Drug-enhanced adhesion prevention

• US 8,394,399 B2
• Filed: 01/29/2008
• Issued: 03/12/2013
• Est. Priority Date: 02/17/2004
• Status: Active Grant

• Current Assignee: Ethicon Incorporated (Johnson & Johnson)
• Original Assignee: Ethicon Incorporated (Johnson & Johnson)
• Inventors: Young, Janel E., Wadsworth, Scott A., Cooper, Kevin, Rosenblatt, Joel, Cui, Han
• Primary Examiner(s): AZPURU, CARLOS A
• Application Number:
  US12/021,546
• Publication Number:
  US 20080119494A1
• Time in Patent Office: 1,869 Days
• Field of Search: None
• US Class Current: 424/423
• CPC Class Codes: A61K 9/1647 Polyesters, e.g. poly(lactide-co-glycolide)
• CPC Class Codes: A61P 41/00 Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution

Abstract

The present invention includes methods for the inhibition of post-operative adhesion formation between tissue surfaces in a body cavity having been subjected to a surgical procedure, which methods involve administering Pemirolast, or an analog thereof, directly to tissue surfaces in the body cavity in amounts and under conditions effective to inhibit formation of adhesions, and to delivery vehicles and compositions suitable for use for local, non-systemic administration of a drug to the body and directly to tissue within a body cavity having been subjected to a surgical procedure.

Claims

1. A method for the inhibition of post-operative adhesion formation in a body between tissue surfaces in a body cavity having been subjected to a surgical procedure comprising administering Pemirolast, or an analog thereof, directly to said tissue surfaces in said body cavity in amounts and under conditions effective to inhibit formation of adhesions thereon, wherein the Pemirolast, or analog thereof, is administered at a level of from about 0.01 milligram Pemirolast, or analog thereof, per kilogram of the body to about 3,000 Pemirolast, or analog thereof, per kilogram of the body.

2. The method of claim 1 wherein said Pemirolast or analog thereof is administered in cooperation with a delivery vehicle suitable for use in the local, non-systemic administration of a therapeutic agent to the body.

3. The method of claim 2 wherein said delivery vehicle is selected from the group consisting of microcapsules, microspheres, barriers, liposomes, lipid foams, solutions, compositions, osmotic pumps, fibers, filaments, gels, foams and films.

4. The method of claim 3 wherein said barrier is absorbable.

5. The method of claim 1 wherein said Pemirolast is administered in combination with a therapeutic agent, said therapeutic agent administered in an amount effective to provide the therapeutic effect intended by administration of said therapeutic agent.

6. The method of claim 5 wherein said therapeutic agent is selected from the group consisting of an anti-platelet, an anti-fibrotic, an anti-inflammatory, an anti-proliferative and an agent that inhibits collagen synthesis.

7. The method of claim 1 wherein said Pemirolast analog is selected from the group consisting of 3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrim-idin-4-one, 7-Methyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin- -4-one, 8-Methyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 7-Ethyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 7-n-Butyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 7-Phenyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 7-Chloro-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 7,9-dimethyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 9-Ethyl-3-(1H-Tetrazol-5-yl)-4H-pyridol[1,2-α

]pyrimidin-4-one, 8,9,1-,11-tetrahydro-3-(1H-Tetrazol-5-yl)-4H-pyrimido[2,1-α

]isoquinol-4-one.

8. The method of claim 1 wherein said Pemirolast or analog thereof is administered in a single dose.

9. The method of claim 1 wherein said Pemirolast or analog thereof is administered by sustained release.

10. The method of claim 1 wherein said Pemirolast or analog thereof is administered by burst/sustained release.

11. The method of claim 1 wherein said Pemirolast or analog thereof is administered at a level of from about 0.01 milligram per kilogram of the body to about 3,000 milligram per kilogram of the body.

12. The method of claim 1 further comprising administering Pemirolast systemically to said body prior to said surgical procedure.

13. The method of claim 1 wherein Pemirolast is administered systemically to said body prior to said surgical procedure in amounts and for a time effective to increase inhibition for formation of adhesions in said body when compared to administration of Pemirolast directly to said tissue surfaces in said body cavity in said body without said systemic administration.