Mechanically Reinforced and Injectable Universal Adhesive Based on a PEI–PAA/Alg Dual-Network Hydrogel Designed by Topological Entanglement and Catechol Chemistry

生物粘附 材料科学 生物相容性 胶粘剂 粘附 自愈水凝胶 壳聚糖 复合材料 聚合物 固化(化学) 纳米技术 化学工程 高分子化学 图层(电子) 工程类 冶金
作者
Buyun Chen,Dandan Zhu,Qiang Li,Chenhao Wang,Jiahua Cui,Zhen Zheng,Xinling Wang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (51): 59826-59837 被引量:28
标识
DOI:10.1021/acsami.3c14743
摘要

Universal adhesion of hydrogels to diverse materials is essential to their extensive applications. Unfortunately, tough adhesion of wet surfaces remains an urgent challenge so far, requiring robust cohesion strength for effective stress dissipation. In this work, a dual-network hydrogel polyethylenimine-poly(acrylic acid)/alginate (PEI-PAA/Alg) with excellent mechanical strength is realized via PEI-PAA complex and calcium alginate coordination for universal adhesion by the synergistic effort of topological entanglement and catechol chemistry. The dual networks of PEI-PAA/Alg provide mechanically reinforced cohesion strength, which is sufficient for energy dissipation during adhesion with universal materials. After the integration of mussel-inspired dopamine into PAA or Alg, the adhesive demonstrates further improved adhesion performance with a solid adherend and capability to bond cancellous bones. Notably, the dopamine-modified adhesive exhibits better instant adhesion and reversibility with wet surfaces compared with commercial fibrin. Adhesion interfaces are investigated by SEM and micro-FTIR to verify the effectiveness of strategies of topological entanglement. Furthermore, the adhesive also possesses great injectability, stability, tissue adhesion, and biocompatibility. In vivo wound healing and histological analysis indicate that the hydrogel can promote wound closure, epidermis regeneration, and tissue refunctionalization, implying its potential application for bioadhesive and wound dressing.
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