IP Library Granted Patent US 8,501,875
Granted Patent B2
US 8,501,875 · App. 13/208,525 · Granted Aug 6, 2013

Surface induced ring-opening polymerization and medical devices formed therefrom

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Quick Facts
Patent No.
US 8,501,875
App. No.
13/208,525
Granted
Aug 6, 2013
Kind
B2
Abstract

The present disclosure relates to coated biodegradable materials having a reduced amount of residual catalysts and methods thereof.

Claims (15)

1. A method of reducing residual catalyst from a biodegradable polymeric material comprising:

providing a container which includes at least one monomer capable of polymerizing via cationic ring-opening polymerization and a biodegradable polymeric material containing a residual catalyst; and

heating the container with the biodegradable polymeric material and the at least one monomer above the glass transition temperature and below the crystallization temperature of the biodegradable polymeric material to release the residual catalyst from the biodegradable polymeric material; and,

polymerizing the monomer with the released residual catalyst at the temperature above the glass transition temperature and below the crystallization temperature of the biodegradable polymeric material.

2. The method of claim 1 wherein the at least one monomer comprises a cyclic ester.

3. The method of claim 2 wherein the cyclic ester comprises an aliphatic cyclic ester.

4. The method of claim 2 wherein the cyclic ester is selected from the group consisting of lactide, glycolide, p-dioxanone, ε-caprolactone, methyl-tetrahydrofuran, ω-pentadecalactone, ω-dodecalactone, δ-valerolactone, β-methyl-β-propiolactone, α-methyl-β-propiolactone, γ-butyrolactone, trimethylene carbonate, tetramethylene carbonate, 2,2-dimethyl trimethylene carbonate and combinations thereof.

5. The method of claim 1 wherein the biodegradable polymeric material is selected from the group consisting of poly-L-lactide, poly-DL-lactide, poly(lactic-co-glycolic acid), poly(glycolic acid), poly(p-dioxanone), poly(ε-caprolactone), poly(trimethylene carbonate), poly(tetramethylene carbonate), poly(hydroxylalkanoates), and combinations thereof.

6. The method of claim 1 wherein the biodegradable polymeric material comprises a biodegradable pellet.

7. The method of claim 1 , wherein the residual catalyst comprises stannous octoate.

8. The method of claim 1 wherein the container is positioned in an oven from about 30 minutes to about 10 days.

9. The method, of claim 1 wherein the container is positioned in an oven from about 6 hours to about 5 days.

10. The method of claim 1 wherein no additional catalyst is used.

11. The method of claim 7 wherein polymerizing the monomer with the released residual catalyst occurs at the temperature above the glass transition temperature and below the crystallization temperature of the biodegradable polymeric material.

12. The method of claim 7 wherein no additional catalyst is used.

Assignments (2)
CHANGE OF NAME Recorded Oct 2, 2012
From: TYCO HEALTHCARE GROUP LP
To: COVIDIEN LP
Reel/Frame 029065/0448 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2011
From: BELCHEVA, NADYA D.; AMINUDDIN, NORMAN
To: TYCO HEALTHCARE GROUP LP
Reel/Frame 026913/0052 →