Synthesis and characterization of a novel biodegradable antimicrobial polymer

被引:157
作者
Woo, GLY
Mittelman, MW
Santerre, JP
机构
[1] Univ Toronto, Fac Dent, Dept Biomat, Toronto, ON M5G 1G6, Canada
[2] Univ Toronto, Fac Engn, Dept Chem Engn & Appl Chem, Toronto, ON, Canada
[3] Altran Corp, Boston, MA USA
基金
英国医学研究理事会;
关键词
biodegradable polymers; antimicrobial; infection; ciprofloxacin; quinolones; polyurethanes;
D O I
10.1016/S0142-9612(00)00003-X
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bacterial infection is a frequent complication associated with the use of medical devices. In an effort to address this problem, antibacterial agents have been incorporated or applied directly onto the surfaces of numerous types of medical devices. This study assessed the feasibility of using a novel biodegradable polymer to release antibiotic drugs in response to inflammatory related enzymes. A model drug polymer was synthesized using 1,6-hexane diisocyanate (HDI), polycaprolactone diol (PCL), and a fluoroquinolone antibiotic, ciprofloxacin. Polymers were characterized by size-exclusion chromatography (SEC), and elemental analysis. Biodegradation studies were carried out by incubating the polymers with solutions of cholesterol esterase (CE) or phosphate buffer (pH 7.0) for 30 days at 37 degrees C. The degradation was assessed by high-performance liquid chromatography (HPLC), mass spectrometry (MS) and C-14 radiolabel release. Subsequently, the activity of the released antibiotic was assessed against a clinical isolate of Pseudomonas aeruginosa. HPLC analysis showed the release of multiple degradation products which were identified, by tandem MS, to include ciprofloxacin and derivatives of ciprofloxacin. The microbiological assessment showed that the released ciprofloxacin possessed antimicrobial activity; 1 mu g/ml was measured after 10 days. The results of this study suggest that these novel bioresponsive antimicrobial polymers or similar analogs show promise for use in the control of medical device associated infections. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1235 / 1246
页数:12
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