Mussel-Inspired Histidine-Based Transient Network Metal Coordination Hydrogels

被引:284
作者
Fullenkamp, Dominic E. [1 ,2 ]
He, Lihong [1 ,2 ]
Barrett, Devin G. [1 ,2 ,3 ]
Burghardt, Wesley R. [4 ]
Messersmith, Phillip B. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Chem Life Proc Inst, Evanston, IL 60208 USA
[3] Northwestern Univ, Inst Bionanotechnol Med, Evanston, IL 60208 USA
[4] Northwestern Univ, Chem & Biol Engn Dept, Evanston, IL 60208 USA
[5] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Evanston, IL 60208 USA
[6] Northwestern Univ, Mat Sci & Engn Dept, Evanston, IL 60208 USA
关键词
BIPYRIDYL-BRANCHED POLYOXAZOLINE; MOLECULE FORCE SPECTROSCOPY; MECHANICAL-PROPERTIES; AFFINITY HYDROGELS; SACRIFICIAL BONDS; POLYMER NETWORKS; HIDDEN LENGTH; CROSS-LINKING; BEHAVIOR; BYSSUS;
D O I
10.1021/ma301791n
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Transient network hydrogels cross-linked through histidine- divalent cation coordination bonds were studied by conventional rheologic methods using histidine-modified star poly(ethylene glycol) (PEG) polymers. These materials were inspired by the mussel, which is thought to use histidine-metal coordination bonds to impart self-healing properties in the mussel byssal thread. Hydrogel viscoelastic mechanical properties were studied as a function of metal, pH, concentration, and ionic strength. The equilibrium metal-binding constants were determined by dilute solution potentiometric titration of monofunctional histidine-modified methoxy-PEG and were found to be consistent with binding constants of small molecule analogues previously studied. pH-dependent speciation curves were then calculated using the equilibrium constants determined by potentiometric titration, providing insight into the pH dependence of histidine-metal ion coordination and guiding the design of metal coordination hydrogels. Gel relaxation dynamics were found to be uncorrelated with the equilibrium constants measured, but were correlated to the expected coordination bond dissociation rate constants.
引用
收藏
页码:1167 / 1174
页数:8
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