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Development of poly(ε-Caprolactone) scaffold loaded with simvastatin and beta-cyclodextrin modified hydroxyapatite inclusion complex for bone tissue engineering

Authors
Lee J.B.Kim J.E.Bae M.S.Park S.A.Balikov D.A.Sung H.-J.Jeon H.B.Park H.K.Um S.H.Lee K.S.Kwon I.K.
Issue Date
Feb-2016
Publisher
MDPI Open Access Publishing
Citation
Polymers, v.8, no.2, pp 1 - 10
Pages
10
Journal Title
Polymers
Volume
8
Number
2
Start Page
1
End Page
10
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147077
DOI
10.3390/polym8020049
ISSN
2073-4360
2073-4360
Abstract
In this study, we developed poly(ε-caprolactone) (PCL) 3D scaffolds using a solid free form fabrication (SFF) technique. β-cyclodextrin (βCD) was grafted to hydroxyapatite (HAp) and this βCD grafted HAp was coated onto the PCL scaffold surface, followed by drug loading through an inclusion complex interaction between the βCD and adamantane (AD) or between βCD and simvastatin (SIM). The scaffold structure was characterized by scanning electron microscopy (SEM). The release profile of simvastatin in the β-CD grafted HAp was also evaluated. Osteogenic differentiation of adipose-derived stromal cells (ADSCs) was examined using an alkaline phosphatase activity (ALP) assay. The results suggest that drug loaded PCL-HAp 3-D scaffolds enhances osteogenic differentiation of ADSCs.
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