Injectable multifunctional chitosan/dextran-based hydrogel accelerates wound healing in combined radiation and burn injury

自愈水凝胶 伤口愈合 化学 生物相容性 壳聚糖 活性氧 促炎细胞因子 炎症 免疫学 医学 生物化学 高分子化学 有机化学
作者
Jintao Shen,Wencheng Jiao,Ziyuan Chen,Chunqing Wang,Xingshuang Song,Lei Ma,Ziyan Tang,Wenrui Yan,Hua Xie,Bochuan Yuan,Li Wang,Jing Dai,Yunbo Sun,Lina Du,Yiguang Jin
出处
期刊:Carbohydrate Polymers [Elsevier]
卷期号:316: 121024-121024 被引量:32
标识
DOI:10.1016/j.carbpol.2023.121024
摘要

Clinical wound management of combined radiation and burn injury (CRBI) remains a huge challenge due to serious injuries induced by redundant reactive oxygen species (ROS), the accompanying hematopoietic, immunologic suppression and stem cell reduction. Herein, the injectable multifunctional Schiff base cross-linked with gallic acid modified chitosan (CSGA)/oxidized dextran (ODex) hydrogels were rationally designed to accelerate wound healing through elimination of ROS in CRBI. CSGA/ODex hydrogels, fabricated by mixing solutions of CSGA and Odex, displayed good self-healing ability, excellent injectability, strong antioxidant activity, and favorable biocompatibility. More importantly, CSGA/ODex hydrogels exhibited excellent antibacterial properties, which is facilitated for wound healing. Furthermore, CSGA/ODex hydrogels significantly suppressed the oxidative damage of L929 cells in an H2O2-induced ROS microenvironment. The recovery of mice with CRBI in mice demonstrated that CSGA/ODex hydrogels significantly reduced the hyperplasia of epithelial cells and the expression of proinflammatory cytokine, and accelerated wound healing which was superior to the treatment with commercial triethanolamine ointment. In conclusion, the CSGA/ODex hydrogels as a wound dressing could accelerate the wound healing and tissue regeneration of CRBI, which provides great potential in clinical treatment of CRBI.
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