Electrotransport drug delivery reservoirs containing inert fillers

• US 6,246,904 B1
• Filed: 11/07/1997
• Issued: 06/12/2001
• Est. Priority Date: 12/17/1996
• Status: Expired due to Term

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Murdock, Thomas O.
• Primary Examiner(s): MENDEZ, MANUEL A
• Application Number:
  US08/965,881
• Time in Patent Office: 1,313 Days
• Field of Search: 604/20-22, 424/449, 424/448, 264/494
• US Class Current: 604/20
• CPC Class Codes: A61N 1/0448 Drug reservoir

Abstract

A novel electrotransport drug delivery system (10) and therapeutic agent-containing reservoir (26, 28) for use therein are provided. An inert filler material effective to reduce the quantity of therapeutic agent otherwise present is incorporated in the reservoir (26, 28) along with the therapeutic agent to be delivered via electrotransport. Methods for making the reservoir (26, 28) and drug delivery system (10) are provided as well.

Claims

1. An electrotransport agent delivery device, comprising a donor electrode, a counter electrode and a source of electrical power adapted to be electrically connected to the donor and counter electrodes, wherein the donor electrode is electrically connected to a donor reservoir having a predetermined volume (V) and being comprised of a polymeric matrix containing a predetermined quantity (q) of a therapeutic agent to be delivered, the polymeric matrix also containing an inert filler material having substantially no tendency to interact with the agent, the inert filler being present in the matrix in a form which allows electrotransport of the agent through and from the reservoir to a patient body surface, the inert filler material being present in the polymeric matrix in an amount which achieves a concentration (ρ

) of therapeutic agent in the matrix which exceeds q/V.

2. The device of claim 1, wherein the polymeric matrix is comprised of a water-swellable polymer selected from the group consisting of polyvinyl alcohols, polyvinylpyrrolidone, cellulosic polymers, polyurethanes, polyethylene oxide, polyanhydrides, polyvinyl pyrrolidone/vinyl acetate copolymers, and mixtures and copolymers thereof.

3. The device of claim 1, wherein the inert filler material has substantially no tendency to bind, absorb, adsorb or react chemically with the therapeutic agent.

4. The device of claim 1, wherein the inert filler material comprises up to about 60 vol. % of the polymeric matrix.

5. The device of claim 1, wherein the inert filler material comprises about 5 vol. % to 60 vol. % of the polymeric matrix.

6. The device of claim 1, wherein the inert filler material comprises about 20 vol. % to 60 vol. % of the polymeric matrix.

7. The device of claim 1, wherein the inert filler material comprises about 40% vol. % to 60 vol. % of the polymeric matrix.

8. The device of claim 1, wherein the inert filler is in the form of solid particles or fibers dispersed in the polymeric matrix.

9. The device of claim 8, wherein the inert filler material is selected from the group consisting of glass beads, polymer powders, polymer beads, polymer solids, cellulose polymers, mineral fillers, and mixtures thereof.

10. The device of claim 1, wherein the inert filler material is comprised of a polymer mesh.

11. The device of claim 10, wherein the polymer mesh is comprised of polypropylene.

12. The device of claim 9, wherein the inert filler is comprised of a polymer powder.

13. The device of claim 12, wherein the polymer powder comprises a micronized polymer with particle size of about 1 μ

m to about 50 μ

m.

14. The device of claim 13, wherein the micronized polymer is selected from the group consisting of polyethylene waxes, polypropylene waxes, polytetrafluoroethylene waxes, Fischer-Tropsch waxes, and mixtures thereof.

15. The device of claim 9, wherein the inert material comprises beads of a crosslinked polymeric material.

16. The device of claim 15, wherein the crosslinked polymeric material is selected from the group consisting of acrylic/divinylbenzene copolymers, styrene/divinylbenzene copolymers, and mixtures thereof.

17. The device of claim 9, wherein the inert filler is comprised of a polymer solid.

18. The device of claim 17, wherein the polymer solid is selected from the group consisting of polyvinyl alcohol, polyvinylpyrrolidone, and mixtures thereof.

19. The device of claim 9, wherein the inert filler is comprised of a mineral filler material.

20. The device of claim 19, wherein the mineral filler material is selected from the group consisting of titanium dioxide, mica, quartz powder, talc, and mixtures thereof.

21. A donor reservoir for an electrotransport agent delivery device, the reservoir having a predetermined volume (V) and being comprised of a polymeric matrix containing a predetermined quantity (q) of a therapeutic agent to be delivered, the polymeric matrix also containing an inert filler material having substantially no tendency to interact with the agent, the inert filler being present in the matrix in a form which allows electrotransport of the agent through and from the reservoir to a patient body surface, the inert filler material being present in the polymeric matrix in an amount which achieves a concentration (ρ

) of therapeutic agent in the matrix which exceeds q/V.

22. The reservoir of claim 21, wherein the polymer matrix comprises a water-swellable polymer selected from the group consisting of polyvinyl alcohols, polyvinyl pyrrolidone, cellulosic polymers, polyurethanes, polyethylene oxide, polyanhydrides, polyvinyl pyrrolidone/vinyl acetate copolymers, and mixtures and copolymers thereof.

23. The reservoir of claim 21, wherein the inert filler material has substantially no tendency to bind, absorb, adsorb or react chemically with the therapeutic agent.

24. The reservoir of claim 21, wherein the inert filler material comprises up to about 60 vol. % of the polymeric matrix.

25. The reservoir of claim 21, wherein the inert filler material comprises about 5 vol. % to 60 vol. % of the polymeric matrix.

26. The reservoir of claim 21, wherein the inert filler material comprises about 20 vol. % to 60 vol. % of the polymeric matrix.

27. The reservoir of claim 21, wherein the inert filler material comprises about 40 vol. % to 60 vol. % of the polymeric matrix.

28. The reservoir of claim 21, wherein the inert filler is in the form of solid particles or fibers dispersed in the polymeric matrix.

29. The reservoir of claim 28, wherein the inert filler material is selected from the group consisting of glass beads, polymer powders, polymer beads, polymer solids, cellulose polymers, mineral fillers, and mixtures thereof.

30. The reservoir of claim 21, wherein the inert filler is comprised of a polymer mesh.

31. A method for increasing the volume (V) of a polymeric donor reservoir for an electrotransport delivery device, the reservoir containing a predetermined quantity (q) of the therapeutic agent to be delivered, without decreasing the concentration (ρ

) of the therapeutic agent in the reservoir, the method comprising placing a predetermined amount of an inert filler material in a polymer matrix, the filler material having substantially no tendency to interact with the therapeutic agent, to produce a donor reservoir comprised of a drug- and inert filler-containing polymer matrix.