JP5899641B2 - Biosensor cartridge, measuring apparatus and measuring method - Google Patents

Description

  The present invention relates to a biosensor provided with a cover film, a biosensor cartridge for continuous measurement having the biosensor, a measuring device using the biosensor cartridge, and a test using the biosensor, biosensor cartridge, and measuring device. The present invention relates to a continuous measurement method for objects.

  Biosensors using electrochemical detection means have been put into practical use as a method for quickly and easily measuring the concentration and the like of a specific component in a biological sample such as blood. An example of such a biosensor is a glucose sensor that electrochemically quantifies glucose in blood.

  A glucose sensor includes an electrode system including a working electrode and a counter electrode, an enzyme, and an electron acceptor as a basic configuration. The enzyme selectively oxidizes glucose in the blood to produce gluconic acid, and at the same time reduces the electron acceptor to produce a reduced form. By applying a constant voltage to the reductant with an electrode system, the reductant is oxidized again, and current is generated at that time. Since this current depends on the glucose concentration in the blood, glucose in the blood can be quantified.

  In diabetic patients requiring self-injection of insulin, control of glucose in blood, that is, blood glucose control, such as after a meal before meals, before going to bed or after waking up, and before and after insulin self-injection, is a serious life-related problem. Since the glucose sensor can be downsized, it is generally used for blood glucose self-measurement by such a diabetic patient. However, a diabetic patient using a glucose sensor has a wide range of measuring devices that can be easily measured from children to the elderly. It has been demanded.

  In the conventional glucose sensor, a sensor chip having a sensor part that can be attached to the measuring device is attached to the device for each measurement. Therefore, the sensor chip is intentionally enlarged so that the patient can easily handle it. However, the method of attaching the sensor chip to the apparatus for each measurement is often difficult to handle, particularly for elderly patients. In order to eliminate such complicated handling, for example, Patent Document 1 discloses a measuring device using a biosensor sheet formed by forming a plurality of biosensors in a sheet shape as a cartridge.

  Further, in the conventional glucose sensor, the electrode system deteriorates due to moisture, and the enzyme in the sensor unit is deactivated. In order to prevent the deactivation of the glucose sensor electrode system and the enzyme due to moisture, for example, Patent Document 2 describes a container containing a desiccant for preventing moisture.

JP 2003-83927 A US Pat. No. 5,911,937

  However, in the measuring apparatus described in Patent Document 1, there is a possibility that the sensor unit is deteriorated with time and certain detection cannot be performed among a plurality of sensor units. When such a measurement failure occurs, it is impossible to accurately measure the blood glucose level, which makes it difficult to control blood glucose by the diabetic patient, which may eventually have a serious effect on the life of the diabetic patient. Further, in the container described in Patent Document 2, even if it is provided with a desiccant, moisture enters the container every time it is opened, so that the moisture-proof guarantee is insufficient.

  As a moisture proof guarantee, there has been a demand for a sufficient amount of desiccant to re-dry the moisture taken into the container due to confidentiality until the glucose sensor in the container is used up and repeated opening and closing during use.

  The present invention solves the above-described problems, and provides a biosensor, a biosensor cartridge, and a measuring apparatus that can provide a sufficient moisture-proof guarantee for an electrode system of a biosensor and that can be measured multiple times by preventing oxidation. The purpose is to provide. Another object of the present invention is to provide a method for continuously measuring a test object, particularly glucose in blood, using the biosensor, biosensor cartridge, and measuring apparatus.

  According to an embodiment of the present invention, a plurality of detection units including an electrode system and a wiring unit are disposed on the first base material, and at least the electrode system is sealed in each of the plurality of detection units. A biosensor comprising: a cover film that is adhered to the first base material and peeled off from the first base material at the time of measurement is provided.

  The biosensor according to an embodiment of the present invention can prevent sufficient moisture-proofing and oxidation from being prevented by bonding the first base material and the cover film so as to seal each of the electrode systems. .

  According to an embodiment of the present invention, at the time of measurement, the electrode system is positioned on the first surface of the first substrate, and a part of the wiring portion is spatially different from the first surface. There is provided a biosensor characterized by being located on the surface.

  In the biosensor according to an embodiment of the present invention, at the time of measurement, a part of the wiring part for transmitting an electrical signal from the electrode system to the measuring device is positioned on a surface spatially different from the electrode system, It is possible to prevent poor conduction due to adhered and coagulated blood, and to accurately measure the blood sugar level.

  In the biosensor, the electrode system and the wiring portion may be positioned on the first surface of the first base material before measurement.

  The biosensor according to an embodiment of the present invention is configured so that a part of a wiring part for transmitting an electrical signal from an electrode system to a measurement device is positioned on a surface spatially different from the electrode system at the time of measurement. In this case, the electrode system and the wiring portion may be arranged on the same surface of the first base material, which makes it easy to manufacture the biosensor, and therefore it is possible to maintain high accuracy of the sensor fabrication.

  In the biosensor, an angle formed by the first surface and the second surface may be 0 ° or more and less than 180 °.

  The biosensor according to an embodiment of the present invention has an angle formed between a surface on which an electrode system is disposed and a surface on which a part of a wiring portion for transmitting an electrical signal from the electrode system to a measuring device is disposed. By setting the angle to 0 ° or more and less than 180 °, it is possible to prevent poor conduction due to blood that has adhered and coagulated, and an accurate blood glucose level can be measured.

  According to one embodiment of the present invention, a first base material on which a plurality of detection units each having an electrode system and a wiring unit are arranged, and the first base material is arranged on the first base material, and among the plurality of detection units A second base material having a cut portion that covers at least the electrode system and penetrates in the thickness direction, and is disposed on the second base material so as to seal at least the cut portion of the second base material. And a cover film to be adhered, wherein the cover film is peeled off from the second substrate at the time of measurement.

  The biosensor according to one embodiment of the present invention includes a second base material that covers at least the electrode system of the detection unit and has a cut portion penetrating in the thickness direction, and the second base material so as to seal the cut portion. Adhesion with the cover film can ensure sufficient moisture protection and oxidation of the electrode system. In addition, the biosensor has a cut portion that penetrates the second base material in the thickness direction, so that the cover film is peeled off during measurement, the second base material is opened at the cut portion, and the sample is detected. It can introduce into the electrode system of and can measure. The electrode system can be protected by the second substrate except during measurement. After the measurement, it is possible to prevent the sample introduced into the electrode system from flowing out.

  In the biosensor, a substrate having water absorption may be provided between the second substrate and the cover film.

  The biosensor according to an embodiment of the present invention can be introduced into the electrode system of the detection unit by providing a substrate having water absorption between the second substrate having a cut portion and the cover film. Absorbs an excessive amount of sample, and also absorbs the sample adhering to the surface of the second substrate to prevent contamination by the sample, particularly blood, to the detection unit, biosensor cartridge, and measurement device before measurement. be able to.

  In the biosensor, the second base material is pushed by pressing the first base material and the second base material from a surface opposite to the surface of the first base material on which the electrode system is disposed. A notch that penetrates the substrate may be opened.

  Since the biosensor according to an embodiment of the present invention has a cut portion that penetrates the second base material, the biosensor protrudes in the surface direction in which the electrode system of the first base material is disposed. By making it deform | transform into, the notch which penetrates a 2nd base material can be opened.

  In the biosensor, at least a part of the wiring part is disposed on a side opposite to the first surface, and at least a part of the electrode system and the wiring part communicate with each other in a thickness direction of the first base material. You may electrically connect through a through-hole.

  In the biosensor according to one embodiment of the present invention, at least a part of the wiring part is disposed on the side opposite to the first surface, and at least a part of the electrode system and the wiring part is in the thickness direction of the first substrate. By being electrically connected through the communicating through-hole, the wiring part can be prevented from directly touching the sample, and poor conduction due to blood that has adhered and coagulated can be prevented. It can be carried out.

  In the biosensor, the electrode system may include a working electrode, a counter electrode, and a reference electrode, and may include an enzyme reaction unit including an enzyme and an electron acceptor located on the working electrode.

  In the biosensor according to one embodiment of the present invention, the electrode system includes a working electrode and a counter electrode, and includes an enzyme reaction unit including an enzyme and an electron acceptor located on the working electrode, thereby adjusting the concentration of the detection target. A corresponding electrical signal can be detected.

  According to one embodiment of the present invention, a biosensor cartridge that houses a biosensor, the first rotation unit around which the biosensor having a detection unit before measurement is wound, and the biosensor having the detection unit after measurement And a cover film containing rotating part in which one end of the cover film is attached and the cover film peeled off from the first base material or the second base material is stored at the time of measurement. A biosensor cartridge comprising: a cover film accommodating portion.

  A biosensor cartridge according to an embodiment of the present invention peels a cover film and places a part of a wiring part for transmitting an electrical signal from an electrode system to a measuring device on a surface spatially different from the electrode system. By housing the biosensor to be positioned, poor conduction due to blood that has adhered and coagulated can be prevented, and an accurate blood glucose level can be measured. Moreover, by providing the 1st rotation part by which the biosensor which has a detection part before a measurement was wound in a container, a biosensor can be supplied for every use, and a cover film is sealed to a detection part. By covering, sufficient moisture-proof guarantee of the detection unit can be obtained. In addition, by providing the cartridge with a recovery unit in which a biosensor having a detection unit after measurement is housed, infection to a third party by blood that has adhered and coagulated can be prevented.

  The biosensor cartridge may further include a connection electrode for receiving an electrical signal from the electrode system in contact with a part of the wiring portion.

  A biosensor cartridge according to an embodiment of the present invention further includes a connection electrode for receiving an electric signal from the electrode system in contact with a part of the wiring unit, thereby measuring an electric signal from the electrode system. Can be transmitted to the device. In addition, since the biosensor and the measurement device do not directly contact each other, contamination of the measurement device with blood can be prevented.

  The biosensor cartridge may further include an extruding unit that pushes the detection unit of the biosensor to the outside.

  The biosensor cartridge according to one embodiment of the present invention further includes an extrusion unit that pushes the detection unit of the biosensor to the outside of the container, so that the detection unit of the biosensor is accommodated inside the biosensor cartridge except during measurement. can do. As a result, when the biosensor cartridge or the measuring device is transported or when the biosensor cartridge is attached to the measuring device, the detecting portion of the biosensor is not exposed to the outside, and the detecting portion can be prevented from being deteriorated or damaged. it can.

  In the biosensor cartridge, the push-out portion may include the connection electrode.

  The biosensor cartridge according to an embodiment of the present invention includes a connection electrode in the extrusion portion, whereby a portion of the wiring portion arranged on the surface of the base material opposite to the electrode system and the connection electrode are provided in the extrusion portion. Can be connected with.

  In the biosensor cartridge, a cover film peeling portion that peels the cover film from the first base material may be provided between the first rotating portion and the cover film accommodating portion.

  The biosensor cartridge according to an embodiment of the present invention includes the cover film peeling portion, and can smoothly peel the cover film during measurement.

  Further, according to one embodiment of the present invention, the measurement device is equipped with a biosensor cartridge that houses the biosensor according to any one of the above, and an arithmetic unit that converts an electrical signal from the electrode system into a measurement value And a display unit for displaying the measurement value.

  A measuring apparatus according to an embodiment of the present invention is configured to peel a cover film and position a part of a wiring portion for transmitting an electric signal from an electrode system to a measuring apparatus on a surface spatially different from the electrode system. By mounting the biosensor cartridge that accommodates the biosensor, it is possible to prevent poor conduction due to blood that has adhered and coagulated, and to accurately measure the blood glucose level. In addition, by providing the calculation unit, an electric signal from the electrode system can be converted into a measured value and provided to the measurer.

  The measurement apparatus may further include a driving unit that drives the rotating unit.

  The measurement apparatus according to an embodiment of the present invention can further include a drive unit that drives the rotation unit, thereby moving the detection unit of the biosensor to the measurement position.

  In the measurement apparatus, the drive unit may arrange one detection unit before the biosensor measurement at an external measurement position.

  The measurement device according to an embodiment of the present invention can reliably measure a patient who is a measurer by disposing one detection unit before measurement of the biosensor at a measurement position outside the measurement device. Can be.

  According to an embodiment of the present invention, a plurality of detection units including an electrode system and a wiring unit are disposed on the first base material, and at least the electrode system is sealed in each of the plurality of detection units. A biosensor comprising a cover film adhered to the first base material and peeled off from the first base material at the time of measurement, the cover film is peeled off, and the electrode system is the first base material The biosensor is arranged so that a part of the wiring portion is located on a second surface that is spatially different from the first surface, and the sample is brought into contact with the electrode system. Measuring an object contained in the sample and receiving an electrical signal from the electrode system from a part of the wiring portion located on the second surface side of the first base material. A characteristic measurement method is provided.

  In the measurement method according to an embodiment of the present invention, the cover film is peeled off, and a part of the wiring part for transmitting an electrical signal from the electrode system to the measurement device is positioned on a surface spatially different from the electrode system. By attaching a biosensor cartridge that accommodates the biosensor, it is possible to prevent conduction failure due to blood that has adhered and coagulated, and to accurately measure the blood glucose level.

  According to one embodiment of the present invention, among the first base material on which a plurality of detection parts having an electrode system and a wiring part are arranged, and among the plurality of detection parts arranged on the first base material A second base material having a cut portion that covers at least the electrode system and penetrates in the thickness direction, and is disposed on the second base material so as to seal at least the cut portion of the second base material. By using a biosensor comprising a cover film to be bonded, peeling the cover film, and deforming the biosensor so as to protrude in the surface direction in which the electrode system of the first substrate is disposed There is provided a measuring method characterized in that a notch passing through the second base material is opened and a sample is contacted with the electrode system to measure a test object.

  In the measurement method according to an embodiment of the present invention, the cover film is peeled off, and the second base material is opened at the cut portion by having a cut portion that penetrates the second base material in the thickness direction. A sample can be introduced into the electrode system of the detection unit for measurement. Moreover, the electrode system can be protected by the second base material except during measurement. After the measurement, it is possible to prevent the sample introduced into the electrode system from flowing out.

  In the measurement method, the biosensor is configured such that a part of the wiring portion is a second surface opposite to the first surface on which the electrode system is disposed via the first base material. May be folded and accommodated in the biosensor cartridge.

  A measurement method according to an embodiment of the present invention includes a surface on which an electrode system of a biosensor is disposed and a surface on which a part of a wiring portion for transmitting an electrical signal from the electrode system to a measurement device is disposed. By bending and arranging, it is possible to prevent poor conduction due to blood that has adhered and coagulated, and an accurate blood glucose level can be measured.

  In the measurement method, the biosensor cartridge includes a first rotation unit that is driven by the drive unit, winds a biosensor having a detection unit before measurement, includes a recovery unit, and a detection unit after measurement. A biosensor having the above may be accommodated, and the cover film peeled off at the time of measurement may be accommodated by providing a third rotating part.

  The measurement method according to an embodiment of the present invention includes a recovery unit, and thus can accommodate a biosensor having a detection unit after measurement, can prevent contamination due to adhered and coagulated blood, Occasional peeling of the cover film can provide sufficient moisture protection for the electrode system and prevent oxidation.

  In the measurement method, the biosensor cartridge may further include a second rotation unit in the collection unit, and the biosensor having the detection unit after the measurement may be wound.

  The measurement method according to an embodiment of the present invention further includes a second rotating unit in the recovery unit, so that the biosensor having the detection unit after measurement can be accommodated in a compact manner. Contamination can be prevented.

  In the measurement method, a cover film peeling part for peeling the cover film from the first base material may be provided between the first rotating part and the cover film accommodating part.

  The measurement method according to an embodiment of the present invention includes a cover film peeling portion, so that the cover film can be smoothly peeled off during measurement, and sufficient moisture-proof guarantee can be obtained for the electrode system before measurement and oxidation can be performed. Can be prevented.

  According to the present invention, there are provided a biosensor, a biosensor cartridge, and a measuring apparatus that can provide a sufficient moisture-proof guarantee for the electrode system of the biosensor and prevent oxidation, and can perform multiple measurements. In addition, a method for continuously measuring a test object, particularly glucose in blood using the biosensor, the biosensor cartridge, and the measuring device is provided.

It is a top view which shows the biosensor before the measurement which concerns on one Embodiment of this invention. It is a schematic diagram which shows the biosensor before the measurement which concerns on one Embodiment of this invention, (a) shows the top view with which the detection part of the biosensor before the measurement was covered with the cover film, (b) shows (a ) Is a cross-sectional view taken along line AA ′. It is a schematic diagram which shows the biosensor before the measurement which concerns on one Embodiment of this invention, (a) shows the top view by which the electrode system of the biosensor before the measurement was covered with the cover film, (b) Sectional drawing of line AA 'of a) is shown. It is a schematic diagram showing a connection between a part of the wiring part and a connection electrode according to an embodiment of the present invention, (a) is a view seen from the surface on which a part of the wiring part of the biosensor is arranged, (B) is the figure which looked at the folded biosensor from the side, (c) shows the example of another form of a connection electrode. It is a figure explaining the biosensor which concerns on one Embodiment of this invention. It is the schematic diagram of the biosensor which expanded the electrode system vicinity which concerns on one Embodiment of this invention. It is a schematic diagram which shows the biosensor before the measurement which concerns on one Embodiment of this invention, (a) shows the top view with which the detection part of the biosensor before the measurement was covered with the cover film, (b) shows (a ) Is a cross-sectional view taken along line AA ′. It is a schematic diagram which shows the biosensor which concerns on one Embodiment of this invention, (a) shows the top view by which the detection part of the biosensor before a measurement was covered with the cover film, (b) is the broken line of (a) Sectional drawing of a part is shown. It is a schematic diagram which shows the measuring method using the biosensor which concerns on one Embodiment of this invention, (a) shows the top view of the biosensor before a measurement, (b) shows the top view of the biosensor at the time of a measurement. (C) shows a cross-sectional view at a broken line part in (a), and (d) shows a cross-sectional view at a broken line part in (b). BRIEF DESCRIPTION OF THE DRAWINGS It is a schematic diagram which shows the biosensor which concerns on one Embodiment of this invention, (a) shows the top view by which the base material which has the water absorption of the biosensor before a measurement was covered with the cover film, (b) Sectional drawing of the broken-line part of (a) is shown. It is a schematic diagram which shows the biosensor cartridge which concerns on one Embodiment of this invention. It is a schematic diagram which shows the biosensor cartridge which concerns on one Embodiment of this invention. It is a schematic diagram which shows the biosensor cartridge which concerns on one Embodiment of this invention. It is a mimetic diagram showing a measuring device concerning one embodiment of the present invention.

  Hereinafter, a biosensor, a biosensor cartridge, a measuring apparatus, and a measuring method according to the present invention will be described with reference to the drawings. However, the biosensor, the biosensor cartridge, the measuring apparatus, and the measuring method of the present invention can be implemented in many different modes, and are limited to the description of the following embodiments and examples. It is not a thing. Note that in the drawings referred to in this embodiment mode and examples, the same portions or portions having similar functions are denoted by the same reference numerals, and repetitive description thereof is omitted.

  As described above, the present inventors have intensively studied to simultaneously solve the protection of the electrode system of the biosensor and the problem of supplying the sample to the electrode system. As a result, the electrode system is sealed with a substrate before measurement. The present inventors have found that the electrode sensor system can be prevented from deteriorating the characteristics of the sample measurement substance due to moisture and oxidation by peeling the sealed substrate at the time of measurement. Hereinafter, a glucose sensor will be described as an example of a biosensor. However, the biosensor, the biosensor cartridge, the measurement device, and the measurement method according to the embodiment of the present invention are not limited to this, and other than blood glucose. It is applicable to various samples and objects to be detected.

[Biosensor]
FIG. 1 is a plan view showing a biosensor 100 before measurement according to an embodiment of the present invention. The biosensor 100 includes a plurality of detection units 101 including an electrode system 10 and a wiring unit 20 on the first base material 1, and a cover film 90 is disposed so as to seal the electrode system 10. The detectors 101 are arranged at predetermined intervals in the longitudinal direction of the first base material 1. The cover film 90 seals each of the electrode systems 10 of the plurality of detection units 101 arranged at predetermined intervals by directly bonding the first base material 1 with heat sealing or the like via an adhesive. Adhering and sealing each electrode system 10 of the biosensor 100 with the first base material 1 and the cover film 90 can provide a sufficient moisture-proof guarantee for the electrode system 10 and is formed in the electrode system 10. Prevents oxidation of enzymes and electron acceptors.

  Here, the predetermined interval at which the detection unit 101 is arranged is an interval at which the detection unit at the measurement position is not contaminated by blood adhered and coagulated on the detection unit after measurement in the biosensor cartridge described later. Therefore, it can be arbitrarily set according to the shape of the biosensor cartridge that houses the biosensor.

  The detection unit 101 includes an electrode system 10 and a wiring unit 20. The electrode system 10 includes a working electrode 11, a counter electrode 13, and a reference electrode 15. A wiring 21, a wiring 23, and a wiring 25 are connected to the working electrode 11, the counter electrode 13, and the reference electrode 15, respectively, thereby configuring the wiring unit 20. In FIG. 1, the straight arrow indicates the feeding direction of the biosensor 100 when it is accommodated in the biosensor cartridge. The biosensor 100 collects a sample in the electrode system 10 at the time of measurement. At this time, in order to transmit an electrical signal from the electrode system 10 to the measuring apparatus, the wiring 21, the wiring 23, and the wiring 25 that are electrically connected to the electrode system 10, and the wiring 21, the wiring 23, and the wiring 25 are not shown. And the corresponding connection electrodes are brought into contact with each other. The connection electrode only needs to be disposed in either a biosensor cartridge or a measurement device described later, and as a result, can transmit an electrical signal to the measurement device.

  Another embodiment of the biosensor according to the present invention will be described. FIG. 2 is a schematic diagram showing a biosensor 200 before measurement according to an embodiment of the present invention. 2A is a plan view in which the detection unit 201 of the biosensor 200 before measurement is covered with the cover film 90, and FIG. 2B is a cross-sectional view taken along line AA ′ in FIG. Show. FIG. 3 is a schematic diagram showing a biosensor 200 before measurement according to an embodiment of the present invention. 3A shows a plan view in which the electrode system 10 of the biosensor 200 before measurement is covered with a cover film 90, and FIG. 3B is a cross-sectional view taken along line AA ′ in FIG. Indicates. The biosensor 200 includes a plurality of detection units 201 on the first substrate 1 and arranges a cover film 90 so as to seal each of the plurality of detection units 201. The detectors 201 are arranged at predetermined intervals in the longitudinal direction of the first base material 1. The cover film 90 seals the detection unit 201 or the electrode system 10 arranged at a predetermined interval.

  Here, the predetermined interval at which the detection unit 201 is arranged refers to a measurement position at which the detection unit at the measurement position is not contaminated by blood adhering to and coagulating on the detection unit after measurement in the biosensor cartridge described later. This is an interval at which the detection unit before measurement is not contaminated with blood during measurement using the detection unit. Therefore, it can be arbitrarily set according to the shape of the biosensor cartridge that houses the biosensor.

  The biosensor 200 shown in FIG. 2A is in a state before measurement and is in a state where the detection unit 201 is covered with a cover film 90 so as to be sealed. The cover film 90 has frame-like adhesive layers 91 arranged at predetermined intervals so as to enclose the respective detection units 201 on the first base material 1, and the detection unit 201 is sealed through the adhesive layer 91. cover. The biosensor 200 is used for measurement by being folded back along the broken line in FIG. Fig.2 (a) has shown the top view of the state before folding. 2 (a) and 2 (b), the detection unit 201 of the biosensor 200 is formed so as to be sealed through the adhesive layer 91, but as shown in FIGS. 3 (a) and 3 (b), It may be formed so as to cover only the electrode system 10 of the detection unit 201 with the adhesive layer 91 interposed therebetween. FIG. 3A shows a plan view of the folded biosensor 200. In the biosensor 200 shown in FIG. 3A, at least the electrode system where the enzyme reaction part is arranged is sealed with a cover film 90. By covering the detection unit 201 or the electrode system 10 of the biosensor 200 so as to be sealed with the cover film 90, sufficient moisture-proof guarantee can be obtained and oxidation of the enzyme / electron acceptor formed on the electrode system 10 can be prevented. it can. Note that the adhesive layer 91 is not essential, and the cover film 90 and the first substrate 1 may be directly bonded by heat sealing or the like. Hereinafter, the biosensor 200 when the cover film 90 is peeled from the biosensor 200 will be described.

  The detection unit 201 includes an electrode system 10 and a wiring unit 20. The electrode system 10 includes a working electrode 11, a counter electrode 13, and a reference electrode 15. A wiring 21, a wiring 23, and a wiring 25 are connected to the working electrode 11, the counter electrode 13, and the reference electrode 15, respectively, thereby configuring the wiring unit 20. A part 130 of the wiring part for transmitting an electric signal from the electrode system 10 to the measuring device is disposed on the opposite side to one end of the wiring part 20 connected to the electrode system 10. In the biosensor, the wiring part 20 is bent, and the electrode system 10 and a part 130 of the wiring part are arranged in parallel on both sides of the first base 1 in the short direction.

  2 (a) and 3 (a), the straight arrow indicates the feed direction of the biosensor when it is accommodated in the biosensor cartridge. At the time of measurement, the biosensor is sampled on the electrode system 10 in a state of being folded along a broken line in FIG. 2 (a) parallel to the longitudinal direction of the biosensor, that is, in a folded state shown in FIG. 3 (a). Collect. At this time, a part 130 of the wiring part for transmitting an electric signal from the electrode system 10 to the measuring device is disposed on the back surface of the electrode system 10 via the first base material 1. In measurement using a biosensor, an electrical signal from the electrode system 10 is measured by bringing a connection electrode into contact with a part 130 of the wiring portion arranged on the back surface of the electrode system 10 via the first base material 1. Communicate to the device. By differentiating the surface from which the sample is collected and the surface in contact with the connection electrode, it is possible to prevent the connection electrode from being contaminated by the sample.

  FIG. 4 is a schematic diagram showing a connection between a part 130 of the wiring portion and the connection electrode 520 according to an embodiment of the present invention. 4A is a view of the biosensor 200 as viewed from the side where the wiring part 130 is disposed, and FIG. 4B is a view of the folded biosensor 200 as viewed from the side. FIG. 4C is a diagram showing an example of another form of the connection electrode 520.

  As shown in FIG. 4A and FIG. 4B, the biosensor 200 includes a wiring 21, a wiring 23, and a wiring 25 arranged on the back surface of the electrode system 10 via the first base material 1. By bringing the connection electrode 521, the connection electrode 523, and the connection electrode 525 into contact with each other, an electrical signal from the electrode system 10 can be transmitted to the measurement device. The connection electrode 521, the connection electrode 523, and the connection electrode 525 may be provided in any of the biosensor cartridge or the measurement device described later and, as a result, can transmit an electrical signal to the measurement device. The connection electrode 521, the connection electrode 523, and the connection electrode 525 can be smoothly brought into contact with the wiring 21, the wiring 23, and the wiring 25 by being held using an elastic body.

  Further, as shown in FIG. 4C, the connection electrode 520 may be configured by arranging the connection electrode 521, the connection electrode 523, and the connection electrode 525 on the support in parallel. When the connection electrode 520 having such a configuration is used, the wiring 21, the wiring 23, and the wiring 25 can be smoothly brought into contact without using an elastic body. In addition, the wiring 21, the wiring 23, and the wiring 25 are not necessarily limited to being arranged in parallel. What is necessary is just to arrange | position along the longitudinal direction of the 1st base material 1 so that each may not cross | intersect another wiring.

  In the present embodiment, the arrangement of the part 130 of the wiring part at the time of measurement has been described as the back surface of the electrode system 10, but the arrangement of the part 130 of the wiring part at the time of measurement is not limited to this. The surface of the first base material 1 on which the electrode system 10 is disposed is defined as the first surface, and the surface of the first base material 1 on which the portion 130 of the wiring portion at the time of measurement is disposed is defined as the second surface. Sometimes, as shown in FIG. 5, the angle θ formed by the first surface and the second surface may be 0 ° or more and less than 180 °. That is, at the time of measurement, the electrode system 10 and the part 130 of the wiring portion may be arranged on spatially different surfaces.

  In the present embodiment, the wiring 21, the wiring 23, and the wiring 25 in the region of the part 130 of the wiring part are arranged along the feed direction of the biosensor 100. For this reason, the biosensor 100 has sufficient length of the wiring 21, the wiring 23, and the wiring 25 in the region of the part 130 of the wiring portion with the connection electrode, thereby aligning each wiring and the connection electrode. Control of the feed direction of the biosensor 200 is facilitated, and the accuracy during measurement can be maintained high. Further, by arranging the wiring 21, the wiring 23, and the wiring 25 along the longitudinal direction of the first base 1 (the biosensor feeding direction), the connection electrode 521, the connection electrode 523, and the connection electrode 525 do not interfere with each other. It becomes easy to arrange in the position.

  The first substrate 1 according to the present embodiment is a substrate that supports the electrode system 10, and at least the surface on which the electrode system 10 is disposed has an insulating property. It is preferable to use a member having electrical insulation and elasticity for the first substrate 1, for example, polyethylene terephthalate (PET) resin, vinyl chloride resin, polystyrene (PS) resin, polypropylene (PP) resin, A film such as polycarbonate (PC) can be suitably used. In particular, PET is excellent in material properties and processability, can reduce manufacturing costs, and is suitable for a glucose sensor used by diabetic patients with high measurement frequency.

  The shape, size, and thickness of the first substrate 1 can be appropriately set depending on the shape of the connection electrode of the device that is used by connecting the biosensor of the present invention. The first base material 1 according to the present embodiment preferably has a strip shape with a width of 0.2 mm or more and 15.0 mm or less. More preferably, the width is 2.5 mm or more and 10.0 mm or less. By using the first substrate 1 having a width in this range, it is possible to realize a biosensor cartridge that can collect blood sufficient for measurement and can be mounted on a small and lightweight measuring device. The thickness of the first base material 1 is preferably 0.004 mm or more and 2.5 mm or less, and more preferably 0.006 mm or more and 0.075 mm or less. The first substrate 1 has a thickness in this range, so that it is easy to roll, and a biosensor cartridge that can be mounted on a small measuring device can be realized.

  FIG. 6 is a schematic view of a biosensor in which the vicinity of the electrode system 10 according to an embodiment of the present invention is enlarged. As described above, the electrode system 10 includes the working electrode 11, the counter electrode 13, and the reference electrode 15. Although not shown, the electrode system 10 is covered with a cover film 90 so as to be sealed before measurement. The working electrode 11 is one electrode for applying a voltage to the reductant electron acceptor, and includes an enzyme reaction unit 17 positioned on the working electrode 11. The enzyme reaction unit 17 includes an enzyme and an electron acceptor. The enzyme reaction unit 17 may be a mixture of an enzyme and an electron acceptor, or may be a laminate of an enzyme and an electron acceptor separately. In the present embodiment, the embodiment in which the enzyme reaction unit 17 is directly disposed on the upper surface of the working electrode 11 is described. However, the enzyme reaction unit 17 is disposed so as to face the working electrode 11 through a space. Also good. The counter electrode 13 is one electrode for measuring a current flowing by electrons emitted from the electron acceptor to the working electrode 11. The reference electrode 15 is an electrode that serves as a reference when determining the potential of the working electrode 11.

  For the electrode system 10, a material excellent in conductivity, corrosion resistance, smoothness and wettability is used. For example, carbon, silver (Ag), silver chloride (AgCl), gold (Au), and palladium (Pd) can be used for the electrode system 10, and carbon is particularly excellent in resistance to oxidation and corrosion, and the manufacturing cost is also low. It can be suppressed, and is suitable for a glucose sensor used by a diabetic patient whose measurement frequency is high. The electrode system 10 can be formed by a mixture of a carbon pigment and an organic binder. Examples of the carbon pigment used in the electrode system 10 according to the embodiment of the present invention include graphite, amorphous carbon, diamond-like carbon, carbon fiber, carbon black, acetylene black, ketjen black (registered trademark), carbon nanotube, and carbon nanohorn. Carbon nanofibers can be used. As the organic binder, acrylic resin, ester resin, vinyl chloride resin, vinyl chloride vinyl acetate copolymer resin, or the like can be used.

  The shape, size, and thickness of the electrode system 10 can be appropriately set according to the material and the object to be detected. The electrode system 10 according to the present embodiment preferably has a rectangular shape with a width of 0.05 mm or more and 2.0 mm or less. More preferably, the width is 0.1 mm or more and 0.5 mm or less. By using the 1st base material 1 which has the width | variety of this range, the area accuracy of each electrode in manufacture of a biosensor and sufficient contact space with each electrode and sample in a measurement can be provided. Further, the thickness of the electrode system 10 is preferably 0.0005 mm or more and 2.0 mm or less, and more preferably 0.001 mm or more and 0.1 mm or less. The electrode system 10 having the thickness in this range can provide the concealability and the resistance value required for the biosensor.

  The enzyme reaction unit 17 according to the present embodiment includes an enzyme and an electron acceptor. When measuring the glucose concentration, glucose oxidase (GOD) or glucose dehydrogenase (GDH) can be used as an enzyme. As the electron acceptor, potassium ferricyanide, a ferrocene derivative, a quinone derivative, an osmume derivative, or the like can be used. The enzyme and electron acceptor are used after appropriately diluted with a solvent. Examples of the solvent according to this embodiment include water, alcohol, and a water-alcohol mixed solvent. Further, it may be uniformly dispersed in a linear or cyclic hydrocarbon poor solvent. It is preferable that the enzyme and the electron acceptor are 0.3 unit or more and 10 units or less and 0.5 μg or more and 200 μg or less, respectively, per test specimen. Glucose oxidase and glucose dehydrogenase preferably have high purity, and the species of origin is not particularly limited as long as it has an activity in the above range. For example, glucose oxidase includes GLO-201 manufactured by Toyobo Co., Ltd. Can be used. The enzyme and the electron acceptor of the enzyme reaction unit 17 can obtain a reaction amount according to the amount of enzyme (titer / unit), but may be a small excess of the optimum weight part that ensures the performance of the enzyme reaction unit 17.

  The enzyme reaction part 17 is preferably formed with a smaller area than the working electrode 11. For example, the enzyme reaction part 17 narrows the width in the range of 0.1 mm to 1.0 mm. The thickness of the enzyme reaction part 17 is preferably in the range of 1 μm to 100 μm. Since a detection current proportional to the area of the enzyme reaction unit 17 is obtained, the area of the enzyme reaction unit 17 is preferably set as wide as possible.

  For the wiring part 20 according to the present embodiment, a material having excellent conductivity is used. Examples of the wiring part 20 include carbon, silver (Ag), silver chloride (AgCl), gold (Au), palladium (Pd), copper (Cu), iron (Fe), aluminum (Al), and stainless steel (SUS). In particular, copper, aluminum and stainless steel are preferable from the viewpoint of the reliability of metal wiring.

  The shape, size, and thickness of the wiring part 20 can be appropriately set according to the material and the object to be detected. The wiring part 20 according to the present embodiment preferably has a rectangular shape with a width of 0.05 mm or more and 2.0 mm or less. More preferably, the width is 0.1 mm or more and 0.5 mm or less. By using the wiring part 20 having a width in this range, the area accuracy of each wiring in the manufacture of the biosensor can be provided. Further, the thickness of the electrode system 10 is preferably 0.002 mm or more and 2.0 mm or less, and more preferably 0.005 mm or more and 1.0 mm. The wiring part 20 can provide the workability and reliability required for the biosensor by having a thickness in this range.

  Next, the adhesive layer 91 for bonding the cover film 90 to the first substrate 1 will be described. The adhesive layer 91 of the cover film 90 is made of incompatible high-density polyethylene and polypropylene, and has a sea-island structure in which the higher component ratio of these resins is the sea and the lower component ratio forms an island.

  In the embodiment of the present invention, the adhesive layer 91 can achieve a desired cohesive peel strength by controlling the sea-island structure by controlling the MFR (melt mass flow rate) of the resin, and adheres to the cover film. Thus, a biosensor excellent in moisture proofing and antioxidation can be obtained.

  The cover film 90 covers the plurality of detection units 101 through the adhesive layer 91 so that each of the detection units 101 is hermetically sealed. As the resin name of the cover film 90 used in the embodiment of the present invention, a resin name commonly used in the industry is used. In the embodiment of the present invention, the density was measured in accordance with “JIS K 7112”.

(1) High-density polyethylene constituting the adhesive layer 91 In the present embodiment, polyethylene includes ethylene homopolymer, and ethylene and other α-olefins (for example, propylene, 1-butene, 1-pentene, 1-hexene, 1 A block or random copolymer with -octene and the like).

High-density polyethylene constituting the adhesive layer 91 has a density is at 0.945 g / cm ³ or more 0.965 g / cm ³ or less, more preferably 0.950 g / cm ³ or more 0.955 g / cm ³ or less, A resin having a relatively high melt viscosity having an MFR (190 ° C.) of 1 g / 10 min to 7 g / 10 min, more preferably 1 g / 10 min to 4 g / 10 min is used. As a result, fuzz at the time of peeling of the cover film 90 can be prevented, and poor conduction due to blood at the time of sample measurement after peeling can be prevented. Here, if the density of the high-density polyethylene constituting the adhesive layer 91 is less than 0.945 g / cm ³ , stringing is likely to occur, and it becomes difficult to introduce measurable blood into the electrode system 10. ^{On the other hand} , if it exceeds 0.965 g / cm ³ , an unmelted product may be produced during film formation, and the cover film 90 may not be smoothly peeled off during measurement. And when MFR (190 degreeC) is less than 1 g / 10min, since flowability falls, manufacture becomes difficult, and also the nonuniformity which raise | generates a compatibility defect with the high MFR polypropylene and is visible. This is not preferable because it occurs. On the other hand, if it exceeds 7 g / 10 minutes, the difference from the MFR of polypropylene disappears, so that the degree of mutual dispersion increases and the desired easy-openability cannot be obtained, which is not preferable. Here, MFR (190 ° C.) was measured according to “JIS K6922”. Suitable high density polyethylene used in the present embodiment includes, for example, Hi-Zex 3300F manufactured by Prime Polymer Co., Ltd., Novatec HJ360 and HJ362N manufactured by Nippon Polyethylene Co., Ltd.

(2) Polypropylene constituting the adhesive layer 91 In the present embodiment, the polypropylene includes a propylene homopolymer and a block or random copolymer of propylene and another α-olefin. As the polypropylene that constitutes the adhesive layer 91, a density of not more than 0.9 g / cm ³ or more 0.91 g / cm ^3, and MFR (230 ° C.) is less than 30 g / 10 min 5 g / 10 minutes or more resins use. In order to obtain an appropriate seal strength, an ethylene / propylene random copolymer is particularly preferable. The block copolymer may have a cohesive fracture strength that is too high to obtain good easy-openability. When the MFR (230 ° C.) of the polypropylene constituting the adhesive layer is less than 5 g / 10 minutes, the fluidity becomes close to that of the low MFR high-density polyethylene, so that it becomes a finely dispersed state. I can't get it. Moreover, when MFR (230 degreeC) exceeds 30 g / 10min, since it is highly fluid, it cannot form into a film by an inflation film forming method. Here, MFR (230 ° C.) was measured according to “JIS K6921”. Examples of polypropylene suitable for use in the present embodiment include ethylene / propylene random copolymer (J235T) manufactured by Prime Polypro Co., Ltd., Novatec FL03H manufactured by Nippon Polypro Co., Ltd., and the like.

(3) Blend ratio The blend ratio of the high-density polyethylene and polypropylene in the adhesive layer 91 is preferably 10 to 50 parts by weight of high-density polyethylene and 50 to 90 parts by weight of polypropylene, but the required adhesive strength. Depending on, the blend ratio can be changed. If the ratio of polypropylene is higher than the above range, the adhesive strength becomes too high and good easy-openability cannot be obtained, and if the ratio is low, sufficient adhesive strength cannot be obtained, and the sealing property can prevent moisture and oxidation. I'm not satisfied.

  Regarding the adhesive layer 91, the layer thickness is 20 μm or less, preferably 10 μm or less. When it exceeds 20 μm, the release layer (aggregated release layer) becomes dirty, and the release surface is inferior in beauty.

Next, the cover film 90 that seals the electrode system of the biosensor will be described. The cover film 90 not only contributes to easy-openability in combination with the adhesive layer 91, but also requires strength and function for forming a film as a lid for the biosensor 100. As a resin satisfying such requirements, it is composed of an ethylene / butene copolymer having a density of 0.93 g / cm ³ or more and 0.94 g / cm ³ or less polymerized using a multi-site catalyst, or a density of 0.945 g / cm ^3. A high density polyethylene of 0.965 g / cm ³ or less is used. Further, it is particularly preferable that the flexural modulus is a numerical value according to “JIS K 7171” of 300 MPa or more. The cover film 90 can be laminated by one layer or two or more layers as necessary.

An ethylene / butene copolymer having a density of 0.93 g / cm ³ or more and 0.94 g / cm ³ or less or a density of 0.945 g / cm ³ or more and 0.965 g polymerized using a suitable multisite catalyst used in the present embodiment. High density polyethylene of / cm ³ or less is, for example, an ethylene / butene copolymer (Neozex 3510F) manufactured by Prime Polymer Co., Ltd., a high density polyethylene (HiZex 3300F) manufactured by Prime Polymer Co., Ltd., or manufactured by Nippon Polyethylene Co., Ltd. High density polyethylene (Novatec HJ360), high density polyethylene (Novatech HJ362N) manufactured by Nippon Polyethylene Co., Ltd., and the like.

  Regarding the cover film 90, a layer thickness of 20 μm to 100 μm is preferable from the viewpoint of easy cutting.

  Next, factors in setting physical properties required for the cover film 90 will be described.

(1) Cohesive failure strength The easy-openability or the cohesive failure strength of the cover film 90 is controlled by changing the blending ratio of high-density polyethylene and polypropylene used for the adhesive layer 91.

(2) Gas barrier property In order to suppress the biosensor 100 from moisture and oxidation, a cover film 90 having oxygen and / or water vapor barrier property may be laminated. The cover film 90 according to the embodiment of the present invention is 2.0 cc / m as a numerical value obtained by a technique based on JIS K 7126 regarding oxygen permeability by further laminating an appropriate base material alone or in some cases. Excellent oxygen barrier properties of ² · day · atm or less can be shown, and regarding water vapor permeability, excellent water vapor of 3.0 g / m ² · day or less as a numerical value obtained by a method according to JIS K 7129 Barrier property can be shown.

  The cover film 90 may be directly bonded so that the electrode system 10 on the first substrate 1 is sealed by heat sealing. What is necessary is just to set a seal | sticker adhesion | attachment width suitably considering opening property. Further, the cover film 90 has frame-like adhesive layers 91 arranged at predetermined intervals so as to enclose the respective detection units 101 on the first base material 1 so that the cover film 90 and the adhesive layer 91 are in contact with each other. You may adhere | attach in the state accumulated on. In this case, cohesive peeling of the adhesive layer 91 occurs at the time of peeling.

  The biosensor 100 according to the present embodiment has sufficient moisture-proof guarantee for the electrode system 10 by sealing the electrode system 10 of the biosensor 100 with the first substrate 1 and the cover film 90 by heat sealing before measurement. It can be obtained and oxidation of the enzyme / electron acceptor formed in the electrode system 10 can be prevented.

  On the other hand, the biosensor 200 according to another embodiment is sealed in the electrode system 10 by adhering the detection unit 101 or the electrode system 10 of the biosensor 100 to the cover film 90 via the adhesive layer 90 before the measurement. Sufficient moisture proof can be obtained and oxidation of the enzyme / electron acceptor formed in the electrode system 10 can be prevented. The biosensor 200 removes the cover film 90 from the first substrate 1 during measurement, and a part 130 of the wiring part for transmitting an electric signal from the electrode system 10 to the measuring device is spatially separated from the electrode system. By positioning them on different surfaces, it is possible to prevent poor conduction due to blood that has adhered and coagulated, and an accurate blood glucose level can be measured. At this time, the angle formed between the surface on which the electrode system is disposed and the surface on which a part of the wiring portion for transmitting an electric signal from the electrode system to the measuring device is set to be 0 ° or more and less than 180 °. Thus, poor conduction due to adhered and coagulated blood can be prevented. In addition, the biosensor according to the present embodiment places a part of the wiring part for transmitting an electrical signal from the electrode system to the measurement device on a plane spatially different from the electrode system at the time of measurement. The electrode system and the wiring part may be arranged on the same surface of the first base material, which facilitates the production of the biosensor, and therefore can maintain high accuracy of the sensor fabrication.

  In the biosensor 200 described above, the electrode system 10 and a part 130 of the wiring part are formed on the same plane of the first base material 1, and the biosensor is bent in parallel with the longitudinal direction of the biosensor. The example of the biosensor which measures so that 10 and some 130 of wiring parts may arrange | position on the different surface was demonstrated. Below, the example of the biosensor 300 which arrange | positions an electrode system and a wiring part on the front and back of the 1st base material 1, respectively, and connects through a through-hole is demonstrated.

  FIG. 7 is a schematic diagram showing a biosensor 300 before measurement according to an embodiment of the present invention. FIG. 7A shows a plan view of the biosensor 300 before measurement, and FIG. 7B shows a cross-sectional view taken along line A-A ′ of FIG. In FIG. 7A, a straight arrow indicates the feed direction of the biosensor 300 when it is accommodated in the biosensor cartridge. The biosensor 300 includes a plurality of detection units 301 on the first base material 1, and a cover film 90 is disposed so as to cover the plurality of detection units 301 so as to be sealed. The detectors 301 are arranged at predetermined intervals in the longitudinal direction of the first base material 1. The cover film 90 covers the detection units 301 arranged at predetermined intervals so as to be sealed. 7 shows an example in which the detection unit 301 is sealed with the cover film 90, but only the electrode system may be sealed with the cover film 90. Further, the cover film 90 and the second base material 3 may be directly bonded by heat sealing or the like without using the adhesive layer 91.

  The detection unit 301 has an electrode system and a wiring part, and connects the electrode system and the wiring part through a through hole. The electrode system includes a working electrode 51 and a counter electrode 53, and the counter electrode 53 is disposed so as to surround the working electrode 51. The wiring part includes a wiring 61 and a wiring 63. The working electrode 51 is connected to the wiring 61 through the through hole 71. Further, the counter electrode 53 is connected to the wiring 63 through the through hole 73. Therefore, in the biosensor 300 according to the present embodiment, the electrode system and the wiring portion are disposed on the opposite sides of the first base 1. Further, as described in the biosensors 100 and 200, the biosensor 300 transmits the electrical signal from the electrode system to the measurement device by connecting the connection electrode and the connection electrode to the wiring and the wiring, respectively, at the time of measurement. can do.

  In the biosensor 300, the detection unit 301 shows an example of a detection unit that functions as a reference electrode using the counter electrode 53. The detection unit 301 applies a voltage to the working electrode 51 and the counter electrode 53 using, for example, a pulse or a triangular wave voltage, performs current measurement as a counter electrode, and shifts a predetermined time to apply a voltage using the counter electrode 53 as a reference electrode. A time-resolved measurement method that applies current to measure current can be applied. Such a measurement method can be realized by switching electrodes to which a voltage is applied by a control unit provided in a measurement apparatus described later, and converting the received electrical signal into a measurement value by a calculation unit. In addition to conducting the front and back using a through-hole, the detection unit 301 may be constituted by a working electrode 51 and a counter electrode 53, and two wires connected to each electrode may be provided. The counter electrode 53 may be disposed so as to surround the working electrode 51. Such a two-pole method has a simpler electrode system configuration than a three-pole method that requires a reference electrode.

  In the biosensor 300 according to the present embodiment, the first base material 1, the electrode system, the other configurations of the wiring portion, and the cover film 90 are the same as those of the biosensors 100 and 200, and thus detailed description thereof is omitted. .

  The biosensor 300 according to the present embodiment covers the detection unit 301 so as to be sealed with the cover film 90 via the adhesive layer 91, thereby eliminating the influence of moisture and oxidation and obtaining sufficient moisture-proof guarantee. In addition, oxidation of the enzyme / electron acceptor formed in the electrode system 10 can be prevented. Further, the biosensor 300 peels off the cover film 90 from the first base material 1 at the time of measurement, and a wiring portion for transmitting an electric signal from the electrode system to the measuring device is provided via the first base material 1. Therefore, it is possible to prevent poor conduction due to blood that has adhered and coagulated without being folded, and to accurately measure the blood sugar level.

(Biosensor manufacturing method)
A method for manufacturing the biosensors 100, 200, and 300 described in the above embodiment will be described. A wiring portion is disposed on the upper surface of the first base material 1. For forming the wiring portion, a printing method, a vapor deposition method, etching, plating, cutting, laser processing (laser tracking), or the like can be used. It can select suitably according to the material of a wiring part.

  Thereafter, an electrode system is formed on the upper surface and side surfaces of the wiring portion. The electrode system can be formed by printing, vapor deposition, etching, plating, cutting, laser processing (laser tracking), or the like. It can select suitably according to the material of a wiring part.

  A solution containing an enzyme and an electron acceptor is applied to the upper surface of one working electrode of the electrode thus formed with a dispenser, and then dried at 40 ° C. to remove the solvent component. In this way, an enzyme reaction part is formed. Next, the cover film 90 is heat-sealed with the first base material 1 so as to seal the electrode system, or the electrode system is encapsulated in a frame shape on the first base material 1. The biosensors 100, 200, and 300 can be manufactured by sticking with a predetermined interval and adhering the cover film 90 to the detection units 101, 201, and 301 so as to be sealed.

  Next, another embodiment of the present invention will be described with reference to the drawings. In addition, the same code | symbol is attached | subjected to the same structure as the biosensor 100,200,300 mentioned above, and description is abbreviate | omitted about the same description. FIG. 8 is a schematic diagram showing a biosensor 400 according to an embodiment of the present invention. FIG. 8A shows a plan view in which the detection part of the biosensor 300 before measurement is covered with a cover film, and FIG. 8B shows a cross-sectional view of a broken line part in FIG. In FIG. 8, a straight arrow indicates the feed direction of the biosensor 400 when it is accommodated in the biosensor cartridge. The biosensor 400 includes a plurality of detection units 401 in the first base material 1, and a third base material 5 having a space at the center of the electrode system 10 of each detection unit 401, cut into the third base material 5. A second base material 3 having a portion, an adhesive layer 91 arranged in a frame shape so as to enclose a cut portion on the second base material 3, and an adhesive so as to seal the cut portion of the second base material 3 A cover film 90 adhered to the layer 91 is provided. The detectors 401 are arranged at predetermined intervals in the longitudinal direction of the first base material 1. Further, the cover film 90 and the second base material 3 may be directly bonded by heat sealing or the like without using the adhesive layer 91.

  The detection unit 401 includes the electrode system 10 and the wiring unit 20, and electrically connects the electrode system 10 and the wiring unit 20 through the through hole 30. The electrode system 10 includes a working electrode 11, a counter electrode 13, and a reference electrode 15. The wiring unit 20 includes a wiring 21, a wiring 23, and a wiring 25. The working electrode 11 is connected to the wiring 21 through the through hole 31. The counter electrode 13 is connected to the wiring 23 through the through hole 33. The reference electrode 15 is connected to the wiring 25 through the through hole 35. Therefore, in the biosensor 400 according to the present embodiment, the electrode system 10 and the wiring unit 20 are arranged on the opposite sides of the first base 1. In addition, the biosensor 300 can transmit an electrical signal from the electrode system 10 to the measuring device by connecting the wiring 21, the wiring 23, and the wiring 25 to the connection electrode, respectively, at the time of measurement.

  In the biosensor 400, the detection unit 401 is provided with a predetermined space 40 and is covered with the second base material 3, and the cover film 90 is disposed on the second base material 3 via the adhesive layer 91. . The second base material 3 has a cut portion 110 penetrating the second base material 3 at a position where the electrode system 10 is disposed, and a frame-like shape is formed on the cut portion 110 of the second base material 3. The adhesive layer 91 is disposed with a predetermined interval, and the cover film 90 is further disposed on the adhesive layer 91. In addition, although the cover film 90 arrange | positioned on the 2nd base material 3 was adhere | attached via the contact bonding layer 91, you may adhere | attach on the 2nd base material 3 directly, without using an contact bonding layer. In this case, the second substrate 3 and the cover film 90 are bonded by heat sealing. The cut portion 110 penetrates the second base material 3 in the thickness direction. The incision part 110 is arranged on the second base material 3 so as to face the position where the electrode system 10 of the first base material 1 is arranged, and the second base material 3 according to the arrangement of the detection unit 401. Are arranged at predetermined intervals in the longitudinal direction. The biosensor 400 can measure the test object contained in the sample by opening the notch 110 and introducing the measurement sample into the electrode system 10.

  A cover film 90 is disposed on the second substrate 3. The cover film 90 may be adhered to the second base material 3 so as to seal the cut portion 110 of the second base material 3, or the adhesive layer 91 is pasted in a frame shape with a predetermined interval. The cover film 90 may be adhered on the adhesive layer 91. The biosensor 400 can measure the specimen contained in the sample by peeling the cover film 90 during measurement and introducing the measurement sample into the electrode system 10.

  FIG. 9 is a schematic diagram illustrating a measurement method using the biosensor 400. FIG. 9A shows a plan view of the biosensor 400 before measurement, and FIG. 9C shows a cross-sectional view taken along a broken line in FIG. 9A. FIG. 9B is a plan view of the biosensor 400 at the time of measurement, and FIG. 9D is a cross-sectional view taken along a broken line in FIG. 9B.

  In the biosensor 400 before the measurement, the cut portion 110 is in a closed state, and by disposing the cover film 90 on the second substrate 3, the influence on the detection unit 401 due to moisture and oxidation is prevented, Sufficient moisture proof can be obtained and oxidation of the enzyme / electron acceptor formed in the electrode system 10 can be prevented. On the other hand, as shown in FIGS. 9 (a) and 9 (c), at the time of measurement, a cover film peeling portion to be described later peels the cover film 90 from the second substrate 3, and the biosensor 400 The biosensor 400 is deformed so as to protrude in the surface direction in which the electrode system 10 of the first substrate 1 is disposed. For example, from the surface opposite to the surface on which the electrode system 10 of the first substrate 1 is disposed, to the surface on which the electrode system 10 of the first substrate 1 is disposed together with the second substrate 3. It is pushed and curved in the orthogonal direction. Thus, by pushing and curving the biosensor 400, the second base material 3 is pulled by a tension in a direction substantially opposite to the direction in which the biosensor 400 is pressed, and the notch 110 penetrating the second base material 3 is opened. At the same time, the electrode system 10 is slightly pushed out and can sufficiently come into contact with the sample. In this way, the sample can be introduced into the electrode system 10 by opening the cut portion 110. Such an operation of pushing the biosensor 400 can be realized by disposing the pushing portion 530 in the biosensor cartridge that houses the biosensor 400, as will be described later.

  In addition, after the sample is introduced into the electrode system 10, by stopping pressing the biosensor 400, the cut portion 110 is brought into the original closed state. At this time, since the predetermined space 40 is arranged in the detection unit 401 covered with the second base material 3, the introduced sample is held in the space 40 while being in contact with the electrode system 10. Can be prevented from flowing out to the outside.

  8 and 9, the cut portion 110 of the biosensor 400 according to the present embodiment has been described as a cross-shaped cut, but the shape of the cut portion 110 is not limited to this. In order to increase the contact efficiency between the sample and the electrode system 10 by opening the notch part more widely, for example, although not shown, the notch part provided with a circular notch in the center part of the notch of the second base material 3 A notch having a rectangular notch at the center of the notch can be provided. By providing a small opening in advance in the center of the notch disposed on the second base material 3, the notch is pulled more greatly at the time of measurement, and the opening can be made larger.

  The third base material 5 according to the present embodiment is a base material in which the space 40 is disposed in the vicinity of the electrode system 10, and at least the surface on which the electrode system 10 is disposed has electrical insulating properties and can be bent. The member which has is used. As the 3rd base material 5, films, such as polyethylene terephthalate (PET) resin, vinyl chloride resin, polystyrene (PS) resin, polypropylene (PP) resin, polycarbonate (PC), can be used conveniently, for example. In particular, PET is excellent in material properties and processability, can reduce manufacturing costs, and is suitable for a glucose sensor used by diabetic patients with high measurement frequency.

  The shape, size, and thickness of the third base material 5 can be appropriately set depending on the shape of the connection electrode of the device that is used by connecting the biosensor of the present invention. The third base material 5 according to the present embodiment preferably has a strip shape with a width of 0.2 mm to 2.5 mm. More preferably, the width is 0.5 mm or more and 1.5 mm or less. By using the third substrate 5 having a width in this range, it is possible to realize a biosensor cartridge that can collect blood sufficient for measurement and that can be mounted on a small and lightweight measuring device. Further, the thickness of the third base material 5 is preferably 0.004 mm or more and 2.5 mm or less, and more preferably 0.006 mm or more and 0.075 mm or less. When the third substrate 5 has a thickness in this range, it becomes easier to roll, and a biosensor cartridge that can be mounted on a small measuring device can be realized. In the biosensor 300, the end portions of the second base material 3 and the third base material 5 are bonded to the first base material 1 via an adhesive layer (not shown). In addition, when the 1st base material 1 and the 2nd base material 3 are adhere | attached by the contact bonding layer (not shown) and the space 40 is formed by the contact bonding layer, the 3rd base material 5 is abbreviate | omitted. Also good.

  As described above, the biosensor 400 according to the embodiment of the present invention has a cut portion that penetrates the second base material 3 in the thickness direction at the position where the electrode system 10 is disposed, and the cut portion is By disposing the cover film 90 on the second substrate 3 having, the electrode system 10 can be protected from moisture, oxidation, etc., and sufficient moisture-proof guarantee can be obtained and the electrode system 10 is formed. Prevents oxidation of enzymes and electron acceptors. At the time of measurement, the first base material 1 and the second base material are peeled from the surface opposite to the surface of the first base material 1 on which the electrode system 10 is disposed, that is, the back surface, by peeling the cover film 90. By pressing 3, the sample can be introduced into the electrode system 10 of the detection unit 301 and measured by opening the second base 3 at the cut portion. Further, after the measurement, it is possible to prevent the sample introduced into the electrode system 10 by the second base material 3 from flowing out.

  Furthermore, although not illustrated, the biosensor 400 according to the embodiment of the present invention disposes the cut portion 110 in the second base material 3 at a position shifted from the position where the electrode system 10 of the first base material 1 is disposed. be able to. By shifting the position of the cut portion 110 in the second base material 3 from the position where the electrode system 10 of the first base material 1 is disposed, the force pushing from the back surface of the first base material 1 Since the electrode system 10 is not directly applied, it is possible to prevent the electrode system 10 from being damaged at the time of measurement, and to reduce measurement errors due to distortion of the electrode system 10.

  In the biosensor 200 described above, an example in which the mountain is folded via a broken line is shown, but the electrode system 10 and the wiring part 20 may be electrically connected to the same surface of the first base 1 and arranged. Good.

(Biosensor with water-absorbing substrate)
In the conventional biosensor, in order to facilitate the introduction of the sample into the electrode system inside the sensor, for example, the outer surface near the introduction portion of the sample has been subjected to water repellent treatment. However, when such a water-repellent treatment is applied to the biosensor according to the present invention having the belt-like shape as described above, an excessive amount of sample that could not be introduced into the space 40 from the cut portion 110 becomes spherical. , It remains on the surface of the second substrate 3. The sample remaining in this way may cause contamination of the measurement device, contamination of the detection unit before measurement, or poor conduction. In particular, when the sample is blood, it may cause serious problems such as spread of infection to third parties.

  It is conceivable to provide a water-absorbing pad inside the biosensor cartridge that houses the biosensor so that the electrode system after measurement or a sample adhering to the vicinity of the electrode system is absorbed by contact. In order to provide a water-absorbing pad in a biosensor cartridge capable of measuring a plurality of times, it is necessary to dispose a large member in order to ensure sufficient water absorption, which hinders downsizing of the measuring device.

  Such a problem can be solved by the biosensor 400 according to an embodiment of the present invention described below. FIG. 10 is a schematic diagram of a biosensor 400 according to an embodiment of the present invention. FIG. 10A shows a plan view in which a substrate having water absorption of the biosensor 400 before measurement is covered with a cover film 90, and FIG. 10B shows a cross-sectional view of a broken line part in FIG. . The biosensor 400 shown in FIG. 10 includes a base material 7 (hereinafter referred to as a water-absorbing base material) having water absorption between the second base material 3 and the cover film 90, and the cover film 90 and the absorbent group. Except for the fact that the material 7 is directly bonded by heat sealing, it has the same configuration as the biosensor shown in FIG. 10 shows an example in which the cover film 90 and the absorbent base material 7 are directly bonded by heat sealing or the like, but frame-like adhesive layers 91 are arranged on the absorbent base material 7 at predetermined intervals. The absorbent base material 7 may be sealed via the adhesive layer 91.

  The biosensor 400 has a cut portion 110 penetrating the second base material 3 at a position where the electrode system 10 is disposed, and an opening portion 75 at a position of the water absorbent base material 7 corresponding to the cut portion 110. The opening 75 of the conductive base material 7 is covered so that the cover film 90 is sealed. For the water-absorbing substrate 7, it is preferable to use a member having good hygroscopicity, such as non-woven fabrics such as spunbond and melt blown, and films or papers containing or coated with a polymer absorbent on various substrates. it can. Nonwoven fabrics are suitable when the sample is blood because the amount of absorption is stable. Moreover, according to the property of a sample, you may use the member which has antimicrobial property for the water absorbing base material 7, or the process which provides antimicrobial property.

  The shape, size, and thickness of the water-absorbing substrate 7 can be appropriately set in consideration of the properties of the sample and the amount that may contact the biosensor. As shown in FIG. 10, it is preferable that the water absorbent base material 7 according to the present embodiment is provided with an opening 75 that is spaced 0.1 mm or more from the notch 110 and the width of the water absorbent base material 7 is the second. The same or narrow width as that of the base material 3 is preferable. By using the water-absorbing substrate 7 having a width in this range, it is possible to realize a biosensor cartridge that can sufficiently absorb an excessive amount of sample and can be mounted on a small and lightweight measuring device. The thickness of the water-absorbing substrate 7 is preferably 0.005 mm to 1.0 mm, and more preferably 0.01 mm to 0.2 mm. Since the water-absorbing substrate 7 has a thickness in this range, it becomes easy to roll, and a biosensor cartridge that can sufficiently absorb an excessive amount of sample and can be mounted on a small measuring device is realized. be able to. Since other configurations are the same as those of the biosensor 100 and the biosensor 200, detailed description thereof is omitted.

  By using the biosensor 400 according to the present embodiment, it is possible to obtain sufficient moisture-proof guarantee against moisture, oxidation, etc. for the electrode system of the biosensor before measurement, and the enzyme / electron acceptor formed in the electrode system 10 Oxidation can be prevented. In addition, an excessive amount of sample that cannot be introduced into the space 40 from the notch 110 during measurement can be absorbed, and contamination of the measurement device, contamination of the detection unit before measurement, and poor conduction can be prevented. Even when the sample is blood, the spread of infectious diseases to third parties can be prevented.

(Biosensor manufacturing method)
As an example of a biosensor manufacturing method, the biosensor 400 manufacturing method described in the above embodiment will be described. A member such as a metal foil is disposed on the upper surface of the first substrate 1, and the wiring portion 20 is disposed. For forming the wiring portion 20, a printing method, a vapor deposition method, etching, plating, cutting, laser processing (laser tracking), or the like can be used. It can be appropriately selected according to the material of the wiring part 20.

  Thereafter, the electrode system 10 is formed on the upper surface and side surfaces of the wiring part 20. The electrode system 10 can be formed by printing, vapor deposition, etching, plating, cutting, laser processing (laser tracking), or the like. It can be appropriately selected according to the material of the wiring part 20.

  A solution containing an enzyme and an electron acceptor is applied to the upper surface of one working electrode 11 of the electrode thus formed with a dispenser, and then dried at 40 ° C. to remove the solvent component. Thus, an enzyme reaction part is formed and the detection part 401 is manufactured.

  The cut part 110 can be formed by cutting the second base material 3 into a roll cut, a die cut, a slit process or the like. The size of the notch 110 is such that the sample can be introduced into the predetermined space 40 held by bringing the sample into contact with the electrode system 10 formed between the first base material 1 and the second base material 3. The size can be set arbitrarily.

  Further, the third base material 5 is formed, and the electrode system 10 formed on the first base material 1 is pasted to manufacture the biosensor 400. An adhesive layer is formed on the surface on which the third base material 5, the first base material 1 and the electrode system 10 are attached, and on the surface on which the second base material 3 is attached. The space 40 is formed by punching the third base material 5 having adhesive layers formed on both the upper surface and the lower surface.

  The second substrate 3 is bonded to one surface of the third substrate 5. Then, it arrange | positions so that the 3rd base material 5 and the electrode system 10 may oppose the other surface of the 3rd base material 5, and the 1st base material 1 is bonded. Thus, the both ends of the 1st base material 1 and the 3rd base material 5 are stuck with an adhesion layer. In addition, after the 3rd base material 5 and the 1st base material 1 are bonded, the 2nd base material 3 may be bonded to the 3rd base material 5 as the order of bonding. Next, the cover film 90 is heat-sealed on the second substrate 3. The biosensor 400 can be manufactured through the above steps. Note that a frame-like adhesive layer 91 may be affixed on the cut portion 110 of the second base material 3 at a predetermined interval, and the cover film 90 may be formed thereon.

  Moreover, after bonding the 2nd base material 3 and the water absorbing base material 7 through an contact bonding layer, the cut | notch part 110 is formed. Next, a biosensor may be manufactured by sticking a frame-like adhesive layer 91 on the absorbent base material 7 at a predetermined interval and adhering a cover film 90 thereon.

[Biosensor cartridge]
A biosensor cartridge 500 according to an embodiment of the present invention that houses the above-described biosensor will be described. FIG. 11 is a schematic diagram showing a biosensor cartridge 500 according to an embodiment of the present invention. The biosensor cartridge 500 includes a collection unit 540, a first rotation unit 551, and a third rotation unit (also referred to as a cover film containing rotation unit) 555 that is a cover film collection unit inside the container 510. 540 includes a second rotating unit 553. The first rotating unit 551 winds and stores the biosensor 100. One end of the biosensor 100 is fixed to the second rotating unit 553 arranged in the collection unit 540, and the measured detection unit 101 is wound around the collection unit 540 and collected. One end of the cover film 90 of the biosensor 100 is fixed to the third rotating unit 555 that is a cover film collecting unit, and the cover film 90 is peeled off during measurement and wound around the cover film collecting unit to be collected.

  The biosensor cartridge 500 is configured such that the biosensor 100 in which the detection unit 101 before measurement is covered with the cover film 90 is passed through the support column 557 and further through the first cover film peeling portion 671 that peels the cover film 90. The biosensor 100 can be compactly accommodated in the biosensor cartridge 500 by being wound around and stored in the rotation unit 555, and the detection unit when foreign matter adheres to the detection unit 101 and the biosensor is stored. And scratches on the detection part of the biosensor during measurement can be prevented. In addition, the biosensor cartridge 500 can ensure the moisture resistance of the biosensor 100 before measurement and can prevent oxidation of the enzyme / electron acceptor formed in the electrode system 10. Furthermore, by including the recovery unit 540, the biosensor 100 having the detection unit 101 after measurement can be accommodated, thereby preventing contamination due to adhered and coagulated blood. By further including the second rotation unit 553 in the recovery unit 540, the biosensor 100 including the detection unit 101 after measurement can be accommodated in a compact manner.

  FIG. 12 is a schematic diagram showing a biosensor cartridge 500 according to an embodiment of the present invention. As shown in FIG. 12, the biosensor cartridge 500 is different from the biosensor cartridge 500 shown in FIG. 11 in that the shape of the second cover film peeling portion 675 is substantially triangular and there is no connection electrode 520. Yes.

  Further, the biosensor cartridge 500 may include an extruding unit 530 that pushes the detection unit 101 of the biosensor 100 to the outside of the container 510 at the time of measurement. The arrows in the figure indicate the directions in which the first to third rotating parts rotate, and indicate the feed direction of the biosensor 100. For example, the extruding unit 530 can be moved back and forth in the direction of the opening of the biosensor cartridge 500 by rotating the elliptical rotating unit 535. Moreover, the extrusion part 530 may be a slide type, and is not limited to these. The biosensor cartridge 500 pushes the detection unit 101 of the biosensor 100 to the outside by the push-out unit 530, and enables sampling and detection of the detection object. By rotating the first rotation unit 551 described above, the detection unit 101 can be moved to a measurement position located at the tip of the pushing unit 530. Here, the biosensor cartridge 500 shown in FIG. 11 is a connection in which the cover form 90 is peeled off by the first cover film peeling portion 671 and arranged in front of the first cover film peeling portion 671, that is, in the direction of the extrusion portion 530. The feed direction of the biosensor 100 is further guided by the electrode 520.

  Although not shown, an opening / closing mechanism can be provided in the opening of the biosensor cartridge 500. The opening / closing mechanism may be a door-shaped mechanism that opens the biosensor cartridge 500 in the pushing direction of the pushing portion 530, or may be a slide shutter. Note that the pushing portion 530 may be fixed, and a cap with high hermeticity may be used to close the opening of the biosensor cartridge 500 except during measurement.

  The biosensor cartridge 500 further includes an extruding unit 530 that pushes the detection unit 101 of the biosensor 100 to the outside, so that the detection unit 101 of the biosensor 100 can be accommodated inside the biosensor cartridge 500 except during measurement. it can. Thereby, when the biosensor cartridge 500 or the measuring device is transported or when the biosensor cartridge 500 is mounted on the measuring device, the detecting unit 101 of the biosensor 100 is not exposed to the outside, and the detecting unit 101 is deteriorated or damaged. Can be prevented.

  As shown in FIG. 11, the biosensor cartridge 500 includes a connection electrode 520 that is in contact with a part of the wiring unit 20 of the detection unit 101 of the biosensor 100 and receives an electrical signal from the electrode system 10. In the drawing, the connection electrode 520 is disposed before the push-out portion 530 with respect to the feed direction of the biosensor 100. Further, instead of the connection electrode 520, the connection electrode 529 can be disposed behind the pushing portion 530 with respect to the position of the connection electrode 529, that is, the feeding direction of the biosensor 100. As shown in FIG. 2 and FIG. 3, when a part 130 of the wiring part is disposed on the back surface of the electrode system 10 via the first base material 1 at the time of measurement, the biosensor cartridge 500 is an extruded part. The connection electrode 520 may be provided in the 530. When the connection part 520 is provided in the pushing part 530, the connection electrode 520 is disposed in the vicinity of the tip part of the pushing part 530 that contacts the part 130 of the wiring part of the detection part 101. When the angle formed between the surface on which the electrode system 10 is disposed and the surface on which the part 130 of the wiring portion is disposed is greater than 0 ° and smaller than 90 °, the connection electrode 520 and the connection electrode 529 are bio- A shape corresponding to the angle of the sensor 100 may be used. In the biosensor cartridge 500 described above, an example in which the wiring portion is bent and a part of the wiring portion and the connection electrode are electrically connected has been described. However, the electrode system and the wiring portion are formed on the same surface, You may electrically connect a wiring part and a connection electrode. In this case, the connection electrode may be arranged so that an electrical signal from the electrode system can be received from the wiring portion.

  The biosensor cartridge 500 further includes a connection electrode for receiving an electric signal from the electrode system in contact with a part of the wiring portion, so that the electric signal from the electrode system can be transmitted to the measuring device. . In addition, since the biosensor cartridge 500 includes the connection electrode, the biosensor and the measurement device are not in direct contact with each other, so that contamination of the measurement device with blood can be prevented.

  As shown in FIG. 2, the biosensor cartridge 500 according to the present embodiment includes a wiring unit for transmitting an electrical signal from the electrode system 10 to the measuring device via the first base 1. The part 130 may be folded in a state of being arranged on the back surface of the electrode system 10 and wound around the first rotating unit 551 for storage. Further, the biosensor 200 may be wound and stored around the first rotating unit 551 without being bent. In this case, the biosensor 200 may be bent at the time of measurement so that the electrode system 10 and the part 130 of the wiring part are respectively arranged on two spatially different surfaces.

  Although not shown, the biosensor cartridge may include a mechanism that bends the biosensor 200 during measurement. In this case, in the biosensor cartridge, the biosensor 200 is arranged such that a part 130 of the wiring part is disposed on the back surface of the electrode system 10 while passing between the support pillars that are the two fulcrums of the bent part. It can be bent. Moreover, the bending mechanism may have a guide. The guide has a structure in which the outlet is narrower than the inlet with respect to the feed direction of the biosensor 200. The biosensor 200 is bent together with the feed by passing through the guide. By using this guide part, the biosensor 200 can be folded back reliably. When the biosensor cartridge according to the present embodiment includes the bent portion, the biosensor 200 can be wound and stored around the first rotating portion 551 without being bent. Compared to the above, it is possible to reduce the bulk in the thickness direction when it is wound and stored in a roll shape, and more biosensors 200 can be accommodated, or the biosensors 200 can be accommodated in a smaller space.

  In the above-described embodiment, the biosensor cartridge including the second rotation unit 553 in the recovery unit has been described. However, the biosensor cartridge according to the present invention is limited to the biosensor cartridge including the second rotation unit 553 in the recovery unit. Not. Although not shown, the biosensor cartridge may include a support column instead of the second rotating unit. In the biosensor cartridge, one end of the biosensor 100 is fixed to a support column disposed in the collection unit, and one end of the cover film 90 of the biosensor 100 is connected to the third rotating unit 555 via the cover film peeling unit. Stick. The biosensor cartridge causes the cover film 90 to be peeled off at the time of measurement by rotating the first rotation unit 551 in the biosensor feed direction, and the detection unit 101 of the biosensor is positioned at the measurement position located at the tip of the extrusion unit 530. Can be moved. By peeling the cover film of the biosensor at the time of measurement, it is possible to ensure the moisture proof of the biosensor 100 before the measurement and to prevent oxidation of the enzyme / electron acceptor formed on the electrode system 10. Furthermore, by sealing a part of the biosensor with a cover film, foreign matter adhesion to the detection unit 101, scratching of the detection unit when the biosensor is stored, and scratching of the detection unit of the biosensor during measurement are prevented. Can do. In addition, by accommodating the biosensor 100 having the detection unit 101 after measurement in the recovery unit 740, contamination due to adhered and coagulated blood can be prevented. The biosensor cartridge is provided with a support column with one end of the biosensor fixed to the collection unit, and accommodates the biosensor having the measured detection unit 101 in the collection unit without separately arranging the second rotation unit. Therefore, it is possible to reduce the size and weight.

  FIG. 13 is a schematic diagram showing a biosensor cartridge 800 according to an embodiment of the present invention. The biosensor cartridge 800 includes a collection unit 740, a first rotation unit 751, and a third rotation unit 755 as a cover film collection unit inside the container 710, and the collection unit 740 includes a second rotation unit 753. Prepare. Each of the first rotating unit 751, the second rotating unit 753, and the third rotating unit 755 rotates in the direction of the arrow in the drawing, and the end of the second rotating unit 753 is manually rotated to The first rotating unit 751 and the third rotating unit 755 rotate in conjunction with each other. The first rotating unit 751 winds and stores the biosensor 100. One end of the biosensor 100 is fixed to the second rotating unit 753 arranged in the collecting unit 740, and the measured detecting unit 101 is wound around the collecting unit 740 and collected. One end of the cover film 90 of the biosensor 100 is fixed to a third rotating unit 755 that is a cover film collecting unit via a cover film peeling unit 765, and the cover film 90 is peeled off during measurement and wound around the cover film collecting unit. Take and collect.

  The biosensor cartridge 800 may include an extruding unit 730 that pushes the detection unit of the biosensor to the outside of the container 710 during measurement. The arrows in the figure indicate the directions in which the first to third rotating parts rotate, and indicate the feed direction of the biosensor. The biosensor cartridge 800 pushes out the detection unit of the biosensor to the outside by the push-out unit 730, and enables collection of a sample and detection of an object to be detected. By rotating the second rotating unit 753 described above, the detecting unit can be moved to the measurement position located at the tip of the pushing unit 730. Note that the pushing portion 730 may be fixed, and a highly airtight cap may be used to close the opening of the biosensor cartridge 800 except during measurement.

  As shown in FIG. 13, the biosensor cartridge 800 includes a connection electrode 729 for receiving an electrical signal from the electrode system in contact with a part of the wiring part of the detection unit of the biosensor. In the drawing, the connection electrode 729 is disposed behind the push-out portion 730 with respect to the feed direction of the biosensor. When a part of the wiring part is disposed on the back surface of the electrode system via the first base material at the time of measurement, the biosensor cartridge 800 may include a connection electrode in the pushing part 730. In the case where the push-out unit 730 is provided with a connection electrode, the connection electrode is disposed near the tip of the push-out unit 730 that comes into contact with a part of the wiring part of the detection unit. Note that when the angle formed by the surface on which the electrode system is disposed and the surface on which a part of the wiring portion is disposed is greater than 0 ° and smaller than 90 °, the connection electrode 729 corresponds to the angle of the biosensor. The shape may be used.

  In the biosensor cartridge 800, before the measurement, the biosensor 100 in which the electrode system 10 is sealed with the cover film 90 is transferred from the first rotating unit 751 to the second rotating unit 553 via the first cover film peeling unit 765. Wrap around. During measurement, the biosensor 100 can be accommodated in a compact manner inside the biosensor cartridge 800 by being wound and stored by the first cover film peeling portion 765 that peels the cover film 90. The effect of oxidation can be prevented. Further, by providing the recovery unit 740, the biosensor 100 having the detection unit 101 after the measurement can be accommodated, and contamination due to adhered and coagulated blood can be prevented. By further including the second rotating unit 753 in the recovery unit 740, the biosensor 100 having the detection unit 101 after measurement can be accommodated in a compact manner.

(measuring device)
Hereinafter, a measuring apparatus according to an embodiment of the present invention equipped with the above-described biosensor cartridge will be described. FIG. 14 is a schematic diagram showing a measuring apparatus 1000 according to an embodiment of the present invention. In FIG. 14, a measuring apparatus 1000 equipped with a biosensor cartridge 500 will be described as an example. Although not shown, measurement apparatus 1000 includes a connection electrode and a calculation unit for receiving an electrical signal generated in electrode system 10 from biosensor cartridge 500. The measuring apparatus 1000 includes a display unit 1100 and a power source.

  In the measuring apparatus 1000, the connection electrode may receive an electrical signal generated in the electrode system 10 via the connection electrode 520 disposed in the biosensor cartridge 500, and the connection electrode is wired without passing through the connection electrode 520. The electrical signal generated by the electrode system 10 may be received by directly connecting to the unit 20. When the connection electrode receives an electrical signal generated in the electrode system 10 via the connection electrode 520 provided in the biosensor cartridge 500, the biosensor and the measurement device are not in direct contact with each other. Contamination due to can be prevented.

  Moreover, the measuring apparatus 1000 converts the electric signal received from the electrode system 10 into a measured value by the calculating part. The obtained measurement value is displayed on the display unit 1100, and the measurer can visually recognize the measurement result.

  Although not shown, measurement apparatus 1000 may further include a drive unit. The driving unit drives the first rotating unit 551, the second rotating unit 553, and the third rotating unit disposed in the biosensor cartridge 500, and the one detecting unit 101 before the measurement of the biosensor 100 is externally connected. Place it at the measurement position. Here, the drive unit according to the present embodiment may be the manual dial shown in FIG. 13 or a motor. When the drive unit is a motor, electronic control can be performed by providing a control unit. By arranging one detection unit 101 before measurement of the biosensor 100 by the drive unit at an external measurement position, it is possible to reliably perform measurement of a patient who is a measurer.

  In the measuring apparatus according to the present embodiment configured as described above, a part of the wiring unit for transmitting an electrical signal from the electrode system to the measuring apparatus is positioned on a plane spatially different from the electrode system at the time of measurement. By mounting the biosensor cartridge that houses the biosensor, it is possible to prevent poor conduction due to blood that has adhered and coagulated, and to accurately measure the blood glucose level. In addition, the measuring apparatus according to the present embodiment can mount the biosensor cartridge 800 in addition to the biosensor cartridge 500, and can also use the biosensors 200, 300, and 400 depending on the biosensor cartridge to be mounted. it can.

(Measuring method)
Below, the measuring method using the measuring apparatus mentioned above is demonstrated. The biosensor cartridge containing the biosensor according to the present embodiment is provided to the measurer by the supplier. When the measuring apparatus according to the present embodiment is, for example, a blood glucose measuring apparatus, the supplier is a doctor, a hospital, a pharmacy, or the like, and the measuring person is a diabetic patient. The measurer attaches the biosensor cartridge to the measurement device. The measurer turns on the power and activates the calculation unit, the display unit 1100, the drive unit, the control unit, and the like.

  It is preferable that the detection unit before the measurement is in a position where it does not come into contact with the extruding unit except when the biosensor cartridge is attached to the measurement device or during measurement. At the time of measurement, the measurer pushes out the biosensor to the outside, drives the rotation unit by the drive unit, and places one detection unit before measurement at the external measurement position. At this time, in the measuring method according to the present embodiment, a part of the wiring part for transmitting the electric signal from the electrode system to the measuring device is positioned on a plane spatially different from the electrode system at the time of measurement. Further, the cover film covering the detection part of the biosensor is peeled off by one detection part by the cover film peeling part provided in the biosensor cartridge by driving the rotation part.

  The measurer supplies a sample containing the test object to the electrode system of the detection unit. When measuring a blood glucose level, the sample is blood, and it is possible to prevent poor conduction of the wiring portion of the detection unit due to blood that has adhered and coagulated, and an accurate blood glucose level can be measured.

  The electrical signal from the electrode system generated by the measurement is received from the biosensor wiring section through the connection electrode of the biosensor cartridge or directly at the connection electrode of the measurement device, and converted into a measurement value by the calculation section. . The converted measurement value is displayed on the display unit, and the measurer can recognize the measurement result.

  After the measurement, the rotation unit is driven by the drive unit, and a part of the biosensor having the measurement unit after measurement is accommodated in the recovery unit, thereby preventing contamination by the adhered / coagulated blood. Since the biosensor cartridge according to the present embodiment accommodates a biosensor having a plurality of detection units, the series of measurement operations can be continuously performed a plurality of times. For this reason, it is not necessary to perform the attachment / detachment operation of the biosensor for every measurement like the past. In addition, a part of the wiring part for transmitting the electrical signal from the electrode system to the measuring device is located on a surface spatially different from the electrode system at the time of measurement, thereby preventing conduction failure due to adhered and coagulated blood. Therefore, accurate blood glucose level can be measured.

  1: first substrate, 3: second substrate, 5: third substrate, 7: absorbent substrate, 10: electrode system, 11: working electrode, 13: counter electrode, 15: reference electrode, 17: enzyme reaction part, 20: wiring part, 21: wiring, 23: wiring, 25: wiring, 51: working electrode, 53: counter electrode, 61: wiring, 63: wiring, 71: through hole, 73: through hole, 75: Opening part, 90: Cover film, 91: Adhesive layer, 100: Biosensor, 101: Detection part, 130: Part of wiring part, 200: Biosensor, 201: Detection part, 300: Biosensor, 301: Detection unit, 400: Biosensor, 401: Detection unit, 500: Biosensor cartridge, 510: Container, 520: Connection electrode, 521: Connection electrode, 523: Connection electrode, 525: Connection electrode, 529: Connection electrode, 530: Extrusion section, 535: elliptical rotating section 540: Recovery unit, 551: First rotation unit, 553: Second rotation unit, 555: Third rotation unit, 557: Support column, 600: Biosensor cartridge, 650: Biosensor cartridge, 671: First Cover film peeling section, 673: second cover film peeling section, 729: connection electrode, 730: extrusion section, 740: recovery section, 751: first rotating section, 753: second rotating section, 755: third Rotating part, 765: Cover film peeling part, 800: Biosensor cartridge, 1000: Measuring device, 1100: Display part.

Claims (25)

A plurality of detection units comprising an electrode system and a wiring unit are disposed on the first base material,
Of the plurality of detection units, at least the electrode system is adhered to the first base material through an adhesive layer having polyethylene and polypropylene so as to be sealed, and is peeled off from the first base material at the time of measurement. A cover film,
During the measurement, the electrode system is located on a first surface of said first substrate, a portion of the wiring portion a position to Luba biosensor to said first plane and spatially different second surface A biosensor cartridge for receiving,
A first rotating unit around which a biosensor having a detection unit before measurement is wound;
A collection unit in which a biosensor having a detection unit after measurement is stored;
One end of the cover film is attached, and a cover film accommodating portion having a cover film accommodating rotating portion that accommodates the cover film peeled off from the first base material at the time of measurement,
Extruding unit provided with connection electrodes for extruding the detection unit of the biosensor to the outside and receiving an electrical signal from the electrode system;
A biosensor cartridge comprising: 2. The biosensor cartridge according to claim 1, wherein the polyethylene has a density of 0.945 g / cm ³ or more and 0.965 g / cm ³ or less. The biosensor cartridge according to claim 2, wherein the polyethylene has an MFR (190 ° C) of 1 g / 10 min or more and 7 g / 10 min or less. The polypropylene biosensor cartridge according to claim 3, wherein the density is less than 0.9 g / cm ³ or more 0.91 g / cm ^3. The biosensor cartridge according to claim 4, wherein the polypropylene has an MFR (230 ° C.) of 5 g / 10 min or more and 30 g / 10 min or less. 6. The biosensor cartridge according to claim 5, wherein the polyethylene and the polypropylene have a blend ratio of 10 to 50 parts by weight of the polyethylene and 50 to 90 parts by weight of the polypropylene. The biosensor cartridge according to claim 6, wherein the adhesive layer has a layer thickness of 20 μm or less, preferably 10 μm or less. The biosensor cartridge according to any one of claims 1 to 7, wherein the electrode system and the wiring portion are positioned on the first surface of the first base material before measurement. The biosensor cartridge according to any one of claims 1 to 7, wherein an angle formed by the first surface and the second surface is not less than 0 ° and less than 180 °. The electrode system includes a working electrode, a counter electrode, and a reference electrode,
The biosensor cartridge according to claim 1, further comprising an enzyme reaction unit including an enzyme and an electron acceptor located on the working electrode. The biosensor cartridge according to claim 1 , further comprising a connection electrode that is in contact with a part of the wiring portion and receives an electrical signal from the electrode system. The biosensor cartridge according to claim 1 , further comprising a cover film peeling portion that peels the cover film from the first base material between the first rotating portion and the cover film accommodating portion. . A measuring device to which the biosensor cartridge according to any one of claims 1 to 12 is attached,
An arithmetic unit for converting an electrical signal from the electrode system into a measured value;
And a display unit for displaying the measurement value. The measuring apparatus according to claim 13 , further comprising a driving unit that drives the rotating unit. The measurement apparatus according to claim 14 , wherein the driving unit arranges one detection unit before the biosensor measurement at an external measurement position. A plurality of detection units each including an electrode system and a wiring unit are disposed on the first base, and among the plurality of detection units, at least the electrode system is sealed with polyethylene and Using a biosensor equipped with a cover film that is bonded through an adhesive layer having polypropylene and peeled off from the first substrate at the time of measurement,
Peeling the cover film,
The biosensor is disposed so that the electrode system is located on a first surface of the first base material, and a part of the wiring portion is located on a second surface spatially different from the first surface. And
A sample is brought into contact with the electrode system, and a test object contained in the sample is measured;
Receiving an electrical signal from the electrode system from a part of the wiring portion located on the second surface side of the first base material ;
The biosensor is folded by bending the biosensor so that a part of the wiring portion becomes a second surface opposite to the first surface on which the electrode system is disposed via the first base material. A measuring method comprising housing in a cartridge. The measurement method according to claim 16 , wherein the polyethylene has a density of 0.945 g / cm ³ or more and 0.965 g / cm ³ or less. The measurement method according to claim 16 , wherein the polyethylene has an MFR (190 ° C.) of 1 g / 10 min or more and 7 g / 10 min or less. The polypropylene, the measuring method according to claim 16, wherein the density is less than 0.9 g / cm ³ or more 0.91 g / cm ^3. The said polypropylene has MFR (230 degreeC) of 5 g / 10min or more and 30 g / 10min or less, The measuring method of Claim 16 characterized by the above-mentioned. The polyethylene and the blending ratio of the polypropylene, the polyethylene is 10 to 50 parts by weight, measuring method according to claim 16, wherein the polypropylene is from 50 to 90 parts by weight. The measuring method according to claim 16 , wherein the adhesive layer has a layer thickness of 20 μm or less, preferably 10 μm or less. The biosensor cartridge includes a first rotating unit driven by the driving unit, and winds a biosensor having a detection unit before measurement,
A recovery unit is provided, containing a biosensor having a detection unit after measurement,
The measurement method according to any one of claims 16 to 22 , further comprising a third rotating unit, wherein the cover film peeled off at the time of measurement is accommodated. The biosensor cartridge further includes a second rotating part in the recovery part,
The measurement method according to claim 23 , wherein the biosensor having the detection unit after the measurement is wound up. The measurement method according to claim 23 , further comprising a cover film peeling portion that peels the cover film from the first base material between the first rotating portion and the third rotating portion. .

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