Hydrazone self-crosslinking of multiphase elastin-like block copolymer networks

被引:26
|
作者
Krishna, Urlam Murali [2 ]
Martinez, Adam W. [3 ]
Caves, Jeffrey M. [1 ,4 ]
Chaikof, Elliot L. [1 ,2 ,3 ,4 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Surg, Boston, MA 02215 USA
[2] Emory Univ, Dept Surg, Atlanta, GA 30322 USA
[3] Emory Univ, Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02215 USA
关键词
Elastin-mimetic; Block copolymer; Self-crosslinking; Viscoelasticity; Recombinant biomaterial; HYALURONIC-ACID; LOCALIZED DELIVERY; PROTEIN POLYMER; HYDROGEL FILMS; TISSUE; POLYPEPTIDES; CONJUGATE; COLLAGEN; BIOMATERIALS; DEGRADATION;
D O I
10.1016/j.actbio.2011.11.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biosynthetic strategies for the production of recombinant elastin-like protein (ELP) triblock copolymers have resulted in elastomeric protein hydrogels, formed through rapid physical crosslinking upon warming of concentrated solutions. However, the strength of physically crosslinked networks can be limited, and options for non-toxic chemical crosslinking of these networks are not optimal. In this report, we modify two recombinant elastin-like proteins with aldehyde and hydrazide functionalities. When combined, these modified recombinant proteins self-crosslink through hydrazone bonding without requiring initiators or producing by-products. Crosslinked materials are evaluated for water content and swelling upon hydration, and subject to tensile and compressive mechanical tests. Hydrazone crosslinking is a viable method for increasing the mechanical strength of elastin-like protein polymers, in a manner that is likely to lend itself to the biocompatible in situ formation of chemically and physically crosslinked ELP hydrogels. (c) 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:988 / 997
页数:10
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