In vitro microbial inhibition and cellular response to novel biodegradable composite wound dressings with controlled release of antibiotics

被引:75
作者
Elsner, J. J. [1 ]
Berdicevsky, I. [2 ]
Zilberman, M. [1 ]
机构
[1] Tel Aviv Univ, Dept Biomed Engn, IL-69978 Tel Aviv, Israel
[2] Technion Israel Inst Technol, Dept Microbiol, IL-32000 Haifa, Israel
基金
以色列科学基金会;
关键词
Fibroblast; Gentamicin; Ceftazidime; Poly-(DL-lactic-co-glycolic acid); Infection; ALAMAR-BLUE ASSAY; BURNED PATIENTS; COLLAGEN; INFECTIONS; VIABILITY; BIOFILMS; DELIVERY; GROWTH; SILVER; DRUGS;
D O I
10.1016/j.actbio.2010.07.013
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
About 70% of all people with severe burns die from related infections, despite advances in treatment regimens and the best efforts of nurses and doctors. Although silver-eluting wound dressings are available for addressing this problem, there is growing evidence of the deleterious effects of such dressings in delaying the healing process owing to cellular toxicity. A new concept of antibiotic-eluting composite wound dressings is described here. These dressings are based on a polyglyconate mesh coated with a porous poly-(DL-lactic-co-glycolic acid) matrix loaded with antibiotic drugs. The effect of antibiotic release on bacterial inhibition was studied, and cell cytotoxicity was examined. The dressings resulted in a 99.99% decrease in the viable counts of Pseudomonas aeruginosa and Staphylococcus albus at very high initial inoculations of 10(7)-10(8) CFU ml(-1) after only 1 day, while such a decrease in Staphylococcus aureus was obtained within 3 days. Bacterial inhibition zones around the dressing material were found to persist for 2 weeks, indicating a long-lasting antimicrobial effect. Despite severe toxicity to bacteria, the dressing material was found to have no toxic effect on cultured fibroblasts, indicating that the new antibiotic-eluting wound dressings represent an effective option for selective treatment of bacterial infections. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:325 / 336
页数:12
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