Modulating Drug Release Rate By Controlling The Kinetics Of The pH Transition In Hydrogels

• US 20110091549A1
• Filed: 03/16/2010
• Published: 04/21/2011
• Est. Priority Date: 10/16/2009
• Status: Abandoned Application

• Current Assignee: Confluent Surgical, Inc. (Medtronic Plc)
• Original Assignee: Confluent Surgical, Inc. (Medtronic Plc)
• Inventors: Blaskovich, Phillip, Costa, Daniel S., Ohri, Rachit
• Application Number:
  US12/724,458
• Publication Number:
  US 20110091549A1
• Time in Patent Office: Days
• US Class Current: 424/484
• CPC Class Codes: A61K 31/445 Non condensed piperidines, e.g. piperocaine
• CPC Class Codes: A61K 9/06 Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels composition of ointments, creams or gels A61K47/00

Abstract

Methods and compositions relate to modulating the release profile of drug molecules from a hydrogel by controlling the kinetics of the pH transition of the hydrogel. The hydrogel is formed by in situ polymerization and includes a drug molecule having a pKa between the pH of the formed hydrogel and the physiologic environment in which the hydrogel is placed.

Claims

1. A method comprising:

contacting a first hydrogel precursor with a first buffer;

contacting a second hydrogel precursor with a second buffer;

adding a bioactive agent to the first hydrogel precursor, the second hydrogel precursor, or both; and

contacting tissue with the first hydrogel precursor and the second hydrogel precursor,

wherein the first hydrogel precursor and second hydrogel precursor form a hydrogel upon contact, and wherein the bioactive agent has a pKa between the initial pH of the hydrogel at formation, and the physiologic pH.

2. The method according to claim 1, wherein forming the hydrogel further comprises a visualization agent.

3. The method according to claim 1, wherein the first hydrogel precursor possesses first functional groups and the second hydrogel precursor possesses second functional groups.

4. The method according to claim 3, further comprising:

delivering the first and second precursors onto an area of tissue so that a crosslinking reaction is facilitated between the first and second precursors.

5. The method according to claim 4, wherein the crosslinking reaction leads to gelation of the hydrogel from about 3 seconds to about 1 minute.

6. The method according to claim 1, wherein the physiologic environment has a pH of about 7.4.

7. The method according to claim 1, wherein the pH of the formed hydrogel is from about 5.0 to about 9.5.

8. The method according to claim 1, wherein the pH of the formed hydrogel is about 8.5.

9. The method according to claim 1, wherein the pKa of the bioactive agent is alkaline.

10. The method according to claim 1, wherein the first buffer, the second buffer, or both, comprises at least one alkalizer.

11. The method according to claim 1, wherein the pKa of the bioactive agent is acidic.

12. The method according to claim 1, wherein the first buffer, the second buffer, or both, comprises at least one acidifier.

13. A kit for producing a hydrogel comprising:

a first precursor;

a second precursor;

a first buffer for the first precursor;

a second buffer for the second precursor;

a bioactive agent; and

an applicator for substantially simultaneously delivering the bioactive agent, and the first and second precursors.

14. A hydrogel comprising:

a first precursor combined with a first buffer;

a second precursor combined with a second buffer;

a bioactive agent; and

wherein the pKa of the bioactive agent is greater than the pH of the hydrogel, and wherein the pH of the first buffer, the second buffer, or both, is selected to increase or decrease the release of the bioactive agent from the hydrogel.

15. The hydrogel of claim 14, wherein the increase or decrease in the release of the bioactive agent comprises an increase or decrease in a rate of release of the bioactive agent from the hydrogel.

16. The hydrogel of claim 14, wherein an amount of bioactive agent released from the hydrogel is increased or decreased at a time from about 30 minutes to about 4 days after administration.

17. The hydrogel of claim 14, wherein an amount of bioactive agent released from the hydrogel is increased or decreased at a time from about 1 day to about 60 days after administration.

18. The hydrogel of claim 14, wherein the pH of the first buffer, the second buffer, or both, is greater than the pKa of the bioactive agent, thereby decreasing the release of the bioactive agent from the hydrogel.

19. The hydrogel of claim 14, wherein the pH of the first buffer, the second buffer, or both, is less than the pKa of the bioactive agent, thereby increasing the release of the bioactive agent from the hydrogel.

20. A hydrogel comprising:

a first precursor combined with a first buffer;

a second precursor combined with a second buffer;

a bioactive agent; and

wherein the pKa of the bioactive agent is less than the pH of the hydrogel, and the pH of the first buffer, the second buffer, or both, is selected to increase or decrease the release of the bioactive agent from the hydrogel.

21. The hydrogel of claim 20, wherein the increase or decrease in the release of the bioactive agent comprises an increase or decrease in a rate of release of the bioactive agent from the hydrogel.

22. The hydrogel of claim 20, wherein an amount of bioactive agent released from the hydrogel is increased or decreased at a time from about 30 minutes to about 4 days after administration.

23. The hydrogel of claim 20, wherein an amount of bioactive agent released from the hydrogel is increased or decreased at a time from about 1 day to about 60 days after administration.

24. The hydrogel of claim 20, wherein the pH of the first buffer, the second buffer, or both, is less than the pKa of the bioactive agent, thereby decreasing the release of the bioactive agent from the hydrogel.

25. The hydrogel of claim 20, wherein the pH of the first buffer, the second buffer, or both, is greater than the pKa of the bioactive agent, thereby increasing the release of the bioactive agent from the hydrogel.