...
首页> 外文期刊>Journal of Applied Polymer Science >Synthesis of unsaturated polyphosphoester as a potential injectable tissue engineering scaffold materials
【24h】

Synthesis of unsaturated polyphosphoester as a potential injectable tissue engineering scaffold materials

机译:合成不饱和聚磷酸酯作为潜在的可注射组织工程支架材料

获取原文
获取原文并翻译 | 示例

摘要

Polyphosphoester is a kind of biodegradable polymer with excellent biocompatibility and have been used in drug delivery, tissue engineering, and other bioapplications. A novel unsaturated polyphosphoester (UPPE) based on bis(1,2-propylene glycol) fumarate (BPGF) and ethyl dichlorophosphate was synthesized by polycondensation reaction, and crosslinkable double bonds was introduced into the resulting polymer through the fumarate groups. NMR results indicate that there are three possible bonding models in polyphosphoester because of three isomers of BPGF. The GPC results express that increase in polymerization time leads to high molecular weight of polyphosphester and narrow distribution of molecular weight. After 18 h of polymerization reaction, the molecular weight reached to 5956 g mol(-1) and the polydispersity index was 1.12. The UPPE was soluble in N-vinyl pyrrolidone and easily crosslinked by free-radical polymerization. At the constant temperature (37 degrees C), the maximum temperature due to heat release during crosslinking reaction varied from 41.1 degrees C to 82.30 degrees C and the setting time was between 1.95 and 10.28 min, according to different formulas. (c) 2006 Wiley Periodicals, Inc.
机译:聚磷酸酯是一种具有良好生物相容性的可生物降解的聚合物,已被用于药物输送,组织工程和其他生物应用中。通过缩聚反应合成了一种新的基于双(1,2-丙二醇)富马酸酯(BPGF)和二氯磷酸乙基酯的不饱和聚磷酸酯(UPPE),并通过富马酸酯基团将可交联的双键引入所得聚合物中。 NMR结果表明,由于BPGF的三个异构体,聚磷酸酯中存在三种可能的键合模型。 GPC结果表明,聚合时间的增加导致聚磷酸酯的高分子量和窄的分子量分布。聚合反应18小时后,分子量达到5956 g mol(-1),多分散指数为1.12。 UPPE可溶于N-乙烯基吡咯烷酮,并易于通过自由基聚合交联。在恒定温度(37摄氏度)下,根据不同的配方,由于交联反应过程中放热而导致的最高温度在41.1摄氏度至82.30摄氏度之间变化,凝固时间在1.95至10.28分钟之间。 (c)2006年Wiley Periodicals,Inc.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号