Gentamicin-impregnated chitosan/nanohydroxyapatite/ethyl cellulose microspheres granules for chronic osteomyelitis therapy

In this article gentamicin (GM) impregnated microspheres were used to extend the drug release time for the treatment of chronic osteomyelitis. The granules were prepared in solution and consisted of nanohydroxyapatite (nHA), chitosan (CS) and GM loaded ethyl cellulose (EC) microspheres. A rabbit mod...

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Published inJournal of biomedical materials research. Part A Vol. 93A; no. 3; pp. 1020 - 1031
Main Authors Shi, Pujiang, Zuo, Yi, Li, Xiaowei, Zou, Qin, Liu, Haohuai, Zhang, Li, Li, Yubao, Morsi, Yos S
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.06.2010
Wiley-Blackwell
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Summary:In this article gentamicin (GM) impregnated microspheres were used to extend the drug release time for the treatment of chronic osteomyelitis. The granules were prepared in solution and consisted of nanohydroxyapatite (nHA), chitosan (CS) and GM loaded ethyl cellulose (EC) microspheres. A rabbit model with chronic osteomyelitis was made by using staphylococcus aureus and morrhuate sodium and special inspection methods were used to test the curative effects of the granules, such as microbiological investigations, tissue, and X‐ray observations. The granules were provided with excellent drug release properties, 49 days in vitro and 45 days in vivo, moreover, they showed almost no cytotoxic for fibroblast and osteoblast. The findings indicated that the GM‐impregnated CS/nHA/EC microspheres granules showed outstanding curative effect. Generally, it can be concluded that the granules containing GM impregnated microspheres may be used effectively in the treatment of the chronic osteomyelitis. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010
Bibliography:ArticleID:JBM32598
China-Netherlands Programme Strategic Alliances - No. 2008DFB50120
China 973 fund - No. 2007CB936102
This article was published online on 9 September 2009. An error was subsequently identified and the article was corrected on 30 September 2009.
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content type line 23
ISSN:1549-3296
1552-4965
1552-4965
DOI:10.1002/jbm.a.32598