聚乙烯亚胺
胶粘剂
儿茶酚
材料科学
水溶液
粘附
单宁酸
化学工程
氢键
纳米技术
高分子化学
化学
有机化学
复合材料
图层(电子)
分子
工程类
基因
生物化学
转染
作者
Yuexin Cui,Liying Yin,Xiaoya Sun,Ning Zhang,Nan Gao,Guangshan Zhu
标识
DOI:10.1021/acsami.1c14231
摘要
The excellent adhesion of mussels under wet conditions has inspired the development of numerous catechol-based wet adhesives. Nevertheless, the performance of catechol-based wet adhesive suffers from the sensitivity toward temperature, pH, or oxidation stimuli. Therefore, it is of great significance to develop non-catechol-based wet adhesives to fully recapitulate nature’s dynamic function. Herein, a novel type of non-catechol-based wet adhesive is reported, which is readily formed by self-assembly of commercially available branched polyethylenimine and phosphotungstic acid in aqueous solution through the combination of electrostatic interaction and hydrogen bonding. This wet adhesive shows reversible, tunable, and strong adhesion on diverse substrates and further exhibits high efficacy in promoting biological wound healing. During the healing of the wound, the as-prepared wet adhesive also possesses inherent antimicrobial properties, thus avoiding inflammations and infections due to microorganism accumulation.
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