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WO2019026796A1 - Adaptor assembly - Google Patents

Adaptor assembly Download PDF

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Publication number
WO2019026796A1
WO2019026796A1 PCT/JP2018/028275 JP2018028275W WO2019026796A1 WO 2019026796 A1 WO2019026796 A1 WO 2019026796A1 JP 2018028275 W JP2018028275 W JP 2018028275W WO 2019026796 A1 WO2019026796 A1 WO 2019026796A1
Authority
WO
WIPO (PCT)
Prior art keywords
adapter
puncture needle
cover
vial
adapter assembly
Prior art date
Application number
PCT/JP2018/028275
Other languages
French (fr)
Japanese (ja)
Inventor
野口央照
沖山忠
Original Assignee
株式会社ジェイ・エム・エス
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 株式会社ジェイ・エム・エス filed Critical 株式会社ジェイ・エム・エス
Publication of WO2019026796A1 publication Critical patent/WO2019026796A1/en

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Classifications

    • 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
    • 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
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/162Needle sets, i.e. connections by puncture between reservoir and tube ; Connections between reservoir and tube

Definitions

  • the present invention relates to an adapter assembly comprising a vial mountable adapter and a cover separably mounted on the adapter.
  • a vial containing a powdered drug is widely distributed.
  • a solution is injected into the vial, the drug is dissolved in the solution to obtain a drug solution, and the drug solution is removed from the vial.
  • the injection of the solution into the vial and the removal of the drug solution are performed via a puncture needle (sometimes called a "bottle needle") pierced in a stopper (rubber stopper) that seals the opening (opening) of the vial.
  • the drug is a dangerous drug such as an anticancer drug, for example, it is necessary to prevent such drug and its drug solution from leaking out to the outside. Therefore, in order to prevent the puncture needle punctured in the stopper of the vial from coming out of the stopper unintentionally, the claw engaging with the enlarged flange surrounding the mouth of the vial is integrally provided with the puncture needle Adapters are often used.
  • the adapter of Patent Document 1 includes a puncture needle and a claw that can be engaged with a flange of a vial.
  • the claws are provided on an elastically bendable arm. With the tip of the puncture needle facing the stopper of the vial, the adapter is pushed toward the vial. The puncture needle punctures the stopper of the vial. The claw is displaced in a direction away from the puncture needle (i.e., radially outward) by abutting on the stopper (or the aluminum cap covering it), and the arm elastically bends and deforms. Thereafter, as the pawl passes the flange, the arm resiliently recovers and the pawl engages the flange of the vial.
  • the adapter When attaching the adapter to the vial, after visually aligning the tip of the puncture needle with the center of the stopper so that the puncture needle punctures the center of the stopper, the adapter is pushed toward the vial.
  • the tip of the puncture needle may be off center of the plug.
  • the adapter can not be properly attached to the vial, such as it becomes difficult to engage the hook of the adapter with the flange of the vial.
  • An object of the present invention is to align the tip of the puncture needle of the adapter with the center of the stopper of the vial.
  • the adapter assembly of the present invention comprises an adapter mountable to a vial, and a cover removably mounted on the adapter from above.
  • the adapter is provided with a puncture needle capable of piercing the stopper of the vial, a plurality of claws engageable with the enlarged flange of the vial, and a plurality of elastically bendable plurality provided with the plurality of claws.
  • the arm of the The cover includes a guide mechanism extending to face the puncture needle. When the cover is attached to the adapter, the guide mechanism extends further downward than the puncture needle.
  • the guide mechanism provided on the cover extends further downward than the puncture needle. Therefore, the tip of the puncture needle can be easily aligned with the center of the plug using the guide mechanism.
  • FIG. 1 is an exploded perspective view of an adapter assembly and a vial according to one embodiment of the present invention.
  • FIG. 2A is a top perspective view of an adapter according to an embodiment of the present invention.
  • FIG. 2B is a perspective view from below of the adapter according to an embodiment of the present invention.
  • FIG. 2C is a cross-sectional view along a plane including the central axis of the adapter according to one embodiment of the present invention.
  • FIG. 3A is a bottom perspective view of a cover according to an embodiment of the present invention.
  • FIG. 3B is a cross-sectional perspective view from below of the cover according to an embodiment of the present invention.
  • FIG. 3C is a plan view of a cover according to an embodiment of the present invention.
  • FIG. 4A is a top perspective view of an adapter assembly according to one embodiment of the present invention.
  • FIG. 4B is a plan view of an adapter assembly in accordance with one embodiment of the present invention.
  • FIG. 4C is a cross-sectional view of the adapter assembly according to an embodiment of the present invention along a plane including the central axis.
  • FIG. 4D is a cross-sectional view of an adapter assembly according to an embodiment of the present invention taken along another plane including the central axis.
  • FIG. 5 is a cross-sectional view of a vial to which an adapter assembly according to an embodiment of the present invention is attached.
  • FIG. 6 is a perspective view showing a state immediately before the puncture needle of the adapter assembly according to an embodiment of the present invention punctures the stopper of the vial.
  • FIG. 7 is a perspective view showing the adapter assembly according to an embodiment of the present invention attached to a vial.
  • the cover may include a plurality of the guide mechanisms.
  • the plurality of guide mechanisms may be disposed along a circle concentric with the puncture needle. According to this aspect, it is possible to improve the accuracy of the alignment of the tip of the puncture needle with respect to the center of the plug.
  • the guide mechanism may be elastically deformable such that its tip is separated from the puncture needle.
  • the adapter assembly can be adapted to a plurality of types of vials in which the outer diameter of the stopper (or flange) is different. Also, even if the guide mechanism collides with the shoulder of the vial in the process of attaching the adapter assembly to the vial, the puncture needle can be pierced to the desired depth to the stopper.
  • the adapter may include a connector in communication with the puncture needle.
  • the cover may include a connector case for housing the connector. According to this aspect, the sanitary condition of the connector can be well maintained. Also, by attaching a cover to a used adapter, the potential for drug exposure can be reduced.
  • the connector case may be disposed on the top of the cover. According to this aspect, when holding the cover, the worker is likely to pick the connector case with his / her finger. This causes the operator to apply a downward force to the arm when attaching the adapter assembly to the vial, which makes it difficult to attach the adapter assembly to the vial or causes the arm to break (break). Reduce the possibility of the situation happening.
  • the peripheral wall of the connector case may be provided with a pair of gripping surfaces parallel to each other. According to this aspect, when holding the adapter assembly, the worker is always directed to pinch the gripping surface. This further reduces the possibility of the operator applying a downward force on the arm when attaching the adapter assembly to the vial.
  • An extension plate may project radially outward from the lower end of the peripheral wall of the connector case. According to this aspect, when attaching the adapter assembly to the vial, the operator can apply a downward force to the expansion plate.
  • the expansion plate also prevents an operator's finger from touching the arm and inadvertently applying a downward force to the arm when attaching the adapter assembly to the vial.
  • the extension plate may have a major axis in a direction in which the pair of gripping surfaces face each other. Such an aspect further facilitates gripping the gripping surface with a finger to apply a downward force to the adapter assembly.
  • the extension plate may be located higher than the plurality of arms. Such an aspect is advantageous for reducing the possibility of the operator's finger touching the arm and inadvertently applying a downward force to the arm when attaching the adapter assembly to the vial.
  • the plurality of arms may be disposed to face in a first direction orthogonal to the longitudinal direction of the puncture needle.
  • the pair of gripping surfaces may be arranged to face in a second direction orthogonal to the first direction and perpendicular to the longitudinal direction of the puncture needle.
  • An alignment structure may be provided on the cover to axially align the cover coaxially with the adapter. According to this aspect, it is possible to improve the accuracy of the alignment of the tip of the puncture needle with respect to the center of the plug.
  • An engagement structure may be provided on the cover to engage the adapter so as to prevent the adapter from falling off the cover. According to this aspect, the mounting operation of the adapter assembly to the vial can be easily performed.
  • FIG. 1 is an exploded perspective view of an adapter assembly 1 and a vial 80 according to an embodiment of the present invention.
  • the adapter assembly 1 includes an adapter 10 attached to a vial 80 and a cover 50 that can be repeatedly attached to and detached from the adapter 10.
  • an XYZ orthogonal coordinate system as illustrated is set.
  • the Z-axis is parallel to the central axis 1a of the adapter assembly 1 (see FIG. 2C described below; the central axis 1a coincides with the central axes of the adapter 10, the cover 50, and the vial 80).
  • the direction parallel to the Z axis is called "vertical direction".
  • the side to which the Z-axis arrow points is called the "upper” side, and the opposite side is called the “lower” side.
  • the direction parallel to the plane (that is, the XY plane) orthogonal to the Z axis is called “horizontal direction”.
  • the direction along the straight line orthogonal to the central axis 1a is called “radial direction”, and the direction rotating around the central axis 1a is called “circumferential direction”.
  • FIG. 2A is a perspective view from above of the adapter 10.
  • FIG. 2B is a perspective view of the adapter 10 as viewed from below.
  • FIG. 2C is a cross-sectional view along a plane including the central axis 1 a of the adapter 10.
  • the adapter 10 is substantially the same as the adapter described in Patent Document 1.
  • the adapter 10 includes a puncture needle (male member) 11 extending along the central axis 1a.
  • the puncture needle 11 is provided with a sharp tip 11 a at its lower end.
  • a flow path 12 through which a liquid (for example, a drug solution) flows is formed along the central axis 1a.
  • the flow channel 12 communicates with an opening 13 provided on the outer peripheral surface near the tip 11 a of the puncture needle 11.
  • the opening 13 opens radially outward.
  • the tubular portion 14 surrounds a portion near the proximal end 11 b of the puncture needle 11.
  • the tubular portion 14 has a hollow cylindrical shape, and is coaxially disposed with the puncture needle 11 and radially spaced from the puncture needle 11.
  • the upper end of the tubular portion 14 is connected to the proximal end 11 b of the puncture needle 11.
  • each arm 20 includes a shoulder 21 extending substantially parallel to the X axis, and a suspension 22 extending downward from the distal end (the end farthest from the puncture needle 1) of the shoulder 21.
  • the suspension 22 faces the puncture needle 11.
  • the suspension portion 22 is inclined so as to approach the puncture needle 11 as it approaches its lower end.
  • a claw 30 is provided at the lower end of the suspension 22 so as to protrude toward the puncture needle 11.
  • the shoulder portion 21 and the suspension portion 22 constituting the arm 20, and the claw 30 are thin plates having a substantially constant dimension in the Y-axis direction.
  • Each pawl 30 includes two ribs 33 extending downwardly from its lower surface.
  • the rib 33 is a thin plate substantially parallel to the XZ plane.
  • the two ribs 33 provided on each of the claws 30 are separated in the Y-axis direction.
  • the rib 33 has an end edge 33a extending downward starting from the tip end of the claw 30 (the portion of the claw 30 closest to the puncture needle 11) 30a.
  • the edge 33a is configured by a smooth convex curve. Viewed as a whole, the edge 33a is inclined away from the puncture needle 11 downward from the tip 30a.
  • the vertical position of the lower end 30 b of the claw 30 is not limited, but is preferably the same as or slightly lower than the tip 11 a of the puncture needle 11. This is because the adapter 10 can be stably left on the horizontal surface in the upright state with the claw 30 down.
  • each rib 30 is provided with two ribs 33.
  • each claw 30 may be provided with one or more ribs 33.
  • the dimension of the rib 33 in the Y-axis direction is arbitrary.
  • the rib 33 may have a dimension in the Y-axis direction substantially the same as that of the claw 30.
  • the arm 20 has a cantilever support structure having a fixed end connected to the tubular portion 14.
  • the shoulder 21 constituting the arm 20 is a thin plate-like member, and can be elastically bent and deformed relatively easily.
  • the pawl 30 is provided at the free end of the arm 20. Therefore, the arm 20 can be elastically deformed in the direction in which the nail 30 is separated from the puncture needle 11. When the arm 20 deforms in this manner, the shoulder 21 bends so that the distal end of the shoulder 21 is displaced upward.
  • an arc-shaped hook portion 16 further protrudes radially outward.
  • the collar 16 is continuous with the shoulder 21 so as to form a substantially flat surface with the shoulder 21 of the arm 20.
  • the arm 20 and the hook portion 16 are integrated with the puncture needle 11 via the tubular portion 14, but the present invention is not limited thereto.
  • the tubular portion 14 may be omitted, and the shoulder 21 and the hook 16 of the arm 20 may be provided directly on the puncture needle 11.
  • a connector 40 is provided above the tubular portion 14. As shown in FIG. 2C, the connector 40 includes a cylindrical portion 41 having a substantially cylindrical shape, and a partition member (sometimes called "septum") 45 provided on the upper end of the cylindrical portion 41; And a cap 47 covered on the partition member 45.
  • the lumen 42 of the cylindrical portion 41 communicates with the flow passage 12 in the puncture needle 11.
  • the partition member 45 is a thin plate having a circular plan view shape. At the center of the partition member 45, a linear slit (cut) 45a penetrating the partition member 45 in the vertical direction is formed.
  • the partition member 45 can be easily deformed by an external force, and returns immediately to the state before deformation when the external force is removed.
  • the outer peripheral surface of the cylindrical portion 41 is a cylindrical surface.
  • the annular protrusion 41 b is continuous in the circumferential direction and slightly spaced downward from the engagement protrusion 41 a.
  • the cap 47 includes a top plate 48 having a disk shape, and a circumferential wall 49 having a cylindrical shape extending from the outer peripheral edge of the top plate 48.
  • a circular opening (through hole) 48 a is formed at the center of the top plate 48.
  • the surrounding wall 49 is formed with a pair of engagement holes 49a.
  • the engagement holes 49 a are through holes radially penetrating the surrounding wall 49.
  • the partition member 45 is held by the upper end of the cylindrical portion 41 and the top plate 48 of the cap 47 in the thickness direction (that is, in the vertical direction).
  • the cap 47 is engaged with the engaging protrusion 41 a by fitting the engaging protrusion 41 a protruding from the cylindrical portion 41 into the engaging hole 49 a of the cap 47.
  • the slit 45a of the partition member 45 is exposed in the opening 48a formed in the top plate 48 of the cap 47 (see FIG. 2A).
  • the annular protrusion 41 b formed in the cylindrical portion 41 is adjacent to the lower side of the peripheral wall 49 of the cap 47.
  • the top surface of the annular protrusion 41 b constitutes a cylindrical surface substantially the same as the outer peripheral surface of the peripheral wall 49.
  • the connector 40 provided with the partition member 45 in which the slit 45a is formed is generally called a needleless port.
  • the slit 45a is closed to form a fluid-tight seal.
  • the partition member 45 has a function of separating the inner cavity 42 of the cylindrical portion 41 from the outside.
  • a cylindrical male luer (not shown) having no sharp tip is inserted into the slit 45 a of the partition wall member 45, the partition wall member 45 is elastically deformed and the lumen 42 of the cylindrical portion 41 and the male luer communicate.
  • the partition member 45 When the male luer is pulled out of the partition member 45, the partition member 45 immediately returns to the initial state, and the slit 45a is closed in a fluid tight manner.
  • the partition member 45 functions as a self-closing valve body.
  • the portion of the adapter 10 excluding the partition wall member 45 and the cap 47 is preferably integrally manufactured as a whole by injection molding a resin material.
  • Resin materials that can be used include, but are not limited to, polyethylene, polypropylene, polycarbonate, styrene ethylene, polyethylene terephthalate, polybutylene terephthalate, butylene styrene block copolymer, etc. In consideration of elastic bending deformation of 20, polyolefin resins such as polyethylene and polypropylene are preferable.
  • the material of the cap 47 is not limited, but is preferably a hard material, and for example, resin materials such as polycarbonate, polypropylene, polyacetal, polyamide, hard polyvinyl chloride, polyethylene and the like can be used.
  • the material of the partition member 45 is not limited, but is preferably a soft material (so-called elastomer) having rubber elasticity (or flexibility), for example, a rubber material such as isoprene rubber, silicone rubber, butyl rubber, or the like A thermoplastic elastomer etc. can be used.
  • FIG. 3A is a perspective view of the cover 50 as viewed from below.
  • FIG. 3B is a cross-sectional perspective view of the cover 50 as viewed from below.
  • FIG. 3C is a plan view of the cover 50.
  • the cover 50 includes a connector case 51, an expansion plate 58, and a guide bar 59 (see FIG. 1).
  • the connector case 51 has a hollow, substantially cylindrical shape, with its upper end closed and its lower end released.
  • the connector 40 (see FIGS. 4C and 4D) is accommodated in the connector case 51 from below.
  • a pair of gripping surfaces 53 parallel to each other is provided on the outer peripheral surface of the peripheral wall 52 extending along the vertical direction of the connector case 51 (only one gripping surface 53 is visible in FIG. 3A).
  • the gripping surface 53 is substantially flat and parallel to the XZ plane.
  • the outer peripheral surface of the peripheral wall 52 excluding the gripping surface 53 is not limited, but in the present embodiment, it is a smooth convex curved surface (for example, a cylindrical surface) (see FIG. 3C).
  • the extension wall 55 protrudes downward from the extension plate 58.
  • the extension wall 55 extends the surrounding wall 52 downward beyond the extension plate 58.
  • the extending wall 55 is not annularly continuous in the circumferential direction, and is divided at two places. That is, the pair of extension walls 55 oppose each other in the Y-axis direction.
  • ribs (protrusions) 56 project from the inner peripheral surface of the connector case 51 (only two ribs 56 are shown in FIG. 3B).
  • the ribs 56 extend from the circumferential wall 52 to the extension wall 55 along the up-down direction (i.e., the Z-axis direction).
  • the four ribs 56 are arranged at equal angular intervals with respect to the central axis.
  • the diameter of the circle inscribed in the four ribs 56 (this circle is along the XY plane) is substantially the same as the outer diameter of the peripheral wall 49 of the cap 47 and the annular projection 41b (see FIG. 2A).
  • a protrusion 57 protrudes toward the central axis.
  • the number of ribs 56 is not limited to four, and may be three or five or more.
  • the projections 57 may be provided on all the ribs 56.
  • An extension plate 58 extends radially outward from the lower end of the peripheral wall 52 of the connector case 51.
  • the upper surface of the expansion plate 58 is substantially parallel to the horizontal plane (XY plane).
  • the expansion plate 58 is annularly continuous around the connector case 51.
  • the plan view shape of the outer peripheral edge of the expansion plate 58 is non-circular in which the dimension along the Y-axis direction is larger than the dimension along the X-axis direction.
  • the expansion plate 58 of the present embodiment is an athletic stadium that is composed of two straight lines 58a parallel to the Y-axis direction and two arcs 58b connecting both ends of the two straight lines. It has a shape similar to a track.
  • the expansion plate 58 has a shape in which a circle concentric with the central axis of the cover 50 is cut by two parallel straight lines 58a.
  • the radial extension length of the expansion plate 58 from the peripheral wall 52 of the connector case 51 is longer in the Y-axis direction than in the X-axis direction. Since the outer peripheral edge of the expansion plate 58 includes two parallel straight lines 58a, a large number of covers 50 can be arranged at high density in the horizontal and vertical directions on the horizontal plane with the connector case 51 facing up. . This facilitates handling of the cover 50, for example, when mass producing the cover 50.
  • the planar view shape of the expansion board 58 is not limited to this embodiment.
  • the extension plate 58 may have an arbitrary planar view shape such as, for example, an oval, an oval, a substantially rhombic, or a polygon (for example, a hexagon or an octagon).
  • the expansion plate 58 preferably has a major axis in the Y-axis direction.
  • the extension plate 58 may not be continuous in the circumferential direction.
  • two straight lines 58 a may be in contact with the surrounding wall 52. In this case, the extension length of the expansion plate 58 from the surrounding wall 52 along the X-axis direction is zero.
  • a plurality of (four in this embodiment) guide bars 59 extend downward from the outer peripheral edge (in particular, the arc 58b) of the expansion plate 58.
  • the guide bar 59 has a narrow thin-plate shape, and can be elastically bent and deformed so that its tip (or lower end) 59a approaches and separates from the central axis.
  • the undeformed initial guide bar 59 is disposed on a circle concentric with the cover 50.
  • the cover 50 is preferably integrally manufactured as a whole by injection molding a resin material.
  • Resin materials which can be used include, but are not limited to, polyethylene, polypropylene, polycarbonate, styrene ethylene, polyethylene terephthalate, polybutylene terephthalate, butylene styrene block copolymer and the like.
  • polyolefin resins such as polyethylene and polypropylene are preferable.
  • FIG. 4A is a perspective view of the adapter assembly 1 with the cover 50 attached to the adapter 10 as viewed from above.
  • FIG. 4B is a plan view of the adapter assembly 1.
  • FIG. 4C is a cross-sectional view of the adapter assembly 1 along the XZ plane including the central axis.
  • FIG. 4D is a cross-sectional view of the adapter assembly 1 along the YZ plane including the central axis.
  • the connector 40 of the adapter 10 is housed in the connector case 51 of the cover 50.
  • the lower end of the extension wall 55 of the cover 50 vertically abuts on the hook portion 16 (see FIG. 2A) of the adapter 10. Thereby, the insertion depth of the adapter 10 with respect to the connector case 51 is defined.
  • the rib 56 (see FIG. 3B) provided on the inner circumferential surface of the connector case 51 abuts on the circumferential wall 49 of the cap 47 and the annular projection 41b (see FIG. 2A). Thereby, the cover 50 is aligned coaxially with the adapter 10. Also, the projection 57 (see FIG. 3B) protruding from the rib 56 engages with the lower edge of the annular projection 41 b. This prevents the adapter 10 from falling out of the cover 50. In the process of attaching the cover 50 to the adapter 10, when the projection 57 passes over the annular projection 41b and engages with the annular projection 41b, the operator feels a click on the fingertip. The operator can recognize that the cover 50 is correctly attached to the adapter 10 by the click feeling.
  • the extension wall 55 and the projection 57 of the cover 50 vertically position the adapter 10 with respect to the cover 50.
  • the guide bar 59 faces the puncture needle 11 and extends further downward than the puncture needle 11. That is, the tip 59 a of the guide bar 59 is located below the tip 11 a of the puncture needle 11. Also preferably, the guide bar 59 extends further downward than the claws 30 (including the rib 33). That is, the tip end 59 a of the guide bar 59 is preferably located below the lower end 30 b of the claw 30.
  • the four guide bars 59 are arranged along a circle concentric with the puncture needle 11.
  • the cover 50 does not vertically abut on the arm 20 (particularly its shoulder 21). For this reason, the cover 50 attached to the adapter 10 does not inhibit the elastic deformation of the arm 20.
  • the expansion plate 58 of the cover 50 is at a higher position than the arm 20.
  • the arms 20 (especially their shoulders 21) project radially outward of the expansion plate 58.
  • the guide bar 59 extends further downward from the extension plate 58 beyond the arm 20.
  • the side edge 59 b (see FIG. 4A) extending along the vertical direction of the guide bar 59 is on the side edge defining the width of the arm 20 in the Y-axis direction. Limited by colliding.
  • the pair of arms 20 are opposed in the X-axis direction, whereas the pair of gripping surfaces 53 of the cover 50 are opposed in the Y-axis direction, and the major axis of the expansion plate 58 of the cover 50 is parallel to the Y-axis It is.
  • the cover 50 can be repeatedly attached to and detached from the adapter 10. When the cover 50 is separated from the adapter 10, a relatively large tensile force is applied to the adapter 10 and the cover 50 in the vertical direction to release the engagement between the annular projection 41b of the adapter 10 and the projection 57 of the cover 50. There is a need to.
  • FIG. 5 is a cross-sectional view of an example of a vial 80 to which the adapter assembly 1 is attached.
  • the vial 80 is a sealed container in which a stopper (rubber stopper) 87 is inserted into a port (opening) 82 facing upward of the bottle body 81 to seal the port 82 airtightly and liquid tight.
  • Powdered medicine (not shown) is contained in the vial 80.
  • an enlarged flange 83 is provided so as to surround the opening 82.
  • the outer peripheral surface of the flange 83 is a substantially cylindrical surface.
  • the bottle body 81 has a neck portion 84 having an outer diameter smaller than the flange 83 downward from the flange 83, a shoulder 85 having an outer diameter gradually increasing downward, and an outer diameter substantially constant in the vertical direction Certain cylindrical portions 86 are provided adjacent to each other in this order.
  • the plug 87 has an outer diameter substantially the same as that of the flange 83.
  • a cap 88 is attached to the plug 87 and the flange 83 in order to prevent the plug 87 from falling off the opening 82 of the bottle body 81.
  • the cap 88 is made of a sheet of metal (for example, aluminum) or resin, and is in close contact with the stopper 87 and the flange 83.
  • the lower end of the cap 88 extends below the outer peripheral surface which is a substantially cylindrical surface of the flange 83.
  • the upper end of the cap 88 extends to the upper surface of the plug 87.
  • the central region of the upper surface of the plug 87 is exposed to the outside through a circular opening 88 a provided in the cap 88 (see FIG. 6 described later).
  • the outer peripheral surface of the plug 87 and the outer peripheral surface of the flange 83 are cylindrical surfaces having substantially the same diameter. Accordingly, the outer peripheral surface 88 c of the cap 88 mounted on the plug 87 and the flange 83 is also a substantially cylindrical surface.
  • the upper end of the outer peripheral surface 88c of the cap 88 (or the outer peripheral edge of the upper surface of the cap 88) is referred to as an upper end edge 88b, and the lower end of the outer peripheral surface 88c is referred to as a lower end edge 88d.
  • the vial 80 may not have the cap 88.
  • the upper end edge 88 b, the lower end edge 88 d and the outer peripheral surface 88 c mean corresponding portions of the plug 87 or the flange 83.
  • the adapter assembly 1 is delivered to a medical institution such as a hospital with the cover 50 attached to the adapter 10 as shown in FIG. 4A.
  • the adapter assembly 1 is attached to the vial 80 as follows.
  • the vial 80 is erected with the stopper 87 up.
  • the tip end 11a of the puncture needle 11 is brought close to the upper surface of the plug 87 while maintaining the adapter assembly 1 such that the central axis (or the puncture needle 11) is parallel in the vertical direction.
  • the guide bar 59 of the cover 50 extends below the tip 11 a of the puncture needle 11 (the vial 80 side). Therefore, before the tip 11 a of the puncture needle 11 contacts the upper surface of the plug 87, a part of the cap 88 (or the plug 87) is stored in the area surrounded by the four guide bars 59. .
  • the four guide bars 59 are arranged along a circle concentric with the puncture needle 11.
  • the adapter assembly 1 is brought close to the vial 80 so that the cap 88 is housed inside the four guide bars 59, the tip 11a of the puncture needle 11 is easily aligned with the center of the stopper 87. be able to.
  • the diameter of the inscribed circle of the four guide bars 59 is set to be substantially the same as the outer diameter of the cap 88.
  • the tip end 11 a of the puncture needle 11 can be more accurately aligned with the center of the plug 87.
  • the diameter of the inscribed circle of the four guide bars 59 may be smaller than the outer diameter of the cap 88.
  • the tip end 59a of the guide bar 59 abuts on the portion of the convex curved surface where the outer diameter near the upper end edge 88b (see FIG. 5) of the cap 88 gradually changes, and the tip end 59a is displaced radially outward.
  • the guide bar 59 bends and deforms as appropriate.
  • the elastic recovery force of the four guide bars 59 aligns the tip 11 a of the puncture needle 11 with the center of the plug 87.
  • the adapter assembly 1 is adapted to a plurality of types of vials in which the outer diameter of the cap 88 is different.
  • the tip 11 a of the puncture needle 11 contacts the plug 87
  • the claws 30 in particular, the end 33 a of the rib 33
  • the claw 30 may contact the cap 88 before the tip 11a of the puncture needle 11 contacts the plug 87.
  • the claw 30 contacts the cap 88 by appropriately setting the length of the guide bar 59 so that the guide bar 59 extends below the claw 30 (including the rib 33).
  • the adapter assembly 1 With the puncture needle 11 aligned with the stopper 87 as shown in FIG. 6, the adapter assembly 1 is strongly pushed toward the vial 80. While the end 33 a of the claw 30 contacts the vicinity of the upper end 88 b of the cap 88, the claw 30 is displaced radially outward away from the puncture needle 11. When the claws 30 are displaced, the arms 20 elastically bend and deform. When the claws 30 pass through the cap 88, the arm 20 elastically recovers.
  • the adapter assembly 1 can be attached to the vial 80, as shown in FIG. Similar to the adapter of Patent Document 1, the claws 30 are fitted into the constricted portion 84 (see FIG. 5) of the vial 80 and the claws 30 engage with the flanges 83.
  • the puncture needle 11 passes through the plug 87, and the opening 13 (see FIG. 1A) is located below the plug 87.
  • the inside of the vial 80 is in communication with the connector 40 via the flow path 12 of the puncture needle 11.
  • the tip 59 a of the guide bar 59 reaches around the shoulder 85 of the bottle body 81.
  • the guide bar 59 may be appropriately elastically bent and deformed so that the tip end 59a of the guide bar 59 is displaced radially outward in accordance with the change in the outer diameter of the bottle main body 81 at the shoulder 85.
  • the cover 50 is removed from the adapter 10.
  • the adapter 10 remains attached to the vial 80.
  • a male connector for example, a male luer
  • the drug in the vial 80 can be used to prepare a drug solution.
  • the guide bar 59 reduces the visibility of the tip 11 a of the puncture needle 11 via the bottle body 81 and the visibility of the drug or liquid in the vial 80. Removing the cover 50 from the adapter 10 improves their visibility.
  • the cover 50 is attached to the adapter 10 again.
  • the used vial 80 is discarded with the adapter assembly 1 attached (see FIG. 7).
  • the adapter assembly 1 of the present embodiment includes the guide bar 59 extending downward (the vial 80 side) than the puncture needle 11, the tip 11a of the puncture needle 11 is at the center of the plug 87. It can be easily aligned.
  • the adapter 10 is attached to the vial 80 without using the cover 50. In this case, it is necessary to visually align the tip 11 a of the puncture needle 11 with the center of the plug 87. In this case, the positional displacement amount of the puncture needle 11 with respect to the plug 87 is likely to be large compared to the present embodiment. If the adapter 10 is pushed toward the vial 80 with the tip 11 a of the puncture needle 11 displaced from the center of the stopper 87, the claw 30 can not be engaged with the flange 83 of the vial 80. In contrast, the puncture needle 11 may be punctured obliquely.
  • the nail 30 may contact the cap 88 before the puncture needle 11 contacts the plug 87.
  • the adapter 10 is pushed toward the vial 80 with the tip 11a of the puncture needle 11 displaced from the center of the plug 87, the claw 30 slides on the cap 88 in the horizontal direction. For this reason, the vial 80 may tip over.
  • the tip 11a of the puncture needle 11 may be caught on the edge of the opening 88a of the cap 88 while the nail 30 slides on the cap 88, and the puncture needle 11 may be bent due to the radial force applied to the tip 11a. is there. In the present embodiment, the possibility of the occurrence of such a problem is reduced.
  • the adapter assembly for the vial 80 is confirmed by confirming the vertical position of the tip 59a of each guide bar 59 with respect to the cap 88 in the state of FIG. 6 before puncturing the puncture needle 11 into the plug 87. It is easy to check the slope of 1 and correct it. For this reason, the puncture needle 11 can be punctured perpendicularly to the plug 87. Even if the tip 11a of the puncture needle 11 punctures the center of the plug 87, if the puncture needle 11 punctures the plug 87 at an angle, for example, the claw 30 can not be engaged with the flange 83 of the vial 80. It can happen. In the present embodiment, such a situation is unlikely to occur.
  • the plurality of guide bars 59 are circumferentially spaced. For this reason, as shown in FIG. 6, the position of the tip 11a of the puncture needle 11 relative to the plug 87 can be visually checked through the space between the adjacent guide bars 59.
  • the plurality of guide bars 59 are arranged along a circle concentric with the puncture needle 11.
  • the guide bar 59 arranged in this manner is advantageous for improving the accuracy of the alignment of the tip 11 a of the puncture needle 11 with the center of the plug 87.
  • the guide bar 59 can be elastically bent and deformed so that its tip 59 a is separated from the puncture needle 11. Therefore, the adapter assembly 1 can be adapted to a plurality of types of vials having different outer diameters of the cap 88. Also, even if the tip 59a of the guide bar 59 collides with the shoulder 85 of the vial 80 in the process of attaching the adapter assembly 1 to the vial 80, the guide bar 59 is appropriately bent and deformed. It can be punctured to the desired depth.
  • the guide bar 59 is provided as a "guide mechanism" for aligning the tip 11a of the puncture needle 11 with the center of the plug 87, but the configuration of the guide mechanism of the present invention is not limited thereto.
  • the shape of the guide mechanism is not limited to this embodiment, and may be changed as appropriate.
  • the guide mechanism does not have to extend linearly in parallel with the puncture needle 11 like the guide bar 59 in a natural state where no external force is applied.
  • the puncture needle approaches the tip (tip 59a) It may be curved away from 11.
  • the guide mechanism may have a substantially "T" shape in which the tip end 59a of the guide bar 59 is circumferentially extended.
  • the guide mechanism may have a substantially "U" shape in which the tips 59a of two guide bars 59 adjacent in the circumferential direction are connected.
  • the cross-sectional shape of the guide mechanism along the horizontal plane is also not limited, and may be, for example, a circle, an ellipse, or an arc concentric with the puncture needle 11.
  • the guide mechanism may be substantially incapable of radial elastic bending.
  • the number and arrangement of the guide mechanisms are not limited to the present embodiment, and may be changed as appropriate.
  • the number of guide mechanisms may be one, but is preferably two or more.
  • the plurality of guide mechanisms can be arranged at equal angular intervals about the puncture needle 11.
  • the pair of guide mechanisms may be spaced apart from each other around the puncture needle 11 in a state where the two guide mechanisms forming the pair face each other with the puncture needle 11 interposed therebetween.
  • the cover 50 includes a connector case 51 capable of housing the connector 40 of the adapter 10.
  • the connector case 51 covers the top plate 48 of the connector 40 and the partition wall member 45 exposed through the opening 48 a.
  • the finger of the person does not touch the connector 40. Therefore, the sanitary condition of the connector 40 can be maintained well.
  • the cover 50 is attached again to the adapter 10 attached to the vial 80 and the vial 80 is discarded, the possibility of exposure to dangerous chemicals can be reduced.
  • the connector case 51 is disposed on the top of the cover 50. Therefore, when holding the cover 50, the worker is likely to pick the connector case 51 with a finger. For example, in the state of FIG. 6, the operator can push the adapter assembly 1 toward the vial 80 by pinching the connector case 51.
  • the worker is likely to apply a downward force to the connector case 51 instead of the arm 20 (particularly the shoulder portion 21). Therefore, the above problems are unlikely to occur.
  • the peripheral wall 52 of the connector case 51 is provided with a pair of gripping surfaces 53 parallel to each other. Therefore, in the state of FIG. 6, the operator can hold the adapter assembly 1 most stably when holding the gripping surface 53 with two fingers. In other words, the worker is always instructed to pick the gripping surface 53. For example, the worker can grasp the gripping surface 53 with the thumb and forefinger (or middle finger) of the right hand. In this state, the operator pushes the adapter assembly 1 toward the vial 80. The operator can attach the adapter assembly 1 to the vial 80 without touching the adapter 10. Therefore, the possibility of the worker touching the arm 20 (especially the shoulder 21) is further reduced.
  • the expansion plate 58 protrudes radially outward from the lower end of the peripheral wall 52 of the connector case 51.
  • the connector case 51 particularly its gripping surface 53
  • the finger can be applied to the upper surface of the expansion plate 58.
  • the spreader plate 58 facilitates applying a downward force to the adapter assembly 1 when attaching the adapter assembly 1 to the vial 80.
  • the extension plate 58 prevents the operator's finger from extending downward from the extension plate 58, the possibility of the finger touching the arm 20 and erroneously applying a downward force to the arm 20 is reduced.
  • the extension plate 58 has a major axis in the direction (Y-axis direction) in which the pair of gripping surfaces 53 face each other.
  • the projecting length of the expansion plate 58 projecting radially outward from the gripping surface 53 is generally larger than the projecting length of the expanding plate 58 projecting radially outward from the peripheral wall 52 other than the gripping surface 53. This is because when the gripping surface 53 is pinched with a finger and a downward force is applied, a finger can be applied to the portion of the expansion plate 58 having a relatively large projecting length, so that the adapter assembly 1 is given a downward force. Makes it easier to add.
  • the extension plate 58 is at a higher position than the arm 20. Since the finger gripping the connector case 51 and the other fingers hit the extension plate 58, the possibility that these fingers touch the arm 20 located lower than the extension plate 58 is low. Therefore, the expansion plate 58 is advantageous for reducing the possibility that the operator's finger touches the arm 20 and erroneously applies a downward force to the arm 20 when attaching the adapter assembly 1 to the vial 80. It is.
  • the direction (Y-axis direction) in which the pair of gripping surfaces 53 face is orthogonal to the direction (X-axis direction) in which the pair of arms 20 face.
  • the middle finger is usually disposed in the vicinity of the forefinger, that is, near the gripping surface 53. Because there is no arm 20 below the middle finger, even if the middle finger extends below the expansion plate 58, there is a possibility that the middle finger will touch the arm 20 and inadvertently apply a downward force to the arm 20. Low.
  • the middle finger when the direction in which the pair of gripping surfaces 53 opposes matches the direction in which the pair of arms 20 opposes, if the middle finger extends below the extension plate 58, It can happen that the middle finger accidentally applies a downward force to the arm 20 (especially its shoulder 21). In this case, the above problem may occur.
  • the direction in which the gripping surface 53 faces is perpendicular to the extending direction of the arm 20, a finger other than the finger holding the gripping surface 53 touches the arm 20 to contact the arm 20. It is unlikely to accidentally apply a downward force.
  • the planar view shape of the expansion board 58 is not limited to this embodiment, It is arbitrary.
  • the expansion plate 58 may be circular, concentric with the cover 50, or non-circular having a major axis in the X-axis direction.
  • the expansion plate 58 does not have to be parallel to the XY plane, and may be inclined, for example, to descend toward its outer peripheral edge.
  • the expansion plate 58 may be omitted.
  • a guide bar 59 may extend downward from the lower end of the peripheral wall 52 of the connector case 51.
  • the gripping surface 53 need not be planar in the strict sense.
  • the gripping surface 53 may be provided with a plurality of protrusions or a plurality of ribs (linear protrusions) in order to improve the gripping property and non-slip property, or the entire gripping surface 53 is a smooth concave surface May be composed of
  • the peripheral wall 52 of the connector case 51 may not be configured to always hold only a specific surface by the operator.
  • the pair of gripping surfaces 53 may be omitted, and the outer peripheral surface of the peripheral wall 52 may have any shape such as a cylindrical surface or a polygonal cylindrical surface (for example, a hexagonal cylindrical surface or an octagonal cylindrical surface).
  • the worker can grip the peripheral wall 52 of the connector case 51 with two fingers in any direction.
  • the rib 56 provided on the inner peripheral surface of the connector case 51 functions as a “axis alignment structure” for making the cover 50 coaxial with the adapter 10.
  • the coaxial arrangement of the case 50 with the adapter 10 is advantageous for improving the accuracy of the alignment of the tip 11 a of the puncture needle 11 with the center of the plug 87.
  • the axial alignment structure is constituted by four ribs 56, but the axial alignment structure of the present invention is not limited to this.
  • the inner peripheral surface of the peripheral wall 52 of the connector case 51 which is configured to omit the rib 56 and has an inner diameter substantially the same as the outer diameter of the peripheral wall 49 of the cap 47 and / or the annular protrusion 41b It may be used as
  • the projections 57 protruding from the ribs 56 function as an "engagement structure" for engaging the adapter 10.
  • the engagement structure prevents the adapter 10 from falling off the cover 50 when the cover 50 (in particular, its connector case 51) is picked up and lifted from the adapter assembly 1 in which the cover 50 is attached to the adapter 10.
  • the mounting operation of the adapter assembly 1 to the vial 80 can be easily performed.
  • the engagement structure is constituted by the projection 57 provided on the rib 56, but the engagement structure of the present invention is not limited to this.
  • the protrusion engaged with the adapter 10 may be provided on the inner peripheral surface of the peripheral wall 52 other than the rib 56 of the connector case 51.
  • a protrusion engaging the adapter 10 may be annularly continuous with the inner circumferential surface of the circumferential wall 52.
  • the protrusions may be configured to engage with the adapter 10 at locations other than the annular protrusion 41 b.
  • the engagement structure need not be a protrusion but may be a recess (including a groove).
  • the engagement structure may be provided at a location of the cover 50 other than the connector case 51.
  • the cover 50 may be provided with a recess or protrusion that engages with a protrusion 17 (see FIG. 2A) radially projecting from the adapter 10.
  • the present invention can be widely used as an adapter assembly attached to a vial. Above all, it can be preferably used in the medical field.
  • the type of drug in the vial is not limited, but is suitable when it is a potent drug such as an anticancer drug.

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Abstract

An adaptor assembly (1) is provided with: an adaptor (10) capable of being mounted to vial (80); and a cover (50) separably mounted to the adaptor from above. The adaptor is provided with: a puncture needle (11) capable of puncturing the plug body (87) of the vial; a plurality of latches (30) capable of engaging with the increased diameter flange (83) of the vial; and a plurality of arms (20) which have the plurality of latches provided thereto and which are elastically bendable and deformable. The cover is provided with a guide mechanism (59) extending so as to face the puncture needle. The guide mechanism extends further downward than the puncture needle while the cover is mounted to the adaptor.

Description

アダプタ組立体Adapter assembly
 本発明は、バイアルに装着可能なアダプタと、アダプタに分離可能に装着されたカバーとを備えたアダプタ組立体に関する。 The present invention relates to an adapter assembly comprising a vial mountable adapter and a cover separably mounted on the adapter.
 粉末状の薬剤を封入したバイアルが広く流通している。薬剤を患者に投与する場合、バイアル内に溶解液を注入し、薬剤を溶解液で溶解して薬液を得、当該薬液をバイアルから取り出す。バイアルに対する溶解液の注入や薬液の取り出しは、バイアルの口(開口)を封止する栓体(ゴム栓)に穿刺した穿刺針(「瓶針」と呼ばれることもある)を介して行われる。 A vial containing a powdered drug is widely distributed. When a drug is administered to a patient, a solution is injected into the vial, the drug is dissolved in the solution to obtain a drug solution, and the drug solution is removed from the vial. The injection of the solution into the vial and the removal of the drug solution are performed via a puncture needle (sometimes called a "bottle needle") pierced in a stopper (rubber stopper) that seals the opening (opening) of the vial.
 薬剤が、例えば抗がん剤のような危険な薬剤である場合、このような薬剤やその薬液が外界に漏れ出るのを防止する必要がある。そこで、バイアルの栓体に穿刺した穿刺針が栓体から意図せずに抜け出ることがないように、バイアルの口を取り囲む拡径したフランジに係合する爪が穿刺針とともに一体的に設けられたアダプタが用いられることが多い。 When the drug is a dangerous drug such as an anticancer drug, for example, it is necessary to prevent such drug and its drug solution from leaking out to the outside. Therefore, in order to prevent the puncture needle punctured in the stopper of the vial from coming out of the stopper unintentionally, the claw engaging with the enlarged flange surrounding the mouth of the vial is integrally provided with the puncture needle Adapters are often used.
 このようなアダプタの一例が、特許文献1に記載されている。特許文献1のアダプタは、穿刺針と、バイアルのフランジに係合可能な爪とを備える。爪は弾性的に曲げ変形可能なアームに設けられている。穿刺針の先端をバイアルの栓体に対向させた状態で、アダプタをバイアルに向かって押し込む。穿刺針はバイアルの栓体を穿刺する。爪は、栓体(またはこれを覆うアルミニウムキャップ)に当接することによって穿刺針から離間する向き(即ち半径方向外向き)に変位し、アームは弾性的に曲げ変形する。その後、爪がフランジを通過すると、アームが弾性回復し、爪はバイアルのフランジに係合する。 An example of such an adapter is described in US Pat. The adapter of Patent Document 1 includes a puncture needle and a claw that can be engaged with a flange of a vial. The claws are provided on an elastically bendable arm. With the tip of the puncture needle facing the stopper of the vial, the adapter is pushed toward the vial. The puncture needle punctures the stopper of the vial. The claw is displaced in a direction away from the puncture needle (i.e., radially outward) by abutting on the stopper (or the aluminum cap covering it), and the arm elastically bends and deforms. Thereafter, as the pawl passes the flange, the arm resiliently recovers and the pawl engages the flange of the vial.
国際公開第2016/152801号(図9A~図11B)WO 2016/152801 (FIGS. 9A to 11B)
 アダプタをバイアルに装着する際には、穿刺針が栓体の中心を穿刺するように、目視にて穿刺針の先端を栓体の中心に位置合わせした後、アダプタをバイアルに向かって押し込む。しかしながら、実際には、穿刺針の先端が栓体の中心から外れてしまうことがある。穿刺針が栓体の中心から外れた位置を穿刺すると、アダプタの爪をバイアルのフランジに係合させることが困難になるなど、アダプタをバイアルに適切に装着することができない。 When attaching the adapter to the vial, after visually aligning the tip of the puncture needle with the center of the stopper so that the puncture needle punctures the center of the stopper, the adapter is pushed toward the vial. However, in practice, the tip of the puncture needle may be off center of the plug. When the puncture needle punctures the off center of the stopper, the adapter can not be properly attached to the vial, such as it becomes difficult to engage the hook of the adapter with the flange of the vial.
 本発明の目的は、アダプタの穿刺針の先端をバイアルの栓体の中心に位置合わせすることにある。 An object of the present invention is to align the tip of the puncture needle of the adapter with the center of the stopper of the vial.
 本発明のアダプタ組立体は、バイアルに装着可能なアダプタと、前記アダプタに上方から分離可能に装着されたカバーとを備える。前記アダプタは、前記バイアルの栓体を穿刺可能な穿刺針と、前記バイアルの拡径したフランジに係合可能な複数の爪と、前記複数の爪が設けられた弾性的に曲げ変形可能な複数のアームとを備える。前記カバーは、前記穿刺針に対向するように延びたガイド機構を備える。前記カバーが前記アダプタに装着された状態において、前記ガイド機構は、前記穿刺針よりも更に下方に向かって延びている。 The adapter assembly of the present invention comprises an adapter mountable to a vial, and a cover removably mounted on the adapter from above. The adapter is provided with a puncture needle capable of piercing the stopper of the vial, a plurality of claws engageable with the enlarged flange of the vial, and a plurality of elastically bendable plurality provided with the plurality of claws. And the arm of the The cover includes a guide mechanism extending to face the puncture needle. When the cover is attached to the adapter, the guide mechanism extends further downward than the puncture needle.
 本発明によれば、カバーがアダプタに装着された状態において、カバーに設けられたガイド機構が、穿刺針よりも更に下方に向かって延びる。このため、ガイド機構を利用して、穿刺針の先端を栓体の中心に容易に位置合わせすることができる。 According to the present invention, in the state where the cover is attached to the adapter, the guide mechanism provided on the cover extends further downward than the puncture needle. Therefore, the tip of the puncture needle can be easily aligned with the center of the plug using the guide mechanism.
図1は、本発明の一実施形態にかかるアダプタ組立体及びバイアルの分解斜視図である。FIG. 1 is an exploded perspective view of an adapter assembly and a vial according to one embodiment of the present invention. 図2Aは、本発明の一実施形態にかかるアダプタの上方から見た斜視図である。FIG. 2A is a top perspective view of an adapter according to an embodiment of the present invention. 図2Bは、本発明の一実施形態にかかるアダプタの下方から見た斜視図である。FIG. 2B is a perspective view from below of the adapter according to an embodiment of the present invention. 図2Cは、本発明の一実施形態にかかるアダプタの中心軸を含む面に沿った断面図である。FIG. 2C is a cross-sectional view along a plane including the central axis of the adapter according to one embodiment of the present invention. 図3Aは、本発明の一実施形態にかかるカバーの下方から見た斜視図である。FIG. 3A is a bottom perspective view of a cover according to an embodiment of the present invention. 図3Bは、本発明の一実施形態にかかるカバーの下方から見た断面斜視図である。FIG. 3B is a cross-sectional perspective view from below of the cover according to an embodiment of the present invention. 図3Cは、本発明の一実施形態にかかるカバーの平面図である。FIG. 3C is a plan view of a cover according to an embodiment of the present invention. 図4Aは、本発明の一実施形態にかかるアダプタ組立体の上方から見た斜視図である。FIG. 4A is a top perspective view of an adapter assembly according to one embodiment of the present invention. 図4Bは、本発明の一実施形態にかかるアダプタ組立体の平面図である。FIG. 4B is a plan view of an adapter assembly in accordance with one embodiment of the present invention. 図4Cは、本発明の一実施形態にかかるアダプタ組立体の、中心軸を含む面に沿った断面図である。FIG. 4C is a cross-sectional view of the adapter assembly according to an embodiment of the present invention along a plane including the central axis. 図4Dは、本発明の一実施形態にかかるアダプタ組立体の、中心軸を含む別の面に沿った断面図である。FIG. 4D is a cross-sectional view of an adapter assembly according to an embodiment of the present invention taken along another plane including the central axis. 図5は、本発明の一実施形態にかかるアダプタ組立体が装着されるバイアルの断面図である。FIG. 5 is a cross-sectional view of a vial to which an adapter assembly according to an embodiment of the present invention is attached. 図6は、本発明の一実施形態にかかるアダプタ組立体の穿刺針がバイアルの栓体を穿刺する直前の状態を示した斜視図である。FIG. 6 is a perspective view showing a state immediately before the puncture needle of the adapter assembly according to an embodiment of the present invention punctures the stopper of the vial. 図7は、本発明の一実施形態にかかるアダプタ組立体をバイアルに装着した状態を示した斜視図である。FIG. 7 is a perspective view showing the adapter assembly according to an embodiment of the present invention attached to a vial.
 上記の本発明のアダプタ組立体において、前記カバーは複数の前記ガイド機構を備えてもよい。前記複数のガイド機構は、前記穿刺針と同心の円に沿って配置されていてもよい。かかる態様によれば、栓体の中心に対する穿刺針の先端の位置合わせの精度を向上させることができる。 In the above-mentioned adapter assembly of the present invention, the cover may include a plurality of the guide mechanisms. The plurality of guide mechanisms may be disposed along a circle concentric with the puncture needle. According to this aspect, it is possible to improve the accuracy of the alignment of the tip of the puncture needle with respect to the center of the plug.
 前記ガイド機構は、その先端が前記穿刺針から離れるように弾性的に変形可能であってもよい。かかる態様によれば、アダプタ組立体を、栓体(またはフランジ)の外径が異なる複数種類のバイアルに適応させることができる。また、アダプタ組立体をバイアルに装着する過程でガイド機構がバイアルの肩部に衝突する場合にも、穿刺針を栓体に所望する深さまで穿刺することができる。 The guide mechanism may be elastically deformable such that its tip is separated from the puncture needle. According to this aspect, the adapter assembly can be adapted to a plurality of types of vials in which the outer diameter of the stopper (or flange) is different. Also, even if the guide mechanism collides with the shoulder of the vial in the process of attaching the adapter assembly to the vial, the puncture needle can be pierced to the desired depth to the stopper.
 前記アダプタは、前記穿刺針に連通したコネクタを備えてもよい。前記カバーは前記コネクタを収納するコネクタケースを備えてもよい。かかる態様によれば、コネクタの衛生状態を良好に維持することができる。また、使用済みのアダプタにカバーを装着することにより、薬剤被曝の可能性を低減することができる。 The adapter may include a connector in communication with the puncture needle. The cover may include a connector case for housing the connector. According to this aspect, the sanitary condition of the connector can be well maintained. Also, by attaching a cover to a used adapter, the potential for drug exposure can be reduced.
 前記コネクタケースは、前記カバーの上部に配置されていてもよい。かかる態様によれば、作業者は、カバーを保持する際、コネクタケースを指で摘まむ可能性が高い。これは、アダプタ組立体をバイアルに装着する際に、作業者がアームに下向きの力を加えてしまうことによってバイアルに対するアダプタ組立体の装着が困難になったり、アームが破損(破断)したりするという事態が起こる可能性を低減する。 The connector case may be disposed on the top of the cover. According to this aspect, when holding the cover, the worker is likely to pick the connector case with his / her finger. This causes the operator to apply a downward force to the arm when attaching the adapter assembly to the vial, which makes it difficult to attach the adapter assembly to the vial or causes the arm to break (break). Reduce the possibility of the situation happening.
 前記コネクタケースの周囲壁に互いに平行な一対の把持面が設けられていてもよい。かかる態様によれば、作業者は、アダプタ組立体を保持する際、常に把持面を摘まむように仕向けられる。これは、アダプタ組立体をバイアルに装着する際に、作業者がアームに下向きの力を加えてしまう可能性が更に低減される。 The peripheral wall of the connector case may be provided with a pair of gripping surfaces parallel to each other. According to this aspect, when holding the adapter assembly, the worker is always directed to pinch the gripping surface. This further reduces the possibility of the operator applying a downward force on the arm when attaching the adapter assembly to the vial.
 前記コネクタケースの前記周囲壁の下端から、半径方向の外向きに拡張板が突出していてもよい。かかる態様によれば、アダプタ組立体をバイアルに装着する際に、作業者は下向きの力を拡張板に加えることができる。また、拡張板は、アダプタ組立体をバイアルに装着する際に、作業者の指がアームに触れてアームに下向きの力を誤って加えてしまうのを防止する。 An extension plate may project radially outward from the lower end of the peripheral wall of the connector case. According to this aspect, when attaching the adapter assembly to the vial, the operator can apply a downward force to the expansion plate. The expansion plate also prevents an operator's finger from touching the arm and inadvertently applying a downward force to the arm when attaching the adapter assembly to the vial.
 前記拡張板は、前記一対の把持面が対向する方向に長軸を有していてもよい。かかる態様は、把持面を指で摘まんでアダプタ組立体に下向き力を加えるのを更に容易にする。 The extension plate may have a major axis in a direction in which the pair of gripping surfaces face each other. Such an aspect further facilitates gripping the gripping surface with a finger to apply a downward force to the adapter assembly.
 前記拡張板は、前記複数のアームよりも高い位置にあってもよい。かかる態様は、アダプタ組立体をバイアルに装着する際に、作業者の指がアームに触れてアームに下向きの力を誤って加えてしまう可能性を低減するのに有利である。 The extension plate may be located higher than the plurality of arms. Such an aspect is advantageous for reducing the possibility of the operator's finger touching the arm and inadvertently applying a downward force to the arm when attaching the adapter assembly to the vial.
 前記複数のアームは、前記穿刺針の長手方向に直交する第1方向に対向するように配置されていてもよい。この場合、前記一対の把持面は、前記第1方向に直交し且つ前記穿刺針の長手方向に直交する第2方向に対向するように配置されていてもよい。かかる態様は、アダプタ組立体をバイアルに装着する際に、把持面を摘まんだ指以外の指がアームに触れてアームに下向きの力を誤って加えてしまう可能性を低減するのに有利である。 The plurality of arms may be disposed to face in a first direction orthogonal to the longitudinal direction of the puncture needle. In this case, the pair of gripping surfaces may be arranged to face in a second direction orthogonal to the first direction and perpendicular to the longitudinal direction of the puncture needle. Such an aspect is advantageous for reducing the possibility that a finger other than the pinched finger may touch the arm and inadvertently apply a downward force to the arm when attaching the adapter assembly to the vial. is there.
 前記カバーを前記アダプタと同軸に軸合わせする軸合わせ構造が、前記カバーに設けられていてもよい。かかる態様によれば、栓体の中心に対する穿刺針の先端の位置合わせの精度を向上させることができる。 An alignment structure may be provided on the cover to axially align the cover coaxially with the adapter. According to this aspect, it is possible to improve the accuracy of the alignment of the tip of the puncture needle with respect to the center of the plug.
 前記カバーから前記アダプタが抜け落ちないように前記アダプタに係合する係合構造が、前記カバーに設けられていてもよい。かかる態様によれば、アダプタ組立体のバイアルへの装着作業を容易に行うことができる。 An engagement structure may be provided on the cover to engage the adapter so as to prevent the adapter from falling off the cover. According to this aspect, the mounting operation of the adapter assembly to the vial can be easily performed.
 以下に、本発明を好適な実施形態を示しながら詳細に説明する。但し、本発明は以下の実施形態に限定されないことはいうまでもない。以下の説明において参照する各図は、説明の便宜上、本発明の実施形態を構成する主要部材を簡略化して示したものである。従って、本発明の範囲内において、図面に示されていない任意の部材を追加したり、あるいは、図面に示された任意の部材を変更もしくは省略したりしてもよい。 Hereinafter, the present invention will be described in detail with reference to preferred embodiments. However, it goes without saying that the present invention is not limited to the following embodiments. Each drawing referred to in the following description is a simplified view of main members constituting an embodiment of the present invention for convenience of explanation. Therefore, within the scope of the present invention, any member not shown in the drawings may be added, or any member shown in the drawings may be changed or omitted.
 図1は、本発明の一実施形態にかかるアダプタ組立体1及びバイアル80の分解斜視図である。アダプタ組立体1は、バイアル80に装着されるアダプタ10と、アダプタ10に対して繰り返し着脱可能なカバー50とを備える。以下の説明の便宜のため、図示したようなXYZ直交座標系を設定する。Z軸は、アダプタ組立体1の中心軸1a(後述する図2Cを参照。中心軸1aは、アダプタ10、カバー50、及びバイアル80の各中心軸と一致する)と平行である。Z軸に平行な方向を「上下方向」という。Z軸の矢印が向いた側を「上」側、その反対側を「下」側という。Z軸に直交する平面(即ち、XY面)に平行な方向を「水平方向」という。中心軸1aに直交する直線に沿った方向を「半径方向」といい、中心軸1aの周りを回転する方向を「周方向」という。 FIG. 1 is an exploded perspective view of an adapter assembly 1 and a vial 80 according to an embodiment of the present invention. The adapter assembly 1 includes an adapter 10 attached to a vial 80 and a cover 50 that can be repeatedly attached to and detached from the adapter 10. For convenience of the following description, an XYZ orthogonal coordinate system as illustrated is set. The Z-axis is parallel to the central axis 1a of the adapter assembly 1 (see FIG. 2C described below; the central axis 1a coincides with the central axes of the adapter 10, the cover 50, and the vial 80). The direction parallel to the Z axis is called "vertical direction". The side to which the Z-axis arrow points is called the "upper" side, and the opposite side is called the "lower" side. The direction parallel to the plane (that is, the XY plane) orthogonal to the Z axis is called "horizontal direction". The direction along the straight line orthogonal to the central axis 1a is called "radial direction", and the direction rotating around the central axis 1a is called "circumferential direction".
 1.アダプタ
 図2Aは、アダプタ10の上方から見た斜視図である。図2Bは、アダプタ10の下方から見た斜視図である。図2Cは、アダプタ10の中心軸1aを含む面に沿った断面図である。アダプタ10は、特許文献1に記載されたアダプタと概略同じである。
1. Adapter FIG. 2A is a perspective view from above of the adapter 10. FIG. 2B is a perspective view of the adapter 10 as viewed from below. FIG. 2C is a cross-sectional view along a plane including the central axis 1 a of the adapter 10. The adapter 10 is substantially the same as the adapter described in Patent Document 1.
 図2Cに示されているように、アダプタ10は、中心軸1aに沿って延びた穿刺針(オス部材)11を備える。穿刺針11は、その下端に鋭利な先端11aを備える。穿刺針11の内部には、液体(例えば薬液)が流れる流路12が中心軸1aに沿って形成されている。流路12は、穿刺針11の先端11a近傍の外周面に設けられた開口13に連通している。開口13は、半径方向外向きに開口している。 As shown in FIG. 2C, the adapter 10 includes a puncture needle (male member) 11 extending along the central axis 1a. The puncture needle 11 is provided with a sharp tip 11 a at its lower end. Inside the puncture needle 11, a flow path 12 through which a liquid (for example, a drug solution) flows is formed along the central axis 1a. The flow channel 12 communicates with an opening 13 provided on the outer peripheral surface near the tip 11 a of the puncture needle 11. The opening 13 opens radially outward.
 穿刺針11の基端11bの近傍の部分を管状部14が取り囲んでいる。管状部14は、中空の円筒形状を有し、穿刺針11と同軸に配置され、穿刺針11から半径方向に離間している。管状部14の上端は、穿刺針11の基端11bに接続されている。 The tubular portion 14 surrounds a portion near the proximal end 11 b of the puncture needle 11. The tubular portion 14 has a hollow cylindrical shape, and is coaxially disposed with the puncture needle 11 and radially spaced from the puncture needle 11. The upper end of the tubular portion 14 is connected to the proximal end 11 b of the puncture needle 11.
 図2Aに示されているように、管状部14の下端に、一対のアーム20が設けられている。一対のアーム20は、X軸方向に対向している。各アーム20は、X軸にほぼ平行に延びた肩部21と、肩部21の遠位端(穿刺針1から最も遠い端部)から下方に向かって延びた懸架部22とを備える。懸架部22は穿刺針11に対向している。懸架部22は、その下端に近づくにしたがって穿刺針11に近づくように傾斜している。 As shown in FIG. 2A, at the lower end of the tubular portion 14, a pair of arms 20 is provided. The pair of arms 20 are opposed in the X-axis direction. Each arm 20 includes a shoulder 21 extending substantially parallel to the X axis, and a suspension 22 extending downward from the distal end (the end farthest from the puncture needle 1) of the shoulder 21. The suspension 22 faces the puncture needle 11. The suspension portion 22 is inclined so as to approach the puncture needle 11 as it approaches its lower end.
 爪30が、穿刺針11に向かって突出するように、懸架部22の下端に設けられている。アーム20を構成する肩部21及び懸架部22と、爪30とは、Y軸方向の寸法が略一定の細い板状物である。各爪30は、その下面から下方に向かって延びる2枚のリブ33を含む。リブ33は、XZ面に略平行な薄板状物である。各爪30に設けられた2枚のリブ33は、Y軸方向に離間している。リブ33は、爪30の先端(爪30のうち穿刺針11に最も接近した部分)30aを始点として、下方に向かって延びた端縁33aを有する。端縁33aは、滑らかな凸曲線で構成されている。全体として見れば、端縁33aは、先端30aから、下方に向かって穿刺針11から離間するように傾斜している。 A claw 30 is provided at the lower end of the suspension 22 so as to protrude toward the puncture needle 11. The shoulder portion 21 and the suspension portion 22 constituting the arm 20, and the claw 30 are thin plates having a substantially constant dimension in the Y-axis direction. Each pawl 30 includes two ribs 33 extending downwardly from its lower surface. The rib 33 is a thin plate substantially parallel to the XZ plane. The two ribs 33 provided on each of the claws 30 are separated in the Y-axis direction. The rib 33 has an end edge 33a extending downward starting from the tip end of the claw 30 (the portion of the claw 30 closest to the puncture needle 11) 30a. The edge 33a is configured by a smooth convex curve. Viewed as a whole, the edge 33a is inclined away from the puncture needle 11 downward from the tip 30a.
 爪30(またはリブ33)の下端30bの上下方向位置は、限定されないが、穿刺針11の先端11aと同じか、これよりわずかに低いことが好ましい。アダプタ10を、爪30を下にした直立状態で、水平面上に安定的に放置しておくことができるからである。 The vertical position of the lower end 30 b of the claw 30 (or the rib 33) is not limited, but is preferably the same as or slightly lower than the tip 11 a of the puncture needle 11. This is because the adapter 10 can be stably left on the horizontal surface in the upright state with the claw 30 down.
 本実施形態では、各爪30に2つのリブ33が設けられているが、各爪30に1つ又は3つ以上のリブ33が設けられていてもよい。リブ33のY軸方向寸法は任意であり、例えばリブ33が爪30と略同じY軸方向寸法を有していてもよい。 In the present embodiment, each rib 30 is provided with two ribs 33. However, each claw 30 may be provided with one or more ribs 33. The dimension of the rib 33 in the Y-axis direction is arbitrary. For example, the rib 33 may have a dimension in the Y-axis direction substantially the same as that of the claw 30.
 アーム20は、管状部14との接続部分を固定端とする片持ち支持構造を有している。アーム20を構成する肩部21は、薄板状の部材であり、比較的容易に弾性的に曲げ変形可能である。爪30は、アーム20の自由端に設けられている。従って、アーム20は、爪30が穿刺針11から離れる向きに弾性的に変形することができる。アーム20がこのように変形するとき、肩部21の遠位端が上方に変位するように、肩部21が曲げ変形する。 The arm 20 has a cantilever support structure having a fixed end connected to the tubular portion 14. The shoulder 21 constituting the arm 20 is a thin plate-like member, and can be elastically bent and deformed relatively easily. The pawl 30 is provided at the free end of the arm 20. Therefore, the arm 20 can be elastically deformed in the direction in which the nail 30 is separated from the puncture needle 11. When the arm 20 deforms in this manner, the shoulder 21 bends so that the distal end of the shoulder 21 is displaced upward.
 管状部14の下端から、更に円弧状の鍔部16が半径方向外向きに突出している。鍔部16は、アーム20の肩部21と略同一平面を構成するように、肩部21と連続している。 From the lower end of the tubular portion 14, an arc-shaped hook portion 16 further protrudes radially outward. The collar 16 is continuous with the shoulder 21 so as to form a substantially flat surface with the shoulder 21 of the arm 20.
 本実施形態では、アーム20及び鍔部16が、管状部14を介して穿刺針11に一体化されているが、本発明はこれに限定されない。例えば、管状部14を省略し、アーム20の肩部21及び鍔部16が穿刺針11に直接設けられていてもよい。 In the present embodiment, the arm 20 and the hook portion 16 are integrated with the puncture needle 11 via the tubular portion 14, but the present invention is not limited thereto. For example, the tubular portion 14 may be omitted, and the shoulder 21 and the hook 16 of the arm 20 may be provided directly on the puncture needle 11.
 管状部14の上方にコネクタ40が設けられている。図2Cに示されているように、コネクタ40は、略円筒形状を有する筒状部41と、筒状部41の上端に設けられた隔壁部材(「セプタム」と呼ばれることがある)45と、隔壁部材45にかぶせられたキャップ47とを備える。筒状部41の内腔42は、穿刺針11内の流路12と連通している。 A connector 40 is provided above the tubular portion 14. As shown in FIG. 2C, the connector 40 includes a cylindrical portion 41 having a substantially cylindrical shape, and a partition member (sometimes called "septum") 45 provided on the upper end of the cylindrical portion 41; And a cap 47 covered on the partition member 45. The lumen 42 of the cylindrical portion 41 communicates with the flow passage 12 in the puncture needle 11.
 隔壁部材45は、円形の平面視形状を有する薄板である。隔壁部材45の中央に、隔壁部材45を上下方向に貫通する直線状のスリット(切り込み)45aが形成されている。隔壁部材45は、外力によって容易に変形可能であり、且つ、外力を取り除くと直ちに変形前の状態に復帰する。 The partition member 45 is a thin plate having a circular plan view shape. At the center of the partition member 45, a linear slit (cut) 45a penetrating the partition member 45 in the vertical direction is formed. The partition member 45 can be easily deformed by an external force, and returns immediately to the state before deformation when the external force is removed.
 筒状部41の外周面は円筒面である。筒状部41の外周面から、一対の係合突起41a及び環状突起41bが外側に向かって突出している。環状突起41bは、周方向に連続しており、係合突起41aに対して下側にわずかに離間している。 The outer peripheral surface of the cylindrical portion 41 is a cylindrical surface. A pair of engagement protrusions 41 a and an annular protrusion 41 b protrude outward from the outer peripheral surface of the cylindrical portion 41. The annular protrusion 41 b is continuous in the circumferential direction and slightly spaced downward from the engagement protrusion 41 a.
 キャップ47は、円板形状を有する天板48と、天板48の外周端縁から延びた円筒形状を有する周囲壁49とを備える。天板48の中央には円形の開口(貫通孔)48aが形成されている。周囲壁49には、一対の係合孔49aが形成されている。係合孔49aは、周囲壁49を半径方向に貫通する貫通孔である。 The cap 47 includes a top plate 48 having a disk shape, and a circumferential wall 49 having a cylindrical shape extending from the outer peripheral edge of the top plate 48. A circular opening (through hole) 48 a is formed at the center of the top plate 48. The surrounding wall 49 is formed with a pair of engagement holes 49a. The engagement holes 49 a are through holes radially penetrating the surrounding wall 49.
 隔壁部材45は、筒状部41の上端とキャップ47の天板48とによって、その厚さ方向(即ち、上下方向)に挟持される。筒状部41から突出した係合突起41aがキャップ47の係合孔49a内に嵌入することによって、キャップ47は係合突起41aに係合される。隔壁部材45のスリット45aは、キャップ47の天板48に形成された開口48a内に露出する(図2A参照)。筒状部41に形成された環状突起41bは、キャップ47の周囲壁49に下側に隣接する。環状突起41bの頂面は、周囲壁49の外周面と略同一の円筒面を構成する。 The partition member 45 is held by the upper end of the cylindrical portion 41 and the top plate 48 of the cap 47 in the thickness direction (that is, in the vertical direction). The cap 47 is engaged with the engaging protrusion 41 a by fitting the engaging protrusion 41 a protruding from the cylindrical portion 41 into the engaging hole 49 a of the cap 47. The slit 45a of the partition member 45 is exposed in the opening 48a formed in the top plate 48 of the cap 47 (see FIG. 2A). The annular protrusion 41 b formed in the cylindrical portion 41 is adjacent to the lower side of the peripheral wall 49 of the cap 47. The top surface of the annular protrusion 41 b constitutes a cylindrical surface substantially the same as the outer peripheral surface of the peripheral wall 49.
 スリット45aが形成された隔壁部材45を備えたコネクタ40は、一般にニードルレスポートと呼ばれる。隔壁部材45が変形していない初期状態では、スリット45aは閉じられて液密なシールを形成する。隔壁部材45は、筒状部41の内腔42を外界から分離する機能を有する。隔壁部材45のスリット45aに、鋭利な先端を有しない筒状のオスルアー(図示せず)を挿入すると、隔壁部材45が弾性変形し、筒状部41の内腔42とオスルアーとが連通する。オスルアーを隔壁部材45から引き抜くと、隔壁部材45は直ちに初期状態に復帰し、スリット45aは液密に閉じられる。このように、隔壁部材45は、自閉式の弁体として機能する。 The connector 40 provided with the partition member 45 in which the slit 45a is formed is generally called a needleless port. In the initial state in which the partition member 45 is not deformed, the slit 45a is closed to form a fluid-tight seal. The partition member 45 has a function of separating the inner cavity 42 of the cylindrical portion 41 from the outside. When a cylindrical male luer (not shown) having no sharp tip is inserted into the slit 45 a of the partition wall member 45, the partition wall member 45 is elastically deformed and the lumen 42 of the cylindrical portion 41 and the male luer communicate. When the male luer is pulled out of the partition member 45, the partition member 45 immediately returns to the initial state, and the slit 45a is closed in a fluid tight manner. Thus, the partition member 45 functions as a self-closing valve body.
 アダプタ10の、隔壁部材45及びキャップ47を除く部分は、樹脂材料を射出成形することにより全体を一部品として一体的に製造されることが好ましい。使用できる樹脂材料は、制限はないが、ポリエチレン、ポリプロピレン、ポリカーボネート、スチレンエチレン、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ブチレンスチレンブロック共重合体などを例示することができるが、医療用に用いられることやアーム20が弾性曲げ変形されることを考慮すると、ポリエチレン、ポリプロピレンなどのポリオレフィン系樹脂が好ましい。キャップ47の材料は、制限はないが、硬質の材料であることが好ましく、例えば、ポリカーボネート、ポリプロピレン、ポリアセタール、ポリアミド、硬質ポリ塩化ビニル、ポリエチレン等の樹脂材料を用いることができる。隔壁部材45の材料は、制限はないが、ゴム弾性(または可撓性)を有する軟質の材料(いわゆるエラストマー)であることが好ましく、例えば、イソプレンゴム、シリコーンゴム、ブチルゴム等のゴム材料や、熱可塑性エラストマー等を用いることができる。 The portion of the adapter 10 excluding the partition wall member 45 and the cap 47 is preferably integrally manufactured as a whole by injection molding a resin material. Resin materials that can be used include, but are not limited to, polyethylene, polypropylene, polycarbonate, styrene ethylene, polyethylene terephthalate, polybutylene terephthalate, butylene styrene block copolymer, etc. In consideration of elastic bending deformation of 20, polyolefin resins such as polyethylene and polypropylene are preferable. The material of the cap 47 is not limited, but is preferably a hard material, and for example, resin materials such as polycarbonate, polypropylene, polyacetal, polyamide, hard polyvinyl chloride, polyethylene and the like can be used. The material of the partition member 45 is not limited, but is preferably a soft material (so-called elastomer) having rubber elasticity (or flexibility), for example, a rubber material such as isoprene rubber, silicone rubber, butyl rubber, or the like A thermoplastic elastomer etc. can be used.
 2.カバー
 図3Aは、カバー50の下方から見た斜視図である。図3Bは、カバー50の下方から見た断面斜視図である。図3Cは、カバー50の平面図である。
2. Cover FIG. 3A is a perspective view of the cover 50 as viewed from below. FIG. 3B is a cross-sectional perspective view of the cover 50 as viewed from below. FIG. 3C is a plan view of the cover 50. FIG.
 カバー50は、コネクタケース51、拡張板58、及び、ガイドバー59を備える(図1参照)。 The cover 50 includes a connector case 51, an expansion plate 58, and a guide bar 59 (see FIG. 1).
 図3Aに示されているように、コネクタケース51は、中空の略筒形状を有し、その上端は閉じられ、その下端は解放されている。後述するように、コネクタケース51に、下方からコネクタ40(図4C及び図4D参照)が収納される。コネクタケース51の上下方向に沿って延びた周囲壁52の外周面には、互いに平行な一対の把持面53が設けられている(図3Aでは一方の把持面53のみが見える)。把持面53は、実質的に平坦面であり、XZ面に平行である。把持面53を除く周囲壁52の外周面は、限定されないが、本実施形態では滑らかな凸曲面(例えば円筒面)である(図3C参照)。 As shown in FIG. 3A, the connector case 51 has a hollow, substantially cylindrical shape, with its upper end closed and its lower end released. As described later, the connector 40 (see FIGS. 4C and 4D) is accommodated in the connector case 51 from below. A pair of gripping surfaces 53 parallel to each other is provided on the outer peripheral surface of the peripheral wall 52 extending along the vertical direction of the connector case 51 (only one gripping surface 53 is visible in FIG. 3A). The gripping surface 53 is substantially flat and parallel to the XZ plane. The outer peripheral surface of the peripheral wall 52 excluding the gripping surface 53 is not limited, but in the present embodiment, it is a smooth convex curved surface (for example, a cylindrical surface) (see FIG. 3C).
 図3Bに示されているように、延長壁55が、拡張板58から下方に向かって突出している。延長壁55は、周囲壁52を拡張板58を越えて下方に延長したものである。但し、周囲壁52と異なり、延長壁55は周方向に環状に連続しておらず、2箇所で分断されている。即ち、一対の延長壁55が、Y軸方向に対向している。 As shown in FIG. 3B, the extension wall 55 protrudes downward from the extension plate 58. The extension wall 55 extends the surrounding wall 52 downward beyond the extension plate 58. However, unlike the surrounding wall 52, the extending wall 55 is not annularly continuous in the circumferential direction, and is divided at two places. That is, the pair of extension walls 55 oppose each other in the Y-axis direction.
 コネクタケース51の内周面から4本のリブ(突起)56が突出している(図3Bでは、2本のリブ56のみが示されている)。リブ56は、上下方向(即ちZ軸方向)に沿って、周囲壁52から延長壁55にまで延びている。4本のリブ56は、中心軸に対して等角度間隔で配置されている。4本のリブ56に内接する円(この円はXY面に沿っている)の直径は、キャップ47の周囲壁49及び環状突起41b(図2A参照)の外径とほぼ同じである。4本のリブ56のうち中心軸を挟んで対向する2本のリブ56からは、中心軸に向かって突起57が突出している。なお、本発明では、リブ56の数は、4本に限定されず、3本又は5本以上であってもよい。突起57が全てのリブ56に設けられていてもよい。 Four ribs (protrusions) 56 project from the inner peripheral surface of the connector case 51 (only two ribs 56 are shown in FIG. 3B). The ribs 56 extend from the circumferential wall 52 to the extension wall 55 along the up-down direction (i.e., the Z-axis direction). The four ribs 56 are arranged at equal angular intervals with respect to the central axis. The diameter of the circle inscribed in the four ribs 56 (this circle is along the XY plane) is substantially the same as the outer diameter of the peripheral wall 49 of the cap 47 and the annular projection 41b (see FIG. 2A). From the two ribs 56 opposed to each other across the central axis among the four ribs 56, a protrusion 57 protrudes toward the central axis. In the present invention, the number of ribs 56 is not limited to four, and may be three or five or more. The projections 57 may be provided on all the ribs 56.
 拡張板58が、コネクタケース51の周囲壁52の下端から、半径方向の外向きに延びている。拡張板58の上面は、水平面(XY面)に対して略平行である。図3Cに示されているように、拡張板58は、コネクタケース51の周囲に環状に連続している。拡張板58の外周端縁の平面視形状は、Y軸方向に沿った寸法がX軸方向に沿った寸法より大きな非円形である。具体的には、本実施形態の拡張板58は、Y軸方向に平行な2本の直線58aと、この2本の直線の両端をつなぐ2つの円弧58bとで構成された、陸上競技場のトラックに近似した形状を有する。換言すれば、拡張板58は、カバー50の中心軸と同心の円を平行な2本の直線58aで切断した形状を有する。この結果、コネクタケース51の周囲壁52からの拡張板58の半径方向のはみ出し長さは、X軸方向よりもY軸方向において、より長い。拡張板58の外周端縁が、平行な2直線58aを含むので、多数のカバー50を、コネクタケース51を上にした直立状態で、水平面上に縦横方向に高密度に並べて配置することができる。これは、例えばカバー50を多量生産する場合に、カバー50の取り扱いを容易にする。 An extension plate 58 extends radially outward from the lower end of the peripheral wall 52 of the connector case 51. The upper surface of the expansion plate 58 is substantially parallel to the horizontal plane (XY plane). As shown in FIG. 3C, the expansion plate 58 is annularly continuous around the connector case 51. The plan view shape of the outer peripheral edge of the expansion plate 58 is non-circular in which the dimension along the Y-axis direction is larger than the dimension along the X-axis direction. Specifically, the expansion plate 58 of the present embodiment is an athletic stadium that is composed of two straight lines 58a parallel to the Y-axis direction and two arcs 58b connecting both ends of the two straight lines. It has a shape similar to a track. In other words, the expansion plate 58 has a shape in which a circle concentric with the central axis of the cover 50 is cut by two parallel straight lines 58a. As a result, the radial extension length of the expansion plate 58 from the peripheral wall 52 of the connector case 51 is longer in the Y-axis direction than in the X-axis direction. Since the outer peripheral edge of the expansion plate 58 includes two parallel straight lines 58a, a large number of covers 50 can be arranged at high density in the horizontal and vertical directions on the horizontal plane with the connector case 51 facing up. . This facilitates handling of the cover 50, for example, when mass producing the cover 50.
 なお、拡張板58の平面視形状は、本実施形態に限定されない。拡張板58は、例えば、楕円形、長円形、略菱形、多角形(例えば六角形、八角形)等の任意の平面視形状を有していてもよい。但し、拡張板58は、本実施形態のように、Y軸方向に長軸を有することが好ましい。拡張板58は、周方向に連続していなくてもよい。例えば、図3Cにおいて、2本の直線58aが周囲壁52に接していてもよい。この場合、周囲壁52からの拡張板58のX軸方向に沿ったはみ出し長さはゼロである。 In addition, the planar view shape of the expansion board 58 is not limited to this embodiment. The extension plate 58 may have an arbitrary planar view shape such as, for example, an oval, an oval, a substantially rhombic, or a polygon (for example, a hexagon or an octagon). However, as in the present embodiment, the expansion plate 58 preferably has a major axis in the Y-axis direction. The extension plate 58 may not be continuous in the circumferential direction. For example, in FIG. 3C, two straight lines 58 a may be in contact with the surrounding wall 52. In this case, the extension length of the expansion plate 58 from the surrounding wall 52 along the X-axis direction is zero.
 図3Aに示されているように、拡張板58の外周端縁(特に円弧58b)から下方に向かって複数本(本実施形態では4本)のガイドバー59が延びている。ガイドバー59は、狭幅の薄板形状を有しており、その先端(または下端)59aが中心軸に対して接離するように弾性的に曲げ変形可能である。Z軸に沿って見たとき、変形していない初期状態のガイドバー59は、カバー50と同心の円上に配置される。 As shown in FIG. 3A, a plurality of (four in this embodiment) guide bars 59 extend downward from the outer peripheral edge (in particular, the arc 58b) of the expansion plate 58. As shown in FIG. The guide bar 59 has a narrow thin-plate shape, and can be elastically bent and deformed so that its tip (or lower end) 59a approaches and separates from the central axis. When viewed along the Z-axis, the undeformed initial guide bar 59 is disposed on a circle concentric with the cover 50.
 カバー50は、樹脂材料を射出成形することにより全体を一部品として一体的に製造されることが好ましい。使用できる樹脂材料は、制限はないが、ポリエチレン、ポリプロピレン、ポリカーボネート、スチレンエチレン、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ブチレンスチレンブロック共重合体などを例示することができる。ガイドバー59が弾性曲げ変形されることを考慮すると、ポリエチレン、ポリプロピレンなどのポリオレフィン系樹脂が好ましい。 The cover 50 is preferably integrally manufactured as a whole by injection molding a resin material. Resin materials which can be used include, but are not limited to, polyethylene, polypropylene, polycarbonate, styrene ethylene, polyethylene terephthalate, polybutylene terephthalate, butylene styrene block copolymer and the like. In consideration of elastic bending deformation of the guide bar 59, polyolefin resins such as polyethylene and polypropylene are preferable.
 3.アダプタ組立体
 図1に示すように、カバー50は、アダプタ10に上方から装着することができる。図4Aは、アダプタ10にカバー50が装着されたアダプタ組立体1の上方から見た斜視図である。図4Bは、アダプタ組立体1の平面図である。図4Cは、アダプタ組立体1の、中心軸を含むXZ面に沿った断面図である。図4Dは、アダプタ組立体1の、中心軸を含むYZ面に沿った断面図である。
3. Adapter Assembly As shown in FIG. 1, the cover 50 can be attached to the adapter 10 from above. FIG. 4A is a perspective view of the adapter assembly 1 with the cover 50 attached to the adapter 10 as viewed from above. FIG. 4B is a plan view of the adapter assembly 1. FIG. 4C is a cross-sectional view of the adapter assembly 1 along the XZ plane including the central axis. FIG. 4D is a cross-sectional view of the adapter assembly 1 along the YZ plane including the central axis.
 図4C及び図4Dに示されているように、アダプタ10のコネクタ40は、カバー50のコネクタケース51内に収納されている。図4Dに示されているように、カバー50の延長壁55の下端が、アダプタ10の鍔部16(図2A参照)に上下方向に当接している。これにより、コネクタケース51に対するアダプタ10の挿入深さが規定される。 As shown in FIGS. 4C and 4D, the connector 40 of the adapter 10 is housed in the connector case 51 of the cover 50. As shown in FIG. 4D, the lower end of the extension wall 55 of the cover 50 vertically abuts on the hook portion 16 (see FIG. 2A) of the adapter 10. Thereby, the insertion depth of the adapter 10 with respect to the connector case 51 is defined.
 図示を省略するが、コネクタケース51の内周面に設けられたリブ56(図3B参照)がキャップ47の周囲壁49及び環状突起41b(図2A参照)に当接する。これにより、カバー50はアダプタ10に対して同軸になるように位置合わせされる。また、リブ56から突出した突起57(図3B参照)は、環状突起41bの下側の端縁に係合する。これにより、カバー50からアダプタ10が落下するのが防止される。アダプタ10にカバー50を装着する過程で、突起57が環状突起41bを乗り越えて環状突起41bに係合するとき、作業者は指先にクリック感を感じる。作業者は、このクリック感により、カバー50がアダプタ10に正しく装着されたことを認識することができる。 Although not shown, the rib 56 (see FIG. 3B) provided on the inner circumferential surface of the connector case 51 abuts on the circumferential wall 49 of the cap 47 and the annular projection 41b (see FIG. 2A). Thereby, the cover 50 is aligned coaxially with the adapter 10. Also, the projection 57 (see FIG. 3B) protruding from the rib 56 engages with the lower edge of the annular projection 41 b. This prevents the adapter 10 from falling out of the cover 50. In the process of attaching the cover 50 to the adapter 10, when the projection 57 passes over the annular projection 41b and engages with the annular projection 41b, the operator feels a click on the fingertip. The operator can recognize that the cover 50 is correctly attached to the adapter 10 by the click feeling.
 カバー50をアダプタ10に装着すると、カバー50の延長壁55及び突起57が、カバー50に対してアダプタ10を上下方向に位置決めする。この状態で、ガイドバー59は、穿刺針11に対向し、穿刺針11よりも更に下方に向かって延びている。即ち、ガイドバー59の先端59aは、穿刺針11の先端11aよりも下側に位置している。また、好ましくは、ガイドバー59は、爪30(リブ33を含む)よりも更に下方に向かって延びている。即ち、ガイドバー59の先端59aは、好ましくは、爪30の下端30bよりも下側に位置している。上述したようにカバー50はアダプタ10と同軸であるので、4つのガイドバー59は、穿刺針11と同心の円に沿って配置される。 When the cover 50 is attached to the adapter 10, the extension wall 55 and the projection 57 of the cover 50 vertically position the adapter 10 with respect to the cover 50. In this state, the guide bar 59 faces the puncture needle 11 and extends further downward than the puncture needle 11. That is, the tip 59 a of the guide bar 59 is located below the tip 11 a of the puncture needle 11. Also preferably, the guide bar 59 extends further downward than the claws 30 (including the rib 33). That is, the tip end 59 a of the guide bar 59 is preferably located below the lower end 30 b of the claw 30. As described above, since the cover 50 is coaxial with the adapter 10, the four guide bars 59 are arranged along a circle concentric with the puncture needle 11.
 図4Cに示されているように、カバー50は、アーム20(特にその肩部21)に上下方向に当接していない。このため、アダプタ10に装着されたカバー50が、アーム20の弾性変形を阻害することはない。 As shown in FIG. 4C, the cover 50 does not vertically abut on the arm 20 (particularly its shoulder 21). For this reason, the cover 50 attached to the adapter 10 does not inhibit the elastic deformation of the arm 20.
 図4Aに示されているように、カバー50の拡張板58は、アーム20よりも高い位置にある。アーム20(特にその肩部21)は、拡張板58よりも半径方向外側に突出している。ガイドバー59は、拡張板58から、アーム20を越えて更に下方に向かって延びている。アダプタ10に対するカバー50の中心軸回りの回転は、ガイドバー59の上下方向に沿って延びた側端縁59b(図4A参照)が、アーム20のY軸方向の幅を規定する側端縁に衝突することによって制限される。一対のアーム20はX軸方向に対向しているのに対して、カバー50の一対の把持面53はY軸方向に対向し、また、カバー50の拡張板58の長軸はY軸に平行である。 As shown in FIG. 4A, the expansion plate 58 of the cover 50 is at a higher position than the arm 20. The arms 20 (especially their shoulders 21) project radially outward of the expansion plate 58. The guide bar 59 extends further downward from the extension plate 58 beyond the arm 20. When the cover 50 is rotated relative to the adapter 10 about the central axis, the side edge 59 b (see FIG. 4A) extending along the vertical direction of the guide bar 59 is on the side edge defining the width of the arm 20 in the Y-axis direction. Limited by colliding. The pair of arms 20 are opposed in the X-axis direction, whereas the pair of gripping surfaces 53 of the cover 50 are opposed in the Y-axis direction, and the major axis of the expansion plate 58 of the cover 50 is parallel to the Y-axis It is.
 カバー50は、アダプタ10に対して繰り返し着脱することができる。アダプタ10からカバー50を分離する際には、アダプタ10及びカバー50のそれぞれに上下方向に比較的大きな引張り力を加えて、アダプタ10の環状突起41bとカバー50の突起57との係合を解除する必要がある。 The cover 50 can be repeatedly attached to and detached from the adapter 10. When the cover 50 is separated from the adapter 10, a relatively large tensile force is applied to the adapter 10 and the cover 50 in the vertical direction to release the engagement between the annular projection 41b of the adapter 10 and the projection 57 of the cover 50. There is a need to.
 4.アダプタ組立体の使用方法
 図5は、アダプタ組立体1が装着されるバイアル80の一例の断面図である。バイアル80は、瓶本体81の上方を向いた口(開口)82に栓体(ゴム栓)87を嵌入して当該口82を気密及び液密に封止した密閉容器である。バイアル80内には、粉末状の薬剤(図示せず)が収容されている。瓶本体81の上端には、口82を取り囲むように、拡径したフランジ83が設けられている。フランジ83の外周面は、略円筒面である。瓶本体81は、フランジ83から下方に向かって、フランジ83よりも小さな外径を有するくびれ部84、外径が下方に向かって徐々に大きくなる肩部85、外径が上下方向において略一定である円筒部86を、この順に互いに隣接して有している。
4. Method of Using Adapter Assembly FIG. 5 is a cross-sectional view of an example of a vial 80 to which the adapter assembly 1 is attached. The vial 80 is a sealed container in which a stopper (rubber stopper) 87 is inserted into a port (opening) 82 facing upward of the bottle body 81 to seal the port 82 airtightly and liquid tight. Powdered medicine (not shown) is contained in the vial 80. At the upper end of the bottle body 81, an enlarged flange 83 is provided so as to surround the opening 82. The outer peripheral surface of the flange 83 is a substantially cylindrical surface. The bottle body 81 has a neck portion 84 having an outer diameter smaller than the flange 83 downward from the flange 83, a shoulder 85 having an outer diameter gradually increasing downward, and an outer diameter substantially constant in the vertical direction Certain cylindrical portions 86 are provided adjacent to each other in this order.
 栓体87は、フランジ83と略同一の外径を有する。栓体87が瓶本体81の口82から脱落するのを防止するために、栓体87及びフランジ83にキャップ88が装着されている。キャップ88は、金属(例えばアルミニウム)または樹脂等のシートからなり、栓体87及びフランジ83に密着している。キャップ88の下端は、フランジ83の略円筒面である外周面よりも下側にまで及んでいる。キャップ88の上端は、栓体87の上面にまで及んでいる。栓体87の上面の中央の領域は、キャップ88に設けられた円形の開口88aを介して外界に露出している(後述する図6参照)。 The plug 87 has an outer diameter substantially the same as that of the flange 83. A cap 88 is attached to the plug 87 and the flange 83 in order to prevent the plug 87 from falling off the opening 82 of the bottle body 81. The cap 88 is made of a sheet of metal (for example, aluminum) or resin, and is in close contact with the stopper 87 and the flange 83. The lower end of the cap 88 extends below the outer peripheral surface which is a substantially cylindrical surface of the flange 83. The upper end of the cap 88 extends to the upper surface of the plug 87. The central region of the upper surface of the plug 87 is exposed to the outside through a circular opening 88 a provided in the cap 88 (see FIG. 6 described later).
 栓体87の外周面とフランジ83の外周面とは、略同一直径の円筒面である。従って、栓体87及びフランジ83に装着されたキャップ88の外周面88cも略円筒面である。キャップ88の外周面88cの上端(または、キャップ88の上面の外周端縁)を上側端縁88bといい、また、当該外周面88cの下端を下側端縁88dという。 The outer peripheral surface of the plug 87 and the outer peripheral surface of the flange 83 are cylindrical surfaces having substantially the same diameter. Accordingly, the outer peripheral surface 88 c of the cap 88 mounted on the plug 87 and the flange 83 is also a substantially cylindrical surface. The upper end of the outer peripheral surface 88c of the cap 88 (or the outer peripheral edge of the upper surface of the cap 88) is referred to as an upper end edge 88b, and the lower end of the outer peripheral surface 88c is referred to as a lower end edge 88d.
 バイアル80はキャップ88を備えていなくてもよい。その場合には、上側端縁88b、下側端縁88d、外周面88cは、栓体87又はフランジ83の対応する箇所を意味する。 The vial 80 may not have the cap 88. In that case, the upper end edge 88 b, the lower end edge 88 d and the outer peripheral surface 88 c mean corresponding portions of the plug 87 or the flange 83.
 アダプタ組立体1は、図4Aに示したようにアダプタ10にカバー50が装着された状態で病院等の医療機関に納品される。バイアル80内の薬剤を用いて薬液を調製する際に、アダプタ組立体1は以下のようにしてバイアル80に装着される。 The adapter assembly 1 is delivered to a medical institution such as a hospital with the cover 50 attached to the adapter 10 as shown in FIG. 4A. When preparing a drug solution using the drug in the vial 80, the adapter assembly 1 is attached to the vial 80 as follows.
 最初に、図6に示すように、バイアル80を栓体87を上にして直立させる。アダプタ組立体1を、その中心軸(または穿刺針11)が上下方向に平行になるように維持しながら、穿刺針11の先端11aを栓体87の上面に接近させる。上述したように、カバー50のガイドバー59は、穿刺針11の先端11aよりも下方(バイアル80側)に延びている。従って、穿刺針11の先端11aが栓体87の上面に接触するよりも前に、キャップ88(または栓体87)の一部が4本のガイドバー59で囲まれた領域内に収納される。4本のガイドバー59は、穿刺針11と同心の円に沿って配置されている。従って、4本のガイドバー59の内側にキャップ88が収納されるようにアダプタ組立体1をバイアル80に接近させれば、穿刺針11の先端11aを栓体87の中心に容易に位置合わせすることができる。 First, as shown in FIG. 6, the vial 80 is erected with the stopper 87 up. The tip end 11a of the puncture needle 11 is brought close to the upper surface of the plug 87 while maintaining the adapter assembly 1 such that the central axis (or the puncture needle 11) is parallel in the vertical direction. As described above, the guide bar 59 of the cover 50 extends below the tip 11 a of the puncture needle 11 (the vial 80 side). Therefore, before the tip 11 a of the puncture needle 11 contacts the upper surface of the plug 87, a part of the cap 88 (or the plug 87) is stored in the area surrounded by the four guide bars 59. . The four guide bars 59 are arranged along a circle concentric with the puncture needle 11. Therefore, if the adapter assembly 1 is brought close to the vial 80 so that the cap 88 is housed inside the four guide bars 59, the tip 11a of the puncture needle 11 is easily aligned with the center of the stopper 87. be able to.
 好ましくは、4本のガイドバー59の内接円の直径は、キャップ88の外径と略同じに設定される。これにより、穿刺針11の先端11aを栓体87の中心により正確に位置合わせすることができる。 Preferably, the diameter of the inscribed circle of the four guide bars 59 is set to be substantially the same as the outer diameter of the cap 88. Thus, the tip end 11 a of the puncture needle 11 can be more accurately aligned with the center of the plug 87.
 4本のガイドバー59の内接円の直径は、キャップ88の外径より小さくてもよい。この場合、ガイドバー59の先端59aが、キャップ88の上側端縁88b(図5参照)の近傍の外径が徐々に変化する凸曲面の部分に当接し、先端59aが半径方向外向きに変位するように、ガイドバー59が適宜曲げ変形する。4本のガイドバー59の弾性回復力が、穿刺針11の先端11aを栓体87の中心に位置合わせする。このように、アダプタ組立体1は、キャップ88の外径が異なる複数種類のバイアルに適応している。 The diameter of the inscribed circle of the four guide bars 59 may be smaller than the outer diameter of the cap 88. In this case, the tip end 59a of the guide bar 59 abuts on the portion of the convex curved surface where the outer diameter near the upper end edge 88b (see FIG. 5) of the cap 88 gradually changes, and the tip end 59a is displaced radially outward. As a result, the guide bar 59 bends and deforms as appropriate. The elastic recovery force of the four guide bars 59 aligns the tip 11 a of the puncture needle 11 with the center of the plug 87. Thus, the adapter assembly 1 is adapted to a plurality of types of vials in which the outer diameter of the cap 88 is different.
 穿刺針11の先端11aが栓体87に接触したとき、爪30(特にリブ33の端縁33a)は、キャップ88に未だ接触していないことが好ましい。但し、キャップ88の外径によっては、穿刺針11の先端11aが栓体87に接触するよりも前に、爪30がキャップ88に接触する場合が起こりうる。この場合であっても、ガイドバー59が爪30(リブ33を含む)よりも下方に延びるように、ガイドバー59の長さを適切に設定することにより、爪30がキャップ88に接触したときに、キャップ88(または栓体87)の一部を4本のガイドバー59で囲まれた領域内に収納させることは可能である。従って、上記の場合にも、穿刺針11の先端11aを栓体87の中心に容易に位置合わせすることができる。 When the tip 11 a of the puncture needle 11 contacts the plug 87, it is preferable that the claws 30 (in particular, the end 33 a of the rib 33) have not yet been in contact with the cap 88. However, depending on the outer diameter of the cap 88, the claw 30 may contact the cap 88 before the tip 11a of the puncture needle 11 contacts the plug 87. Even in this case, when the claw 30 contacts the cap 88 by appropriately setting the length of the guide bar 59 so that the guide bar 59 extends below the claw 30 (including the rib 33). In addition, it is possible to accommodate a part of the cap 88 (or the plug 87) in the area surrounded by the four guide bars 59. Therefore, also in the above case, the tip end 11 a of the puncture needle 11 can be easily aligned with the center of the plug 87.
 図6のように栓体87に対して穿刺針11を位置合わせした状態で、アダプタ組立体1をバイアル80に向かって強く押し込む。爪30の端縁33aがキャップ88の上側端縁88b近傍に接触しながら、爪30が穿刺針11から離れるように半径方向外向きに変位する。爪30が変位するとき、アーム20は弾性的に曲げ変形する。爪30がキャップ88を通過し終えると、アーム20が弾性回復する。図7に示すように、アダプタ組立体1をバイアル80に装着することができる。特許文献1のアダプタと同様に、爪30がバイアル80のくびれ部84(図5参照)に嵌入し、爪30がフランジ83に係合する。図示を省略するが、穿刺針11は栓体87を貫通し、その開口13(図1A参照)は栓体87よりも下側に位置する。バイアル80の内部は穿刺針11の流路12を介してコネクタ40と連通される。ガイドバー59の先端59aは、瓶本体81の肩部85のあたりに達している。肩部85での瓶本体81の外径の変化に応じてガイドバー59の先端59aが半径方向外向きに変位するように、ガイドバー59が適宜弾性的に曲げ変形してもよい。 With the puncture needle 11 aligned with the stopper 87 as shown in FIG. 6, the adapter assembly 1 is strongly pushed toward the vial 80. While the end 33 a of the claw 30 contacts the vicinity of the upper end 88 b of the cap 88, the claw 30 is displaced radially outward away from the puncture needle 11. When the claws 30 are displaced, the arms 20 elastically bend and deform. When the claws 30 pass through the cap 88, the arm 20 elastically recovers. The adapter assembly 1 can be attached to the vial 80, as shown in FIG. Similar to the adapter of Patent Document 1, the claws 30 are fitted into the constricted portion 84 (see FIG. 5) of the vial 80 and the claws 30 engage with the flanges 83. Although not shown, the puncture needle 11 passes through the plug 87, and the opening 13 (see FIG. 1A) is located below the plug 87. The inside of the vial 80 is in communication with the connector 40 via the flow path 12 of the puncture needle 11. The tip 59 a of the guide bar 59 reaches around the shoulder 85 of the bottle body 81. The guide bar 59 may be appropriately elastically bent and deformed so that the tip end 59a of the guide bar 59 is displaced radially outward in accordance with the change in the outer diameter of the bottle main body 81 at the shoulder 85.
 その後、アダプタ10からカバー50を取り外す。アダプタ10はバイアル80に装着されたままである。コネクタ40にオスコネクタ(例えばオスルアー)を接続してバイアル80内の薬剤を用いて薬液の調製を行うことができる。図7から理解できるように、ガイドバー59は、瓶本体81を介した穿刺針11の先端11aの視認性や、バイアル80内の薬剤や液体の視認性を低下させる。アダプタ10からカバー50を取り外すことにより、これらの視認性が向上する。 Thereafter, the cover 50 is removed from the adapter 10. The adapter 10 remains attached to the vial 80. A male connector (for example, a male luer) is connected to the connector 40, and the drug in the vial 80 can be used to prepare a drug solution. As can be understood from FIG. 7, the guide bar 59 reduces the visibility of the tip 11 a of the puncture needle 11 via the bottle body 81 and the visibility of the drug or liquid in the vial 80. Removing the cover 50 from the adapter 10 improves their visibility.
 薬液調製後、アダプタ10にカバー50を再度装着する。使用済みのバイアル80は、アダプタ組立体1が装着された状態(図7参照)で廃棄される。アダプタ10にカバー50を装着することによって、コネクタ40の天板48や、その開口48aを介して露出された隔壁部材45に付着しているかも知れない薬液による薬剤被曝を防止することができる。 After preparation of the drug solution, the cover 50 is attached to the adapter 10 again. The used vial 80 is discarded with the adapter assembly 1 attached (see FIG. 7). By mounting the cover 50 on the adapter 10, it is possible to prevent the chemical exposure to a chemical solution that may be attached to the top plate 48 of the connector 40 and the partition wall member 45 exposed through the opening 48a.
 5.作用
 以上のように、本実施形態のアダプタ組立体1は、穿刺針11よりも下方(バイアル80側)に延びたガイドバー59を備えるので、穿刺針11の先端11aを栓体87の中心に容易に位置合わせすることができる。
5. As described above, since the adapter assembly 1 of the present embodiment includes the guide bar 59 extending downward (the vial 80 side) than the puncture needle 11, the tip 11a of the puncture needle 11 is at the center of the plug 87. It can be easily aligned.
 本実施形態とは異なり、カバー50を用いることなく、アダプタ10をバイアル80に装着することは可能である。この場合、目視にて穿刺針11の先端11aを栓体87の中心に位置合わせする必要がある。この場合には、栓体87に対する穿刺針11の位置ズレ量は、本実施形態に比べて大きくなる可能性が高い。穿刺針11の先端11aが栓体87の中心から位置ズレした状態でアダプタ10をバイアル80に向かって押し込むと、爪30をバイアル80のフランジ83に係合させることができなかったり、バイアル80に対して穿刺針11が斜めに穿刺されてしまったりする。また、キャップ88の外径によっては、穿刺針11が栓体87に接触するよりも前に爪30がキャップ88に接触する場合がある。この場合に、穿刺針11の先端11aが栓体87の中心から位置ズレした状態でアダプタ10をバイアル80に向かって押し込むと、爪30がキャップ88上を水平方向に滑ってしまう。このため、バイアル80が転倒することがある。あるいは、爪30がキャップ88上を滑る過程で穿刺針11の先端11aがキャップ88の開口88aの端縁に引っかかり、先端11aに半径方向の力が加わることによって穿刺針11が折れ曲がってしまうことがある。本実施形態では、このような問題が生じる可能性が低減される。 Unlike the present embodiment, it is possible to attach the adapter 10 to the vial 80 without using the cover 50. In this case, it is necessary to visually align the tip 11 a of the puncture needle 11 with the center of the plug 87. In this case, the positional displacement amount of the puncture needle 11 with respect to the plug 87 is likely to be large compared to the present embodiment. If the adapter 10 is pushed toward the vial 80 with the tip 11 a of the puncture needle 11 displaced from the center of the stopper 87, the claw 30 can not be engaged with the flange 83 of the vial 80. In contrast, the puncture needle 11 may be punctured obliquely. Further, depending on the outer diameter of the cap 88, the nail 30 may contact the cap 88 before the puncture needle 11 contacts the plug 87. In this case, when the adapter 10 is pushed toward the vial 80 with the tip 11a of the puncture needle 11 displaced from the center of the plug 87, the claw 30 slides on the cap 88 in the horizontal direction. For this reason, the vial 80 may tip over. Alternatively, the tip 11a of the puncture needle 11 may be caught on the edge of the opening 88a of the cap 88 while the nail 30 slides on the cap 88, and the puncture needle 11 may be bent due to the radial force applied to the tip 11a. is there. In the present embodiment, the possibility of the occurrence of such a problem is reduced.
 本実施形態では、穿刺針11を栓体87に穿刺する前の図6の状態で、キャップ88に対する各ガイドバー59の先端59aの上下方向の位置を確認することより、バイアル80に対するアダプタ組立体1の傾きを確認し、それを修正するのが容易である。このため、栓体87に対して穿刺針11を垂直に穿刺することができる。穿刺針11の先端11aが栓体87の中心を穿刺したとしても、穿刺針11が栓体87を斜めに穿刺すると、例えば爪30をバイアル80のフランジ83に係合させることができないという事態が起こりうる。本実施形態では、このような事態が起こる可能性は低い。 In the present embodiment, the adapter assembly for the vial 80 is confirmed by confirming the vertical position of the tip 59a of each guide bar 59 with respect to the cap 88 in the state of FIG. 6 before puncturing the puncture needle 11 into the plug 87. It is easy to check the slope of 1 and correct it. For this reason, the puncture needle 11 can be punctured perpendicularly to the plug 87. Even if the tip 11a of the puncture needle 11 punctures the center of the plug 87, if the puncture needle 11 punctures the plug 87 at an angle, for example, the claw 30 can not be engaged with the flange 83 of the vial 80. It can happen. In the present embodiment, such a situation is unlikely to occur.
 複数のガイドバー59は周方向に離間している。このため、図6に示されているように、隣り合うガイドバー59の間を介して、栓体87に対する穿刺針11の先端11aの位置を目視することができる。 The plurality of guide bars 59 are circumferentially spaced. For this reason, as shown in FIG. 6, the position of the tip 11a of the puncture needle 11 relative to the plug 87 can be visually checked through the space between the adjacent guide bars 59.
 複数のガイドバー59は、穿刺針11と同心の円に沿って配置されている。このように配置されたガイドバー59は、栓体87の中心に対する穿刺針11の先端11aの位置合わせの精度を向上させるのに有利である。 The plurality of guide bars 59 are arranged along a circle concentric with the puncture needle 11. The guide bar 59 arranged in this manner is advantageous for improving the accuracy of the alignment of the tip 11 a of the puncture needle 11 with the center of the plug 87.
 ガイドバー59は、その先端59aが穿刺針11から離れるように弾性的に曲げ変形が可能である。このため、アダプタ組立体1を、キャップ88の外径が異なる複数種類のバイアルに適応させることができる。また、アダプタ組立体1をバイアル80に装着する過程でガイドバー59の先端59aがバイアル80の肩部85に衝突しても、ガイドバー59は適宜曲げ変形するので、穿刺針11を栓体87に所望する深さまで穿刺することができる。 The guide bar 59 can be elastically bent and deformed so that its tip 59 a is separated from the puncture needle 11. Therefore, the adapter assembly 1 can be adapted to a plurality of types of vials having different outer diameters of the cap 88. Also, even if the tip 59a of the guide bar 59 collides with the shoulder 85 of the vial 80 in the process of attaching the adapter assembly 1 to the vial 80, the guide bar 59 is appropriately bent and deformed. It can be punctured to the desired depth.
 本実施形態では、栓体87の中心に対して穿刺針11の先端11aを位置合わせする「ガイド機構」としてガイドバー59を備えたが、本発明のガイド機構の構成はこれに限定されない。例えば、ガイド機構の形状は本実施形態に限定されず、適宜変更してよい。ガイド機構が、外力が印加されていない自然状態において、ガイドバー59のように穿刺針11と平行に直線状に延びている必要はなく、例えば、その先端(先端59a)に近づくにしたがって穿刺針11から離れるように湾曲していてもよい。ガイド機構が、ガイドバー59の先端59aが周方向に延ばされた略「T」字状を有していてもよい。あるいは、ガイド機構が、周方向に隣り合う2本のガイドバー59の先端59aが接続された略「U」状を有していてもよい。ガイド機構の水平面に沿った断面形状についても制限はなく、例えば、円形、楕円形、穿刺針11と同心の円弧などであってもよい。ガイド機構は、半径方向の弾性曲げ変形が実質的に不可能であってもよい。ガイド機構の数や配置も、本実施形態に限定されず、適宜変更してよい。ガイド機構の数は、1つでもよいが、2以上であることが好ましい。複数のガイド機構は、穿刺針11を中心として等角度間隔で配置することができる。あるいは、一対以上のガイド機構の対を、対をなす2つのガイド機構を穿刺針11を挟んで対向させた状態で、穿刺針11の周囲に離間して配置してもよい。 In the present embodiment, the guide bar 59 is provided as a "guide mechanism" for aligning the tip 11a of the puncture needle 11 with the center of the plug 87, but the configuration of the guide mechanism of the present invention is not limited thereto. For example, the shape of the guide mechanism is not limited to this embodiment, and may be changed as appropriate. The guide mechanism does not have to extend linearly in parallel with the puncture needle 11 like the guide bar 59 in a natural state where no external force is applied. For example, the puncture needle approaches the tip (tip 59a) It may be curved away from 11. The guide mechanism may have a substantially "T" shape in which the tip end 59a of the guide bar 59 is circumferentially extended. Alternatively, the guide mechanism may have a substantially "U" shape in which the tips 59a of two guide bars 59 adjacent in the circumferential direction are connected. The cross-sectional shape of the guide mechanism along the horizontal plane is also not limited, and may be, for example, a circle, an ellipse, or an arc concentric with the puncture needle 11. The guide mechanism may be substantially incapable of radial elastic bending. The number and arrangement of the guide mechanisms are not limited to the present embodiment, and may be changed as appropriate. The number of guide mechanisms may be one, but is preferably two or more. The plurality of guide mechanisms can be arranged at equal angular intervals about the puncture needle 11. Alternatively, the pair of guide mechanisms may be spaced apart from each other around the puncture needle 11 in a state where the two guide mechanisms forming the pair face each other with the puncture needle 11 interposed therebetween.
 カバー50は、アダプタ10のコネクタ40を収納することができるコネクタケース51を備える。コネクタケース51は、コネクタ40の天板48や、その開口48aを介して露出された隔壁部材45を覆う。例えば、上述したように、コネクタ40にオスコネクタを接続する直前までアダプタ10にカバー50を装着しておけば、バイアル80へのアダプタ組立体1の装着や、その後のバイアル80の移動などにおいて作業者の指などがコネクタ40に触れることはない。従って、コネクタ40の衛生状態を良好に維持することができる。また、薬液調製後、バイアル80に装着されたアダプタ10に、再度、カバー50を装着して、バイアル80を廃棄すれば、危険な薬剤による被曝の可能性を低減することができる。 The cover 50 includes a connector case 51 capable of housing the connector 40 of the adapter 10. The connector case 51 covers the top plate 48 of the connector 40 and the partition wall member 45 exposed through the opening 48 a. For example, as described above, if the cover 50 is attached to the adapter 10 just before connecting the male connector to the connector 40, the operation in attachment of the adapter assembly 1 to the vial 80, movement of the vial 80 thereafter, etc. The finger of the person does not touch the connector 40. Therefore, the sanitary condition of the connector 40 can be maintained well. In addition, after the chemical solution is prepared, if the cover 50 is attached again to the adapter 10 attached to the vial 80 and the vial 80 is discarded, the possibility of exposure to dangerous chemicals can be reduced.
 コネクタケース51は、カバー50の上部に配置されている。このため、作業者は、カバー50を保持する際、コネクタケース51を指で摘まむ可能性が高い。例えば、図6の状態において、作業者は、コネクタケース51を摘まんで、アダプタ組立体1をバイアル80に向かって押し込むことができる。 The connector case 51 is disposed on the top of the cover 50. Therefore, when holding the cover 50, the worker is likely to pick the connector case 51 with a finger. For example, in the state of FIG. 6, the operator can push the adapter assembly 1 toward the vial 80 by pinching the connector case 51.
 上記とは異なり、アダプタ組立体1をバイアル80に装着する際に、作業者が、カバー50から半径方向外向きに突出したアーム20の肩部21に下向きの力を加えてしまう場合を考える。上述したように、爪30がバイアル80のキャップ88を乗り越えるためには、爪30は半径方向外向きに変位する必要があり、このとき、アーム20は肩部21が上方に持ち上がるように曲げ変形する。作業者が肩部21に加える下向きの力は、アーム20のこの曲げ変形を阻害するように作用する。このため、バイアル80に対するアダプタ組立体1の装着作業が困難になったり、アーム20が破損(破断)したりするという問題が生じうる。 Differently from the above, it is assumed that when attaching the adapter assembly 1 to the vial 80, the operator applies a downward force to the shoulder 21 of the arm 20 projecting radially outward from the cover 50. As mentioned above, in order for the claw 30 to move over the cap 88 of the vial 80, the claw 30 needs to be displaced radially outward, and at this time, the arm 20 is bent and deformed so that the shoulder 21 is lifted upward. Do. The downward force applied by the operator to the shoulder 21 acts to inhibit this bending deformation of the arm 20. For this reason, the mounting operation of the adapter assembly 1 with respect to the vial 80 may be difficult, or the arm 20 may be broken (broken).
 カバー50の上部にコネクタケース51を設けた本実施形態では、作業者が、アーム20(特に肩部21)ではなく、コネクタケース51に下向きの力を加える可能性が高い。従って、上記の問題が生じる可能性は低い。 In the present embodiment in which the connector case 51 is provided on the top of the cover 50, the worker is likely to apply a downward force to the connector case 51 instead of the arm 20 (particularly the shoulder portion 21). Therefore, the above problems are unlikely to occur.
 コネクタケース51の周囲壁52には、互いに平行な一対の把持面53が設けられている。このため、図6の状態において、作業者は、2本の指で把持面53を摘まんだときに、アダプタ組立体1を最も安定的に保持することができる。換言すれば、作業者は、常に把持面53を摘まむように仕向けられる。例えば、作業者は、把持面53を、右手の親指と人差し指(または中指)とで摘まむことができる。この状態で、作業者は、アダプタ組立体1をバイアル80に向かって押し込む。作業者は、アダプタ10に触れることなく、アダプタ組立体1をバイアル80に装着することができる。従って、作業者がアーム20(特に肩部21)に触れる可能性が更に低減される。 The peripheral wall 52 of the connector case 51 is provided with a pair of gripping surfaces 53 parallel to each other. Therefore, in the state of FIG. 6, the operator can hold the adapter assembly 1 most stably when holding the gripping surface 53 with two fingers. In other words, the worker is always instructed to pick the gripping surface 53. For example, the worker can grasp the gripping surface 53 with the thumb and forefinger (or middle finger) of the right hand. In this state, the operator pushes the adapter assembly 1 toward the vial 80. The operator can attach the adapter assembly 1 to the vial 80 without touching the adapter 10. Therefore, the possibility of the worker touching the arm 20 (especially the shoulder 21) is further reduced.
 本実施形態では、コネクタケース51の周囲壁52の下端から、半径方向外向きに拡張板58が突出している。コネクタケース51(特にその把持面53)を片方の手の指で摘まんで下向きの力を加えるときに、指を拡張板58の上面に当てることができる。従って、拡張板58は、アダプタ組立体1をバイアル80に装着する際に、アダプタ組立体1に下向きの力を加えるのを容易にする。また、拡張板58は、作業者の指が拡張板58から下方に延びるのを防止するので、指がアーム20に触れてアーム20に下向きの力を誤って加えてしまう可能性を低減する。 In the present embodiment, the expansion plate 58 protrudes radially outward from the lower end of the peripheral wall 52 of the connector case 51. When the connector case 51 (particularly its gripping surface 53) is pinched by the finger of one hand to apply a downward force, the finger can be applied to the upper surface of the expansion plate 58. Thus, the spreader plate 58 facilitates applying a downward force to the adapter assembly 1 when attaching the adapter assembly 1 to the vial 80. In addition, since the extension plate 58 prevents the operator's finger from extending downward from the extension plate 58, the possibility of the finger touching the arm 20 and erroneously applying a downward force to the arm 20 is reduced.
 拡張板58は、一対の把持面53が対向する方向(Y軸方向)に長軸を有する。この結果、把持面53から半径方向外向きに突出した拡張板58の突出長さは、把持面53以外の周囲壁52から半径方向外向きに突出した拡張板58の突出長さより概して大きくなる。これは、把持面53を指で摘まんで下向きの力を加えるときに、相対的に大きな突出長さを有する拡張板58の部分に指を当てることができるので、アダプタ組立体1に下向き力を加えるのを更に容易にする。 The extension plate 58 has a major axis in the direction (Y-axis direction) in which the pair of gripping surfaces 53 face each other. As a result, the projecting length of the expansion plate 58 projecting radially outward from the gripping surface 53 is generally larger than the projecting length of the expanding plate 58 projecting radially outward from the peripheral wall 52 other than the gripping surface 53. This is because when the gripping surface 53 is pinched with a finger and a downward force is applied, a finger can be applied to the portion of the expansion plate 58 having a relatively large projecting length, so that the adapter assembly 1 is given a downward force. Makes it easier to add.
 拡張板58は、アーム20よりも高い位置にある。コネクタケース51を摘まんでいる指やそれ以外の指は拡張板58に当たるので、これらの指が拡張板58より低い位置にあるアーム20に触れる可能性は低い。従って、拡張板58は、アダプタ組立体1をバイアル80に装着する際に、作業者の指がアーム20に触れてアーム20に下向きの力を誤って加えてしまう可能性を低減するのに有利である。 The extension plate 58 is at a higher position than the arm 20. Since the finger gripping the connector case 51 and the other fingers hit the extension plate 58, the possibility that these fingers touch the arm 20 located lower than the extension plate 58 is low. Therefore, the expansion plate 58 is advantageous for reducing the possibility that the operator's finger touches the arm 20 and erroneously applies a downward force to the arm 20 when attaching the adapter assembly 1 to the vial 80. It is.
 一対の把持面53が対向する方向(Y軸方向)は、一対のアーム20が対向する方向(X軸方向)と直交する。例えば一対の把持面53を右手の親指と人差し指とで摘まんでアダプタ組立体1をバイアル80に向かって押し込む場合、通常、中指は、人差し指の近傍、即ち把持面53の近傍、に配置される。中指の下方にはアーム20は存在しないので、たとえ中指が拡張板58よりも下に延びたとしても、その中指がアーム20に触れてアーム20に下向きの力を誤って加えてしまう可能性は低い。これに対して、本実施形態と異なり、一対の把持面53が対向する方向が一対のアーム20が対向する方向と一致している場合、中指が拡張板58よりも下に延びてしまうと、中指がアーム20(特にその肩部21)に下向きの力を誤って加えてしまう事態が起こりうる。この場合、上記の問題が生じる可能性がある。このように、本実施形態では、把持面53が向く方向が、アーム20が延びる方向に対して直角であるので、把持面53を摘まんだ指以外の指がアーム20に触れてアーム20に下向きの力を誤って加えてしまう可能性が低い。 The direction (Y-axis direction) in which the pair of gripping surfaces 53 face is orthogonal to the direction (X-axis direction) in which the pair of arms 20 face. For example, when the pair of gripping surfaces 53 is pinched with the right thumb and forefinger and the adapter assembly 1 is pushed toward the vial 80, the middle finger is usually disposed in the vicinity of the forefinger, that is, near the gripping surface 53. Because there is no arm 20 below the middle finger, even if the middle finger extends below the expansion plate 58, there is a possibility that the middle finger will touch the arm 20 and inadvertently apply a downward force to the arm 20. Low. On the other hand, unlike the present embodiment, when the direction in which the pair of gripping surfaces 53 opposes matches the direction in which the pair of arms 20 opposes, if the middle finger extends below the extension plate 58, It can happen that the middle finger accidentally applies a downward force to the arm 20 (especially its shoulder 21). In this case, the above problem may occur. As described above, in the present embodiment, since the direction in which the gripping surface 53 faces is perpendicular to the extending direction of the arm 20, a finger other than the finger holding the gripping surface 53 touches the arm 20 to contact the arm 20. It is unlikely to accidentally apply a downward force.
 なお、本発明では、拡張板58の平面視形状は、本実施形態に限定されず、任意である。例えば、拡張板58は、カバー50と同心の円形であってもよく、あるいはX軸方向に長軸を有する非円形であってもよい。拡張板58は、XY面に平行である必要はなく、例えばその外周端縁に向かって下降するように傾斜していてもよい。 In addition, in this invention, the planar view shape of the expansion board 58 is not limited to this embodiment, It is arbitrary. For example, the expansion plate 58 may be circular, concentric with the cover 50, or non-circular having a major axis in the X-axis direction. The expansion plate 58 does not have to be parallel to the XY plane, and may be inclined, for example, to descend toward its outer peripheral edge.
 また、本発明では、拡張板58を省略してもよい。例えば、コネクタケース51の周囲壁52の下端からガイドバー59が下方に向かって延びていてもよい。 In the present invention, the expansion plate 58 may be omitted. For example, a guide bar 59 may extend downward from the lower end of the peripheral wall 52 of the connector case 51.
 把持面53は、厳密な意味で平面である必要はない。把持性や滑り止め性を向上させるために、把持面53に、複数の突起または複数のリブ(直線状の突起)が設けられていてもよく、あるいは、把持面53の全体が滑らかな凹曲面で構成されていてもよい。 The gripping surface 53 need not be planar in the strict sense. The gripping surface 53 may be provided with a plurality of protrusions or a plurality of ribs (linear protrusions) in order to improve the gripping property and non-slip property, or the entire gripping surface 53 is a smooth concave surface May be composed of
 コネクタケース51の周囲壁52は、作業者が常に特定の面のみを把持するように構成されていなくてもよい。例えば、一対の把持面53を省略し、周囲壁52の外周面が、円筒面、多角柱面(例えば、六角柱面、八角柱面)等の任意の形状を有していてもよい。この場合、作業者は、コネクタケース51の周囲壁52を、2本の指で任意の方向に把持しうる。 The peripheral wall 52 of the connector case 51 may not be configured to always hold only a specific surface by the operator. For example, the pair of gripping surfaces 53 may be omitted, and the outer peripheral surface of the peripheral wall 52 may have any shape such as a cylindrical surface or a polygonal cylindrical surface (for example, a hexagonal cylindrical surface or an octagonal cylindrical surface). In this case, the worker can grip the peripheral wall 52 of the connector case 51 with two fingers in any direction.
 コネクタケース51の内周面に設けられたリブ56は、カバー50をアダプタ10と同軸にするための「軸合わせ構造」として機能する。ケース50がアダプタ10と同軸に配置されることは、栓体87の中心に対する穿刺針11の先端11aの位置合わせの精度を向上させるのに有利である。 The rib 56 provided on the inner peripheral surface of the connector case 51 functions as a “axis alignment structure” for making the cover 50 coaxial with the adapter 10. The coaxial arrangement of the case 50 with the adapter 10 is advantageous for improving the accuracy of the alignment of the tip 11 a of the puncture needle 11 with the center of the plug 87.
 本実施形態では軸合わせ構造が4本のリブ56で構成されたが、本発明の軸合わせ構造はこれに限定されない。例えば、リブ56を省略し、キャップ47の周囲壁49及び/又は環状突起41bの外径とほぼ同じ内径を有するように構成されたコネクタケース51の周囲壁52の内周面を、軸合わせ構造として使用してもよい。 In the present embodiment, the axial alignment structure is constituted by four ribs 56, but the axial alignment structure of the present invention is not limited to this. For example, the inner peripheral surface of the peripheral wall 52 of the connector case 51 which is configured to omit the rib 56 and has an inner diameter substantially the same as the outer diameter of the peripheral wall 49 of the cap 47 and / or the annular protrusion 41b It may be used as
 リブ56から突出した突起57は、アダプタ10に係合する「係合構造」として機能する。係合構造は、カバー50がアダプタ10に装着されたアダプタ組立体1をカバー50(特にそのコネクタケース51)を摘まんで持ち上げたとき、アダプタ10がカバー50から抜け落ちるのを防ぐ。このため、アダプタ組立体1のバイアル80への装着作業を容易に行うことができる。 The projections 57 protruding from the ribs 56 function as an "engagement structure" for engaging the adapter 10. The engagement structure prevents the adapter 10 from falling off the cover 50 when the cover 50 (in particular, its connector case 51) is picked up and lifted from the adapter assembly 1 in which the cover 50 is attached to the adapter 10. Thus, the mounting operation of the adapter assembly 1 to the vial 80 can be easily performed.
 本実施形態では係合構造はリブ56に設けられた突起57で構成されたが、本発明の係合構造はこれに限定されない。例えば、アダプタ10に係合する突起を、コネクタケース51のリブ56以外の周囲壁52の内周面に設けてもよい。アダプタ10に係合する突起が、周囲壁52の内周面に環状に連続していてもよい。突起は、アダプタ10の環状突起41b以外の箇所に係合するように構成されていてもよい。係合構造は、突起である必要はなく、凹部(溝を含む)であってもよい。また、係合構造は、カバー50の、コネクタケース51以外の箇所に設けてもよい。例えば、アダプタ10から半径方向に突出した凸部17(図2A参照)と係合する凹部又は突起をカバー50に設けてもよい。 In the present embodiment, the engagement structure is constituted by the projection 57 provided on the rib 56, but the engagement structure of the present invention is not limited to this. For example, the protrusion engaged with the adapter 10 may be provided on the inner peripheral surface of the peripheral wall 52 other than the rib 56 of the connector case 51. A protrusion engaging the adapter 10 may be annularly continuous with the inner circumferential surface of the circumferential wall 52. The protrusions may be configured to engage with the adapter 10 at locations other than the annular protrusion 41 b. The engagement structure need not be a protrusion but may be a recess (including a groove). In addition, the engagement structure may be provided at a location of the cover 50 other than the connector case 51. For example, the cover 50 may be provided with a recess or protrusion that engages with a protrusion 17 (see FIG. 2A) radially projecting from the adapter 10.
 本発明は、バイアルに装着されるアダプタ組立体として広範囲に利用することができる。中でも医療分野において好ましく利用することができる。バイアル内の薬剤の種類は限定されないが、抗がん剤のような劇薬である場合に好適である。 The present invention can be widely used as an adapter assembly attached to a vial. Above all, it can be preferably used in the medical field. The type of drug in the vial is not limited, but is suitable when it is a potent drug such as an anticancer drug.
1 アダプタ組立体
10 アダプタ
11 穿刺針
20 アーム
30 爪
40 コネクタ
50 カバー
51 コネクタケース
52 コネクタケースの周囲壁
53 把持面
56 リブ(軸合わせ構造)
57 突起(係合構造)
58 拡張板
59 ガイドバー(ガイド機構)
59a ガイドバーの先端
80 バイアル
83 フランジ
87 栓体
Reference Signs List 1 adapter assembly 10 adapter 11 puncture needle 20 arm 30 claw 40 connector 50 cover 51 connector case 52 peripheral wall of connector case 53 grip surface 56 rib (alignment structure)
57 Protrusion (engagement structure)
58 Expansion plate 59 Guide bar (guide mechanism)
59a Guide bar tip 80 vial 83 flange 87 stopper

Claims (12)

  1.  バイアルに装着可能なアダプタと、前記アダプタに上方から分離可能に装着されたカバーとを備えたアダプタ組立体であって、
     前記アダプタは、前記バイアルの栓体を穿刺可能な穿刺針と、前記バイアルの拡径したフランジに係合可能な複数の爪と、前記複数の爪が設けられた弾性的に曲げ変形可能な複数のアームとを備え、
     前記カバーは、前記穿刺針に対向するように延びたガイド機構を備え、
     前記カバーが前記アダプタに装着された状態において、前記ガイド機構は、前記穿刺針よりも更に下方に向かって延びていることを特徴とするアダプタ組立体。
    An adapter assembly comprising: a vial mountable adapter; and a cover separably mounted from above on said adapter, comprising:
    The adapter is provided with a puncture needle capable of piercing the stopper of the vial, a plurality of claws engageable with the enlarged flange of the vial, and a plurality of elastically bendable plurality provided with the plurality of claws. Equipped with an arm,
    The cover includes a guide mechanism extending to face the puncture needle.
    An adapter assembly characterized in that the guide mechanism extends further downward than the puncture needle when the cover is attached to the adapter.
  2.  前記カバーは複数の前記ガイド機構を備え、
     前記複数のガイド機構は、前記穿刺針と同心の円に沿って配置されている請求項1に記載のアダプタ組立体。
    The cover includes a plurality of the guide mechanisms,
    The adapter assembly according to claim 1, wherein the plurality of guide mechanisms are arranged along a circle concentric with the puncture needle.
  3.  前記ガイド機構は、その先端が前記穿刺針から離れるように弾性的に変形可能である請求項1又は2に記載のアダプタ組立体。 The adapter assembly according to claim 1 or 2, wherein the guide mechanism is elastically deformable such that its tip is separated from the puncture needle.
  4.  前記アダプタは、前記穿刺針に連通したコネクタを備え、
     前記カバーは前記コネクタを収納するコネクタケースを備える請求項1~3のいずれか一項に記載のアダプタ組立体。
    The adapter comprises a connector in communication with the puncture needle,
    The adapter assembly according to any one of claims 1 to 3, wherein the cover comprises a connector case for housing the connector.
  5.  前記コネクタケースは、前記カバーの上部に配置されている請求項4に記載のアダプタ組立体。 The adapter assembly according to claim 4, wherein the connector case is disposed on the top of the cover.
  6.  前記コネクタケースの周囲壁に互いに平行な一対の把持面が設けられている請求項4又は5に記載のアダプタ組立体。 The adapter assembly according to claim 4 or 5, wherein the peripheral wall of the connector case is provided with a pair of gripping surfaces parallel to each other.
  7.  前記コネクタケースの前記周囲壁の下端から、半径方向の外向きに拡張板が突出している請求項6に記載のアダプタ組立体。 The adapter assembly according to claim 6, wherein an expansion plate protrudes radially outward from the lower end of the peripheral wall of the connector case.
  8.  前記拡張板は、前記一対の把持面が対向する方向に長軸を有する請求項7に記載のアダプタ組立体。 The adapter assembly according to claim 7, wherein the expansion plate has a major axis in a direction in which the pair of gripping surfaces face each other.
  9.  前記拡張板は、前記複数のアームよりも高い位置にある請求項7又は8に記載のアダプタ組立体。 The adapter assembly according to claim 7, wherein the extension plate is at a higher position than the plurality of arms.
  10.  前記複数のアームは、前記穿刺針の長手方向に直交する第1方向に対向するように配置されており、
     前記一対の把持面は、前記第1方向に直交し且つ前記穿刺針の長手方向に直交する第2方向に対向するように配置されている請求項6~9のいずれか一項に記載のアダプタ組立体。
    The plurality of arms are disposed to face each other in a first direction orthogonal to the longitudinal direction of the puncture needle,
    The adapter according to any one of claims 6 to 9, wherein the pair of gripping surfaces are arranged to face in a second direction orthogonal to the first direction and orthogonal to the longitudinal direction of the puncture needle. Assembly.
  11.  前記カバーを前記アダプタと同軸に軸合わせする軸合わせ構造が、前記カバーに設けられている請求項1~10のいずれか一項に記載のアダプタ組立体。 The adapter assembly according to any one of the preceding claims, wherein an alignment structure is provided on the cover for coaxial alignment of the cover with the adapter.
  12.  前記カバーから前記アダプタが抜け落ちないように前記アダプタに係合する係合構造が、前記カバーに設けられている請求項1~11のいずれか一項に記載のアダプタ組立体。 The adapter assembly according to any one of the preceding claims, wherein an engagement structure is provided on the cover for engaging the adapter so as to prevent the adapter from falling off the cover.
PCT/JP2018/028275 2017-08-03 2018-07-27 Adaptor assembly WO2019026796A1 (en)

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