The in vitro hydrolysis of poly(ester urethane)s consisting of poly[(R)-3-hydroxybutyrate] and poly(ethylene glycol)

被引:114
|
作者
Loh, XJ
Tan, KK
Li, X
Li, J
机构
[1] Natl Univ Singapore, Fac Engn, Div Bioengn, Singapore 117576, Singapore
[2] Natl Univ Singapore, IMRE, Singapore 117602, Singapore
关键词
poly(ester urethane); poly[(R)-3-hydroxybutyrate; poly(ethylene glycol); hydrolytic degradation;
D O I
10.1016/j.biomaterials.2005.10.038
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This paper reports the study of the complete degradation process for a series of newly synthesized multi-block poly(ester urethane)s consisting of poly[(R)-3-hydroxybutyrate] (PHB) as hard and hydrophobic block and poly(ethylene glycol) (PEG) as soft and hydrophilic segment. The initial stages of degradation of the poly(PHB/PEG urethane)s were monitored by carrying out the degradation experiments at pH 7.4 and 37 degrees C. The weight loss of the copolymer films was traced. and the degraded copolymer films were characterized by GPC, H-1 NMR, TGA, and SEM. The induction phase of the polymer degradation was characterized by a random chain scission of the ester backbone bonds of the PHB segments and an insignificant decline in the weight of the polymer films. An accelerated degradation process was carried out at pH 11.5 and 37 degrees C to investigate the long-term degradation behaviour. The characterization of the degraded polymer films was similar to that for the experiment at pH 7.4. In addition. the water-soluble degradation products were characterized by GPC, H-1 NMR, and FTIR. The main components of the water-soluble degradation products were found to be PEG blocks (monomeric up to quadmeric), 3-hydroxybutyric acid, and crotonic acid. It was found that the copolymer incorporating the highest amount of PEG degraded at the highest rate of all the copolymers studied. The complete degradation of the poly(PHB/PEG urethane)s was monitored using a combination of the physiological and accelerated hydrolytic degradation. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1841 / 1850
页数:10
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