| CPC A61K 47/36 (2013.01) [A61K 9/7007 (2013.01); A61K 31/00 (2013.01); A61K 31/7036 (2013.01); A61K 38/14 (2013.01); A61L 15/28 (2013.01); A61L 15/44 (2013.01); A61L 27/20 (2013.01); A61L 27/58 (2013.01); A61L 29/043 (2013.01); A61L 29/146 (2013.01); A61L 29/148 (2013.01); A61L 29/16 (2013.01); A61L 31/042 (2013.01); A61L 31/146 (2013.01); A61L 31/148 (2013.01); A61L 31/16 (2013.01); C08B 37/003 (2013.01); C08J 5/18 (2013.01); C08L 5/08 (2013.01); A61K 9/0024 (2013.01); A61L 2300/232 (2013.01); A61L 2300/25 (2013.01); A61L 2300/406 (2013.01); C08J 2305/08 (2013.01)] | 4 Claims |
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1. A medical device for implantation comprising an acid-treated chitosan composition, prepared by a method comprising:
(a) dissolving chitosan in one or more acids in an aqueous solvent;
(b) forming the chitosan of step (a) into a film by pouring the chitosan into a thin layer and heating the chitosan to form a dehydrated chitosan film;
(c) lyophilizing the chitosan film under conditions that reduce the water content by about 10%-100%;
(d) neutralizing the chitosan film by contacting the film with water, a neutral, or a basic solution, wherein the water, neutral, or basic solution is selected to modulate a physical-mechanical property of the fiber;
(e) washing the chitosan film with water until neutral; and
(f) lyophilizing the film of step (e) to reduce the water content by about 80%-100%, thereby producing a biodegradable chitosan film.
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