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含载地塞米松壳聚糖微球的聚己内酯纤维支架对人骨髓间充质干细胞的体外成骨诱导作用

In vitro osteogenic induction of human marrow-derived mesenchymal stem cells by PCL fibrous scaffolds containing dexamethazone-loaded chitosan microspheres.

作者信息

Omidvar Noushin, Ganji Fariba, Eslaminejad Mohamadreza Baghaban

机构信息

Biomedical Engineering Group, Chemical Engineering Faculty, Tarbiat Modares University, Tehran, Iran.

Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

出版信息

J Biomed Mater Res A. 2016 Jul;104(7):1657-67. doi: 10.1002/jbm.a.35695. Epub 2016 Mar 16.

DOI:10.1002/jbm.a.35695
PMID:26916786
Abstract

This research reports the encapsulation of dexamethasone (Dex) within the chitosan microspheres (CSMs) embedded in a fibrous structure of poly(ɛ-caprolactone) (PCL) to provide a platform for osteogenic differentiation of human mesenchymal stem cells (hMSCs). Dex loaded CSMs were prepared by spray drying a mixture of chitosan and Dex. Then, they were electrospun with PCL solution to create a bilayer fibrous scaffold (PCL/CSMs-Dex). The CSMs act as good depots for sustained release of Dex over a period of 14 days, without noticeable burst release. This is mainly attributed to the core-shell structure of the final PCL/CSMs-Dex-matrix, which could prolong the release and eliminate the initial burst. The water contact angle of PCL scaffolds decreased from 141.4 ± 3.8 to 118.4 ± 7.6 in the presence of CSMs. Improved proliferation of hMSCs cultured on PCL/CSMs-Dex scaffolds was also evidenced. Furthermore, osteogenic assays showed an increase in alkaline phosphatase activity and mineral deposits. The expression of bone-specific genes also confirmed the osteogenic differentiation of cells cultured on these Dex-loaded core-shell structures. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1657-1667, 2016.

摘要

本研究报告了将地塞米松(Dex)包裹于壳聚糖微球(CSMs)中,并嵌入聚(ε-己内酯)(PCL)纤维结构内,以为人间充质干细胞(hMSCs)的成骨分化提供一个平台。负载Dex的CSMs通过喷雾干燥壳聚糖和Dex的混合物制备而成。然后,将它们与PCL溶液进行电纺丝,以创建双层纤维支架(PCL/CSMs-Dex)。CSMs可作为良好的储存库,使Dex在14天内持续释放,且无明显的突释现象。这主要归因于最终的PCL/CSMs-Dex基质的核壳结构,其可延长释放时间并消除初始突释。在存在CSMs的情况下,PCL支架的水接触角从141.4±3.8降至118.4±7.6。在PCL/CSMs-Dex支架上培养的hMSCs的增殖也得到了改善。此外,成骨试验显示碱性磷酸酶活性和矿物质沉积增加。骨特异性基因的表达也证实了在这些负载Dex的核壳结构上培养的细胞的成骨分化。©2016威利期刊公司。《生物医学材料研究杂志》A部分:104A:1657 - 1667,2016年。

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