Medicament Device

• US 20170028132A1
• Filed: 12/01/2014
• Published: 02/02/2017
• Est. Priority Date: 12/01/2013
• Status: Active Grant

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Raj, Abhijitsinh, Charvin, Matthieu, Booth, David, Cronenberg, Richard
• Granted Patent: US 10,391,245 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61M 2005/206 With automatic needle insertion
• CPC Class Codes: A61M 2005/2414 from the side
• CPC Class Codes: A61M 2005/247 with fixed or steady piercing means, e.g. piercing under movement of ampoule
• CPC Class Codes: A61M 5/142 Pressure infusion, e.g. using pumps
• CPC Class Codes: A61M 5/1454 spring-actuated, e.g. by a clockwork
• CPC Class Codes: A61M 5/162 Needle sets, i.e. connections by puncture between reservoir and tube ; Connections between reservoir and tube in jet-action syringes A61M5/30; connectors for tubes having sealed ends and a needle for piercing them A61M39/14
• CPC Class Codes: A61M 5/20 Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically A61M5/142 , A61M5/46 take precedence; hypodermic projectiles F42B12/54
• CPC Class Codes: A61M 5/2455 with sealing means to be broken or opened
• CPC Class Codes: A61M 5/2459 upon internal pressure increase, e.g. pierced or burst A61M5/2429 takes precedence
• CPC Class Codes: A61M 5/2466 by piercing without internal pressure increase A61M5/2429 takes precedence
• CPC Class Codes: A61M 5/31568 Means keeping track of the total dose administered, e.g. since the cartridge was inserted

Abstract

A method for creating a sterile connection with a fluid in a container. The container has a sealing member sealing a first end of the container, and a barrier sealing a chamber in fluid communication with the sealing member. The method includes providing a valve sleeve assembly that includes a flexible sleeve having a barrier portion at an end of the flexible sleeve, a hollow first penetrator disposed within the flexible sleeve, and a hollow second penetrator at least partially disposed within the first penetrator. An interior of the flexible sleeve is sterile. The method also includes piercing the barrier portion and the barrier with the first penetrator, and displacing the second penetrator relative to the first penetrator and the sealing member to pierce the sealing member and establish the sterile connection with an interior of the container.

Claims

1. An apparatus for making a sterile connection, comprising:

a container;

a sealing member sealing a first end of the container;

a barrier sealing a chamber in fluid communication with the sealing member; and

a valve sleeve assembly, comprising;

a flexible sleeve having a barrier portion at an end of the flexible sleeve, an interior of the flexible sleeve being sterile;

a hollow first penetrator adapted to displace relative to the flexible sleeve; and

a hollow second penetrator at least partially disposed within the first penetrator and adapted to displace relative to the first penetrator and the flexible sleeve;

wherein in an initial state, the flexible sleeve encloses the first penetrator and a penetrating end of the second penetrator;

wherein one of the container and the valve sleeve assembly is adapted to displace relative to the remaining one of the container and the valve sleeve assembly;

wherein the flexible sleeve is adapted to collapse, thereby displacing the outer penetrator relative to the flexible sleeve to pierce the barrier portion and the barrier; and

wherein upon further relative displacement between the container and the valve sleeve assembly, subsequent to the piercing of the barrier portion and the barrier, the second penetrator is adapted displace relative to the first penetrator, through the chamber, to pierce the sealing member to create a sterile connection with the interior of the container.

2. The apparatus according to claim 1, further comprising a spacing member interposed between the sealing member and the barrier, and at least partially defining the chamber.

3. The apparatus according to claim 1, wherein a piercing end of the second penetrator that pierces the sealing member does not contact the first penetrator.

4. The apparatus according to claim 1, wherein the first penetrator further comprises:

a penetrating portion; and

a collapsing portion connected to the penetrating portion.

5. The apparatus according to claim 4, wherein the collapsing portion comprises an elastomeric material.

6. The apparatus according to claim 4, wherein the collapsing portion comprises:

a base having a hole therethrough for passage of the second penetrator; and

at least one leg connecting the base and the penetrating portion.

7. A medical device in which the apparatus according to claim 1 is disposed, wherein the medical device is adapted for delivering medicament within the container to a patient, the medical device comprising:

a plunger adapted to induce the relative displacement between the container and the valve sleeve assembly; and

a patient needle fluidly connected to the second penetrator.

8. The device according to claim 7, further comprising:

a dose status indicator indicating an operating status of the medical device;

wherein the plunger comprises a cantilevered arm adapted to control timing of withdrawal of the patient needle back into the medical device and timing of a status change indicated by the dose status indicator.

9. The device according to claim 8, further comprising:

a needle actuator displaceably disposed within the medical device and adapted to control insertion of the patient needle; and

a release flipper displaceably disposed within the medical device and adapted to contact the plunger'"'"'s cantilevered arm and, subsequent to the patient needle'"'"'s extension outside the medical device, prevent displacement of the needle actuator until a predetermined displacement of the plunger has occurred and the cantilevered arm no longer contacts the release flipper.

10. The device according to claim 9, wherein the dose status indicator is fixedly disposed on the needle actuator.

11. The medical device according to claim 7, further comprising

a needle actuator displaceably disposed within the medical device and adapted to control insertion of the patient needle;

a release gate displaceably disposed within the medical device and adapted to selectively engage the plunger and prevent plunger displacement; and

an activation flipper displaceably disposed within the medical device and adapted to contact the needle actuator and release gate and, upon activation of the medical device and displacement of the needle actuator, induce disengagement of the release gate with the plunger to permit plunger displacement.

12. The medical device according to claim 7, further comprising:

a needle actuator displaceably disposed within the medical device and adapted to control insertion of the patient needle;

a trolley displaceably disposed within the medical device and adapted to hold the container and control displacement of the container toward the valve sleeve assembly; and

a locking mechanism, comprising;

a stop selectively engaging the trolley; and

a latch adapted to, upon displacement of the latch by the needle actuator, disengage the stop from the trolley, thereby permitting displacement of the trolley toward the valve sleeve assembly.

13. The medical device according to claim 7, further comprising a stopper displaceably disposed in a second end of the container opposite to the first end to define the interior volume of the container;

wherein the stopper is connected with the plunger.

14. The medical device according to claim 7, wherein:

the container is fixedly disposed within the medical device; and

the flexible sleeve is connected with an end of the plunger and the valve sleeve assembly displaces toward container as plunger displaces.

15. The medical device according to claim 14, wherein the sealing member comprises a stopper movably disposed within the container.

16. The medical device according to claim 14, wherein:

the first penetrator includes a cavity;

the second penetrator is fixedly disposed with respect to the plunger; and

the plunger comprises a protrusion on its distal end that enters into the cavity to advance the second penetrator relative to the first penetrator.

17. The medical device according to claim 1, wherein the barrier portion of the flexible sleeve comprises a membrane disposed across an opening at an end of the flexible sleeve.

18. The medical device according to claim 1, wherein the first penetrator comprises at least one internal rib frictionally engaging the second penetrator.

19. The medical device according to claim 1, further comprising:

a protective cap having;

a first portion thereof at least partially surrounding the first end of the container; and

a second portion thereof inserted into a recess in the sealing member;

wherein the barrier seals on opening in the second portion; and

an outer cap at least partially surrounding the protective cap and adapted to prevent the protective cap from disengaging from the container.

20. The medical device according to claim 19, wherein the second portion forms at least a portion of the chamber.

21. The medical device according to claim 19, wherein the first portion includes at least one cantilevered arm with a hook at its free end adapted to engage a catch disposed at the first end of the container.

22. A method for creating a sterile connection with a fluid in a container, the container having a sealing member sealing a first end of the container, and a barrier sealing a chamber in fluid communication with the sealing member, the method comprising:

providing a valve sleeve assembly, comprising;

a flexible sleeve having a barrier portion at an end of the flexible sleeve, an interior of the flexible sleeve being sterile;

a hollow first penetrator disposed within the flexible sleeve; and

a hollow second penetrator at least partially disposed within the first penetrator;

piercing the barrier portion and the barrier with the first penetrator;

displacing the second penetrator relative to the first penetrator and the sealing member to pierce the sealing member and establish the sterile connection with an interior of the container.

23. The method according to claim 22, wherein piercing the barrier portion and the barrier with the first penetrator comprises:

displacing the container toward the valve sleeve assembly;

contacting the valve sleeve assembly with the container; and

collapsing at least a portion of the flexible sleeve to pierce the barrier portion and the barrier with the first penetrator.