In vitro gentamicin sustained and controlled release from chitosan cross-linked films

被引:26
作者
Campos, Maria G. N. [1 ,2 ]
Rawls, Henry R. [2 ]
Innocentini-Mei, Lucia H. [1 ]
Satsangi, Neera [2 ]
机构
[1] State Univ Campinas UNICAMP, Sch Chem Engn, Dept Polymer Technol, BR-13083970 Campinas, SP, Brazil
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Restorat Dent, Biomat Div, Sch Dent, San Antonio, TX 78229 USA
关键词
BLOCKED DIISOCYINATE; MICROSPHERES; DELIVERY; HYDROGELS; LINKING; GENIPIN; GEL;
D O I
10.1007/s10856-008-3611-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A novel wound dressing film was investigated for controlled and sustained delivery of gentamicin, while covering and protecting the wound. Chitosan was cross-linked with Hexamethylene 1,6-bis (aminocarboxysulfonate) to prepare the wound dressing films. Cross-linking reaction was required to control the water retention and release of encapsulated gentamicin. Cross-linked films swell less and became more hydrophilic than chitosan film itself. However, this behavior was inversely proportional to the degree of cross-linking. In vitro gentamicin release from the cross-linked films, at physiological conditions of pH and temperature, was studied for 2 weeks. The effects of gentamicin initial concentration and cross-linking ratio on the kinetics of gentamicin release were evaluated. Results showed that the diffusion rate was governed by initial concentration of gentamicin and degree of cross-linking, since higher gentamicin initial concentration and degree of cross-linking promoted the slower release, while lower gentamicin initial concentration and degree of cross-linking promoted the faster one.
引用
收藏
页码:537 / 542
页数:6
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