Microporous nanofibrous fibrin-based scaffolds for bone tissue engineering

被引:121
|
作者
Osathanon, Thanaphum [1 ,2 ]
Linnes, Michael L. [2 ]
Rajachar, Rupak M. [2 ]
Ratner, Buddy D. [2 ]
Somerman, Martha J. [1 ,3 ]
Giachelli, Cecilia M. [1 ,2 ]
机构
[1] Univ Washington, Sch Dent, Dept Oral Biol, Seattle, WA 98195 USA
[2] Univ Washington, Coll Engn, Dept Bioengn, Seattle, WA 98195 USA
[3] Univ Washington, Sch Dent, Dept Periodont, Seattle, WA 98195 USA
关键词
Fibrin; Calcium phosphate; Hydroxyapatite; Bone tissue engineering;
D O I
10.1016/j.biomaterials.2008.06.030
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The fibrotic response of the body to synthetic polymers limits their success in tissue engineering and other applications. Though porous polymers have demonstrated improved healing, difficulty in controlling their pore sizes and pore interconnections has clouded the understanding of this phenomenon. In this study, a novel method to fabricate natural polymer/calcium phosphate composite scaffolds with tightly controllable pore size, Pore interconnection, and calcium phosphate deposition was developed. Microporous, nanofibrous fibrin scaffolds were fabricated using sphere-templating methods. Composite scaffolds were created by solution deposition of calcium phosphate on fibrin Surfaces OF by direct incorporation of nanocrystalline hydroxyapatite (nHA). The SEM results showed that fibrin scaffolds exhibited a highly porous and interconnected structure. Osteoblast-like cells, obtained from murine calvaria, attached, Spread and showed a polygonal morphology on the Surface of the biomaterial. Multiple cell layers and fibrillar Matrix deposition were observed. Moreover, cells seeded on mineralized fibrin scaffolds exhibited significantly higher alkaline phosphatase activity as well as osteoblast marker gene expression compared to fibrin scaffolds and nHA incorporated fibrin scaffolds (0.25 and 0.5 g). All types of scaffolds were degraded both in vitro and in vivo. Furthermore, these scaffolds promoted bone formation in a mouse calvarial defect model and the bone formation was enhanced by addition of FhBMP-2. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4091 / 4099
页数:9
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