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Photocrosslinkable Biodegradable Elastomers Based on Cinnamate-Functionalized Polyesters

机译:基于肉桂酸酯官能化聚酯的可光交联的可生物降解弹性体

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摘要

Synthetic biodegradable elastomers are an emerging class of materials that play a critical role in supporting innovations in bioabsorbable medical implants. This work describes the synthesis and characterization of poly (glycerol-co-sebacate)-cinnamate (PGS-CinA), a biodegradable elastomer based on hyperbranched polyesters derivatized with pendant cinnamate groups. PGS-CinA can be prepared via photodimerization in the absence of photoinitiator using monomers that are found in common foods. The resulting network exhibits a Young’s modulus of 50.5 to 152.1 kPa and a projected in vitro degradation half-life time between 90 and 140 days. PGS-CinA elastomers are intrinsically cell adherent and support rapid proliferation of fibroblasts. Spreading and proliferation of fibroblasts are loosely governed by the substrate stiffness within the range of Young’s moduli in PGS-CinA networks that were prepared. The thermo-mechanical properties, biodegradability, and intrinsic support of cell attachment and proliferation suggest that PGS-CinA networks abroadly applicable for use in next generation bioabsorable materials including temporary medical devices and scaffolds for soft tissue engineering.
机译:合成生物可降解弹性体是一类新兴的材料,在支持生物可吸收医疗植入物的创新方面起着至关重要的作用。这项工作描述了聚(甘油-癸二酸癸二酸酯)-肉桂酸酯(PGS-CinA)的合成和表征,聚甘油(肉桂酸酯-癸二酸酯)是一种可生物降解的弹性体,它基于肉桂酸酯侧基衍生的超支化聚酯。 PGS-CinA可以在不存在光引发剂的情况下,使用常见食品中的单体通过光二聚制备。最终的网络显示出的杨氏模量为50.5至152.1 kPa,预计的体外降解半衰期为90至140天。 PGS-CinA弹性体本质上是细胞粘附的,并支持成纤维细胞的快速增殖。在制备的PGS-CinA网络中,成纤维细胞的扩散和增殖大致由杨氏模量范围内的底物刚度决定。热力学性质,生物降解性以及细胞附着和增殖的内在支持表明,PGS-CinA网络在国外可用于下一代可生物吸收的材料,包括临时医疗器械和用于软组织工程的支架。

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