生物污染
自愈水凝胶
生物相容性
材料科学
粘附
蛋白质吸附
聚合
化学工程
吸附
氢键
纳米技术
高分子化学
有机化学
聚合物
复合材料
分子
化学
生物化学
膜
工程类
冶金
作者
Meng Li,Mengyuan Zhang,Zheng Liu,Ruilin Xie,Yuxuan Yang,Kaixiang Shen,Aimin Yang,Yilong Cheng
标识
DOI:10.1007/s40843-023-2763-1
摘要
The design and fabrication of injectable barriers with promising antifouling capability to prevent the formation of adhesions after surgery remains challenging. Herein, we introduce amino acid derivative with hydroxyl group (N-acryloyl serine (ASer)) into the preparation of hydrogels to develop a novel hydrogen bond-crosslinked hydrogel (PASer) by free radical polymerization. It is found that one substituted methyl group can cause considerable disruption to the hydrogen bonding interaction and result in increased initial gelling concentration and significant decrease in the mechanical properties of poly(N-acryloyl threonine) (PAThr) hydrogel compared with PASer hydrogel. Moreover, it is worth noting that the hydrophilic hydroxyl groups enable PASer hydrogel to efficiently resist protein adsorption and cell adhesion. The PASer hydrogel possesses excellent mechanical performance, injectability, self-fusion, good biocompatibility and appropriate in vivo residence time, which are consistent with the requirements of postoperative anti-adhesion materials in clinical practice. In vivo studies reveal that the advanced hydrogel shows satisfactory preventive effect on postoperative peritoneal adhesions in the established mice abdominal wall defect model.
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