...
首页> 外文期刊>Biomacromolecules >Synthesis and Evaluation of Novel Biodegradable Hydrogels Based on Poly(ethylene glycol)and Sebacic Acid as Tissue Engineering Scaffolds
【24h】

Synthesis and Evaluation of Novel Biodegradable Hydrogels Based on Poly(ethylene glycol)and Sebacic Acid as Tissue Engineering Scaffolds

机译:基于聚乙二醇和癸二酸作为组织工程支架的新型可生物降解水凝胶的合成与评价

获取原文
获取原文并翻译 | 示例

摘要

Novel biodegradable poly(ethylene glycol)(PEG)based hydrogels,namely,PEG sebacate diacrylate(PEGSDA)were synthesized,and their properties were evaluated.Chemical structures of these polymers were confirmed by Fourier transform infrared and proton nuclear magnetic resonance(~1H NMR)spectroscopy.After photopoly-merization,the dynamic shear modulus of the hydrogels was up to 0.2 MPa for 50% PEGSDA hydrogel,significantly higher than conventional hydrogels such as PEG diacrylate(PEGDA).The swelling ratios of these macromers were significantly lower than PEGDA.The in vitro degradation study demonstrated that these hydrogels were biodegradable with weight losses about 66% and 32% for 25% and 50% PEGSDA after 8 weeks of incubation in phosphate-buffered saline at 37 °C.In vitro biocompatibility was assessed using cultured rat bone marrow stromal cells(MSCs)in the presence of unreacted monomers or degradation products.Unlike conventional PEGDA hydrogels,PEGSDA hydrogel without RGD peptide modification induced MSC cell adhesion similar to tissue culture polystyrene.Finally,complex three-dimensional structures of PEGSDA hydrogels using solid free form technique were fabricated and their structure integrity was better maintained than PEGDA hydrogels.These hydrogels may find use as scaffolds for tissue engineering applications.
机译:合成了新型的可生物降解的聚乙二醇(PEG)基水凝胶,即PEG癸二酸二丙烯酸酯(PEGSDA),并对其性质进行了评估。通过傅立叶变换红外和质子核磁共振(〜1H NMR)证实了这些聚合物的化学结构光聚合后,对于50%的PEGSDA水凝胶,水凝胶的动态剪切模量高达0.2 MPa,显着高于常规水凝胶如PEG二丙烯酸酯(PEGDA)。体外降解研究表明,这些水凝胶在37°C的磷酸盐缓冲盐水中孵育8周后,可降解25%和50%PEGSDA的重量分别约为66%和32%,可生物降解。大鼠骨髓基质细胞(MSCs)存在未反应的单体或降解产物。与常规PEGDA水凝胶不同,没有RGD肽修饰的PEGSDA水凝胶阳离子诱导的MSC细胞粘附力与组织培养聚苯乙烯相似。 。

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