Design of infection-resistant antibiotic-releasing polymers: I. Fabrication and formulation

被引:45
作者
Kwok, CS
Wan, CX
Hendricks, S
Bryers, JD
Horbett, TA
Ratner, BD
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[3] Montana State Univ, Coll Engn, Dept Chem Engn, Bozeman, MT 59717 USA
[4] Univ Connecticut, Ctr Hlth, Ctr Biomat, Farmington, CT 06030 USA
关键词
controlled release; coating; infection; ciprofloxacin; polyurethane;
D O I
10.1016/S0168-3659(99)00106-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biomaterials-related infections are often observed with prosthetic implants and in many cases result in the failure of the devices. To design a biomedically useful polymer that is intrinsically infection-resistant, we have developed a ciprofloxacin-loaded polyurethane (PU) matrix that releases antibiotic locally at the implant surface, thereby minimizing bacterial accumulation. We report here the methods of fabrication and formulation for making such antibiotic-loaded devices, as well as evidence of their bactericidal properties. Specifically, various pore-forming agents and drug loadings were examined. An optimum formulation consisting of BIOSPAN(R) PU, poly(ethylene glycol) and ciprofloxacin offered the longest effective period of sustained release (5 days). The bactericidal efficacy of the released ciprofloxacin against Pseudomonas aeruginosa (PA) was four times that of the control PU without antibiotics. This bactericidal efficiency was due to an increase in the PA detachment from the surface. These observations suggested that the released ciprofloxacin was biologically active in preventing the bacteria from permanently adhering to the substratum, and thus decreasing the possibility of biofilm-related infection. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:289 / 299
页数:11
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