自愈水凝胶
胶粘剂
聚合物
共价键
粘附
化学
贻贝
甲基丙烯酸酯
非共价相互作用
材料科学
高分子化学
纳米技术
分子
有机化学
氢键
聚合
生态学
图层(电子)
生物
作者
Bum Jin Kim,Dongyeop X. Oh,Sangsik Kim,Jeong Hyun Seo,Dong Soo Hwang,Admir Mašić,Dong Keun Han,Hyung Joon
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2014-04-08
卷期号:15 (5): 1579-1585
被引量:270
摘要
Hydrogel systems based on cross-linked polymeric materials which could provide both adhesion and cohesion in wet environment have been considered as a promising formulation of tissue adhesives. Inspired by marine mussel adhesion, many researchers have tried to exploit the 3,4-dihydroxyphenylalanine (DOPA) molecule as a cross-linking mediator of synthetic polymer-based hydrogels which is known to be able to achieve cohesive hardening as well as adhesive bonding with diverse surfaces. Beside DOPA residue, composition of other amino acid residues and structure of mussel adhesive proteins (MAPs) have also been considered important elements for mussel adhesion. Herein, we represent a novel protein-based hydrogel system using DOPA-containing recombinant MAP. Gelation can be achieved using both oxdiation-induced DOPA quinone-mediated covalent and Fe3+-mediated coordinative noncovalent cross-linking. Fe3+-mediated hydrogels show deformable and self-healing viscoelastic behavior in rheological analysis, which is also well-reflected in bulk adhesion strength measurement. Quinone-mediated hydrogel has higher cohesive strength and can provide sufficient gelation time for easier handling. Collectively, our newly developed MAP hydrogel can potentially be used as tissue adhesive and sealant for future applications.
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