Catch bond-inspired hydrogels with repeatable and loading rate-sensitive specific adhesion

自愈水凝胶 胶粘剂 材料科学 粘附 韧性 氢键 复合材料 单宁酸 纳米技术 化学工程 高分子化学 图层(电子) 化学 分子 有机化学 工程类
作者
Zuoying Yuan,Xiaocen Duan,Xing Su,Zhuoling Tian,Anqi Jiang,Zhuo Wan,Hao Wang,Pengfei Wei,Bo Zhao,Xiaozhi Liu,Jianyong Huang
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:21: 566-575 被引量:11
标识
DOI:10.1016/j.bioactmat.2022.09.002
摘要

Biological receptor-ligand adhesion governed by mammalian cells involves a series of mechanochemical processes that can realize reversible, loading rate-dependent specific interfacial bonding, and even exhibit a counterintuitive behavior called catch bonds that tend to have much longer lifetimes when larger pulling forces are applied. Inspired by these catch bonds, we designed a hydrogen bonding-meditated hydrogel made from acrylic acid-N-acryloyl glycinamide (AA-NAGA) copolymers and tannic acids (TA), which formed repeatable specific adhesion to polar surfaces in an ultra-fast and robust way, but hardly adhered to nonpolar materials. It demonstrated up to five-fold increase in shear adhesive strength and interfacial adhesive toughness with external loading rates varying from 5 to 500 mm min-1. With a mechanochemical coupling model based on Monte Carlo simulations, we quantitatively revealed the nonlinear dependence of rate-sensitive interfacial adhesion on external loading, which was in good agreement with the experimental data. Likewise, the developed hydrogels were biocompatible, possessed antioxidant and antibacterial properties and promoted wound healing. This work not only reports a stimuli-responsive hydrogel adhesive suitable for multiple biomedical applications, but also offers an innovative strategy for bionic designs of smart hydrogels with loading rate-sensitive specific adhesion for various emerging areas including flexible electronics and soft robotics.
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