Biomimetic composite coating on rapid prototyped scaffolds for bone tissue engineering

被引:106
作者
Arafat, M. Tarik [1 ,2 ]
Lam, Christopher X. F. [3 ]
Ekaputra, Andrew K. [3 ]
Wong, Siew Yee [1 ]
Li, Xu [1 ]
Gibson, Ian [2 ,4 ]
机构
[1] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[2] Natl Univ Singapore, Dept Mech Engn, Singapore 117576, Singapore
[3] Natl Univ Singapore, Div Bioengn, Singapore 119260, Singapore
[4] Inst Politech Leiria, Lab Rapid & Sustainable Prod Dev, Leiria, Portugal
关键词
Rapid prototyping scaffolds; Biomimetic composite coating; Carbonated hydroxyapatite-gelatin composite; Bone tissue engineering; MESENCHYMAL STEM-CELLS; IN-VITRO; OSTEOBLAST DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; SURFACE MODIFICATION; HYDROXYAPATITE; APATITE; FABRICATION; DEPOSITION; DESIGN;
D O I
10.1016/j.actbio.2010.09.010
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The objective of this present study was to improve the functional performance of rapid prototyped scaffolds for bone tissue engineering through biomimetic composite coating. Rapid prototyped poly(epsilon-caprolactone)/tri-calcium phosphate (PCL/TCP) scaffolds were fabricated using the screw extrusion system (SES). The fabricated PCL/TCP scaffolds were coated with a carbonated hydroxyapatite (CHA)-gelatin composite via biomimetic co-precipitation. The structure of the prepared CHA-gelatin composite coating was studied by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. Compressive mechanical testing revealed that the coating process did not have any detrimental effect on the mechanical properties of the scaffolds. The cell-scaffold interaction was studied by culturing porcine bone marrow stromal cells (BMSCs) on the scaffolds and assessing the proliferation and bone-related gene and protein expression capabilities of the cells. Confocal laser microscopy and SEM images of the cell-scaffold constructs showed a uniformly distributed cell sheet and accumulation of extracellular matrix in the interior of CHA-gelatin composite-coated PCL/TCP scaffolds. The proliferation rate of BMSCs on CHA-gelatin composite-coated PCL/TCP scaffolds was about 2.3 and 1.7 times higher than that on PCL/TCP scaffolds and CHA-coated PCL/TCP scaffolds, respectively, by day 10. Furthermore, reverse transcription polymerase chain reaction and Western blot analysis revealed that CHA-gelatin composite-coated PCL/TCP scaffolds stimulate osteogenic differentiation of BMSCs the most, compared with PCL/TCP scaffolds and CHA-coated PCL/TCP scaffolds. These results demonstrate that CHA-gelatin composite-coated rapid prototyped PCL/TCP scaffolds are promising for bone tissue engineering. (C) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:809 / 820
页数:12
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