丙烯酰胺
胶粘剂
聚合
粘附
氰基丙烯酸酯
自愈水凝胶
高分子化学
材料科学
化学
聚合物
纳米技术
复合材料
共聚物
图层(电子)
作者
Tingwu Liu,Wen Sun,Changjun Mu,Xu Zhang,Donghua Xu,Qiuyan Yan,Shifang Luan
标识
DOI:10.1016/j.ijbiomac.2024.132360
摘要
Injectable adhesive hydrogels combining rapid gelling with robust adhesion to wet tissues are highly required for fast hemostasis in surgical and major trauma scenarios. Inspired by the cross-linking mechanism of mussel adhesion proteins, we developed a bionic double-crosslinked (BDC) hydrogel of poly (γ-glutamic acid) (PGA)/poly (N-(2-hydroxyethyl) acrylamide) (PHEA) fabricated through a combination of photo-initiated radical polymerization and hydrogen bonding cross-linking. The BDC hydrogel exhibited an ultrafast gelling process within 1 s. Its maximum adhesion strength to wet porcine skin reached 254.5 kPa (9 times higher than that of cyanoacrylate (CA) glue) and could withstand an ultrahigh burst pressure of 626.4 mmHg (24 times higher than that of CA glue). Notably, the BDC hydrogel could stop bleeding within 10 s from a rat liver incision 10 mm long and 5 mm deep. The wound treated with the BDC hydrogel healed faster than the control groups, underlining the potential for emergency rescue and wound care scenarios.
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