pH-Based Regulation of Hydrogel Mechanical Properties Through Mussel-Inspired Chemistry and Processing

被引:223
作者
Barrett, Devin G. [1 ]
Fullenkamp, Dominic E. [2 ]
He, Lihong [2 ]
Holten-Andersen, Niels [3 ]
Lee, Ka Yee C. [3 ]
Messersmith, Phillip B. [4 ]
机构
[1] Northwestern Univ, Dept Biomed Engn, Chem Life Proc Inst, Inst Bionanotechnol Med, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Biomed Engn, Chem Life Proc Inst, Evanston, IL 60208 USA
[3] Univ Chicago, Inst Biophys Dynam, James Franck Inst, Dept Chem, Chicago, IL 60637 USA
[4] Northwestern Univ, Dept Biomed Engn, Mat Sci & Engn Dept,Robert H Lurie Comprehens Can, Chem & Biol Engn Dept,Chem Life Proc Inst,Inst Bi, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
biomimetics; hydrogels; polymeric materials; structure-property relationships; VISCOELASTIC PROPERTIES; SACRIFICIAL BONDS; HIDDEN LENGTH; CROSS-LINKING; SPIDER SILKS; POLYMER; ADHESIVES; PROTEIN; COORDINATION; EQUILIBRIA;
D O I
10.1002/adfm.201201922
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The mechanical holdfast of the mussel, the byssus, is processed at acidic pH yet functions at alkaline pH. Byssi are enriched in Fe3+ and catechol-containing proteins, species with chemical interactions that vary widely over the pH range of byssal processing. Currently, the link between pH, Fe3+-catechol reactions, and mechanical function is poorly understood. Herein, it is described how pH influences the mechanical performance of materials formed by reacting synthetic catechol polymers with Fe3+. Processing Fe3+-catechol polymer materials through a mussel-mimetic acidic-to-alkaline pH change leads to mechanically tough materials based on a covalent network fortified by sacrificial Fe3+-catechol coordination bonds. These findings offer the first direct evidence of Fe3+-induced covalent cross-linking of catechol polymers, reveal additional insight into the pH dependence and mechanical role of Fe3+-catechol interactions in mussel byssi, and illustrate the wide range of physical properties accessible in synthetic materials through mimicry of mussel-protein chemistry and processing.
引用
收藏
页码:1111 / 1119
页数:9
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