Implantable electrophoretic pump for ionic drugs and associated methods

• US 4,639,244 A
• Filed: 07/12/1985
• Issued: 01/27/1987
• Est. Priority Date: 05/03/1983
• Status: Expired due to Term

• Current Assignee: Robinson John D Dr
• Original Assignee: Nabil I. Rizk
• Inventors: Rizk, Nabil I., Stevens, Charles L.
• Primary Examiner(s): Coven, Edward M.
• Assistant Examiner(s): Hindenburg, Max F.
• Application Number:
  US06/754,629
• Time in Patent Office: 564 Days
• Field of Search: 604/20, 604/21, 604/19, 604/140, 604/145, 604/150, 604/891-897, 604/151, 204/299 R
• US Class Current: 604/19
• CPC Class Codes: A61N 1/306 Arrangements where at least part of the apparatus is introduced into the body

Abstract

An implantable electrophoretic pump for ionic drugs and the method of using the same is provided. A reservoir is provided with a filler opening and a discharge opening. The discharge opening has a diffusion membrane and a pair of associated electrodes. A battery and electronic components provide for energizing the electrodes so as to effect ion transfer of the ionic drugs into other portions of the patient'"'"'s body through the voltage induced between the two electrodes. The pump is particularly useful for ionic drugs such as insulin, blood thinners, antibiotics and the like. A method of making a porous electrode.

Claims

1. An implantable electrophoretic pump for ionic drugs comprising

a housing,

a substantially fixed volume reservoir for storing said ionic drugs having a filler opening and a discharge opening,

said housing having opening means disposed generally adjacent to said filler opening and said discharge opening,

a filler member disposed within said filler opening and being self-sealing and adapted to be pierced by a reservoir filling member and upon removal of said filling member will resist leakage therethrough,

a reservoir discharge member disposed within said discharge opening and having a diffusion membrane and a pair of associated electrodes,

electrical energizing means for energizing said electrodes, and

the polarity of said electrodes being adapted to be connected such that when said electrodes are energized increased flow of said ionic drug through said discharge member will occur as compared with flow induced solely through diffusion when said electrodes are not energized, whereby said pump can deliver said ionic drugs electrophoretically.

2. The implantable electrophoretic pump of claim 1 wherein said electrical means includes battery means.

3. The implantable electrophoretic pump of claim 2 wherein said diffusion membrane is a passive diffusion membrane.

4. The implantable electrophoretic pump of claim 1 including said discharge member being in communication with the exterior of the housing through said opening means, and

said filler member being in communication with the exterior of said housing through said opening means.

5. The implantable electrophoretic pump of claim 3 including said passive diffusion membrane permitting the passage of said ionic drug therethrough under the influence of diffusion or electrophoresis or both.

6. The implantable electrophoretic pump of claim 1 including said diffusion membrane being an active membrane.

7. The implantable electrophoretic pump of claim 6 including said active membrane being an ion exchange membrane.

8. The implantable electrophoretic pump of claim 5 including said filler opening being disposed in a first wall of said reservoir, and

said discharge opening being disposed in a second wall of said reservoir.

9. The implantable electrophoretic pump of claim 8 including said first wall and said second wall being substantially perpendicular to each other.

10. The implantable electrophoretic pump of claim 5 including said electrodes being of porous construction.

11. The implantable electrophoretic pump of claim 5 including said electrodes being composed of a material selected from the group consisting of silver/silver chloride, carbon, carbon mesh and platinum.

12. The implantable electrophoretic pump of claim 5 including said reservoir having a chamber with a storage volume of about 15 to 25 milliliters.

13. The implantable electrophoretic pump of claim 5 including the interior of said reservoir except for the regions of said filler opening and said discharge opening having an interior coating of a material selected from a group consisting of resinous plastic and silicon rubber.

14. The implantable electrophoretic pump of claim 5 including electronic means energized by said battery means for energizing said electrodes during predetermined periods.

15. The implantable electrophoretic pump of claim 10 including electronic means having means for bolus activation which when activated is adapted to deliver additional quantities of said ionic drug.

16. The implantable electrophoretic pump of claim 15 including said bolus means adapted to be activated by means disposed exteriorly of the user.

17. The implantable electrophoretic pump of claim 14 including said electronic means having means for reversing the polarity of said electrodes.

18. The electrophoretic pump of claim 17 wherein said electronic means have means for charging the said electrode disposed closer to the interior of said reservoir with a charge of the type possessed by said ionic drug.

19. The implantable electrophoretic pump of claim 5 including said housing having an average height of about 15 to 25 mm., a maximum length of about 90 to 110 cm. and an average width of about 35 to 50 mm.

20. The implantable electrophoretic pump of claim 5 including said membrane being a passive membrane and said membrane being selected from the group consisting of cellulose esters, cellulose acetate, nylon polyvinylidene fluoride, polytetraflouroethylene and cellulose nitrates.

21. The implantable electrophoretic pump of claim 20 including said passive membrane having a thickness of about 100 to 200 microns and an area of about 0.5 to 5 cm².

22. The implantable electrophoretic pump of claim 5 including said reservoir being substantially cylindrical, and

said filler opening being disposed on one of the end walls.

23. The implantable electrophoretic pump of claim 22 including said discharge opening being disposed in a lateral wall of said reservoir.

24. The implantable electrophoretic pump of claim 23 including said housing having a generally triangular shape in plan.

25. The implantable electrophoretic pump of claim 1 including

said reservoir disposed within said housing.

26. The implantable electrophoretic pump of claim 1 including

said reservoir disposed externally of said housing and being in electrical communication therewith.

27. The implantable electrophoretic pump of claim 14 including said electronic means including capacitor means.

28. The implantable electrophoretic pump of claim 13 wherein said material is an ion exchange resin.

29. A reservoir for an implantable electrophoretic pump including

a hollow body defining a substantially fixed volume drug storage chamber,

a filler opening defined within said body,

a self-sealing member sealingly secured within said filler opening,

a discharge opening defined within said body,

a diffusion membrane sealingly secured within said discharge opening, and

a pair of electrodes having an electrode disposed on each side of said diffusion membrane whereby said reservoir can deliver said drug electrophoretically.

30. The reservoir of claim 29 including said diffusion membrane being a passive membrane.

31. The reservoir of claim 29 including said diffusion membrane being an active membrane.

32. The reservoir of claim 29 including said diffusion membrane being an ion exchange membrane.

33. The reservoir of claim 29 including said reservoir body being of substantially rigid construction.

34. The reservoir of claim 33 including said filler opening being in a wall oriented generally perpendicularly with respect to the wall in which said discharge opening is defined.

35. The reservoir of claim 34 including said reservoir being of generally cylindrical shape.

36. The reservoir of claim 30 including said passive membrane being of a material selected from the group consisting of cellulose esters, cellulose acetate, nylon, polyvinylidene flouride, polytetraflouroethylene and cellulose nitrates.

37. The reservoir of claim 35 including said passive membrane having a thickness of about 100 to 200 microns.

38. The reservoir of claim 37 including said passive membrane having an area of about 0.5 to 5 cm².

39. The reservoir of claim 37 including resilient member having reinforcing members.

40. A method of delivering an ionic drug within a patient comprising

providing an implantable electrophoretic pump having a housing within which is disposed a substantially fixed volume ionic drug storage reservoir having a filler opening sealed by a self-sealing membrane and a discharge opening sealed by a diffusion membrane having electrode means disposed on opposite sides of said diffusion membrane,

introducing an ionic drug into said reservoir,

implanting said pump in said patient,

effecting basal rate delivery of said ionic drug to said patient by diffusion, and

periodically energizing said electrode to effect alteration of the diffusion induced flow of ions out of said reservoir whereby said drug can be delivered electrophoretically.

41. The method of claim 40 wherein said diffusion membrane is a passive membrane.

42. The method of delivering an ionic drug of claim 40 including introducing said ionic drug into said reservoir prior to implantation of said pump.

43. The method of delivering an ionic drug of claim 40 including introducing said ionic drug into said reservoir after implantation of said pump.

44. The method of delivering an ionic drug of claim 40 including implanting said pump in said patient'"'"'s peritoneum.

45. The method of delivering an ionic drug of claim 42 including providing electronic means operatively associated with said electrode means within said pump, and

batteries disposed within said pump for energizing said electrodes.

46. The method of delivering an ionic drug of claim 45 including maintaining a substantially continuous flow of said ionic drug out of said reservoir by means of diffusion, and

periodically enhancing or retarding said diffusion rate of flow through energizing said electrodes.

47. The method of delivering an ionic drug of claim 46 including reversing polarity of said electrodes when it is desired to retard diffusion induced flow of said ionic drug.

48. The method of delivering an ionic drug of claim 47 including periodically replenishing the supply of said ionic drug by introducing a hypodermic needle into said reservoir through said self-sealing membrane.