Fabrication and characterization of injection molded poly (ε-caprolactone) and poly (ε-caprolactone)/hydroxyapatite scaffolds for tissue engineering

被引:39
|
作者
Cui, Zhixiang [2 ]
Nelson, Brenton [1 ]
Peng, YiYan [1 ]
Li, Ke [3 ]
Pilla, Srikanth [1 ]
Li, Wan-Ju [1 ]
Turng, Lih-Sheng [1 ,3 ,4 ]
Shen, Changyu [2 ]
机构
[1] Univ Wisconsin, Madison, WI 53706 USA
[2] Zhengzhou Univ, Zhengzhou, Henan, Peoples R China
[3] S China Univ Technol, Guangzhou, Guangdong, Peoples R China
[4] Huazhong Univ Sci & Technol, Wuhan 430074, Peoples R China
关键词
Injection molding; Tissue engineering scaffolds; Porous and interconnected structures; Particulate leaching; Biocompatibility; COMPOSITE SCAFFOLDS; POLYCAPROLACTONE SCAFFOLDS; IN-VITRO; BONE; CELLS; MATRICES; DESIGN; SYSTEM; BLEND;
D O I
10.1016/j.msec.2012.04.064
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this study, poly(epsilon-caprolactone) (PCL)/sodium chloride (NaCl), PCL/poly(ethylene oxide) (PEO)/NaCl and PCL/PEO/NaCl/hydroxyapatite (HA) composites were injection molded and characterized. The water soluble and sacrificial polymer. PEO, and NaCl particulates in the composites were leached by deionized water to produce porous and interconnected microstructures. The effect of leaching time on porosity, and residual contents of NaCl and NaCl/HA, as well as the effect of HA addition on mechanical properties was investigated. In addition, the biocompatibility was observed via seeding human mesenchymal stem cells (hMSCs) on PCL and PCL/HA scaffolds. The results showed that the leaching time depends on the spatial distribution of sacrificial PEO phase and NaCl particulates. The addition of HA has significantly improved the elastic (E') and loss moduli (E '') of PCL/HA scaffolds. Human MSCs were observed to have attached and proliferated on both PCL and PCL/HA scaffolds. Taken together, the molded PCL and PCL/HA scaffolds could be good candidates as tissue engineering scaffolds. Additionally, injection molding would be a potential and high throughput technology to fabricate tissue scaffolds. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1674 / 1681
页数:8
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