップ101(実施の形態1におけるセンサチップ11に対応)の平面図である。
図25(c)は、基板12の平面図である。基板12の上面には、図25(b)に示すスペーサ103(実施の形態1におけるスペーサ13に対応)が貼り付けられる。
図28は、本実施の形態9におけるセンサチップ111(実施の形態1におけるセンサチップ11に対応)の平面図である。
図27(a)~図27(c)は、センサチップ111の分解平面図である。
図30は、実施の形態10におけるセンサチップ141(実施の形態9におけるセンサチップ111に対応)の平面図である。
図29(c)は、基板125の平面図である。
図31は、上記実施の形態9,10で示したセンサチップ111,141を用いて血糖値の測定等を行う血液検査装置151の部品配置図である。
穿刺部153は、上ホルダ153aと下ホルダ153bとを有している。下ホルダ153bは、板ばね153eによって上ホルダ153a側に付勢されている。コネクタ159は、上ホルダ153aと下ホルダ153bとの間に挟まれたセンサチップ111の接続端子117a,118a,119a,120a(図28参照)と接続され、電気回路部157へ信号を伝送する。
図34は、本実施の形態12におけるセンサチップ161(実施の形態1におけるセンサチップ11に対応)の平面図である。
図33(c)は、基板165の平面図である。基板165上には、基板165の長手方向に沿って、検出電極166(対極)、検出電極167(作用極)、検出電極168(検知極)が互いに平行に設けられている。
本実施の形態では、これらの部材(基板165、スペーサ169およびカバー170)を組み合わせることで、センサチップ161が構成される。
図36は、本実施の形態13におけるセンサチップ171(実施の形態12におけるセンサチップ161に対応)の平面図である。
図35(c)は、基板165の平面図である。基板165の上面には、図35(b)に示すスペーサ174(実施の形態12におけるスペーサ169に対応)が貼り付けられる。スペーサ174では、略長方形状の一方の短辺174aの両端部分を除く部分に、余剰血液貯留部172を形成する凹面174bが形成されている。そして、スペーサ174の長辺174cには、供給路163を形成する溝169dが、両側面間を貫通するように設けられている。スペーサ174の上面には、図33(a)に示すカバー175が貼り付けられる。カバー175には、余剰血液貯留部172の奥部に対応する位置に、スリット状の空気孔176が形成されている。
図38は、本実施の形態14におけるセンサチップ181(実施の形態13におけるセンサチップ171に対応)の平面図である。
図40は、本実施の形態15におけるセンサチップ191(実施の形態1におけるセンサチップ11に対応)の平面図である。
図39(c)は、基板195の平面図である。略長方形状の基板195には、長辺方向に沿って、一方の長辺から中央に向かって順に検知電極196(C極)、検知電極197(W極)、検知電極198が互いに平行に敷設されている。検知電極196,197,198は、一方の長辺側から中央までの間に敷設されている。
スペーサ199には、一方の長辺側から中央に向かって、供給路193を形成するスリット199aが設けられている。また、スペーサ199には、他方の長辺から中央までの間に、余剰血液貯留部194を形成する切り込み199bが設けられている。スリット199aと切り込み199bとは、離間した位置に独立して形成されている。
図42は、本実施の形態16におけるセンサチップ201(実施の形態3におけるセンサチップ51に対応)の平面図である。
図41(a)は、上述した実施の形態3における血液測定部55(図15参照)である。血液測定部55は、図14に示す基板43と、基板43の上面に貼り付けられたスペーサ44と、スペーサ44の上面に貼り付けられたカバー45とを有している。
本発明のセンサチップは、血液などの生体試料の成分を分析するセンサチップであって、板体状の基体と、流入口と、供給路と、検出電極と、を備えている。流入口は、この基体の一端に設けられるとともに分析用の生体試料が流入する。供給路は、この流入口に連通し、生体試料が導入される。検出電極は、この供給路に設けられ、分析用の信号を検出する。基体には、分析に使用されなかった余分な生体試料である余剰血液を吸引するとともに、この吸引した余剰血液を貯える余剰血液貯留部を有している。
さらに、本発明の測定器は、筐体と、センサ挿入部と、コネクタと、測定回路部と、表示部と、を備えている。センサ挿入部は、上記センサチップが挿入されるとともに、筐体の一方に設けられる。コネクタは、センサ挿入部に設けられている。測定回路部は、コネクタに接続されている。表示部は、測定回路部の出力に接続されている。コネクタは、センサチップに余剰血液が吸引されたことを検出する余剰血液検出電極用の端子を有している。
(効果)
以上のように本発明によれば、ユーザは、従来のように余剰血液を拭き取るためのティシュや洗浄綿等を持ち歩く必要がなく、しかも測定が終わり余剰血液が吸引されたセンサチップごと廃棄することができる。この結果、余剰血液を容易に処理することができ、作業効率を向上させることができる。
3a 余剰血液
11 センサチップ
12 基板
13 スペーサ
13b 切り込み
14 カバー
15 センサチップの基体
17,18,19 検出電極
20 流入口
21 供給路
23 検出部
25 余剰血液貯留部
Claims (42)
- 生体試料の成分を分析するセンサチップにおいて、
板体状の基体と、
前記基体の一端に設けられるとともに、分析用の前記生体試料が流入する流入口と、
前記流入口に連通し、前記生体試料が導入される供給路と、
前記供給路に設けられ、分析用の信号を検出する検出電極と、
前記基体に設けられており、前記分析に使用されなかった余分な生体試料である余剰血液を吸引して貯える余剰血液貯留部と、
を備えているセンサチップ。 - 前記基体は、前記基体の端部に設けられるとともに前記余剰血液貯留部に連通する余剰血液流入口を有し、
前記余剰血液流入口は、毛細管現象によって前記余剰血液を前記余剰血液貯留部へと吸引する、
請求項1に記載のセンサチップ。 - 前記流入口は、前記基体の一方の端面に設けられるとともに、
前記余剰血液流入口は、前記流入口が設けられた端面とは異なる前記基体の端面に設けられる、
請求項2に記載のセンサチップ。 - 前記余剰血液貯留部は、前記基体の一面または二面以上の面において開口している、
請求項1に記載のセンサチップ。 - 前記余剰血液貯留部の容積は、前記供給路の容積より大きい、
請求項1に記載のセンサチップ。 - 前記余剰血液貯留部の容積は、前記基体の体積の3分の2以下である、
請求項1から5のいずれかに記載のセンサチップ。 - 前記余剰血液流入口は、複数設けられている、
請求項2に記載のセンサチップ。 - 前記余剰血液流入口は、前記基体の長手方向の中心線を基準に対称位置に配置されている、
請求項7に記載のセンサチップ。 - 複数設けられている前記余剰血液流入口は、互いに隣接する位置に配置されている、
請求項7に記載のセンサチップ。 - 前記余剰血液貯留部は、複数設けられている、
請求項1または2に記載のセンサチップ。 - 複数の前記余剰血液貯留部は、前記基体の長手方向の中心線を基準に対称位置に配置されている、
請求項10に記載のセンサチップ。 - 複数の前記余剰血液貯留部の形状は、それぞれ同一形状に形成されている、
請求項10に記載のセンサチップ。 - 複数の前記余剰血液貯留部の形状は、それぞれ異なる形状に形成されている、
請求項10に記載のセンサチップ。 - 前記供給路と前記余剰血液貯留部とは、同一部材で形成されている、
請求項1に記載のセンサチップ。 - 前記基体は、基板とスペーサとカバーとが積層されて形成されている、
請求項14に記載のセンサチップ。 - 前記供給路と前記余剰血液貯留部とは、同一の層に形成されている、
請求項15に記載のセンサチップ。 - 前記供給路と前記余剰血液貯留部とは、前記スペーサによって形成される空間として形成されている、
請求項15に記載のセンサチップ。 - 前記供給路と前記余剰血液貯留部とは、異なる層に形成されている、
請求項1に記載のセンサチップ。 - 前記供給路と前記余剰血液貯留部とは、別部材で形成されている、
請求項18に記載のセンサチップ。 - 前記基体は、基板とスペーサとカバーと余剰血液吸引用スペーサとが積層されて形成されている、
請求項18または19に記載のセンサチップ。 - 前記基体は、基板とスペーサとカバーと余剰血液吸引用スペーサと余剰血液吸引用カバーとが積層されて形成されている、
請求項18または19に記載のセンサチップ。 - 前記余剰血液貯留部内には、複数個の凸が設けられている、
請求項1、15、18および19のいずれか1つに記載のセンサチップ。 - 前記基体は、前記余剰血液貯留部内へ流入した血液を検知する余剰血液検知電極を有している、
請求項1に記載のセンサチップ。 - 前記流入口は、前記基体の第1の辺側に設けられるとともに、
前記余剰血液流入口は、前記流入口側の第2の辺に設けられている、
請求項2に記載のセンサチップ。 - 前記流入口は、前記基体の第1の辺側に設けられ、
前記余剰血液流入口は、前記基体の第2の辺側に設けられるとともに、
前記余剰血液貯留部内には、複数個の凸が形成されている、
請求項2に記載のセンサチップ。 - 前記基体の第1の辺側に、前記余剰血液流入口が設けられているとともに、
前記基体の第2の辺側に、測定用血液の流入口が設けられている、
請求項2に記載のセンサチップ。 - 前記基体の第1の辺全体に、前記余剰血液流入口が設けられているとともに、
前記基体の第2の辺の略中央に前記流入口が設けられている、
請求項2に記載のセンサチップ。 - 前記基体の第1の辺全体に前記余剰血液流入口が設けられているとともに、
前記余剰血液貯留部内には、複数個の凸が形成されており、
前記基体の互いに対向する辺間を貫通する供給路をさらに備えている、
請求項2に記載のセンサチップ。 - 前記基体の第1の辺に前記余剰血液流入口が設けられているとともに、
前記基体の互いに対向する辺間を貫通する供給路をさらに備えている、
請求項2に記載のセンサチップ。 - 前記基体の第1の辺側に前記流入口が設けられているとともに、
前記基体の第2の辺側に前記余剰血液流入口が設けられている、
請求項2に記載のセンサチップ。 - 前記基体は、略長方形状を有しており、
前記流入口は、前記略長方形の第1の短辺に設けられており、
前記余剰血液貯留部は、前記基体の上面あるいは下面に貼り付けられた余剰血液吸引部材である、
請求項1に記載のセンサチップ。 - 前記供給路は、前記流入口側とは反対の位置に設けられ、外気に連通する第1の空気孔を有している、
請求項1に記載のセンサチップ。 - 前記余剰血液貯留部は、余剰血液を吸引するために設けられており、外気に連通する第2の空気孔を有している、
請求項1または32に記載のセンサチップ。 - 前記余剰血液流入口及びその周辺部分は、撥水処理されている、または撥水性部材で形成されている、
請求項2に記載のセンサチップ。 - 前記余剰血液貯留部は、前記基体に設けられ前記分析に使用されなかった余分な生体試料である余剰血液を吸収する吸収部材である、
請求項1に記載のセンサチップ。 - 前記吸収部材は、前記基体の一面に取りつけられた薄膜形状を有している、
請求項35に記載のセンサチップ。 - 前記吸収部材は、不織布で形成されている、
請求項35に記載のセンサチップ。 - 筐体と、
請求項1から37のいずれか1つに記載のセンサチップが挿入され、前記筐体の一方に設けられるセンサ挿入部と、
前記センサ挿入部に設けられたコネクタと、
前記コネクタに接続された測定回路部と、
前記測定回路部の出力に接続されており、前記測定回路部において測定された前記センサチップに導入された生体試料の分析データの測定結果を表示する表示部と、
を備えている測定器。 - 前記センサ挿入部に挿入される前記センサチップは、前記余剰血液貯留部内へ流入した血液を検知する余剰血液検知電極を有し、
前記コネクタに設けられており、前記センサチップに余剰血液が吸引されたことを検出する余剰血液検出電極用の端子を、さらに備えている、
請求項38に記載の測定器。 - 前記余剰血液検出電極用端子は、前記分析用の検出電極と接続する接続端子の一部または全部の端子を兼用している、
請求項39に記載の測定器。 - 筐体と、
請求項1から37のいずれか1つに記載のセンサチップが挿入され、前記筐体の一部に設けられるセンサ挿入部と、
前記センサ挿入部に対向する位置または近傍する位置に設けられており、皮膚を穿刺する穿刺手段と、
前記センサ挿入部に設けられたコネクタと、
前記コネクタに接続され、生体試料の分析を行なう電気回路部と、
前記電気回路部の出力に接続された表示部と、
を備えた血液検査装置。 - 前記センサチップは、前記余剰血液貯留部内へ流入した血液を検知する余剰血液検知電極を有し、
前記センサチップに取り込んだ余剰血液の検出を行なう余剰血液検出回路部を、さらに備えている、
請求項41に記載の血液検査装置。
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JP2011508209A JP5080687B2 (ja) | 2009-04-07 | 2010-03-17 | センサチップとこれを用いる測定器及び血液検査装置 |
US13/258,641 US9176090B2 (en) | 2009-04-07 | 2010-03-17 | Sensor chip, and measurement device and blood test device in which this sensor chip is used |
EP10761332.5A EP2418479B1 (en) | 2009-04-07 | 2010-03-17 | Sensor chip and measuring device and blood test device in which this sensor chip is used |
CN201080014402.7A CN102369431B (zh) | 2009-04-07 | 2010-03-17 | 传感器芯片、使用该传感器芯片的测定器及血液检查装置 |
US13/860,570 US9255902B2 (en) | 2009-04-07 | 2013-04-11 | Sensor chip, and measurement device and blood test device in which this sensor chip is used |
US14/978,158 US9513249B2 (en) | 2009-04-07 | 2015-12-22 | Sensor chip, and measurement device and blood test device in which this sensor chip is used |
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US13/258,641 A-371-Of-International US9176090B2 (en) | 2009-04-07 | 2010-03-17 | Sensor chip, and measurement device and blood test device in which this sensor chip is used |
US13/860,570 Division US9255902B2 (en) | 2009-04-07 | 2013-04-11 | Sensor chip, and measurement device and blood test device in which this sensor chip is used |
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US (3) | US9176090B2 (ja) |
EP (1) | EP2418479B1 (ja) |
JP (2) | JP5080687B2 (ja) |
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WO2019189777A1 (ja) * | 2018-03-30 | 2019-10-03 | 株式会社Provigate | センサチップ、センシング装置、カバー、体液収集デバイス及びセンサ |
JP3234519U (ja) * | 2021-04-07 | 2021-10-14 | 杭州安旭生物科技股▲ふん▼有限公司Assure Tech. (Hangzhou) Co., Ltd. | 採血構造、全血及び指先血検出装置 |
JP2022108166A (ja) * | 2021-01-12 | 2022-07-25 | 大成化工株式会社 | 積層チューブ容器 |
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CN108398470B (zh) * | 2018-04-13 | 2024-01-30 | 广州万孚生物技术股份有限公司 | 血液活化凝血时间测定生物传感器及其制作方法 |
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US20130220838A1 (en) | 2013-08-29 |
JPWO2010116624A1 (ja) | 2012-10-18 |
US20120010486A1 (en) | 2012-01-12 |
EP2418479A4 (en) | 2012-11-07 |
CN102369431A (zh) | 2012-03-07 |
US20160153926A1 (en) | 2016-06-02 |
JP2013033049A (ja) | 2013-02-14 |
US9255902B2 (en) | 2016-02-09 |
JP5216930B2 (ja) | 2013-06-19 |
CN102369431B (zh) | 2014-04-09 |
JP5080687B2 (ja) | 2012-11-21 |
EP2418479B1 (en) | 2013-10-23 |
US9176090B2 (en) | 2015-11-03 |
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US9513249B2 (en) | 2016-12-06 |
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