WO2014203365A1 - Suction syringe - Google Patents

Suction syringe Download PDF

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Publication number
WO2014203365A1
WO2014203365A1 PCT/JP2013/066922 JP2013066922W WO2014203365A1 WO 2014203365 A1 WO2014203365 A1 WO 2014203365A1 JP 2013066922 W JP2013066922 W JP 2013066922W WO 2014203365 A1 WO2014203365 A1 WO 2014203365A1
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WO
WIPO (PCT)
Prior art keywords
syringe
syringe barrel
pusher
suction
shaft portion
Prior art date
Application number
PCT/JP2013/066922
Other languages
French (fr)
Japanese (ja)
Inventor
一美 後藤
保 片柳
Original Assignee
テルモ・クリニカルサプライ株式会社
株式会社プラスチック・ホンダ
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・クリニカルサプライ株式会社, 株式会社プラスチック・ホンダ filed Critical テルモ・クリニカルサプライ株式会社
Priority to PCT/JP2013/066922 priority Critical patent/WO2014203365A1/en
Publication of WO2014203365A1 publication Critical patent/WO2014203365A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/22Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
    • A61B17/22031Gripping instruments, e.g. forceps, for removing or smashing calculi
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/22Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/31Details
    • A61M5/315Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
    • A61M5/31501Means for blocking or restricting the movement of the rod or piston
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/31Details
    • A61M5/315Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
    • A61M5/31511Piston or piston-rod constructions, e.g. connection of piston with piston-rod
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/50Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2217/00General characteristics of surgical instruments
    • A61B2217/002Auxiliary appliance
    • A61B2217/005Auxiliary appliance with suction drainage system

Definitions

  • the present invention relates to a suction syringe having a syringe barrel having a suction port and a pusher provided with a gasket slidable in the syringe barrel at the tip.
  • a method using a suction catheter in which a suction lumen is formed in a long shaft is performed.
  • This suction catheter sucks and removes foreign matter from the suction port at the distal end to the suction lumen.
  • this suction catheter is connected to the hub at the proximal end. A syringe is used.
  • This suction syringe can generate a negative pressure in the syringe barrel by moving the pusher in the direction of pulling it out of the syringe barrel.
  • the suction catheter as described above, the foreign substance such as a thrombus is removed outside the body by being sucked into the syringe through the suction catheter. Therefore, in order to hold the sucked foreign matter in the syringe barrel, it is necessary to regulate the movement of the pusher so that the pusher does not return to the syringe barrel in a state where a negative pressure is generated in the syringe barrel.
  • Patent Document 1 discloses a container in which a locking piece is rotatably mounted on an eccentric shaft formed on a plunger rod, and a medicine and a solution are filled therein.
  • a technique is disclosed in which the plunger rod is locked so as not to move by setting the outer peripheral edge of the locking piece to the outside of the inner diameter of the main body and locking the locking piece to the container main body.
  • Patent Document 1 is a technique of a prefilled syringe in which a container body is prefilled with a medicine and a solution, and is not a technique related to a suction syringe that generates a negative pressure in a syringe barrel.
  • the prefilled syringe of Patent Document 1 has a complicated structure because the pusher is composed of three components, that is, a gasket, a locking piece, and a plunger rod. Therefore, when handling the prefilled syringe of Patent Document 1 having a complicated structure as described above, the handler rotates the locking piece while holding both the container main body and the plunger rod to lock and unlock the plunger rod. An operation must be performed. As described above, the prefilled syringe of Patent Document 1 is not good in operability because the work of the handler becomes complicated. In particular, when performing treatment to remove foreign substances such as blood clots clogged in the blood vessel as described above, the handling of the operator may be troublesome because the treatment may be hindered. It is desirable that it can be engaged (locked).
  • An object of the present invention is to provide a syringe for suction that can be used.
  • a syringe for suction which is a bottomed cylinder having an open base end, and is movable to the syringe barrel connected to the suction catheter And a pusher that generates a negative pressure in the syringe barrel by being moved in a direction of pulling out from the syringe barrel, and the pusher has a tip portion to which a gasket is attached, and the tip portion A shaft portion that fits into the syringe barrel, and when the shaft portion is positioned outside the syringe barrel by moving the pusher in a direction of pulling out from the syringe barrel, the shaft portion is outside the diameter of the syringe barrel.
  • the return of the pusher when negative pressure is generated is regulated by moving in the direction and engaging with the base end.
  • the pusher has a simple structure including a tip portion and a shaft portion.
  • the suction syringe can easily regulate the return of the pusher when negative pressure is generated by moving the shaft portion outwardly of the syringe barrel and engaging with the proximal end portion. In this manner, the suction syringe can easily regulate the return of the pusher under a state where a negative pressure is generated in the syringe barrel with a simple structure.
  • the distal end portion and the shaft portion are fitted by a groove formed in the distal end portion and a protrusion formed in the shaft portion and slidably fitted into the groove.
  • the shaft portion can move in the radially outward direction of the syringe barrel while being guided by the groove. Therefore, the operability of the suction syringe is improved.
  • the fitting portion of the groove with the protrusion is formed so as to be inclined with respect to the radial direction of the pusher in the direction of pulling out the pusher from the syringe barrel. It is preferable.
  • the shaft portion can be naturally moved in the radially outward direction of the syringe barrel simply by moving the pusher in the direction of pulling out the syringe barrel. Therefore, the operability of the suction syringe is significantly improved.
  • the fitting portion of the groove with the protrusion is formed along the radial direction of the syringe barrel.
  • the pusher can easily move in the radially outward direction of the syringe barrel. Therefore, the operability of the suction syringe is significantly improved.
  • the protrusion is formed at a position that is eccentric to a side opposite to a side where the shaft portion moves in a radially outward direction of the syringe barrel with respect to a main body portion of the shaft portion. It is preferable.
  • the suction syringe can reliably regulate the return of the pusher under a state in which a negative pressure is generated in the syringe barrel.
  • the return of the pusher can be easily regulated under a simple structure under a state in which a negative pressure is generated in the syringe barrel.
  • FIG. 2 is a cross-sectional view taken along the line AA in FIG.
  • FIG. 3 is a sectional view taken along line BB in FIG.
  • FIG. 3 is a cross-sectional view taken along the line CC of FIG.
  • FIG. 6 is a DD sectional view of FIG. 5.
  • FIG. 7 is a cross-sectional view taken along line EE in FIG. 6.
  • FIG. 9 is a sectional view taken along line FF in FIG. 8.
  • FIG. 10 is a sectional view taken along line GG in FIG. 9.
  • FIG. 10 is a cross-sectional view taken along line HH in FIG. 9.
  • FIG. 1 is an external perspective view of the suction syringe 1 according to the first embodiment, in which no negative pressure is generated in the syringe barrel 10, and the pusher 12 is disposed in the syringe barrel 10. It is a figure which shows the state made.
  • FIG. 2 is a cross-sectional view taken along the line AA in FIG. 3 is a cross-sectional view taken along the line BB in FIG. 2, and
  • FIG. 4 is a cross-sectional view taken along the line CC in FIG. FIG.
  • FIG. 5 is an external perspective view of the suction syringe 1 according to the first embodiment, in which a negative pressure is generated in the syringe barrel 10, and the shaft portion 22 of the pusher 12 is the syringe barrel 10. It is a figure which shows the state engaged with the base end part 10a.
  • FIG. 6 is a sectional view taken along the line DD of FIG.
  • FIG. 7 is a cross-sectional view taken along the line EE of FIG.
  • the suction syringe 1 has a syringe barrel 10 and a pusher 12.
  • the injection tube 10 is formed in a bottomed tube shape having an open base end portion 10a. Further, the syringe barrel 10 is integrally formed at the tip portion thereof, that is, at the center portion of the bottom portion on the tip side, so that a mouth portion 10b having a small diameter with respect to the barrel portion of the syringe barrel 10 protrudes from the bottom portion. ing. A suction catheter (not shown) is connected to the mouth portion 10b.
  • the syringe barrel 10 is integrally formed with a flange-shaped finger rest 10c on the outer periphery of the base end 10a.
  • the finger rests 10c are a pair of plate-like portions formed so as to protrude in opposite directions with respect to the central axis of the syringe barrel 10.
  • the finger pad 10c is formed in a longitudinal shape having a longitudinal direction in one direction orthogonal to the central axis of the syringe barrel 10.
  • the syringe barrel 10 may be provided with a scale (not shown) indicating the amount of liquid on the outer peripheral surface 10e.
  • the pusher 12 includes a tip portion 20 and a shaft portion 22.
  • the distal end portion 20 is disposed closer to the mouth portion 10 b (bottom portion) of the syringe barrel 10 than the shaft portion 22.
  • the distal end portion 20 includes a first portion 20a, a second portion 20b, and a third portion 20c in order from the mouth portion 10b side of the syringe barrel 10.
  • tip part 20 is mounted
  • the second portion 20 b has a substantially cross-shaped cross section in the radial direction orthogonal to the axial direction of the pusher 12.
  • the third portion 20c is formed in a substantially cylindrical shape, and a groove 30 is formed therein.
  • the groove 30 is open on one end side in the radial direction of the pusher 12 and is closed on the other end side in the radial direction of the pusher 12 inside the inner peripheral surface 10 d of the syringe barrel 10.
  • the fitting portion 30 a with the protrusion 32 of the shaft portion 22 in the groove 30 is formed to be inclined with respect to the radial direction of the pusher 12.
  • the fitting portion 30 a moves from the closed side to the open side of the groove 30, that is, the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.
  • the inclination angle ⁇ (see FIGS. 2 and 6) of the fitting portion 30a with respect to the radial direction of the pusher 12 is considered to be 5 ° to 50 °, and particularly preferably 10 ° to 30 °. . In FIG. 2 and FIG. 6, as an example, the inclination angle ⁇ is shown as 10 °.
  • the shaft portion 22 is fitted to the tip portion 20.
  • the main-body part 22a of the axial part 22 has comprised the cross section of the radial direction orthogonal to the axial direction (left-right direction of FIG. 2) in substantially cross shape.
  • the shaft portion 22 includes a convex portion 22c that protrudes toward the distal end portion 20 on the end surface 22b of the main body portion 22a on the distal end portion 20 side.
  • the shaft part 22 is provided with a projection 32 projecting in the radial direction of the shaft part 22 (perpendicular to the plane of FIG. 2 and up and down in FIG. 4) on the projection 22c.
  • the protrusion 32 is formed in a substantially rectangular parallelepiped shape, and is fitted to the groove 30 in a slidable state.
  • the position of the central axis Lt of the convex portion 22 c and the protrusion 32 is deviated from the position of the central axis Lj of the main body portion 22 a of the shaft portion 22. . That is, the convex portion 22 c and the protrusion 32 are eccentric with respect to the main body portion 22 a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.
  • the position of the central axis Lj coincides with the position of the central axis Ls of the distal end portion 20 and the position of the central axis of the syringe barrel 10.
  • the shaft portion 22 includes an engaging portion 34 that abuts on the proximal end portion 10a of the syringe barrel 10 when negative pressure is generated in the syringe barrel 10 at the end surface 22b, as will be described later. Yes.
  • the shaft portion 22 is provided with a flange 36 at the end opposite to the tip 20 side.
  • the flange 36 is a portion that the operator grips with a finger when the handler of the suction syringe 1 moves the pusher 12 in the direction in which the pusher 12 is pulled out from the syringe barrel 10.
  • Such a pusher 12 is movably inserted inside the inner peripheral surface 10d of the syringe barrel 10 and moves in a direction in which it is pulled out of the syringe barrel 10, thereby generating a negative pressure in the syringe barrel 10. it can.
  • “generating negative pressure in the syringe barrel 10” means that the pressure inside the syringe barrel 10 is made lower than the pressure outside the syringe barrel 10.
  • the suction syringe 1 has a structure in which the pusher 12 is not completely removed from the syringe barrel 10.
  • the suction syringe 1 has an inner peripheral surface of the syringe barrel 10 before use, that is, before negative pressure is generated in the syringe barrel 10. It is stored in a state of being pushed inside 10d.
  • the shaft portion 22 of the pusher 12 is formed so that the position of the central axis Lj of the main body portion 22a coincides with the position of the central axis Ls of the distal end portion 20.
  • the position of the central axis Ls of the distal end portion 20 matches the position of the central axis of the syringe barrel 10.
  • the engaging portion 34 of the shaft portion 22 contacts and engages with the proximal end portion 10 a of the syringe barrel 10.
  • the pusher 12 is restricted from returning in the direction opposite to the direction in which the pusher 12 is pulled out from the syringe barrel 10.
  • the projection 32 (convex portion 22 c) of the shaft portion 22 contacts the inner peripheral surface 10 d of the syringe barrel 10.
  • the shaft portion 22 is further restricted from moving outward in the radial direction of the pusher 12.
  • the pusher 12 is locked (locked) under a state where a negative pressure is generated in the syringe barrel 10 as shown in FIGS. . Therefore, the operator can easily restrict the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
  • the stopper 22 is used to restrict the shaft portion 22 of the pusher 12 from returning in the direction opposite to the direction in which the pusher 12 is pulled out of the syringe barrel 10. As a stopping means).
  • the engaging portion 34 of the shaft portion 22 is engaged with the base end portion 10 a as shown in FIGS. 5 and 6.
  • the shaft portion 22 is moved inward in the radial direction of the syringe barrel 10.
  • the protrusion 32 of the shaft portion 22 moves toward the inside in the radial direction of the syringe barrel 10 while sliding the fitting portion 30a of the groove 30 of the distal end portion 20.
  • the engaging part 34 of the shaft part 22 is separated from the base end part 10a, and the engagement with the base end part 10a is released.
  • the axial part 22 moves to the direction pushed inside 10d of the internal peripheral surface of the injection cylinder 10.
  • the suction syringe 1 enters the state shown in FIGS. 1 to 4, and the generation of the negative pressure in the syringe barrel 10 is released.
  • the suction syringe 1 has a bottomed cylindrical shape with an open proximal end portion 10a, and is inserted into the syringe barrel 10 connected to the suction catheter and the syringe barrel 10 so as to be movable. And a pusher 12 that generates a negative pressure in the syringe barrel 10 by being moved in a direction in which the syringe 10 is pulled out.
  • the pusher 12 includes a distal end portion 20 to which the gasket 14 is attached, and a shaft portion 22 that is fitted to the distal end portion 20.
  • the pusher 12 has a simple structure including the tip portion 20 and the shaft portion 22.
  • the suction syringe 1 moves the shaft portion 22 to the outside in the radial direction of the syringe barrel 10 and engages the engaging portion 34 with the proximal end portion 10a, thereby returning the pusher 12 when negative pressure is generated.
  • the suction syringe 1 can easily regulate the return of the pusher 12 under a simple structure under a state in which a negative pressure is generated in the syringe barrel 10.
  • the distal end portion 20 and the shaft portion 22 are fitted by a groove 30 formed in the distal end portion 20 and a protrusion 32 that is formed in the shaft portion 22 and slidably fits into the groove 30. . Then, by sliding the protrusion 32 into the groove 30, the shaft portion 22 can be moved outward in the radial direction of the syringe barrel 10 while being guided by the groove 30. Therefore, the operability of the suction syringe 1 is improved.
  • the fitting portion 30 a of the groove 30 with the protrusion 32 is formed so as to be inclined with respect to the radial direction of the pusher 12 in the direction in which the pusher 12 is pulled out from the syringe barrel 10. Specifically, as shown in FIGS. 2 and 6, in the cross section in the axial direction of the pusher 12, the fitting portion 30 a moves from the closed side to the open side of the groove 30, that is, the shaft portion 22. When moving the outer side of the syringe barrel 10 in the radial direction, the pusher 12 is moved relative to the radial direction of the pusher 12 (vertical direction in FIGS. 2 and 6) as it moves in the direction in which the shaft portion 22 is moved.
  • the protrusion 32 is formed at a position that is eccentric with respect to the main body portion 22a of the shaft portion 22 on the side opposite to the side on which the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.
  • FIG. 8 is an external perspective view of the suction syringe 2 of Example 2, in which no negative pressure is generated in the syringe barrel 10, and the pusher 12 is disposed in the syringe barrel 10. It is a figure which shows the state made.
  • FIG. 9 is a cross-sectional view taken along the line FF in FIG. 10 is a GG cross-sectional view of FIG. 9, and FIG. 11 is a HH cross-sectional view of FIG. FIG.
  • FIG. 12 is an external perspective view of the suction syringe 2 according to the second embodiment, in which a negative pressure is generated in the syringe barrel 10, and the shaft portion 22 of the pusher 12 is connected to the syringe barrel 10. It is a figure which shows the state engaged with the base end part 10a.
  • FIG. 13 is a cross-sectional view taken along the line II of FIG.
  • FIG. 14 is a sectional view taken along line JJ of FIG.
  • the pusher 12 in the suction syringe 2 of the second embodiment is different from the first embodiment.
  • the distal end portion 20 has a groove 40 in the third portion 20 c. I have.
  • the groove 40 one end side in the radial direction of the pusher 12 is opened inside the inner peripheral surface 10 d of the syringe barrel 10, and the other end side in the radial direction of the pusher 12 is closed.
  • the fitting portion 40a with the protrusion 42 in the groove 40 is in the radial direction of the pusher 12 (the vertical direction in FIGS. 9 and 13).
  • parallel that is, perpendicular to the axial direction of the pusher 12.
  • the shaft portion 22 is provided with a projection 42 protruding in the radial direction of the shaft portion 22 on the convex portion 22d.
  • the protrusion 42 is formed in a disk shape and engages with the groove 40 in a slidable state. Further, as shown in FIG. 9, in the axial section of the pusher 12, the position of the central axis Lt of the convex portion 22 d and the protrusion 42 is deviated from the position of the central axis Lj of the main body portion 22 a of the shaft portion 22. .
  • the convex portion 22 d and the protrusion 42 are eccentric with respect to the main body portion 22 a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.
  • two grooves 40 and two protrusions 42 are formed.
  • the suction syringe 2 has an inner peripheral surface of the syringe barrel 10 before use, that is, before negative pressure is generated in the syringe barrel 10. It is stored in a state of being pushed inside 10d.
  • the position of the central axis Lj of the main body portion 22a of the shaft portion 22 deviates from the position of the central axis Ls of the distal end portion 20. That is, the shaft portion 22 moves to a position eccentric with respect to the distal end portion 20 and the syringe barrel 10.
  • the engaging portion 34 of the shaft portion 22 comes into contact with and engages with the proximal end portion 10 a of the syringe barrel 10.
  • the pusher 12 is restricted from returning in the direction opposite to the direction in which the pusher 12 is pulled out from the syringe barrel 10.
  • the protrusion 42 (projection 22 d) of the shaft portion 22 comes into contact with the inner peripheral surface 10 d of the syringe barrel 10.
  • the shaft portion 22 is further restricted from moving outward in the radial direction of the pusher 12.
  • the pusher 12 is locked under a state where a negative pressure is generated in the syringe barrel 10 as shown in FIGS. 12 to 14. Therefore, the operator can easily restrict the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
  • the engaging portion 34 of the shaft portion 22 is engaged with the proximal end portion 10a.
  • the shaft 22 is moved inward in the radial direction of the syringe barrel 10 while rotating.
  • the protrusion 42 of the shaft portion 22 slides along the groove 40 of the distal end portion 20 and moves toward the inside in the radial direction of the syringe barrel 10.
  • the engaging part 34 of the shaft part 22 is separated from the base end part 10a, and the engagement with the base end part 10a is released.
  • the axial part 22 moves to the direction pushed inside 10d of the internal peripheral surface of the injection cylinder 10. As shown in FIG.
  • the suction syringe 2 enters the state shown in FIGS. 8 to 11, and the generation of the negative pressure in the syringe barrel 10 is released.
  • the suction syringe 2 has a bottomed cylindrical shape with an open proximal end portion 10a, and is inserted into the syringe barrel 10 connected to the suction catheter and the syringe barrel 10 so as to be movable. And a pusher 12 that generates a negative pressure in the syringe barrel 10 by being moved in a direction in which the syringe 10 is pulled out.
  • the pusher 12 includes a distal end portion 20 to which the gasket 14 is attached, and a shaft portion 22 that is fitted to the distal end portion 20.
  • the pusher 12 has a simple structure including the tip portion 20 and the shaft portion 22.
  • the suction syringe 2 moves the shaft portion 22 to the outside in the radial direction of the syringe barrel 10 and engages the engaging portion 34 with the base end portion 10a, thereby returning the pusher 12 when negative pressure is generated.
  • the suction syringe 2 can easily regulate the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10 with a simple structure.
  • the tip portion 20 and the shaft portion 22 are fitted by a groove 40 formed in the tip portion 20 and a projection 42 formed in the shaft portion 22 and slidably fitted to the groove 40. . Then, by sliding the protrusion 42 into the groove 40, the shaft portion 22 can be moved outward in the radial direction of the syringe barrel 10 while being guided by the groove 40. Therefore, the operability of the suction syringe 2 is improved.
  • the fitting portion 40 a with the protrusion 42 in the groove 40 is formed along the radial direction of the syringe barrel 10.
  • the pusher 12 can easily move outward in the radial direction of the syringe barrel 10. Therefore, the operability of the suction syringe 2 is significantly improved.
  • the protrusion 42 is formed at a position eccentric with respect to the main body portion 22a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.

Abstract

A suction syringe (1) is configured in such a manner that a pusher (12) comprises a front end section (20) on which a gasket is mounted and a shaft section (22) which fits to the front end section (20) and in such a manner that, when the pusher (12) is moved in the direction of pulling the pusher (12) out of a syringe cylinder (10) and the shaft section (22) is positioned outside the syringe cylinder (10), the shaft section (22) moves toward the outside of the syringe cylinder (10) in the radial direction thereof and engages with the base end section (10a) of the syringe cylinder (10), thereby restricting the return of the pusher (12) when a negative pressure is created.

Description

吸引用シリンジSyringe for suction
 本発明は、吸引口を有する注射筒と、当該注射筒内で摺動自在なガスケットを先端に設けた押し子と、を有する吸引用シリンジに関する。 The present invention relates to a suction syringe having a syringe barrel having a suction port and a pusher provided with a gasket slidable in the syringe barrel at the tip.
 血管内に詰まった血栓等の異物を除去する治療方法として、長尺なシャフト内に吸引ルーメンが形成された吸引カテーテルを用いた方法が行われる。この吸引カテーテルは、先端の吸引口から吸引ルーメンへと異物を吸引して外部に除去するものであるが、異物を吸引するための陰圧の発生源として、基端のハブに接続された吸引用シリンジが用いられる。 As a treatment method for removing a foreign substance such as a thrombus clogged in a blood vessel, a method using a suction catheter in which a suction lumen is formed in a long shaft is performed. This suction catheter sucks and removes foreign matter from the suction port at the distal end to the suction lumen. As a source of negative pressure for sucking foreign matter, this suction catheter is connected to the hub at the proximal end. A syringe is used.
 この吸引用シリンジは、押し子を注射筒内から引き抜く方向に移動させることにより、注射筒内に陰圧を発生させることができる。このとき、前記のように吸引カテーテルを用いて血管内に詰まった血栓等の異物を除去するときには、血栓等の異物を吸引カテーテルを介して注射筒に吸引することにより体外へと除去する。そのため、吸引した異物を注射筒内に保持するために、注射筒内に陰圧を発生させた状態下で押し子が注射筒内に戻らないように押し子の移動を規制する必要がある。 This suction syringe can generate a negative pressure in the syringe barrel by moving the pusher in the direction of pulling it out of the syringe barrel. At this time, when removing a foreign substance such as a thrombus clogged in a blood vessel using the suction catheter as described above, the foreign substance such as a thrombus is removed outside the body by being sucked into the syringe through the suction catheter. Therefore, in order to hold the sucked foreign matter in the syringe barrel, it is necessary to regulate the movement of the pusher so that the pusher does not return to the syringe barrel in a state where a negative pressure is generated in the syringe barrel.
 ここで、押し子の移動を規制する従来技術として、特許文献1には、プランジャロッドに形成した偏心軸に係止駒が回動自在に装着され、内部に薬剤と溶解液が充填された容器本体の内径の外側に係止駒の外周縁部を突出させた状態でセットして係止駒を容器本体に係止することにより、プランジャロッドを移動しないようにロックする技術が開示されている。 Here, as a conventional technique for restricting the movement of the pusher, Patent Document 1 discloses a container in which a locking piece is rotatably mounted on an eccentric shaft formed on a plunger rod, and a medicine and a solution are filled therein. A technique is disclosed in which the plunger rod is locked so as not to move by setting the outer peripheral edge of the locking piece to the outside of the inner diameter of the main body and locking the locking piece to the container main body.
特開2005-006675号公報JP 2005-006675 A
 しかしながら、特許文献1の技術は、予め容器本体内に薬剤と溶解液が充填されたプレフィルドシリンジの技術であり、注射筒内に陰圧を発生させる吸引用シリンジに関する技術ではない。 However, the technique of Patent Document 1 is a technique of a prefilled syringe in which a container body is prefilled with a medicine and a solution, and is not a technique related to a suction syringe that generates a negative pressure in a syringe barrel.
 また、特許文献1のプレフィルドシリンジは、押し子がガスケットと係止駒とプランジャロッドの3つの構成部品で構成されているので、構造が複雑である。そのため、取扱者は、前記のように複雑な構造の特許文献1のプレフィルドシリンジを取り扱うに際して、容器本体とプランジャロッドの両方を持ちながら係止駒を回転させて、プランジャロッドのロック操作やロック解除操作を行わなければならない。このように、特許文献1のプレフィルドシリンジは、取扱者の作業が煩雑となってしまうので、操作性が良くない。特に、前記のように血管内に詰まった血栓等の異物を除去する治療を行うに際して、このように取扱者の作業が煩雑となるのは治療の支障をきたす恐れがあるため、押し子は容易に係合(ロック)できることが望ましい。 In addition, the prefilled syringe of Patent Document 1 has a complicated structure because the pusher is composed of three components, that is, a gasket, a locking piece, and a plunger rod. Therefore, when handling the prefilled syringe of Patent Document 1 having a complicated structure as described above, the handler rotates the locking piece while holding both the container main body and the plunger rod to lock and unlock the plunger rod. An operation must be performed. As described above, the prefilled syringe of Patent Document 1 is not good in operability because the work of the handler becomes complicated. In particular, when performing treatment to remove foreign substances such as blood clots clogged in the blood vessel as described above, the handling of the operator may be troublesome because the treatment may be hindered. It is desirable that it can be engaged (locked).
 そこで、本発明は上記した問題点を解決するためになされたものであり、簡便な構造のもと、注射筒内にて陰圧を発生させている状態下で押し子の戻りを容易に規制することができる吸引用シリンジを提供することを目的とする。 Therefore, the present invention has been made to solve the above-described problems, and the return of the pusher is easily regulated under a state where a negative pressure is generated in the syringe barrel with a simple structure. An object of the present invention is to provide a syringe for suction that can be used.
 上記課題を解決するためになされた本発明の一態様は、吸引用シリンジにおいて、開放した基端部を備える有底筒状で、吸引カテーテルに接続される注射筒と、前記注射筒に移動可能に挿入され、前記注射筒から引き抜く方向へ移動させることにより前記注射筒内に陰圧を発生させる押し子と、を有し、前記押し子は、ガスケットが装着される先端部と、前記先端部に嵌合する軸部と、を備え、前記押し子を前記注射筒から引き抜く方向へ移動させて前記軸部を前記注射筒外に位置させたときに、前記軸部が前記注射筒の径外方向に移動して前記基端部に係合することにより、陰圧発生時における前記押し子の戻りを規制すること、を特徴とする。 One aspect of the present invention made to solve the above problems is a syringe for suction, which is a bottomed cylinder having an open base end, and is movable to the syringe barrel connected to the suction catheter And a pusher that generates a negative pressure in the syringe barrel by being moved in a direction of pulling out from the syringe barrel, and the pusher has a tip portion to which a gasket is attached, and the tip portion A shaft portion that fits into the syringe barrel, and when the shaft portion is positioned outside the syringe barrel by moving the pusher in a direction of pulling out from the syringe barrel, the shaft portion is outside the diameter of the syringe barrel. The return of the pusher when negative pressure is generated is regulated by moving in the direction and engaging with the base end.
 この態様によれば、押し子は、先端部と軸部を備えた簡便な構造である。そして、吸引用シリンジは、軸部を注射筒の径外方向に移動させて基端部に係合させることにより、陰圧発生時における押し子の戻りを容易に規制することができる。このようにして、吸引用シリンジは、簡便な構造のもと、注射筒内にて陰圧を発生させている状態下で押し子の戻りを容易に規制することができる。 According to this aspect, the pusher has a simple structure including a tip portion and a shaft portion. The suction syringe can easily regulate the return of the pusher when negative pressure is generated by moving the shaft portion outwardly of the syringe barrel and engaging with the proximal end portion. In this manner, the suction syringe can easily regulate the return of the pusher under a state where a negative pressure is generated in the syringe barrel with a simple structure.
 また、上記の態様においては、前記先端部と前記軸部は、前記先端部に形成される溝と、前記軸部に形成され前記溝に対して摺動可能に嵌合する突起とにより、嵌合していること、が好ましい。 In the above aspect, the distal end portion and the shaft portion are fitted by a groove formed in the distal end portion and a protrusion formed in the shaft portion and slidably fitted into the groove. Are preferred.
 この態様によれば、突起を溝に摺動させることにより、軸部は溝に案内されながら注射筒の径外方向に移動することができる。そのため、吸引用シリンジの操作性が向上する。 According to this aspect, by sliding the protrusion in the groove, the shaft portion can move in the radially outward direction of the syringe barrel while being guided by the groove. Therefore, the operability of the suction syringe is improved.
 また、上記の態様においては、前記溝における前記突起との嵌合部は、前記押し子の径方向に対して、前記押し子を前記注射筒から引き抜く方向側へ傾斜するように形成されていること、が好ましい。 In the above aspect, the fitting portion of the groove with the protrusion is formed so as to be inclined with respect to the radial direction of the pusher in the direction of pulling out the pusher from the syringe barrel. It is preferable.
 この態様によれば、押し子を注射筒から引き抜く方向へ移動させるだけで、自然に軸部を注射筒の径外方向に移動させることができる。そのため、吸引用シリンジの操作性が顕著に向上する。 According to this aspect, the shaft portion can be naturally moved in the radially outward direction of the syringe barrel simply by moving the pusher in the direction of pulling out the syringe barrel. Therefore, the operability of the suction syringe is significantly improved.
 また、上記の態様においては、前記溝における前記突起との嵌合部は、前記注射筒の径方向に沿って形成されていること、が好ましい。 In the above aspect, it is preferable that the fitting portion of the groove with the protrusion is formed along the radial direction of the syringe barrel.
 この態様によれば、押し子は、容易に注射筒の径外方向に移動することができる。そのため、吸引用シリンジの操作性が顕著に向上する。 According to this aspect, the pusher can easily move in the radially outward direction of the syringe barrel. Therefore, the operability of the suction syringe is significantly improved.
 また、上記の態様においては、前記突起は、前記軸部の本体部分に対して前記軸部が前記注射筒の径外方向に移動する側とは反対側に偏心させた位置に形成されていること、が好ましい。 Further, in the above aspect, the protrusion is formed at a position that is eccentric to a side opposite to a side where the shaft portion moves in a radially outward direction of the syringe barrel with respect to a main body portion of the shaft portion. It is preferable.
 この態様によれば、軸部が注射筒の径外方向に移動して基端部に係合するときに、軸部における基端部との係合部の面積を大きくすることができる。そのため、軸部と基端部との係合状態が安定する。したがって、吸引用シリンジは、注射筒内にて陰圧を発生させている状態下で、押し子の戻りを確実に規制することができる。 According to this aspect, when the shaft portion moves in the radially outward direction of the syringe barrel and engages with the base end portion, the area of the engaging portion with the base end portion in the shaft portion can be increased. Therefore, the engagement state between the shaft portion and the base end portion is stabilized. Therefore, the suction syringe can reliably regulate the return of the pusher under a state in which a negative pressure is generated in the syringe barrel.
 本発明の吸引用シリンジによれば、簡便な構造のもと、注射筒内にて陰圧を発生させている状態下で押し子の戻りを容易に規制することができる。 According to the suction syringe of the present invention, the return of the pusher can be easily regulated under a simple structure under a state in which a negative pressure is generated in the syringe barrel.
実施例1の吸引用シリンジの外観斜視図であり、押し子が注射筒内に配置された状態を示す図である。It is an external appearance perspective view of the syringe for suction of Example 1, and is a figure showing the state where the pusher was arranged in the syringe barrel. 図1のA-A断面図である。FIG. 2 is a cross-sectional view taken along the line AA in FIG. 図2のB-B断面図である。FIG. 3 is a sectional view taken along line BB in FIG. 図2のC-C断面図である。FIG. 3 is a cross-sectional view taken along the line CC of FIG. 実施例1の吸引用シリンジの外観斜視図であり、押し子の軸部が注射筒の基端部に係合している状態を示す図である。It is an external appearance perspective view of the syringe for suction of Example 1, and is a figure which shows the state which the axial part of the pusher is engaging with the base end part of the injection cylinder. 図5のD-D断面図である。FIG. 6 is a DD sectional view of FIG. 5. 図6のE-E断面図である。FIG. 7 is a cross-sectional view taken along line EE in FIG. 6. 実施例2の吸引用シリンジの外観斜視図であり、押し子が注射筒内に配置された状態を示す図である。It is an external appearance perspective view of the suction syringe of Example 2, and is a figure which shows the state by which the pusher was arrange | positioned in the syringe barrel. 図8のF-F断面図である。FIG. 9 is a sectional view taken along line FF in FIG. 8. 図9のG-G断面図である。FIG. 10 is a sectional view taken along line GG in FIG. 9. 図9のH-H断面図である。FIG. 10 is a cross-sectional view taken along line HH in FIG. 9. 実施例2の吸引用シリンジの外観斜視図であり、押し子の軸部が注射筒の基端部に係合している状態を示す図である。It is an external appearance perspective view of the syringe for suction of Example 2, and is a figure which shows the state which the axial part of the pusher is engaging with the base end part of the injection cylinder. 図12のI-I断面図である。It is II sectional drawing of FIG. 図13のJ-J断面図である。It is JJ sectional drawing of FIG.
 以下、本発明の吸引用シリンジを具体化した実施の形態について、図面に基づき詳細に説明する。 Hereinafter, embodiments of the suction syringe of the present invention will be described in detail with reference to the drawings.
<実施例1>
〔吸引用シリンジの構成〕
 まず、実施例1の吸引用シリンジ1の構成について説明する。ここで、図1は、実施例1の吸引用シリンジ1の外観斜視図であり、注射筒10内にて陰圧を発生させていない状態であって、押し子12が注射筒10内に配置された状態を示す図である。また、図2は、図1のA-A断面図である。また、図3は図2のB-B断面図であり、図4は図2のC-C断面図である。また、図5は、実施例1の吸引用シリンジ1の外観斜視図であり、注射筒10内にて陰圧を発生させている状態であって、押し子12の軸部22が注射筒10の基端部10aに係合している状態を示す図である。また、図6は、図5のD-D断面図である。さらに、図7は、図6のE-E断面図である。
<Example 1>
[Configuration of suction syringe]
First, the configuration of the suction syringe 1 of Example 1 will be described. Here, FIG. 1 is an external perspective view of the suction syringe 1 according to the first embodiment, in which no negative pressure is generated in the syringe barrel 10, and the pusher 12 is disposed in the syringe barrel 10. It is a figure which shows the state made. FIG. 2 is a cross-sectional view taken along the line AA in FIG. 3 is a cross-sectional view taken along the line BB in FIG. 2, and FIG. 4 is a cross-sectional view taken along the line CC in FIG. FIG. 5 is an external perspective view of the suction syringe 1 according to the first embodiment, in which a negative pressure is generated in the syringe barrel 10, and the shaft portion 22 of the pusher 12 is the syringe barrel 10. It is a figure which shows the state engaged with the base end part 10a. FIG. 6 is a sectional view taken along the line DD of FIG. Further, FIG. 7 is a cross-sectional view taken along the line EE of FIG.
 図1~図7に示すように、吸引用シリンジ1は、注射筒10と、押し子12を有する。 As shown in FIGS. 1 to 7, the suction syringe 1 has a syringe barrel 10 and a pusher 12.
 注射筒10は、開放した基端部10aを備える有底筒状に形成されている。また、注射筒10は、その先端部、すなわち、先端側の底部の中央部分に、注射筒10の胴部に対して径が小さい口部10bが底部から突出するようにして一体的に形成されている。この口部10bには、不図示の吸引カテーテルが接続される。 The injection tube 10 is formed in a bottomed tube shape having an open base end portion 10a. Further, the syringe barrel 10 is integrally formed at the tip portion thereof, that is, at the center portion of the bottom portion on the tip side, so that a mouth portion 10b having a small diameter with respect to the barrel portion of the syringe barrel 10 protrudes from the bottom portion. ing. A suction catheter (not shown) is connected to the mouth portion 10b.
 また、注射筒10は、基端部10aの外周に、フランジ形状の指当て部10cが一体的に形成されている。この指当て部10cは、注射筒10の中心軸に対して互いに反対方向に突出するように形成された1対の板状の部分である。なお、指当て部10cは、注射筒10の中心軸に直交する一方向を長手方向とする長手形状に形成されている。 Further, the syringe barrel 10 is integrally formed with a flange-shaped finger rest 10c on the outer periphery of the base end 10a. The finger rests 10c are a pair of plate-like portions formed so as to protrude in opposite directions with respect to the central axis of the syringe barrel 10. The finger pad 10c is formed in a longitudinal shape having a longitudinal direction in one direction orthogonal to the central axis of the syringe barrel 10.
 なお、注射筒10は、その外周面10eに、液量を示す不図示の目盛りが付されていてもよい。 The syringe barrel 10 may be provided with a scale (not shown) indicating the amount of liquid on the outer peripheral surface 10e.
 押し子12は、先端部20と軸部22を備えている。先端部20は、軸部22よりも注射筒10の口部10b(底部)側に配置されている。先端部20は、注射筒10の口部10b側から順に、第1部位20aと第2部位20bと第3部位20cを備えている。そして、先端部20は、第1部位20aにおける注射筒10の口部10b側に、ガスケット14が装着されている。また、第2部位20bは、押し子12の軸方向に直交する径方向の横断面が略十文字状をなしている。 The pusher 12 includes a tip portion 20 and a shaft portion 22. The distal end portion 20 is disposed closer to the mouth portion 10 b (bottom portion) of the syringe barrel 10 than the shaft portion 22. The distal end portion 20 includes a first portion 20a, a second portion 20b, and a third portion 20c in order from the mouth portion 10b side of the syringe barrel 10. And the front-end | tip part 20 is mounted | worn with the gasket 14 at the opening | mouth part 10b side of the injection cylinder 10 in the 1st site | part 20a. Further, the second portion 20 b has a substantially cross-shaped cross section in the radial direction orthogonal to the axial direction of the pusher 12.
 また、第3部位20cは、略円筒形状に形成され、その内部に溝30が形成されている。この溝30は、注射筒10の内周面10dの内側において、押し子12の径方向の一端側が開放されており、押し子12の径方向の他端側が閉塞されている。 Further, the third portion 20c is formed in a substantially cylindrical shape, and a groove 30 is formed therein. The groove 30 is open on one end side in the radial direction of the pusher 12 and is closed on the other end side in the radial direction of the pusher 12 inside the inner peripheral surface 10 d of the syringe barrel 10.
 そして、図2に示すように、押し子12の軸方向の断面において、溝30における軸部22の突起32との嵌合部30aは、押し子12の径方向に対して傾斜するように形成されている。具体的には、押し子12の軸方向の断面において、嵌合部30aは、溝30の閉塞側から開放側に向かうに連れて、すなわち、軸部22を注射筒10の径方向の外側に移動させる際に軸部22を移動させる方向に向かうに連れて、押し子12の径方向(図2の上下方向)に対して、押し子12を注射筒10から引き抜く方向側(図2の右側)へ傾斜するように形成されている。なお、押し子12の径方向に対する嵌合部30aの傾斜角θ(図2や図6参照)は、5°~50°とすることが考えられ、特に好ましくは、10°~30°である。図2や図6においては、一例として、傾斜角θは10°として示している。 As shown in FIG. 2, in the axial section of the pusher 12, the fitting portion 30 a with the protrusion 32 of the shaft portion 22 in the groove 30 is formed to be inclined with respect to the radial direction of the pusher 12. Has been. Specifically, in the axial cross section of the pusher 12, the fitting portion 30 a moves from the closed side to the open side of the groove 30, that is, the shaft portion 22 moves outward in the radial direction of the syringe barrel 10. When moving the shaft portion 22 in the direction of movement, the direction side in which the pusher 12 is pulled out of the syringe barrel 10 with respect to the radial direction of the pusher 12 (vertical direction in FIG. 2) (right side in FIG. 2). ). It should be noted that the inclination angle θ (see FIGS. 2 and 6) of the fitting portion 30a with respect to the radial direction of the pusher 12 is considered to be 5 ° to 50 °, and particularly preferably 10 ° to 30 °. . In FIG. 2 and FIG. 6, as an example, the inclination angle θ is shown as 10 °.
 軸部22は、先端部20に嵌合している。そして、軸部22の本体部分22aは、その軸方向(図2の左右方向)に直交する径方向の横断面が略十文字状をなしている。また、軸部22は、本体部分22aの先端部20側の端面22bに、先端部20側に突出する凸部22cを備えている。 The shaft portion 22 is fitted to the tip portion 20. And the main-body part 22a of the axial part 22 has comprised the cross section of the radial direction orthogonal to the axial direction (left-right direction of FIG. 2) in substantially cross shape. Further, the shaft portion 22 includes a convex portion 22c that protrudes toward the distal end portion 20 on the end surface 22b of the main body portion 22a on the distal end portion 20 side.
 そして、軸部22は、その凸部22cに、軸部22の径方向(図2の紙面垂直方向、図4の上下方向)に突出する突起32を備えている。この突起32は、略直方体形状に形成されており、溝30に対してスライド(摺動)可能な状態で嵌合している。 And the shaft part 22 is provided with a projection 32 projecting in the radial direction of the shaft part 22 (perpendicular to the plane of FIG. 2 and up and down in FIG. 4) on the projection 22c. The protrusion 32 is formed in a substantially rectangular parallelepiped shape, and is fitted to the groove 30 in a slidable state.
 また、図2に示すように、押し子12の軸方向の断面において、凸部22cと突起32の中心軸Ltの位置は、軸部22の本体部分22aの中心軸Ljの位置から外れている。すなわち、凸部22cと突起32は、軸部22の本体部分22aに対して、軸部22が注射筒10の径方向の外側に移動する側とは反対側に、偏心している。なお、図2において、中心軸Ljの位置は、先端部20の中心軸Lsの位置および注射筒10の中心軸の位置と一致している。 Further, as shown in FIG. 2, in the axial section of the pusher 12, the position of the central axis Lt of the convex portion 22 c and the protrusion 32 is deviated from the position of the central axis Lj of the main body portion 22 a of the shaft portion 22. . That is, the convex portion 22 c and the protrusion 32 are eccentric with respect to the main body portion 22 a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10. In FIG. 2, the position of the central axis Lj coincides with the position of the central axis Ls of the distal end portion 20 and the position of the central axis of the syringe barrel 10.
 また、軸部22は、その端面22bにて、後述するように、注射筒10内に陰圧を発生させたときに、注射筒10の基端部10aに当接する係合部34を備えている。 In addition, the shaft portion 22 includes an engaging portion 34 that abuts on the proximal end portion 10a of the syringe barrel 10 when negative pressure is generated in the syringe barrel 10 at the end surface 22b, as will be described later. Yes.
 また、軸部22は、先端部20側とは反対側の端部に、フランジ36を備えている。このフランジ36は、吸引用シリンジ1の取扱者が押し子12を注射筒10内から引き抜く方向へ移動させるときに、取扱者が指で掴む部分である。 Further, the shaft portion 22 is provided with a flange 36 at the end opposite to the tip 20 side. The flange 36 is a portion that the operator grips with a finger when the handler of the suction syringe 1 moves the pusher 12 in the direction in which the pusher 12 is pulled out from the syringe barrel 10.
 このような押し子12は、注射筒10の内周面10dの内側に移動可能に挿入され、注射筒10から引き抜かれる方向に移動することにより、注射筒10内に陰圧を発生させることができる。ここで、「注射筒10内に陰圧を発生させる」とは、注射筒10の内部の圧力を注射筒10の外部の圧力よりも低くする、ということである。なお、吸引用シリンジ1は、押し子12が注射筒10から完全に抜けてしまうことがないような構造になっている。 Such a pusher 12 is movably inserted inside the inner peripheral surface 10d of the syringe barrel 10 and moves in a direction in which it is pulled out of the syringe barrel 10, thereby generating a negative pressure in the syringe barrel 10. it can. Here, “generating negative pressure in the syringe barrel 10” means that the pressure inside the syringe barrel 10 is made lower than the pressure outside the syringe barrel 10. The suction syringe 1 has a structure in which the pusher 12 is not completely removed from the syringe barrel 10.
〔吸引用シリンジの作用〕
 次に、このような構成の吸引用シリンジ1の作用について説明する。まず、吸引用シリンジ1は、使用前、すなわち、注射筒10内に陰圧を発生させる前において、図1と図2と図4に示すように、押し子12が注射筒10の内周面10dの内側に押し込まれた状態で保管されている。このとき、図2に示すように、押し子12の軸部22は、その本体部分22aの中心軸Ljの位置が先端部20の中心軸Lsの位置に一致するようにして、注射筒10の内周面10dの内側に配置されている。なお、先端部20の中心軸Lsの位置は、注射筒10の中心軸の位置と一致している。
[Operation of suction syringe]
Next, the operation of the suction syringe 1 having such a configuration will be described. First, as shown in FIGS. 1, 2, and 4, the suction syringe 1 has an inner peripheral surface of the syringe barrel 10 before use, that is, before negative pressure is generated in the syringe barrel 10. It is stored in a state of being pushed inside 10d. At this time, as shown in FIG. 2, the shaft portion 22 of the pusher 12 is formed so that the position of the central axis Lj of the main body portion 22a coincides with the position of the central axis Ls of the distal end portion 20. Arranged inside the inner peripheral surface 10d. The position of the central axis Ls of the distal end portion 20 matches the position of the central axis of the syringe barrel 10.
 そこで、吸引用シリンジ1の取扱者が押し子12を注射筒10から引き抜く方向へ移動させると、注射筒10内に陰圧が発生する。そして、取扱者がさらに押し子12を注射筒10から引き抜く方向へ移動させると、注射筒10内に発生する陰圧が大きくなる。 Therefore, when the operator of the suction syringe 1 moves the pusher 12 in the direction of pulling out the syringe barrel 10, a negative pressure is generated in the syringe barrel 10. When the handler further moves the pusher 12 in the direction of pulling out the syringe barrel 10, the negative pressure generated in the syringe barrel 10 increases.
 やがて、図5と図6に示すように、軸部22の本体部分22aを注射筒10の外に位置させると、軸部22は注射筒10から解放される。すると、図6と図7に示すように、軸部22の突起32が、先端部20の溝30の嵌合部30aをスライドする。このようにして、図5と図6に示すように、軸部22が、注射筒10の径方向の外側に向かって移動する。そして、軸部22の本体部分22aの中心軸Ljの位置が、自然に先端部20の中心軸Lsの位置から外れる。すなわち、軸部22が、自然に先端部20および注射筒10に対して偏心した位置に移動する。 Eventually, as shown in FIGS. 5 and 6, when the main body portion 22 a of the shaft portion 22 is positioned outside the syringe barrel 10, the shaft portion 22 is released from the syringe barrel 10. Then, as shown in FIGS. 6 and 7, the protrusion 32 of the shaft portion 22 slides on the fitting portion 30 a of the groove 30 of the tip portion 20. In this way, as shown in FIGS. 5 and 6, the shaft portion 22 moves toward the outside in the radial direction of the syringe barrel 10. Then, the position of the central axis Lj of the main body portion 22a of the shaft portion 22 is naturally deviated from the position of the central axis Ls of the distal end portion 20. That is, the shaft portion 22 naturally moves to a position eccentric with respect to the distal end portion 20 and the syringe barrel 10.
 すると、図5と図6に示すように、軸部22の係合部34が、注射筒10の基端部10aに当接して係合する。これにより、押し子12は、注射筒10から引き抜かれる方向とは反対方向に戻ることが規制される。また、このとき、図6に示すように、軸部22の突起32(凸部22c)が、注射筒10の内周面10dに当接する。これにより、軸部22は、さらに押し子12の径方向の外側に向かって移動することが規制される。 Then, as shown in FIGS. 5 and 6, the engaging portion 34 of the shaft portion 22 contacts and engages with the proximal end portion 10 a of the syringe barrel 10. As a result, the pusher 12 is restricted from returning in the direction opposite to the direction in which the pusher 12 is pulled out from the syringe barrel 10. Further, at this time, as shown in FIG. 6, the projection 32 (convex portion 22 c) of the shaft portion 22 contacts the inner peripheral surface 10 d of the syringe barrel 10. As a result, the shaft portion 22 is further restricted from moving outward in the radial direction of the pusher 12.
 以上のようにして、吸引用シリンジ1は、図5~図7に示すように、注射筒10内にて陰圧を発生させている状態下で、押し子12がロック(係止)される。したがって、取扱者は、注射筒10内にて陰圧を発生させている状態下で、押し子12の戻りを容易に規制させることができる。 As described above, in the syringe 1 for suction, the pusher 12 is locked (locked) under a state where a negative pressure is generated in the syringe barrel 10 as shown in FIGS. . Therefore, the operator can easily restrict the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
 このように、実施例1の吸引用シリンジ1においては、押し子12の軸部22自体が押し子12が注射筒10から引き抜かれる方向とは反対方向に戻ることを規制するためのストッパー(係止手段)としての役割を有している。 Thus, in the suction syringe 1 according to the first embodiment, the stopper 22 is used to restrict the shaft portion 22 of the pusher 12 from returning in the direction opposite to the direction in which the pusher 12 is pulled out of the syringe barrel 10. As a stopping means).
 その後、取扱者は、注射筒10内の陰圧の発生を解除する際には、図5と図6に示すように軸部22の係合部34が基端部10aに係合している状態から、軸部22を注射筒10の径方向の内側に移動させる。すると、軸部22の突起32が、先端部20の溝30の嵌合部30aをスライドしながら、注射筒10の径方向の内側に向かって移動する。これにより、軸部22の係合部34は、基端部10aから離れて、基端部10aとの係合が解除される。そして、軸部22は、注射筒10の内周面10dの内側に押し込まれる方向へ移動する。これにより、吸引用シリンジ1は、図1~図4に示す状態となり、注射筒10内の陰圧の発生が解除される。 Thereafter, when the handler releases the generation of the negative pressure in the syringe barrel 10, the engaging portion 34 of the shaft portion 22 is engaged with the base end portion 10 a as shown in FIGS. 5 and 6. From the state, the shaft portion 22 is moved inward in the radial direction of the syringe barrel 10. Then, the protrusion 32 of the shaft portion 22 moves toward the inside in the radial direction of the syringe barrel 10 while sliding the fitting portion 30a of the groove 30 of the distal end portion 20. Thereby, the engaging part 34 of the shaft part 22 is separated from the base end part 10a, and the engagement with the base end part 10a is released. And the axial part 22 moves to the direction pushed inside 10d of the internal peripheral surface of the injection cylinder 10. As shown in FIG. As a result, the suction syringe 1 enters the state shown in FIGS. 1 to 4, and the generation of the negative pressure in the syringe barrel 10 is released.
〔本実施例の効果〕
 本実施例によれば、吸引用シリンジ1は、開放した基端部10aを備える有底筒状で、吸引カテーテルに接続される注射筒10と、注射筒10に移動可能に挿入され、注射筒10から引き抜く方向へ移動させることにより注射筒10内に陰圧を発生させる押し子12と、を有する。そして、押し子12は、ガスケット14が装着される先端部20と、先端部20に嵌合する軸部22と、を備える。そして、吸引用シリンジ1は、押し子12を注射筒10から引き抜く方向へ移動させて軸部22を注射筒10外に位置させたときに、軸部22が注射筒10の径方向の外側に移動して基端部10aに係合することにより、陰圧発生時における押し子12の戻りを規制する。
[Effect of this embodiment]
According to the present embodiment, the suction syringe 1 has a bottomed cylindrical shape with an open proximal end portion 10a, and is inserted into the syringe barrel 10 connected to the suction catheter and the syringe barrel 10 so as to be movable. And a pusher 12 that generates a negative pressure in the syringe barrel 10 by being moved in a direction in which the syringe 10 is pulled out. The pusher 12 includes a distal end portion 20 to which the gasket 14 is attached, and a shaft portion 22 that is fitted to the distal end portion 20. When the suction syringe 1 moves the pusher 12 in the direction in which the pusher 12 is pulled out of the syringe barrel 10 and positions the shaft portion 22 outside the syringe barrel 10, the shaft portion 22 is placed on the outer side in the radial direction of the syringe barrel 10. By moving and engaging with the base end portion 10a, the return of the pusher 12 when negative pressure is generated is regulated.
 このように、押し子12は、先端部20と軸部22を備えた簡便な構造である。そして、吸引用シリンジ1は、軸部22を注射筒10の径方向の外側に移動させて係合部34を基端部10aに係合させることにより、陰圧発生時における押し子12の戻りを容易に規制することができる。このようにして、吸引用シリンジ1は、簡便な構造のもと、注射筒10内にて陰圧を発生させている状態下で押し子12の戻りを容易に規制することができる。 Thus, the pusher 12 has a simple structure including the tip portion 20 and the shaft portion 22. The suction syringe 1 moves the shaft portion 22 to the outside in the radial direction of the syringe barrel 10 and engages the engaging portion 34 with the proximal end portion 10a, thereby returning the pusher 12 when negative pressure is generated. Can be easily regulated. In this manner, the suction syringe 1 can easily regulate the return of the pusher 12 under a simple structure under a state in which a negative pressure is generated in the syringe barrel 10.
 また、先端部20と軸部22は、先端部20に形成される溝30と、軸部22に形成され溝30に対して摺動可能に嵌合する突起32とにより、嵌合している。そして、突起32を溝30にスライドさせることにより、軸部22は溝30に案内されながら注射筒10の径方向の外側に移動することができる。そのため、吸引用シリンジ1の操作性が向上する。 Further, the distal end portion 20 and the shaft portion 22 are fitted by a groove 30 formed in the distal end portion 20 and a protrusion 32 that is formed in the shaft portion 22 and slidably fits into the groove 30. . Then, by sliding the protrusion 32 into the groove 30, the shaft portion 22 can be moved outward in the radial direction of the syringe barrel 10 while being guided by the groove 30. Therefore, the operability of the suction syringe 1 is improved.
 また、溝30における突起32との嵌合部30aは、押し子12の径方向に対して、押し子12を注射筒10から引き抜く方向側へ傾斜するように形成されている。具体的には、図2や図6に示すように、押し子12の軸方向の断面において、嵌合部30aは、溝30の閉塞側から開放側に向かうに連れて、すなわち、軸部22を注射筒10の径方向の外側に移動させる際に軸部22を移動させる方向に向かうに連れて、押し子12の径方向(図2や図6の上下方向)に対して、押し子12を注射筒10から引き抜く方向側(図2や図6の右側)へ傾斜するように形成されている。これにより、押し子12を注射筒10から引き抜く方向へ移動させるだけで、自然に軸部22を注射筒の径方向の外側に移動させることができる。そのため、吸引用シリンジ1の操作性が顕著に向上する。 In addition, the fitting portion 30 a of the groove 30 with the protrusion 32 is formed so as to be inclined with respect to the radial direction of the pusher 12 in the direction in which the pusher 12 is pulled out from the syringe barrel 10. Specifically, as shown in FIGS. 2 and 6, in the cross section in the axial direction of the pusher 12, the fitting portion 30 a moves from the closed side to the open side of the groove 30, that is, the shaft portion 22. When moving the outer side of the syringe barrel 10 in the radial direction, the pusher 12 is moved relative to the radial direction of the pusher 12 (vertical direction in FIGS. 2 and 6) as it moves in the direction in which the shaft portion 22 is moved. It is formed so that it may incline to the direction side (right side of FIG. 2 and FIG. 6) which pulls out from the injection cylinder 10. As shown in FIG. Thereby, the shaft part 22 can be naturally moved to the outer side in the radial direction of the syringe barrel simply by moving the pusher 12 in the direction of pulling out the syringe barrel 10. Therefore, the operability of the suction syringe 1 is significantly improved.
 また、突起32は、軸部22の本体部分22aに対して、軸部22が注射筒10の径方向の外側に移動する側とは反対側に偏心させた位置に形成されている。これにより、軸部22が注射筒10の径方向の外側に移動して基端部10aに係合するときに、軸部22の係合部34の係合面積を大きくすることができる。そのため、軸部22と基端部10aとの係合状態が安定する。したがって、吸引用シリンジ1は、注射筒10内にて陰圧を発生させている状態下で、押し子12の戻りを確実に規制することができる。 Also, the protrusion 32 is formed at a position that is eccentric with respect to the main body portion 22a of the shaft portion 22 on the side opposite to the side on which the shaft portion 22 moves outward in the radial direction of the syringe barrel 10. Thereby, when the axial part 22 moves to the outer side of the radial direction of the injection cylinder 10, and engages with the base end part 10a, the engagement area of the engaging part 34 of the axial part 22 can be enlarged. Therefore, the engagement state between the shaft portion 22 and the base end portion 10a is stabilized. Therefore, the suction syringe 1 can reliably regulate the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
<実施例2>
 次に、実施例2について説明するが、実施例1と同等の構成要素については、同一の符号を付して説明を省略し、異なった点を中心に述べる。ここで、図8は、実施例2の吸引用シリンジ2の外観斜視図であり、注射筒10内にて陰圧を発生させていない状態であって、押し子12が注射筒10内に配置された状態を示す図である。また、図9は、図8のF-F断面図である。また、図10は図9のG-G断面図であり、図11は図9のH-H断面図である。また、図12は、実施例2の吸引用シリンジ2の外観斜視図であり、注射筒10内にて陰圧を発生させている状態であって、押し子12の軸部22が注射筒10の基端部10aに係合している状態を示す図である。また、図13は、図12のI-I断面図である。さらに、図14は、図13のJ-J断面図である。
<Example 2>
Next, the second embodiment will be described. The same components as those of the first embodiment are denoted by the same reference numerals, the description thereof will be omitted, and different points will be mainly described. Here, FIG. 8 is an external perspective view of the suction syringe 2 of Example 2, in which no negative pressure is generated in the syringe barrel 10, and the pusher 12 is disposed in the syringe barrel 10. It is a figure which shows the state made. FIG. 9 is a cross-sectional view taken along the line FF in FIG. 10 is a GG cross-sectional view of FIG. 9, and FIG. 11 is a HH cross-sectional view of FIG. FIG. 12 is an external perspective view of the suction syringe 2 according to the second embodiment, in which a negative pressure is generated in the syringe barrel 10, and the shaft portion 22 of the pusher 12 is connected to the syringe barrel 10. It is a figure which shows the state engaged with the base end part 10a. FIG. 13 is a cross-sectional view taken along the line II of FIG. Further, FIG. 14 is a sectional view taken along line JJ of FIG.
〔吸引用シリンジの構成〕
 実施例2の吸引用シリンジ2における押し子12は、実施例1と異なる点として、図8や図9などに示すように、先端部20は、その第3部位20cの内部に、溝40を備えている。この溝40は、注射筒10の内周面10dの内側において、押し子12の径方向の一端側は開放されており、押し子12の径方向の他端側は閉塞されている。そして、図9と図13に示すように、押し子12の軸方向の断面において、溝40における突起42との嵌合部40aは、押し子12の径方向(図9と図13の上下方向)に沿って平行に、すなわち、押し子12の軸方向に直交するようにして、形成されている。
[Configuration of suction syringe]
As shown in FIGS. 8 and 9, the pusher 12 in the suction syringe 2 of the second embodiment is different from the first embodiment. As shown in FIGS. 8 and 9, the distal end portion 20 has a groove 40 in the third portion 20 c. I have. In the groove 40, one end side in the radial direction of the pusher 12 is opened inside the inner peripheral surface 10 d of the syringe barrel 10, and the other end side in the radial direction of the pusher 12 is closed. 9 and 13, in the axial section of the pusher 12, the fitting portion 40a with the protrusion 42 in the groove 40 is in the radial direction of the pusher 12 (the vertical direction in FIGS. 9 and 13). ) In parallel, that is, perpendicular to the axial direction of the pusher 12.
 また、軸部22は、その凸部22dに、軸部22の径方向に突出する突起42を備えている。この突起42は、円盤形状に形成されており、溝40に対してスライド可能な状態で係合している。また、図9に示すように、押し子12の軸方向の断面において、凸部22dと突起42の中心軸Ltの位置は、軸部22の本体部分22aの中心軸Ljの位置から外れている。すなわち、凸部22dと突起42は、軸部22の本体部分22aに対して、軸部22が注射筒10の径方向の外側に移動する側とは反対側に、偏心している。 Further, the shaft portion 22 is provided with a projection 42 protruding in the radial direction of the shaft portion 22 on the convex portion 22d. The protrusion 42 is formed in a disk shape and engages with the groove 40 in a slidable state. Further, as shown in FIG. 9, in the axial section of the pusher 12, the position of the central axis Lt of the convex portion 22 d and the protrusion 42 is deviated from the position of the central axis Lj of the main body portion 22 a of the shaft portion 22. . That is, the convex portion 22 d and the protrusion 42 are eccentric with respect to the main body portion 22 a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10.
 なお、本実施例では、溝40と突起42は、各々2つ形成されている。 In this embodiment, two grooves 40 and two protrusions 42 are formed.
〔吸引用シリンジの作用〕
 次に、このような構成の吸引用シリンジ2の作用について説明する。まず、吸引用シリンジ2は、使用前、すなわち、注射筒10内に陰圧を発生させる前において、図8と図9と図11に示すように、押し子12が注射筒10の内周面10dの内側に押し込まれた状態で保管されている。
[Operation of suction syringe]
Next, the operation of the suction syringe 2 having such a configuration will be described. First, as shown in FIGS. 8, 9, and 11, the suction syringe 2 has an inner peripheral surface of the syringe barrel 10 before use, that is, before negative pressure is generated in the syringe barrel 10. It is stored in a state of being pushed inside 10d.
 そこで、吸引用シリンジ2の取扱者が押し子12を注射筒10から引き抜く方向へ移動させると、注射筒10内に陰圧が発生する。やがて、図12と図13に示すように、軸部22の本体部分22aが注射筒10の外に位置すると、軸部22は注射筒10から解放される。そこで、取扱者は、軸部22を中心軸Ljを中心にして回転させる。すると、図13と図14に示すように、軸部22の突起42が回転しながら溝40をスライドすることにより、軸部22が注射筒10の径方向の外側に向かって移動する。このようにして、軸部22の本体部分22aの中心軸Ljの位置が、先端部20の中心軸Lsの位置から外れる。すなわち、軸部22が、先端部20および注射筒10に対して偏心した位置に移動する。 Therefore, when the operator of the suction syringe 2 moves the pusher 12 in the direction of pulling out the syringe barrel 10, a negative pressure is generated in the syringe barrel 10. Eventually, as shown in FIGS. 12 and 13, when the main body portion 22 a of the shaft portion 22 is positioned outside the syringe barrel 10, the shaft portion 22 is released from the syringe barrel 10. Therefore, the handler rotates the shaft portion 22 around the central axis Lj. Then, as shown in FIG. 13 and FIG. 14, the shaft portion 22 moves toward the outside in the radial direction of the syringe barrel 10 by sliding the groove 40 while the projection 42 of the shaft portion 22 rotates. In this way, the position of the central axis Lj of the main body portion 22a of the shaft portion 22 deviates from the position of the central axis Ls of the distal end portion 20. That is, the shaft portion 22 moves to a position eccentric with respect to the distal end portion 20 and the syringe barrel 10.
 すると、図12と図13に示すように、軸部22の係合部34が、注射筒10の基端部10aに当接して係合する。これにより、押し子12は、注射筒10から引き抜かれる方向とは反対方向に戻ることが規制される。また、このとき、図13に示すように、軸部22の突起42(凸部22d)が、注射筒10の内周面10dに当接する。これにより、軸部22は、さらに押し子12の径方向の外側に向かって移動することが規制される。 Then, as shown in FIGS. 12 and 13, the engaging portion 34 of the shaft portion 22 comes into contact with and engages with the proximal end portion 10 a of the syringe barrel 10. As a result, the pusher 12 is restricted from returning in the direction opposite to the direction in which the pusher 12 is pulled out from the syringe barrel 10. Further, at this time, as shown in FIG. 13, the protrusion 42 (projection 22 d) of the shaft portion 22 comes into contact with the inner peripheral surface 10 d of the syringe barrel 10. As a result, the shaft portion 22 is further restricted from moving outward in the radial direction of the pusher 12.
 以上のようにして、吸引用シリンジ2は、図12~図14に示すように、注射筒10内にて陰圧を発生させている状態下で、押し子12がロックされる。したがって、取扱者は、注射筒10内にて陰圧を発生させている状態下で、押し子12の戻りを容易に規制させることができる。 As described above, in the suction syringe 2, the pusher 12 is locked under a state where a negative pressure is generated in the syringe barrel 10 as shown in FIGS. 12 to 14. Therefore, the operator can easily restrict the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
 その後、取扱者は、注射筒10内の陰圧の発生を解除する際には、図12と図13に示すように軸部22の係合部34が基端部10aに係合している状態にて、軸部22を回転させながら注射筒10の径方向の内側に移動させる。すると、軸部22の突起42が、先端部20の溝40に沿ってスライドして、注射筒10の径方向の内側に向かって移動する。これにより、軸部22の係合部34は、基端部10aから離れて、基端部10aとの係合が解除される。そして、軸部22は、注射筒10の内周面10dの内側に押し込まれる方向へ移動する。これにより、吸引用シリンジ2は、図8~図11に示す状態となり、注射筒10内の陰圧の発生が解除される。 Thereafter, when the handler releases the generation of the negative pressure in the syringe barrel 10, as shown in FIGS. 12 and 13, the engaging portion 34 of the shaft portion 22 is engaged with the proximal end portion 10a. In the state, the shaft 22 is moved inward in the radial direction of the syringe barrel 10 while rotating. Then, the protrusion 42 of the shaft portion 22 slides along the groove 40 of the distal end portion 20 and moves toward the inside in the radial direction of the syringe barrel 10. Thereby, the engaging part 34 of the shaft part 22 is separated from the base end part 10a, and the engagement with the base end part 10a is released. And the axial part 22 moves to the direction pushed inside 10d of the internal peripheral surface of the injection cylinder 10. As shown in FIG. As a result, the suction syringe 2 enters the state shown in FIGS. 8 to 11, and the generation of the negative pressure in the syringe barrel 10 is released.
〔本実施例の効果〕
 本実施例によれば、吸引用シリンジ2は、開放した基端部10aを備える有底筒状で、吸引カテーテルに接続される注射筒10と、注射筒10に移動可能に挿入され、注射筒10から引き抜く方向へ移動させることにより注射筒10内に陰圧を発生させる押し子12と、を有する。そして、押し子12は、ガスケット14が装着される先端部20と、先端部20に嵌合する軸部22と、を備える。そして、吸引用シリンジ2は、押し子12を注射筒10から引き抜く方向へ移動させて軸部22を注射筒10外に位置させたときに、軸部22が注射筒10の径方向の外側に移動して基端部10aに係合することにより、陰圧発生時における押し子12の戻りを規制する。
[Effect of this embodiment]
According to the present embodiment, the suction syringe 2 has a bottomed cylindrical shape with an open proximal end portion 10a, and is inserted into the syringe barrel 10 connected to the suction catheter and the syringe barrel 10 so as to be movable. And a pusher 12 that generates a negative pressure in the syringe barrel 10 by being moved in a direction in which the syringe 10 is pulled out. The pusher 12 includes a distal end portion 20 to which the gasket 14 is attached, and a shaft portion 22 that is fitted to the distal end portion 20. When the suction syringe 2 moves the pusher 12 in the direction in which the pusher 12 is pulled out from the syringe barrel 10 and positions the shaft portion 22 outside the syringe barrel 10, the shaft portion 22 is placed on the outer side in the radial direction of the syringe barrel 10. By moving and engaging with the base end portion 10a, the return of the pusher 12 when negative pressure is generated is regulated.
 このように、押し子12は、先端部20と軸部22を備えた簡便な構造である。そして、吸引用シリンジ2は、軸部22を注射筒10の径方向の外側に移動させて係合部34を基端部10aに係合させることにより、陰圧発生時における押し子12の戻りを容易に規制することができる。このようにして、吸引用シリンジ2は、簡便な構造のもと、注射筒10内にて陰圧を発生させている状態下で押し子12の戻りを容易に規制することができる。 Thus, the pusher 12 has a simple structure including the tip portion 20 and the shaft portion 22. The suction syringe 2 moves the shaft portion 22 to the outside in the radial direction of the syringe barrel 10 and engages the engaging portion 34 with the base end portion 10a, thereby returning the pusher 12 when negative pressure is generated. Can be easily regulated. In this manner, the suction syringe 2 can easily regulate the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10 with a simple structure.
 また、先端部20と軸部22は、先端部20に形成される溝40と、軸部22に形成され溝40に対して摺動可能に嵌合する突起42とにより、嵌合している。そして、突起42を溝40にスライドさせることにより、軸部22は溝40に案内されながら注射筒10の径方向の外側に移動することができる。そのため、吸引用シリンジ2の操作性が向上する。 Further, the tip portion 20 and the shaft portion 22 are fitted by a groove 40 formed in the tip portion 20 and a projection 42 formed in the shaft portion 22 and slidably fitted to the groove 40. . Then, by sliding the protrusion 42 into the groove 40, the shaft portion 22 can be moved outward in the radial direction of the syringe barrel 10 while being guided by the groove 40. Therefore, the operability of the suction syringe 2 is improved.
 また、溝40における突起42との嵌合部40aは、注射筒10の径方向に沿って形成されている。これにより、押し子12は、容易に注射筒10の径方向の外側に移動することができる。そのため、吸引用シリンジ2の操作性が顕著に向上する。 Further, the fitting portion 40 a with the protrusion 42 in the groove 40 is formed along the radial direction of the syringe barrel 10. As a result, the pusher 12 can easily move outward in the radial direction of the syringe barrel 10. Therefore, the operability of the suction syringe 2 is significantly improved.
 また、突起42は、軸部22の本体部分22aに対して、軸部22が注射筒10の径方向の外側に移動する側とは反対側に偏心させた位置に形成されている。これにより、軸部22が注射筒10の径方向の外側に移動して基端部10aに係合するときに、軸部22の係合部34の係合面積を大きくすることができる。そのため、軸部22と基端部10aとの係合状態が安定する。したがって、吸引用シリンジ2は、注射筒10内にて陰圧を発生させている状態下で、押し子12の戻りを確実に規制することができる。 Further, the protrusion 42 is formed at a position eccentric with respect to the main body portion 22a of the shaft portion 22 on the side opposite to the side where the shaft portion 22 moves outward in the radial direction of the syringe barrel 10. Thereby, when the axial part 22 moves to the outer side of the radial direction of the injection cylinder 10, and engages with the base end part 10a, the engagement area of the engaging part 34 of the axial part 22 can be enlarged. Therefore, the engagement state between the shaft portion 22 and the base end portion 10a is stabilized. Therefore, the suction syringe 2 can reliably regulate the return of the pusher 12 under a state where a negative pressure is generated in the syringe barrel 10.
 なお、上記した実施の形態は単なる例示にすぎず、本発明を何ら限定するものではなく、その要旨を逸脱しない範囲内で種々の改良、変形が可能であることはもちろんである。 It should be noted that the above-described embodiment is merely an example, and does not limit the present invention in any way, and various improvements and modifications can be made without departing from the scope of the invention.
 1  吸引用シリンジ
 2  吸引用シリンジ
 10 注射筒
 10a 基端部
 10d 内周面
 12 押し子
 20 先端部
 22 軸部
 22a 本体部分
 22b 端面
 30 溝
 30a 嵌合部
 32 突起
 34 係合部
 40 溝
 40a 嵌合部
 42 突起
 Ls (先端部の)中心軸
 Lj (軸部の本体部分の)中心軸
 Lt (突起の)中心軸
DESCRIPTION OF SYMBOLS 1 Syringe syringe 2 Suction syringe 10 Injection cylinder 10a Base end part 10d Inner peripheral surface 12 Pusher 20 Tip part 22 Shaft part 22a Main body part 22b End surface 30 Groove 30a Fitting part 32 Protrusion 34 Engagement part 40 Groove 40a Fitting Part 42 Projection Ls Center axis Lj (at the tip) Lj Center axis (at the main part of the shaft part) Lt (Projection) center axis

Claims (5)

  1.  開放した基端部を備える有底筒状で、吸引カテーテルに接続される注射筒と、
     前記注射筒に移動可能に挿入され、前記注射筒から引き抜く方向へ移動させることにより前記注射筒内に陰圧を発生させる押し子と、
    を有し、
     前記押し子は、ガスケットが装着される先端部と、前記先端部に嵌合する軸部と、を備え、
     前記押し子を前記注射筒から引き抜く方向へ移動させて前記軸部を前記注射筒外に位置させたときに、前記軸部が前記注射筒の径外方向に移動して前記基端部に係合することにより、陰圧発生時における前記押し子の戻りを規制すること、
     を特徴とする吸引用シリンジ。
    A syringe barrel connected to a suction catheter in a bottomed cylinder with an open proximal end;
    A pusher that is movably inserted into the syringe barrel and generates a negative pressure in the syringe barrel by moving it in a direction of being pulled out of the syringe barrel;
    Have
    The pusher includes a tip portion to which a gasket is attached, and a shaft portion fitted to the tip portion,
    When the pusher is moved in the direction of pulling out from the syringe barrel and the shaft portion is positioned outside the syringe barrel, the shaft portion moves in the radially outward direction of the syringe barrel and engages with the base end portion. By restricting the return of the pusher when negative pressure is generated,
    A syringe for suction.
  2.  請求項1の吸引用シリンジにおいて、
     前記先端部と前記軸部は、前記先端部に形成される溝と、前記軸部に形成され前記溝に対して摺動可能に嵌合する突起とにより、嵌合していること、
     を特徴とする吸引用シリンジ。
    The suction syringe of claim 1, wherein
    The tip portion and the shaft portion are fitted by a groove formed in the tip portion and a protrusion formed in the shaft portion and slidably fitted to the groove;
    A syringe for suction.
  3.  請求項2の吸引用シリンジにおいて、
     前記溝における前記突起との嵌合部は、前記押し子の径方向に対して、前記押し子を前記注射筒から引き抜く方向側へ傾斜するように形成されていること、
     を特徴とする吸引用シリンジ。
    The syringe for suction according to claim 2,
    The fitting portion with the protrusion in the groove is formed so as to incline toward the direction in which the pusher is pulled out from the syringe barrel with respect to the radial direction of the pusher.
    A syringe for suction.
  4.  請求項2の吸引用シリンジにおいて、
     前記溝における前記突起との嵌合部は、前記注射筒の径方向に沿って形成されていること、
     を特徴とする吸引用シリンジ。
    The syringe for suction according to claim 2,
    The fitting portion with the protrusion in the groove is formed along the radial direction of the syringe barrel,
    A syringe for suction.
  5.  請求項1乃至4のいずれか1つの吸引用シリンジにおいて、
     前記突起は、前記軸部の本体部分に対して前記軸部が前記注射筒の径外方向に移動する側とは反対側に偏心させた位置に形成されていること、
     を特徴とする吸引用シリンジ。
    The syringe for suction according to any one of claims 1 to 4,
    The protrusion is formed at a position that is eccentric to a side opposite to a side where the shaft portion moves in a radially outward direction of the syringe barrel with respect to a main body portion of the shaft portion;
    A syringe for suction.
PCT/JP2013/066922 2013-06-20 2013-06-20 Suction syringe WO2014203365A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/066922 WO2014203365A1 (en) 2013-06-20 2013-06-20 Suction syringe

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/066922 WO2014203365A1 (en) 2013-06-20 2013-06-20 Suction syringe

Publications (1)

Publication Number Publication Date
WO2014203365A1 true WO2014203365A1 (en) 2014-12-24

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ID=52104127

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Application Number Title Priority Date Filing Date
PCT/JP2013/066922 WO2014203365A1 (en) 2013-06-20 2013-06-20 Suction syringe

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Country Link
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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000296178A (en) * 1999-02-08 2000-10-24 Fuji Photo Optical Co Ltd Adapter device for syringe
JP2010528825A (en) * 2007-06-12 2010-08-26 ベクトン・ディキンソン・アンド・カンパニー Syringe assembly including anti-reuse mechanism

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000296178A (en) * 1999-02-08 2000-10-24 Fuji Photo Optical Co Ltd Adapter device for syringe
JP2010528825A (en) * 2007-06-12 2010-08-26 ベクトン・ディキンソン・アンド・カンパニー Syringe assembly including anti-reuse mechanism

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