Song Fuyu, Zhang Jiahui, Lu Jie, Cheng Yi, Tao Yehan, Shao Changyou, Wang Haisong
Liaoning Key Laboratory of Lignocellulose Chemistry and BioMaterials, School of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian 116034, China.
Liaoning Key Laboratory of Lignocellulose Chemistry and BioMaterials, School of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian 116034, China.
Int J Biol Macromol. 2021 Oct 31;189:183-193. doi: 10.1016/j.ijbiomac.2021.08.132. Epub 2021 Aug 21.
The significant progress in efforts to design hydrogel adhesive mimicking mussels' functions has been witnessed in recent years. However, it is still an arduous challenge to fabricate self-adhesive hydrogel adhesive that tradeoff of exalting features containing scalability, self-healing, degradability, biocompatibility, and antibacterial properties. Herein, we manufactured a multi-functional physical hydrogel adhesive by integrating catechol groups modified chitosan and polyvinyl alcohol (PVA). Intriguingly, the physical gels reinforce durable and repeatable adhesiveness due to the limited auto-oxidation of catechol groups of the 3-(3,4-dihydroxyphenyl) propionic acid modified chitosan (DCS), which can be adhered diametrically on human skin without shedding and residue. Additionally, the dynamic H-bonds between DCS and PVA endows the hydrogel to self-heal under a relatively mild stimulation. The assembly of silver nano armor remarkably enhances the mechanical strength and antibacterial of the hydrogel. Meanwhile, the metal coordination formed between the nano-silver and the hydroxyl groups of catechol and the electrostatic interaction between the silver ions and the hydroxyl groups also contribute to the hydrogel to achieve self-healing. This work provides a neoteric prospect in designing degradable hydrogels with stretchability, self-adhesion, self-healing, antibacterial and biocompatibility for potential applications in tissue adhesion and wound healing.
近年来,在设计模仿贻贝功能的水凝胶粘合剂方面已取得显著进展。然而,制造具有可扩展性、自愈性、可降解性、生物相容性和抗菌性能等优异特性的自粘性水凝胶粘合剂仍然是一项艰巨的挑战。在此,我们通过整合儿茶酚基团修饰的壳聚糖和聚乙烯醇(PVA)制备了一种多功能物理水凝胶粘合剂。有趣的是,由于3-(3,4-二羟基苯基)丙酸修饰的壳聚糖(DCS)的儿茶酚基团的自动氧化受限,物理凝胶增强了持久且可重复的粘附性,它可以直接粘附在人体皮肤上而不脱落和残留。此外,DCS和PVA之间的动态氢键使水凝胶在相对温和的刺激下能够自愈。银纳米铠甲的组装显著提高了水凝胶的机械强度和抗菌性能。同时,纳米银与儿茶酚羟基之间形成的金属配位以及银离子与羟基之间的静电相互作用也有助于水凝胶实现自愈。这项工作为设计具有拉伸性、自粘性、自愈性、抗菌性和生物相容性的可降解水凝胶提供了新的前景,有望用于组织粘附和伤口愈合。