Volume 104, Issue 7 pp. 1657-1667
Original Article

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

Noushin Omidvar

Noushin Omidvar

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

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Fariba Ganji

Corresponding Author

Fariba Ganji

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

Correspondence to: F. Ganji; e-mail: [email protected] or M. B. Eslaminejad; e-mail: [email protected]Search for more papers by this author
Mohamadreza Baghaban Eslaminejad

Corresponding Author

Mohamadreza Baghaban Eslaminejad

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

Correspondence to: F. Ganji; e-mail: [email protected] or M. B. Eslaminejad; e-mail: [email protected]Search for more papers by this author
First published: 25 February 2016
Citations: 17

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.

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