胶粘剂
粘附
组织粘连
止血
肿胀 的
材料科学
甲基丙烯酸酯
自愈水凝胶
生物医学工程
共聚物
高分子化学
复合材料
外科
聚合物
图层(电子)
医学
作者
Hongjian Huang,Renfeng Xu,Peng Ni,Zhenghong Zhang,Caixia Sun,Huaying He,Xinyue Wang,Lidan Zhang,Ziyi Liang,Haiqing Liu
标识
DOI:10.1016/j.mtbio.2022.100369
摘要
Tissue adhesive with on-demand detachment feature is critically important since it can minimize hurt to patient when it is stripped away. Herein, a water-driven noninvasively detachable wet tissue adhesive hydrogel (w-TAgel) was produced by UV-initiated radical copolymerization of N-isopropylacrylamide (NIPAM), acrylamide (AAm), gelatin methacrylate (GelMA), and urushiol. As a w-TAgel, its robust and tough mechanical property makes it suitable for dynamic wound tissue. The polyurushiol segments of it are crucial to the formation of tough adhesion interface with various wet tissues, while polyNIPAM units play an indispensable role in on-demand detachment via thermo-responsive swelling behavior because the hydrophobic aggregation among isopropyl groups is destroyed upon water treatment with temperature of 25 °C or less. Additionally, it exhibits multiple merits including good hemocompatibility, cytocompatibility as well as pro-coagulant activity and hemostasis. Therefore, our w-TAgel with strong adhesion and facile detachment is an advanced prospective dressing for wound closure and rapid hemostasis. The wet tissue adhesion and water-driven detachable mechanism may shed new light on the development of on-demand noninvasively detachable wet tissue adhesives.
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