Polymeric foam reservoirs for an electrotransport delivery device

• US 6,650,934 B2
• Filed: 11/07/1997
• Issued: 11/18/2003
• Est. Priority Date: 12/17/1996
• Status: Expired due to Term

• Current Assignee: Thomas O. Murdock
• Original Assignee: Thomas O. Murdock
• Inventors: Murdock, Thomas O.
• Primary Examiner(s): Casler, Brian L.
• Assistant Examiner(s): Thissell, Jeremy
• Application Number:
  US08/966,437
• Publication Number:
  US 20020042587A1
• Time in Patent Office: 2,202 Days
• Field of Search: 604/20-22, 424/449, 424/448, 264/494, 521/141
• US Class Current: 604/20
• CPC Class Codes: A61K 9/0009 involving or responsive to electricity, magnetism or acoustic waves; Galenical aspects of sonophoresis, iontophoresis, electroporation or electroosmosis microelectromechanical systems A61K9/0097
• CPC Class Codes: A61N 1/0448 Drug reservoir

Abstract

A method is provided for preparing a novel therapeutic agent-containing reservoir (26, 28) for use in conjunction with an electrotransport drug delivery system (10). A polymeric matrix is foamed in a selected atmosphere and then cross-linked to form a polymeric closed-cell foam matrix reservoir (26, 28). The method enables relatively smaller quantities of therapeutic agent to be loaded into the electrotransport system (10) and is especially useful for the transdermal delivery of more costly drugs, such as peptides and proteins produced from genetically engineered cell lines, and/or highly potent drugs for which a small dosage is efficacious. Reservoirs (26, 28) prepared according to this method and electrotransport devices (10) containing such reservoirs are also provided.

Claims

1. A method of making a therapeutic agent-containing polymeric reservoir having a predetermined volume, the reservoir to be incorporated into an electrotransport agent delivery system adapted to deliver the therapeutic agent by electrotransport through an animal body surface, comprising the steps of:

(a) providing a polymer matrix;

(b) performing a step selected from the group consisting of;

i. placing a predetermined amount of the therapeutic agent in the polymer matrix and then foaming the polymer matrix with a gas to produce a polymeric foam matrix;

ii. simultaneously adding a predetermined amount of the therapeutic agent to the polymer matrix while foaming the polymer matrix with a gas to produce a polymeric foam matrix; and

iii. foaming the polymeric matrix with a gas to produce a polymeric foam matrix and then adding a predetermined amount of the therapeutic agent to the polymeric foam matrix;

(c) cross-linking the polymeric foam matrix to produce a polymeric closed-cell foam matrix reservoir having a predetermined pore volume, the matrix, upon hydration with a liquid solvent used to solubilize the therapeutic agent, having closed foam cells containing the gas and said closed foam cells being substantially free of the therapeutic agent and the liquid solvent and wherein the closed foam cells comprise about 25 to about 90 vol % of the polymeric foam matrix.

2. The method of claim 1, wherein the polymeric foam matrix is cross-linked using electromagnetic radiation, a chemical cross-linking agent or a freeze/thaw cycle.

3. The method of claim 2, wherein the polymer is selected from the group consisting of polyvinyl alcohols, polyvinyl pyrrolidones, cellulosic polymers, polyurethanes, polyethylene oxides, polyanhydrides, polyvinyl pyrrolidone/vinyl acetate copolymers, and mixtures thereof.

4. The method of claim 2, wherein the cross-linking is accomplished by means of a chemical cross-linking agent.

5. The method of claim 4, wherein the chemical cross-linking agent is selected from the group consisting of aldehydes, epoxides, borax, diisocyanates, and mixtures thereof.

6. The method of claim 1, wherein the cross linking of the foamed matrix is accomplished by freezing and thawing the matrix.

7. The method of claim 6, wherein the polymer comprises polyvinyl alcohol.

8. The method of claim 1, wherein the therapeutic agent is a protein, a polypeptide, or a fragment thereof.

9. The method of claim 1, wherein the gas is selected from the group consisting of air, carbon dioxide, oxygen, nitrogen, noble gases, and mixtures thereof.

10. A therapeutic agent-containing polymeric reservoir for an electrotransport therapeutic agent delivery system, the reservoir having a predetermined volume, the reservoir comprising a cross-linked polymeric closed-cell aqueous foam matrix containing a predetermined amount of the therapeutic agent and a predetermined volume percent of closed foam cells, the matrix, upon hydration with a liquid solvent used to solubilize the therapeutic agent, having closed foam cells containing a gas and being substantially free of the therapeutic agent and the liquid solvent wherein said closed foam cells comprise about 25 to about 90 vol % of the polymeric matrix.

11. The reservoir of claim 10, wherein the polymer matrix is electromagnetic radiation cross-linked, chemically cross-linked or freeze/thaw cross-linked.

12. The reservoir of claim 10, wherein the polymer is an electron beam cross-linked polymer selected from the group consisting of polyvinyl alcohols, polyvinyl pyrrolidones, cellulosic polymers, polyurethanes, polyethylene oxides, polyanhydrides, polyvinyl pyrrolidone/vinyl acetate copolymers, and mixtures thereof.

13. The reservoir of claim 10, wherein the polymer is a chemically cross-linked polymer selected from the group consisting of polyvinyl alcohols, polyvinyl pyrrolidones, cellulosic polymers, polyurethanes, polyethylene oxides, polyanhydrides, polyvinyl pyrrolidone/vinyl acetate copolymers, and mixtures thereof.

14. The reservoir of claim 10, wherein the polymer comprises a freeze/thaw cross-linked polyvinyl alcohol.

15. The reservoir of claim 10, wherein the therapeutic agent is a drug.

16. The reservoir of claim 10, wherein the therapeutic agent is a protein, a polypeptide, or a fragment thereof.

17. The reservoir of claim 10, wherein the gas is selected from the group consisting of air, carbon dioxide, oxygen, nitrogen, noble gases, and mixtures thereof.

18. An electrotransport delivery device comprising the reservoir of claim 10.

19. An electrotransport device for delivering a therapeutic agent through an animal body surface, the device comprising a donor electrode, a counter electrode, and a source of electrical power adapted to be electrically connected to the donor electrode and the counter electrode, the donor electrode being electrically connected to the therapeutic agent-containing reservoir of claim 10.