生物相容性
自愈水凝胶
丙烯酸酯
超分子化学
材料科学
聚合
自愈
共价键
纳米技术
化学
分子
高分子化学
聚合物
复合材料
有机化学
共聚物
冶金
替代医学
病理
医学
作者
Zhifang Wang,Yipeng Ren,Ye Zhu,Lijing Hao,Yunhua Chen,Geng An,Hongkai Wu,Xuetao Shi,Chuanbin Mao
标识
DOI:10.1002/anie.201804400
摘要
Abstract It is still a challenge to achieve both excellent mechanical strength and biocompatibility in hydrogels. In this study, we exploited two interactions to form a novel biocompatible, slicing‐resistant, and self‐healing hydrogel. The first was molecular host–guest recognition between a host (isocyanatoethyl acrylate modified β‐cyclodextrin) and a guest (2‐(2‐(2‐(2‐(adamantyl‐1‐oxy)ethoxy)ethoxy)ethoxy)ethanol acrylate) to form “three‐arm” host–guest supramolecules (HGSMs), and the second was covalent bonding between HGSMs (achieved by UV‐initiated polymerization) to form strong cross‐links in the hydrogel. The host–guest interaction enabled the hydrogel to rapidly self‐heal. When it was cut, fresh surfaces were formed with dangling host and guest molecules (due to the breaking of host–guest recognition), which rapidly recognized each other again to heal the hydrogel by recombination of the cut surfaces. The smart hydrogels hold promise for use as biomaterials for soft‐tissue repair.
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