Please use this identifier to cite or link to this item: https://doi.org/10.1163/092050611X597807
Title: Electrospun poly(L-lactic acid) nanofibres loaded with dexamethasone to induce osteogenic differentiation of human mesenchymal stem cells
Authors: Nguyen, L.T.H.
Liao, S.
Chan, C.K. 
Ramakrishna, S. 
Keywords: Bone
Dexamethasone
Electrospinning
Nanofibre
Osteoinductive
Poly(L-lactic acid)
Issue Date: 2012
Citation: Nguyen, L.T.H., Liao, S., Chan, C.K., Ramakrishna, S. (2012). Electrospun poly(L-lactic acid) nanofibres loaded with dexamethasone to induce osteogenic differentiation of human mesenchymal stem cells. Journal of Biomaterials Science, Polymer Edition 23 (14) : 1771-1791. ScholarBank@NUS Repository. https://doi.org/10.1163/092050611X597807
Abstract: Dexamethasone (Dex), a synthetic corticosteroid, was loaded into poly(L-lactic acid) (PLLA) nanofibrous scaffolds with a concentration of 0.333 wt% by electrospinning. The Dex-loaded PLLA nanofibres increased the mechanical strength in comparison with pure PLLA nanofibres. A sustained release profile for over 2 months with an initial burst release after 12 h of 17% was shown. Importantly, the amounts of Dex released from the PLLA nanofibres every 3 days were close to the ones used for the standard osteogenic medium. The sustained osteoinductive environment created by released Dex strongly differentiated human mesenchymal stem cells (hMSCs) cultured in the Ost-Dex medium. ALP activity, BSP expression and calcium deposition were significantly higher than those of the cells cultured on the PLLA scaffolds without Dex. A large amount of hydroxyapatite-like minerals was observed on the Dex-loaded PLLA scaffolds after 21 days culture. The cells on these scaffolds also indicated an osteoblastic morphology on the 14th day. Besides, these scaffolds slightly increased the cell proliferation comparing to the scaffolds without Dex. As such, the PLLA nanofibres loaded with 0.333 wt% Dex was an effective osteoinductive scaffold which acts as a promising strategy for bone treatment. © 2011 Koninklijke Brill NV, Leiden.
Source Title: Journal of Biomaterials Science, Polymer Edition
URI: http://scholarbank.nus.edu.sg/handle/10635/85118
ISSN: 09205063
DOI: 10.1163/092050611X597807
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