Iontophoretic delivery device and method of making same

• US 5,543,098 A
• Filed: 02/17/1994
• Issued: 08/06/1996
• Est. Priority Date: 03/11/1991
• Status: Expired due to Term

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Landrau, Felix A., Myers, Robert M.
• Primary Examiner(s): Green, Randall L.
• Assistant Examiner(s): Bockelman, Mark
• Application Number:
  US08/197,665
• Time in Patent Office: 901 Days
• Field of Search: 604/20, 607/149, 607/152, 264/104-105, 264/126, 264/160, 424/422-438, 424/447-449
• US Class Current: 264/104
• CPC Class Codes: A61N 1/0436 Material of the electrode
• CPC Class Codes: A61N 1/0448 Drug reservoir
• CPC Class Codes: A61N 1/30 Apparatus for iontophoresis, i.e. transfer of media in ionic state by an electromotoric force into the body, or cataphoresis

Abstract

An electrically powered transdermal iontophoretic delivery device (10, 20) and a method of making same is provided. The device utilizes electrode assemblies (8, 9) composed of a substantially homogenous blend of a polymeric matrix containing about 5 to 50 vol % of a conductive filler which forms a conductive network through the matrix, and up to about 50 vol % of the agent to be iontophoretically delivered through the skin. In the case of the donor electrode assembly, the agent is typically a drug and preferably a water soluble drug salt. In the case of the counter electrode assembly, the agent is typically an electrolyte salt. The homogenous blend eliminates the need for separate electrode and agent containing layers which require lamination.

Claims

1. A method of making an electrode assembly for an electrically powered iontophoretic delivery device, comprising:

homogeneously blending a mixture of about 5 to 50 vol % of a conductive filler, from about 1 to 50 vol % of a therapeutic agent to be iontophoretically delivered in order to obtain a therapeutic effect and the remainder a polymeric matrix; and

forming the agent-containing blended mixture into a sheet having a predetermined thickness, wherein the filler forms an electrically conductive network through the entire thickness of the matrix.

2. The method of claim 1, wherein the sheet is formed by pre-mixing the conductive filler and the therapeutic agent in the polymeric matrix and passing the matrix through a pair of opposing rollers rotating at different speeds and in opposite directions.

3. The method of claim 2, wherein the pair of opposed rolls rotating at different speeds and in opposite directions comprises a rubber mill.

4. The method of claim 2, further including calendering the sheet to a uniform thickness.

5. The method of claim 4, wherein the calendering comprises passing the sheet through a plurality of pairs of opposed calender rolls.

6. The method of claim 1, wherein the sheet is formed by pre-mixing the conductive filler and the therapeutic agent in the polymeric matrix and passing the matrix through multiple pairs of opposing rollers rotating at different speeds and in opposite directions.

7. The method of claim 6, further including calendering the sheet to a uniform thickness.

8. The method of claim 7, wherein the calendering comprises passing the sheet through a plurality of pairs of opposed calender rolls.

9. The method of claim 1, wherein the conductive filler comprises an electrochemically reactive material able to undergo oxidation or reduction during operation of the device.

10. The method of claim 9, wherein the electrochemically reactive material is selected from the group consisting of Ag, Zn, Cu, silver halides, copper halides and Ag₄ Fe(CN)₆.

11. The method of claim 1, wherein the conductive filler comprises an electrochemically inert material.

12. The method of claim 11, wherein the conductive filler is selected from the group consisting of carbon or graphite fibers, powdered carbon, graphite and electrochemically inert metals.

13. The method of claim 12, wherein the inert metal is selected from the group consisting of platinum, gold and stainless steel.

14. The method of claim 1, including homogenously blending about 10 to 50 vol % of a pore forming agent in the mixture.

15. The method of claim 1, wherein the polymeric matrix is selected from the group consisting of hydrophilic polymers, hydrophobic polymers and blends thereof.

16. The method of claim 1, wherein the polymeric matrix is comprised of a hydrophobic polymer selected from the group consisting of ethylene vinyl acetate copolymers, polyalkylenes, polyisoprenes, rubbers, polyisobutylene, polyvinylacetate, polyamides, polyurethanes, polyvinylchlorides, and modified cellulosic polymers.

17. The method of claim 1, wherein the polymeric matrix comprises an ethylene vinyl acetate copolymer.

18. The method of claim 1, wherein the polymeric matrix is comprised of a hydrophilic polymer selected from the group consisting of hydrogels, polyethylene oxides, cellulosic polymers, polyacrylic acids and polyvinyl pyrrolidones.

19. The method of claim 1, wherein the polymeric matrix comprises polyvinyl pyrrolidone.