In vivo biocompatibility and biodegradation of poly(ethylene carbonate)

被引:66
作者
Dadsetan, M
Christenson, EM
Unger, F
Ausborn, M
Kissel, T
Hiltner, A
Anderson, JM
机构
[1] Case Western Reserve Univ, Dept Macromol Sci, Ctr Appl Polymer Res, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[3] Novartis Pharma AG, Basel, Switzerland
[4] Univ Marburg, Dept Pharmaceut & Biopharm, D-35032 Marburg, Germany
关键词
poly(ethylene carbonate); biodegradation; cage implant; biocompatibility; surface erosion;
D O I
10.1016/j.jconrel.2003.08.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biodegradation and biocompatibility of poly(ethylene carbonate) (PEC) was examined using an in vivo cage implant system. Exudate analysis showed that PEC and PEC degradation products were biocompatible and induced minimal inflammatory and wound healing responses. Adherent foreign body giant cells (FBGCs) caused pitting on the PEC surface, which led to extensive degradation over time. Data obtained from molecular weight and examination of film cross-sections in the scanning electron microscope (SEM) indicated that PEC underwent surface erosion with no change to the remaining bulk. Attenuated total reflectance infrared (ATR-FTIR) spectroscopy was used to characterize the chemical degradation. Superoxide anion released from inflammatory cells appeared to initiate an "unzipping" mechanism of degradation by deprotonation of PEC hydroxyl end groups. The resulting alkoxide ion participated in a concerted mechanism involving water and the carbonate carbonyl, leading to elimination of ethylene glycol. Carbonate ions decomposed further with release of carbon dioxide to regenerate alkoxide ion. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:259 / 270
页数:12
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