个人信息Personal Information
副教授
博士生导师
硕士生导师
主要任职:Null
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理
办公地点:西部校区化工实验楼A306
联系方式:13841142437
电子邮箱:zywei@dlut.edu.cn
Biodegradable radiopaque iodinated poly(ester urethane)s containing poly(epsilon-caprolactone) blocks: Synthesis, characterization, and biocompatibility
点击次数:
论文类型:期刊论文
发表时间:2014-04-01
发表刊物:JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
收录刊物:EI、PubMed、SCIE
卷号:102
期号:4
页面范围:1121-1130
ISSN号:1549-3296
关键字:poly(ester-urethane)s; radiopacity; iodinated bisphenol A; biocompatibility
摘要:Biodegradable radiopaque iodinated poly(ester-urethane) (I-PU), consisting of poly(epsilon-caprolactone) (PCL) diol and iodinated bisphenol A (IBPA), has been successfully synthesized via a coupling reaction of PCL-diisocyanate and IBPA with varying compositions. The IBPA with four iodine atoms per molecule was applied as a chain extender to endow the I-PUs with intrinsic X-ray visibility. The chemical structure and molecular weights of I-PUs were characterized by Fourier transform infrared spectroscopy (FT-IR), proton-nuclear magnetic resonance, and gel permeation chromatography (GPC). The effects of IBPA on the physical properties of I-PUs were systematically studied by means of differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and wide-angle X-ray diffraction (WAXD). The DSC results showed that the crystallization of PCL segments in I-PUs was restrained with increasing amount of IBPA, which was also confirmed by WAXD. In the X-radiography analysis, all the synthesized I-PUs exhibited high radiopacity compared with an aluminum wedge of equivalent thickness. Enzymatic degradation tests showed that the incorporation of IBPA prolonged the degradation of I-PUs and distinct mass loss and degradation happened in the third month. Basic cytocompatibility conducted using rat adipose-derived cells proved that all the I-PUs and their biodegradation products were nontoxic. The radiopaque I-PUs is expected to possess a significant advantage over the traditional polymer counterparts in some related biomedical fields. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 1121-1130, 2014.