JP4631030B2 - Needle integrated biosensor - Google Patents

Description

  The present invention relates to a needle-integrated biosensor. More specifically, a needle integrated type having a configuration in which a puncture needle for piercing the skin to obtain a body fluid (blood etc.) and a biosensor for collecting and analyzing the body fluid taken out on the surface of the skin are integrated. It relates to biosensors.

Conventionally, a diabetic patient himself collects blood and measures a blood glucose level which is a glucose level in blood. In this case, the patient uses a blood collection device called a lancet that attaches and detaches the blood collection needle, collects blood by inserting a blood collection needle into his fingertip or arm, and moves the collected blood to a blood glucose analyzer to measure the blood glucose level. is doing. In such a measurement method, the patient must carry a set of measuring instruments consisting of several points such as a blood glucose analyzer, a lancet, a blood collection needle and an analytical element, and combine them when necessary to perform the measurement. However, it takes a lot of training and it takes a considerable amount of time before the patient can make reliable measurements. Actually, measurements at sites other than the fingertips and forearms (abdominal wall, earlobe, etc.) are difficult even for an expert. In recent years, biosensors that can be measured with a sample volume of 1 μl or less have been developed due to the need for less invasive specimen supply with less pain. The work of supplying accurately becomes very difficult. As a result, the measurement fails, and the patient who is the subject needs to puncture again and replace the biosensor, and the measurement must be performed again.
JP-A-9-266898 Japanese Patent Publication No. 8-20412

Thus, several needle-integrated biosensors have been devised. First, in the needle-integrated biosensor disclosed in Patent Document 3, the puncture needle and the biosensor are set at different positions inside a pen-type (two-color ballpoint pen-like) measuring device equipped with a puncture needle drive unit. In this case, the tip of the pen-like measuring device is applied to the skin of the subject and punctured, and then the biosensor is exposed to the tip and blood sampling is performed to measure blood glucose. However, this method does not eliminate the troublesomeness of setting the needle and the biosensor in the measuring device.
JP 2000-217804 A

Moreover, in the needle-integrated biosensor disclosed in Patent Document 4, the puncture needle is entrusted to external driving, and the puncture needle moves in parallel along the longitudinal direction of the elongated piece-like biosensor. Have taken. However, in this type, since the puncture needle moves in the blood collection conveyance path and the reagent layer of the biosensor, there is a risk that the surface of the puncture needle is contaminated with the reagent before the puncture needle pierces the skin of the subject.
Republished 2002-056769

  In addition, due to insufficient disposal of infectious diseases for disposal after use, a puncture drive is provided on the measurement device side, and the needle-integrated biosensor unit cannot withstand the impact of the drive during puncture Many problems remain, such as structure.

The object of the present invention is that the puncture driving unit as seen in a lancet is not required, so that the configuration is very simple, so that the assembly is easy, and the sample body fluid can be collected reliably in a small amount without waste. It is to provide a needle-integrated biosensor.

  The object of the present invention is achieved by a needle-integrated biosensor in which at least two electrodes and a puncture needle (non-perforated needle) are penetrated or embedded perpendicularly to the substrate, and a columnar cover is disposed so as to cover them. Is done.

  The needle-integrated biosensor according to the present invention does not require a puncture driving unit such as that found in a lancet for collecting a sample body fluid, and thus has a very simple configuration, and therefore is easy to assemble, and also has capillary action or By providing a blood collection means by any one of the suction blood collection method and the vacuum blood collection method, the sample body fluid is reliably collected in a small amount without waste. Since such a biosensor can be used as a cartridge, it can be easily carried by simple packaging and has an effect of being hygienic after use.

  The needle-integrated biosensor of the present invention includes at least two electrode systems arranged perpendicular to an electrically insulating substrate such as plastic, a puncture rod-shaped needle, and a columnar cover that covers the outside of the electrode (forming substrate). Composed of a combination. This biosensor will be described in more detail.

At least two electrodes of the biosensor are penetrated or embedded perpendicular to the substrate. Specifically, a method of arranging two flat electrodes at intervals, a method of forming three or more flat electrodes at intervals and forming a hollow prismatic structure, or a plate electrode having a curved surface Examples include a method of forming a hollow cylindrical structure by arranging two or more at intervals. Each of these three types of electrodes will be described.

  The two flat electrodes are preferably flat members each having a part or all of them as electrodes. Further, the hollow prismatic structure is formed by arranging three or more flat plate members each having part or all of an electrode, and the hollow columnar structure is a curved member having part or all of an electrode. It is formed by arranging two or more.

  When a part of the plate member is an electrode, the part other than the electrode (electrode forming substrate) is an insulating material, for example, an inorganic material such as plastic or ceramic, a biodegradable material, paper, etc., preferably polyethylene terephthalate. Used.

  The electrode forming a part of the plate member is formed by depositing a conductive material on the surface of the electrode forming substrate or by bonding the electrode member and the electrode forming substrate.

  Film formation of the conductive material on the electrode forming substrate surface is performed by a screen printing method, a vapor deposition method, a sputtering method, a foil bonding method, a plating method, etc., and the bonding between the electrode member and the electrode forming substrate is This is done with an adhesive.

  Examples of the conductive material include carbon, silver, silver / silver chloride, platinum, gold, nickel, copper, palladium, titanium, iridium, lead, tin oxide, and platinum black. As carbon, carbon nanotubes, carbon microcoils, carbon nanohorns, fullerenes, dendrimers, or derivatives thereof can be used.

  The electrode may be a two-pole method formed by a working electrode and a counter electrode or a three-pole method formed by a working electrode and a counter electrode, a reference electrode, or a number of poles larger than that. Two or more electrodes can be formed.

  A substrate is used to form the columnar structure. The material of the substrate is sufficient if it is electrically insulative, and the electrode (forming substrate) is disposed by penetrating or being embedded perpendicularly to the substrate. At this time, a spacer can also be provided between the electrodes (forming substrate). When the electrode (formation substrate) penetrates the substrate, the opposite side of the electrode from the substrate is the terminal that sends the electrical signal from the biosensor to the measurement device, and the electrode (formation substrate) penetrates the substrate If not, a terminal is provided on a part of the substrate, preferably a side surface.

  A reagent layer is formed on the electrode (forming substrate) as necessary. The reagent layer is preferably immobilized on the electrode surface or the plate member surface. In this case, the reagent layer is formed by a screen printing method or a dispenser method, and is immobilized on the surface of the electrode (forming substrate) by an adsorption method with drying or a covalent bonding method. The reagent varies depending on the detection target. For example, when a needle-integrated biosensor is configured for blood glucose measurement, a reagent containing glucose oxidase that is an oxidase and potassium ferricyanide as a mediator is employed. When these reagents are dissolved by blood, the enzyme reaction is started. As a result, potassium ferricyanide coexisting in the reagent layer is reduced, and potassium ferrocyanide which is a reduced electron carrier is accumulated. The amount is proportional to the substrate concentration, ie the glucose concentration in the blood. The reduced electron carrier accumulated for a certain time is oxidized by an electrochemical reaction. The glucose concentration (blood glucose level) is calculated from the anode current measured at this time.

Needle-integrated biosensor A needle-integrated biosensor is formed by incorporating a puncture portion into a part of a biosensor having a hollow prismatic structure or a cylindrical structure. The puncture unit is composed of a puncture stick needle.

  The rod-shaped needle is a needle that does not have a hole, and is disposed inside, preferably in the center of, a prismatic structure or a cylindrical structure composed of two or more electrode plate members. The rod-shaped needle is embedded perpendicularly to the substrate or fixed by a spacer provided between electrodes (forming substrate). In the latter case, there is an advantage that the electrode interval can be fixed together. The rod-like needle in this case is preferably made of the same material as that of a commercially available lancet puncture needle, and may be processed using, for example, stainless steel.

  In the needle-integrated biosensor incorporating a rod-like needle, the outer side of the electrode plate member is covered with a hollow columnar cover. In this case, the columnar cover has a prismatic or cylindrical shape, and preferably has the same shape as that of the electrode (forming substrate). The columnar cover is fixed to the substrate so as to withstand the stress during puncturing.

  The rod-shaped needle needs to protrude beyond the columnar cover after fixing. The length is sufficient if blood can be collected by puncturing the skin of the subject, and is fixed so as to protrude 0.1 to 2 mm, preferably 0.5 to 1 mm. Here, in order to be able to adjust the protruding length of the puncture needle, it is preferable to use a mechanism in which the height of the spacer provided between the electrodes can be adjusted stepwise with screws or the like.

  A needle-integrated biosensor incorporating a rod-like needle enables puncturing by the user piercing the protruding portion of the puncture needle directly into the skin of the subject. The bleeding blood is transferred through the columnar cover to the biosensor electrode reaction part by capillary action. At this time, depending on the blood, the electrode may not be sufficiently covered, for example, when the hematocrit value is high. Therefore, the electrode (formation substrate) portion away from the blood collection introducing portion is preferably covered with a resist. Thereby, even when the hematocrit value is high, the electrode can be filled at a minimum, so that the sample liquid can be transferred without being influenced by the state. On the other hand, when the hematocrit value is low and blood transfer is performed smoothly, it is necessary to stop capillary action in order to prevent excessive blood collection. Examples of this means include a method in which an air outlet is provided in the columnar cover, and a substrate connection portion of the columnar cover is narrowed or expanded.

  In order to improve the adhesion of the puncture part to the skin and to reliably introduce blood collection at the puncture blood collection port, a blood collection introduction guide is preferably provided at the tip of the columnar cover, that is, the puncture blood collection port. Examples of the material for the blood collection introduction guide include gels, elastic materials, and foamable materials.

  As a blood collection method, a suction blood collection method or a vacuum blood collection method may be mentioned in addition to the method using the capillary phenomenon. An example of a needle-integrated biosensor that uses a suction blood collection method is one in which a syringe-like aspirator is placed on the back side of the biosensor substrate, specifically, the substrate with a negative pressure inside the syringe and a septum. At the same time as puncturing the skin with a needle that is fixed at both ends and puncturing at the time of use, the puncture needle is also inserted into the diaphragm on the opposite side of the skin. Is a negative pressure. Thereby, blood collection can be performed smoothly.

  Examples of the needle-integrated biosensor using the vacuum blood collection method include a method in which the puncture blood collection port in the columnar cover is covered with a diaphragm and the inside is evacuated. At this time, since the tip of the puncture needle protrudes from the columnar structure, the diaphragm and the puncture needle need to be fixed in a state of keeping the airtightness inside. Such a biosensor has a structure in which the puncture needle slightly moves toward the inside of the needle-integrated biosensor at the time of puncturing, whereby the diaphragm is broken by the movement of the puncture needle, and the negative pressure inside the needle-integrated biosensor is reduced. Since it is applied to the skin after puncture, blood can be collected using this negative pressure.

  In any case, in order to enhance the adhesion to the skin, a blood collection introduction guide is preferably provided so as to border the outside of the diaphragm, that is, the columnar cover. The blood collection introduction guide also has an effect of maintaining the internal airtightness. In addition, since the hematocrit value also affects the vacuum blood collection method, the electrode area is defined within a range where the minimum blood collection is possible even in the case of a high hematocrit value, that is, the electrode portion of the electrode plate member is located near the puncture blood collection port. It is preferable to use the resist described above as a method for defining the electrode area.

  The puncture needle preferably has a photocatalytic function effective for antibacterial and antiviral effects on its surface, and a titanium oxide or titanium dioxide film is formed by vapor deposition or sputtering.

  Since such a needle-integrated biosensor is of a cartridge type, it can be stored in a dedicated container that is convenient to carry, and anyone can easily and reliably attach it to the measuring device. By adopting this cartridge type aspect, the convenience of the needle-integrated biosensor can be dramatically improved as compared with the conventional method. Moreover, simple packaging is possible, and it can be kept hygienic from start to finish before and after use. In more detail, a packaging form is described.

Packaging Form As a packaging form of the needle-integrated biosensor, first, packaging of individual needle-integrated biosensors, particularly one that protects the puncture blood collection part at the tip of the needle-integrated biosensor. As such a package, a cap-shaped simple package that protects the tip is preferable. Thereby, the puncture blood collection part can be protected hygienically and safely until use. Furthermore, by having such a form, repackaging after use is possible, and it is possible to prevent infectious diseases that are a concern after disposal, and as another method of use, body fluid after puncture collection is stored. It is also possible.

  As a second packaging form, a container in which a plurality of needle-integrated biosensor cartridges that are simply packaged can be carried together is exemplified. Since the needle-integrated biosensor cartridge of the present invention is extremely small even if it includes the bulk of the simple packaging, even if a plurality of needle-integrated biosensor cartridges are stored together in a container, the overall size of the packaging container is small. Specifically, it is desirable that the pocket size is easy to carry.

  As a third packaging form, a packaging container itself is capable of individually packaging and storing a needle-integrated biosensor cartridge inside. In this case, for example, a form in which the needle-integrated biosensor cartridge is individually stored in a well-shaped tray and individually wrapped with a packaging film or the like in order to maintain airtightness may be used.

Measuring device The measuring device for the needle-integrated biosensor is easy to carry and secures operability and durability for repeated and reliable measurement using a cartridge-type needle-integrating biosensor. preferable.

  Specifically, a form in which a cartridge-type needle-integrated biosensor is slid sideways or inserted in the vertical direction into the introduction part at the lower part of the measuring apparatus is preferable. At this time, the terminal of the biosensor is connected to the connector of the measuring device so that measurement is possible. After that, when the user decides the puncture portion and starts puncturing, puncturing, blood sampling and measurement are automatically performed, and finally the measurement result is derived.

  An example of structural features will be described in more detail. This measuring device includes a cartridge introduction part, a connector, an electrochemical measurement circuit, a memory part, an operation panel, a measurement part for measuring electrical values in the electrodes of the biosensor, and a display part for displaying the measurement values in the measurement part. In addition, the apparatus can be equipped with radio waves such as Bluetooth (registered trademark) as wireless means.

  In addition, an illumination function can be provided in consideration of use by a dark place or a low vision person. In this case, it is preferable that the user can improve the operability when attaching and puncturing the needle-integrated biosensor cartridge. For example, the illumination light is emitted from the introduction portion of the cartridge of the measuring device. By irradiating, the user can easily introduce the cartridge into the measuring apparatus, and the puncture portion is illuminated by illumination from the introduction portion even after the cartridge is attached. Therefore, it is preferable that a material such as a spacer or a diaphragm that fixes the electrode plate member of the needle-integrated biosensor cartridge having an illumination function is a transparent material.

  In addition to the automatic illumination function of the display unit and puncture unit in the dark place, the measurement device has a voice guide function and a voice recognition function corresponding to visual impairment due to diabetes, a measurement data management function built in a radio clock, measurement data A communication function for a medical institution, a charging function, and the like can be provided.

  The measuring method in the measuring unit of the measuring device is not particularly limited, and potential step chronoamperometry, coulometry, cyclic voltammetry, or the like can be used.

As described above, the needle-integrated biosensor, the needle-integrated biosensor cartridge, and the package thereof according to the present invention do not limit the user, that is, can support universal planning.

  The needle-integrated biosensor and the needle-integrated biosensor cartridge according to the embodiment of the present invention will be described in detail with reference to the drawings. However, the present invention is limited to the following examples as long as the gist thereof is not exceeded. is not.

  FIG. 1 is a diagram showing an example of a needle-integrated biosensor in which a rod-like puncture needle is arranged at the center of a cylindrical electrode plate member 18 and a cylindrical cover 4 is arranged on the outside thereof. 1a is a configuration diagram, FIG. 1b is a longitudinal sectional view of the center line in FIG. 1a, FIG. 1c is a front view when the substrate 5 is viewed from the puncture blood sampling port 9, and FIG. Each figure is shown.

  In the case of the needle-integrated biosensor shown in FIG. 1, two electrode plate members 18 are arranged, and the two electrode plate members 18 form a cylindrical shape, and the puncture needle 6 is arranged at the center thereof. Has been. The puncture blood collection port 9 provided at the tip of the cylindrical cover 4 is provided with a puncture introduction guide 7 for the purpose of improving the adhesion with the skin as the subject. In use, blood is collected by puncturing with the puncture needle 6 protruding from the cylindrical cover 4 and introduced to the air discharge port 8 (22) for stopping the capillary phenomenon.

  FIG. 2 is a diagram showing an example of a needle-integrated biosensor in which a rod-like puncture needle is arranged at the center of an electrode plate member arranged in parallel and facing, and a cylindrical cover is arranged on the outside thereof. 2a is a configuration diagram, FIG. 2b is a cross-sectional view taken along the line AA ′ in FIG. 2a, FIG. 2c is a front view when the substrate 5 is viewed from the puncture blood sampling port 9, and FIG. The rear views are shown respectively.

  In the case of the needle-integrated biosensor shown in FIG. 2, two electrode plate members 1 are arranged, these two electrode plate members 1 are arranged facing each other in parallel, and a spacer 2 is sandwiched in the center thereof. A puncture needle 6 is arranged. The spacer 2 fixes the positional relationship between the electrodes and the puncture needle. In this case, the puncture blood inlet 9 provided at the tip of the cylindrical cover 4 is provided with a puncture introduction guide 7 for the purpose of improving the adhesion with the skin as the subject. In use, blood is collected by puncturing with the puncture needle 6 protruding from the cylindrical cover 4 and introduced to the air discharge port 8 (22) for stopping the capillary phenomenon.

  FIG. 3 is a diagram showing an example of a needle-integrated biosensor in which a rod-like puncture needle is arranged at the center of a prismatic electrode plate member and a cylindrical cover 4 is arranged on the outside thereof. 3a is a configuration diagram, FIG. 3b is a cross-sectional view taken along line AA ′ in FIG. 3a, FIG. 3c is a front view when the substrate 5 is viewed from the puncture blood sampling port 9, and FIG. The rear views are shown respectively.

  In the case of the needle-integrated biosensor shown in FIG. 3, three electrode plate members 1 are arranged, a triangular prism shape is formed by these three electrode plate members 1, and a spacer 2 is sandwiched between the center portions. A puncture needle 6 is arranged. The spacer 2 fixes the positional relationship between the electrodes and the puncture needle. In this case, the puncture blood inlet 9 provided at the tip of the cylindrical cover 4 is provided with a puncture introduction guide 7 for the purpose of improving the adhesion with the skin as the subject. In use, blood is collected by puncturing with the puncture needle 6 protruding from the cylindrical cover 4 and introduced to the air discharge port 8 (22) for stopping the capillary phenomenon.

  FIG. 4 is a diagram showing an example of a suction blood collection type needle integrated biosensor in which a rod-like puncture needle is arranged at the center of a prismatic electrode plate member and a cylindrical cover 4 is arranged on the outside thereof. 4A is a configuration diagram, FIG. 4B is a cross-sectional view taken along line AA ′ in FIG. 4A, and FIG. 4C is a front view when the substrate 5 is viewed from the puncture blood collection port 9.

  The suction blood collection type needle-integrated biosensor shown in FIG. 4 includes the needle-integrated biosensor shown in FIG. 3 and a suction device 13 having a negative internal pressure, and the puncture needle is defined by the substrate 5 and the substrate 5. Provided with a mechanism capable of moving the formed through hole. Unlike the case of the needle-integrated biosensor shown in FIG. 3, the protruding portion of the puncture needle 6 when not in use is slightly longer. This is because the puncture needle 6 has puncture portions at both ends, and both puncture the skin and the diaphragm 12 simultaneously. Here, in order to keep the inside of the needle-integrated biosensor airtight, unlike FIG. 3, no air outlet is provided. Since the suction device 13 is fixed to the back surface of the substrate 5, the terminal 3 is provided on the side surface of the substrate 5. Further, the aspirator 13 is in close contact with the substrate 5 with the diaphragm 12 in between, and the diaphragm 12 connected to the aspirator 13 in parallel with the puncture of the skin is broken by the puncture needle when used. The internal negative pressure reaches the puncture blood collection port 9. Here, the puncture needle support 11 is required to reliably puncture the skin and the diaphragm 12 with the puncture needle 6. The puncture needle support 11 is designed so that the puncture needle 6 does not reach the aspirator 13 by defining the puncture depth of the diaphragm 12 when puncturing both the skin and the diaphragm 12 simultaneously. As a result, it is possible to automatically perform a series of blood collection / measurement operations after puncture. The electrode 1 shown here is also hardly affected by the state of blood collection by defining the electrode area in the vicinity of the puncture blood collection port with a resist. The suction device used here is a dropper-shaped one made of a plastic material or a shape memory material that can be easily formed.

  FIG. 5 is a cross-sectional view showing a state of the puncture operation of the aspirated blood collection type needle integrated biosensor shown in FIG. By puncturing the diaphragm 12, the air inside the biosensor is sucked into the aspirator.

  FIG. 6 shows a puncture blood collection port 9 of the vacuum blood collection type needle integrated biosensor shown in FIG. 5 provided with a diaphragm 12 and further provided with a puncture introduction guide 7 on its edge. 6a is a configuration diagram, FIG. 6b is a cross-sectional view taken along line AA ′ in FIG. 6a, FIG. 6c is a front view when the substrate 5 is viewed from the puncture blood collection port 9, and FIG. Each rear view is shown. In this case as well, the puncture needle 6 is movable, and when the puncture is directed toward the substrate, the diaphragm 12 is broken, and the vacuum state inside the needle-integrated biosensor is released toward the skin. At this time, since the skin is in close contact with the puncture introduction guide 7, blood collection is efficiently taken into the needle-integrated biosensor.

  FIG. 7 is a cross-sectional view showing a state of the vacuum blood collection type needle integrated biosensor shown in FIG. 6 at the time of puncturing (immediately after puncturing). The diaphragm 12 is broken by the puncture, and the outside air enters the vacuum needle-integrated biosensor.

  FIG. 8 is a sectional view showing an example of use of the vacuum blood collection type needle integrated biosensor shown in FIGS. By inserting the puncture portion of the vacuum blood collection type needle integrated biosensor perpendicular to the skin of the subject (FIG. 8a), the diaphragm is broken (FIG. 8b), and the blood collection 17 is transferred into the sensor from the gap (FIG. 8b). FIG. 8c).

  FIG. 9 shows a packaging example of the needle-integrated biosensor cartridge of the present invention and one usage example with a measuring device. FIG. 9a shows a packaging container 23 that can store a plurality of cartridges, and FIG. 9b shows the inside. In the form of this packaging container, since the cartridge itself is small, it becomes a small pocket size as a whole. Furthermore, in this case, each cartridge is stored in a space provided in a well shape and is packaged by the simple packaging film 26. At the time of use, this simple packaging film 26 can be used by peeling it along the perforation 30 from the knob portion 28 which is a non-adhesive layer. At this time, only the portion of the weak adhesive layer 27 is peeled off from the simple packaging film 26 and the strong adhesive layer 29 portion is not peeled off, thereby preventing the film 26 portion from dropping off (generation of dust). Furthermore, if the weak adhesive layer 27 can be re-adhered, the used cartridge can be returned to its original state. In this case, it is also convenient when the needle-integrated biosensor cartridge is used as a sampling container for blood collection or the like as in a normal syringe.

  FIG. 9c shows a simple packaging example of the needle-integrated biosensor cartridge 15 and is housed in the packaging container 23 in this state. This simple package 24 is in the form of a cap and can be easily removed and reattached after use, and can be applied to a method of use for collecting and storing body fluids. In addition, by using a transparent material for the spacer 25 of the needle-integrated biosensor cartridge, when attached to a measuring device with an illumination function, illumination is performed through the spacer even in the dark, so that the puncture part can be easily determined. can do.

  FIG. 9d shows a measuring device for a needle-integrated biosensor cartridge. The measuring device 31 includes an operation panel 32, a display unit 33, a button 34, a hook 35, a non-slip 36, and a needle-integrated biosensor cartridge introduction unit 37. It is attached to the needle-integrated biosensor cartridge introduction part 37 below. If it is the shape of this measuring device 31, it is easy to carry and operability is also excellent.

  FIG. 10 shows an example of the operation when the needle-integrated biosensor cartridge is used for measurement in a dark place. FIG. 10 a shows a state in which one cartridge 15 packaging portion in the packaging container 23 is illuminated by the illumination 14 from the needle-integrated biosensor cartridge introduction portion 37 of the measuring device 31. FIG. 10 b shows a state in which the illumination 14 illuminates the planned puncture portion of the subject through the transparent spacer of the cartridge 15 attached to the measuring device 31. FIG. 10c shows a state where a spot specified by the illumination 14 is punctured, and blood is collected and measured. In this case, the visibility of the display unit can also be enhanced by a backlight or the like.

It is a figure which shows the example of 1 structure of the needle | hook integrated biosensor by which a rod-shaped puncture needle is arrange | positioned in the center part of a cylindrical electrode plate member, and the cylindrical cover is arrange | positioned on the outer side. It is a figure which shows the example of 1 structure of the needle | hook integrated biosensor by which the rod-shaped puncture needle is arrange | positioned in the center part of the electrode plate member arrange | positioned facing in parallel, and the cylindrical cover is arrange | positioned on the outer side. It is a figure which shows one structural example of the needle | hook integrated biosensor by which the rod-shaped puncture needle is arrange | positioned in the center part of the prismatic electrode plate member, and the cylindrical cover is arrange | positioned on the outer side. It is a figure which shows the example of 1 structure of the suction blood collection type | mold needle | hook integrated biosensor by which the rod-shaped puncture needle is arrange | positioned in the center part of the prismatic electrode plate member, and the cylindrical cover is arrange | positioned on the outer side. It is a figure which shows one example of operation | movement of the suction blood collection type | mold needle integrated biosensor. It is a figure which shows the example of 1 structure of the vacuum blood collection type | mold needle integrated biosensor by which the rod-shaped puncture needle is arrange | positioned in the center part of the prismatic electrode plate member, and the cylindrical cover is arrange | positioned on the outer side. It is a figure which shows one operation example of a vacuum blood-collecting type needle-integrated biosensor. It is a figure which shows one usage example of a vacuum blood-collecting type needle-integrated biosensor. It is a figure which shows the example of a packaging with the biosensor cartridge with integrated needle | hook, and the usage example accompanied by a measuring apparatus. It is a figure which shows one usage example in the dark place of a biosensor cartridge and a measuring apparatus with a needle.

Explanation of symbols

1 Flat electrode (electrode plate member)
2 Spacer 3 Terminal 4 Cylindrical cover 6 Puncture needle 7 Blood sampling introduction guide 8 Air outlet 9 Puncture blood sampling port 10 Electrode reaction part (reagent layer)
DESCRIPTION OF SYMBOLS 11 Puncture needle support body 12 Diaphragm 13 Aspirator 15 Needle integrated biosensor 16 Subject 17 Blood collection 18 Cylindrical electrode (electrode plate member)
22 Capillary phenomenon stop part 23 Packaging container 24 Cap for packaging 25 Transparent substrate 26 Packaging film 27 Weak adhesive layer 28 Non-adhesive layer (pick)
29 Strong adhesive layer 30 Perforation 31 Measuring device 32 Operation panel 33 Display unit 34 Button 35 Hook 36 Non-slip 37 Needle-integrated biosensor cartridge introduction unit

Claims (22)

  A needle-integrated biosensor in which at least two electrodes and a puncture rod-like needle are vertically penetrated or embedded with respect to a substrate, and a columnar cover is disposed so as to cover them.   The needle-integrated biosensor according to claim 1, wherein a terminal for sending an electrical signal to the measuring device is provided on the opposite side of the substrate from the substrate.   The needle-integrated biosensor according to claim 1, wherein a terminal for sending an electric signal to the measuring device is formed on a side surface of the substrate in which the electrode is embedded.   The needle-integrated biosensor according to claim 1, wherein the electrode is formed on a substrate for electrode formation by film formation or bonding to the substrate for electrode formation.   The needle-integrated biosensor according to claim 1, wherein an electrode area is defined by a resist.   The needle-integrated biosensor according to claim 1, wherein a reagent layer is formed on the electrode.   The needle-integrated biosensor according to claim 1, wherein a puncture rod-like needle having a photocatalytic function is used.   The needle-integrated biosensor according to claim 1, further comprising a body fluid collection stop portion due to capillary action.   The needle-integrated biosensor according to any one of claims 1 to 8, wherein a blood collection introduction guide is provided at a puncture blood collection port of the columnar cover.   The needle-integrated biosensor according to any one of claims 1 to 9, wherein a diaphragm is provided at a puncture blood collection port having a columnar structure.   The needle-integrated biosensor according to claim 10, wherein blood collection is performed by a suction blood collection method.   The needle-integrated biosensor according to claim 10, wherein blood collection is performed by a vacuum blood collection method.   The needle-integrated biosensor according to any one of claims 1 to 11, wherein the substrate is transparent.   The needle-integrated biosensor according to any one of claims 1 to 12, which is of a cartridge type.   The needle-integrated biosensor cartridge according to claim 14, which is a disposable type.   The needle-integrated biosensor cartridge according to claim 14, which is in a packaged state.   The needle-integrated biosensor cartridge according to claim 16, wherein the cartridge is packaged in a repackable state.   A needle-integrated biosensor cartridge package containing a plurality of the needle-integrated biosensor cartridges according to any one of claims 14 to 17.   A needle-integrated biosensor cartridge according to any one of claims 14 to 18, a needle-integrated biosensor cartridge introduction portion for inserting and setting the cartridge, a connector portion for capturing an electrical signal at an electrode of the cartridge, Measuring unit for measuring electrical values via a connector unit, operation panel unit for measurement, display unit for displaying measured values in the measuring unit, memory unit for storing measured values, driving unit for puncture needle, driving unit A measuring device for a needle-integrated biosensor provided with a trigger start button and a puncture start button for starting puncturing with a puncture needle.   The measurement apparatus for a needle-integrated biosensor according to claim 19, wherein a potential step chronoamperometry method, a coulometry method, or a cyclic voltammetry method is applied as a measurement method in the measurement unit.   21. The measuring device for a needle integrated biosensor according to claim 19 or 20, wherein the insertion port of the needle integrated biosensor cartridge can be illuminated. The needle according to any one of claims 19 to 21, comprising at least one of a voice guide function and a voice recognition function, a measurement data management function by incorporating a radio clock, a communication function of measurement data to a medical institution, and a charging function. Integrated biosensor measuring device.

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