4.6 Article

Preparation and characterization of a novel 3D scaffold from poly(ε-caprolactone)/biphasic calcium phosphate hybrid composite microspheres adhesion

期刊

BIOCHEMICAL ENGINEERING JOURNAL
卷 64, 期 -, 页码 76-83

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bej.2012.02.005

关键词

PCL/BCP-HCM 3D scaffold; GF-SEDA; In vitro study; Composite; Adhesion; Porous

资金

  1. Ministry of Health & Welfare, Republic of Korea [A111084]
  2. Korea Health Promotion Institute [A111084] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The use of scaffold-based strategies in tissue engineering applications requires that the micro-architecture of the scaffold satisfies key micro-structural and biological requirements. In this study, we examined the effects of experimental fabrication conditions on the synthesis of a scaffold formed by a poly(epsilon-caprolactone)/biphasic calcium phosphate (PCL/BCP) hybrid composite microspheres adhesion. The goal of our study was to identify the optimal fabrication conditions. An optimized poly(epsilon-caprolactone)/biphasic calcium phosphate hybrid composite microspheres (PCL/BCP-HCM) 3D scaffold was prepared using the gas foaming and spontaneous emulsion droplets adherence (GF-SEDA) technique. Optical microscopy, mu CT, SEM, mercury porosimeter, EDS, XRD, a universal testing machine, and MTT assays were used to characterize the assembled scaffolds. When the GF-SEDA technique was used under optimal conditions, the resulting novel PCL/BCP-HCM 3D scaffold had a micro-porous homogenous structure composed of PCL and BCP with a large distribution of pore sizes (ranging from 0.01 to 1000 mu m) and highly interconnected micro-pores. In addition, the total porosity of the scaffold was 74% with a compressive strength of 0.82 MPa. Furthermore, an in vitro study of cell-scaffold interaction demonstrated that cell adhesion, growth, and proliferation were significant over the course of 5 days in culture. (C) 2012 Elsevier B.V. All rights reserved.

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