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在静电纺聚己内酯纳米纤维上接枝明胶,以改善内皮细胞的铺展和增殖并控制细胞取向。

Grafting of gelatin on electrospun poly(caprolactone) nanofibers to improve endothelial cell spreading and proliferation and to control cell Orientation.

作者信息

Ma Zuwei, He Wei, Yong Thomas, Ramakrishna S

机构信息

Nanoscience and Nanotechnology Initiative, National University of Singapore.

出版信息

Tissue Eng. 2005 Jul-Aug;11(7-8):1149-58. doi: 10.1089/ten.2005.11.1149.

DOI:10.1089/ten.2005.11.1149
PMID:16144451
Abstract

We modified the surface of electrospun poly(caprolactone) (PCL) nanofibers to improve their compatibility with endothelial cells (ECs) and to show the potential application of PCL nanofibers as a blood vessel tissue-engineering scaffold. Nonwoven PCL nanofibers (PCL NF) and aligned PCL nanofibers (APCL NF) were fabricated by electrospinning technology. To graft gelatin on the nanofiber surface, PCL nanofibers were first treated with air plasma to introduce -COOH groups on the surface, followed by covalent grafting of gelatin molecules, using water-soluble carbodiimide as the coupling agent. The chemical change in the material surface during surface modification was confirmed by X-ray photoelectron spectroscopy and quantified by colorimetric methods. ECs were cultured to evaluate the cytocompatibility of surface-modified PCL NF and APCL NF. Gelatin grafting can obviously enhance EC spreading and proliferation compared with the original material. Moreover, gelatin-grafted APCL NF readily orients ECs along the fibers whereas unmodified APCL NF does not. Immunostaining micrographs showed that ECs cultured on gelatin-grafted PCL NF were able to maintain the expression of three characteristic markers: platelet-endothelial cell adhesion molecule 1 (PECAM-1), intercellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1). The surface-modified PCL nanofibrous material is a potential candidate material in blood vessel tissue engineering.

摘要

我们对静电纺聚己内酯(PCL)纳米纤维的表面进行了改性,以提高其与内皮细胞(ECs)的相容性,并展示PCL纳米纤维作为血管组织工程支架的潜在应用。通过静电纺丝技术制备了非织造PCL纳米纤维(PCL NF)和取向PCL纳米纤维(APCL NF)。为了在纳米纤维表面接枝明胶,首先对PCL纳米纤维进行空气等离子体处理,以在表面引入-COOH基团,然后使用水溶性碳二亚胺作为偶联剂,将明胶分子共价接枝。通过X射线光电子能谱确认了表面改性过程中材料表面的化学变化,并通过比色法进行了定量。培养ECs以评估表面改性的PCL NF和APCL NF的细胞相容性。与原始材料相比,明胶接枝可以明显增强EC的铺展和增殖。此外,明胶接枝的APCL NF易于使ECs沿纤维取向,而未改性的APCL NF则不能。免疫染色显微照片显示,在明胶接枝的PCL NF上培养的ECs能够维持三种特征性标志物的表达:血小板内皮细胞黏附分子1(PECAM-1)、细胞间黏附分子1(ICAM-1)和血管细胞黏附分子1(VCAM-1)。表面改性的PCL纳米纤维材料是血管组织工程中一种潜在的候选材料。

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