Novel thermosensitive chitosan hydrogels: In vivo evaluation

被引:35
|
作者
Patois, Emilie [1 ]
Osorio-da Cruz, Suzanne [2 ]
Tille, Jean-Christophe [3 ]
Walpoth, Beat [2 ]
Gurny, Robert [1 ]
Jordan, Olivier [1 ]
机构
[1] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, Dept Pharmaceut & Biopharmaceut, CH-1211 Geneva, Switzerland
[2] Univ Hosp Geneva, Dept Surg, CH-1211 Geneva 14, Switzerland
[3] Univ Hosp Geneva, Dept Clin Pathol, CH-1211 Geneva 14, Switzerland
关键词
chitosan; thermosensitive hydrogels; in situ forming implants; biodegradation; in vivo evaluation; FIELD-FLOW FRACTIONATION; BIOCOMPATIBILITY; DEGRADATION; POLYMERS; SYSTEMS; CHITIN; VITRO; FILMS;
D O I
10.1002/jbm.a.32211
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chitosan is an attractive biopolymer for the preparation of hydrogels. Its unique combination of biocompatibility, biodegradability, bioadhesivity, and tissue-promoting abilities allows pharmaceutical applications. We investigated novel thermosensitive hydrogels based on chitosan homogeneously reacetylated to a deacetylation degree of about 50%, combined with selected polyols or polyoses such as trehalose, a nontoxic polysaccharide. The latter, a gel-inducing and lyoprotective agent enabled the formulation to be lyophilized and rehydrated without affecting the thermosensitive behavior. This made possible long-term storage and promoted its use in a clinical setup. The thermally induced sot-gel transition allowed injectability and in situ setting. Rheological characterization revealed that storage moduli could be increased by one decade by increasing the chitosan concentration from 1.4 to 2.2% (w/w). Evaluation in vivo provided evidence of in situ implant formation in Subcutaneous tissue of Sprague-Dawley rats and permanence for Lip to 3 months. Histopathological analysis demonstrated a mild, chronic, inflammatory reaction that disappeared with the complete absorption of the gel implant over a few months period. Such in situ forming hydrogels could be advantageous for specific applications in drug delivery and tissue engineering. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 91A: 324-330, 2009
引用
收藏
页码:324 / 330
页数:7
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