Resveratrol-conjugated poly-epsilon-caprolactone facilitates in vitro mineralization and in vivo bone regeneration
2011 (English)In: ACTA BIOMATERIALIA, ISSN 1742-7061, Vol. 7, no 2, 751-758 p.Article in journal (Refereed) Published
Incorporation of osteoinductive factors in a suitable scaffold is considered a promising strategy for generating osteogenic biomaterials. Resveratrol is a polyphenol found in parts of certain plants, including nuts, berries and grapes. It is known to increase DNA synthesis and alkaline phosphatase (ALP) activity in osteoblasts and to prevent femoral bone loss in ovariectomized (OVX) rats. In the present study resveratrol was coupled through a hydrolysable covalent bond with the carboxylic acid groups in porous poly-epsilon-caprolactone (PCL) surface grafted with acrylic acid (AA). The osteogenic effect of this new scaffold was evaluated in mesenchymal cell culture and in the rat calvarial defect model. We found that the incorporation of resveratrol caused increased ALP activity of rat bone marrow stromal cells and enhanced mineralization of the cell-scaffold composites in vitro. After 8 weeks the calvarial defects implanted with resveratrol-conjugated PCL displayed a higher X-ray density than the defects implanted with control PCL. Bone-like structures, positively immunostained for bone sialoprotein, were shown to be more extensively formed in the resveratrol-conjugated PCL These results show that incorporation of resveratrol into the AA-functionalized porous PCL scaffold led to a significant increase in osteogenesis. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Place, publisher, year, edition, pages
2011. Vol. 7, no 2, 751-758 p.
Resveratrol, Biodegradable scaffolds, Bone regeneration, Vapor phase grafting, Tissue engineering
Industrial Biotechnology Materials Engineering
IdentifiersURN: urn:nbn:se:kth:diva-31031DOI: 10.1016/j.actbio.2010.09.008ISI: 000286707700032ScopusID: 2-s2.0-78650744947OAI: oai:DiVA.org:kth-31031DiVA: diva2:402185
QC 201103072011-03-072011-03-072011-03-07Bibliographically approved