WO2011132657A1 - Liquid-medicine dosing device - Google Patents

Liquid-medicine dosing device Download PDF

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Publication number
WO2011132657A1
WO2011132657A1 PCT/JP2011/059585 JP2011059585W WO2011132657A1 WO 2011132657 A1 WO2011132657 A1 WO 2011132657A1 JP 2011059585 W JP2011059585 W JP 2011059585W WO 2011132657 A1 WO2011132657 A1 WO 2011132657A1
Authority
WO
WIPO (PCT)
Prior art keywords
port
container
state
drug
puncture needle
Prior art date
Application number
PCT/JP2011/059585
Other languages
French (fr)
Japanese (ja)
Inventor
等 沖原
美緒 百貫
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 JP2012511659A priority Critical patent/JPWO2011132657A1/en
Publication of WO2011132657A1 publication Critical patent/WO2011132657A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/22Valves or arrangement of valves
    • A61M39/223Multiway valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14Details; Accessories therefor
    • A61J1/20Arrangements for transferring or mixing fluids, e.g. from vial to syringe
    • A61J1/2003Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
    • A61J1/2006Piercing means
    • A61J1/201Piercing means having one piercing end
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14Details; Accessories therefor
    • A61J1/20Arrangements for transferring or mixing fluids, e.g. from vial to syringe
    • A61J1/2003Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
    • A61J1/2048Connecting means
    • A61J1/2058Connecting means having multiple connecting ports
    • A61J1/2062Connecting means having multiple connecting ports with directional valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/14Details; Accessories therefor
    • A61J1/20Arrangements for transferring or mixing fluids, e.g. from vial to syringe
    • A61J1/2096Combination of a vial and a syringe for transferring or mixing their contents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/22Valves or arrangement of valves
    • A61M2039/229Stopcocks

Definitions

  • the present invention relates to a drug solution administration device.
  • the drug when a patient self-injects a drug solution such as a blood product, the drug may be dissolved or diluted with a liquid, and the drug solution may be sucked with a syringe and used.
  • An object of the present invention is to provide a drug administration device that can easily and quickly dissolve or dilute a drug to obtain a drug solution and allow the drug solution to flow out of a puncture needle.
  • the present invention provides: A first port; a second port; and a third port.
  • a multiway cock that can take a first state in which the first port communicates with the second port and a second state in which the first port communicates with the third port;
  • a connecting device provided in the second port;
  • a second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
  • the first container is connected to the connecting device, the second container is connected to the first port, and the liquid is discharged from the second container in a state where the multiway cock is in the first state.
  • the drug solution After being introduced into the first container and dissolving or diluting the drug to obtain a drug solution, the drug solution is inhaled from the first container into the second container, Next, the multi-way cock is in the second state, the chemical solution is discharged from the second container, and the chemical solution is configured to flow out of the puncture needle through the tube. It is an instrument.
  • the present invention includes a first port, a second port, and a third port, and the first port, the second port, and the third port.
  • a multiway stopcock capable of taking a first state in which the first port and the second port are in communication with each other and a second state in which the first port and the third port are in communication with each other ,
  • a connecting device provided in the second port;
  • a first container in which a medicine connected to the second port via the connection device is stored;
  • a tube having one end connected to the third port and a puncture needle connected to the other end;
  • a filter that is detachably attached to the first port and that allows gas to pass but bacteria not to pass through;
  • a second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
  • the filter has a housing that is detachably attached to the first port, and a filter member that is installed in the housing and through which gas passes but bacteria do not pass.
  • the inside of the first container has a negative pressure, and when the first container is connected to the second port via the connecting device, the air that has passed through the filter is introduced into the first container. It is preferable that it is comprised so that.
  • the first port and the third port are arranged on a straight line, and the second port protrudes to the side of the first port. It is preferable.
  • the puncture needle is preferably a winged needle.
  • the drug solution administration device of the present invention it is provided in the vicinity of the puncture needle in the middle of the tube, and has an easy-to-break portion that breaks more easily than the surrounding portion, It is preferable that the breakable portion is broken so that the first portion including the puncture needle can be separated from the second portion other than the first portion.
  • the easily breakable portion is provided separately from the puncture needle and in a region within 10 cm from the proximal end of the puncture needle of the tube.
  • the tube includes a distal tube connected to the puncture needle, a proximal tube positioned proximal to the distal tube, the distal tube, and the A connecting member that connects the proximal tube, It is preferable that the breakable part is formed in the connecting member.
  • the connecting member includes a distal end portion connected to the distal end side tube, a proximal end portion connected to the proximal end tube, the distal end portion, and the proximal end portion. Having an intermediate part for connecting The intermediate part has a thin part thinner than the distal end part and the base end part, It is preferable that the thin portion constitutes the easily breakable portion.
  • the multi-way stopcock has a cylindrical shape, and a cylindrical portion in which the first port, the second port, and the third port are respectively disposed on an outer peripheral portion thereof.
  • a cock having a cylindrical body portion that is rotatably inserted into the cylindrical portion and has flow paths corresponding to the first port, the second port, and the third port, respectively. And by turning the cock, the first state and the second state can be taken, It is preferable to further include a detachment mechanism that prevents the connection tool from being detached from the second port in the first state, and allows the connection tool to be detached from the second port in the second state. .
  • connection device has a tubular portion for connection to the second port
  • the detachment mechanism is provided on the cock with a protruding piece formed on the outer peripheral portion of the tubular portion and on a circumference centering on the central axis of the trunk portion in conjunction with the turning operation of the cock.
  • An engaging piece that moves, In the first state, the engagement piece engages with the protruding piece to prevent the connection tool from being detached from the second port, and in the second state, the engagement is released. It is preferable that the connecting device can be detached from the second port.
  • a pair of the projecting pieces are provided on opposite sides via the central axis of the second port, It is preferable that a pair of the engaging pieces are provided corresponding to the pair of protruding pieces.
  • FIG. 1 is a side view (partially sectional view) showing a first embodiment of a drug solution administration device of the present invention.
  • FIG. 2 is a perspective view showing a drug solution administration device body of the drug solution administration device shown in FIG.
  • FIG. 3 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 4 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 5 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 6 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 7 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 1 is a side view (partially sectional view) showing a first embodiment of a drug solution administration device of the present invention.
  • FIG. 2 is a perspective view showing a drug solution administration device body of the drug solution administration device shown in FIG.
  • FIG. 8 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1.
  • FIG. 9 is a perspective view showing the vicinity of the puncture needle of the drug solution administration device (second embodiment) of the present invention.
  • 10 is a schematic cross-sectional view of a connecting member in the drug solution administration device shown in FIG. 9.
  • 11 is a perspective view showing a separated state in the vicinity of the puncture needle of the drug solution administration device shown in FIG.
  • FIG. 12 is a perspective view sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention.
  • FIG. 9 is a perspective view showing the vicinity of the puncture needle of the drug solution administration device (second embodiment) of the present invention.
  • 10 is a schematic cross-sectional view of a connecting member in the drug solution administration device shown in FIG. 9.
  • 11 is a perspective view showing a separated state in the vicinity of the puncture needle of the drug solution administration device shown in
  • FIG. 13 is a perspective view sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention.
  • 14 is a cross-sectional view taken along line AA in FIG.
  • FIG. 15 is a cross-sectional view taken along line BB in FIG.
  • FIG. 1 is a side view (partially sectional view) showing a first embodiment of a drug solution administration device of the present invention
  • FIG. 2 is a perspective view showing a drug solution administration device body of the drug solution administration device shown in FIG.
  • FIG. 8 is a side view for explaining the procedure for using the drug solution administration device shown in FIG.
  • FIG. 1 the right side in FIG. 1, FIG. 3 to FIG. 6 and FIG. 8 is the “front end”, the left side is the “base end (rear end)”, and the left side in FIG. Is described as “base end”.
  • the drug solution administration device 1 of the present embodiment shown in these drawings is a device used when performing self-injection of a drug solution.
  • the drug solution administration device 1 is a drug solution administration device body 2.
  • a syringe 6 as a second container (inhalation / discharge device) capable of inhaling and discharging liquid
  • a vial (drug container) 7 as a first container in which a medicine is stored.
  • the first container is not limited to a vial as long as it is a container in which a medicine is stored, and other examples include an ampoule.
  • the second container is not limited to a syringe as long as it can inhale and discharge liquid, and other examples include a container made of an elastic body or the like.
  • medical solution administration instrument 1 can be used also when not only self-injection but medical workers, such as a doctor and a nurse, inject with respect to a patient, for example.
  • medical workers such as a doctor and a nurse
  • the drug solution administration device body 2 includes a three-way stopcock (multi-way stopcock) 3, a tube 4, a puncture needle 5, a filter 8 through which gas passes but bacteria do not pass, and a connection device 9 to which a vial 7 is connected. Part 11.
  • the three-way cock 3 includes a main body 31 and a cock 35.
  • the main body 31 is formed on the outer periphery of the cylindrical portion 32 and the cylindrical portion 32, and the first port 331, the second port 332, and the third port that protrude outward in the radial direction of the cylindrical portion 32. 333.
  • the first port 331, the second port 332, and the third port 333 each have a tubular shape and are arranged at equal angular intervals, that is, at an angle of 90 °.
  • the first port 331 and the third port 333 are arranged at an angle of 180 °, that is, arranged on a straight line.
  • the second port 332 protrudes toward the side of the first port 331 and the second port 332, that is, an angle of 90 ° with respect to each of the first port 331 and the second port 332.
  • the flow paths 341, 342, and 343 formed inside the first port 331, the second port 332, and the third port 333 are respectively located in the lumen 320 of the cylindrical portion 32 at the same height position. Communicate.
  • a flange-like protrusion 334 is formed on the outer peripheral portion of the base end of the first port 331.
  • the shape of the protrusion 334 is non-circular when viewed from the axial direction of the first port 331, that is, has a shape in which one of the two orthogonal directions is longer than the other.
  • the screw adapter 63 can be screwed with the thread formed on the lock adapter 63 and the thread formed on the housing 81 of the filter 8.
  • the protrusion 334 is not limited to the protrusion 334 as long as it can be screwed with the thread, and may be a thread, for example.
  • the cock 35 has a trunk portion 36 and a lever 38 formed on the upper portion of the trunk portion 36.
  • the body portion 36 has a columnar shape or a cylindrical shape (columnar shape in the illustrated configuration), and is rotatably inserted into the inner cavity 320 of the cylindrical portion 32 with airtightness or liquidtightness.
  • flow paths 371, 372, and 373 corresponding to the flow paths 341, 342, and 343 of the first port 331, the second port 332, and the third port 333 are formed in a T shape. ing. That is, three flow paths 371, 372, and 373 extending in the radial direction of the body part 36 at an angle of 90 ° are communicated with each other in the vicinity of the center part of the body part 36 inside the body part 36. It is formed to do.
  • the flow paths 371, 372, and 373 coincide with the flow paths 341, 342, and 343 of the first port 331, the second port 332, and the third port 333 with the cock 35 inserted into the main body 31. It is formed at a height position. Each of the flow paths 371, 372, and 373 is opened on the outer peripheral surface of the body portion 36 to form an opening.
  • the lever 38 is formed to protrude in the opposite direction to the flow path 372 at the upper portion of the body portion 36, that is, at a portion protruding above the cylindrical portion 32 in the body portion 36.
  • the lever 38 is gripped with fingers, and the cock 35 is rotated.
  • the three-way stopcock 3 is in the first state in which the first port 331 and the second port 332 communicate when the lever 38 is positioned on the third port 333 side as shown in FIG. As shown in FIG. 8, when positioned on the second port 332 side, the first port 331 and the third port 333 communicate with each other in a second state. Although not shown, when the lever 38 is positioned on the first port 331 side, the second port 332 and the third port 333 communicate with each other, and when the lever 38 is positioned on the opposite side of the second port 332. The first port 331, the second port 332, and the third port 333 communicate with each other.
  • the constituent material of each part of the three-way stopcock 3 is not particularly limited.
  • polyolefin such as polypropylene, polycarbonate, or the like can be used.
  • the connecting device 9 is provided at the second port 332 of the three-way stopcock 3.
  • the connecting device 9 includes a main body 91 and a hollow needle 92 that can be pierced with a stopper 72 of a vial 7 described later.
  • the main body portion 91 has a bottomed cylindrical holder 911 surrounding the hollow needle 92 and a tubular portion 912 formed at the bottom of the holder 911 so as to protrude in the axial direction of the holder 911.
  • the tubular portion 912 is fixed to the second port 332 and communicates with the flow path 342 of the second port 332.
  • the diameter of the tubular portion 912 is set smaller than the diameter of the holder 911.
  • the hollow needle 92 is located in the holder 911 and is formed on the bottom of the holder 911 so as to protrude in the axial direction of the holder 911. Further, the hollow needle 92 is disposed at a position corresponding to the tubular portion 912 and communicates with the flow path 342 of the second port 332 via the tubular portion 912. Further, a hole 921 is formed in the middle of the hollow needle 92, and the inside and outside of the hollow needle 92 communicate with each other through the hole 921. Thus, when the hollow needle 92 pierces the stopper 72 of the vial 7, the inside of the vial 7 and the flow path 342 of the second port 332 communicate with each other via the hollow needle 92.
  • connection instrument 9 it does not specifically limit as a constituent material of the connection instrument 9,
  • the thing similar to what was illustrated as a constituent material of the three-way cock 3 mentioned above can be used.
  • connection device 9 is fixed to the second port 332.
  • the present invention is not limited to this, and the connection device 9 is detachably attached to the second port 332 as in a third embodiment to be described later. You may be comprised so that.
  • the connecting portion 11 has a cylindrical shape, and a base end portion thereof is fixed to the third port 333 of the three-way stopcock 3.
  • the constituent material of the connecting portion 11 is not particularly limited, and for example, the same materials as those exemplified as the constituent material of the three-way cock 3 described above can be used.
  • the proximal end of the tube 4 is fixed to the distal end of the connecting portion 11. That is, the tube 4 is connected to the third port 333 via the connecting portion 11 and communicates with the flow path 343 of the third port 333.
  • a hollow puncture needle 5 having a sharp needle tip is connected to the distal end portion of the tube 4, and a cap 52 is detachably attached to the puncture needle 5.
  • a pair of wings 51 a and 51 b are formed on the side of the proximal end side of the puncture needle 5. That is, the puncture needle 5 is a winged needle.
  • Each of the wings 51a and 51b has flexibility and can be opened and closed by bending or bending the wings 51a and 51b.
  • the wings 51a and 51b are picked up with fingers and closed, and the puncture operation can be performed. It is also possible to puncture the other parts without picking the wings 51a and 51b. After puncturing the puncture needle 5, the wings 51a and 51b are opened, and the wings 51a and 51b are fixed to the skin with an adhesive tape or the like.
  • the length of the tube 4 is not particularly limited, but is preferably about 15 to 40 cm, and more preferably about 20 to 30 cm. Thereby, self-injection can be performed more easily.
  • the filter 8 is detachably attached to the first port 331 of the three-way stopcock 3, and the syringe 6 is detachably connected. That is, the filter 8 and the syringe 6 are selectively attached to the first port 331.
  • the method of attaching the filter 8 and the syringe 6 to the first port 331 is not particularly limited, and examples thereof include fitting and screwing. In this embodiment, a screwing method is adopted. Yes.
  • the filter 8 has a housing 81 and a filter member 82 which is installed in the housing 81 and through which gas passes but bacteria do not pass.
  • the housing 81 includes a cylindrical portion 811 having a bottomed cylindrical shape, and a tubular portion 812 formed on the bottom portion of the cylindrical portion 811 so as to protrude in the axial direction of the cylindrical portion 811.
  • the diameter of the tubular portion 812 is set smaller than the diameter of the tubular portion 811.
  • an opening is formed in a portion corresponding to the tubular portion 812 at the bottom of the cylindrical portion 811.
  • the filter member 82 is being fixed to the bottom part of the cylindrical part 811 so that the said opening may be covered.
  • a thread that is a screwing portion that is screwed with the protrusion 334 of the first port 331 of the three-way stopcock 3 is formed on the inner peripheral surface of the tubular portion 812.
  • the filter 8 is detachably attached to the first port 331 by screwing the screw thread into the protrusion 334.
  • the filter member 82 includes, for example, non-woven fabric and paper such as polypropylene, polysulfone, regenerated cellulose, polyamide, and polyester, or those obtained by applying a sealing process thereto.
  • the syringe 6 includes an outer cylinder 61, a gasket 66 that can slide within the outer cylinder 61, and a pusher 65 that moves the gasket 66 along the axial direction (longitudinal direction) of the outer cylinder 61.
  • the gasket 66 is connected to the tip of the pusher 65.
  • the outer cylinder 61 is formed of a bottomed cylindrical member, and a mouth portion 62 whose diameter is reduced with respect to the body portion of the outer cylinder 61 is integrally formed at the tip portion thereof, that is, the center portion of the bottom portion on the tip side. Has been. From the mouth 62, a liquid such as a chemical solution is sucked or discharged. In addition, the first port 331 of the three-way cock 3 is detachably connected to the mouth portion 62.
  • a flange 64 is integrally formed on the outer periphery of the base end (rear end) of the outer cylinder 61. Further, a scale indicating the liquid amount is attached to the outer peripheral surface of the outer cylinder 61.
  • the constituent material of the outer cylinder 61 is not particularly limited, and examples thereof include various resins such as polypropylene and cyclic polyolefin. In addition, it is preferable that the constituent material of the outer cylinder 61 is substantially transparent in order to ensure internal visibility.
  • a gasket 66 made of an elastic material is accommodated (inserted).
  • a plurality (two in this embodiment) of ring-shaped protrusions are formed on the outer periphery of the gasket 66 over the entire periphery, and these protrusions are in close contact with the inner peripheral surface of the outer cylinder 61.
  • the gasket 66 has a hollow portion that opens to the base end surface. In this hollow portion, a head portion of a pusher 65 described later is screwed. A female screw is formed on the inner surface of the hollow portion of the gasket 66.
  • the constituent material of the gasket 66 is not particularly limited, and examples thereof include various rubber materials and various thermoplastic elastomers.
  • the pusher 65 has a rod-like main body 67 whose cross section is cross-shaped.
  • a head portion that is inserted into the hollow portion of the gasket 66 and connected to the gasket 66 is formed on the distal end side of the main body portion 67.
  • the gasket 66 and the pusher 65 are connected by screwing the male screw with the female screw.
  • gasket 66 and the pusher 65 are not limited to the connection by screwing, but may be, for example, a structure connected by uneven fitting, a structure fixed by adhesion, fusion, or the like, or an integrally molded structure. .
  • a disc-shaped flange 68 is formed on the base end side of the main body 67.
  • a lock adapter 63 is provided on the outer peripheral side of the mouth portion 62 of the outer cylinder 61.
  • the lock adapter 63 has, on its inner peripheral surface, a thread that is a screwing portion that is screwed with the protrusion 334 of the first port 331 of the three-way cock 3.
  • the lock adapter 63 is fixed to the distal end portion of the outer cylinder 61.
  • the mouth portion 62 of the syringe 6 is inserted into the first port 331, the syringe 6 (lock adapter 63) is rotated, and the protrusion 334 of the first port 331 is inserted. Then, the thread of the lock adapter 63 is screwed.
  • the first port 331 and the mouth portion 62 of the syringe 6 are connected, and the protrusion 334 and the screw thread of the lock adapter 63 are screwed together, whereby the syringe 6 is held in the first port 331.
  • a space (liquid storage space) surrounded by the outer cylinder 61 and the gasket 66 of the syringe 6 is filled with a liquid that dissolves or dilutes the medicine stored in the vial 7.
  • the liquid is not particularly limited and may be appropriately selected depending on the drug. Examples thereof include water for injection, physiological saline, and glucose solution.
  • the liquid may be sealed in the syringe 6 in advance, or the liquid may be sucked into the syringe 6 when used.
  • the lock adapter 63 is fixed to the outer cylinder 61, but is not limited thereto, and for example, the lock adapter 63 moves along the axial direction of the outer cylinder 61 with respect to the mouth portion 62. It may be one that can be installed, one that can rotate about the axis (concentrically), one that can move along the axial direction, and one that can rotate about the axis.
  • constituent materials of the lock adapter 63 and the pusher 65 are not particularly limited, and for example, the same materials as those exemplified as the constituent material of the outer cylinder 61 described above can be used.
  • the vial 7 has a bottomed cylindrical rigid main body 71 in which a medicine is stored, and a stopper 72 that is provided in an upper mouth portion of the main body 71 and hermetically seals the space in the main body 71. ing.
  • An annular member 73 is attached around the mouth of the main body 71 and the plug body 72, thereby preventing the plug body 72 from being detached from the main body 71. Further, the inside of the vial 7 has a negative pressure.
  • the vial 7 is connected to the second port 332 through the connecting device 9 described above.
  • the drug is not particularly limited, and examples thereof include blood preparations such as dried human blood coagulation factor VIII, hormone preparations such as insulin preparations, and antiviral agents such as interferon preparations.
  • the form of the drug is not particularly limited, and examples thereof include solids (tablets, granules, etc.), solids such as powders (powder, etc.), liquids (liquids, etc.) and the like.
  • the constituent material of the main body 71 is not particularly limited, and examples thereof include various glasses and various resins.
  • the plug body 72 can be pierced by the hollow needle 92 of the connection tool 9, and the constituent material thereof is not particularly limited.
  • various rubber materials and elastic materials such as various thermoplastic elastomers can be used. Can be mentioned.
  • the vial 7 is connected to the connection device 9 with the filter 8 attached to the first port 331.
  • the vial 7 is pushed into the holder 911 of the connection tool 9 from the stopper 72 side.
  • the hollow needle 92 of the connection device 9 penetrates the stopper 72 of the vial 7, and the inside of the vial 7 and the second port 332 communicate with each other through the hollow needle 92. Since the inside of the vial 7 has a negative pressure, external air passes through the filter 8 and is introduced into the vial 7 through the three-way cock 3, and the inside of the vial 7 becomes atmospheric pressure.
  • the filter 8 can prevent bacteria from entering the chemical liquid administration device 1 such as the three-way stopcock 3 or the vial 7.
  • the filter 8 is removed from the first port 331 as shown in FIG. 4, and the mouth portion 62 of the syringe 6 is connected to the first port 331 as shown in FIG.
  • the pusher 65 is pressed and moved in the distal direction, the liquid sealed in the syringe 6 is introduced into the vial 7 from the syringe 6, and the vial 7 is shaken several times. Thereby, the medicine in the vial 7 is dissolved or diluted with the inflowing liquid, and the medicine liquid is stored in the vial 7.
  • the vertical direction of the vial 7 is reversed, the pusher 65 is pulled and moved in the proximal direction, and the drug solution in the vial 7 is sucked into the syringe 6 from the vial 7.
  • the lever 38 of the three-way cock 3 is aligned with the position of the second port 332, so that the first port 331 and the third port 333 communicate with each other.
  • the cap 52 is removed from the puncture needle 5 and priming is performed.
  • the tip of the puncture needle 5 is punctured at the target site, and the drug solution in the syringe 6 is administered. That is, the pusher 65 is moved while being pushed in the distal direction. Thereby, the chemical
  • the first port 331 to which the syringe 6 is connected and the third port 333 to which the tube 4 is connected via the connecting portion 11 are arranged on a straight line, air is not supplied during priming. It is difficult to remain, and resistance during administration of the drug solution is also reduced.
  • the second port 332 protrudes to the side of the first port 331 and the third port 333, a straight line connecting the first port 331 and the third port 333 is used as a central axis.
  • the vial 7 can be rotated, so that it is possible to easily change the vertical direction of the vial 7 in the operation of inverting the vertical direction of the vial 7 as shown in FIG. 7 from the state shown in FIG. Can do.
  • the drug in the vial 7 is dissolved or diluted to obtain a drug solution, and the drug solution is sucked into the syringe 6 and discharged from the puncture needle 5 with ease. Can be done quickly.
  • FIG. 9 is a perspective view showing the vicinity of the puncture needle of the drug solution administration device of the present invention (second embodiment)
  • FIG. 10 is a schematic cross-sectional view of a connecting member in the drug solution administration device shown in FIG.
  • FIG. 10 is a perspective view showing a separated state in the vicinity of the puncture needle of the drug solution administration device shown in FIG. 9.
  • the left side in FIGS. 9 to 11 is referred to as “front end” and the right side is referred to as “base end (rear end)”.
  • This embodiment is the same as the first embodiment except that the configuration near the puncture needle is different.
  • an easily breakable portion 57 is formed in the middle of the tube 4 in the vicinity of the puncture needle 5 of the drug solution administration device 1.
  • Such an easily breakable portion 57 is configured to break more easily than the surroundings, specifically, the portions near the distal end side and the proximal end side.
  • the medicinal solution administration device 1 can be divided into a first part 5a including the puncture needle 5 and a second part 5b on the base end side. Can be separated (see FIG. 11).
  • Trash including the puncture needle 5 must be properly treated as “needle trash” in accordance with various laws and regulations. Therefore, like this embodiment, it is only necessary to dispose only the first part 5a as needle dust by separating the first part 5a including the puncture needle 5 and the other second part 5b. The amount of needle dust is reduced. As a result, the economical efficiency at the time of discarding the chemical solution administration instrument 1 is improved. In other words, it is possible to reduce the frequency of dust removal as needle dust, and to suppress the cost for disposal. By breaking the easily breakable portion 57, the first portion 5a and the second portion 5b can be easily separated, so that there is no trouble in disposal and the operability is excellent.
  • the tube 4 includes a distal end side tube 54 whose distal end portion is connected to the puncture needle 5, and a proximal end side with respect to the distal end side tube 54, and the proximal end portion is a connecting portion 11. And a tubular connecting member 56 that connects the distal tube 54 and the proximal tube 55 to each other.
  • the connecting member 56 includes a distal end portion 561 connected to the distal end side tube 54, a proximal end portion 562 connected to the proximal end side tube 55, and an intermediate portion 563 that connects the distal end portion 561 and the proximal end portion 562. And have.
  • the tip 561 is formed with a pair of knobs 561a and 561b projecting on both sides thereof, and the base end 562 is formed with a pair of knobs 562a and 562b projecting on both sides thereof.
  • Each of these knobs 561a, 561b, 562a, 562b has a flat plate shape.
  • each of the knobs 561a, 561b, 562a, 562b has a shape in which both surfaces thereof are recessed except for the edges so that the fingers can be easily hooked.
  • the intermediate portion 563 has a thin portion 563a that is thinner than the distal end portion 561 and the base end portion 562, and the thin portion 563a constitutes the easily breakable portion 57. Since the thin portion 563a is thinner than the distal end portion 561 and the base end portion 562, the thin portion 563a is more fragile than the distal end portion 561 and the base end portion 562, and breaks with a small force. Therefore, by constituting the easy break portion 57 with such a thin portion 563a, it is possible to form the easy break portion 57 that can reliably exhibit its function and has a simple structure.
  • Such a breakable portion 57 is, for example, gripping the distal end portion 561 with one hand and the proximal end portion 562 with the other hand, and at least one of the distal end portion 561 and the proximal end portion 562 with respect to the other. By twisting and rotating, it is broken so that it can be twisted. According to such a method, the easily breakable portion 57 can be easily broken.
  • the above-described procedure is also referred to as a “rupture procedure”.
  • a pair of knobs 561a and 561b are formed at the distal end portion 561, and a pair of knobs 562a and 562b are formed at the proximal end portion 562.
  • the thin portion 563a (easy to break portion 57) has flexibility (flexibility), specifically, stretchability or stretchability.
  • flexibility flexibility
  • the breakable easy portion 57 is deformed to be extended as the rotation angle between the distal end portion 561 and the proximal end portion 562 increases, and the rotation angle exceeds a predetermined angle. At that time, the stretching limit is exceeded and the breakable portion 57 is broken so that it can be twisted.
  • liquid tightness in the tube 4 can be ensured until immediately before the break, that is, in a state where the easily breakable portion 57 is being deformed. Therefore, for example, even if the easy breakable portion 57 is deformed unintentionally, if the easy breakable portion 57 is not broken, the liquid tightness in the tube 4 is ensured. Liquid leakage from the tube 4 can be prevented.
  • the predetermined angle is preferably 45 ° or more, and more preferably 90 ° or more.
  • the breakable portion 57 is preferably provided in the middle of the tube 4 and within a region within 10 cm from the proximal end of the puncture needle 5, and more preferably within a region within 3 to 6 cm. preferable.
  • part 5a can be made smaller, and the generation amount of needle dust can be suppressed more.
  • the length is 3 to 6 cm, the above-described effects can be exhibited, and the easily breakable portion 57 can be appropriately separated from the puncture needle 5, so that the operability of the puncture needle 5 is not impaired.
  • the thin portion 563a (easy to break portion 57) is formed by forming a substantially V-shaped groove 563b on the outer periphery of the intermediate portion 563.
  • channel 563b becomes a mark and the user can visually recognize the easily breakable part 57 easily. Therefore, it becomes easy to perform the breaking procedure mentioned above, and operativity improves.
  • the groove 563b is formed so as not to penetrate the inside of the connecting member 56 (the lumen of the tube 4), thereby ensuring the liquid tightness of the tube 4.
  • the cross-sectional shape of the groove 563b is not limited to the V shape, and may be, for example, a substantially semicircle.
  • Such a groove 563b is preferably formed over the entire circumference of the intermediate portion 563. That is, it is preferable that the groove 563b has a ring shape. Thereby, the easy break portion 57 can be formed over the entire circumference of the intermediate portion 563. Therefore, the easy-to-break portion 57 has a configuration suitable for the act of twisting off by the above-described breaking procedure, and the breaking procedure can be performed easily and reliably.
  • the thickness of the thin portion 563a (easy to break portion 57) varies depending on the constituent material of the connecting member 56, but is about 0.2 to 1.0 mm at a portion corresponding to the bottom of the groove 563b.
  • the thickness is preferably about 0.3 to 0.5 mm.
  • the thickness of the thin portion 563a is set to the above value, when there is no intention of breaking such as during use of the instrument, the breakage can be reliably prevented, and when there is an intention of breaking such as when discarding after use.
  • constituent materials of the connecting member 56 include various resins such as polyvinyl chloride, polyethylene, polypropylene, and polyamide.
  • the puncture needle 5 is removed after completion of the administration of the drug solution, and then the breaking operation is performed.
  • the distal end portion 561 is grasped with one hand and the proximal end portion 562 is grasped with the other hand, and at least one of the distal end portion 561 and the proximal end portion 562 is held with respect to the other.
  • the breakable easy portion 57 positioned between them is twisted off. Thereby, as shown in FIG. 11, it isolate
  • FIGS. 12 and 13 are perspective views sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention
  • FIG. FIG. 15 is a sectional view taken along line BB in FIG.
  • the upper side in FIGS. 14 and 15 is referred to as “upper” or “upper”, and the lower side is referred to as “lower” or “lower”.
  • This embodiment is the same as the first embodiment except that the drug administration device further includes a release mechanism.
  • connection tool 9 is detachably connected to the second port 332.
  • a cylindrical sealing member 39c made of an elastic material is disposed between the inner peripheral portion of the connection tool 9 and the outer peripheral portion of the second port 332.
  • the sealing member 39c maintains liquid tightness when the connection tool 9 is connected to the second port 332. As a result, the liquid is prevented from leaking unintentionally when the liquid goes back and forth between the vial 7 and the three-way cock 3.
  • the sealing member 39c is a method such as fitting, fusing (thermal fusing, high frequency fusing, ultrasonic fusing, etc.), adhesion (adhesion with an adhesive or a solvent), etc., to the second port 332. It is fixed by.
  • the outer peripheral surface of the sealing member 39c has a tapered shape whose outer shape gradually decreases upward.
  • the sealing member 39c may be fixed to the connection tool 9 side.
  • the outer peripheral surface of the second port 332 has a tapered shape whose outer diameter gradually decreases upward.
  • leave from the 2nd port 332 of the connection tool 9 are selected.
  • a separation mechanism 30 is used.
  • the detachment mechanism 30 prevents the connection tool 9 from being detached from the second port 332 in the first state, and enables the connection tool 9 to be detached from the second port 332 in the second state. It is configured.
  • the detachment mechanism 30 corresponds to a pair of projecting pieces 931 and 932 that project from the lower part of the outer peripheral portion of the tubular portion 912 of the connecting device 9 and a pair of projecting pieces 931 and 932. And a pair of engagement pieces 351 and 352 provided on the cock 35.
  • the protruding piece 931 and the protruding piece 932 protrude toward opposite sides (outside) through the central axis of the connecting device 9.
  • the upper surfaces of the projecting pieces 931 and 932 are each curved in an arc shape like the outer peripheral portion of the cylindrical portion 32. Further, the lower surfaces of the projecting pieces 931 and 932 are flat surfaces.
  • the engagement piece 351 is provided on a side plate portion 362 provided at one end of the body portion 36
  • the engagement piece 352 is a plate on the end portion on the opposite side of the lever 38 of the body portion 36 of the cock 35.
  • the flange portion 361 is provided.
  • the engagement piece 351 and the engagement piece 352 are arranged to face each other and project toward the second port 332 side (inner side).
  • the engagement pieces 351 and 352 are curved in an arc shape like the protrusion pieces 931 and 932, respectively.
  • the engagement piece 351 moves on the circumference around the central axis of the cock body 36 in conjunction with the operation and engages with the protrusion 931.
  • the engagement piece 352 can be in an engagement / disengagement state with respect to the protruding piece 932.
  • the engaging piece 351 can be engaged (contacted) with the protruding piece 931 from the upper side when the three-way cock 3 is in the first state.
  • the engaging piece 352 can be engaged with the protruding piece 932 from above when the three-way cock 3 is in the first state. Such engagement can reliably prevent the connection tool 9 from being detached from the second port 332 (moving upward).
  • the lower portion of the inner peripheral surface of the tubular portion 912 of the connection device 9 is pressed (closely contacted) with the lower portion of the outer peripheral surface forming the tapered shape of the sealing member 39c by the engagement.
  • the liquid tightness between the connecting device 9 and the sealing member 39c is maintained. Note that, as described above, when the sealing member 39c is fixed to the connecting device 9 side, the inner peripheral surface of the tubular portion 912 of the connecting device 9 is in close contact with the outer peripheral surface of the second port 332.
  • the vial 7 in which the medicinal solution is sucked into the syringe 6 is not used in the operation after the suction operation, if it is removed from the three-way stopcock 3 as described above, the subsequent operation is obstructed. In addition, the drug solution administration operation can be easily performed.
  • the drug solution administration device of the present invention may be a combination of any two or more configurations (features) of the above embodiments.
  • a three-way cock is used as a multi-way cock.
  • the present invention is not limited to this, and for example, a cock having four or more ports may be used.
  • the medicinal-solution administration device of the present invention has a first port, a second port, and a third port, and the first port, the second port, and the third port are selected from the first port, the second port, and the third port.
  • a multi-way stopcock capable of taking a first state in which the first port and the second port communicate with each other and a second state in which the first port and the third port communicate with each other;
  • a connecting device provided in the port, a first container containing a medicine connected to the second port via the connecting device, one end side connected to the third port, and a puncture on the other end side A tube to which a needle is connected; and a second container that is detachably connected to the first port, in which a liquid for dissolving or diluting the drug is enclosed, and capable of inhaling and discharging the liquid.
  • the liquid is introduced from the second container into the first container, and the drug is dissolved or diluted to obtain a drug solution , Inhaling the medicinal solution from the first container into the second container, then setting the multi-way stopcock in the second state, discharging the medicinal solution from the second container, and passing the medicinal solution through the tube
  • the puncture needle is configured to flow out. Therefore, it is possible to easily and quickly perform an operation of dissolving or diluting the drug to obtain a drug solution and causing the drug solution to flow out of the puncture needle.

Abstract

A liquid-medicine dosing device comprises a main body, a syringe for taking in and discharging a liquid medicine, and a vial in which a drug is contained. The main body of the liquid-medicine dosing device comprises: a three-way stopcock; a tube which has one end thereof connected to a third port of the three-way stopcock and the other end connected to a puncture needle; a filter which is detachably attached to a first port of the three-way stopcock, and allows a gas to flow and blocks bacteria; and a connection tool and a linking part which are provided at a second port of the three-way stopcock, and are connected to the vial.

Description

薬液投与器具Chemical administration device
 本発明は、薬液投与器具に関するものである。 The present invention relates to a drug solution administration device.
 例えば、患者が血液製剤等の薬液を自己注射する場合、薬剤を液体で溶解または希釈し、その薬液をシリンジで吸引して用いる場合がある。これらの操作は、下記のようにして行われる。 For example, when a patient self-injects a drug solution such as a blood product, the drug may be dissolved or diluted with a liquid, and the drug solution may be sucked with a syringe and used. These operations are performed as follows.
 まず、両頭針または中空針を備えたアダプタを用い、その両頭針または中空針の一端側に、薬剤が収納された薬剤容器を接続し、他端側に、液体が収納された液体容器を接続し、液体容器内の液体を薬剤容器内に移送する。これにより、薬剤容器内の薬剤が液体で溶解または希釈され、薬液が得られる(例えば、特許文献1参照)。 First, using a double-ended needle or an adapter with a hollow needle, connect the drug container containing the drug to one end of the double-ended needle or hollow needle, and connect the liquid container containing the liquid to the other end. Then, the liquid in the liquid container is transferred into the drug container. Thereby, the chemical | medical agent in a chemical | medical agent container is melt | dissolved or diluted with a liquid, and a chemical | medical solution is obtained (for example, refer patent document 1).
 次に、薬剤容器からアダプタを抜去し、先端に鋭利な針先を有する穿刺針が接続されたシリンジを用い、その穿刺針を薬剤容器の栓体に刺通し、薬剤容器内の薬液をシリンジの外筒内に吸引、充填する。 Next, remove the adapter from the drug container, use a syringe with a puncture needle with a sharp needle tip at the tip, pierce the puncture needle through the plug of the drug container, and remove the drug solution in the drug container from the syringe. Suction and fill into the cylinder.
 しかしながら、このような従来のアダプタと、穿刺針が接続されたシリンジとを用いる手法では、操作が煩雑であり、手間と時間がかかるという欠点がある。 However, the method using such a conventional adapter and a syringe to which a puncture needle is connected has a drawback that the operation is complicated and takes time and effort.
 また、穿刺針を薬剤容器の栓体に穿刺する操作が必要であるので、その操作の際、穿刺針で手指を誤って刺してしまう虞がある。 Also, since an operation for puncturing the plug of the drug container is necessary, there is a risk that the finger may be accidentally punctured with the puncture needle during the operation.
特表2005-516696号公報JP 2005-516696 A
 本発明の目的は、容易かつ迅速に、薬剤を溶解または希釈して薬液を得、その薬液を穿刺針から流出させることができる薬液投与器具を提供することにある。 An object of the present invention is to provide a drug administration device that can easily and quickly dissolve or dilute a drug to obtain a drug solution and allow the drug solution to flow out of a puncture needle.
 上記目的を達成するために、本発明は、
 第1のポートと、第2のポートと、第3のポートとを有し、前記第1のポート、前記第2のポートおよび前記第3のポートのうちの前記第1のポートと前記第2のポートとが連通した第1の状態と、前記第1のポートと前記第3のポートとが連通した第2の状態とをとり得る多方活栓と、
 前記第2のポートに設けられる接続器具と、
 前記接続器具を介して前記第2のポートに接続される薬剤が収納された第1容器と、
 一端側が前記第3のポートに接続され、他端側に穿刺針が接続されたチューブと、
 前記第1のポートに着脱自在に接続され、前記薬剤を溶解または希釈する液体が封入され、液体の吸入・排出が可能な第2容器とを備え、
 前記接続器具に前記第1容器を接続するとともに、前記第1のポートに前記第2容器を接続し、前記多方活栓を前記第1の状態とした状態で、前記第2容器から前記液体を前記第1容器内に導入し、前記薬剤を溶解または希釈して薬液を得た後、前記第1容器から前記薬液を前記第2容器内に吸入し、
 次いで、前記多方活栓を前記第2の状態とし、前記第2容器から前記薬液を排出し、該薬液を前記チューブを介して前記穿刺針から流出させるよう構成されていることを特徴とする薬液投与器具である。
In order to achieve the above object, the present invention provides:
A first port; a second port; and a third port. The first port, the second port, and the third port of the first port, the second port, and the third port. A multiway cock that can take a first state in which the first port communicates with the second port and a second state in which the first port communicates with the third port;
A connecting device provided in the second port;
A first container in which a medicine connected to the second port via the connection device is stored;
A tube having one end connected to the third port and a puncture needle connected to the other end;
A second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
The first container is connected to the connecting device, the second container is connected to the first port, and the liquid is discharged from the second container in a state where the multiway cock is in the first state. After being introduced into the first container and dissolving or diluting the drug to obtain a drug solution, the drug solution is inhaled from the first container into the second container,
Next, the multi-way cock is in the second state, the chemical solution is discharged from the second container, and the chemical solution is configured to flow out of the puncture needle through the tube. It is an instrument.
 上記目的を達成するために、本発明は、第1のポートと、第2のポートと、第3のポートとを有し、前記第1のポート、前記第2のポートおよび前記第3のポートのうちの前記第1のポートと前記第2のポートとが連通した第1の状態と、前記第1のポートと前記第3のポートとが連通した第2の状態とをとり得る多方活栓と、
 前記第2のポートに設けられる接続器具と、
 前記接続器具を介して前記第2のポートに接続される薬剤が収納された第1容器と、
 一端側が前記第3のポートに接続され、他端側に穿刺針が接続されたチューブと、
 前記第1のポートに着脱自在に装着され、気体は通過するが細菌は通過しないフィルタと、
 前記第1のポートに着脱自在に接続され、前記薬剤を溶解または希釈する液体が封入され、液体の吸入・排出が可能な第2容器とを備え、
 前記多方活栓を前記第1の状態とし、前記第1のポートに前記フィルタが装着された状態で、前記接続器具に前記第1容器を接続し、
 次いで、前記第1のポートから前記フィルタを取り外し、前記第1のポートに前記第2容器を接続し、
 次いで、前記第2容器から前記液体を前記第1容器内に導入し、前記薬剤を溶解または希釈して薬液を得た後、前記第1容器から前記薬液を前記第2容器内に吸入し、
 次いで、前記多方活栓を前記第2の状態とし、前記第2容器から前記薬液を排出し、該薬液を前記チューブを介して前記穿刺針から流出させるよう構成されていることを特徴とする薬液投与器具である。
In order to achieve the above object, the present invention includes a first port, a second port, and a third port, and the first port, the second port, and the third port. A multiway stopcock capable of taking a first state in which the first port and the second port are in communication with each other and a second state in which the first port and the third port are in communication with each other ,
A connecting device provided in the second port;
A first container in which a medicine connected to the second port via the connection device is stored;
A tube having one end connected to the third port and a puncture needle connected to the other end;
A filter that is detachably attached to the first port and that allows gas to pass but bacteria not to pass through;
A second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
With the multi-way stopcock in the first state, with the filter attached to the first port, connect the first container to the connection device,
Then, removing the filter from the first port, connecting the second container to the first port,
Next, after introducing the liquid from the second container into the first container and dissolving or diluting the drug to obtain a drug solution, the drug solution is inhaled from the first container into the second container,
Next, the multi-way cock is in the second state, the chemical solution is discharged from the second container, and the chemical solution is configured to flow out of the puncture needle through the tube. It is an instrument.
 また、本発明の薬液投与器具では、前記フィルタは、前記第1のポートに着脱自在に装着されるハウジングと、該ハウジング内に設置され、気体は通過するが細菌は通過しないフィルタ部材とを有し、
 前記第1容器内は、陰圧になっており、前記接続器具を介して前記第2のポートに前記第1容器を接続した際、前記フィルタを通過した空気が前記第1容器内に導入されるよう構成されているのが好ましい。
In the medicinal-solution administration device of the present invention, the filter has a housing that is detachably attached to the first port, and a filter member that is installed in the housing and through which gas passes but bacteria do not pass. And
The inside of the first container has a negative pressure, and when the first container is connected to the second port via the connecting device, the air that has passed through the filter is introduced into the first container. It is preferable that it is comprised so that.
 また、本発明の薬液投与器具では、前記第1のポートと前記第3のポートとは、直線上に配置され、前記第2のポートは、前記第1のポートの側方に向って突出しているのが好ましい。 In the medicinal-solution administration device of the present invention, the first port and the third port are arranged on a straight line, and the second port protrudes to the side of the first port. It is preferable.
 また、本発明の薬液投与器具では、前記穿刺針は、翼付き針であるのが好ましい。 In the drug solution administration device of the present invention, the puncture needle is preferably a winged needle.
 また、本発明の薬液投与器具では、前記チューブの途中であって前記穿刺針の近傍に設けられ、その周囲の部分よりも容易に破断する破断容易部とを有し、
 前記破断容易部が破断することで、前記穿刺針を含む第1の部位と、それ以外の第2の部位とに分離することができるよう構成されているのが好ましい。
Further, in the drug solution administration device of the present invention, it is provided in the vicinity of the puncture needle in the middle of the tube, and has an easy-to-break portion that breaks more easily than the surrounding portion,
It is preferable that the breakable portion is broken so that the first portion including the puncture needle can be separated from the second portion other than the first portion.
 また、本発明の薬液投与器具では、前記破断容易部は、前記穿刺針と別体かつ前記チューブの前記穿刺針の基端から10cm以内の領域に設けられているのが好ましい。 In the medicinal-solution administration device of the present invention, it is preferable that the easily breakable portion is provided separately from the puncture needle and in a region within 10 cm from the proximal end of the puncture needle of the tube.
 また、本発明の薬液投与器具では、前記チューブは、前記穿刺針に接続された先端側チューブと、前記先端側チューブよりも基端側に位置する基端側チューブと、前記先端側チューブと前記基端側チューブとを連結する連結部材とを有し、
 前記連結部材に、前記破断容易部が形成されているのが好ましい。
Further, in the drug solution administration device according to the present invention, the tube includes a distal tube connected to the puncture needle, a proximal tube positioned proximal to the distal tube, the distal tube, and the A connecting member that connects the proximal tube,
It is preferable that the breakable part is formed in the connecting member.
 また、本発明の薬液投与器具では、前記連結部材は、前記先端側チューブに接続された先端部と、前記基端側チューブに接続された基端部と、前記先端部と前記基端部とを連結する中間部を有し、
 前記中間部には、前記先端部および前記基端部よりも薄肉化された薄肉部を有し、
 前記薄肉部が前記破断容易部を構成しているのが好ましい。
In the drug solution administration device of the present invention, the connecting member includes a distal end portion connected to the distal end side tube, a proximal end portion connected to the proximal end tube, the distal end portion, and the proximal end portion. Having an intermediate part for connecting
The intermediate part has a thin part thinner than the distal end part and the base end part,
It is preferable that the thin portion constitutes the easily breakable portion.
 また、本発明の薬液投与器具では、前記多方活栓は、円筒状をなし、その外周部に前記第1のポート、前記第2のポートおよび前記第3のポートがそれぞれ配置される筒状部と、該筒状部内に回動自在に挿入され、前記第1のポート、前記第2のポートおよび前記第3のポートにそれぞれ対応する流路が形成された円柱状の胴部を有するコックとを備え、該コックを回動操作することにより、前記第1の状態と前記第2の状態とを取り得るものであり、
 前記第1の状態で前記接続器具の前記第2のポートからの離脱を防止し、前記第2の状態で前記接続器具を前記第2のポートから離脱可能となる離脱機構をさらに備えるのが好ましい。
Further, in the drug solution administration device of the present invention, the multi-way stopcock has a cylindrical shape, and a cylindrical portion in which the first port, the second port, and the third port are respectively disposed on an outer peripheral portion thereof. A cock having a cylindrical body portion that is rotatably inserted into the cylindrical portion and has flow paths corresponding to the first port, the second port, and the third port, respectively. And by turning the cock, the first state and the second state can be taken,
It is preferable to further include a detachment mechanism that prevents the connection tool from being detached from the second port in the first state, and allows the connection tool to be detached from the second port in the second state. .
 また、本発明の薬液投与器具では、前記接続器具は、前記第2のポートに接続するための管状部を有し、
 前記離脱機構は、前記管状部の外周部に突出形成された突片と、前記コックに設けられ、該コックの回動操作に連動して前記胴部の中心軸を中心とする円周上を移動する係合片とを有し、
 前記第1の状態では、前記係合片が前記突片と係合して、前記接続器具の前記第2のポートからの離脱を防止し、前記第2の状態では、前記係合が解除され、前記接続器具の前記第2のポートからの離脱が可能となるのが好ましい。
Further, in the drug solution administration device of the present invention, the connection device has a tubular portion for connection to the second port,
The detachment mechanism is provided on the cock with a protruding piece formed on the outer peripheral portion of the tubular portion and on a circumference centering on the central axis of the trunk portion in conjunction with the turning operation of the cock. An engaging piece that moves,
In the first state, the engagement piece engages with the protruding piece to prevent the connection tool from being detached from the second port, and in the second state, the engagement is released. It is preferable that the connecting device can be detached from the second port.
 また、本発明の薬液投与器具では、前記突片は、前記第2のポートの中心軸を介して互いに反対側に一対設けられ、
 前記係合片は、前記一対の突片に対応して一対設けられているのが好ましい。
Further, in the drug solution administration device of the present invention, a pair of the projecting pieces are provided on opposite sides via the central axis of the second port,
It is preferable that a pair of the engaging pieces are provided corresponding to the pair of protruding pieces.
図1は、本発明の薬液投与器具の第1実施形態を示す側面図(一部断面図)である。FIG. 1 is a side view (partially sectional view) showing a first embodiment of a drug solution administration device of the present invention. 図2は、図1に示す薬液投与器具の薬液投与器具本体を示す斜視図である。FIG. 2 is a perspective view showing a drug solution administration device body of the drug solution administration device shown in FIG. 図3は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 3 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図4は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 4 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図5は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 5 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図6は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 6 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図7は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 7 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図8は、図1に示す薬液投与器具の使用手順を説明するための側面図である。FIG. 8 is a side view for explaining the procedure for using the drug solution administration device shown in FIG. 1. 図9は、本発明の薬液投与器具(第2実施形態)の穿刺針の近傍を示す斜視図である。FIG. 9 is a perspective view showing the vicinity of the puncture needle of the drug solution administration device (second embodiment) of the present invention. 図10は、図9に示す薬液投与器具における連結部材の模式的断面図である。10 is a schematic cross-sectional view of a connecting member in the drug solution administration device shown in FIG. 9. 図11は、図9に示す薬液投与器具の穿刺針の近傍の分離状態を示す斜視図である。11 is a perspective view showing a separated state in the vicinity of the puncture needle of the drug solution administration device shown in FIG. 図12は、本発明の薬液投与器具(第3実施形態)が備える多方活栓の操作(第1の状態から第2の状態)を順に示す斜視図である。FIG. 12 is a perspective view sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention. 図13は、本発明の薬液投与器具(第3実施形態)が備える多方活栓の操作(第1の状態から第2の状態)を順に示す斜視図である。FIG. 13 is a perspective view sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention. 図14は、図12中のA-A線断面図である。14 is a cross-sectional view taken along line AA in FIG. 図15は、図13中のB-B線断面図である。FIG. 15 is a cross-sectional view taken along line BB in FIG.
 以下、本発明の薬液投与器具を添付図面に示す好適な実施形態に基づいて詳細に説明する。 Hereinafter, the drug solution administration device of the present invention will be described in detail based on preferred embodiments shown in the accompanying drawings.
 <第1実施形態>
 図1は、本発明の薬液投与器具の第1実施形態を示す側面図(一部断面図)、図2は、図1に示す薬液投与器具の薬液投与器具本体を示す斜視図、図3~図8は、それぞれ、図1に示す薬液投与器具の使用手順を説明するための側面図である。
<First Embodiment>
FIG. 1 is a side view (partially sectional view) showing a first embodiment of a drug solution administration device of the present invention, FIG. 2 is a perspective view showing a drug solution administration device body of the drug solution administration device shown in FIG. FIG. 8 is a side view for explaining the procedure for using the drug solution administration device shown in FIG.
 なお、以下では、図1、図3~図6および図8中の右側を「先端」、左側を「基端(後端)」とし、図2および図7中の左側を「先端」、右側を「基端」として説明を行う。 In the following, the right side in FIG. 1, FIG. 3 to FIG. 6 and FIG. 8 is the “front end”, the left side is the “base end (rear end)”, and the left side in FIG. Is described as “base end”.
 これらの図に示す本実施形態の薬液投与器具1は、薬液の自己注射を行う場合に用いられる器具であり、図1および図2に示すように、薬液投与器具1は、薬液投与器具本体2と、液体の吸入・排出が可能な第2容器(吸入・排出器具)であるシリンジ6と、薬剤が収納された第1容器であるバイアル(薬剤容器)7とを備えている。 The drug solution administration device 1 of the present embodiment shown in these drawings is a device used when performing self-injection of a drug solution. As shown in FIGS. 1 and 2, the drug solution administration device 1 is a drug solution administration device body 2. And a syringe 6 as a second container (inhalation / discharge device) capable of inhaling and discharging liquid, and a vial (drug container) 7 as a first container in which a medicine is stored.
 なお、第1容器としては、薬剤が収納された容器であればバイアルに限らず、この他、例えば、アンプル等が挙げられる。また、第2容器としては、液体の吸入・排出が可能なものであれば、シリンジに限らず、この他、例えば、弾性体等で構成された容器等が挙げられる。また、薬液投与器具1は、自己注射以外にも、例えば医師や看護師等の医療従事者が患者に対して注射を行う場合にも使用することができる。以下、各構成要素について順次説明する。 Note that the first container is not limited to a vial as long as it is a container in which a medicine is stored, and other examples include an ampoule. In addition, the second container is not limited to a syringe as long as it can inhale and discharge liquid, and other examples include a container made of an elastic body or the like. Moreover, the chemical | medical solution administration instrument 1 can be used also when not only self-injection but medical workers, such as a doctor and a nurse, inject with respect to a patient, for example. Hereinafter, each component will be sequentially described.
 薬液投与器具本体2は、三方活栓(多方活栓)3と、チューブ4と、穿刺針5と、気体は通過するが細菌は通過しないフィルタ8と、バイアル7が接続される接続器具9と、連結部11とを有している。 The drug solution administration device body 2 includes a three-way stopcock (multi-way stopcock) 3, a tube 4, a puncture needle 5, a filter 8 through which gas passes but bacteria do not pass, and a connection device 9 to which a vial 7 is connected. Part 11.
 三方活栓3は、本体31と、コック35とを有している。
 本体31は、筒状部32と、筒状部32の外周に形成され、筒状部32の径方向外方に向けて突出する第1のポート331、第2のポート332および第3のポート333とを有している。
The three-way cock 3 includes a main body 31 and a cock 35.
The main body 31 is formed on the outer periphery of the cylindrical portion 32 and the cylindrical portion 32, and the first port 331, the second port 332, and the third port that protrude outward in the radial direction of the cylindrical portion 32. 333.
 第1のポート331、第2のポート332、第3のポート333は、それぞれ、管状をなし、等角度間隔、すなわち、90°の角度を隔てて配置されている。この場合、第1のポート331と第3のポート333とは、180°の角度を隔てて配置、すなわち、直線上に配置されている。また、第2のポート332は、第1のポート331および第2のポート332の側方に向って突出、すなわち、第1のポート331および第2のポート332のそれぞれに対し、90°の角度を隔てて配置されている。また、第1のポート331、第2のポート332、第3のポート333の内部に形成された流路341、342および343は、それぞれが等しい高さ位置で筒状部32の内腔320に連通している。 The first port 331, the second port 332, and the third port 333 each have a tubular shape and are arranged at equal angular intervals, that is, at an angle of 90 °. In this case, the first port 331 and the third port 333 are arranged at an angle of 180 °, that is, arranged on a straight line. Further, the second port 332 protrudes toward the side of the first port 331 and the second port 332, that is, an angle of 90 ° with respect to each of the first port 331 and the second port 332. Are arranged apart from each other. The flow paths 341, 342, and 343 formed inside the first port 331, the second port 332, and the third port 333 are respectively located in the lumen 320 of the cylindrical portion 32 at the same height position. Communicate.
 また、第1のポート331の基端の外周部には、フランジ状の突起334が形成されている。突起334の形状は、第1のポート331の軸方向から見たとき、非円形、すなわち、直交する2方向のうちの一方が他方よりも長くなるような形状をなしており、後述するシリンジ6のロックアダプタ63に形成されているネジ山およびフィルタ8のハウジング81に形成されているネジ山のぞれぞれと螺合し得るようになっている。なお、突起334は、前記ネジ山と螺合し得るものであれば、前記突起334に限らず、例えば、ネジ山等であってもよい。 Further, a flange-like protrusion 334 is formed on the outer peripheral portion of the base end of the first port 331. The shape of the protrusion 334 is non-circular when viewed from the axial direction of the first port 331, that is, has a shape in which one of the two orthogonal directions is longer than the other. The screw adapter 63 can be screwed with the thread formed on the lock adapter 63 and the thread formed on the housing 81 of the filter 8. The protrusion 334 is not limited to the protrusion 334 as long as it can be screwed with the thread, and may be a thread, for example.
 コック35は、胴部36と、胴部36の上部に形成されたレバー38とを有している。胴部36は、円柱形状または円筒形状(図示の構成では円柱形状)をなし、筒状部32の内腔320内に気密性または液密性をもって回動自在に挿入されている。 The cock 35 has a trunk portion 36 and a lever 38 formed on the upper portion of the trunk portion 36. The body portion 36 has a columnar shape or a cylindrical shape (columnar shape in the illustrated configuration), and is rotatably inserted into the inner cavity 320 of the cylindrical portion 32 with airtightness or liquidtightness.
 胴部36の内部には、第1のポート331、第2のポート332および第3のポート333の流路341、342および343に対応する流路371、372および373がT字状に形成されている。すなわち、胴部36の内部には、90°の角度を隔てて胴部36の径方向に延在する3本の流路371、372、373が、胴部36の中心部付近にて互いに連通するように形成されている。 In the body portion 36, flow paths 371, 372, and 373 corresponding to the flow paths 341, 342, and 343 of the first port 331, the second port 332, and the third port 333 are formed in a T shape. ing. That is, three flow paths 371, 372, and 373 extending in the radial direction of the body part 36 at an angle of 90 ° are communicated with each other in the vicinity of the center part of the body part 36 inside the body part 36. It is formed to do.
 また、各流路371、372、373は、コック35を本体31に挿入した状態で、第1のポート331、第2のポート332、第3のポート333の流路341、342、343と一致する高さ位置に形成されている。各流路371、372、373は、それぞれ、胴部36の外周面に開口し、開口を形成している。 The flow paths 371, 372, and 373 coincide with the flow paths 341, 342, and 343 of the first port 331, the second port 332, and the third port 333 with the cock 35 inserted into the main body 31. It is formed at a height position. Each of the flow paths 371, 372, and 373 is opened on the outer peripheral surface of the body portion 36 to form an opening.
 レバー38は、胴部36の上部、すなわち、胴部36における筒状部32の上方に突出した部位に、流路372と逆方向に突出するように形成されている。このレバー38を手指で把持し、コック35の回動操作を行う。 The lever 38 is formed to protrude in the opposite direction to the flow path 372 at the upper portion of the body portion 36, that is, at a portion protruding above the cylindrical portion 32 in the body portion 36. The lever 38 is gripped with fingers, and the cock 35 is rotated.
 なお、三方活栓3は、レバー38を図1に示すように第3のポート333側に位置させると、第1のポート331と第2のポート332とが連通した第1の状態となり、また、図8に示すように第2のポート332側に位置させると、第1のポート331と第3のポート333とが連通した第2の状態となる。また、図示しないが、レバー38を第1のポート331側に位置させると、第2のポート332と第3のポート333とが連通し、また、第2のポート332の反対側に位置させると、第1のポート331と第2のポート332と第3のポート333とのすべてが連通する。 The three-way stopcock 3 is in the first state in which the first port 331 and the second port 332 communicate when the lever 38 is positioned on the third port 333 side as shown in FIG. As shown in FIG. 8, when positioned on the second port 332 side, the first port 331 and the third port 333 communicate with each other in a second state. Although not shown, when the lever 38 is positioned on the first port 331 side, the second port 332 and the third port 333 communicate with each other, and when the lever 38 is positioned on the opposite side of the second port 332. The first port 331, the second port 332, and the third port 333 communicate with each other.
 三方活栓3の各部の構成材料としては、それぞれ、特に限定されず、例えば、ポリプロピレン等のポリオレフィンや、ポリカーボネート等を用いることができる。 The constituent material of each part of the three-way stopcock 3 is not particularly limited. For example, polyolefin such as polypropylene, polycarbonate, or the like can be used.
 接続器具9は、三方活栓3の第2のポート332に設けられている。
 この接続器具9は、本体部91と、後述するバイアル7の栓体72を刺通可能な中空針92とを有している。本体部91は、中空針92の周囲を囲う有底筒状のホルダー911と、ホルダー911の底部に、ホルダー911の軸方向に突出するように形成された管状部912とを有している。管状部912は、第2のポート332に固定され、その第2のポート332の流路342に連通している。なお、管状部912の径は、ホルダー911の径よりも小さく設定されている。
The connecting device 9 is provided at the second port 332 of the three-way stopcock 3.
The connecting device 9 includes a main body 91 and a hollow needle 92 that can be pierced with a stopper 72 of a vial 7 described later. The main body portion 91 has a bottomed cylindrical holder 911 surrounding the hollow needle 92 and a tubular portion 912 formed at the bottom of the holder 911 so as to protrude in the axial direction of the holder 911. The tubular portion 912 is fixed to the second port 332 and communicates with the flow path 342 of the second port 332. The diameter of the tubular portion 912 is set smaller than the diameter of the holder 911.
 中空針92は、ホルダー911内に位置し、そのホルダー911の底部に、ホルダー911の軸方向に突出するように形成されている。また、中空針92は、管状部912に対応する位置に配置され、管状部912を介して第2のポート332の流路342に連通している。また、中空針92の途中の側部には、孔921が形成されており、この孔921を介して中空針92の内部と外部とが連通している。これにより、中空針92がバイアル7の栓体72を刺通すると、中空針92を介して、バイアル7内と第2のポート332の流路342とが連通する。 The hollow needle 92 is located in the holder 911 and is formed on the bottom of the holder 911 so as to protrude in the axial direction of the holder 911. Further, the hollow needle 92 is disposed at a position corresponding to the tubular portion 912 and communicates with the flow path 342 of the second port 332 via the tubular portion 912. Further, a hole 921 is formed in the middle of the hollow needle 92, and the inside and outside of the hollow needle 92 communicate with each other through the hole 921. Thus, when the hollow needle 92 pierces the stopper 72 of the vial 7, the inside of the vial 7 and the flow path 342 of the second port 332 communicate with each other via the hollow needle 92.
 なお、接続器具9の構成材料としては、特に限定されず、例えば、前述した三方活栓3の構成材料として例示したものと同様のものを用いることができる。 In addition, it does not specifically limit as a constituent material of the connection instrument 9, For example, the thing similar to what was illustrated as a constituent material of the three-way cock 3 mentioned above can be used.
 また、接続器具9は、本実施形態では、第2のポート332に固定されているが、これに限らず、後述する第3実施形態のように、第2のポート332に着脱自在に装着されるように構成されていてもよい。 In the present embodiment, the connection device 9 is fixed to the second port 332. However, the present invention is not limited to this, and the connection device 9 is detachably attached to the second port 332 as in a third embodiment to be described later. You may be comprised so that.
 連結部11は、筒状をなしており、その基端部は、三方活栓3の第3のポート333に固定されている。この連結部11の構成材料としては、特に限定されず、例えば、前述した三方活栓3の構成材料として例示したものと同様のものを用いることができる。 The connecting portion 11 has a cylindrical shape, and a base end portion thereof is fixed to the third port 333 of the three-way stopcock 3. The constituent material of the connecting portion 11 is not particularly limited, and for example, the same materials as those exemplified as the constituent material of the three-way cock 3 described above can be used.
 連結部11の先端部には、チューブ4の基端部が固定されている。すなわち、チューブ4は、この連結部11を介して、第3のポート333に接続され、第3のポート333の流路343に連通している。 The proximal end of the tube 4 is fixed to the distal end of the connecting portion 11. That is, the tube 4 is connected to the third port 333 via the connecting portion 11 and communicates with the flow path 343 of the third port 333.
 また、チューブ4の先端部には、鋭利な針先を有する中空の穿刺針5が接続されており、その穿刺針5には、キャップ52が着脱自在に装着されている。また、穿刺針5の基端側の側方には、1対の翼51a、51bが形成されている。すなわち、穿刺針5は、翼付き針である。翼51a、51bは、それぞれ可撓性を有し、翼51a、51bが屈曲または湾曲することにより、開閉可能に構成されている。 Further, a hollow puncture needle 5 having a sharp needle tip is connected to the distal end portion of the tube 4, and a cap 52 is detachably attached to the puncture needle 5. In addition, a pair of wings 51 a and 51 b are formed on the side of the proximal end side of the puncture needle 5. That is, the puncture needle 5 is a winged needle. Each of the wings 51a and 51b has flexibility and can be opened and closed by bending or bending the wings 51a and 51b.
 穿刺針5を穿刺する際には、翼51a、51bを手指で摘んで閉じた状態とし、穿刺の操作を行うことができる。なお、翼51a、51bを摘まず、他の部位を摘んで穿刺することもできる。穿刺針5を穿刺した後は、翼51a、51bを開いた状態とし、翼51a、51bを粘着テープ等により皮膚に固定する。 When puncturing the puncture needle 5, the wings 51a and 51b are picked up with fingers and closed, and the puncture operation can be performed. It is also possible to puncture the other parts without picking the wings 51a and 51b. After puncturing the puncture needle 5, the wings 51a and 51b are opened, and the wings 51a and 51b are fixed to the skin with an adhesive tape or the like.
 なお、チューブ4の長さは、特に限定されないが、15~40cm程度であることが好ましく、20~30cm程度であることがより好ましい。これにより、自己注射をより容易に行うことができる。 The length of the tube 4 is not particularly limited, but is preferably about 15 to 40 cm, and more preferably about 20 to 30 cm. Thereby, self-injection can be performed more easily.
 三方活栓3の第1のポート331には、フィルタ8が着脱自在に装着され、また、シリンジ6が着脱自在に接続されるようになっている。すなわち、第1のポート331には、フィルタ8とシリンジ6とが選択的に取り付けられる。この場合、第1のポート331にフィルタ8、シリンジ6を取り付ける方法は、それぞれ、特に限定されず、例えば、嵌合、螺合等が挙げられ、本実施形態では、螺合方式を採用している。 The filter 8 is detachably attached to the first port 331 of the three-way stopcock 3, and the syringe 6 is detachably connected. That is, the filter 8 and the syringe 6 are selectively attached to the first port 331. In this case, the method of attaching the filter 8 and the syringe 6 to the first port 331 is not particularly limited, and examples thereof include fitting and screwing. In this embodiment, a screwing method is adopted. Yes.
 フィルタ8は、ハウジング81と、ハウジング81内に設置され、気体は通過するが細菌は通過しないフィルタ部材82とを有している。 The filter 8 has a housing 81 and a filter member 82 which is installed in the housing 81 and through which gas passes but bacteria do not pass.
 ハウジング81は、有底筒状の筒状部811と、筒状部811の底部に、筒状部811の軸方向に突出するように形成された管状部812とを有している。管状部812の径は、筒状部811の径よりも小さく設定されている。また、筒状部811の底部の管状部812に対応する部位には、開口が形成されている。そして、フィルタ部材82は、前記開口を覆うように、筒状部811の底部に固定されている。 The housing 81 includes a cylindrical portion 811 having a bottomed cylindrical shape, and a tubular portion 812 formed on the bottom portion of the cylindrical portion 811 so as to protrude in the axial direction of the cylindrical portion 811. The diameter of the tubular portion 812 is set smaller than the diameter of the tubular portion 811. In addition, an opening is formed in a portion corresponding to the tubular portion 812 at the bottom of the cylindrical portion 811. And the filter member 82 is being fixed to the bottom part of the cylindrical part 811 so that the said opening may be covered.
 また、管状部812の内周面には、三方活栓3の第1のポート331の突起334と螺合する螺合部であるネジ山が形成されている。前記ネジ山を突起334に螺合させることにより、第1のポート331にフィルタ8が着脱自在に装着される。 Further, on the inner peripheral surface of the tubular portion 812, a thread that is a screwing portion that is screwed with the protrusion 334 of the first port 331 of the three-way stopcock 3 is formed. The filter 8 is detachably attached to the first port 331 by screwing the screw thread into the protrusion 334.
 なお、フィルタ部材82としては、例えば、ポリプロピレン、ポリスルホン、再生セルロース、ポリアミド、ポリエステル等の不織布や紙、またはそれらに目止め加工を施したもの等が挙げられる。 The filter member 82 includes, for example, non-woven fabric and paper such as polypropylene, polysulfone, regenerated cellulose, polyamide, and polyester, or those obtained by applying a sealing process thereto.
 シリンジ6は、外筒61と、外筒61内で摺動し得るガスケット66と、ガスケット66を外筒61の軸方向(長手方向)に沿って移動操作する押し子65とを備えている。ガスケット66は、押し子65の先端に連結されている。 The syringe 6 includes an outer cylinder 61, a gasket 66 that can slide within the outer cylinder 61, and a pusher 65 that moves the gasket 66 along the axial direction (longitudinal direction) of the outer cylinder 61. The gasket 66 is connected to the tip of the pusher 65.
 外筒61は、有底筒状の部材で構成され、その先端部、すなわち、先端側底部の中央部には、外筒61の胴部に対し縮径した口部62が一体的に突出形成されている。この口部62からは、薬液等の液体が吸入または排出される。また、口部62には、三方活栓3の第1のポート331が着脱自在に接続されるようになっている。 The outer cylinder 61 is formed of a bottomed cylindrical member, and a mouth portion 62 whose diameter is reduced with respect to the body portion of the outer cylinder 61 is integrally formed at the tip portion thereof, that is, the center portion of the bottom portion on the tip side. Has been. From the mouth 62, a liquid such as a chemical solution is sucked or discharged. In addition, the first port 331 of the three-way cock 3 is detachably connected to the mouth portion 62.
 外筒61の基端(後端)外周には、フランジ64が一体的に形成されている。
  また、外筒61の外周面には、液量を示す目盛りが付されている。
A flange 64 is integrally formed on the outer periphery of the base end (rear end) of the outer cylinder 61.
Further, a scale indicating the liquid amount is attached to the outer peripheral surface of the outer cylinder 61.
 外筒61の構成材料としては、特に限定されず、例えば、ポリプロピレン、環状ポリオレフィンのような各種樹脂等が挙げられる。なお、外筒61の構成材料は、内部の視認性を確保するために、実質的に透明であるのが好ましい。 The constituent material of the outer cylinder 61 is not particularly limited, and examples thereof include various resins such as polypropylene and cyclic polyolefin. In addition, it is preferable that the constituent material of the outer cylinder 61 is substantially transparent in order to ensure internal visibility.
 このような外筒61内には、弾性材料で構成されたガスケット66が収納されて(挿入されて)いる。ガスケット66の外周部には、複数(本実施形態では2つ)のリング状の突部が全周に亘って形成されており、これらの突部が外筒61の内周面に密着しつつ摺動することで、液密性をより確実に保持するとともに、摺動性の向上が図れる。 In such an outer cylinder 61, a gasket 66 made of an elastic material is accommodated (inserted). A plurality (two in this embodiment) of ring-shaped protrusions are formed on the outer periphery of the gasket 66 over the entire periphery, and these protrusions are in close contact with the inner peripheral surface of the outer cylinder 61. By sliding, liquid-tightness can be more reliably maintained and slidability can be improved.
 また、ガスケット66には、その基端面に開放する中空部が形成されている。この中空部は、後述する押し子65のヘッド部が螺入される。ガスケット66の中空部の内面には、雌ネジが形成されている。 In addition, the gasket 66 has a hollow portion that opens to the base end surface. In this hollow portion, a head portion of a pusher 65 described later is screwed. A female screw is formed on the inner surface of the hollow portion of the gasket 66.
 ガスケット66の構成材料としては、特に限定されず、例えば、各種ゴム材料や、各種熱可塑性エラストマー等が挙げられる。 The constituent material of the gasket 66 is not particularly limited, and examples thereof include various rubber materials and various thermoplastic elastomers.
 押し子65は、横断面が十文字状をなす棒状の本体部67を有している。
 本体部67の先端側には、ガスケット66の中空部内に挿入され、ガスケット66と連結されるヘッド部が形成されている。ヘッド部の外周には、ガスケット66の中空部の内面の雌ネジと螺合し得る雄ネジが形成されている。この雄ネジを雌ネジと螺合することにより、ガスケット66と押し子65とが連結される。なお、ガスケット66と押し子65は、螺合による連結に限らず、例えば凹凸嵌合等により連結された構成、接着、融着等により固着された構成、一体成形された構成であってもよい。
The pusher 65 has a rod-like main body 67 whose cross section is cross-shaped.
A head portion that is inserted into the hollow portion of the gasket 66 and connected to the gasket 66 is formed on the distal end side of the main body portion 67. On the outer periphery of the head portion, a male screw that can be screwed with a female screw on the inner surface of the hollow portion of the gasket 66 is formed. The gasket 66 and the pusher 65 are connected by screwing the male screw with the female screw. In addition, the gasket 66 and the pusher 65 are not limited to the connection by screwing, but may be, for example, a structure connected by uneven fitting, a structure fixed by adhesion, fusion, or the like, or an integrally molded structure. .
 また、本体部67の基端側には、円盤状のフランジ68が形成されている。
 また、外筒61の口部62の外周側には、ロックアダプタ63が設けられている。ロックアダプタ63は、その内周面に、三方活栓3の第1のポート331の突起334と螺合する螺合部であるネジ山を有している。本実施形態では、このロックアダプタ63は、外筒61の先端部に固定されている。
A disc-shaped flange 68 is formed on the base end side of the main body 67.
A lock adapter 63 is provided on the outer peripheral side of the mouth portion 62 of the outer cylinder 61. The lock adapter 63 has, on its inner peripheral surface, a thread that is a screwing portion that is screwed with the protrusion 334 of the first port 331 of the three-way cock 3. In the present embodiment, the lock adapter 63 is fixed to the distal end portion of the outer cylinder 61.
 第1のポート331にシリンジ6を接続する際は、第1のポート331にシリンジ6の口部62を挿入し、シリンジ6(ロックアダプタ63)を回転させ、第1のポート331の突起334に、ロックアダプタ63のネジ山を螺合させる。これにより、第1のポート331とシリンジ6の口部62とが接続され、突起334とロックアダプタ63のネジ山とが螺合することにより、第1のポート331にシリンジ6が保持される。 When connecting the syringe 6 to the first port 331, the mouth portion 62 of the syringe 6 is inserted into the first port 331, the syringe 6 (lock adapter 63) is rotated, and the protrusion 334 of the first port 331 is inserted. Then, the thread of the lock adapter 63 is screwed. Thus, the first port 331 and the mouth portion 62 of the syringe 6 are connected, and the protrusion 334 and the screw thread of the lock adapter 63 are screwed together, whereby the syringe 6 is held in the first port 331.
 また、シリンジ6の外筒61とガスケット66とで囲まれた空間(貯液空間)には、バイアル7に収納された薬剤を溶解または希釈する液体が封入されている。この液体としては、特に限定されず、前記薬剤に応じて適宜選択されるものであるが、例えば、注射用水、生理食塩水、ブドウ糖溶液等が挙げられる。 Further, a space (liquid storage space) surrounded by the outer cylinder 61 and the gasket 66 of the syringe 6 is filled with a liquid that dissolves or dilutes the medicine stored in the vial 7. The liquid is not particularly limited and may be appropriately selected depending on the drug. Examples thereof include water for injection, physiological saline, and glucose solution.
 なお、シリンジ6への前記液体の封入は、予め行われていてもよく、また、使用する際に、前記液体をシリンジ6内に吸引するようにしてもよい。 The liquid may be sealed in the syringe 6 in advance, or the liquid may be sucked into the syringe 6 when used.
 また、本実施形態では、ロックアダプタ63は、外筒61に固定されているが、これに限らず、例えば、ロックアダプタ63が、口部62に対し、外筒61の軸方向に沿って移動可能に設置されているもの、軸回りに(同心的に)回転可能なもの、軸方向に沿って移動可能で、かつ軸回りに回転可能なもの等であってもよい。 In the present embodiment, the lock adapter 63 is fixed to the outer cylinder 61, but is not limited thereto, and for example, the lock adapter 63 moves along the axial direction of the outer cylinder 61 with respect to the mouth portion 62. It may be one that can be installed, one that can rotate about the axis (concentrically), one that can move along the axial direction, and one that can rotate about the axis.
 また、ロックアダプタ63および押し子65の構成材料としては、それぞれ、特に限定されず、例えば、前述した外筒61の構成材料として例示したものと同様のものを用いることができる。 Further, the constituent materials of the lock adapter 63 and the pusher 65 are not particularly limited, and for example, the same materials as those exemplified as the constituent material of the outer cylinder 61 described above can be used.
 バイアル7は、薬剤が収納された有底筒状の硬質の本体71と、本体71の上側の口部に設けられ、本体71内の空間を気密的に封止する栓体72とを有している。本体71の口部と栓体72との周囲には、環状部材73が装着され、これにより、栓体72の本体71からの離脱が防止される。また、バイアル7内は、陰圧になっている。このバイアル7は、前述した接続器具を9介して第2のポート332に接続される。 The vial 7 has a bottomed cylindrical rigid main body 71 in which a medicine is stored, and a stopper 72 that is provided in an upper mouth portion of the main body 71 and hermetically seals the space in the main body 71. ing. An annular member 73 is attached around the mouth of the main body 71 and the plug body 72, thereby preventing the plug body 72 from being detached from the main body 71. Further, the inside of the vial 7 has a negative pressure. The vial 7 is connected to the second port 332 through the connecting device 9 described above.
 また、薬剤としては、特に限定されないが、例えば、乾燥人血液凝固第VIII因子等の血液製剤、インスリン製剤等のホルモン製剤、インターフェロン製剤等の抗ウイルス剤等が挙げられる。 The drug is not particularly limited, and examples thereof include blood preparations such as dried human blood coagulation factor VIII, hormone preparations such as insulin preparations, and antiviral agents such as interferon preparations.
 また、薬剤の形態としては、特に限定されず、例えば、固体(錠剤、顆粒剤等)、粉体(散剤等)等の固形のものや、液体(液剤等)等が挙げられる。 Also, the form of the drug is not particularly limited, and examples thereof include solids (tablets, granules, etc.), solids such as powders (powder, etc.), liquids (liquids, etc.) and the like.
 また、本体71の構成材料としては、特に限定されず、例えば、各種ガラスや、各種樹脂等が挙げられる。 The constituent material of the main body 71 is not particularly limited, and examples thereof include various glasses and various resins.
 また、栓体72は、接続器具9の中空針92で刺通可能なものであり、その構成材料としては、特に限定されず、例えば、各種ゴム材料や、各種熱可塑性エラストマー等の弾性材料が挙げられる。 The plug body 72 can be pierced by the hollow needle 92 of the connection tool 9, and the constituent material thereof is not particularly limited. For example, various rubber materials and elastic materials such as various thermoplastic elastomers can be used. Can be mentioned.
 次に、自己注射を行う際の薬液投与器具1の使用手順(作用)を説明する。
 まず、図1に示すように、三方活栓3のレバー38を第3のポート333の位置に合わせ、第1のポート331と第2のポート332とが連通した第1の状態とする。
Next, the use procedure (action) of the drug solution administration device 1 when performing self-injection will be described.
First, as shown in FIG. 1, the lever 38 of the three-way stopcock 3 is aligned with the position of the third port 333 so that the first port 331 and the second port 332 communicate with each other.
 次いで、図3に示すように、第1のポート331にフィルタ8が装着された状態で、接続器具9にバイアル7を接続する。この際は、バイアル7をその栓体72側から接続器具9のホルダー911内に押し込む。これにより、接続器具9の中空針92がバイアル7の栓体72を刺通し、中空針92を介してバイアル7内と第2のポート332とが連通する。バイアル7内は陰圧になっているので、外部の空気がフィルタ8を通過し、三方活栓3を経てバイアル7内に導入され、バイアル7内が大気圧となる。この際、フィルタ8により、三方活栓3内やバイアル7内等の薬液投与器具1内への細菌の侵入を防止することができる。 Next, as shown in FIG. 3, the vial 7 is connected to the connection device 9 with the filter 8 attached to the first port 331. At this time, the vial 7 is pushed into the holder 911 of the connection tool 9 from the stopper 72 side. As a result, the hollow needle 92 of the connection device 9 penetrates the stopper 72 of the vial 7, and the inside of the vial 7 and the second port 332 communicate with each other through the hollow needle 92. Since the inside of the vial 7 has a negative pressure, external air passes through the filter 8 and is introduced into the vial 7 through the three-way cock 3, and the inside of the vial 7 becomes atmospheric pressure. At this time, the filter 8 can prevent bacteria from entering the chemical liquid administration device 1 such as the three-way stopcock 3 or the vial 7.
 次いで、図4に示すように、第1のポート331からフィルタ8を取り外し、図5に示すように、第1のポート331にシリンジ6の口部62を接続する。 Next, the filter 8 is removed from the first port 331 as shown in FIG. 4, and the mouth portion 62 of the syringe 6 is connected to the first port 331 as shown in FIG.
 次いで、図6に示すように、押し子65を先端方向に押圧して移動し、シリンジ6内に封入されている液体をそのシリンジ6からバイアル7内に導入し、バイアル7を数回振る。これにより、バイアル7内の薬剤は、流入した液体で溶解または希釈され、バイアル7内に薬液が収納された状態となる。 Next, as shown in FIG. 6, the pusher 65 is pressed and moved in the distal direction, the liquid sealed in the syringe 6 is introduced into the vial 7 from the syringe 6, and the vial 7 is shaken several times. Thereby, the medicine in the vial 7 is dissolved or diluted with the inflowing liquid, and the medicine liquid is stored in the vial 7.
 次いで、図7に示すように、バイアル7の上下の向きを反転させ、押し子65を基端方向に引っ張って移動し、バイアル7内の薬液をそのバイアル7からシリンジ6内に吸入する。 Next, as shown in FIG. 7, the vertical direction of the vial 7 is reversed, the pusher 65 is pulled and moved in the proximal direction, and the drug solution in the vial 7 is sucked into the syringe 6 from the vial 7.
 次いで、図8に示すように、三方活栓3のレバー38を第2のポート332の位置に合わせ、第1のポート331と第3のポート333とが連通した第2の状態とする。 Next, as shown in FIG. 8, the lever 38 of the three-way cock 3 is aligned with the position of the second port 332, so that the first port 331 and the third port 333 communicate with each other.
 次いで、穿刺針5からキャップ52を取り外し、プライミングを行う。
 次いで、穿刺針5の針先を目的部位に穿刺し、シリンジ6内の薬液を投与する。すなわち、押し子65を先端方向に押圧して移動する。これにより、シリンジ6内の薬液は、そのシリンジ6から排出され、三方活栓3およびチューブ4を介して穿刺針5から流出し、投与される。
Next, the cap 52 is removed from the puncture needle 5 and priming is performed.
Next, the tip of the puncture needle 5 is punctured at the target site, and the drug solution in the syringe 6 is administered. That is, the pusher 65 is moved while being pushed in the distal direction. Thereby, the chemical | medical solution in the syringe 6 is discharged | emitted from the syringe 6, flows out from the puncture needle 5 through the three-way cock 3 and the tube 4, and is administered.
 ここで、シリンジ6が接続された第1のポート331と、チューブ4が連結部11を介して接続されている第3のポート333とは、直線上に配置されているので、プライミング時に空気が残留し難く、また、薬液を投与する際の抵抗も少なくなる。 Here, since the first port 331 to which the syringe 6 is connected and the third port 333 to which the tube 4 is connected via the connecting portion 11 are arranged on a straight line, air is not supplied during priming. It is difficult to remain, and resistance during administration of the drug solution is also reduced.
 また、第2のポート332は、第1のポート331および第3のポート333の側方に向って突出しているので、第1のポート331と第3のポート333とを結ぶ直線を中心軸としてバイアル7を回動させることができ、これにより、図6に示す状態から図7に示すようにバイアル7の上下の向きを反転させる操作の際、容易に、バイアル7の上下の向きを変えることができる。 Further, since the second port 332 protrudes to the side of the first port 331 and the third port 333, a straight line connecting the first port 331 and the third port 333 is used as a central axis. The vial 7 can be rotated, so that it is possible to easily change the vertical direction of the vial 7 in the operation of inverting the vertical direction of the vial 7 as shown in FIG. 7 from the state shown in FIG. Can do.
 以上説明したように、この薬液投与器具1によれば、バイアル7内の薬剤を溶解または希釈して薬液を得、その薬液をシリンジ6内に吸入し、穿刺針5から流出させる操作を容易かつ迅速に行うことができる。 As described above, according to the drug administration device 1, the drug in the vial 7 is dissolved or diluted to obtain a drug solution, and the drug solution is sucked into the syringe 6 and discharged from the puncture needle 5 with ease. Can be done quickly.
 また、前記操作において、穿刺針5をバイアル7の栓体72に刺通する操作が不要であるので、操作者にとって安全である。 Further, in the above operation, an operation for inserting the puncture needle 5 into the stopper 72 of the vial 7 is unnecessary, and thus it is safe for the operator.
 <第2実施形態>
  図9は、本発明の薬液投与器具(第2実施形態)の穿刺針の近傍を示す斜視図、図10は、図9に示す薬液投与器具における連結部材の模式的断面図、図11は、図9に示す薬液投与器具の穿刺針の近傍の分離状態を示す斜視図である。なお、以下では、説明の都合上、図9~図11中の左側を「先端」、右側を「基端(後端)」という。
Second Embodiment
FIG. 9 is a perspective view showing the vicinity of the puncture needle of the drug solution administration device of the present invention (second embodiment), FIG. 10 is a schematic cross-sectional view of a connecting member in the drug solution administration device shown in FIG. FIG. 10 is a perspective view showing a separated state in the vicinity of the puncture needle of the drug solution administration device shown in FIG. 9. In the following, for convenience of explanation, the left side in FIGS. 9 to 11 is referred to as “front end” and the right side is referred to as “base end (rear end)”.
 以下、これらの図を参照して本発明の薬液投与器具の第2実施形態について説明するが、前述した実施形態との相違点を中心に説明し、同様の事項はその説明を省略する。 Hereinafter, the second embodiment of the drug solution administration device of the present invention will be described with reference to these drawings. However, the difference from the above-described embodiment will be mainly described, and description of similar matters will be omitted.
 本実施形態は、穿刺針の近傍の構成が異なること以外は前記第1実施形態と同様である。 This embodiment is the same as the first embodiment except that the configuration near the puncture needle is different.
 図9、図10に示すように、薬液投与器具1の穿刺針5付近では、チューブ4の途中に、破断容易部57が形成されている。このような破断容易部57は、その周囲、具体的には、その先端側直近および基端側直近の部位よりも容易に破断するように構成されている。 9 and 10, an easily breakable portion 57 is formed in the middle of the tube 4 in the vicinity of the puncture needle 5 of the drug solution administration device 1. Such an easily breakable portion 57 is configured to break more easily than the surroundings, specifically, the portions near the distal end side and the proximal end side.
 このような破断容易部57を破断させることで、薬液投与器具1を、それよりも先端側に位置し穿刺針5を含む第1の部位5aと、基端側の第2の部位5bとに分離することができる(図11参照)。 By breaking such a breakable part 57, the medicinal solution administration device 1 can be divided into a first part 5a including the puncture needle 5 and a second part 5b on the base end side. Can be separated (see FIG. 11).
 穿刺針5を含むゴミは、「針ゴミ」として、各種法律、規則に則って適切に処理する必要がある。そのため、本実施形態のように、穿刺針5を含む第1の部位5aと、それ以外の第2の部位5bとに分離することで、第1の部位5aだけを針ゴミとして処分すればよく、針ゴミの発生量が減少する。その結果、薬液投与器具1を廃棄する際の経済性が向上する。すなわち、針ゴミとしてのゴミ出しの頻度を少なくすることができるとともに、廃棄に係る費用を抑えることができる。破断容易部57を破断させることで簡単に第1の部位5aと第2の部位5bに分離することができるため、廃棄の際の煩わしさがなく、その操作性に優れている。 Trash including the puncture needle 5 must be properly treated as “needle trash” in accordance with various laws and regulations. Therefore, like this embodiment, it is only necessary to dispose only the first part 5a as needle dust by separating the first part 5a including the puncture needle 5 and the other second part 5b. The amount of needle dust is reduced. As a result, the economical efficiency at the time of discarding the chemical solution administration instrument 1 is improved. In other words, it is possible to reduce the frequency of dust removal as needle dust, and to suppress the cost for disposal. By breaking the easily breakable portion 57, the first portion 5a and the second portion 5b can be easily separated, so that there is no trouble in disposal and the operability is excellent.
 以下、破断容易部57について詳細に説明する。
 図9および図10に示すように、チューブ4は、先端部が穿刺針5に接続された先端側チューブ54と、先端側チューブ54よりも基端側に位置し、基端部が連結部11に接続された基端側チューブ55と、先端側チューブ54と基端側チューブ55とを連結する筒状の連結部材56とを有している。
Hereinafter, the easy break portion 57 will be described in detail.
As shown in FIGS. 9 and 10, the tube 4 includes a distal end side tube 54 whose distal end portion is connected to the puncture needle 5, and a proximal end side with respect to the distal end side tube 54, and the proximal end portion is a connecting portion 11. And a tubular connecting member 56 that connects the distal tube 54 and the proximal tube 55 to each other.
 また、連結部材56は、先端側チューブ54に接続された先端部561と、基端側チューブ55に接続された基端部562と、先端部561と基端部562とを連結する中間部563とを有している。 The connecting member 56 includes a distal end portion 561 connected to the distal end side tube 54, a proximal end portion 562 connected to the proximal end side tube 55, and an intermediate portion 563 that connects the distal end portion 561 and the proximal end portion 562. And have.
 先端部561には、その両側に突出する一対のツマミ561a、561bが形成されており、基端部562には、その両側に突出する一対のツマミ562a、562bが形成されている。これらツマミ561a、561b、562a、562bは、それぞれ平板状をなしている。また、各ツマミ561a、561b、562a、562bは、指を引っ掛け易いように、その両面が縁部を除いて凹没した形状をなしている。 The tip 561 is formed with a pair of knobs 561a and 561b projecting on both sides thereof, and the base end 562 is formed with a pair of knobs 562a and 562b projecting on both sides thereof. Each of these knobs 561a, 561b, 562a, 562b has a flat plate shape. Also, each of the knobs 561a, 561b, 562a, 562b has a shape in which both surfaces thereof are recessed except for the edges so that the fingers can be easily hooked.
 中間部563は、先端部561および基端部562よりも薄肉化された薄肉部563aを有しており、この薄肉部563aが破断容易部57を構成している。薄肉部563aは、先端部561および基端部562よりも薄肉化されている分、先端部561および基端部562よりも脆弱であり、小さい力で破断する。そのため、このような薄肉部563aによって破断容易部57を構成することにより、その機能を確実に発揮でき、かつ構成が簡単な破断容易部57を形成することができる。 The intermediate portion 563 has a thin portion 563a that is thinner than the distal end portion 561 and the base end portion 562, and the thin portion 563a constitutes the easily breakable portion 57. Since the thin portion 563a is thinner than the distal end portion 561 and the base end portion 562, the thin portion 563a is more fragile than the distal end portion 561 and the base end portion 562, and breaks with a small force. Therefore, by constituting the easy break portion 57 with such a thin portion 563a, it is possible to form the easy break portion 57 that can reliably exhibit its function and has a simple structure.
 このような破断容易部57は、例えば、一方の手で先端部561を把持するとともに他方の手で基端部562を把持し、先端部561および基端部562の少なくとも一方を、他方に対して捩るように回転させることにより、捩り切られるように破断する。このような方法によれば、簡単に、破断容易部57を破断させることができる。なお、以下、説明の便宜上、上述したような手順を「破断手順」とも言う。 Such a breakable portion 57 is, for example, gripping the distal end portion 561 with one hand and the proximal end portion 562 with the other hand, and at least one of the distal end portion 561 and the proximal end portion 562 with respect to the other. By twisting and rotating, it is broken so that it can be twisted. According to such a method, the easily breakable portion 57 can be easily broken. Hereinafter, for convenience of explanation, the above-described procedure is also referred to as a “rupture procedure”.
 特に、本実施形態では、先端部561に一対のツマミ561a、561bが形成されているとともに、基端部562に一対のツマミ562a、562bが形成されている。これらツマミ561a、561b、562a、562bに指を引っ掛けることにより、先端部561および基端部562を把持し易くなるとともに、先端部561および基端部562を回転させ易くなる。そのため、上述した破断手順をより簡単かつスムーズに行うことができる。 In particular, in this embodiment, a pair of knobs 561a and 561b are formed at the distal end portion 561, and a pair of knobs 562a and 562b are formed at the proximal end portion 562. By hooking a finger on these knobs 561a, 561b, 562a, 562b, the distal end portion 561 and the proximal end portion 562 are easily grasped, and the distal end portion 561 and the proximal end portion 562 are easily rotated. Therefore, the breaking procedure described above can be performed more easily and smoothly.
 また、薄肉部563a(破断容易部57)は、可撓性(柔軟性)、具体的には延伸性もしくは伸縮性を有しているのが好ましい。これにより、上述した破断手順を実行する場合、先端部561と基端部562との回転角が大きくなるに連れて破断容易部57が引き延ばされるように変形し、回転角が所定角度を超えた時点で前記引き延ばしの限界を超え、破断容易部57が捩じ切れるように破断する。 Further, it is preferable that the thin portion 563a (easy to break portion 57) has flexibility (flexibility), specifically, stretchability or stretchability. As a result, when the above-described breaking procedure is executed, the breakable easy portion 57 is deformed to be extended as the rotation angle between the distal end portion 561 and the proximal end portion 562 increases, and the rotation angle exceeds a predetermined angle. At that time, the stretching limit is exceeded and the breakable portion 57 is broken so that it can be twisted.
 このような構成によれば、破断直前まで、すなわち、破断容易部57が変形途中の状態では、チューブ4内の液密性を確保することができる。そのため、例えば、破断容易部57が意図せずに変形したとしても、破断容易部57が破断していなければ、チューブ4内の液密性が確保されているため、チューブ4内の汚染や、チューブ4からの液漏れ等を防止することができる。 According to such a configuration, liquid tightness in the tube 4 can be ensured until immediately before the break, that is, in a state where the easily breakable portion 57 is being deformed. Therefore, for example, even if the easy breakable portion 57 is deformed unintentionally, if the easy breakable portion 57 is not broken, the liquid tightness in the tube 4 is ensured. Liquid leakage from the tube 4 can be prevented.
 なお、前記所定角度としては、45°以上であるのが好ましく、90°以上であるのがより好ましい。これにより、多少の回転では破断容易部57が破断しないため、破断容易部57の不本意な破断、意図しない破断を効果的に防止することができる。 It should be noted that the predetermined angle is preferably 45 ° or more, and more preferably 90 ° or more. Thereby, since the easy-to-break part 57 does not break by some rotation, the unintentional break and the unintended break of the easy-to-break part 57 can be effectively prevented.
 また、破断容易部57は、チューブ4の途中であって、穿刺針5の基端から10cm以内の領域に設けられているのが好ましく、3~6cm以内の領域に設けられているのがより好ましい。これにより、第1の部位5aの体積(嵩)をより小さくすることができ、針ゴミの発生量をより抑えることがでる。特に、3~6cmとすれば、前述の効果を発揮することができるとともに、破断容易部57を穿刺針5から適度に離すことができるため、穿刺針5の操作性を損なうことがない。 Further, the breakable portion 57 is preferably provided in the middle of the tube 4 and within a region within 10 cm from the proximal end of the puncture needle 5, and more preferably within a region within 3 to 6 cm. preferable. Thereby, the volume (bulk) of the 1st site | part 5a can be made smaller, and the generation amount of needle dust can be suppressed more. In particular, when the length is 3 to 6 cm, the above-described effects can be exhibited, and the easily breakable portion 57 can be appropriately separated from the puncture needle 5, so that the operability of the puncture needle 5 is not impaired.
 薄肉部563a(破断容易部57)は、中間部563の外周に略V字状の溝563bを形成することにより形成されている。これにより、簡単に、薄肉部563a(破断容易部57)を形成することができるとともに、溝563bが目印となって、使用者が破断容易部57を簡単に視認することができる。そのため、上述した破断手順を行い易くなり、操作性が向上する。 The thin portion 563a (easy to break portion 57) is formed by forming a substantially V-shaped groove 563b on the outer periphery of the intermediate portion 563. Thereby, while being able to form the thin part 563a (easy to break part 57) easily, the groove | channel 563b becomes a mark and the user can visually recognize the easily breakable part 57 easily. Therefore, it becomes easy to perform the breaking procedure mentioned above, and operativity improves.
 なお、溝563bは、連結部材56の内部(チューブ4の内腔)に貫通しないように形成されており、これにより、チューブ4の液密性が確保されている。また、溝563bの横断面形状は、V字状に限定されず、例えば、略半円であってもよい。 The groove 563b is formed so as not to penetrate the inside of the connecting member 56 (the lumen of the tube 4), thereby ensuring the liquid tightness of the tube 4. Further, the cross-sectional shape of the groove 563b is not limited to the V shape, and may be, for example, a substantially semicircle.
 このような溝563bは、中間部563の全周にわたって形成されているのが好ましい。すなわち、溝563bは、リング状をなしているのが好ましい。これにより、中間部563の全周にわたって破断容易部57を形成することができる。そのため、破断容易部57が、上述した破断手順によって捩じ切るという行為に適した構成となり、破断手順を簡単かつ確実に行うことができる。 Such a groove 563b is preferably formed over the entire circumference of the intermediate portion 563. That is, it is preferable that the groove 563b has a ring shape. Thereby, the easy break portion 57 can be formed over the entire circumference of the intermediate portion 563. Therefore, the easy-to-break portion 57 has a configuration suitable for the act of twisting off by the above-described breaking procedure, and the breaking procedure can be performed easily and reliably.
 このような薄肉部563a(破断容易部57)の厚さとしては、連結部材56の構成材料等によっても異なるが、溝563bの底部に相当する部位で、0.2~1.0mm程度であるのが好ましく、0.3~0.5mm程度であるのがより好ましい。これにより、破断容易部57が適度な機械的強度となり、破断容易部57が脆弱過ぎて使用途中に意図しない不本意な破断が生じたり、反対に、破断容易部57を強靭過ぎて破断に大きな力が必要となってしまったりするのを効果的に防止することができる。 The thickness of the thin portion 563a (easy to break portion 57) varies depending on the constituent material of the connecting member 56, but is about 0.2 to 1.0 mm at a portion corresponding to the bottom of the groove 563b. The thickness is preferably about 0.3 to 0.5 mm. As a result, the easily breakable portion 57 has an appropriate mechanical strength, and the easily breakable portion 57 is too fragile to cause unintentional breakage during use, or on the contrary, the easily breakable portion 57 is too strong and is large in breaking. It is possible to effectively prevent the need for force.
 すなわち、薄肉部563aの厚さを上記数値とすることにより、器具の使用中など破断させる意思がない場合には、破断を確実に防止でき、使用後破棄する際など破断させる意思がある場合には、簡単に破断させることのできる破断容易部57を構成することができる。 That is, by setting the thickness of the thin portion 563a to the above value, when there is no intention of breaking such as during use of the instrument, the breakage can be reliably prevented, and when there is an intention of breaking such as when discarding after use. Can constitute an easily breakable portion 57 that can be easily broken.
 なお、先端部561、基端部562および中間部563は、一体的に形成されている。また、これらの構成材料、すなわち連結部材56の構成材料としては、例えば、ポリ塩化ビニル、ポリエチレン、ポリプロピレン、ポリアミドのような各種樹脂が挙げられる。 In addition, the front-end | tip part 561, the base end part 562, and the intermediate part 563 are integrally formed. Examples of these constituent materials, that is, constituent materials of the connecting member 56 include various resins such as polyvinyl chloride, polyethylene, polypropylene, and polyamide.
 このような構成の破断容易部57を破断するタイミングとしては、薬液の投与完了後に穿刺針5を抜去してから、その破断操作を行う。当該破断操作は、前述したように、一方の手で先端部561を把持するとともに他方の手で基端部562を把持し、先端部561および基端部562の少なくとも一方を、他方に対して捩るように回転させることにより、これらの間に位置する破断容易部57を捩じ切ることにより行なわれる。これにより、図11に示すように、穿刺針5を含む第1の部位5aとその他の第2の部位5bとに分離する。
 そして、分離した第1の部位5aのみを針ゴミとして処分することができる。
As the timing for breaking the breakable portion 57 having such a configuration, the puncture needle 5 is removed after completion of the administration of the drug solution, and then the breaking operation is performed. As described above, in the breaking operation, the distal end portion 561 is grasped with one hand and the proximal end portion 562 is grasped with the other hand, and at least one of the distal end portion 561 and the proximal end portion 562 is held with respect to the other. By rotating to twist, the breakable easy portion 57 positioned between them is twisted off. Thereby, as shown in FIG. 11, it isolate | separates into the 1st site | part 5a containing the puncture needle 5, and the other 2nd site | part 5b.
Then, only the separated first portion 5a can be disposed as needle dust.
 <第3実施形態>
  図12および図13は、それぞれ、本発明の薬液投与器具(第3実施形態)が備える多方活栓の操作(第1の状態から第2の状態)を順に示す斜視図、図14は、図12中のA-A線断面図、図15は、図13中のB-B線断面図である。なお、以下では、説明の都合上、図14および図15中の上側を「上」または「上方」、下側を「下」または「下方」と言う。
<Third Embodiment>
FIGS. 12 and 13 are perspective views sequentially illustrating the operation (from the first state to the second state) of the multiway cock provided in the drug solution administration device (third embodiment) of the present invention, and FIG. FIG. 15 is a sectional view taken along line BB in FIG. In the following, for convenience of explanation, the upper side in FIGS. 14 and 15 is referred to as “upper” or “upper”, and the lower side is referred to as “lower” or “lower”.
 以下、これらの図を参照して本発明の薬液投与器具の第3実施形態について説明するが、前述した実施形態との相違点を中心に説明し、同様の事項はその説明を省略する。 Hereinafter, the third embodiment of the drug solution administration device of the present invention will be described with reference to these drawings, but the description will focus on the differences from the above-described embodiment, and description of similar matters will be omitted.
 本実施形態は、薬液投与器具が離脱機構をさらに備えること以外は前記第1実施形態と同様である。 This embodiment is the same as the first embodiment except that the drug administration device further includes a release mechanism.
 図12~図15に示すように、本実施形態では、第2のポート332には、接続器具9が着脱自在に接続されている。 As shown in FIGS. 12 to 15, in the present embodiment, the connection tool 9 is detachably connected to the second port 332.
 なお、接続器具9の内周部と第2のポート332の外周部との間には、弾性材料で構成された筒状の封止部材39cが配置されている。封止部材39cは、接続器具9が第2のポート332に接続されているときの液密性を維持するものである。これにより、バイアル7と三方活栓3との間を液体が行き来する際に不本意に漏出するのが防止される。なお、封止部材39cは、第2のポート332に対し例えば嵌合や、融着(熱融着、高周波融着、超音波融着等)、接着(接着剤や溶媒による接着)等の方法により固定されている。また、封止部材39cに外周面は、その外形が上方に向かって漸減したテーパ状をなしている。なお、封止部材39cは、接続器具9側に固定されていてもよい。この場合、第2のポート332の外周面は、その外径が上方に向かって漸減したテーパ状をなしている。 A cylindrical sealing member 39c made of an elastic material is disposed between the inner peripheral portion of the connection tool 9 and the outer peripheral portion of the second port 332. The sealing member 39c maintains liquid tightness when the connection tool 9 is connected to the second port 332. As a result, the liquid is prevented from leaking unintentionally when the liquid goes back and forth between the vial 7 and the three-way cock 3. The sealing member 39c is a method such as fitting, fusing (thermal fusing, high frequency fusing, ultrasonic fusing, etc.), adhesion (adhesion with an adhesive or a solvent), etc., to the second port 332. It is fixed by. In addition, the outer peripheral surface of the sealing member 39c has a tapered shape whose outer shape gradually decreases upward. In addition, the sealing member 39c may be fixed to the connection tool 9 side. In this case, the outer peripheral surface of the second port 332 has a tapered shape whose outer diameter gradually decreases upward.
 そして、薬液投与器具1では、接続器具9の第2のポート332からの離脱を防止することができる状態と、接続器具9の第2のポート332からの離脱が可能となる状態とを選択するのに離脱機構30が用いられる。なお、離脱機構30は、第1の状態で接続器具9の第2のポート332からの離脱を防止し、第2の状態で接続器具9の第2のポート332からの離脱を可能とするよう構成されている。 And in the chemical | medical solution administration instrument 1, the state which can detach | leave from the 2nd port 332 of the connection tool 9 and the state which can detach | leave from the 2nd port 332 of the connection tool 9 are selected. For this purpose, a separation mechanism 30 is used. The detachment mechanism 30 prevents the connection tool 9 from being detached from the second port 332 in the first state, and enables the connection tool 9 to be detached from the second port 332 in the second state. It is configured.
 以下、離脱機構30について説明する。
 図12~図15に示すように、離脱機構30は、接続器具9の管状部912の外周部の下部に突出形成された一対の突片931、932と、一対の突片931、932に対応してコック35に設けられた一対の係合片351、352とで構成されている。
Hereinafter, the separation mechanism 30 will be described.
As shown in FIGS. 12 to 15, the detachment mechanism 30 corresponds to a pair of projecting pieces 931 and 932 that project from the lower part of the outer peripheral portion of the tubular portion 912 of the connecting device 9 and a pair of projecting pieces 931 and 932. And a pair of engagement pieces 351 and 352 provided on the cock 35.
 突片931と突片932とは、接続器具9の中心軸を介して互いに反対側(外側)に向かって突出している。突片931、932は、それぞれ、その上面が筒状部32の外周部と同じように円弧状に湾曲している。また、突片931、932の下面は、それぞれ、平面となっている。 The protruding piece 931 and the protruding piece 932 protrude toward opposite sides (outside) through the central axis of the connecting device 9. The upper surfaces of the projecting pieces 931 and 932 are each curved in an arc shape like the outer peripheral portion of the cylindrical portion 32. Further, the lower surfaces of the projecting pieces 931 and 932 are flat surfaces.
 一方、係合片351は、胴部36の一端に設けられた側板部362に設けられており、係合片352は、コック35の胴部36のレバー38と反対側の端部にある板状のフランジ部361に設けられている。係合片351と係合片352とは、互いに対向して配置され、第2のポート332側(内側)に向かって突出している。また、係合片351、352は、それぞれ、突片931、932と同様に、円弧状に湾曲している。 On the other hand, the engagement piece 351 is provided on a side plate portion 362 provided at one end of the body portion 36, and the engagement piece 352 is a plate on the end portion on the opposite side of the lever 38 of the body portion 36 of the cock 35. The flange portion 361 is provided. The engagement piece 351 and the engagement piece 352 are arranged to face each other and project toward the second port 332 side (inner side). In addition, the engagement pieces 351 and 352 are curved in an arc shape like the protrusion pieces 931 and 932, respectively.
 そして、コック35を回動操作すると、その操作に連動して、係合片351は、コックの胴部36の中心軸を中心とする円周上を移動し、突片931に対し係合・非係合状態とすることができ、係合片352は、突片932に対し係合・非係合状態とすることができる。 Then, when the cock 35 is turned, the engagement piece 351 moves on the circumference around the central axis of the cock body 36 in conjunction with the operation and engages with the protrusion 931. The engagement piece 352 can be in an engagement / disengagement state with respect to the protruding piece 932.
 図12、図14に示すように、係合片351は、三方活栓3が第1の状態では、当該突片931にその上側から係合(当接)することができる。また、係合片351と同様に、係合片352も、三方活栓3が第1の状態では、当該突片932にその上側から係合することができる。このような係合により、接続器具9の第2のポート332からの離脱(上方への移動)を確実に防止することができる。 As shown in FIGS. 12 and 14, the engaging piece 351 can be engaged (contacted) with the protruding piece 931 from the upper side when the three-way cock 3 is in the first state. Similarly to the engaging piece 351, the engaging piece 352 can be engaged with the protruding piece 932 from above when the three-way cock 3 is in the first state. Such engagement can reliably prevent the connection tool 9 from being detached from the second port 332 (moving upward).
 さらに、前記係合により、接続器具9の管状部912の内周面の下側の部分が、封止部材39cのテーパ状をなす外周面の下側の部分に押し付けられた(密着した)状態となり、接続器具9と封止部材39cとの液密性が保たれる。なお、前述したように封止部材39cが接続器具9側に固定されている場合、接続器具9の管状部912の内周面が第2のポート332の外周面と密着した状態となる。 Further, the lower portion of the inner peripheral surface of the tubular portion 912 of the connection device 9 is pressed (closely contacted) with the lower portion of the outer peripheral surface forming the tapered shape of the sealing member 39c by the engagement. Thus, the liquid tightness between the connecting device 9 and the sealing member 39c is maintained. Note that, as described above, when the sealing member 39c is fixed to the connecting device 9 side, the inner peripheral surface of the tubular portion 912 of the connecting device 9 is in close contact with the outer peripheral surface of the second port 332.
 図13、図15に示すように、コック35のレバー38を当該レバー38に向かって時計回りに90度回転操作して、三方活栓を第2の状態とすると、係合片351は、突片931に対して非係合状態となり、係合片352も、突片932に対して非係合状態となる。このような離間により、突片931、932のそれぞれに対する係合が解除され、よって、接続器具9を第2のポート332から確実に離脱させることができる。そして、この離脱により、バイアル7を接続器具9ごと三方活栓3から取り外すことができる。 As shown in FIGS. 13 and 15, when the lever 38 of the cock 35 is rotated 90 degrees clockwise toward the lever 38 and the three-way cock is in the second state, the engaging piece 351 becomes the protruding piece. The engagement piece 352 is also disengaged from the protrusion 932. By such separation, the engagement with each of the projecting pieces 931 and 932 is released, and thus the connecting device 9 can be reliably detached from the second port 332. And by this detachment | leave, the vial 7 can be removed from the three-way cock 3 together with the connection tool 9.
 薬液投与器具1では、シリンジ6内に薬液が吸引されたバイアル7は、吸引操作以降の操作では用いられないものであるため、前述のように三方活栓3から取り外されれば、以降の操作の邪魔にならず、薬液投与操作を容易に行なうことができる。 In the medicinal solution administration device 1, since the vial 7 in which the medicinal solution is sucked into the syringe 6 is not used in the operation after the suction operation, if it is removed from the three-way stopcock 3 as described above, the subsequent operation is obstructed. In addition, the drug solution administration operation can be easily performed.
 以上、本発明の薬液投与器具を、図示の実施形態に基づいて説明したが、本発明はこれに限定されるものではなく、各部の構成は、同様の機能を有する任意の構成のものに置換することができる。また、本発明に、他の任意の構成物が付加されていてもよい。 As mentioned above, although the chemical | medical solution administration device of this invention was demonstrated based on embodiment of illustration, this invention is not limited to this, The structure of each part is substituted by the thing of the arbitrary structures which have the same function. can do. In addition, any other component may be added to the present invention.
 また、本発明の薬液投与器具は、前記各実施形態のうちの、任意の2以上の構成(特徴)を組み合わせたものであってもよい。 Further, the drug solution administration device of the present invention may be a combination of any two or more configurations (features) of the above embodiments.
 また、前記各実施形態では、多方活栓として、三方活栓を用いたが、本発明では、これに限らず、例えば、ポートの数が4以上のものを用いてもよい。 In each of the above embodiments, a three-way cock is used as a multi-way cock. However, the present invention is not limited to this, and for example, a cock having four or more ports may be used.
 本発明の薬液投与器具は、第1のポートと、第2のポートと、第3のポートとを有し、前記第1のポート、前記第2のポートおよび前記第3のポートのうちの前記第1のポートと前記第2のポートとが連通した第1の状態と、前記第1のポートと前記第3のポートとが連通した第2の状態とをとり得る多方活栓と、前記第2のポートに設けられる接続器具と、前記接続器具を介して前記第2のポートに接続される薬剤が収納された第1容器と、一端側が前記第3のポートに接続され、他端側に穿刺針が接続されたチューブと、前記第1のポートに着脱自在に接続され、前記薬剤を溶解または希釈する液体が封入され、液体の吸入・排出が可能な第2容器とを備え、前記接続器具に前記第1容器を接続するとともに、前記第1のポートに前記第2容器を接続し、前記多方活栓を前記第1の状態とした状態で、前記第2容器から前記液体を前記第1容器内に導入し、前記薬剤を溶解または希釈して薬液を得た後、前記第1容器から前記薬液を前記第2容器内に吸入し、次いで、前記多方活栓を前記第2の状態とし、前記第2容器から前記薬液を排出し、該薬液を前記チューブを介して前記穿刺針から流出させるよう構成されている。そのため、薬剤を溶解または希釈して薬液を得て、その薬液を穿刺針から流出させる操作を容易かつ迅速に行うことができる。また、前記操作において、穿刺針を第1容器の栓体等に刺通する操作が不要であるので、操作者にとって安全である。従って、薬液投与器具は、産業上の利用可能性を有する。 The medicinal-solution administration device of the present invention has a first port, a second port, and a third port, and the first port, the second port, and the third port are selected from the first port, the second port, and the third port. A multi-way stopcock capable of taking a first state in which the first port and the second port communicate with each other and a second state in which the first port and the third port communicate with each other; A connecting device provided in the port, a first container containing a medicine connected to the second port via the connecting device, one end side connected to the third port, and a puncture on the other end side A tube to which a needle is connected; and a second container that is detachably connected to the first port, in which a liquid for dissolving or diluting the drug is enclosed, and capable of inhaling and discharging the liquid. And connecting the first container to the first port. After two containers are connected and the multiway cock is in the first state, the liquid is introduced from the second container into the first container, and the drug is dissolved or diluted to obtain a drug solution , Inhaling the medicinal solution from the first container into the second container, then setting the multi-way stopcock in the second state, discharging the medicinal solution from the second container, and passing the medicinal solution through the tube The puncture needle is configured to flow out. Therefore, it is possible to easily and quickly perform an operation of dissolving or diluting the drug to obtain a drug solution and causing the drug solution to flow out of the puncture needle. In addition, in the above operation, it is not necessary to pierce the puncture needle through the plug of the first container and the like, which is safe for the operator. Therefore, the chemical solution administration device has industrial applicability.

Claims (7)

  1.  第1のポートと、第2のポートと、第3のポートとを有し、前記第1のポート、前記第2のポートおよび前記第3のポートのうちの前記第1のポートと前記第2のポートとが連通した第1の状態と、前記第1のポートと前記第3のポートとが連通した第2の状態とをとり得る多方活栓と、
     前記第2のポートに設けられる接続器具と、
     前記接続器具を介して前記第2のポートに接続される薬剤が収納された第1容器と、
     一端側が前記第3のポートに接続され、他端側に穿刺針が接続されたチューブと、
     前記第1のポートに着脱自在に接続され、前記薬剤を溶解または希釈する液体が封入され、液体の吸入・排出が可能な第2容器とを備え、
     前記接続器具に前記第1容器を接続するとともに、前記第1のポートに前記第2容器を接続し、前記多方活栓を前記第1の状態とした状態で、前記第2容器から前記液体を前記第1容器内に導入し、前記薬剤を溶解または希釈して薬液を得た後、前記第1容器から前記薬液を前記第2容器内に吸入し、
     次いで、前記多方活栓を前記第2の状態とし、前記第2容器から前記薬液を排出し、該薬液を前記チューブを介して前記穿刺針から流出させるよう構成されていることを特徴とする薬液投与器具。
    A first port; a second port; and a third port. The first port, the second port, and the third port of the first port, the second port, and the third port. A multiway cock that can take a first state in which the first port communicates with the second port and a second state in which the first port communicates with the third port;
    A connecting device provided in the second port;
    A first container in which a medicine connected to the second port via the connection device is stored;
    A tube having one end connected to the third port and a puncture needle connected to the other end;
    A second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
    The first container is connected to the connecting device, the second container is connected to the first port, and the liquid is discharged from the second container in a state where the multiway cock is in the first state. After being introduced into the first container and dissolving or diluting the drug to obtain a drug solution, the drug solution is inhaled from the first container into the second container,
    Next, the multi-way cock is in the second state, the chemical solution is discharged from the second container, and the chemical solution is configured to flow out of the puncture needle through the tube. Instruments.
  2.  第1のポートと、第2のポートと、第3のポートとを有し、前記第1のポート、前記第2のポートおよび前記第3のポートのうちの前記第1のポートと前記第2のポートとが連通した第1の状態と、前記第1のポートと前記第3のポートとが連通した第2の状態とをとり得る多方活栓と、
     前記第2のポートに設けられる接続器具と、
     前記接続器具を介して前記第2のポートに接続される薬剤が収納された第1容器と、
     一端側が前記第3のポートに接続され、他端側に穿刺針が接続されたチューブと、
     前記第1のポートに着脱自在に装着され、気体は通過するが細菌は通過しないフィルタと、
     前記第1のポートに着脱自在に接続され、前記薬剤を溶解または希釈する液体が封入され、液体の吸入・排出が可能な第2容器とを備え、
     前記多方活栓を前記第1の状態とし、前記第1のポートに前記フィルタが装着された状態で、前記接続器具に前記第1容器を接続し、
     次いで、前記第1のポートから前記フィルタを取り外し、前記第1のポートに前記第2容器を接続し、
     次いで、前記第2容器から前記液体を前記第1容器内に導入し、前記薬剤を溶解または希釈して薬液を得た後、前記第1容器から前記薬液を前記第2容器内に吸入し、
     次いで、前記多方活栓を前記第2の状態とし、前記第2容器から前記薬液を排出し、該薬液を前記チューブを介して前記穿刺針から流出させるよう構成されていることを特徴とする薬液投与器具。
    A first port; a second port; and a third port. The first port, the second port, and the third port of the first port, the second port, and the third port. A multiway cock that can take a first state in which the first port communicates with the second port and a second state in which the first port communicates with the third port;
    A connecting device provided in the second port;
    A first container in which a medicine connected to the second port via the connection device is stored;
    A tube having one end connected to the third port and a puncture needle connected to the other end;
    A filter that is detachably attached to the first port and that allows gas to pass but bacteria not to pass through;
    A second container that is detachably connected to the first port, encloses a liquid that dissolves or dilutes the drug, and is capable of inhaling and discharging the liquid;
    With the multi-way stopcock in the first state, with the filter attached to the first port, connect the first container to the connection device,
    Then, removing the filter from the first port, connecting the second container to the first port,
    Next, after introducing the liquid from the second container into the first container and dissolving or diluting the drug to obtain a drug solution, the drug solution is inhaled from the first container into the second container,
    Next, the multi-way cock is in the second state, the chemical solution is discharged from the second container, and the chemical solution is configured to flow out of the puncture needle through the tube. Instruments.
  3.  前記フィルタは、前記第1のポートに着脱自在に装着されるハウジングと、該ハウジング内に設置され、気体は通過するが細菌は通過しないフィルタ部材とを有し、
     前記第1容器内は、陰圧になっており、前記接続器具を介して前記第2のポートに前記第1容器を接続した際、前記フィルタを通過した空気が前記第1容器内に導入されるよう構成されている請求項2に記載の薬液投与器具。
    The filter has a housing that is detachably attached to the first port, and a filter member that is installed in the housing and through which gas passes but bacteria do not pass,
    The inside of the first container has a negative pressure, and when the first container is connected to the second port via the connecting device, the air that has passed through the filter is introduced into the first container. The medicinal-solution administration device according to claim 2 configured to be configured as described above.
  4.  前記第1のポートと前記第3のポートとは、直線上に配置され、前記第2のポートは、前記第1のポートの側方に向って突出している請求項1または2に記載の薬液投与器具。 3. The chemical solution according to claim 1, wherein the first port and the third port are arranged on a straight line, and the second port protrudes toward a side of the first port. Dosing device.
  5.  前記穿刺針は、翼付き針である請求項1または2に記載の薬液投与器具。 3. The drug solution administration device according to claim 1, wherein the puncture needle is a winged needle.
  6.  前記チューブの途中であって前記穿刺針の近傍に設けられ、その周囲の部分よりも容易に破断する破断容易部をさらに備え、
     前記破断容易部が破断することで、前記穿刺針を含む第1の部位と、それ以外の第2の部位とに分離することができるよう構成されている請求項1または2に記載の薬液投与器具。
    In the middle of the tube, provided in the vicinity of the puncture needle, further comprising a breakable portion that breaks more easily than the surrounding portion,
    The medicinal solution administration according to claim 1 or 2, wherein the easy-to-break portion is broken so that it can be separated into a first portion including the puncture needle and a second portion other than the first portion. Instruments.
  7.  前記多方活栓は、円筒状をなし、その外周部に前記第1のポート、前記第2のポートおよび前記第3のポートがそれぞれ配置される筒状部と、該筒状部内に回動自在に挿入され、前記第1のポート、前記第2のポートおよび前記第3のポートにそれぞれ対応する流路が形成された円柱状の胴部を有するコックとを備え、該コックを回動操作することにより、前記第1の状態と前記第2の状態とを取り得るものであり、
     前記第1の状態で前記接続器具の前記第2のポートからの離脱を防止し、前記第2の状態で前記接続器具を前記第2のポートから離脱可能となる離脱機構をさらに備える請求項1または2に記載の薬液投与器具。
    The multi-way stopcock has a cylindrical shape, and a cylindrical portion in which the first port, the second port, and the third port are arranged on an outer peripheral portion thereof, and is rotatable in the cylindrical portion. A cock having a cylindrical body portion that is inserted and formed with flow paths corresponding to the first port, the second port, and the third port, respectively, and rotating the cock Can take the first state and the second state,
    The detachment mechanism further prevents the detachment of the connection tool from the second port in the first state and enables the connection tool to be detached from the second port in the second state. Or the chemical | medical solution administration device of 2.
PCT/JP2011/059585 2010-04-20 2011-04-19 Liquid-medicine dosing device WO2011132657A1 (en)

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