| Literature DB >> 27612772 |
Arash Khojasteh1, Farahnaz Fahimipour2, Mohamadreza Baghaban Eslaminejad3, Mohammad Jafarian4, Shahrbanoo Jahangir5, Farshid Bastami6, Mohammadreza Tahriri7, Akbar Karkhaneh8, Lobat Tayebi9.
Abstract
Bone tissue engineering is sought to apply strategies for bone defects healing without limitations and short-comings of using either bone autografts or allografts and xenografts. The aim of this study was to fabricate a thin layer poly(lactic-co-glycolic) acid (PLGA) coated beta-tricalcium phosphate (β-TCP) scaffold with sustained release of vascular endothelial growth factor (VEGF). PLGA coating increased compressive strength of the β-TCP scaffolds significantly. For in vitro evaluations, canine mesenchymal stem cells (cMSCs) and canine endothelial progenitor cells (cEPCs) were isolated and characterized. Cell proliferation and attachment were demonstrated and the rate of cells proliferation on the VEGF released scaffold was significantly more than compared to the scaffolds with no VEGF loading. A significant increase in expression of COL1 and RUNX2 was indicated in the scaffolds loaded with VEGF and MSCs compared to the other groups. Consequently, PLGA coated β-TCP scaffold with sustained and localized release of VEGF showed favourable results for bone regeneration in vitro, and this scaffold has the potential to use as a drug delivery device in the future.Entities:
Keywords: PLGA; Scaffold; Tissue engineering; VEGF; β-TCP
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Year: 2016 PMID: 27612772 DOI: 10.1016/j.msec.2016.07.011
Source DB: PubMed Journal: Mater Sci Eng C Mater Biol Appl ISSN: 0928-4931 Impact factor: 7.328