Ruthenium-catalyzed photo cross-linking of fibrin-based engineered tissue

被引:75
作者
Bjork, Jason W. [2 ]
Johnson, Sandra L. [2 ]
Tranquillo, Robert T. [1 ,2 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
Arterial tissue engineering; Cross-linking; Dityrosine; Fibrin; Fibroblast; I COLLAGEN; MECHANICAL-PROPERTIES; CYCLIC DISTENSION; MEDIA EQUIVALENT; SCAFFOLD; CELLS; VITRO; ASSAY;
D O I
10.1016/j.biomaterials.2010.12.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Most cross-linking methods utilize chemistry or physical processes that are detrimental to cells and tissue development. Those that are not as harmful often do not provide a level of strength that ultimately meets the required application. The purpose of this work was to investigate the use of a ruthenium sodium persulfate cross-linking system to form dityrosine in fibrin-based engineered tissue. By utilizing the tyrosine residues inherent to fibrin and cell-deposited proteins, at least 3-fold mechanical strength increases and 10-fold stiffness increases were achieved after cross-linking. This strengthening and stiffening effect was found to increase with culture duration prior to cross-linking such that physiologically relevant properties were obtained. Fibrin was not required for this effect as demonstrated by testing with collagen-based engineered tissue. Cross-linked tissues were implanted subcutaneously and shown to have minimal inflammation after 30 days, similar to non-cross-linked controls. Overall, the method employed is rapid, non-toxic, minimally inflammatory, and is capable of increasing strength and stiffness of engineered tissues to physiological levels. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2479 / 2488
页数:10
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