简介概要

The Degradation Rate of Polyanhydride (Poly(sebacic acid), diacetoxy terminated, PSADT)

来源期刊:Journal Of Wuhan University Of Technology Materials Science Edition2013年第4期

论文作者:崔志香 PENG Yiyan LI Ke PENG Jun ZHAO Haibin TURNG Lih-Sheng SHEN Changyu

文章页码:793 - 797

摘    要:The in vitro degradation rate of polyanhydride (poly(sebacic acid), diacetoxy terminated), also known as PSADT, was investigated. PSADT tablets with a circular cross-section were formed using a compression molding device, and then immersed into phosphate buffer saline (PBS) for in vitro degradation experiments. The mechanisms of degradation and the degradation rate were characterized by the change in molecular weight and reduction in specimen mass. In addition, the effects of processing temperature and the geometry of the formed PSADT tablets on the rate of degradation were studied. The surface morphology at different degradation times was observed by scanning electron microscopy (SEM). The experimental results showed that PSADT exhibited surface erosion due to the fact that near zero-order degradation kinetics was observed during its degradation process. Moreover, it is found that the geometry of tablets played an important role on the rate of degradation, while the processing temperature had no significant effect on the PSADT degradation rate.

详情信息展示

The Degradation Rate of Polyanhydride (Poly(sebacic acid), diacetoxy terminated, PSADT)

崔志香1,PENG Yiyan2,LI Ke3,PENG Jun3,ZHAO Haibin3,TURNG Lih-Sheng2,3,SHEN Changyu4

1. School of Materials Science and Engineering, Fujian University of Technology2. Polymer Engineering Center, University of Wisconsin-Madison3. National Engineering Research Center of Novel Technology, South China University of Technology4. School of Materials Science and Engineering, Zhengzhou University

摘 要:The in vitro degradation rate of polyanhydride (poly(sebacic acid), diacetoxy terminated), also known as PSADT, was investigated. PSADT tablets with a circular cross-section were formed using a compression molding device, and then immersed into phosphate buffer saline (PBS) for in vitro degradation experiments. The mechanisms of degradation and the degradation rate were characterized by the change in molecular weight and reduction in specimen mass. In addition, the effects of processing temperature and the geometry of the formed PSADT tablets on the rate of degradation were studied. The surface morphology at different degradation times was observed by scanning electron microscopy (SEM). The experimental results showed that PSADT exhibited surface erosion due to the fact that near zero-order degradation kinetics was observed during its degradation process. Moreover, it is found that the geometry of tablets played an important role on the rate of degradation, while the processing temperature had no significant effect on the PSADT degradation rate.

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