Modification of fibrous poly(L-lactic acid) scaffolds with self-assembling triblock molecules

被引:20
作者
Stendahl, JC
Li, LM
Claussen, RC
Stupp, SI
机构
[1] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
基金
美国国家科学基金会;
关键词
cell adhesion; polylactic acid; scaffold; self-assembly; surface modification;
D O I
10.1016/j.biomaterials.2004.01.042
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Molecular self-assembly offers an effective method to modify the surface properties of common biomaterials by presenting biologically relevant chemistry in a controlled, ordered fashion. This work reports on self-assembling triblock molecules containing rigid cholesteryl segments followed by flexible oligomers Of L-(lactic acid) and second generation L-lysine dendrons. Second harmonic generation and small angle X-ray scattering indicate these molecules self-assemble into multilayer polar structures when cast from ethyl acetate solutions and segregate into polar polydomains when annealed. These self-assembled layers significantly improve water wettability when coated onto poly(L-lactic acid) fibers. Scaffolds formed from fibers modified by self-assembly enhance adhesion of 3T3 mouse calvaria cells and produce greater population growth rates. These results demonstrate the use of self-assembly to present biologically relevant chemistry on surfaces of biomaterials. Applications of this technology include the modification of substrates for cell culture, tissue engineering, and cell transplantation. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5847 / 5856
页数:10
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