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基于肉桂酸酯功能化聚酯的光交联可生物降解弹性体。

Photocrosslinkable biodegradable elastomers based on cinnamate-functionalized polyesters.

机构信息

Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

出版信息

Acta Biomater. 2013 Jul;9(7):7362-70. doi: 10.1016/j.actbio.2013.03.041. Epub 2013 Apr 6.

Abstract

Synthetic biodegradable elastomers are an emerging class of materials that play a critical role in supporting innovations in bioabsorbable medical implants. This paper 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 photoinitiators using monomers that are found in common foods. The resulting network exhibits a Young's modulus of 50.5-152.1kPa and a projected in vitro degradation half-life time between 90 and 140days. 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 are broadly applicable for use in next generation bioabsorable materials including temporary medical devices and scaffolds for soft tissue engineering.

摘要

合成可生物降解弹性体是一类新兴材料,在支持可吸收医疗植入物的创新方面发挥着关键作用。本文描述了聚(甘油-co-癸二酸)-肉桂酸酯(PGS-CinA)的合成与表征,这是一种基于衍生有肉桂酸酯侧基的超支化聚酯的可生物降解弹性体。可以使用在常见食品中发现的单体,通过无引发剂的光二聚化来制备 PGS-CinA。所得网络的杨氏模量为 50.5-152.1kPa,预计体外降解半衰期为 90-140 天。PGS-CinA 弹性体具有内在的细胞黏附性,并支持成纤维细胞的快速增殖。成纤维细胞的铺展和增殖在 PGS-CinA 网络的杨氏模量范围内受到基质硬度的松散控制,该范围较广。热机械性能、生物降解性以及对细胞附着和增殖的固有支持表明,PGS-CinA 网络广泛适用于下一代可吸收材料,包括临时医疗器械和软组织工程支架。

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