WO2022064966A1 - Component measurement apparatus - Google Patents

Component measurement apparatus Download PDF

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Publication number
WO2022064966A1
WO2022064966A1 PCT/JP2021/031666 JP2021031666W WO2022064966A1 WO 2022064966 A1 WO2022064966 A1 WO 2022064966A1 JP 2021031666 W JP2021031666 W JP 2021031666W WO 2022064966 A1 WO2022064966 A1 WO 2022064966A1
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WO
WIPO (PCT)
Prior art keywords
measuring device
unit
housing
puncture
contact surface
Prior art date
Application number
PCT/JP2021/031666
Other languages
French (fr)
Japanese (ja)
Inventor
隆行 杉山
浩明 佐藤
健行 森内
Original Assignee
テルモ株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by テルモ株式会社 filed Critical テルモ株式会社
Priority to JP2022551224A priority Critical patent/JPWO2022064966A1/ja
Publication of WO2022064966A1 publication Critical patent/WO2022064966A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/15Devices for taking samples of blood
    • A61B5/157Devices characterised by integrated means for measuring characteristics of blood
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/66Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood sugars, e.g. galactose

Definitions

  • the present invention relates to a component measuring device for measuring components in body fluid such as blood.
  • test strip test strip having a reagent
  • the user punctures the skin such as a finger using the attached puncture device, and a small amount of blood exuded from the skin is instilled on the inspection part (sample chamber) of the test strip.
  • the instrument measures the amount of glucose (concentration) in the blood by reacting the blood (whole blood) instilled on the test strip with the reagent based on the electrochemical or colorimetric method, and the result is the blood glucose level. Is displayed on the display unit.
  • the instrument used in the system disclosed in Patent Document 1 is provided on the lid of the container for accommodating the test strip, and the puncture device is integrally attached to the side surface of the container, so that the instrument can be carried on the go.
  • the user can measure the blood glucose level by himself / herself. Therefore, in this type of device including the instrument of Patent Document 1, it is required to improve the portability so that it can be easily carried on the go.
  • At least one embodiment of the present invention has been made in view of the above circumstances, and specifically, in a configuration including a puncture device for blood sampling and a measurement device for measuring the amount of a predetermined component in a body fluid. It is an object of the present invention to provide a component measuring device having excellent portability and design.
  • the component measuring device is a puncture device configured to pierce the surface of a living body to exude body fluid, and a predetermined component contained in the body fluid by introducing the body fluid into a test medium.
  • a component measuring device comprising a measuring device configured to measure a component amount, wherein the piercing device is a surface of at least one of a first housing and an outer surface of the first housing.
  • the measuring device is provided on at least one surface of the second housing and the outer surface of the second housing.
  • the piercing device and the measuring device have a second contact surface and a second connecting portion that can be connected to the first connecting portion, and the first contact surface and the second contact surface face each other.
  • the first housing and the second housing are integrated to form a housing of the component measuring device.
  • the first contact surface and the second contact surface become separate surfaces with the puncture device.
  • the measuring device is configured to be a separate body, and the first housing and the second housing have a portion protruding from the outer surface of the housing in a region to be the outer surface of the housing. do not have.
  • a component measuring device having excellent portability and design is provided in a configuration including a puncture device for blood sampling and a measuring device for measuring the amount of a predetermined component in a body fluid. Can be done.
  • XYZ coordinates are set as shown in the figure. That is, the "Z direction” is a direction along the vertical direction, the "X direction” is one direction orthogonal to the Z direction and parallel to the horizontal plane, and the “Y direction” is orthogonal to the Z direction and parallel to the horizontal plane. Of the other directions (directions orthogonal to the X direction), the direction is orthogonal to the X direction.
  • the Z direction coincides with the thickness direction (vertical direction) of the housing 110
  • the X direction coincides with the longitudinal direction (front-back direction) along the long axis direction of the housing 110.
  • the Y direction coincides with the lateral direction (width direction) of the housing 110.
  • the component measuring device 100 punctures the living body surface (for example, skin) of the user as the puncture site to exude body fluid, and measures the component amount of a predetermined component contained in this body fluid. It is a device.
  • the component measuring device 100 is a self-monitoring blood glucose (self-monitoring of blood glucose; SMBG) device that measures the amount (blood glucose level) of the glucose component contained in the body fluid (blood) by the user himself / herself. This will be described as the form adopted in.
  • SMBG self-monitoring of blood glucose
  • the component measuring device 100 is not limited to the SMBG device, but can also be used as a POCT (Point of Care Testing) device mainly operated by a medical worker. Further, since the component measuring device 100 is a device for measuring the specific amount of the component contained in the body fluid, the type of the body fluid and the amount of the component of the component to be measured are not limited to the configuration of the present embodiment.
  • POCT Point of Care Testing
  • the component measuring device 100 punctures the puncture site of the user to exude blood (whole blood), and a predetermined component contained in the blood exuded by the puncture device 10.
  • a measuring device 20 for measuring the amount of components of the above is provided.
  • the component measuring device 100 has a configuration in which the puncture device 10 and the measuring device 20 are separably integrated along a separation surface 101 extending along the axial direction (X direction).
  • the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 are brought into contact with each other to bring them into contact with each other.
  • the component measuring device 100 shown in FIGS. 1 and 2 shows an aspect when not in use.
  • the contact state between the first contact surface 10a and the second contact surface 20a is released during use (during puncture and measurement).
  • the first contact surface 10a is exposed as a part of the housing of the puncture device 10
  • the second contact surface 20a is exposed as a part of the housing of the measurement device 20.
  • the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measuring device 20 form a separation surface 101 that functions as a split surface of the component measuring device 100.
  • the separation surface 101 is provided at least along the longitudinal direction of the component measuring device 100, and is a surface on which the puncture device 10 and the measuring device 20 are separated.
  • the separation surface 101 may be, for example, a vertical surface extending perpendicular to the width direction of the component measuring device 100.
  • the separation cross-sectional end 102 which is the end surface of the separation surface 101 when the component measuring device 100 is viewed from the side of the needle mounting unit 12 (or the side of the needle eject operation unit 14), coincides with the Z direction and is separated at this time.
  • the area of the surface 101 is minimized.
  • the separated cross-sectional end 102 may be tilted in the axial direction by a predetermined angle when viewed from the side of the needle mounting portion 12 (or the side of the needle eject operating portion 14). .. More specifically, the separation surface 101 is an inclined surface that inclines in the width direction toward the thickness direction. When the separation surface 101 is an inclined surface inclined with respect to the Z direction, the separation surface 101 can be wider than when it is a vertical surface, so that the holding force of the puncture device 10 and the measurement device 20 can be appropriately maintained. Further, when connecting the puncture device 10 and the measurement device 20, the user can visually recognize the correct connection direction.
  • the position of the separation surface 101 with respect to the width direction (Y direction) of the component measuring device 100 may be appropriately determined according to the sizes of the puncture device 10 and the measurement device 20, but the separation surface 101 is the puncture device 10 and the like. When they come into contact with the measuring device 20, they are configured to complement each other.
  • the shape of the separation surface 101 may be a flat surface, a curved surface, or a combination of irregularities, but the separation surface 101, that is, the first contact surface 10a and the second contact surface 20a is a flat surface or a surface in consideration of hygiene.
  • a smooth curved surface is preferable, and a flat surface is more preferable. It is preferable that the footprints of the first contact surface 10a and the second contact surface 20a are substantially the same.
  • first contact surface 10a and the second contact surface 20a are both configured to have the same shape and the same size. Thereby, when the puncture device 10 and the measurement device 20 are combined, the portion protruding from the outer surface of the housing 110 can be eliminated.
  • the separated cross-sectional end 102 is located between the first opening 12a and the second opening 22a, which will be described later, or between the medium eject operation unit 23 and the needle eject operation unit 14.
  • the separated cross-sectional end 102 may have a straight line, a curved line, or a combination thereof as long as it does not interfere with the functions of the medium eject operation unit 23 and the needle eject operation unit 14.
  • the housing of the puncture device 10 (first housing 11) and the housing of the measurement device 20 (second housing 21) are the first contact surface 10a of the puncture device 10 and the measurement device 20.
  • the component is measured by connecting the first connecting portion 15 of the puncture device 10 (see FIGS. 5A and 5B) and the second connecting portion 24 of the measuring device 20 in a state where the second contact surface 20a is brought into contact with the puncture device 10.
  • the housing 110 of the device 100 is configured.
  • the first connecting portion 15 of the puncture device 10 and the second connecting portion 24 of the measuring device 20 function as a connecting portion of the component measuring device 100. Through this connecting portion, the puncture device 10 and the measuring device 20 are connected so that the user can arbitrarily attach / detach and connect them.
  • the component measuring device 100 does not have a portion protruding from the outer surface of the housing 110 in a state where the puncture device 10 and the measuring device 20 are connected (that is, when not in use). Specifically, in a state where the puncture device 10 and the measurement device 20 are connected, the outer surface regions of the first housing 11 and the second housing 21 constituting the housing 110 have an outwardly convex shape (convex shape toward the outside). Does not have a bulge).
  • the outer shape of the component measuring device 100 has a pillar shape having a substantially rounded rectangular cross section in a state where the puncture device 10 and the measuring device 20 are integrated, and has a convex shape on the outer surface. It is configured so that there is no such thing.
  • the component measuring device 100 does not have a convex shape on the outer surface of the housing 110 when not in use, it is prevented from being caught by other parts around it when it is carried, and the portability is improved. Further, in the component measuring device 100, when both devices are connected to each other when not in use, the outer surface of the housing 110 does not have a convex shape and becomes a smooth surface. Therefore, the component measuring device 100 is difficult to be recognized as a medical device in appearance and has excellent design. Further, in the component measuring device 100, the puncture device 10 and the measuring device 20 can be separated by the user at the time of use. Therefore, the operability of each device is improved.
  • FIGS. 4 to 8 are diagrams mainly for explaining the configuration of the puncture device 10
  • FIGS. 7 and 8 are diagrams mainly for explaining the configuration of the measurement device 20.
  • FIG. 4 is a diagram for explaining a control system of the measuring device 20.
  • the puncture device 10 punctures the needle mounting portion 12 on which the puncture needle cartridge N is mounted and the puncture needle cartridge N mounted on the needle mounting portion 12 in the first housing 11.
  • the puncture operation unit 13 that advances and retreats the needle N2 to puncture the puncture site of the user, and the needle eject operation unit that is operated when removing (ejecting) the used puncture needle cartridge N attached to the needle mounting unit 12.
  • a first connecting portion 15 for maintaining the connected state of the 14 and the measuring device 20, and a depth adjusting portion 16 for adjusting the puncture depth of the puncture needle N2 with respect to the puncture site are provided.
  • the first housing 11 of the puncture device 10 includes a first contact surface 10a.
  • the first contact surface 10a faces the second contact surface 20a of the measurement device 20 when connected to the measurement device 20.
  • the first contact surface 10a functions as a separation surface 101 of the component measuring device 100, and the state of contact with the second contact surface 20a of the measuring device 20 is maintained when the component measuring device 100 is not used.
  • the puncture device 10 is connected to the measuring device 20 to form the housing 110 of the component measuring device 100, the gap between the first housing 11 and the second housing 21 is eliminated as much as possible.
  • the sense of unity of the housing 110 can be enhanced. Therefore, it is preferable that the first contact surface 10a is formed so as not to have a portion protruding from the surface. Further, the first contact surface 10a can be configured so as not to have a convex portion protruding from the first contact surface 10a, so that the contact state with the second contact surface 20a can be stabilized.
  • the first housing 11 is provided with a first flat portion 11a made of a flat surface at least a part of the outer surface. Therefore, the puncture device 10 can prevent rolling that may occur when the puncture device 10 is placed on a mounting surface such as a table in a state of being separated from the measuring device 20.
  • the first flat portion 11a may be arranged at a part or a plurality of places on the outer surface other than the first contact surface 10a in the first housing 11. Further, when the first contact surface 10a is formed substantially flat, it may function as the first flat portion 11a.
  • the needle mounting portion 12 has a first opening 12a, and the puncture needle cartridge N is inserted and mounted.
  • the puncture needle cartridge N is a medical device for collecting blood provided with a puncture needle N2 that is retractably accommodated from a hole provided on the front end side of the needle holder N1.
  • the puncture needle cartridge N is used in contact with the puncture site. Examples of the puncture site include the surface of the user's body (skin, mucous membrane, etc.) such as the fingertip, palm, upper arm, abdomen, thigh, and earlobe. Therefore, the puncture needle cartridge N is considered to be single-use in order to prevent risks such as infectious diseases, and is removed from the puncture device 10 and discarded after use.
  • the puncture device 10 is used repeatedly.
  • the needle mounting portion 12 has a needle engaging portion 12b.
  • the rear end portion of the puncture needle cartridge N (the rear end portion of the needle holder N1) engages with the needle engaging portion 12b, so that the puncture needle cartridge N is held by the puncture device 10.
  • the needle engaging portion 12b holds the rear end portion of the hub of the puncture needle N2 in the puncture needle cartridge N so as to be able to move forward and backward along the axial direction.
  • the needle engaging portion 12b includes an elastic member (coil spring or the like) that can expand and contract along the axial direction, and based on the operation of the puncture operation portion 13, puncture in the puncture needle cartridge N by utilizing the urging force of the elastic member.
  • the needle N2 is moved forward and backward along the axial direction.
  • the needle mounting portion 12 includes a puncture spring for advancing the needle tip of the puncture needle N2 of the puncture needle cartridge N by a predetermined length (predetermined puncture depth), and a needle of the advanced puncture needle N2. It has a return spring as an elastic member for retracting the tip to the original position (standby position).
  • the puncture operation unit 13 is composed of a mechanical switch that causes the puncture needle cartridge N to perform a puncture operation.
  • the puncture operation unit 13 may be configured by a button-type switch mechanism for causing the puncture needle cartridge N to execute the puncture operation by using the pressing operation of the puncture operation unit 13 as a trigger.
  • the puncture operation unit 13 is preferably arranged in the first contact surface 10a region, for example, so as not to protrude from the outer surface of the housing 110 of the component measuring device 100 in the first housing 11. By arranging the puncture operation unit 13 on the first contact surface 10a, the operation surface is not exposed to the outer surface of the housing 110 when not in use, and the aesthetic appearance of the component measuring device 100 is not spoiled.
  • the needle eject operation unit 14 is operated when the used puncture needle cartridge N is removed from the puncture device 10.
  • the needle eject operation unit 14 may be composed of a lever member for the user to perform an eject operation by pressing along the major axis direction.
  • the needle eject operating unit 14 has a first operating body 14a formed along the outer shape of the first housing 11. That is, the first operating body 14a does not protrude from the outer shape of the first housing 11 when not in use.
  • the first operating body 14a is provided so as to be movable along the axial direction by a predetermined eject operation (pushing operation) by the user, and is provided via an engaging member (not shown) housed in the first housing 11. Remove the puncture needle cartridge N from the needle mounting portion 12.
  • the engaging member is a member that engages with the puncture needle cartridge N and moves in conjunction with the axial direction according to the amount of operation of the first operating body 14a.
  • the first operating body 14a is provided with an elastic member (coil spring or the like) (not shown), and when an eject operation is performed when the puncture needle cartridge N is removed, the first operating body 14a moves from the initial position to the eject position, and the puncture needle cartridge N is removed. After that, it moves to the initial position by the urging force of the elastic member.
  • the first connecting portion 15 is connected to the second connecting portion 24 to maintain the connected state of the puncture device 10 and the measuring device 20.
  • the first connecting portion 15 is configured by, for example, a first magnetic member 15a made of a magnetic material or a magnet.
  • the constituent material of the first connecting portion 15 can be appropriately selected according to the form of the second connecting portion 24. That is, when the second magnetic member 24a that functions as the second connecting portion 24 is made of a magnetic material, the first magnetic member 15a may be made of a magnet so that it can be connected to the second magnetic member 24a.
  • the first magnetic member 15a is composed of a magnetic material or a magnet having a magnetic pole different from that of the second magnetic member 24a so as to be connectable to the second magnetic member 24a. good.
  • the first connecting portion 15 is arranged inside the first housing 11 in the vicinity of the first contact surface 10a so as to face the second connecting portion 24 arranged on the second contact surface 20a of the measuring device 20. Will be done. As a result, when the puncture device 10 and the measurement device 20 are connected, the connected state of both devices is maintained without disturbing the contact state between the first contact surface 10a and the second contact surface 20a. Can be done.
  • the length at which the puncture needle N2 of the puncture needle cartridge N mounted on the needle mounting portion 12 advances is the depth adjusting portion 16.
  • the depth adjusting unit 16 adjusts the amount of advancement (puncture depth) of the puncture needle N2 of the puncture needle cartridge N.
  • the depth adjusting unit 16 adjusts the length at which the puncture needle N2 advances from the opening of the needle holder N1, that is, the puncture depth from the surface of the living body, according to the individual difference of the user who is the blood sampler and the puncture site. It is operated when you do.
  • the puncture depth (advancement amount of the puncture needle N2) by the depth adjusting unit 16 can be adjusted in multiple stages by an adjustment dial or the like.
  • the puncture device 10 is operated when the blood sampling device 10 is used to collect blood necessary for measuring the blood glucose level.
  • the puncture needle cartridge N is mounted on the needle mounting portion 12 by the user. At this time, the rear end portion of the puncture needle cartridge N engages with the needle engaging portion 12b. Subsequently, as shown in FIG. 6B, when the puncture operation unit 13 is operated by the user, the needle mounting unit 12 advances the needle tip of the puncture needle cartridge N to a predetermined advance position by the urging force of the puncture spring. .. As shown in FIG. 6C, when the operation of the puncture operation unit 13 is completed, the needle tip of the advanced puncture needle cartridge N is retracted to the original position (standby position) by the urging force of the return spring. In this way, in the puncture needle cartridge N mounted on the needle mounting portion 12, the puncture needle N2 reciprocates along the axial direction between the standby position and the advance position by operating the puncture operation portion 13. Puncture the user's predetermined biological surface.
  • the user presses the first operating body 14a along the axial direction to displace the engaging member inside the first housing 11 along the axial direction. It is moved to the side to release the engagement state between the needle mounting portion 12 (specifically, the needle engaging portion 12b) and the puncture needle cartridge N.
  • the puncture device 10 is in the state shown in FIG. 6E (that is, the state before use) by removing the puncture needle cartridge N after use from the puncture device 10 without the user touching it.
  • the puncture needle cartridge N is detached from the puncture device 10
  • the first operating body 14a returns from the eject position to the initial position before the operation due to the urging force of the elastic member.
  • the measuring device 20 is attached to the medium mounting portion 22 on which the disposable type inspection medium T is mounted and the medium mounting portion 22 in the second housing 21.
  • the medium eject operation unit 23, which is operated when the used inspection medium T is removed, and the second connection unit 24 for maintaining the connection state with the puncture device 10 are provided.
  • the measuring device 20 communicates with the measuring unit 31, the temperature detecting unit 32, and the device detecting unit 33 as a control system in order to execute various processes related to the measurement of the amount of components in the body fluid. It includes a unit 34, a notification unit 35, a display unit 36, a power supply unit 37, a storage unit 38, and a control unit 39.
  • the second housing 21 of the measuring device 20 has a second contact surface 20a facing the first contact surface 10a of the puncture device 10 when connected to the puncture device 10. .
  • the second contact surface 20a functions as a separation surface 101 of the component measuring device 100, and the state of contact with the first contact surface 10a of the puncture device 10 is maintained when the component measuring device 100 is not used.
  • the second contact surface 20a is formed so as not to have a portion protruding from the surface, like the first contact surface 10a.
  • the second contact surface 20a is formed so as not to have a convex shape on the surface, the contact state with the first contact surface 10a can be stabilized, and the second contact surface 20a is formed on the outer surface of the housing 110.
  • the gap to be obtained can be eliminated as much as possible.
  • the second housing 21 is provided with a second flat portion 21a made of a flat surface at least a part of the outer surface. Therefore, the measuring device 20 can prevent rolling that may occur when the measuring device 20 is placed on a mounting surface such as a table in a state of being separated from the puncturing device 10.
  • the second flat portion 21a may be arranged at a part or a plurality of places on the outer surface other than the second contact surface 20a in the second housing 21. Further, when the second contact surface 20a is formed substantially flat, it may function as the second flat portion 21a. Alternatively, two second flat portions 21a may be provided and arranged as a pair of surfaces facing each other.
  • the second flat portion 21a is preferably arranged on the same surface as the first flat portion 11a in the housing 110. That is, the first flat portion 11a and the second flat portion 21a form one surface of the housing 110. By arranging the first flat portion 11a and the second flat portion 21a on the same surface of the housing 110, both flat portions function as mounting surfaces and the mounting stability of the component measuring device 100 can be improved. ..
  • the medium mounting portion 22 has a second opening 22a, and the inspection medium T is inserted into the medium mounting portion 22.
  • the inspection medium T is, for example, a disposable type test strip having an inspection unit T1 (see FIG. 8D) having a predetermined reagent at the front end, and is discarded after measurement.
  • the inspection unit T1 holds a reagent (coloring reagent) that specifically reacts with the substance to be measured in blood.
  • the reagent may be held on a carrier such as a porous membrane capable of absorbing blood. By reacting with the reagent, blood develops a color with a color concentration corresponding to the amount of glucose contained in the blood.
  • the opening shape of the second opening 22a may be formed according to the shape (cross-sectional shape) of the inspection medium T to be mounted.
  • the opening shape of the second opening 22a is set according to the shape of the inspection medium T to be mounted. Therefore, when the inspection medium T is not a plate shape like a test strip but a substantially columnar chip, the second opening 22a has a shape to which the chip can be mounted.
  • the medium mounting portion 22 holds the mounted inspection medium T, and also holds the medium holding portion (not shown) for advancing the rear end portion of the inspection medium T from the second opening 22a at the time of removal. ) Is provided.
  • the medium holding portion is provided so as to be movable along the axial direction inside the second housing 21 of the measuring device 20.
  • the medium holding portion is a position (measurement position) in which at least a part (particularly near the tip portion) of the inspection medium T is held and measured in the second housing 21 and a position (eject position) in which the inspection medium T is removed. ) And move along the axial direction.
  • the medium holding unit holds the inspection medium T inserted from the second opening 22a, and when the medium eject operation unit 23 is operated after the measurement is completed, the medium holding unit holds the inspection medium T and is far away in the long axis direction. Move toward the end side. Since the inspection medium T is extruded from the second opening 22a of the second housing 21 by a predetermined length, the inspection medium T after measurement can be removed from the measurement device 20 without being touched by the user. ..
  • the amount of extrusion of the inspection medium T by the medium holding unit (corresponding to the operation amount of the medium eject operation unit 23) is the size of the second housing 21, the length of the inspection medium T in the longitudinal direction, and the second required for gripping. Although it is appropriately determined by the amount of protrusion (exposed length) from the opening 22a, it is preferable that the inspection medium T is at least long enough to be detached from the second opening 22a.
  • the medium eject operation unit 23 is operated when the used inspection medium T is removed from the measuring device 20.
  • the medium eject operation unit 23 may be composed of a lever member provided so that the user can move along the axial direction.
  • the medium eject operation unit 23 has a second operation body 23a formed along the outer shape of the second housing 21 and operated by the user.
  • the second operating body 23a is provided so as to be movable along the axial direction by a predetermined eject operation (pressing operation) by the user, and is engaged with the medium holding portion in the second housing 21.
  • the medium holding portion moves toward the front end side in the long axis direction in the second housing 21 as the second operating body 23a moves in the long axis direction.
  • the inspection medium T held in the medium holding portion gradually increases in the amount of protrusion (exposure amount) from the second opening 22a as the second operating body 23a moves.
  • the inspection medium T is separated from the measuring device 20.
  • the medium holding portion moves toward the rear end side in the axial direction as the second operating body 23a moves. And return to the original position (measurement position).
  • the return operation of the second operating body 23a may be performed manually by the user, or may be moved by the urging force of an elastic member (coil spring or the like) (not shown).
  • the second connecting portion 24 brings the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measuring device 20 into contact with each other to maintain the connected state.
  • the second connecting portion 24 is configured by, for example, a second magnetic member 24a made of a magnetic material or a magnet.
  • the constituent material of the second connecting portion 24 may be appropriately selected according to the form of the first connecting portion 15. That is, when the first magnetic member 15a is made of a magnetic material, the second magnetic member 24a may be made of a magnet so that it can be connected to the first magnetic member 15a.
  • the second magnetic member 24a is composed of a magnetic material or a magnet having a magnetic pole different from that of the first magnetic member 15a so that the first magnetic member 15a can be connected to the first magnetic member 15a. good.
  • the second connecting portion 24 is arranged inside the second housing 21 in the vicinity of the second contact surface 20a so as to face the first connecting portion 15 arranged on the first contact surface 10a of the puncture device 10. Will be done. As a result, when the puncture device 10 and the measurement device 20 are connected, the connected state of both devices is maintained without disturbing the contact state between the first contact surface 10a and the second contact surface 20a. Can be done.
  • the measuring unit 31 measures the amount of the component of the body fluid to be measured.
  • the measuring unit 31 optically measures the amount of the glucose component component in the blood.
  • the measuring unit 31 has a light emitting element and a light receiving element (not shown), and is an optical system measuring device that irradiates the blood spread in the inspection unit T1 with the irradiation light from the light emitting element and detects the transmitted light by the light receiving element. It is configured.
  • the measurement unit 31 is arranged in the second housing 21 at a position where the inspection medium T held at the measurement position by the medium holding unit can be inspected (for example, above the inspection unit T1 at the measurement position).
  • the measuring unit 31 intermittently emits light of a single or a plurality of predetermined wavelengths from the light emitting element, receives the light transmitted through the inspection unit T1 by the light receiving element, and outputs an electric signal proportional to the amount of the received light.
  • the control unit 39 captures the electric signal as a digitized measured value. Since this measured value changes depending on the state, it is a data series for each wavelength.
  • the inspection medium T is mounted on the medium mounting unit 22 by the operation of the user.
  • the measuring unit 31 detects that the inspection medium T has been mounted on the medium mounting unit 22 by acquiring a change in the amount of light before and after mounting the inspection medium T in the measuring device 20, and via the control unit 39. Then, the notification unit 35 and the display unit 36 of the device are notified and displayed to urge the user to instill blood.
  • the user applies 0.5 to 10 ⁇ L of blood obtained by the puncture device 10 to the spotting port T2 at the distal end of the test medium T.
  • blood is introduced along a capillary channel (not shown) provided inside the test medium T, it is mixed with a reagent and the reaction with glucose proceeds.
  • the color is developed in an amount corresponding to the glucose level in the blood.
  • the inspection unit T1 is in a position corresponding to the measurement unit 31 when the inspection medium T is attached to the measurement device 20.
  • the blood mixed with the reagent spreads along the capillary tract and reaches the examination unit T1.
  • the inspection medium T may have an air vent hole (not shown) for promoting blood introduction into the capillary passage, and the air vent hole is provided at the end opposite to the spotting port T2 in the capillary passage. It will be provided.
  • the measurement unit 31 emits light having a predetermined wavelength from the light emitting element and the reagent corresponding to the glucose value in the blood.
  • the reagent reaction amount based on the reaction is measured from the amount of light transmitted through the inspection unit T1.
  • the inspection unit T1 is transmitted until the blood mixed with the reagent flows into the inspection unit T1 from the state where there is no sample and the reaction proceeds.
  • a time-series electric signal corresponding to the amount of light is output, and the control unit 39 captures it as a data series of measured values.
  • the control unit 39 detects that blood mixed with the reagent has flowed in from a state where there is no sample (blood) in the inspection unit T1, and the measurement process is started using this as a trigger.
  • the measurement end is processed when the control unit 39 determines from the passage of a predetermined time or the passage of the measured value (for example, when the change of the measured value reaches the plateau). From the start of measurement to the end of measurement
  • the control unit 39 notifies and displays the notification unit 35 and the display unit 36 of the device from the start of measurement to the end of measurement.
  • the measuring unit 31 is configured to perform measurement by a colorimetric method that optically detects the blood glucose level in blood
  • other measuring methods can also be applied.
  • a method for measuring the blood glucose level for example, an enzyme electrode method in which a reagent is applied around an electrode to detect an electrical change accompanying a reaction between the reagent and blood, that is, a current generated between a detection electrode and a counter electrode is used.
  • a current generated between a detection electrode and a counter electrode is used.
  • the measuring unit 31 since the measuring unit 31 only needs to be able to measure the amount of the component in the body fluid to be measured, it is possible to appropriately change the device configuration according to the component to be measured.
  • the temperature detection unit 32 is composed of a known thermometer that measures the environmental temperature at the time of measurement.
  • the temperature detection unit 32 outputs a temperature value based on the measured environmental temperature to the control unit 39.
  • the device detection unit 33 is in a state where the puncture device 10 is connected or separated from the measuring device 20, that is, a state in which the puncturing device 10 is connected to the measuring device 20 (when the component measuring device 100 is not used, the first contact surface 10a is used. And the second contact surface 20a are in contact with each other and connected to each other) and the separated state of the puncture device 10 (when the component measuring device 100 is used, the first contact surface 10a and the second contact surface 20a are separated from each other). State) is detected.
  • the device detection unit 33 can adopt a method corresponding to the method of connecting the puncture device 10 and the measurement device 20 as a method of detecting the attachment / detachment state of both.
  • the puncture device 10 and the measuring device 20 are magnetically connected. Therefore, the device detection unit 33 may be configured by, for example, a magnetic sensor using a Hall element or the like that can detect the presence or absence of a magnetically connected state.
  • the device detection unit 33 punctures a state in which the first contact surface 10a and the second contact surface 20a are in contact with each other and the puncture device 10 is connected, and the first contact surface 10a and the second contact surface 20a are separated from each other. The separated state of the device 10 is magnetically detected.
  • the device detection unit 33 outputs the detected state information (connection state information, separation state information) indicating the detected connection state or separation state to the control unit 39.
  • the device detection unit 33 since the device detection unit 33 only needs to have a configuration capable of detecting the connection and separation state (detachment state) of the puncture device 10 with respect to the measurement device 20, the method of detecting the attachment / detachment state of both is limited to the above configuration. Not done.
  • the communication unit 34 is wired or connected to another device (for example, an external server of a medical facility, various mobile terminals owned by a doctor in charge, etc.) connected via a communication network according to a predetermined protocol. It is a network interface that controls wireless communication (including short-range wireless communication).
  • the communication unit 34 transmits transmission data including a measured value indicating the measured component amount (blood glucose level) to the communication destination.
  • the notification unit 35 is composed of a notification device such as a speaker that outputs a notification sound such as a voice or a buzzer, a light emitting device that lights or blinks in various colors, a vibrator that generates a predetermined vibration, and the like. (For example, the start or end of a predetermined operation, a warning when an error occurs, a procedure guide, etc.) are notified to the user in an identifiable manner. Further, the notification unit 35, under the control of the control unit 39, performs notification from the medium mounting unit 22 to prompt the removal of the inspection medium T, notification to prompt the connection between the puncture device 10 and the measurement device 20, and the like. This prevents the user from forgetting to remove the inspection medium T or misplaceing the component measuring device 100.
  • a notification device such as a speaker that outputs a notification sound such as a voice or a buzzer, a light emitting device that lights or blinks in various colors, a vibrator that generates a predetermined vibration, and the like.
  • the display unit 36 is composed of a display device such as an LCD (Liquid Crystal Display), an OLED (Organic Light Emitting Diode), or a micro LED (Micro Light Emitting Diode) display, and the display content is visible to the user (characters). , Numbers, figures, and other symbols).
  • the display unit 36 displays, for example, the amount of components in the body fluid measured by the measurement unit 31 (specifically, the value calculated by the calculation unit 39b of the control unit 39), and the notification content required for operation. It also displays (guidance display, measurement start / end display, etc.).
  • the display content (display data) displayed on the display surface 36a of the display unit 36 is output from the control unit 39.
  • the display surface 36a of the display unit 36 is arranged on the second contact surface 20a. Therefore, in the component measuring device 100, the display surface 36a is not exposed to the outside of the housing 110 when not in use. For this reason, the design is improved and it becomes difficult for the surroundings to recognize it as a medical device. It is suitable when the user wants to make it difficult for others to notice that he / she is carrying a glucose meter.
  • the power supply unit 37 is housed in the second housing 21, and stores and mounts the battery that is the power source of the component measuring device 100.
  • the battery is preferably a small battery such as a button battery in consideration of the portability of the component measuring device 100.
  • the battery used in the power supply unit 37 may be either a primary battery or a secondary battery. Further, the power supply unit 37 may use a physical battery such as a solar cell in combination with a chemical battery such as a button battery. Further, the power supply unit 37 may be provided with a function capable of supplying power or charging by connecting to an external power source (commercial power source or the like) by wire or wirelessly.
  • the power supply unit 37 is a unit (measurement unit 31, temperature detection unit 32, communication unit 34, notification unit 35, display unit 36) that constitutes the measurement device 20 based on the separated state and the connected state of the puncture device 10 and the measuring device 20. , The amount of power supplied to the circuits of the storage unit 38 and the control unit 39) can be changed, which contributes to power saving.
  • the storage unit 38 is a measuring device 20 such as various control programs necessary for driving the measuring device 20, data transmitted to a communication destination including the measured values measured by the measuring unit 31, and past values related to measurements for a predetermined period. It is composed of a known storage medium for storing various data used.
  • the control unit 39 is composed of various processors including, for example, a CPU (Central Processing Unit), a ROM (Read only memory), a RAM (Random Access Memory), and the like.
  • the control unit 39 controls each unit constituting the measurement device 20 in an integrated manner while activating a predetermined processing program to execute a predetermined processing.
  • the control unit 39 includes, for example, a time measuring unit 39a composed of an RTC (Real-Time Clock), and measures the time according to a reference clock having a predetermined cycle supplied from a clock unit (not shown).
  • the time clock by the time measuring unit 39a is used for generating the date and time when the measurement was performed and for measuring from the start of the measurement to the end of the measurement.
  • control unit 39 calculates the component amount (blood glucose level) of the component in the body fluid to be measured based on the detection value (color concentration and light amount in the case of the specific color type) detected by the measurement unit 31.
  • a calculation unit 39b is provided.
  • the calculation unit 39b has a function of appropriately performing correction processing in consideration of measured value fluctuation factors such as the environmental temperature (temperature value by the temperature detection unit 32) at the time of calculation processing. As a result, the calculation unit 39b can obtain a value closer to the true value with less measurement error. The calculation unit 39b outputs the calculated measured value to the display unit 36.
  • control unit 39 controls ON / OFF of power supply to each unit by the power supply unit 37 based on the state information from the device detection unit 33.
  • the control unit 39 outputs a control signal for stopping the power supply to the power supply unit 37.
  • the power of the measuring device 20 is turned off.
  • the control unit 39 outputs a control signal for starting the power supply to the power supply unit 37. As a result, the measuring device 20 is turned on and becomes an idle state.
  • control unit 39 outputs a control signal to the measurement unit 31 when the power is turned on and becomes an idle state. Using this control signal as a trigger, the measuring unit 31 starts controlling light emission / reception and outputting an electric signal proportional to the amount of light. The control unit 39 starts a process of capturing an electric signal as a digitized measured value. This control continues intermittently until the device detection unit 33 detects the connection between the puncture device 10 and the measurement device 20 and the power is turned off.
  • control unit 39 includes a determination unit 39c that makes a predetermined determination (determination of connection of the puncture device 10, determination of attachment of the inspection medium T, determination of measurement start / end).
  • the control unit 39 takes in as a data series of measured values according to the amount of transmitted light of the inspection unit T1 from the measurement unit 31 that continues the intermittent measurement.
  • the determination unit 39c detects that blood has flowed in from the state where there is no blood in the examination unit T1, it determines that the measurement has started, and starts the measurement process using this as a trigger.
  • the judgment unit 39c Judges that the measurement is completed.
  • the control unit 39 displays the value calculated by the calculation unit 39b on the display unit 36, and notifies the notification unit 35 of the end of the measurement.
  • the determination unit 39c observes the signal from the measurement unit 31 and determines whether or not the inspection medium T mounted on the medium mounting unit 22 has been removed within a predetermined time (for example, several minutes).
  • a predetermined time for example, several minutes.
  • the determination unit 39c causes the notification unit 35 to execute a notification prompting the user to remove the inspection medium T.
  • the determination of the inspection medium T by the determination unit 39c may be determined, for example, depending on whether or not the medium eject operation unit 23 is operated.
  • the inspection medium T is attached to the measurement unit 31 by comparing the blank signal acquired by the measurement unit 31 before the measurement value acquisition with the signal acquired by the measurement unit 31 after a predetermined time has elapsed from the measurement value acquisition. You may decide whether or not it is.
  • the test medium T usually has an air vent hole at the distal end of the capillary tract to facilitate the introduction of blood. If the blood is left for a long time with the blood introduced into the capillary channel in the test medium T, the blood may seep out of the test medium T through the air vent holes. Therefore, it is preferable to remove the inspection medium T from the measuring device 20 within a predetermined time from the measurement.
  • the determination unit 39c determines whether the puncture device 10 and the measurement device 20 are connected within a predetermined time (for example, several minutes) after the inspection medium T is removed based on the state information from the device detection unit 33. Make a judgment.
  • the determination unit 39c determines that the puncture device 10 is not connected within a predetermined time from the acquisition of the measured value (that is, when the connection state information is waiting to be input)
  • the determination unit 39c measures the puncture device 10 with the user.
  • the notification unit 35 is made to execute the notification for prompting the connection with the device 20. As a result, the user can prevent forgetting to connect the puncture device 10 after the measurement is completed.
  • control unit 39 processes and generates transmission data in which the measurement value calculated by the calculation unit 39b is associated with the measurement condition information (temperature information indicating the environmental temperature, the measurement time required for the measurement, etc.). It is provided with a generation processing unit 39d that performs a process of storing the transmitted data in the storage unit 38 and a process of controlling the transmission of the transmitted data toward the communication destination via the communication unit 34.
  • timekeeping unit 39a, the calculation unit 39b, and the generation processing unit 39d are all described as being included in the control unit 39, they may be configured separately from the control unit 39, respectively. Some of them may be included in the control unit 39.
  • control unit 39 when the control unit 39 is in a state where measurement by the measurement unit 31 is possible (a state in which the puncture device 10 is separated from the measurement device 20) and the inspection medium T is not attached within a predetermined time, the user It is also possible to control the notification unit 35 so as to notify the user to attach the inspection medium T. Further, the control unit 39 may be configured to interrupt the measurement process when an unexpected situation such as the puncture device 10 being attached to the measurement device 20 occurs during measurement or the like. At that time, the control unit 39 may cause the notification unit 35 to execute notification indicating a measurement error.
  • the measuring device 20 is operated when measuring the blood glucose level in the blood collected by using the puncture device 10.
  • the inspection medium T is inserted from the second opening 22a by the user and mounted on the medium mounting portion 22.
  • the blood collected by the puncture device 10 is introduced into the inspection unit T1 of the inspection medium T through the opening of the instillation port T2 through the capillary passage of the inspection medium T.
  • the measuring device 20 starts measuring the mounted inspection medium T.
  • the measurement result (measured value) by the measuring unit 31 is displayed on the display unit 36.
  • the user presses the second operation body 23a of the medium eject operation unit 23 along the long axis direction of the component measuring device 100 by the eject operation, and the inside of the second housing 21
  • the medium holding portion on the side is moved along the long axis direction from the measurement position to the eject position.
  • the inspection medium T is pushed out from the second opening 22a and removed.
  • the second operating body 23a moves to the position (initial position) before the operation. Further, as the second operating body 23a moves, the medium holding portion also moves toward the base end side in the long axis direction and returns to the original position (measurement position).
  • the user when using the component measuring device 100 according to the present embodiment, as a first process, the user separates the puncture device 10 and the measuring device 20 (S1), and powers the measuring device 20. Turn it on (S2).
  • step S1 when the control unit 39 inputs the separation state information indicating that the puncture device 10 has been separated from the measurement device 20, the control unit 39 outputs a control signal for starting the power supply to the power supply unit 37. As a result, the power of the measuring device 20 is turned on and the measuring device 20 is in an idle state.
  • control unit 39 determines whether or not the inspection medium T is mounted on the medium mounting unit 22 (S3).
  • step S3 when the control unit 39 determines that the test medium T is mounted on the medium mounting unit 22 (S3-Yes), the control unit 39 ends the mounting detection process of the test medium T and waits for the detection of blood instillation. Start. On the other hand, when the control unit 39 determines that the inspection medium T is not mounted on the medium mounting unit 22 (S3-No), the control unit 39 displays a display prompting the user to mount the inspection medium T (S4). , The processing of step S3 and step S4 is looped until the inspection medium T is attached.
  • control unit 39 observes the signal from the measurement unit 31 and determines whether or not the blood mixed with the reagent has flowed in from the state where the test medium T has no sample (S5).
  • step S5 when the control unit 39 observes the signal from the measurement unit 31 and detects that the blood mixed with the reagent has flowed in from the state where the test medium T has no sample (S5-Yes), the measurement is performed. It is determined to start, and the measurement process is started using this as a trigger (S7). On the other hand, when the inflow of blood mixed with the reagent cannot be detected (S5-No), the control unit 39 displays a display prompting the user to instill blood (S6), and the instillation of blood is confirmed. The process of step S5 and step S6 is looped until the result is reached.
  • control unit 39 starts the measurement (S7), and determines whether or not the reaction is completed by the follow-up observation of the predetermined time by the timing unit 39a or the follow-up observation of the data series of the measured values by the judgment unit 39c. (S8).
  • the determination unit 39c determines that the measurement is completed, and proceeds to the measurement end process (S10). On the other hand, if the reaction is not completed (S8-No), the measurement state is continued (S9), and the process returns to step S8 again.
  • control unit 39 displays the value calculated by the calculation unit 39b on the display unit 36, stores the measurement result and the measurement date and time in the storage unit 38, and notifies the notification unit 35 of the end of the measurement. S10).
  • control unit 39 observes the signal from the measurement unit 31 and determines whether or not the inspection medium T mounted on the medium mounting unit 22 has been removed within a predetermined time (for example, several minutes). (S11).
  • step S11 when the control unit 39 determines that the inspection medium T has been removed from the medium mounting unit 22 within a predetermined time (S11-Yes), the control unit 39 determines whether or not the puncture device 10 is connected to the measurement device 20. (S13). On the other hand, when the control unit 39 determines that the inspection medium T has not been removed from the medium mounting unit 22 within a predetermined time (S11-No), the control unit 39 transfers the inspection medium T from the medium mounting unit 22 to the user. The notification unit 35 is controlled so as to notify the user to remove it, and the display of the measured value is continued (S12). After that, the control unit 39 loops the processes of steps S11 and S12 until the inspection medium T is removed.
  • step S13 when the control unit 39 determines that the puncture device 10 is connected within a predetermined time (S13-Yes), the control unit 39 outputs a control signal for stopping the power supply to the power supply unit 37 (S15), and ends the process. do. As a result, the power of the measuring device 20 is turned off, and the process ends.
  • the control unit 39 determines that the puncture device 10 is not connected within a predetermined time (S13-No)
  • the control unit 39 notifies the user to notify the user to prompt the connection with the puncture device 10.
  • the unit 35 is controlled (S14). After that, the control unit 39 loops the processes of steps S13 and S14 until the puncture device 10 is connected.
  • the component measuring device 100a of the modified example shown below has a different connection form between the puncture device 10 and the measuring device 20 from the above-mentioned form.
  • FIG. 10A shows the configuration of the puncture device 10 as a modified example
  • FIG. 10B shows the configuration of the measuring device 20 as a modified example.
  • the first contact surface 10a of the puncture device 10 is fitted with the measurement device 20 when it is connected to the measurement device 20, so that the first engagement portion functions as the first connection portion 15. 15b is provided.
  • the second contact surface 20a of the measuring device 20 is fitted with the puncturing device 10 when connected to the puncturing device 10, so that the second engaging portion functions as the second connecting portion 24. 24b is provided.
  • the first engaging portion 15b and the second engaging portion 24b form a connecting mechanism composed of members (concave grooves, ridge members) that are fitted to each other.
  • the puncture device 10 and the measurement device 20 have a first engagement portion by sliding at least one device along the axial direction in a state where the first contact surface 10a and the second contact surface 20a are butted against each other.
  • the 15b and the second engaging portion 24b are fitted and connected.
  • the first engaging portion 15b is composed of a pair of concave grooves extending in the axial direction along the longitudinal peripheral edge of the first contact surface 10a.
  • the second engaging portion 24b extends axially along the longitudinal peripheral edge of the second contact surface 20a and protrudes outward from the second contact surface 20a as a pair of protrusions. It consists of strip members. Both the ridge member and the concave groove have the same continuous cross-sectional shape in the axial direction.
  • the ridge member and the concave groove each have a cross-sectional shape having substantially the same shape so that they can be fitted to each other.
  • the first engaging portion 15b is composed of a concave groove and the second engaging portion 24b is composed of a convex member, but the first engaging portion 15b is a convex member.
  • the second engaging portion 24b may be a concave groove.
  • the puncture device 10 is in contact with the first contact surface 10a and the second contact surface 20a, and is slidably moved along the axial direction with the first engaging portion 15b.
  • the second engaging portion 24b By fitting the second engaging portion 24b, it is connected to the measuring device 20.
  • the engagement between the second engaging portion 24b and the first engaging portion 15b provided in the second housing 21 is performed by a predetermined operation (for example, a slide operation). It will be released.
  • the puncture device 10 can be separated from the measurement device 20 by sliding and moving the puncture device 10 in the direction opposite to that at the time of connection in this released state.
  • the first engaging portion 15b and the second engaging portion 24b may be configured such that at least the puncture device 10 and the measuring device 20 can be detachably connected to each other. Therefore, the first engaging portion 15b and the second engaging portion 24b are not limited to the ridge members and the concave grooves that are attached and detached by the slide movement as shown in FIGS. 10A and 10B.
  • the device detection unit 33 is configured to detect the separated state of the puncture device 10 and the measuring device 20 and the connected state by fitting.
  • the device detection unit 33 has a detection piece that moves in a predetermined direction by sliding movement when the puncture device 10 is fitted, and a detection piece in a state where the puncture device 10 is normally fitted to the measurement device 20. It may be a detection mechanism having a detection unit (detection circuit) for electrically detecting the moving position of the above.
  • the device detection unit 33 detects the connection state and the separation state with the puncture device 10 by detecting that the detection piece has moved to a predetermined position, and the state according to the connection state or the separation state between the devices.
  • the information is output to the control unit 39.
  • the configuration of the device detection unit 33 is not limited as long as it has a function of detecting the connection between the puncture device 10 and the measurement device 20.
  • FIG. 12 shows an example of a connection operation between the puncture device 10 and the measurement device 20 in the component measuring device 100a of the modified example.
  • FIG. 12A shows a state in which the measurement by the measuring device 20 is completed and before the puncture device 10 is connected to the measuring device 20.
  • FIG. 12B when the puncture device 10 and the measurement device 20 are connected, the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 face each other.
  • the engaging portion 15b is inserted into the second engaging portion 24b.
  • the puncture device 10 is slid and moved along the axial direction so that the front end portion of the puncture device 10 and the front end portion of the measurement device 20 are parallel to each other in the direction intersecting the axial direction.
  • slide movement for example, one device may be fixed and the other device may be slid.
  • the first engaging portion 15b and the second engaging portion 24b are fitted to each other, and the first contact surface 10a and the second contact surface 20a are in contact with each other.
  • the puncture device 10 and the measurement device 20 are connected.
  • the component measuring device 100 has a piercing device 10 configured to puncture the surface of the living body and exude blood, and the blood exuded from the surface of the living body is contained in the test medium T.
  • a measuring device 20 configured to measure the amount of glucose component (blood glucose level) contained in blood by introducing the puncturing device 10 is provided, and the puncturing device 10 includes a first housing 11 and a first housing 11.
  • the measuring device 20 has a first contact surface 10a and a first connecting portion 15 provided on at least one of the outer surfaces of the above, and the measuring device 20 is a second housing 21 and a second housing 21.
  • the puncture device 10 and the measuring device 20 are in a state where the first contact surface 10a and the second contact surface 20a face each other and are in contact with each other, and the first connecting portion 15 and the second connecting portion are in contact with each other.
  • the first housing 11 and the second housing 21 are integrated to form the housing 110 of the component measuring device 100, and the first connecting portion 15 and the second connecting portion are connected.
  • the first contact surface 10a and the second contact surface 20a become the separation surface 101, and the puncture device 10 and the measurement device 20 are configured to be separate bodies.
  • the housing 11 and the second housing 21 do not have a portion protruding from the outer surface of the housing 110 in the region to be the outer surface of the housing 110.
  • the component measuring device 100 can be attached and detached in a state where the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 are butted against each other when not in use. Since the housing 110 is formed when they are connected and integrated, the device is excellent in portability and design. When the puncture device 10 and the measuring device 20 are integrated, the outer surface of the housing 110 of the component measuring device 100 has no convex shape. Therefore, the component measuring device 100 is prevented from being caught by other parts when being carried, and is difficult to be recognized as a medical device from the surroundings, so that the portability and design are improved. Further, since the component measuring device 100 can separate the puncture device 10 and the measuring device 20 at the time of use, each device can be used separately and the operability is good.
  • the first housing 11 preferably, when the first housing 11 abuts the first contact surface 10a and the second contact surface 20a via the separation surface 101, the first housing 11 is brought into contact with the first contact surface 10a. , May be configured to be connected complementarily to each other and integrated.
  • the device has excellent portability and design.
  • the outer shape of the first contact surface 10a may preferably have the same shape as the outer shape of the second contact surface 20a.
  • the first connecting portion 15 is a first magnetic member provided inside the first housing 11 facing the first contact surface 10a.
  • the second connecting portion 24 is a second magnetic member 24a provided inside the second housing 21 facing the second contact surface 20a, and is the first magnetic member 15a and the second magnetic member.
  • One of the members 24a may be made of a magnet, and the other may be made of a magnet or a magnetic material having a magnetic pole different from that of the magnet.
  • the puncture device 10 and the measurement device 20 can be magnetically connected to the first connecting portion 15 made of the first magnetic member 15a and the second connecting portion 24 made of the second magnetic member 24a, both devices can be connected.
  • the configuration to be connected is not complicated, and it can be easily separated even during use.
  • the first connecting portion 15 is a first engaging portion 15b provided on the first contact surface 10a
  • the second connecting portion 24 is a second connecting portion 24. It may be a second engaging portion 24b provided on the second contact surface 20a and fitted to the first engaging portion 15b by sliding movement along the axial direction.
  • the puncture device 10 and the measuring device 20 have a connecting structure including a first connecting portion 15 including a first engaging portion 15b and a second connecting portion 24 composed of a second engaging portion 24b, both devices are connected or connected.
  • separating at least one device can be connected and separated by a simple operation of sliding along the axial direction.
  • the measuring device 20 is a display unit 36 that displays a blood measurement result (blood glucose level) on a display surface 36a arranged on the second contact surface 20a. It may be configured with.
  • the display surface 36a is not exposed on the outer surface of the housing 110, so that medical treatment is performed from the surroundings. It becomes difficult to be recognized as an instrument.
  • the first housing and the second housing may preferably have a configuration in which a flat surface is formed at least partially.
  • each device when both devices are placed on a mounting surface such as a table with the puncture device 10 and the measuring device 20 separated, each device may have rolling that may occur when the device is placed on the mounting surface. Be prevented.
  • the measuring device 20 has a power supply unit 37 that controls the supply of driving power to the measuring device 20, and a separated state between the puncturing device 10 and the measuring device 20.
  • the configuration may include a device detection unit 33 that detects the connected state, and a control unit 39 that controls the power supply unit 37 and changes the drive power to be supplied based on the detection result by the device detection unit 33.
  • the component measuring device 100 can change the amount of electric power supplied based on the separated state and the connected state of the puncture device 10 and the measuring device 20, so that power saving can be achieved.
  • the measuring device 20 includes a measuring unit 31 for measuring the component amount of the glucose component contained in blood and a notifying unit 35 for performing predetermined notification.
  • the control unit 39 determines that the inspection medium T has not been removed within a predetermined time after the measurement by the measurement unit 31 is completed, the control unit 39 causes the notification unit 35 to execute a notification prompting the removal of the inspection medium T. It may be configured as.
  • the component measuring device 100 can make the user recognize that the inspection medium T has not been removed after the measurement of the measuring unit 31 is completed, so that the inspection medium T is forgotten to be removed. Can be prevented.
  • the control unit 39 is a puncture device within a predetermined time based on the detection result by the device detection unit 33 after the inspection medium T is removed.
  • the notification unit 35 may be configured to execute a notification prompting the connection between the puncture device 10 and the measuring device 20.
  • the puncture device 10 and the measuring device 20 are separable at the time of use, and both are miniaturized devices, so that it is easy to misplace them somewhere after use. ..
  • the component measuring device 100 gives a notification prompting the connection between the puncturing device 10 and the measuring device 20 at a predetermined timing after the blood component measuring process is completed, it is necessary to prevent the puncturing device 10 and the measuring device 20 from being misplaced. Can be done.
  • the body fluid is preferably the blood of the user, and the component may be a glucose component contained in the blood.
  • the component measuring device 100 is excellent in portability and goes out by being adopted in a blood glucose self-measuring device (SMBG device) that measures a blood glucose level based on the amount of glucose component contained in the user's blood as a component to be measured, for example. It can be a device that is difficult to be recognized as a medical device in the future.
  • SMBG device blood glucose self-measuring device
  • Puncture device (10a first contact surface), 11 First housing (11a first flat portion), 12 needle mounting part (12a opening, 12b needle engaging part), 13 Puncture operation part, 14-needle eject operation unit (14a first operation unit), 15 First connecting portion (15a first magnetic member, 15b first engaging portion), 16 Depth adjustment unit, 20 Measuring device (20a second contact surface), 21 Second housing (21a second flat part), 22 Medium mounting portion (22a second opening), 23 Medium eject operation unit (23a second operation unit), 24 Second connecting portion (24a second magnetic member, 24b second engaging portion), 31 Measuring unit, 32 Temperature detector, 33 Device detector, 34 Communication Department, 35 Notification unit, 36 display unit (36a display surface), 37 Power supply, 38 Memory 39 Control unit (39a timekeeping unit, 39b calculation unit, 39c judgment unit, 39d generation processing unit), 100, 100a component measuring device (101 separation surface, 102 separation cross-section end, 110 housing), N puncture needle cartridge (N1 needle holder, N2 puncture needle), T inspection medium (

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  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Abstract

A component measurement apparatus (100) comprising a puncture device (10) configured so as to puncture a living body surface and cause a body fluid to exude therefrom, and a measurement device (20) configured so as to measure the quantity of a prescribed component included in the body fluid using an examination medium (T) into which the body fluid can be introduced, the component measurement apparatus (100) being configured such that when the apparatus is not in use, when a first connecting part (15) and a second connecting part (24) are connected in a state in which a first contacting surface (10a) of the puncture device (10) and a second contacting surface (20a) of the measurement device (20) are butted against each other, and the puncture device (10) and the measurement device (20) are integrated, a casing (110) of the component measurement apparatus (100) is formed by a first casing (11) and a second casing (21), and when the apparatus is in use, the puncture device (10) and the measurement device (20) can be separated by disconnection of the first connecting part (15) and the second connecting part (24).

Description

成分測定装置Component measuring device
 本発明は、血液などの体液中の成分を測定する成分測定装置に関するものである。 The present invention relates to a component measuring device for measuring components in body fluid such as blood.
 血液などの体液中の成分を測定する成分測定装置として、例えば下記特許文献1に開示されるような血糖値を測定する技術が知られている。 As a component measuring device for measuring components in body fluids such as blood, for example, a technique for measuring a blood glucose level as disclosed in Patent Document 1 below is known.
 下記特許文献1のシステムを用いて血糖値測定を行う場合、使用者は、最初に試薬を有する検査用媒体(テストストリップ)を計器に装着させる。続いて、使用者は、付属する穿刺デバイスを用いて手指などの皮膚を穿刺し、その皮膚から滲出した少量の血液を、テストストリップの検査部(サンプルチャンバ)に点着させる。計器は、電気化学的あるいは比色法に基づき、テストストリップに点着された血液(全血)と試薬とを反応させることで、血液中のグルコース量(濃度)を測定し、血糖値として結果を表示部に表示させる。 When measuring the blood glucose level using the system of Patent Document 1 below, the user first attaches a test medium (test strip) having a reagent to the instrument. Subsequently, the user punctures the skin such as a finger using the attached puncture device, and a small amount of blood exuded from the skin is instilled on the inspection part (sample chamber) of the test strip. The instrument measures the amount of glucose (concentration) in the blood by reacting the blood (whole blood) instilled on the test strip with the reagent based on the electrochemical or colorimetric method, and the result is the blood glucose level. Is displayed on the display unit.
特表2007-520699号公報Special Table 2007-520699 Gazette
 ところで、特許文献1に開示されるシステムに用いられる計器は、テストストリップを収容する容器の蓋部に設けられ、容器の側面には穿刺装置が一体に取り付けられているため、外出先などに携帯して使用者自ら血糖値を測定することができる。そのため、特許文献1の計器を含むこの種の装置では、外出先へ手軽に持ち運び可能なように携帯性の向上が求められている。 By the way, the instrument used in the system disclosed in Patent Document 1 is provided on the lid of the container for accommodating the test strip, and the puncture device is integrally attached to the side surface of the container, so that the instrument can be carried on the go. The user can measure the blood glucose level by himself / herself. Therefore, in this type of device including the instrument of Patent Document 1, it is required to improve the portability so that it can be easily carried on the go.
 しかし、特許文献1の計器は、穿刺装置が容器に対してむき出しの状態で取り付けられているため、持ち運ぶ際に、穿刺装置の出っ張り部分(凸形状の部分)が周囲にある他の部分(例えば使用者の衣服、鞄のような服飾雑貨など)と引っ掛かり易く、携帯性の面で改善の余地があった。 However, in the instrument of Patent Document 1, since the puncture device is attached to the container in a bare state, another part (for example, a convex portion) around which the puncture device has a protruding portion (convex shape portion) when carried is carried. It was easy to get caught in the user's clothes, fashion accessories such as bags, etc., and there was room for improvement in terms of portability.
 また、特許文献1の計器は、穿刺装置がむき出しのまま容器に取り付けられているため、いかにも医療器具かのような外観を呈しており、意匠的な改善も望まれている。 Further, since the instrument of Patent Document 1 is attached to the container with the puncture device exposed, it looks like a medical instrument, and improvement in design is also desired.
 本発明の少なくとも一実施形態は、上述の事情に鑑みてなされたものであり、具体的には、採血用の穿刺デバイスと体液中の所定成分の成分量を測定する測定デバイスを備えた構成において、携帯性および意匠性に優れた成分測定装置を提供することにある。 At least one embodiment of the present invention has been made in view of the above circumstances, and specifically, in a configuration including a puncture device for blood sampling and a measurement device for measuring the amount of a predetermined component in a body fluid. It is an object of the present invention to provide a component measuring device having excellent portability and design.
 本実施形態に係る成分測定装置は、生体表面を穿刺して体液を滲出させるように構成された穿刺デバイスと、前記体液を検査用媒体内に導入させることで前記体液に含まれる所定の成分の成分量を測定するように構成された測定デバイスと、を備えた成分測定装置であって、前記穿刺デバイスは、第1筐体と、前記第1筐体の外表面のうち、少なくとも一の面に設けられた第1当接面と、第1連結部とを有し、前記測定デバイスは、第2筐体と、前記第2筐体の外表面のうち、少なくとも一の面に設けられた第2当接面と、前記第1連結部と連結可能な第2連結部とを有し、前記穿刺デバイスと前記測定デバイスは、前記第1当接面と前記第2当接面とが対向して当接した状態で前記第1連結部と前記第2連結部が連結されることにより、前記第1筐体と前記第2筐体が一体化されて前記成分測定装置の筐体を形成するように構成され、前記第1連結部と前記第2連結部との連結が解除されることにより、前記第1当接面および前記第2当接面が分離面となって前記穿刺デバイスと前記測定デバイスが別体となるように構成され、前記第1筐体と前記第2筐体は、前記筐体の外表面となる領域に前記筐体の外表面から突出する部分を有していない。 The component measuring device according to the present embodiment is a puncture device configured to pierce the surface of a living body to exude body fluid, and a predetermined component contained in the body fluid by introducing the body fluid into a test medium. A component measuring device comprising a measuring device configured to measure a component amount, wherein the piercing device is a surface of at least one of a first housing and an outer surface of the first housing. The measuring device is provided on at least one surface of the second housing and the outer surface of the second housing. The piercing device and the measuring device have a second contact surface and a second connecting portion that can be connected to the first connecting portion, and the first contact surface and the second contact surface face each other. By connecting the first connecting portion and the second connecting portion in the state of being in contact with each other, the first housing and the second housing are integrated to form a housing of the component measuring device. By breaking the connection between the first connecting portion and the second connecting portion, the first contact surface and the second contact surface become separate surfaces with the puncture device. The measuring device is configured to be a separate body, and the first housing and the second housing have a portion protruding from the outer surface of the housing in a region to be the outer surface of the housing. do not have.
 本発明の一実施形態によれば、採血用の穿刺デバイスと体液中の所定成分の成分量を測定する測定デバイスを備えた構成において、携帯性および意匠性に優れた成分測定装置を提供することができる。 According to one embodiment of the present invention, a component measuring device having excellent portability and design is provided in a configuration including a puncture device for blood sampling and a measuring device for measuring the amount of a predetermined component in a body fluid. Can be done.
本実施形態に係る成分測定装置を前面側からみた概略斜視図である。It is a schematic perspective view which looked at the component measuring apparatus which concerns on this embodiment from the front side. 本実施形態に係る成分測定装置を後面側からみた概略斜視図である。It is a schematic perspective view which looked at the component measuring apparatus which concerns on this embodiment from the rear surface side. 本実施形態に係る成分測定装置の穿刺デバイスと測定デバイスとを分離した状態を示す概略斜視図である。It is a schematic perspective view which shows the state which separated the puncture device and the measurement device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る測定デバイスの機能ブロック図である。It is a functional block diagram of the measurement device which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスの針装着部側からみた概略斜視図である。It is a schematic perspective view seen from the needle mounting part side of the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスの針イジェクト操作部側からみた概略斜視図である。It is a schematic perspective view seen from the needle eject operation part side of the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスに穿刺針カートリッジが装着された状態を示す概念図である。It is a conceptual diagram which shows the state which the puncture needle cartridge is attached to the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスにより穿刺針が進出した状態を示す概念図である。It is a conceptual diagram which shows the state which the puncture needle has advanced by the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスにより穿刺針が退避した状態を示す概念図である。It is a conceptual diagram which shows the state which the puncture needle retracted by the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスがイジェクト操作された状態を示す概念図である。It is a conceptual diagram which shows the state which the puncture device of the component measuring apparatus which concerns on this embodiment is eject operated. 本実施形態に係る成分測定装置の穿刺デバイスから穿刺針カートリッジが取り外された状態を示す概念図である。It is a conceptual diagram which shows the state which the puncture needle cartridge was removed from the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の測定デバイスの媒体装着部側からみた概略斜視図である。It is a schematic perspective view seen from the medium mounting part side of the measuring device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の穿刺デバイスの媒体イジェクト操作部側からみた概略斜視図である。It is a schematic perspective view seen from the medium eject operation part side of the puncture device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の測定デバイスによる検査用媒体を装着した状態を示す概念図である。It is a conceptual diagram which shows the state which attached the inspection medium by the measuring device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の測定デバイスによる測定状態を示す概念図である。It is a conceptual diagram which shows the measurement state by the measuring device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の測定デバイスがイジェクト操作された状態を示す概念図である。It is a conceptual diagram which shows the state which the measuring device of the component measuring apparatus which concerns on this embodiment is eject operated. 本実施形態に係る成分測定装置の測定デバイスから検査用媒体を取り外した状態を示す概念図である。It is a conceptual diagram which shows the state which removed the inspection medium from the measuring device of the component measuring apparatus which concerns on this embodiment. 本実施形態に係る成分測定装置の使用時における一連の動作例を示すフローチャートである。It is a flowchart which shows a series of operation examples at the time of using the component measuring apparatus which concerns on this embodiment. 改変例となる本実施形態に係る成分測定装置の穿刺デバイスの第1当接面側からみた概略斜視図である。It is a schematic perspective view seen from the 1st contact surface side of the puncture device of the component measuring apparatus which concerns on this embodiment which is a modification. 改変例となる本実施形態に係る成分測定装置の測定デバイスの第2当接面側からみた概略斜視図である。It is a schematic perspective view seen from the 2nd contact surface side of the measuring device of the component measuring apparatus which concerns on this embodiment which is a modification. 改変例となる本実施形態に係る成分測定装置の穿刺デバイスと測定デバイスを連結した状態を示す概略斜視図である。It is a schematic perspective view which shows the state which connected the puncture device and the measuring device of the component measuring apparatus which concerns on this embodiment which is a modification. 改変例となる本実施形態に係る成分測定装置の穿刺デバイスと測定デバイスの連結前の状態を示す概念図である。It is a conceptual diagram which shows the state before connection of the puncture device and the measurement device of the component measuring apparatus which concerns on this embodiment which is a modification. 改変例となる本実施形態に係る成分測定装置の穿刺デバイスと測定デバイスの連結中の状態を示す概念図である。It is a conceptual diagram which shows the state during connection of the puncture device and the measurement device of the component measuring apparatus which concerns on this embodiment which is a modification. 改変例となる本実施形態に係る成分測定装置の穿刺デバイスと測定デバイスの連結後の状態を示す概念図である。It is a conceptual diagram which shows the state after connection of the puncture device and the measurement device of the component measuring apparatus which concerns on this embodiment which is a modification.
 以下、本発明を実施するための形態について、図面を参照しながら詳細に説明する。ここで示す実施形態は、本発明の技術的思想を具体化するために例示するものであって、本発明を限定するものではない。また、本発明の要旨を逸脱しない範囲で当業者などにより考え得る実施可能な他の形態、実施例および運用技術などは全て本発明の範囲、要旨に含まれると共に、特許請求の範囲に記載された発明とその均等の範囲に含まれる。 Hereinafter, embodiments for carrying out the present invention will be described in detail with reference to the drawings. The embodiments shown here are examples for embodying the technical idea of the present invention, and do not limit the present invention. In addition, all other feasible forms, examples, operational techniques, etc. that can be considered by those skilled in the art without departing from the gist of the present invention are included in the scope and gist of the present invention, and are described in the claims. It is included in the scope of the invention and its equality.
 さらに、本明細書に添付する図面は、図示と理解のしやすさの便宜上、適宜縮尺、縦横の寸法比、形状などについて、実物から変更し模式的に表現される場合があるが、あくまで一例であって、本発明の解釈を限定するものではない。 Further, the drawings attached to the present specification may be represented schematically by changing the scale, aspect ratio, shape, etc. from the actual product for convenience of illustration and comprehension. However, it does not limit the interpretation of the present invention.
 なお、本明細書において、説明の便宜上、図示のようにXYZ座標を設定する。すなわち、「Z方向」は鉛直方向に沿った方向であり、「X方向」はZ方向と直交して水平面に平行な一方向であり、「Y方向」はZ方向と直交して水平面に平行な別の一方向(X方向に直交する方向)のうち、X方向と直交する方向である。本実施形態に係る成分測定装置100において、Z方向は筐体110の厚み方向(上下方向)と一致し、X方向は筐体110の長軸方向に沿った長手方向(前後方向)と一致し、Y方向は筐体110の短手方向(幅方向)と一致する。 In this specification, for convenience of explanation, XYZ coordinates are set as shown in the figure. That is, the "Z direction" is a direction along the vertical direction, the "X direction" is one direction orthogonal to the Z direction and parallel to the horizontal plane, and the "Y direction" is orthogonal to the Z direction and parallel to the horizontal plane. Of the other directions (directions orthogonal to the X direction), the direction is orthogonal to the X direction. In the component measuring device 100 according to the present embodiment, the Z direction coincides with the thickness direction (vertical direction) of the housing 110, and the X direction coincides with the longitudinal direction (front-back direction) along the long axis direction of the housing 110. , The Y direction coincides with the lateral direction (width direction) of the housing 110.
 また、以下の説明において、「第1」、「第2」のような序数詞を付して説明する場合は、特に言及しない限り、便宜上用いるものであって何らかの順序を規定するものではない。 Further, in the following explanation, when the explanations are given with ordinal numbers such as "first" and "second", they are used for convenience and do not specify any order unless otherwise specified.
 本発明の一実施形態に係る成分測定装置100は、穿刺部位となる使用者の生体表面(例えば皮膚)を穿刺して体液を滲出させ、この体液に含まれる所定の成分の成分量を測定する装置である。以下の実施形態において、成分測定装置100は、使用者自身が体液(血液)中に含まれるグルコース成分の成分量(血糖値)を測定する血糖自己測定(self-monitoring of blood glucose;SMBG)機器に採用した形態として説明する。 The component measuring device 100 according to the embodiment of the present invention punctures the living body surface (for example, skin) of the user as the puncture site to exude body fluid, and measures the component amount of a predetermined component contained in this body fluid. It is a device. In the following embodiment, the component measuring device 100 is a self-monitoring blood glucose (self-monitoring of blood glucose; SMBG) device that measures the amount (blood glucose level) of the glucose component contained in the body fluid (blood) by the user himself / herself. This will be described as the form adopted in.
 なお、成分測定装置100は、SMBG機器に限定されず、主として医療従事者が操作するPOCT(Point of Care Testing)機器としても使用可能である。また、成分測定装置100は、体液中に含まれる特定の成分量を測定する装置であるため、体液の種別および測定対象となる成分の成分量については、本実施形態の構成に限定されない。 The component measuring device 100 is not limited to the SMBG device, but can also be used as a POCT (Point of Care Testing) device mainly operated by a medical worker. Further, since the component measuring device 100 is a device for measuring the specific amount of the component contained in the body fluid, the type of the body fluid and the amount of the component of the component to be measured are not limited to the configuration of the present embodiment.
 [構成]
 まず、図1~図8を適宜参照しながら、本実施形態に係る成分測定装置100の構成について説明する。
[Constitution]
First, the configuration of the component measuring device 100 according to the present embodiment will be described with reference to FIGS. 1 to 8 as appropriate.
 図1または図2に示すように、成分測定装置100は、使用者の穿刺部位を穿刺して血液(全血)を滲出させる穿刺デバイス10と、穿刺デバイス10により滲出した血液に含まれる所定成分の成分量を測定する測定デバイス20と、を備える。 As shown in FIG. 1 or 2, the component measuring device 100 punctures the puncture site of the user to exude blood (whole blood), and a predetermined component contained in the blood exuded by the puncture device 10. A measuring device 20 for measuring the amount of components of the above is provided.
 成分測定装置100は、軸方向(X方向)に沿って延在する分離面101に沿って穿刺デバイス10と測定デバイス20とが分離可能に一体化された構成とされる。成分測定装置100は、非使用時(測定終了後の携帯時など)において、穿刺デバイス10の第1当接面10aと、測定デバイス20の第2当接面20aとを当接させて両デバイスを連結させる。図1および図2に示す成分測定装置100は、非使用時の態様が示されている。 The component measuring device 100 has a configuration in which the puncture device 10 and the measuring device 20 are separably integrated along a separation surface 101 extending along the axial direction (X direction). When the component measuring device 100 is not in use (such as when it is carried after the measurement is completed), the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 are brought into contact with each other to bring them into contact with each other. To concatenate. The component measuring device 100 shown in FIGS. 1 and 2 shows an aspect when not in use.
 図3に示すように、成分測定装置100は、使用時(穿刺時および測定時)においては、第1当接面10aと第2当接面20aとの当接状態が解除される。このとき、第1当接面10aは穿刺デバイス10の筐体の一部として露出し、第2当接面20aは測定デバイス20の筐体の一部として露出する。これにより、使用者は、穿刺デバイス10と測定デバイス20を分離してそれぞれ独立して使用できる。穿刺デバイス10の第1当接面10aと、測定デバイス20の第2当接面20aは、成分測定装置100の割り面として機能する分離面101を構成する。 As shown in FIG. 3, in the component measuring device 100, the contact state between the first contact surface 10a and the second contact surface 20a is released during use (during puncture and measurement). At this time, the first contact surface 10a is exposed as a part of the housing of the puncture device 10, and the second contact surface 20a is exposed as a part of the housing of the measurement device 20. As a result, the user can separate the puncture device 10 and the measurement device 20 and use them independently. The first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measuring device 20 form a separation surface 101 that functions as a split surface of the component measuring device 100.
 本実施形態に係る成分測定装置100において、分離面101は、少なくとも成分測定装置100の長手方向に沿って設けられ、穿刺デバイス10と測定デバイス20が分離される面である。分離面101は、例えば成分測定装置100の幅方向に対して垂直に延在する垂直面としてもよい。この場合、針装着部12(または針イジェクト操作部14の側)の側から成分測定装置100をみたときの分離面101の端面である分離断面端102は、Z方向と一致し、このとき分離面101の面積は最小となる。あるいは、図1や図2に示すように、分離断面端102が、針装着部12の側(または針イジェクト操作部14の側)からみたときに所定角度だけ軸周り方向に傾斜させることもできる。より詳細には、分離面101は、厚み方向に向かうに連れて幅方向へ傾斜する傾斜面である。分離面101を、Z方向に対して傾斜する傾斜面とすると、垂直面としたときに比べて分離面101が広くとれるため、穿刺デバイス10と測定デバイス20の保持力を適度に維持できる。また、穿刺デバイス10と測定デバイス20とを接続する際に、使用者へ正しい接続方向を視認させることができる。 In the component measuring device 100 according to the present embodiment, the separation surface 101 is provided at least along the longitudinal direction of the component measuring device 100, and is a surface on which the puncture device 10 and the measuring device 20 are separated. The separation surface 101 may be, for example, a vertical surface extending perpendicular to the width direction of the component measuring device 100. In this case, the separation cross-sectional end 102, which is the end surface of the separation surface 101 when the component measuring device 100 is viewed from the side of the needle mounting unit 12 (or the side of the needle eject operation unit 14), coincides with the Z direction and is separated at this time. The area of the surface 101 is minimized. Alternatively, as shown in FIGS. 1 and 2, the separated cross-sectional end 102 may be tilted in the axial direction by a predetermined angle when viewed from the side of the needle mounting portion 12 (or the side of the needle eject operating portion 14). .. More specifically, the separation surface 101 is an inclined surface that inclines in the width direction toward the thickness direction. When the separation surface 101 is an inclined surface inclined with respect to the Z direction, the separation surface 101 can be wider than when it is a vertical surface, so that the holding force of the puncture device 10 and the measurement device 20 can be appropriately maintained. Further, when connecting the puncture device 10 and the measurement device 20, the user can visually recognize the correct connection direction.
 また、成分測定装置100の幅方向(Y方向)に対する分離面101の位置は、穿刺デバイス10と測定デバイス20のサイズなどに応じて適宜決定されてよいが、分離面101は、穿刺デバイス10と測定デバイス20とが当接した際に、互いに相補的に一致する構成とされる。分離面101の形状は、平面、曲面、または凸凹の組み合わせであってもよいが、分離面101、すなわち、第1当接面10aと第2当接面20aは、衛生面を考慮すると平面や滑らかな曲面であるのが好ましく、平面がより好ましい。第1当接面10aと第2当接面20aとのフットプリントはほぼ同じが好ましい。第1当接面10aと第2当接面20aは、共に同一形状、同一サイズで構成するのがより好ましい。これにより、穿刺デバイス10と測定デバイス20を組み合わせた際に、筐体110の外表面から突出する部分をなくすことができる。分離断面端102は、後述の第1開口部12aと第2開口部22aとの間、あるいは、媒体イジェクト操作部23と針イジェクト操作部14との間に位置する。分離断面端102は、媒体イジェクト操作部23と針イジェクト操作部14の機能を妨げない限り、直線、曲線、あるいはそれらの組み合わせた形状であってもよい。 Further, the position of the separation surface 101 with respect to the width direction (Y direction) of the component measuring device 100 may be appropriately determined according to the sizes of the puncture device 10 and the measurement device 20, but the separation surface 101 is the puncture device 10 and the like. When they come into contact with the measuring device 20, they are configured to complement each other. The shape of the separation surface 101 may be a flat surface, a curved surface, or a combination of irregularities, but the separation surface 101, that is, the first contact surface 10a and the second contact surface 20a is a flat surface or a surface in consideration of hygiene. A smooth curved surface is preferable, and a flat surface is more preferable. It is preferable that the footprints of the first contact surface 10a and the second contact surface 20a are substantially the same. It is more preferable that the first contact surface 10a and the second contact surface 20a are both configured to have the same shape and the same size. Thereby, when the puncture device 10 and the measurement device 20 are combined, the portion protruding from the outer surface of the housing 110 can be eliminated. The separated cross-sectional end 102 is located between the first opening 12a and the second opening 22a, which will be described later, or between the medium eject operation unit 23 and the needle eject operation unit 14. The separated cross-sectional end 102 may have a straight line, a curved line, or a combination thereof as long as it does not interfere with the functions of the medium eject operation unit 23 and the needle eject operation unit 14.
 図3に示すように、穿刺デバイス10の筐体(第1筐体11)と測定デバイス20の筐体(第2筐体21)は、穿刺デバイス10の第1当接面10aと測定デバイス20の第2当接面20aを当接させた状態で穿刺デバイス10の第1連結部15(図5A、図5Bを参照)と測定デバイス20の第2連結部24が連結することにより、成分測定装置100の筐体110を構成する。穿刺デバイス10の第1連結部15と測定デバイス20の第2連結部24は、成分測定装置100の連結部として機能する。この連結部により、穿刺デバイス10と測定デバイス20とは、使用者が任意に脱着、連結可能となるように連結する。 As shown in FIG. 3, the housing of the puncture device 10 (first housing 11) and the housing of the measurement device 20 (second housing 21) are the first contact surface 10a of the puncture device 10 and the measurement device 20. The component is measured by connecting the first connecting portion 15 of the puncture device 10 (see FIGS. 5A and 5B) and the second connecting portion 24 of the measuring device 20 in a state where the second contact surface 20a is brought into contact with the puncture device 10. The housing 110 of the device 100 is configured. The first connecting portion 15 of the puncture device 10 and the second connecting portion 24 of the measuring device 20 function as a connecting portion of the component measuring device 100. Through this connecting portion, the puncture device 10 and the measuring device 20 are connected so that the user can arbitrarily attach / detach and connect them.
 成分測定装置100は、穿刺デバイス10と測定デバイス20とを連結した状態(すなわち、非使用時)において、筐体110の外表面から突出する部位を有していない。具体的には、穿刺デバイス10と測定デバイス20が連結された状態において、筐体110を構成する第1筐体11および第2筐体21の外表面の領域は、外方へ向かう凸形状(出っ張り)を有していない。本実施形態において、成分測定装置100の外形は、穿刺デバイス10と測定デバイス20とが一体化した状態において、断面が略角丸長方形をなす柱形状を成しており、外表面に凸形状が無いように構成される。 The component measuring device 100 does not have a portion protruding from the outer surface of the housing 110 in a state where the puncture device 10 and the measuring device 20 are connected (that is, when not in use). Specifically, in a state where the puncture device 10 and the measurement device 20 are connected, the outer surface regions of the first housing 11 and the second housing 21 constituting the housing 110 have an outwardly convex shape (convex shape toward the outside). Does not have a bulge). In the present embodiment, the outer shape of the component measuring device 100 has a pillar shape having a substantially rounded rectangular cross section in a state where the puncture device 10 and the measuring device 20 are integrated, and has a convex shape on the outer surface. It is configured so that there is no such thing.
 このように、成分測定装置100は、非使用時において筐体110の外表面に凸形状が存在しないため、携帯時に周囲にある他の部分との引っ掛かりが防止され、携帯性が向上する。また、成分測定装置100は、非使用時において両デバイスが連結されることにより、筐体110の外表面は凸形状を有さず滑らかな表面となる。そのため、成分測定装置100は、外観的に医療器具として認知され難く、意匠性にも優れている。さらに、成分測定装置100は、使用時には、穿刺デバイス10と測定デバイス20とが使用者によって分離可能とされる。このため、各デバイスの操作性が向上する。 As described above, since the component measuring device 100 does not have a convex shape on the outer surface of the housing 110 when not in use, it is prevented from being caught by other parts around it when it is carried, and the portability is improved. Further, in the component measuring device 100, when both devices are connected to each other when not in use, the outer surface of the housing 110 does not have a convex shape and becomes a smooth surface. Therefore, the component measuring device 100 is difficult to be recognized as a medical device in appearance and has excellent design. Further, in the component measuring device 100, the puncture device 10 and the measuring device 20 can be separated by the user at the time of use. Therefore, the operability of each device is improved.
 次に、図4~図8を適宜参照しながら、成分測定装置100を構成する各部について説明する。図5および図6は、主に穿刺デバイス10の構成に関する説明をするための図であり、図7および図8は、主に測定デバイス20の構成に関する説明をするための図である。また、図4は、測定デバイス20の制御系を説明するための図である。 Next, each part constituting the component measuring device 100 will be described with reference to FIGS. 4 to 8 as appropriate. 5 and 6 are diagrams mainly for explaining the configuration of the puncture device 10, and FIGS. 7 and 8 are diagrams mainly for explaining the configuration of the measurement device 20. Further, FIG. 4 is a diagram for explaining a control system of the measuring device 20.
 〈穿刺デバイス〉
 図5Aまたは図5Bに示すように、穿刺デバイス10は、第1筐体11内に、穿刺針カートリッジNが装着される針装着部12と、針装着部12に取り付けた穿刺針カートリッジNの穿刺針N2を進退させて使用者の穿刺部位に穿刺させる穿刺操作部13と、針装着部12に取り付けられた使用済みの穿刺針カートリッジNを取り外す(イジェクトする)際に操作される針イジェクト操作部14と、測定デバイス20との連結状態を維持するための第1連結部15と、穿刺部位に対する穿刺針N2の穿刺深度を調整するための深度調整部16を備えている。
<Puncture device>
As shown in FIG. 5A or FIG. 5B, the puncture device 10 punctures the needle mounting portion 12 on which the puncture needle cartridge N is mounted and the puncture needle cartridge N mounted on the needle mounting portion 12 in the first housing 11. The puncture operation unit 13 that advances and retreats the needle N2 to puncture the puncture site of the user, and the needle eject operation unit that is operated when removing (ejecting) the used puncture needle cartridge N attached to the needle mounting unit 12. A first connecting portion 15 for maintaining the connected state of the 14 and the measuring device 20, and a depth adjusting portion 16 for adjusting the puncture depth of the puncture needle N2 with respect to the puncture site are provided.
 また、図5Aまたは図5Bに示すように、穿刺デバイス10の第1筐体11は、第1当接面10aを備える。第1当接面10aは、測定デバイス20と連結したときに測定デバイス20の第2当接面20aと対向する。第1当接面10aは、成分測定装置100の分離面101として機能し、成分測定装置100の非使用時において、測定デバイス20の第2当接面20aと当接した状態が維持される。 Further, as shown in FIG. 5A or FIG. 5B, the first housing 11 of the puncture device 10 includes a first contact surface 10a. The first contact surface 10a faces the second contact surface 20a of the measurement device 20 when connected to the measurement device 20. The first contact surface 10a functions as a separation surface 101 of the component measuring device 100, and the state of contact with the second contact surface 20a of the measuring device 20 is maintained when the component measuring device 100 is not used.
 また、穿刺デバイス10は、測定デバイス20に連結されて成分測定装置100の筐体110を構成する際に、第1筐体11と第2筐体21との間の隙間を極力無くすことにより、筐体110の一体感を高めることができる。そのため、第1当接面10aは、その面から突出する部位を有さないように形成するのが好ましい。また、第1当接面10aは、第1当接面10aから突出する凸形状部を有さない構成にすることにより、第2当接面20aと当接状態を安定化させることができる。 Further, when the puncture device 10 is connected to the measuring device 20 to form the housing 110 of the component measuring device 100, the gap between the first housing 11 and the second housing 21 is eliminated as much as possible. The sense of unity of the housing 110 can be enhanced. Therefore, it is preferable that the first contact surface 10a is formed so as not to have a portion protruding from the surface. Further, the first contact surface 10a can be configured so as not to have a convex portion protruding from the first contact surface 10a, so that the contact state with the second contact surface 20a can be stabilized.
 また、第1筐体11は、外表面の少なくとも一部に平坦面からなる第1平坦部11aが設けられている。そのため、穿刺デバイス10は、測定デバイス20から分離させた状態でテーブルなどの載置面に載置したときに生じ得る転がりを防止することができる。第1平坦部11aは、第1筐体11において、第1当接面10a以外の外表面の一部または複数箇所に配置されてよい。また、第1当接面10aが略平坦に形成された場合、第1平坦部11aとして機能させてもよい。 Further, the first housing 11 is provided with a first flat portion 11a made of a flat surface at least a part of the outer surface. Therefore, the puncture device 10 can prevent rolling that may occur when the puncture device 10 is placed on a mounting surface such as a table in a state of being separated from the measuring device 20. The first flat portion 11a may be arranged at a part or a plurality of places on the outer surface other than the first contact surface 10a in the first housing 11. Further, when the first contact surface 10a is formed substantially flat, it may function as the first flat portion 11a.
 針装着部12は、第1開口部12aを有し、穿刺針カートリッジNが挿入されて装着される。穿刺針カートリッジNは、針ホルダーN1の前端側に設けられた孔部から進退可能に収納される穿刺針N2を備えた採血用の医療器具である。穿刺針カートリッジNは、穿刺部位に当接させて使用される。穿刺部位としては、例えば指先、掌、上腕、腹部、大腿部、耳たぶのような使用者の生体表面(皮膚、粘膜など)があげられる。そのため、穿刺針カートリッジNは、感染症などのリスクを防ぐため、シングルユースとされ、使用後に穿刺デバイス10から取り外されて廃棄される。なお、穿刺デバイス10は繰返し使用される。 The needle mounting portion 12 has a first opening 12a, and the puncture needle cartridge N is inserted and mounted. The puncture needle cartridge N is a medical device for collecting blood provided with a puncture needle N2 that is retractably accommodated from a hole provided on the front end side of the needle holder N1. The puncture needle cartridge N is used in contact with the puncture site. Examples of the puncture site include the surface of the user's body (skin, mucous membrane, etc.) such as the fingertip, palm, upper arm, abdomen, thigh, and earlobe. Therefore, the puncture needle cartridge N is considered to be single-use in order to prevent risks such as infectious diseases, and is removed from the puncture device 10 and discarded after use. The puncture device 10 is used repeatedly.
 針装着部12は、針係合部12bを有する。穿刺針カートリッジNの後端部(針ホルダーN1の後端部)は針係合部12bと係合することで、穿刺針カートリッジNは穿刺デバイス10に保持される。 The needle mounting portion 12 has a needle engaging portion 12b. The rear end portion of the puncture needle cartridge N (the rear end portion of the needle holder N1) engages with the needle engaging portion 12b, so that the puncture needle cartridge N is held by the puncture device 10.
 針係合部12bは、穿刺針カートリッジN内の穿刺針N2のハブの後端部を軸方向に沿って進退可能に保持する。針係合部12bは、軸方向に沿って伸縮可能な弾性部材(コイルばねなど)を備え、穿刺操作部13の操作に基づき、弾性部材の付勢力を利用して穿刺針カートリッジN内の穿刺針N2を軸方向に沿って進退させる。本実施形態において、針装着部12は、図示しないが穿刺針カートリッジNの穿刺針N2の針先を所定長(所定の穿刺深度)だけ進出させるための穿刺ばねと、進出した穿刺針N2の針先を元の位置(待機位置)まで退避させるための戻しばねを弾性部材として有している。 The needle engaging portion 12b holds the rear end portion of the hub of the puncture needle N2 in the puncture needle cartridge N so as to be able to move forward and backward along the axial direction. The needle engaging portion 12b includes an elastic member (coil spring or the like) that can expand and contract along the axial direction, and based on the operation of the puncture operation portion 13, puncture in the puncture needle cartridge N by utilizing the urging force of the elastic member. The needle N2 is moved forward and backward along the axial direction. In the present embodiment, although not shown, the needle mounting portion 12 includes a puncture spring for advancing the needle tip of the puncture needle N2 of the puncture needle cartridge N by a predetermined length (predetermined puncture depth), and a needle of the advanced puncture needle N2. It has a return spring as an elastic member for retracting the tip to the original position (standby position).
 穿刺操作部13は、穿刺針カートリッジNに穿刺動作を実行させる機械式スイッチで構成される。本実施形態に係る成分測定装置100において、穿刺操作部13は、穿刺操作部13の押下操作をトリガとし、穿刺針カートリッジNに穿刺動作を実行させるためのボタン式スイッチ機構で構成してよい。穿刺操作部13は、第1筐体11において、成分測定装置100の筐体110の外表面から突出しないように、例えば第1当接面10a領域内に配置するのが好ましい。穿刺操作部13は、第1当接面10aに配置されることにより、非使用時において操作面が筐体110の外表面に露出されず、成分測定装置100の美観を損なうことがない。 The puncture operation unit 13 is composed of a mechanical switch that causes the puncture needle cartridge N to perform a puncture operation. In the component measuring device 100 according to the present embodiment, the puncture operation unit 13 may be configured by a button-type switch mechanism for causing the puncture needle cartridge N to execute the puncture operation by using the pressing operation of the puncture operation unit 13 as a trigger. The puncture operation unit 13 is preferably arranged in the first contact surface 10a region, for example, so as not to protrude from the outer surface of the housing 110 of the component measuring device 100 in the first housing 11. By arranging the puncture operation unit 13 on the first contact surface 10a, the operation surface is not exposed to the outer surface of the housing 110 when not in use, and the aesthetic appearance of the component measuring device 100 is not spoiled.
 針イジェクト操作部14は、使用済みの穿刺針カートリッジNを穿刺デバイス10から取り外す際に操作される。針イジェクト操作部14は、一例として使用者が長軸方向に沿った押下によるイジェクト操作を行うためのレバー部材で構成されてよい。針イジェクト操作部14は、第1筐体11の外形に沿って形成された第1操作体14aを有する。すなわち、第1操作体14aは、非使用時において第1筐体11の外形から突出しない。 The needle eject operation unit 14 is operated when the used puncture needle cartridge N is removed from the puncture device 10. As an example, the needle eject operation unit 14 may be composed of a lever member for the user to perform an eject operation by pressing along the major axis direction. The needle eject operating unit 14 has a first operating body 14a formed along the outer shape of the first housing 11. That is, the first operating body 14a does not protrude from the outer shape of the first housing 11 when not in use.
 第1操作体14aは、使用者による所定のイジェクト操作(押下操作)により軸方向に沿って移動可能に設けられており、第1筐体11内に収納される図示しない係合部材を介して針装着部12から穿刺針カートリッジNを取り外す。係合部材は、穿刺針カートリッジNと係合し、第1操作体14aの操作量に応じて軸方向に連動して移動する部材である。第1操作体14aは、図示しない弾性部材(コイルばねなど)を備え、穿刺針カートリッジNを取り外す際にイジェクト操作されると、初期位置からイジェクト位置まで移動し、穿刺針カートリッジNが取り外された後は、弾性部材の付勢力により初期位置まで移動する。 The first operating body 14a is provided so as to be movable along the axial direction by a predetermined eject operation (pushing operation) by the user, and is provided via an engaging member (not shown) housed in the first housing 11. Remove the puncture needle cartridge N from the needle mounting portion 12. The engaging member is a member that engages with the puncture needle cartridge N and moves in conjunction with the axial direction according to the amount of operation of the first operating body 14a. The first operating body 14a is provided with an elastic member (coil spring or the like) (not shown), and when an eject operation is performed when the puncture needle cartridge N is removed, the first operating body 14a moves from the initial position to the eject position, and the puncture needle cartridge N is removed. After that, it moves to the initial position by the urging force of the elastic member.
 第1連結部15は、第2連結部24と連結して穿刺デバイス10と測定デバイス20の連結状態を維持させる。第1連結部15は、一例として磁性体または磁石からなる第1磁性部材15aにより構成される。第1連結部15は、第2連結部24の形態に応じて構成材料が適宜選択され得る。すなわち、第1磁性部材15aは、第2連結部24として機能する第2磁性部材24aが磁性体で構成された場合、第2磁性部材24aと連結可能なように磁石によって構成されてよい。また、第1磁性部材15aは、第2磁性部材24aが磁石で構成された場合、第2磁性部材24aと連結可能なように磁性体または第2磁性部材24aと磁極の異なる磁石によって構成されてよい。 The first connecting portion 15 is connected to the second connecting portion 24 to maintain the connected state of the puncture device 10 and the measuring device 20. The first connecting portion 15 is configured by, for example, a first magnetic member 15a made of a magnetic material or a magnet. The constituent material of the first connecting portion 15 can be appropriately selected according to the form of the second connecting portion 24. That is, when the second magnetic member 24a that functions as the second connecting portion 24 is made of a magnetic material, the first magnetic member 15a may be made of a magnet so that it can be connected to the second magnetic member 24a. Further, when the second magnetic member 24a is composed of a magnet, the first magnetic member 15a is composed of a magnetic material or a magnet having a magnetic pole different from that of the second magnetic member 24a so as to be connectable to the second magnetic member 24a. good.
 第1連結部15は、測定デバイス20の第2当接面20aに配置される第2連結部24と対向するように第1当接面10aの近傍における第1筐体11の内方に配置される。これにより、穿刺デバイス10と測定デバイス20を連結した際には、第1当接面10aと第2当接面20aとの当接状態を阻害することなく、両デバイスの連結状態を維持することができる。 The first connecting portion 15 is arranged inside the first housing 11 in the vicinity of the first contact surface 10a so as to face the second connecting portion 24 arranged on the second contact surface 20a of the measuring device 20. Will be done. As a result, when the puncture device 10 and the measurement device 20 are connected, the connected state of both devices is maintained without disturbing the contact state between the first contact surface 10a and the second contact surface 20a. Can be done.
 針装着部12に装着された穿刺針カートリッジNの穿刺針N2が進出する長さ(使用者の穿刺部位(皮膚などの生体表面)に穿刺される際の穿刺深さ)は、深度調整部16により任意の長さに調整可能である。深度調整部16は、穿刺針カートリッジNの穿刺針N2の進出量(穿刺深度)を調整する。深度調整部16は、被採血者である使用者の個人差や穿刺部位に応じて、穿刺針N2が針ホルダーN1の開口部からの進出する長さ、すなわち生体表面からの穿刺深さを調整する際に操作される。深度調整部16による穿刺深度(穿刺針N2の進出量)は、調整ダイヤル等によって多段階で調整可能となっている。 The length at which the puncture needle N2 of the puncture needle cartridge N mounted on the needle mounting portion 12 advances (the puncture depth when puncturing the puncture site (living body surface such as skin) of the user) is the depth adjusting portion 16. Can be adjusted to any length. The depth adjusting unit 16 adjusts the amount of advancement (puncture depth) of the puncture needle N2 of the puncture needle cartridge N. The depth adjusting unit 16 adjusts the length at which the puncture needle N2 advances from the opening of the needle holder N1, that is, the puncture depth from the surface of the living body, according to the individual difference of the user who is the blood sampler and the puncture site. It is operated when you do. The puncture depth (advancement amount of the puncture needle N2) by the depth adjusting unit 16 can be adjusted in multiple stages by an adjustment dial or the like.
 次に、図6A~図6Eを参照しながら、穿刺デバイス10の使用例について説明する。穿刺デバイス10は、測定デバイス20を用いて血糖値を測定するために必要な採血を行う際に操作される。 Next, an example of using the puncture device 10 will be described with reference to FIGS. 6A to 6E. The puncture device 10 is operated when the blood sampling device 10 is used to collect blood necessary for measuring the blood glucose level.
 図6Aに示すように、穿刺針カートリッジNは、使用者によって針装着部12に装着される。この際、穿刺針カートリッジNの後端部は、針係合部12bと係合する。続いて、図6Bに示すように、使用者により穿刺操作部13が操作されると、針装着部12は、穿刺ばねの付勢力により穿刺針カートリッジNの針先を所定の進出位置まで進出させる。図6Cに示すように、穿刺操作部13の操作が終わると、進出した穿刺針カートリッジNの針先は、戻しばねの付勢力により元の位置(待機位置)まで退避する。このように、針装着部12に装着された穿刺針カートリッジNは、穿刺操作部13が操作されることにより、穿刺針N2が待機位置と進出位置の間を軸方向に沿って往復移動し、使用者の所定の生体表面を穿刺する。 As shown in FIG. 6A, the puncture needle cartridge N is mounted on the needle mounting portion 12 by the user. At this time, the rear end portion of the puncture needle cartridge N engages with the needle engaging portion 12b. Subsequently, as shown in FIG. 6B, when the puncture operation unit 13 is operated by the user, the needle mounting unit 12 advances the needle tip of the puncture needle cartridge N to a predetermined advance position by the urging force of the puncture spring. .. As shown in FIG. 6C, when the operation of the puncture operation unit 13 is completed, the needle tip of the advanced puncture needle cartridge N is retracted to the original position (standby position) by the urging force of the return spring. In this way, in the puncture needle cartridge N mounted on the needle mounting portion 12, the puncture needle N2 reciprocates along the axial direction between the standby position and the advance position by operating the puncture operation portion 13. Puncture the user's predetermined biological surface.
 次に、図6Dに示すように、使用者は、軸方向に沿って第1操作体14aを押下して第1筐体11の内方にある係合部材を軸方向に沿って遠位端側に移動させ、針装着部12(詳細には針係合部12b)と穿刺針カートリッジNとの係合状態を解除する。 Next, as shown in FIG. 6D, the user presses the first operating body 14a along the axial direction to displace the engaging member inside the first housing 11 along the axial direction. It is moved to the side to release the engagement state between the needle mounting portion 12 (specifically, the needle engaging portion 12b) and the puncture needle cartridge N.
 そして、穿刺デバイス10は、使用者が手で触れることなく、使用後の穿刺針カートリッジNを穿刺デバイス10から取り外すことで、図6Eに示された状態(つまり、使用前の状態)となる。穿刺針カートリッジNが穿刺デバイス10から離脱されると、第1操作体14aは、弾性部材の付勢力により、イジェクト位置から操作前の初期位置へと戻った状態となる。 Then, the puncture device 10 is in the state shown in FIG. 6E (that is, the state before use) by removing the puncture needle cartridge N after use from the puncture device 10 without the user touching it. When the puncture needle cartridge N is detached from the puncture device 10, the first operating body 14a returns from the eject position to the initial position before the operation due to the urging force of the elastic member.
 〈測定デバイス〉
 図7A、図7Bのいずれかに示すように、測定デバイス20は、第2筐体21内に、ディスポーザブルタイプの検査用媒体Tが装着される媒体装着部22と、媒体装着部22に取り付けられた使用済みの検査用媒体Tを取り外す際に操作される媒体イジェクト操作部23と、穿刺デバイス10との連結状態を維持するための第2連結部24とを備える。
<Measurement device>
As shown in either FIG. 7A or FIG. 7B, the measuring device 20 is attached to the medium mounting portion 22 on which the disposable type inspection medium T is mounted and the medium mounting portion 22 in the second housing 21. The medium eject operation unit 23, which is operated when the used inspection medium T is removed, and the second connection unit 24 for maintaining the connection state with the puncture device 10 are provided.
 また、図4に示すように、測定デバイス20は、体液中の成分量の測定に関する各種処理を実行するため、制御系として測定部31と、温度検出部32と、デバイス検出部33と、通信部34と、報知部35と、表示部36と、電源部37と、記憶部38と、制御部39を備える。 Further, as shown in FIG. 4, the measuring device 20 communicates with the measuring unit 31, the temperature detecting unit 32, and the device detecting unit 33 as a control system in order to execute various processes related to the measurement of the amount of components in the body fluid. It includes a unit 34, a notification unit 35, a display unit 36, a power supply unit 37, a storage unit 38, and a control unit 39.
 図7Aまたは図7Bに示すように、測定デバイス20の第2筐体21は、穿刺デバイス10と連結したときに穿刺デバイス10の第1当接面10aと対向する第2当接面20aを有する。第2当接面20aは、成分測定装置100の分離面101として機能し、成分測定装置100の非使用時において、穿刺デバイス10の第1当接面10aと当接した状態が維持される。 As shown in FIG. 7A or FIG. 7B, the second housing 21 of the measuring device 20 has a second contact surface 20a facing the first contact surface 10a of the puncture device 10 when connected to the puncture device 10. .. The second contact surface 20a functions as a separation surface 101 of the component measuring device 100, and the state of contact with the first contact surface 10a of the puncture device 10 is maintained when the component measuring device 100 is not used.
 また、第2当接面20aは、第1当接面10aと同様、その面から突出する部位を有さないように形成するのが好ましい。第2当接面20aは、面上に凸形状を有さない構成とすることにより、第1当接面10aと当接状態を安定化させることができると共に、筐体110の外表面に生じ得る隙間を極力無くすことができる。 Further, it is preferable that the second contact surface 20a is formed so as not to have a portion protruding from the surface, like the first contact surface 10a. By forming the second contact surface 20a so as not to have a convex shape on the surface, the contact state with the first contact surface 10a can be stabilized, and the second contact surface 20a is formed on the outer surface of the housing 110. The gap to be obtained can be eliminated as much as possible.
 また、第2筐体21は、外表面の少なくとも一部に平坦面からなる第2平坦部21aが設けられている。そのため、測定デバイス20は、穿刺デバイス10から分離させた状態でテーブルなどの載置面に載置したときに生じ得る転がりを防止することができる。第2平坦部21aは、第2筐体21において、第2当接面20a以外の外表面の一部または複数箇所に配置されてよい。また、第2当接面20aが略平坦に形成された場合、第2平坦部21aとして機能させてもよい。あるいは、第2平坦部21aを2つ設けて、互いに向かい合う一対の面として配置してもよい。 Further, the second housing 21 is provided with a second flat portion 21a made of a flat surface at least a part of the outer surface. Therefore, the measuring device 20 can prevent rolling that may occur when the measuring device 20 is placed on a mounting surface such as a table in a state of being separated from the puncturing device 10. The second flat portion 21a may be arranged at a part or a plurality of places on the outer surface other than the second contact surface 20a in the second housing 21. Further, when the second contact surface 20a is formed substantially flat, it may function as the second flat portion 21a. Alternatively, two second flat portions 21a may be provided and arranged as a pair of surfaces facing each other.
 なお、穿刺デバイス10と測定デバイス20とが連結したときに、第2平坦部21aは、筐体110において第1平坦部11aと同一面上に配置されるのが好ましい。すなわち、第1平坦部11aと第2平坦部21aは、筐体110の一面を構成する。第1平坦部11aと第2平坦部21aを筐体110の同一面上に配置させることにより、両平坦部が載置面として機能して成分測定装置100の載置安定性を高めることができる。 When the puncture device 10 and the measurement device 20 are connected, the second flat portion 21a is preferably arranged on the same surface as the first flat portion 11a in the housing 110. That is, the first flat portion 11a and the second flat portion 21a form one surface of the housing 110. By arranging the first flat portion 11a and the second flat portion 21a on the same surface of the housing 110, both flat portions function as mounting surfaces and the mounting stability of the component measuring device 100 can be improved. ..
 媒体装着部22は、第2開口部22aを有し、検査用媒体Tが挿入される。検査用媒体Tは、一例として前端に所定の試薬を有する検査部T1(図8Dを参照)を有するディスポーザブルタイプのテストストリップであり、測定後に廃棄される。検査部T1は、血液中の被測定物質と特異的に反応する試薬(発色試薬)が保持されている。血液を吸収可能な多孔性膜などの担体に、試薬を保持させてもよい。血液は、試薬と反応することで、血液内に含まれたグルコース量に応じた色濃度で呈色する。 The medium mounting portion 22 has a second opening 22a, and the inspection medium T is inserted into the medium mounting portion 22. The inspection medium T is, for example, a disposable type test strip having an inspection unit T1 (see FIG. 8D) having a predetermined reagent at the front end, and is discarded after measurement. The inspection unit T1 holds a reagent (coloring reagent) that specifically reacts with the substance to be measured in blood. The reagent may be held on a carrier such as a porous membrane capable of absorbing blood. By reacting with the reagent, blood develops a color with a color concentration corresponding to the amount of glucose contained in the blood.
 第2開口部22aの開口形状は、装着される検査用媒体Tの形状(断面形状)に合わせて形成されてよい。なお、第2開口部22aは、装着される検査用媒体Tの形状に応じて、その開口形状が設定される。そのため、検査用媒体Tがテストストリップのような板状ではなく、略円柱状のチップの場合、第2開口部22aは、チップが装着可能な形状を有することとなる。 The opening shape of the second opening 22a may be formed according to the shape (cross-sectional shape) of the inspection medium T to be mounted. The opening shape of the second opening 22a is set according to the shape of the inspection medium T to be mounted. Therefore, when the inspection medium T is not a plate shape like a test strip but a substantially columnar chip, the second opening 22a has a shape to which the chip can be mounted.
 また、媒体装着部22は、装着された検査用媒体Tを保持すると共に、取り外しの際に検査用媒体Tの後端部を第2開口部22aから進出させるための媒体保持部(図示せず)を備えている。 Further, the medium mounting portion 22 holds the mounted inspection medium T, and also holds the medium holding portion (not shown) for advancing the rear end portion of the inspection medium T from the second opening 22a at the time of removal. ) Is provided.
 媒体保持部は、測定デバイス20の第2筐体21の内方において軸方向に沿って移動可能に設けられている。媒体保持部は、第2筐体21内において検査用媒体Tの少なくとも一部(特に先端部近傍)を保持して測定を行う位置(測定位置)と検査用媒体Tが取り外される位置(イジェクト位置)との間を軸方向に沿って移動する。 The medium holding portion is provided so as to be movable along the axial direction inside the second housing 21 of the measuring device 20. The medium holding portion is a position (measurement position) in which at least a part (particularly near the tip portion) of the inspection medium T is held and measured in the second housing 21 and a position (eject position) in which the inspection medium T is removed. ) And move along the axial direction.
 媒体保持部は、第2開口部22aから挿入された検査用媒体Tを保持し、測定終了後に媒体イジェクト操作部23が操作されると、検査用媒体Tを保持した状態で長軸方向の遠位端側に向かって移動する。検査用媒体Tは、第2筐体21の第2開口部22aから所定長だけ押し出されるため、使用者が手で触れることなく、測定後の検査用媒体Tを測定デバイス20から取り外すことができる。媒体保持部による検査用媒体Tの押し出し量(媒体イジェクト操作部23の操作量に相当)は、第2筐体21のサイズ、検査用媒体Tの長手方向の長さ、把持に必要な第2開口部22aからの突出量(露出長さ)によって適宜決定されるが、少なくとも検査用媒体Tを第2開口部22aから離脱できる程度の長さとするのが好ましい。 The medium holding unit holds the inspection medium T inserted from the second opening 22a, and when the medium eject operation unit 23 is operated after the measurement is completed, the medium holding unit holds the inspection medium T and is far away in the long axis direction. Move toward the end side. Since the inspection medium T is extruded from the second opening 22a of the second housing 21 by a predetermined length, the inspection medium T after measurement can be removed from the measurement device 20 without being touched by the user. .. The amount of extrusion of the inspection medium T by the medium holding unit (corresponding to the operation amount of the medium eject operation unit 23) is the size of the second housing 21, the length of the inspection medium T in the longitudinal direction, and the second required for gripping. Although it is appropriately determined by the amount of protrusion (exposed length) from the opening 22a, it is preferable that the inspection medium T is at least long enough to be detached from the second opening 22a.
 媒体イジェクト操作部23は、使用済みの検査用媒体Tを測定デバイス20から取り外す際に操作される。媒体イジェクト操作部23は、一例として使用者が軸方向に沿って移動可能に設けられたレバー部材で構成されてよい。媒体イジェクト操作部23は、第2筐体21の外形に沿って形成され、使用者によって操作される第2操作体23aを有する。 The medium eject operation unit 23 is operated when the used inspection medium T is removed from the measuring device 20. As an example, the medium eject operation unit 23 may be composed of a lever member provided so that the user can move along the axial direction. The medium eject operation unit 23 has a second operation body 23a formed along the outer shape of the second housing 21 and operated by the user.
 第2操作体23aは、使用者による所定のイジェクト操作(押下操作)により軸方向に沿って移動可能に設けられており、第2筐体21内で媒体保持部と係合している。媒体保持部は、第2操作体23aの長軸方向への移動に伴い、第2筐体21内において長軸方向の前端側へと移動する。媒体保持部に保持された検査用媒体Tは、第2操作体23aの移動に連れて第2開口部22aからの突出量(露出量)が徐々に増大する。第2操作体23aの操作によって媒体保持部がイジェクト位置まで移動すると、検査用媒体Tは、測定デバイス20から離脱する。第2操作体23aは、検査用媒体Tを取り外された後、操作前の位置(初期位置)まで移動すると、第2操作体23aの移動に連れて媒体保持部が軸方向の後端側へと移動して元の位置(測定位置)まで戻る。第2操作体23aの戻り動作は、使用者が手動で行ってもよいし、図示しない弾性部材(コイルばねなど)の付勢力によって移動させてもよい。 The second operating body 23a is provided so as to be movable along the axial direction by a predetermined eject operation (pressing operation) by the user, and is engaged with the medium holding portion in the second housing 21. The medium holding portion moves toward the front end side in the long axis direction in the second housing 21 as the second operating body 23a moves in the long axis direction. The inspection medium T held in the medium holding portion gradually increases in the amount of protrusion (exposure amount) from the second opening 22a as the second operating body 23a moves. When the medium holding portion moves to the eject position by the operation of the second operating body 23a, the inspection medium T is separated from the measuring device 20. When the second operating body 23a moves to the position (initial position) before the operation after the inspection medium T is removed, the medium holding portion moves toward the rear end side in the axial direction as the second operating body 23a moves. And return to the original position (measurement position). The return operation of the second operating body 23a may be performed manually by the user, or may be moved by the urging force of an elastic member (coil spring or the like) (not shown).
 第2連結部24は、穿刺デバイス10の第1当接面10aと、測定デバイス20の第2当接面20aとを当接させて連結状態を維持させる。第2連結部24は、一例として磁性体または磁石からなる第2磁性部材24aにより構成される。第2連結部24は、第1連結部15の形態に応じて構成材料が適宜選択され得る。すなわち、第2磁性部材24aは、第1磁性部材15aが磁性体で構成された場合、第1磁性部材15aと連結可能なように磁石によって構成されてよい。また、第2磁性部材24aは、第1磁性部材15aが磁石で構成された場合、第1磁性部材15aと連結可能なように磁性体または第1磁性部材15aと磁極の異なる磁石によって構成されてよい。 The second connecting portion 24 brings the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measuring device 20 into contact with each other to maintain the connected state. The second connecting portion 24 is configured by, for example, a second magnetic member 24a made of a magnetic material or a magnet. The constituent material of the second connecting portion 24 may be appropriately selected according to the form of the first connecting portion 15. That is, when the first magnetic member 15a is made of a magnetic material, the second magnetic member 24a may be made of a magnet so that it can be connected to the first magnetic member 15a. Further, when the first magnetic member 15a is composed of a magnet, the second magnetic member 24a is composed of a magnetic material or a magnet having a magnetic pole different from that of the first magnetic member 15a so that the first magnetic member 15a can be connected to the first magnetic member 15a. good.
 第2連結部24は、穿刺デバイス10の第1当接面10aに配置される第1連結部15と対向するように第2当接面20aの近傍における第2筐体21の内方に配置される。これにより、穿刺デバイス10と測定デバイス20を連結した際には、第1当接面10aと第2当接面20aとの当接状態を阻害することなく、両デバイスの連結状態を維持することができる。 The second connecting portion 24 is arranged inside the second housing 21 in the vicinity of the second contact surface 20a so as to face the first connecting portion 15 arranged on the first contact surface 10a of the puncture device 10. Will be done. As a result, when the puncture device 10 and the measurement device 20 are connected, the connected state of both devices is maintained without disturbing the contact state between the first contact surface 10a and the second contact surface 20a. Can be done.
 次に、図4を参照しながら測定デバイス20の制御系について説明する。 Next, the control system of the measuring device 20 will be described with reference to FIG.
 測定部31は、測定対象となる体液の成分量を測定する。本実施形態に係る成分測定装置100において、測定部31は、血液中のグルコース成分の成分量を光学的に測定する。測定部31は、図示しない発光素子及び受光素子を有し、検査部T1内で拡がった血液に対し発光素子から照射光を照射して、その透過光を受光素子により検出する光学系測定器として構成されている。測定部31は、第2筐体21内において、媒体保持部により測定位置で保持される検査用媒体Tが検査可能な位置(例えば測定位置にある検査部T1の上方)に配置される。測定部31は、発光素子から単一または複数の所定波長の光を断続的に出射し、検査部T1を透過した光を受光素子で受光し、受光光量に比例した電気信号を出力する。制御部39は電気信号をデジタル化した測定値として取り込む。この測定値は状態により変化するため、波長ごとのデータ系列である。 The measuring unit 31 measures the amount of the component of the body fluid to be measured. In the component measuring device 100 according to the present embodiment, the measuring unit 31 optically measures the amount of the glucose component component in the blood. The measuring unit 31 has a light emitting element and a light receiving element (not shown), and is an optical system measuring device that irradiates the blood spread in the inspection unit T1 with the irradiation light from the light emitting element and detects the transmitted light by the light receiving element. It is configured. The measurement unit 31 is arranged in the second housing 21 at a position where the inspection medium T held at the measurement position by the medium holding unit can be inspected (for example, above the inspection unit T1 at the measurement position). The measuring unit 31 intermittently emits light of a single or a plurality of predetermined wavelengths from the light emitting element, receives the light transmitted through the inspection unit T1 by the light receiving element, and outputs an electric signal proportional to the amount of the received light. The control unit 39 captures the electric signal as a digitized measured value. Since this measured value changes depending on the state, it is a data series for each wavelength.
 使用者の操作により、検査用媒体Tは、媒体装着部22に装着される。測定部31は、測定デバイス20内への検査用媒体Tの装着前後における光量変化を取得することで、検査用媒体Tが媒体装着部22に装着されたことを検知し、制御部39を介して、装置の報知部35および表示部36に使用者に血液の点着を促す報知および表示を行う。 The inspection medium T is mounted on the medium mounting unit 22 by the operation of the user. The measuring unit 31 detects that the inspection medium T has been mounted on the medium mounting unit 22 by acquiring a change in the amount of light before and after mounting the inspection medium T in the measuring device 20, and via the control unit 39. Then, the notification unit 35 and the display unit 36 of the device are notified and displayed to urge the user to instill blood.
 使用者は検査用媒体Tの遠位端部にある点着口T2に、穿刺デバイス10によって得た0.5~10μLの血液を塗布する。検査用媒体Tの内部に設けられた毛管路(図示せず)に沿って、血液が導入されたのち、試薬と混合されてグルコースとの反応が進行する。これにより血液中のグルコース値に応じた量の発色を呈する。検査用媒体T内の毛管路において検査部T1は、検査用媒体Tを測定デバイス20に装着した際に測定部31に対応した位置にある。試薬と混合された血液は、毛管路に沿って拡がり、検査部T1に到達する。なお、検査用媒体Tは毛管路内への血液導入を促すための空気抜き孔(図示せず)を有していてもよく、空気抜き孔は、毛管路において点着口T2と反対の端部に設けられる。試薬と混合された血液が検査部T1に到達して、検査部T1の間隙内に拡がると、測定部31は、発光素子から所定波長の光を出射し、血液中のグルコース値に応じた試薬反応に基づく試薬反応量を、検査部T1を透過した光量から計測する。 The user applies 0.5 to 10 μL of blood obtained by the puncture device 10 to the spotting port T2 at the distal end of the test medium T. After blood is introduced along a capillary channel (not shown) provided inside the test medium T, it is mixed with a reagent and the reaction with glucose proceeds. As a result, the color is developed in an amount corresponding to the glucose level in the blood. In the capillary line in the inspection medium T, the inspection unit T1 is in a position corresponding to the measurement unit 31 when the inspection medium T is attached to the measurement device 20. The blood mixed with the reagent spreads along the capillary tract and reaches the examination unit T1. The inspection medium T may have an air vent hole (not shown) for promoting blood introduction into the capillary passage, and the air vent hole is provided at the end opposite to the spotting port T2 in the capillary passage. It will be provided. When the blood mixed with the reagent reaches the test unit T1 and spreads in the gap of the test unit T1, the measurement unit 31 emits light having a predetermined wavelength from the light emitting element and the reagent corresponding to the glucose value in the blood. The reagent reaction amount based on the reaction is measured from the amount of light transmitted through the inspection unit T1.
 測定部31は断続的に出射光と受光強度測定を継続しているので、検査部T1にまだ検体が無い状態から試薬と混合された血液が流入しその反応が進むまで、検査部T1の透過光量に応じた時系列の電気信号を出力し、制御部39は測定値のデータ系列として取り込む。 Since the measuring unit 31 continues to measure the emitted light and the light receiving intensity intermittently, the inspection unit T1 is transmitted until the blood mixed with the reagent flows into the inspection unit T1 from the state where there is no sample and the reaction proceeds. A time-series electric signal corresponding to the amount of light is output, and the control unit 39 captures it as a data series of measured values.
 検査部T1に検体(血液)が無い状態から、試薬と混合された血液が流入したことを制御部39で検知し、これをトリガとして測定処理を開始する。測定終了は、制御部39が既定時間の経過もしくは測定値の経過より判断した時点(例えば、測定値の変化がプラトーに達した時点)で測定終了の処理を行う。測定開始から測定終了に至るまで制御部39は、装置の報知部35および表示部36に測定開始から測定終了に至るまでの報知および表示を行う。 The control unit 39 detects that blood mixed with the reagent has flowed in from a state where there is no sample (blood) in the inspection unit T1, and the measurement process is started using this as a trigger. The measurement end is processed when the control unit 39 determines from the passage of a predetermined time or the passage of the measured value (for example, when the change of the measured value reaches the plateau). From the start of measurement to the end of measurement The control unit 39 notifies and displays the notification unit 35 and the display unit 36 of the device from the start of measurement to the end of measurement.
 なお、測定部31は、血液中の血糖値を光学的に検出する比色式による測定を行う構成としたが、他の測定方式も適用することができる。血糖値の測定方式としては、例えば電極の周辺に試薬を塗布して、試薬と血液との反応に伴う電気的変化、つまり検出電極と対極の間に生じた電流を検出する酵素電極式などが挙げられる。また、当然のことながら、測定部31は、測定対象となる体液中の成分の成分量が測定できればよいため、測定対象となる成分に応じて適宜機器構成を変更することも可能である。 Although the measuring unit 31 is configured to perform measurement by a colorimetric method that optically detects the blood glucose level in blood, other measuring methods can also be applied. As a method for measuring the blood glucose level, for example, an enzyme electrode method in which a reagent is applied around an electrode to detect an electrical change accompanying a reaction between the reagent and blood, that is, a current generated between a detection electrode and a counter electrode is used. Can be mentioned. Further, as a matter of course, since the measuring unit 31 only needs to be able to measure the amount of the component in the body fluid to be measured, it is possible to appropriately change the device configuration according to the component to be measured.
 温度検出部32は、測定時の環境温度を測定する公知の温度計で構成される。温度検出部32は、測定した環境温度に基づく温度値を制御部39に出力する。 The temperature detection unit 32 is composed of a known thermometer that measures the environmental temperature at the time of measurement. The temperature detection unit 32 outputs a temperature value based on the measured environmental temperature to the control unit 39.
 デバイス検出部33は、測定デバイス20に対する穿刺デバイス10の連結または分離した状態、すなわち測定デバイス20に対する穿刺デバイス10の連結状態(成分測定装置100の非使用時であって、第1当接面10aと第2当接面20aが当接し連結した状態)と、穿刺デバイス10の分離状態(成分測定装置100の使用時であって、第1当接面10aと第2当接面20aが離隔した状態)を検出する。 The device detection unit 33 is in a state where the puncture device 10 is connected or separated from the measuring device 20, that is, a state in which the puncturing device 10 is connected to the measuring device 20 (when the component measuring device 100 is not used, the first contact surface 10a is used. And the second contact surface 20a are in contact with each other and connected to each other) and the separated state of the puncture device 10 (when the component measuring device 100 is used, the first contact surface 10a and the second contact surface 20a are separated from each other). State) is detected.
 デバイス検出部33は、両者の着脱状態を検出する方法として、穿刺デバイス10と測定デバイス20との連結方法に即した方法を採用することができる。本実施形態に係る成分測定装置100において、穿刺デバイス10と測定デバイス20は、磁気的に連結する構成となっている。そのため、デバイス検出部33は、一例として磁気的な連結状態の有無が検出可能なホール素子などを用いた磁気センサで構成されてよい。デバイス検出部33は、第1当接面10aと第2当接面20aが当接して穿刺デバイス10が連結した状態と、第1当接面10aと第2当接面20aが離隔して穿刺デバイス10が分離した状態を磁気的に検出する。デバイス検出部33は、検出した連結状態または分離状態を示す状態情報(連結状態情報、分離状態情報)を制御部39に出力する。 The device detection unit 33 can adopt a method corresponding to the method of connecting the puncture device 10 and the measurement device 20 as a method of detecting the attachment / detachment state of both. In the component measuring device 100 according to the present embodiment, the puncture device 10 and the measuring device 20 are magnetically connected. Therefore, the device detection unit 33 may be configured by, for example, a magnetic sensor using a Hall element or the like that can detect the presence or absence of a magnetically connected state. The device detection unit 33 punctures a state in which the first contact surface 10a and the second contact surface 20a are in contact with each other and the puncture device 10 is connected, and the first contact surface 10a and the second contact surface 20a are separated from each other. The separated state of the device 10 is magnetically detected. The device detection unit 33 outputs the detected state information (connection state information, separation state information) indicating the detected connection state or separation state to the control unit 39.
 なお、デバイス検出部33は、測定デバイス20に対する穿刺デバイス10の連結および分離状態(着脱状態)が検出可能な構成を有していればよいため、両者の着脱状態の検出方法は上記構成に限定されない。 Since the device detection unit 33 only needs to have a configuration capable of detecting the connection and separation state (detachment state) of the puncture device 10 with respect to the measurement device 20, the method of detecting the attachment / detachment state of both is limited to the above configuration. Not done.
 通信部34は、所定のプロトコルに従い通信ネットワークを介して接続される他の装置(通信先となる、例えば医療施設の外部サーバ、担当医が所有する各種の移動端末など)との間の有線または無線通信(近距離無線通信も含む)を制御するネットワークインターフェースである。通信部34は、測定した成分量(血糖値)を示す測定値を含む送信データを通信先に送信する。 The communication unit 34 is wired or connected to another device (for example, an external server of a medical facility, various mobile terminals owned by a doctor in charge, etc.) connected via a communication network according to a predetermined protocol. It is a network interface that controls wireless communication (including short-range wireless communication). The communication unit 34 transmits transmission data including a measured value indicating the measured component amount (blood glucose level) to the communication destination.
 報知部35は、音声やブザー音のような報知音を出力するスピーカなどの報知器、種々の色で点灯または点滅する発光機器、所定の振動を発生させるバイブレータなどで構成され、所定の報知内容(例えば、所定動作の開始または終了、エラー発生に伴う警告、手順の案内など)を使用者が識別可能に報知する。また、報知部35は、制御部39からの制御により、媒体装着部22から検査用媒体Tの取り外しを促す報知、穿刺デバイス10と測定デバイス20との連結を促す報知などの報知を行う。これにより、使用者による、検査用媒体Tの取り外し忘れや、成分測定装置100の置き忘れなどが防止される。 The notification unit 35 is composed of a notification device such as a speaker that outputs a notification sound such as a voice or a buzzer, a light emitting device that lights or blinks in various colors, a vibrator that generates a predetermined vibration, and the like. (For example, the start or end of a predetermined operation, a warning when an error occurs, a procedure guide, etc.) are notified to the user in an identifiable manner. Further, the notification unit 35, under the control of the control unit 39, performs notification from the medium mounting unit 22 to prompt the removal of the inspection medium T, notification to prompt the connection between the puncture device 10 and the measurement device 20, and the like. This prevents the user from forgetting to remove the inspection medium T or misplaceing the component measuring device 100.
 表示部36は、例えばLCD(Liquid Crystal Display)、OLED(Organic Light Emitting Diode)、マイクロLED(Micro Light Emmiting Diode)ディスプレイなどの表示デバイスで構成され、表示内容を使用者に視認可能な形式(文字、数字、図形など記号)で出力するインターフェースである。表示部36は、例えば測定部31で測定された体液中の成分量(詳細には、制御部39の算出部39bで算出された値)を表示する他、操作する上で必要となる通知内容(案内表示、測定開始・終了の表示など)の表示も行う。表示部36の表示面36aに表示される表示内容(表示データ)は、制御部39から出力される。 The display unit 36 is composed of a display device such as an LCD (Liquid Crystal Display), an OLED (Organic Light Emitting Diode), or a micro LED (Micro Light Emitting Diode) display, and the display content is visible to the user (characters). , Numbers, figures, and other symbols). The display unit 36 displays, for example, the amount of components in the body fluid measured by the measurement unit 31 (specifically, the value calculated by the calculation unit 39b of the control unit 39), and the notification content required for operation. It also displays (guidance display, measurement start / end display, etc.). The display content (display data) displayed on the display surface 36a of the display unit 36 is output from the control unit 39.
 表示部36の表示面36aは、第2当接面20aに配置される。そのため、成分測定装置100は、非使用時において表示面36aが筐体110の外部に露出されない。このため、意匠性が向上すると共に、周囲から医療器具と認識され難くなる。使用者が血糖計を携帯していることを、他人に気づかれ難くしたい場合に好適である。 The display surface 36a of the display unit 36 is arranged on the second contact surface 20a. Therefore, in the component measuring device 100, the display surface 36a is not exposed to the outside of the housing 110 when not in use. For this reason, the design is improved and it becomes difficult for the surroundings to recognize it as a medical device. It is suitable when the user wants to make it difficult for others to notice that he / she is carrying a glucose meter.
 電源部37は、第2筐体21内に収納され、成分測定装置100の電源である電池を収納し、装着させる。電池は、成分測定装置100の携帯性を考慮すると、ボタン電池のような小型電池が好ましい。なお、電源部37で使用される電池は、一次電池または二次電池のいずれでもよい。また、電源部37は、ボタン電池のような化学電池の他、太陽電池などの物理電池を併用することもできる。さらに、電源部37は、外部電源(商用電源など)と有線または無線接続して電源供給または充電可能な機能を具備させてもよい。電源部37は、穿刺デバイス10と測定デバイス20との分離状態および連結状態に基づき、測定デバイス20を構成する各部(測定部31、温度検出部32、通信部34、報知部35、表示部36、記憶部38および制御部39)の回路に供給する電力量を変化させることができ、省電力に寄与する。 The power supply unit 37 is housed in the second housing 21, and stores and mounts the battery that is the power source of the component measuring device 100. The battery is preferably a small battery such as a button battery in consideration of the portability of the component measuring device 100. The battery used in the power supply unit 37 may be either a primary battery or a secondary battery. Further, the power supply unit 37 may use a physical battery such as a solar cell in combination with a chemical battery such as a button battery. Further, the power supply unit 37 may be provided with a function capable of supplying power or charging by connecting to an external power source (commercial power source or the like) by wire or wirelessly. The power supply unit 37 is a unit (measurement unit 31, temperature detection unit 32, communication unit 34, notification unit 35, display unit 36) that constitutes the measurement device 20 based on the separated state and the connected state of the puncture device 10 and the measuring device 20. , The amount of power supplied to the circuits of the storage unit 38 and the control unit 39) can be changed, which contributes to power saving.
 記憶部38は、測定デバイス20の駆動に必要な各種制御プログラム、測定部31で測定された測定値が含まれる通信先への送信データ、所定期間分の測定に関する過去値など、測定デバイス20で使用される各種データを記憶する公知の記憶媒体で構成される。 The storage unit 38 is a measuring device 20 such as various control programs necessary for driving the measuring device 20, data transmitted to a communication destination including the measured values measured by the measuring unit 31, and past values related to measurements for a predetermined period. It is composed of a known storage medium for storing various data used.
 制御部39は、例えばCPU(Central Processing Unit)、ROM(Read only memory)、RAM(Random Access Memory)などを含む各種プロセッサで構成される。制御部39は、所定の処理プログラムを起動させながら測定デバイス20を構成する各部を統括制御して所定の処理を実行させる。制御部39は、例えばRTC(Real-Time Clock)で構成される計時部39aを備え、図示しないクロック部から供給される所定周期の基準クロックに従って時刻を計時する。計時部39aによる時刻計時は、測定を実施した年月日時分の生成や、測定開始から測定終了までの計時に用いられる。 The control unit 39 is composed of various processors including, for example, a CPU (Central Processing Unit), a ROM (Read only memory), a RAM (Random Access Memory), and the like. The control unit 39 controls each unit constituting the measurement device 20 in an integrated manner while activating a predetermined processing program to execute a predetermined processing. The control unit 39 includes, for example, a time measuring unit 39a composed of an RTC (Real-Time Clock), and measures the time according to a reference clock having a predetermined cycle supplied from a clock unit (not shown). The time clock by the time measuring unit 39a is used for generating the date and time when the measurement was performed and for measuring from the start of the measurement to the end of the measurement.
 また、制御部39は、測定部31により検出された検出値(比色式の場合は、色濃度や光量)に基づいて測定対象となる体液中の成分の成分量(血糖値)を算出する算出部39bを備える。 Further, the control unit 39 calculates the component amount (blood glucose level) of the component in the body fluid to be measured based on the detection value (color concentration and light amount in the case of the specific color type) detected by the measurement unit 31. A calculation unit 39b is provided.
 算出部39bは、算出処理の際の環境温度(温度検出部32による温度値)などの測定値変動要因を考慮して適宜補正処理を行う機能を備えている。これにより、算出部39bは、測定誤差が少なく、より真値に近い値を得ることができる。算出部39bは、算出した測定値を表示部36に出力する。 The calculation unit 39b has a function of appropriately performing correction processing in consideration of measured value fluctuation factors such as the environmental temperature (temperature value by the temperature detection unit 32) at the time of calculation processing. As a result, the calculation unit 39b can obtain a value closer to the true value with less measurement error. The calculation unit 39b outputs the calculated measured value to the display unit 36.
 また、制御部39は、デバイス検出部33からの状態情報に基づいて電源部37による各部への電源供給のON/OFF制御を行う。制御部39は、デバイス検出部33から連結状態情報が入力されると、電源部37に電源供給を停止させる制御信号を出力する。これにより、測定デバイス20は、電源がOFFとなる。また、制御部39は、デバイス検出部33から分離状態情報が入力されると、電源部37に電源供給を開始させる制御信号を出力する。これにより、測定デバイス20は、電源がONしてアイドル状態となる。 Further, the control unit 39 controls ON / OFF of power supply to each unit by the power supply unit 37 based on the state information from the device detection unit 33. When the connection state information is input from the device detection unit 33, the control unit 39 outputs a control signal for stopping the power supply to the power supply unit 37. As a result, the power of the measuring device 20 is turned off. Further, when the separation state information is input from the device detection unit 33, the control unit 39 outputs a control signal for starting the power supply to the power supply unit 37. As a result, the measuring device 20 is turned on and becomes an idle state.
 また、制御部39は、電源がONしてアイドル状態となると、測定部31に制御信号を出力する。この制御信号をトリガとして、測定部31は、発光・受光の制御および光量に比例した電気信号の出力を開始する。制御部39は電気信号をデジタル化した測定値として取り込む処理を開始する。この制御は、デバイス検出部33が穿刺デバイス10と測定デバイス20との連結を検知し電源がOFFとなるまで断続的に継続する。 Further, the control unit 39 outputs a control signal to the measurement unit 31 when the power is turned on and becomes an idle state. Using this control signal as a trigger, the measuring unit 31 starts controlling light emission / reception and outputting an electric signal proportional to the amount of light. The control unit 39 starts a process of capturing an electric signal as a digitized measured value. This control continues intermittently until the device detection unit 33 detects the connection between the puncture device 10 and the measurement device 20 and the power is turned off.
 また、制御部39は、所定の判断(穿刺デバイス10の連結判断、検査用媒体Tの装着判断、測定開始終了判断)を行う判断部39cを備えている。制御部39は、断続的な測定を継続している測定部31から、検査部T1の透過光量に応じた測定値のデータ系列として取り込む。判断部39cは、検査部T1に血液が無い状態から、血液が流入したことを検知したとき、測定開始と判断し、これをトリガとして測定処理を開始する。検査部T1で試薬と血液の反応が進み、計時部39aで測定開始から既定時間を経過したとき、もしくは判断部39cで測定値のデータ系列の経過より測定終了条件となったとき、判断部39cは測定終了と判断する。制御部39は、測定終了処理として、算出部39bで算出された値を表示部36に表示し、報知部35に測定終了の報知を行う。 Further, the control unit 39 includes a determination unit 39c that makes a predetermined determination (determination of connection of the puncture device 10, determination of attachment of the inspection medium T, determination of measurement start / end). The control unit 39 takes in as a data series of measured values according to the amount of transmitted light of the inspection unit T1 from the measurement unit 31 that continues the intermittent measurement. When the determination unit 39c detects that blood has flowed in from the state where there is no blood in the examination unit T1, it determines that the measurement has started, and starts the measurement process using this as a trigger. When the reaction between the reagent and blood progresses in the inspection unit T1 and the predetermined time elapses from the start of measurement in the timing unit 39a, or when the measurement end condition is reached from the progress of the data series of the measured values in the judgment unit 39c, the judgment unit 39c Judges that the measurement is completed. As the measurement end process, the control unit 39 displays the value calculated by the calculation unit 39b on the display unit 36, and notifies the notification unit 35 of the end of the measurement.
 測定終了後に判断部39cは測定部31からの信号を観察し、媒体装着部22に装着された検査用媒体Tが所定時間(例えば数分)内に取り外されたか否かの判断を行う。判断部39cは、所定時間内に検査用媒体Tが取り外されていないと判断した場合、使用者に対して検査用媒体Tを取り外すように促す報知を報知部35に実行させる。これにより、使用者は、測定終了後における検査用媒体Tの取り外し忘れを防止することができる。判断部39cによる検査用媒体Tの取り外しの判断は、例えば媒体イジェクト操作部23の操作の有無に応じて判断してよい。あるいは、測定値取得前に測定部31が取得したブランク信号と、測定値取得から所定時間経過後に測定部31が得た信号とを比較することで、測定部31に検査用媒体Tが装着されているかどうかを判断してもよい。検査用媒体Tは通常、毛管路の遠位部に血液を導入しやすくするための空気抜き孔を有する。検査用媒体T内の毛管路に血液が導入されたまま長時間放置されると、この空気抜き孔を通じて、血液が検査用媒体Tの外部へ染み出す可能性がある。このため、検査用媒体Tは、測定から所定時間内に測定デバイス20から取り外すのが好ましい。 After the measurement is completed, the determination unit 39c observes the signal from the measurement unit 31 and determines whether or not the inspection medium T mounted on the medium mounting unit 22 has been removed within a predetermined time (for example, several minutes). When the determination unit 39c determines that the inspection medium T has not been removed within a predetermined time, the determination unit 39c causes the notification unit 35 to execute a notification prompting the user to remove the inspection medium T. As a result, the user can prevent forgetting to remove the inspection medium T after the measurement is completed. The determination of the inspection medium T by the determination unit 39c may be determined, for example, depending on whether or not the medium eject operation unit 23 is operated. Alternatively, the inspection medium T is attached to the measurement unit 31 by comparing the blank signal acquired by the measurement unit 31 before the measurement value acquisition with the signal acquired by the measurement unit 31 after a predetermined time has elapsed from the measurement value acquisition. You may decide whether or not it is. The test medium T usually has an air vent hole at the distal end of the capillary tract to facilitate the introduction of blood. If the blood is left for a long time with the blood introduced into the capillary channel in the test medium T, the blood may seep out of the test medium T through the air vent holes. Therefore, it is preferable to remove the inspection medium T from the measuring device 20 within a predetermined time from the measurement.
 また、判断部39cは、デバイス検出部33からの状態情報に基づき、検査用媒体Tが取り外された後、所定時間(例えば数分)内に穿刺デバイス10と測定デバイス20とが連結されたか否かの判断を行う。判断部39cは、測定値取得から所定時間内に穿刺デバイス10が連結されていないと判断した場合(つまり、連結状態情報の入力待ちの状態のとき)、使用者に対して穿刺デバイス10と測定デバイス20との連結を促すための報知を報知部35に実行させる。これにより、使用者は、測定終了後における穿刺デバイス10の連結し忘れを防止することができる。 Further, the determination unit 39c determines whether the puncture device 10 and the measurement device 20 are connected within a predetermined time (for example, several minutes) after the inspection medium T is removed based on the state information from the device detection unit 33. Make a judgment. When the determination unit 39c determines that the puncture device 10 is not connected within a predetermined time from the acquisition of the measured value (that is, when the connection state information is waiting to be input), the determination unit 39c measures the puncture device 10 with the user. The notification unit 35 is made to execute the notification for prompting the connection with the device 20. As a result, the user can prevent forgetting to connect the puncture device 10 after the measurement is completed.
 また、制御部39は、算出部39bで算出された測定値と、測定条件情報(環境温度を示す温度情報、測定に要した測定時間など)とを関連付けた送信データを生成する処理と、生成した送信データを記憶部38に記憶させる処理と、通信部34を介して通信先に向けて送信データを送信制御させる処理を行う生成処理部39dを備えている。 Further, the control unit 39 processes and generates transmission data in which the measurement value calculated by the calculation unit 39b is associated with the measurement condition information (temperature information indicating the environmental temperature, the measurement time required for the measurement, etc.). It is provided with a generation processing unit 39d that performs a process of storing the transmitted data in the storage unit 38 and a process of controlling the transmission of the transmitted data toward the communication destination via the communication unit 34.
 なお、計時部39a、算出部39b、および生成処理部39dは、共に制御部39に含まれた構成として説明しているが、それぞれが制御部39と別体の構成としてもよいし、これらの中から幾つかが制御部39に含まれた構成としてもよい。 Although the timekeeping unit 39a, the calculation unit 39b, and the generation processing unit 39d are all described as being included in the control unit 39, they may be configured separately from the control unit 39, respectively. Some of them may be included in the control unit 39.
 また、制御部39は、測定部31による測定が可能な状態(測定デバイス20から穿刺デバイス10が分離された状態)となり、検査用媒体Tが所定時間以内に装着されていないときは、使用者に対して検査用媒体Tの装着を促す報知を行うように報知部35を制御することもできる。さらに、制御部39は、測定中などに穿刺デバイス10が測定デバイス20に装着されるなどの不測の事態が生じた場合、測定処理を中断させる構成とすることもできる。その際、制御部39は、報知部35に測定エラーを示す報知を実行させてもよい。 Further, when the control unit 39 is in a state where measurement by the measurement unit 31 is possible (a state in which the puncture device 10 is separated from the measurement device 20) and the inspection medium T is not attached within a predetermined time, the user It is also possible to control the notification unit 35 so as to notify the user to attach the inspection medium T. Further, the control unit 39 may be configured to interrupt the measurement process when an unexpected situation such as the puncture device 10 being attached to the measurement device 20 occurs during measurement or the like. At that time, the control unit 39 may cause the notification unit 35 to execute notification indicating a measurement error.
 次に、図8A~図8Dを参照しながら、測定デバイス20の使用例について説明する。測定デバイス20は、穿刺デバイス10を用いて採血した血液中の血糖値を測定する際に操作される。 Next, an example of using the measuring device 20 will be described with reference to FIGS. 8A to 8D. The measuring device 20 is operated when measuring the blood glucose level in the blood collected by using the puncture device 10.
 図8Aに示すように、検査用媒体Tは、使用者により第2開口部22aから挿入されて媒体装着部22に装着される。検査用媒体Tの検査部T1には、穿刺デバイス10によって採血された血液が、点着口T2の開口を介して、検査用媒体Tの毛管路を通じて導入される。続いて、測定デバイス20は、装着された検査用媒体Tの測定を開始する。図8Bに示すように、測定部31による測定結果(測定値)は、表示部36に表示される。 As shown in FIG. 8A, the inspection medium T is inserted from the second opening 22a by the user and mounted on the medium mounting portion 22. The blood collected by the puncture device 10 is introduced into the inspection unit T1 of the inspection medium T through the opening of the instillation port T2 through the capillary passage of the inspection medium T. Subsequently, the measuring device 20 starts measuring the mounted inspection medium T. As shown in FIG. 8B, the measurement result (measured value) by the measuring unit 31 is displayed on the display unit 36.
 次に、図8Cに示すように、使用者は、イジェクト操作により媒体イジェクト操作部23の第2操作体23aを成分測定装置100の長軸方向に沿って押下し、第2筐体21の内方にある媒体保持部を、測定位置からイジェクト位置まで長軸方向に沿って移動させる。これにより、図8Cに示すように、検査用媒体Tは、第2開口部22aから押し出されて、取り外される。図8Dに示すように、検査用媒体Tを取り外した後、第2操作体23aは、操作前の位置(初期位置)まで移動する。また、第2操作体23aの移動に連れて、媒体保持部についても、長軸方向の基端側へと移動して元の位置(測定位置)まで戻る。 Next, as shown in FIG. 8C, the user presses the second operation body 23a of the medium eject operation unit 23 along the long axis direction of the component measuring device 100 by the eject operation, and the inside of the second housing 21 The medium holding portion on the side is moved along the long axis direction from the measurement position to the eject position. As a result, as shown in FIG. 8C, the inspection medium T is pushed out from the second opening 22a and removed. As shown in FIG. 8D, after the inspection medium T is removed, the second operating body 23a moves to the position (initial position) before the operation. Further, as the second operating body 23a moves, the medium holding portion also moves toward the base end side in the long axis direction and returns to the original position (measurement position).
 [動作]
 次に、図9を参照しながら本実施形態に係る成分測定装置100の使用時における一連の動作例について説明する。なお、以下に説明する動作については、例示的な順序でステップの要素を提示しており、提示した特定の順序に限定されない。また、各処理は、成分測定装置100を使用する上で、必要なタイミングで適宜行われるものとする。
[motion]
Next, a series of operation examples when the component measuring device 100 according to the present embodiment is used will be described with reference to FIG. 9. The operations described below are presented in an exemplary order, and are not limited to the specific order in which they are presented. Further, each process shall be appropriately performed at a timing necessary for using the component measuring device 100.
 図9に示すように、本実施形態に係る成分測定装置100を使用する際、最初の処理として、使用者は、穿刺デバイス10と測定デバイス20を分離させ(S1)、測定デバイス20の電源をONにする(S2)。 As shown in FIG. 9, when using the component measuring device 100 according to the present embodiment, as a first process, the user separates the puncture device 10 and the measuring device 20 (S1), and powers the measuring device 20. Turn it on (S2).
 ステップS1において、制御部39は、測定デバイス20から穿刺デバイス10が分離されたことを示す分離状態情報を入力すると、電源部37に電源供給を開始させるための制御信号を出力する。これにより、測定デバイス20は、電源がONとなり、アイドル状態となる。 In step S1, when the control unit 39 inputs the separation state information indicating that the puncture device 10 has been separated from the measurement device 20, the control unit 39 outputs a control signal for starting the power supply to the power supply unit 37. As a result, the power of the measuring device 20 is turned on and the measuring device 20 is in an idle state.
 次処理として、制御部39は、検査用媒体Tが媒体装着部22に装着されたか否かの判断を行う(S3)。 As a next process, the control unit 39 determines whether or not the inspection medium T is mounted on the medium mounting unit 22 (S3).
 ステップS3において、制御部39は、検査用媒体Tが媒体装着部22に装着されたと判断した場合(S3-Yes)、検査用媒体Tの装着検知処理を終了し血液点着の検知待ち処理を開始する。一方、制御部39は、検査用媒体Tが媒体装着部22に装着されていないと判断した場合(S3-No)、使用者に対して検査用媒体Tの装着を促す表示を行い(S4)、検査用媒体Tが装着されるまでステップS3およびステップS4の処理をループする。 In step S3, when the control unit 39 determines that the test medium T is mounted on the medium mounting unit 22 (S3-Yes), the control unit 39 ends the mounting detection process of the test medium T and waits for the detection of blood instillation. Start. On the other hand, when the control unit 39 determines that the inspection medium T is not mounted on the medium mounting unit 22 (S3-No), the control unit 39 displays a display prompting the user to mount the inspection medium T (S4). , The processing of step S3 and step S4 is looped until the inspection medium T is attached.
 次に、制御部39は、測定部31からの信号を観察し、検査用媒体Tに検体が無い状態から試薬と混合された血液が流入したか否かの判断を行う(S5)。 Next, the control unit 39 observes the signal from the measurement unit 31 and determines whether or not the blood mixed with the reagent has flowed in from the state where the test medium T has no sample (S5).
 ステップS5において、制御部39は、測定部31からの信号を観察し、検査用媒体Tに検体が無い状態から試薬と混合された血液が流入したことを検知した場合(S5-Yes)、測定開始と判断し、これをトリガとして測定処理を開始する(S7)。一方、制御部39は、試薬と混合された血液の流入が検知できない場合(S5-No)は、使用者に対して血液点着を促す表示を行い(S6)、血液の点着が確認されるまでステップS5およびステップS6の処理をループする。 In step S5, when the control unit 39 observes the signal from the measurement unit 31 and detects that the blood mixed with the reagent has flowed in from the state where the test medium T has no sample (S5-Yes), the measurement is performed. It is determined to start, and the measurement process is started using this as a trigger (S7). On the other hand, when the inflow of blood mixed with the reagent cannot be detected (S5-No), the control unit 39 displays a display prompting the user to instill blood (S6), and the instillation of blood is confirmed. The process of step S5 and step S6 is looped until the result is reached.
 次処理として、制御部39は、測定を開始し(S7)、計時部39aによる既定時間の経過観察、若しくは判断部39cで測定値のデータ系列の経過観察より、反応終了したか否かの判断を行う(S8)。 As the next process, the control unit 39 starts the measurement (S7), and determines whether or not the reaction is completed by the follow-up observation of the predetermined time by the timing unit 39a or the follow-up observation of the data series of the measured values by the judgment unit 39c. (S8).
 検査部T1で試薬と血液の反応が進み、計時部39aにより測定開始から既定時間を経過したとき、若しくは判断部39cで測定値のデータ系列の経過より測定終了条件となった場合(S8-Yes)、判断部39cは測定終了と判断し測定終了処理(S10)に進む。一方、反応終了に至らない場合(S8-No)、測定状態を継続し(S9)、再度ステップS8へと戻る。 When the reaction between the reagent and blood progresses in the inspection unit T1 and the predetermined time has elapsed from the start of measurement by the timing unit 39a, or when the measurement end condition is reached from the progress of the data series of the measured values in the judgment unit 39c (S8-Yes). ), The determination unit 39c determines that the measurement is completed, and proceeds to the measurement end process (S10). On the other hand, if the reaction is not completed (S8-No), the measurement state is continued (S9), and the process returns to step S8 again.
 制御部39は、測定終了処理として、算出部39bで算出された値を表示部36に表示し、測定結果と測定日時を記憶部38に記憶し、報知部35に測定終了の報知を行う(S10)。 As the measurement end process, the control unit 39 displays the value calculated by the calculation unit 39b on the display unit 36, stores the measurement result and the measurement date and time in the storage unit 38, and notifies the notification unit 35 of the end of the measurement. S10).
 測定終了処理の後、制御部39は、測定部31からの信号を観察し、媒体装着部22に装着された検査用媒体Tが所定時間(例えば数分)内に取り外されたか否かの判断を行う(S11)。 After the measurement end processing, the control unit 39 observes the signal from the measurement unit 31 and determines whether or not the inspection medium T mounted on the medium mounting unit 22 has been removed within a predetermined time (for example, several minutes). (S11).
 ステップS11において、制御部39は、所定時間内に媒体装着部22から検査用媒体Tが取り外されたと判断した場合(S11-Yes)、穿刺デバイス10が測定デバイス20に連結したか否かの判断を行う(S13)。一方、制御部39は、所定時間内に媒体装着部22から検査用媒体Tが取り外されていないと判断した場合(S11-No)、使用者に対して検査用媒体Tを媒体装着部22から取り外すように促す報知を行うように報知部35を制御すると共に測定値の表示を継続する(S12)。この後、制御部39は、検査用媒体Tが取り外されるまでステップS11およびステップS12の処理をループする。 In step S11, when the control unit 39 determines that the inspection medium T has been removed from the medium mounting unit 22 within a predetermined time (S11-Yes), the control unit 39 determines whether or not the puncture device 10 is connected to the measurement device 20. (S13). On the other hand, when the control unit 39 determines that the inspection medium T has not been removed from the medium mounting unit 22 within a predetermined time (S11-No), the control unit 39 transfers the inspection medium T from the medium mounting unit 22 to the user. The notification unit 35 is controlled so as to notify the user to remove it, and the display of the measured value is continued (S12). After that, the control unit 39 loops the processes of steps S11 and S12 until the inspection medium T is removed.
 ステップS13において、制御部39は、所定時間内に穿刺デバイス10が連結されたと判断した場合(S13-Yes)、電源部37に電源供給を停止させる制御信号を出力し(S15)、処理を終了する。これにより、測定デバイス20の電源はOFFとなり、処理を終了する。一方、制御部39は、所定時間内に穿刺デバイス10が連結されていないと判断した場合(S13-No)、使用者に対して穿刺デバイス10との連結を促すための報知を行うように報知部35を制御する(S14)。この後、制御部39は、穿刺デバイス10が連結されるまでステップS13およびステップS14の処理をループする。 In step S13, when the control unit 39 determines that the puncture device 10 is connected within a predetermined time (S13-Yes), the control unit 39 outputs a control signal for stopping the power supply to the power supply unit 37 (S15), and ends the process. do. As a result, the power of the measuring device 20 is turned off, and the process ends. On the other hand, when the control unit 39 determines that the puncture device 10 is not connected within a predetermined time (S13-No), the control unit 39 notifies the user to notify the user to prompt the connection with the puncture device 10. The unit 35 is controlled (S14). After that, the control unit 39 loops the processes of steps S13 and S14 until the puncture device 10 is connected.
 [改変例]
 次に、図10~図12を適宜参照しながら、本発明に係る成分測定装置100の改変例について説明する。以下に説明する改変例は、上述した実施形態と同一の機能を有する構成要件について同一の符号を付して詳細な説明を省略する。また、改変例において、特に言及しない構成、部材、および使用方法などについては、上述した実施形態と同様のものとしてよい。
[Modification example]
Next, a modified example of the component measuring device 100 according to the present invention will be described with reference to FIGS. 10 to 12 as appropriate. In the modification described below, the same reference numerals are given to the constituent elements having the same functions as those in the above-described embodiment, and detailed description thereof will be omitted. Further, in the modified example, the configuration, members, usage method and the like not particularly mentioned may be the same as those in the above-described embodiment.
 以下に示す改変例の成分測定装置100aは、穿刺デバイス10と測定デバイス20との連結形態が上述した形態と異なる。 The component measuring device 100a of the modified example shown below has a different connection form between the puncture device 10 and the measuring device 20 from the above-mentioned form.
 図10Aには、改変例となる穿刺デバイス10の構成が示されており、図10Bには、改変例となる測定デバイス20の構成が示されている。 FIG. 10A shows the configuration of the puncture device 10 as a modified example, and FIG. 10B shows the configuration of the measuring device 20 as a modified example.
 図10Aに示すように、穿刺デバイス10の第1当接面10aには、測定デバイス20と連結する際に測定デバイス20と嵌着するため、第1連結部15として機能する第1係合部15bが設けられている。図10Bに示すように、測定デバイス20の第2当接面20aには、穿刺デバイス10と連結する際に穿刺デバイス10と嵌着するため、第2連結部24として機能する第2係合部24bが設けられている。第1係合部15bおよび第2係合部24bは、互いに嵌合し合う部材(凹溝、凸条部材)からなる連結機構を構成する。穿刺デバイス10と測定デバイス20は、第1当接面10aと第2当接面20aとを突き合せた状態で少なくとも一方のデバイスを軸方向に沿ってスライド移動させることにより、第1係合部15bと第2係合部24bが嵌合して連結される。 As shown in FIG. 10A, the first contact surface 10a of the puncture device 10 is fitted with the measurement device 20 when it is connected to the measurement device 20, so that the first engagement portion functions as the first connection portion 15. 15b is provided. As shown in FIG. 10B, the second contact surface 20a of the measuring device 20 is fitted with the puncturing device 10 when connected to the puncturing device 10, so that the second engaging portion functions as the second connecting portion 24. 24b is provided. The first engaging portion 15b and the second engaging portion 24b form a connecting mechanism composed of members (concave grooves, ridge members) that are fitted to each other. The puncture device 10 and the measurement device 20 have a first engagement portion by sliding at least one device along the axial direction in a state where the first contact surface 10a and the second contact surface 20a are butted against each other. The 15b and the second engaging portion 24b are fitted and connected.
 ここで、第1係合部15bおよび第2係合部24bの形状について詳述する。図10Aに示すように、第1係合部15bは、第1当接面10aの長手方向の周縁に沿って軸方向に延在する一対の凹溝からなる。図10Bに示すように、第2係合部24bは、第2当接面20aの長手方向の周縁に沿って軸方向に延在し第2当接面20aから外方に突出する一対の凸条部材からなる。凸条部材および凹溝は、いずれも軸方向に同一の断面形状が連続する。また、凸条部材と凹溝は、それぞれ互いの嵌合が可能となるように、略同形状の断面形状を有している。なお、本実施形態に係る成分測定装置100aにおいて、第1係合部15bは凹溝、第2係合部24bは凸状部材で構成されているが、第1係合部15bを凸状部材とし、第2係合部24bを凹溝としてもよい。 Here, the shapes of the first engaging portion 15b and the second engaging portion 24b will be described in detail. As shown in FIG. 10A, the first engaging portion 15b is composed of a pair of concave grooves extending in the axial direction along the longitudinal peripheral edge of the first contact surface 10a. As shown in FIG. 10B, the second engaging portion 24b extends axially along the longitudinal peripheral edge of the second contact surface 20a and protrudes outward from the second contact surface 20a as a pair of protrusions. It consists of strip members. Both the ridge member and the concave groove have the same continuous cross-sectional shape in the axial direction. Further, the ridge member and the concave groove each have a cross-sectional shape having substantially the same shape so that they can be fitted to each other. In the component measuring device 100a according to the present embodiment, the first engaging portion 15b is composed of a concave groove and the second engaging portion 24b is composed of a convex member, but the first engaging portion 15b is a convex member. The second engaging portion 24b may be a concave groove.
 図11に示すように、穿刺デバイス10は、第1当接面10aと第2当接面20aとを当接させた状態で、軸方向に沿ってスライド移動させながら第1係合部15bと第2係合部24bを嵌合させることにより、測定デバイス20に連結される。また、穿刺デバイス10と測定デバイス20との連結状態は、第2筐体21に設けられた第2係合部24bと第1係合部15bとの係合を所定操作(例えばスライド操作)により解除される。穿刺デバイス10は、この解除状態において連結時と逆方向にスライド移動させことにより測定デバイス20との分離が可能となる。 As shown in FIG. 11, the puncture device 10 is in contact with the first contact surface 10a and the second contact surface 20a, and is slidably moved along the axial direction with the first engaging portion 15b. By fitting the second engaging portion 24b, it is connected to the measuring device 20. Further, in the connected state between the puncture device 10 and the measuring device 20, the engagement between the second engaging portion 24b and the first engaging portion 15b provided in the second housing 21 is performed by a predetermined operation (for example, a slide operation). It will be released. The puncture device 10 can be separated from the measurement device 20 by sliding and moving the puncture device 10 in the direction opposite to that at the time of connection in this released state.
 なお、第1係合部15bと第2係合部24bは、少なくとも穿刺デバイス10と測定デバイス20が着脱可能に連結できる構成であればよい。よって、第1係合部15bおよび第2係合部24bは、図10A、図10Bに示すような、スライド移動によって着脱される凸条部材および凹溝に限定されない。 The first engaging portion 15b and the second engaging portion 24b may be configured such that at least the puncture device 10 and the measuring device 20 can be detachably connected to each other. Therefore, the first engaging portion 15b and the second engaging portion 24b are not limited to the ridge members and the concave grooves that are attached and detached by the slide movement as shown in FIGS. 10A and 10B.
 また、改変例の成分測定装置100aにおいて、デバイス検出部33は、穿刺デバイス10と測定デバイス20との分離状態および嵌合による連結状態を検出する構成となる。デバイス検出部33は、一例として、測定デバイス20に対して穿刺デバイス10が正常に嵌合された状態において、穿刺デバイス10の嵌合時のスライド移動により所定方向に移動する検出片と、検出片の移動位置を電気的に検出する検出部(検出回路)と、を有する検出機構としてよい。デバイス検出部33は、検出片が所定位置まで移動したことを検出部で検出することにより、穿刺デバイス10との連結状態および分離状態を検出し、デバイス同士の連結状態または分離状態に応じた状態情報を制御部39に出力する。 Further, in the component measuring device 100a of the modified example, the device detection unit 33 is configured to detect the separated state of the puncture device 10 and the measuring device 20 and the connected state by fitting. As an example, the device detection unit 33 has a detection piece that moves in a predetermined direction by sliding movement when the puncture device 10 is fitted, and a detection piece in a state where the puncture device 10 is normally fitted to the measurement device 20. It may be a detection mechanism having a detection unit (detection circuit) for electrically detecting the moving position of the above. The device detection unit 33 detects the connection state and the separation state with the puncture device 10 by detecting that the detection piece has moved to a predetermined position, and the state according to the connection state or the separation state between the devices. The information is output to the control unit 39.
 なお、デバイス検出部33は、穿刺デバイス10と測定デバイス20との連結が検出可能な機能を有していれば、その構成は限定されない。 The configuration of the device detection unit 33 is not limited as long as it has a function of detecting the connection between the puncture device 10 and the measurement device 20.
 図12には、改変例の成分測定装置100aにおける穿刺デバイス10と測定デバイス20の連結動作例が示されている。 FIG. 12 shows an example of a connection operation between the puncture device 10 and the measurement device 20 in the component measuring device 100a of the modified example.
 図12Aには、測定デバイス20による測定が終了し、穿刺デバイス10を測定デバイス20に連結させる前の状態が示されている。図12Bに示すように、穿刺デバイス10と測定デバイス20を連結させる場合は、穿刺デバイス10の第1当接面10aと測定デバイス20の第2当接面20aとを対向させた状態で第1係合部15bを第2係合部24bに挿入させる。この挿入状態において、穿刺デバイス10の前端部と測定デバイス20の前端部が軸方向と交差する方向で並列するように、例えば穿刺デバイス10を軸方向に沿ってスライド移動させる。スライド移動は、例えば一方のデバイスを固定した状態で他方のデバイスをスライド移動させればよい。これにより、図12Cに示すように、第1係合部15bと第2係合部24bは、互いに嵌合し合い、第1当接面10aと第2当接面20aが当接した状態で穿刺デバイス10と測定デバイス20が連結される。 FIG. 12A shows a state in which the measurement by the measuring device 20 is completed and before the puncture device 10 is connected to the measuring device 20. As shown in FIG. 12B, when the puncture device 10 and the measurement device 20 are connected, the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 face each other. The engaging portion 15b is inserted into the second engaging portion 24b. In this inserted state, for example, the puncture device 10 is slid and moved along the axial direction so that the front end portion of the puncture device 10 and the front end portion of the measurement device 20 are parallel to each other in the direction intersecting the axial direction. For slide movement, for example, one device may be fixed and the other device may be slid. As a result, as shown in FIG. 12C, the first engaging portion 15b and the second engaging portion 24b are fitted to each other, and the first contact surface 10a and the second contact surface 20a are in contact with each other. The puncture device 10 and the measurement device 20 are connected.
 [作用効果]
 以上説明したように、本実施形態に係る成分測定装置100は、生体表面を穿刺して血液を滲出させるように構成された穿刺デバイス10と、生体表面から滲出した血液を検査用媒体T内に導入させることで血液に含まれるグルコース成分の成分量(血糖値)を測定するように構成された測定デバイス20と、を備え、穿刺デバイス10は、第1筐体11と、第1筐体11の外表面のうち、少なくとも一の面に設けられた第1当接面10aと、第1連結部15とを有し、測定デバイス20は、第2筐体21と、第2筐体21の外表面のうち、少なくとも一の面に設けられた第2当接面20aと、第1連結部15と連結可能な第2連結部24とを有している。また、成分測定装置100において、穿刺デバイス10と測定デバイス20は、第1当接面10aと第2当接面20aとが対向して当接した状態で第1連結部15と第2連結部24が連結されることにより、第1筐体11と第2筐体21が一体化されて成分測定装置100の筐体110を形成するように構成され、第1連結部15と第2連結部24との連結が解除されることにより、第1当接面10aおよび第2当接面20aが分離面101となって穿刺デバイス10と測定デバイス20が別体となるように構成され、第1筐体11と第2筐体21は、筐体110の外表面となる領域に筐体110の外表面から突出する部分を有していない。
[Action effect]
As described above, the component measuring device 100 according to the present embodiment has a piercing device 10 configured to puncture the surface of the living body and exude blood, and the blood exuded from the surface of the living body is contained in the test medium T. A measuring device 20 configured to measure the amount of glucose component (blood glucose level) contained in blood by introducing the puncturing device 10 is provided, and the puncturing device 10 includes a first housing 11 and a first housing 11. The measuring device 20 has a first contact surface 10a and a first connecting portion 15 provided on at least one of the outer surfaces of the above, and the measuring device 20 is a second housing 21 and a second housing 21. It has a second contact surface 20a provided on at least one surface of the outer surface, and a second connecting portion 24 that can be connected to the first connecting portion 15. Further, in the component measuring device 100, the puncture device 10 and the measuring device 20 are in a state where the first contact surface 10a and the second contact surface 20a face each other and are in contact with each other, and the first connecting portion 15 and the second connecting portion are in contact with each other. By connecting 24, the first housing 11 and the second housing 21 are integrated to form the housing 110 of the component measuring device 100, and the first connecting portion 15 and the second connecting portion are connected. When the connection with the 24 is released, the first contact surface 10a and the second contact surface 20a become the separation surface 101, and the puncture device 10 and the measurement device 20 are configured to be separate bodies. The housing 11 and the second housing 21 do not have a portion protruding from the outer surface of the housing 110 in the region to be the outer surface of the housing 110.
 このような構成とすることで、成分測定装置100は、非使用時において穿刺デバイス10の第1当接面10aと、測定デバイス20の第2当接面20aを突き合せた状態で着脱可能に連結させて一体化したときに筐体110が形成されるため、携帯性および意匠性に優れた装置となる。穿刺デバイス10と測定デバイス20を一体化させた場合において、成分測定装置100の筐体110の外表面に凸形状がない状態となる。そのため、成分測定装置100は、携帯時に他の部分との引っ掛かりが防止されると共に、周囲から医療器具として認識され難くなり、携帯性と意匠性が向上する。さらに、成分測定装置100は、使用時において、穿刺デバイス10と測定デバイス20を分離可能なため、各デバイスを別体で使用することができ、操作性もよい。 With such a configuration, the component measuring device 100 can be attached and detached in a state where the first contact surface 10a of the puncture device 10 and the second contact surface 20a of the measurement device 20 are butted against each other when not in use. Since the housing 110 is formed when they are connected and integrated, the device is excellent in portability and design. When the puncture device 10 and the measuring device 20 are integrated, the outer surface of the housing 110 of the component measuring device 100 has no convex shape. Therefore, the component measuring device 100 is prevented from being caught by other parts when being carried, and is difficult to be recognized as a medical device from the surroundings, so that the portability and design are improved. Further, since the component measuring device 100 can separate the puncture device 10 and the measuring device 20 at the time of use, each device can be used separately and the operability is good.
 また、本実施形態に係る成分測定装置100において、好適には、第1筐体11は、分離面101を介して第1当接面10aと第2当接面20aを当接させた際に、互いに相補的に接続されて一体化する構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, when the first housing 11 abuts the first contact surface 10a and the second contact surface 20a via the separation surface 101, the first housing 11 is brought into contact with the first contact surface 10a. , May be configured to be connected complementarily to each other and integrated.
 このような構成とすれば、穿刺デバイス10と測定デバイス20とを接続させた際に、第1筐体11と第2筐体21とが一体化して成分測定装置100の筐体110を構成することができるため、携帯性および意匠性に優れた装置となる。 With such a configuration, when the puncture device 10 and the measuring device 20 are connected, the first housing 11 and the second housing 21 are integrated to form the housing 110 of the component measuring device 100. Therefore, the device has excellent portability and design.
 また、本実施形態に係る成分測定装置100において、好適には、第1当接面10aの外形は、第2当接面20aの外形と同一形状を有する構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, the outer shape of the first contact surface 10a may preferably have the same shape as the outer shape of the second contact surface 20a.
 このような構成とすれば、穿刺デバイス10と測定デバイス20を組み合わせた際に、筐体110の外表面から突出する部分をなくすことができる。 With such a configuration, when the puncture device 10 and the measurement device 20 are combined, the portion protruding from the outer surface of the housing 110 can be eliminated.
 また、本実施形態に係る成分測定装置100において、好適には、第1連結部15は、第1当接面10aと対向して第1筐体11の内方に設けられた第1磁性部材15aであり、第2連結部24は、第2当接面20aと対向して第2筐体21の内方に設けられた第2磁性部材24aであり、第1磁性部材15aと第2磁性部材24aのうち、いずれか一方は磁石で構成され、他方は磁石と磁極の異なる磁石または磁性体で構成されてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, the first connecting portion 15 is a first magnetic member provided inside the first housing 11 facing the first contact surface 10a. 15a, the second connecting portion 24 is a second magnetic member 24a provided inside the second housing 21 facing the second contact surface 20a, and is the first magnetic member 15a and the second magnetic member. One of the members 24a may be made of a magnet, and the other may be made of a magnet or a magnetic material having a magnetic pole different from that of the magnet.
 穿刺デバイス10と測定デバイス20は、第1磁性部材15aからなる第1連結部15と、第2磁性部材24aからなる第2連結部24との磁気的な連結が可能であるため、両デバイスを連結させる構成が複雑化せず、使用時も容易に分離させることができる。 Since the puncture device 10 and the measurement device 20 can be magnetically connected to the first connecting portion 15 made of the first magnetic member 15a and the second connecting portion 24 made of the second magnetic member 24a, both devices can be connected. The configuration to be connected is not complicated, and it can be easily separated even during use.
 また、本実施形態に係る成分測定装置100において、好適には、第1連結部15は、第1当接面10aに設けられた第1係合部15bであり、第2連結部24は、第2当接面20aに設けられて第1係合部15bに対して軸方向に沿ったスライド移動により嵌着される第2係合部24bとしてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, the first connecting portion 15 is a first engaging portion 15b provided on the first contact surface 10a, and the second connecting portion 24 is a second connecting portion 24. It may be a second engaging portion 24b provided on the second contact surface 20a and fitted to the first engaging portion 15b by sliding movement along the axial direction.
 穿刺デバイス10と測定デバイス20は、第1係合部15bからなる第1連結部15と、第2係合部24bからなる第2連結部24からなる連結構造を有するため、両デバイスを連結または分離させる際は、少なくとも一方のデバイスを軸方向に沿ってスライド移動という簡易的な操作によって連結および分離が可能となる。 Since the puncture device 10 and the measuring device 20 have a connecting structure including a first connecting portion 15 including a first engaging portion 15b and a second connecting portion 24 composed of a second engaging portion 24b, both devices are connected or connected. When separating, at least one device can be connected and separated by a simple operation of sliding along the axial direction.
 また、本実施形態に係る成分測定装置100において、好適には、測定デバイス20は、第2当接面20aに配置された表示面36aに血液の測定結果(血糖値)を表示させる表示部36を備えた構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, the measuring device 20 is a display unit 36 that displays a blood measurement result (blood glucose level) on a display surface 36a arranged on the second contact surface 20a. It may be configured with.
 このような構成とすることで、成分測定装置100は、穿刺デバイス10と測定デバイス20を連結させて一体化した状態において、筐体110の外表面に表示面36aが露出しないため、周囲から医療器具として認識され難くなる。 With such a configuration, in the component measuring device 100, when the puncture device 10 and the measuring device 20 are connected and integrated, the display surface 36a is not exposed on the outer surface of the housing 110, so that medical treatment is performed from the surroundings. It becomes difficult to be recognized as an instrument.
 また、本実施形態に係る成分測定装置100において、好適には、前記第1筐体および前記第2筐体は、少なくとも一部に平坦面が形成される構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, the first housing and the second housing may preferably have a configuration in which a flat surface is formed at least partially.
 このような構成により、穿刺デバイス10と測定デバイス20を分離した状態で両デバイスをテーブルなどの載置面に載置したとき、各デバイスは、載置面に載置したときに生じ得る転がりが防止される。 With such a configuration, when both devices are placed on a mounting surface such as a table with the puncture device 10 and the measuring device 20 separated, each device may have rolling that may occur when the device is placed on the mounting surface. Be prevented.
 また、本実施形態に係る成分測定装置100において、好適には、測定デバイス20は、測定デバイス20に対する駆動電力の供給制御を行う電源部37と、穿刺デバイス10と測定デバイス20との分離状態および連結状態を検出するデバイス検出部33と、デバイス検出部33による検出結果に基づき、電源部37を制御して供給する駆動電力を変化させる制御部39と、を備えた構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, the measuring device 20 has a power supply unit 37 that controls the supply of driving power to the measuring device 20, and a separated state between the puncturing device 10 and the measuring device 20. The configuration may include a device detection unit 33 that detects the connected state, and a control unit 39 that controls the power supply unit 37 and changes the drive power to be supplied based on the detection result by the device detection unit 33.
 このような構成により、成分測定装置100は、穿刺デバイス10と測定デバイス20との分離状態および連結状態に基づいて供給する電力量を変化させることができるため、省電力化を図ることができる。 With such a configuration, the component measuring device 100 can change the amount of electric power supplied based on the separated state and the connected state of the puncture device 10 and the measuring device 20, so that power saving can be achieved.
 また、本実施形態に係る成分測定装置100において、好適には、測定デバイス20は、血液に含まれるグルコース成分の成分量を測定する測定部31と、所定の報知を行う報知部35を備え、制御部39は、測定部31による測定が終了した後、検査用媒体Tが所定時間内に取り外されていないと判断した場合、検査用媒体Tの取り外しを促す報知を報知部35に実行させるように構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, preferably, the measuring device 20 includes a measuring unit 31 for measuring the component amount of the glucose component contained in blood and a notifying unit 35 for performing predetermined notification. When the control unit 39 determines that the inspection medium T has not been removed within a predetermined time after the measurement by the measurement unit 31 is completed, the control unit 39 causes the notification unit 35 to execute a notification prompting the removal of the inspection medium T. It may be configured as.
 このような構成により、成分測定装置100は、測定部31の測定が終了した後、検査用媒体Tが取り外されていないことを使用者に認識させることができるため、検査用媒体Tの取り外し忘れを防止することができる。 With such a configuration, the component measuring device 100 can make the user recognize that the inspection medium T has not been removed after the measurement of the measuring unit 31 is completed, so that the inspection medium T is forgotten to be removed. Can be prevented.
 また、本実施形態に係る成分測定装置100において、好適には、さらに、制御部39は、検査用媒体Tが取り外された後、デバイス検出部33による検出結果に基づき、所定時間内に穿刺デバイス10と測定デバイス20とが連結されていないと判断した場合、穿刺デバイス10と測定デバイス20との連結を促す報知を報知部35に実行させる構成としてもよい。 Further, in the component measuring device 100 according to the present embodiment, more preferably, the control unit 39 is a puncture device within a predetermined time based on the detection result by the device detection unit 33 after the inspection medium T is removed. When it is determined that the 10 and the measuring device 20 are not connected, the notification unit 35 may be configured to execute a notification prompting the connection between the puncture device 10 and the measuring device 20.
 成分測定装置100は、携帯性を向上させるため、穿刺デバイス10と測定デバイス20は使用時に分離可能であって共に小型化が図られたデバイスとなっているため、使用後にどこかへ置き忘れし易い。しかしながら、成分測定装置100は、血液の成分測定処理が終了した後に所定タイミングで穿刺デバイス10と測定デバイス20との連結を促す報知を行うため、穿刺デバイス10と測定デバイス20の置き忘れを防止することができる。 In the component measuring device 100, in order to improve portability, the puncture device 10 and the measuring device 20 are separable at the time of use, and both are miniaturized devices, so that it is easy to misplace them somewhere after use. .. However, since the component measuring device 100 gives a notification prompting the connection between the puncturing device 10 and the measuring device 20 at a predetermined timing after the blood component measuring process is completed, it is necessary to prevent the puncturing device 10 and the measuring device 20 from being misplaced. Can be done.
 また、本実施形態に係る成分測定装置100において、好適には、体液は、使用者の血液であり、成分は、血液に含まれるグルコース成分としてもよい。 Further, in the component measuring device 100 according to the present embodiment, the body fluid is preferably the blood of the user, and the component may be a glucose component contained in the blood.
 成分測定装置100は、例えば測定する成分として使用者の血液に含まれるグルコース成分量に基づく血糖値を測定する血糖自己測定機器(SMBG機器)に採用されることにより、携帯性に優れ、かつ外出先において医療器具として認識され難い機器と成り得る。 The component measuring device 100 is excellent in portability and goes out by being adopted in a blood glucose self-measuring device (SMBG device) that measures a blood glucose level based on the amount of glucose component contained in the user's blood as a component to be measured, for example. It can be a device that is difficult to be recognized as a medical device in the future.
 本出願は、2020年9月23日に出願された日本国特許出願第2020-158863号に基づいており、その開示内容は、参照により全体として引用されている。 This application is based on Japanese Patent Application No. 2020-158863 filed on September 23, 2020, and the disclosure content is cited as a whole by reference.
 10 穿刺デバイス(10a 第1当接面)、
 11 第1筐体(11a 第1平坦部)、
 12 針装着部(12a 開口部、12b 針係合部)、
 13 穿刺操作部、
 14 針イジェクト操作部(14a 第1操作体)、
 15 第1連結部(15a 第1磁性部材、15b 第1係合部)、
 16 深度調整部、
 20 測定デバイス(20a 第2当接面)、
 21 第2筐体(21a 第2平坦部)、
 22 媒体装着部(22a 第2開口部)、
 23 媒体イジェクト操作部(23a 第2操作体)、
 24 第2連結部(24a 第2磁性部材、24b 第2係合部)、
 31 測定部、
 32 温度検出部、
 33 デバイス検出部、
 34 通信部、
 35 報知部、
 36 表示部(36a 表示面)、
 37 電源部、
 38 記憶部、
 39 制御部(39a 計時部、39b 算出部、39c 判断部、39d 生成処理部)、
 100、100a 成分測定装置(101 分離面、102 分離断面端、110 筐体)、
 N 穿刺針カートリッジ(N1 針ホルダー、N2 穿刺針)、
 T 検査用媒体(T1 検査部、T2 点着口)。
10 Puncture device (10a first contact surface),
11 First housing (11a first flat portion),
12 needle mounting part (12a opening, 12b needle engaging part),
13 Puncture operation part,
14-needle eject operation unit (14a first operation unit),
15 First connecting portion (15a first magnetic member, 15b first engaging portion),
16 Depth adjustment unit,
20 Measuring device (20a second contact surface),
21 Second housing (21a second flat part),
22 Medium mounting portion (22a second opening),
23 Medium eject operation unit (23a second operation unit),
24 Second connecting portion (24a second magnetic member, 24b second engaging portion),
31 Measuring unit,
32 Temperature detector,
33 Device detector,
34 Communication Department,
35 Notification unit,
36 display unit (36a display surface),
37 Power supply,
38 Memory
39 Control unit (39a timekeeping unit, 39b calculation unit, 39c judgment unit, 39d generation processing unit),
100, 100a component measuring device (101 separation surface, 102 separation cross-section end, 110 housing),
N puncture needle cartridge (N1 needle holder, N2 puncture needle),
T inspection medium (T1 inspection unit, T2 point arrival).

Claims (11)

  1.  生体表面を穿刺して体液を滲出させるように構成された穿刺デバイスと、
     前記体液を検査用媒体内に導入させることで前記体液に含まれる所定の成分の成分量を測定するように構成された測定デバイスと、を備えた成分測定装置であって、
     前記穿刺デバイスは、第1筐体と、前記第1筐体の外表面のうち、少なくとも一の面に設けられた第1当接面と、第1連結部とを有し、
     前記測定デバイスは、第2筐体と、前記第2筐体の外表面のうち、少なくとも一の面に設けられた第2当接面と、前記第1連結部と連結可能な第2連結部とを有し、
     前記穿刺デバイスと前記測定デバイスは、前記第1当接面と前記第2当接面とが対向して当接した状態で前記第1連結部と前記第2連結部が連結されることにより、前記第1筐体と前記第2筐体が一体化されて前記成分測定装置の筐体を形成するように構成され、
     前記第1連結部と前記第2連結部との連結が解除されることにより、前記第1当接面および前記第2当接面が分離面となって前記穿刺デバイスと前記測定デバイスが別体となるように構成され、
     前記第1筐体と前記第2筐体は、前記筐体の外表面となる領域に前記筐体の外表面から突出する部分を有していない、成分測定装置。
    A puncture device configured to puncture the surface of a living body and exude body fluids,
    A component measuring device comprising a measuring device configured to measure the amount of a predetermined component contained in the body fluid by introducing the body fluid into a test medium.
    The puncture device has a first housing, a first contact surface provided on at least one surface of the outer surface of the first housing, and a first connecting portion.
    The measuring device includes a second housing, a second contact surface provided on at least one surface of the outer surface of the second housing, and a second connecting portion that can be connected to the first connecting portion. And have
    In the puncture device and the measuring device, the first connecting portion and the second connecting portion are connected in a state where the first contact surface and the second contact surface face each other and are in contact with each other. The first housing and the second housing are integrated to form a housing of the component measuring device.
    When the connection between the first connecting portion and the second connecting portion is released, the first contact surface and the second contact surface become separate surfaces, and the puncture device and the measurement device are separated from each other. Is configured to be
    The first housing and the second housing are component measuring devices having no portion protruding from the outer surface of the housing in a region to be the outer surface of the housing.
  2.  前記第1筐体と前記第2筐体は、前記分離面を介して前記第1当接面と前記第2当接面を当接させた際に、互いに相補的に接続されて一体化する、請求項1に記載の成分測定装置。 The first housing and the second housing are complementary to each other and integrated when the first contact surface and the second contact surface are brought into contact with each other via the separation surface. , The component measuring apparatus according to claim 1.
  3.  前記第1当接面の外形は、前記第2当接面の外形と同一形状を有する、請求項1または2に記載の成分測定装置。 The component measuring device according to claim 1 or 2, wherein the outer shape of the first contact surface has the same shape as the outer shape of the second contact surface.
  4.  前記第1連結部は、前記第1当接面と対向して前記第1筐体の内方に設けられた第1磁性部材であり、
     前記第2連結部は、前記第2当接面と対向して前記第2筐体の内方に設けられた第2磁性部材であり、
     前記第1磁性部材と前記第2磁性部材のうち、いずれか一方は磁石で構成され、他方は前記磁石と磁極の異なる磁石または磁性体で構成される、請求項1~3のいずれか1項に記載の成分測定装置。
    The first connecting portion is a first magnetic member provided inside the first housing so as to face the first contact surface.
    The second connecting portion is a second magnetic member provided inside the second housing so as to face the second contact surface.
    Any one of claims 1 to 3, wherein one of the first magnetic member and the second magnetic member is composed of a magnet, and the other is composed of a magnet or a magnetic material having a magnetic pole different from that of the magnet. The component measuring device according to.
  5.  前記第1連結部は、前記第1当接面に設けられた第1係合部であり、
     前記第2連結部は、前記第2当接面に設けられて前記第1係合部に対して軸方向に沿ったスライド移動により嵌着される第2係合部である、請求項1~3のいずれか1項に記載の成分測定装置。
    The first connecting portion is a first engaging portion provided on the first contact surface, and is a first engaging portion.
    Claims 1 to 1, wherein the second connecting portion is a second engaging portion provided on the second contact surface and fitted to the first engaging portion by sliding movement along an axial direction. Item 3. The component measuring apparatus according to any one of 3.
  6.  前記測定デバイスは、前記第2当接面に配置された表示面に前記体液の測定結果を表示させる表示部を備えた、請求項1~5のいずれか1項に記載の成分測定装置。 The component measuring device according to any one of claims 1 to 5, wherein the measuring device includes a display unit for displaying the measurement result of the body fluid on a display surface arranged on the second contact surface.
  7.  前記第1筐体および前記第2筐体は、少なくとも一部に平坦面が形成される、請求項1~6のいずれか1項に記載の成分測定装置。 The component measuring device according to any one of claims 1 to 6, wherein the first housing and the second housing have a flat surface formed at least in a part thereof.
  8.  前記測定デバイスは、前記測定デバイスに対する駆動電力の供給制御を行う電源部と、
     前記穿刺デバイスと前記測定デバイスとの分離状態および連結状態を検出するデバイス検出部と、
     前記デバイス検出部による検出結果に基づき、前記電源部を制御して供給する前記駆動電力を変化させる制御部と、を備える、請求項1~7のいずれか1項に記載の成分測定装置。
    The measuring device includes a power supply unit that controls the supply of driving power to the measuring device.
    A device detection unit that detects the separated state and the connected state of the puncture device and the measuring device, and
    The component measuring device according to any one of claims 1 to 7, further comprising a control unit that controls and supplies the power supply unit based on a detection result by the device detection unit.
  9.  前記測定デバイスは、前記体液に含まれる前記成分の成分量を測定する測定部と、
     所定の報知を行う報知部を備え、
     前記制御部は、前記測定部による測定が終了した後、前記検査用媒体が所定時間内に取り外されていないと判断した場合、前記検査用媒体の取り外しを促す報知を前記報知部に実行させる、請求項8に記載の成分測定装置。
    The measuring device includes a measuring unit that measures the amount of the component contained in the body fluid, and a measuring unit.
    Equipped with a notification unit that performs predetermined notification
    When the control unit determines that the inspection medium has not been removed within a predetermined time after the measurement by the measurement unit is completed, the control unit causes the notification unit to execute a notification prompting the removal of the inspection medium. The component measuring device according to claim 8.
  10.  さらに、前記制御部は、前記検査用媒体が取り外された後、前記デバイス検出部による前記検出結果に基づき、所定時間内に前記穿刺デバイスと前記測定デバイスとが連結されていないと判断した場合、前記穿刺デバイスと前記測定デバイスとの連結を促す報知を前記報知部に実行させる、請求項9に記載の成分測定装置。 Further, when the control unit determines that the puncture device and the measurement device are not connected within a predetermined time based on the detection result by the device detection unit after the inspection medium is removed. The component measuring device according to claim 9, wherein the notification unit is made to execute a notification prompting the connection between the puncture device and the measuring device.
  11.  前記体液は、使用者の血液であり、前記成分は、前記血液に含まれるグルコース成分である、請求項1~10のいずれか1項に記載の成分測定装置。 The component measuring device according to any one of claims 1 to 10, wherein the body fluid is the blood of the user, and the component is a glucose component contained in the blood.
PCT/JP2021/031666 2020-09-23 2021-08-30 Component measurement apparatus WO2022064966A1 (en)

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JP2001524680A (en) * 1997-11-28 2001-12-04 ロシュ ダイアグノスティックス ゲーエムベーハー Analytical measuring instrument with incision instrument
JP2002515302A (en) * 1998-05-20 2002-05-28 ノボ ノルディスク アクティーゼルスカブ Medical devices for use by patients for self-medication of diabetes
JP2011064597A (en) * 2009-09-17 2011-03-31 Terumo Corp Blood sugar meter and method of measuring blood sugar value
JP2016515024A (en) * 2013-03-14 2016-05-26 ニプロ ダイアグナスティックス,インコーポレーテッド Measuring instrument with replaceable modules

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001524680A (en) * 1997-11-28 2001-12-04 ロシュ ダイアグノスティックス ゲーエムベーハー Analytical measuring instrument with incision instrument
JP2002515302A (en) * 1998-05-20 2002-05-28 ノボ ノルディスク アクティーゼルスカブ Medical devices for use by patients for self-medication of diabetes
JP2011064597A (en) * 2009-09-17 2011-03-31 Terumo Corp Blood sugar meter and method of measuring blood sugar value
JP2016515024A (en) * 2013-03-14 2016-05-26 ニプロ ダイアグナスティックス,インコーポレーテッド Measuring instrument with replaceable modules

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