Composite scaffolds: Bridging nanofiber and microsphere architectures to improve bioactivity of mechanically competent constructs

被引:30
作者
Brown, Justin L. [2 ]
Peach, M. Sean [3 ]
Nair, Lakshmi S. [1 ]
Kumbar, Sangamesh G. [1 ]
Laurencin, Cato T. [1 ,4 ]
机构
[1] Univ Connecticut, Dept Orthopaed Surg, Farmington, CT 06030 USA
[2] Penn State Univ, Dept Bioengn, University Pk, PA 16802 USA
[3] Univ Virginia, Dept Physiol, Charlottesville, VA 22904 USA
[4] Univ Connecticut, Dept Chem Mat & Biomol Engn, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
biomaterials; nanofiber; microsphere; polyphosphazene; osteoblast; OSTEOBLAST DIFFERENTIATION; BONE; ADHESION; MATRIX; CELL; EXPRESSION; RUNX2; FAK;
D O I
10.1002/jbm.a.32934
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
Tissue engineering often benefits from the use of composites to produce an ideal scaffold. We present the focused development of a novel structure that combines the biomimetic properties of nanofibers with the robust mechanical aspects of the sintered microsphere scaffold to produce a composite scaffold that demonstrates an ability to mimic the mechanical environment of trabecular bone while also promoting the phenotype progression of osteoblast progenitor cells. These composite nanofiber/microsphere scaffolds exhibited a mechanical modulus and compressive strength similar to trabecular bone and exhibited degradation resulting in a mass loss of 30% after 24 weeks. The nanofiber portion of these scaffolds was sufficiently porous to allow cell migration throughout the fibrous portion of the scaffold and promoted phenotype progression through focal adhesion kinase-mediated activation of the transcription factor Runx2, control scaffolds not containing nanofibers did not demonstrate extensive cell migration or phenotype progression. Ultimately, the focal adhesion kinase activity on the composite nanofiber/microsphere scaffolds demonstrated causality over the production of the mature osteoblast marker, osteocalcin, and the development of a calcified matrix. (C) 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 95A: 1150-1158,2010.
引用
收藏
页码:1150 / 1158
页数:9
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