Robust, superabsorbent and antibacterial polysaccharide-based hybrid-network hydrogels for wound repair

自愈水凝胶 生物相容性 壳聚糖 聚丙烯酰胺 极限抗拉强度 材料科学 黄原胶 肿胀 的 抗压强度 化学工程 化学 生物医学工程 复合材料 高分子化学 流变学 有机化学 医学 工程类 冶金
作者
Qin He,Xia Gao,Zhifang Wu,Junlin Zhu,Hang Chen,Xinyao Liu,Xiaonan Zhang
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:279: 134626-134626
标识
DOI:10.1016/j.ijbiomac.2024.134626
摘要

Hydrogel dressings with multiple functions are ideal options for wound repair. This study developed hydrogel dressings by interpenetrating the physically crosslinked xanthan gum (XG)/carboxylated chitosan (CCS) network and the chemically crosslinked polyacrylamide (PAAm) network via a one-pot method. The XG-CCS/PAAm hydrogels were found to display tunable mechanical properties, due to the formation of strong network structure. The hydrogels exhibited the strongest tensile strength of 0.6 MPa at an XG/CCS ratio of 40/60, while the largest compressive strength of 4.5 MPa is achieved at an XG/CCS ratio of 60/40. Moreover, the hydrogel with an XG/CCS ratio of 60/40 exhibited desirable adhesion strength on porcine skin, which was 3.7 kPa. It also had a swelling ratio, as high as 1200 %. After loading with cephalexin, the XG-CCS/PAAm hydrogels can deliver the antibacterial drugs following a first-order kinetic. As a result, both E. coli and S. aureus can be completely inactivated by the cefalexin-loaded hydrogels after 12 h. Furthermore, the XG-CCS/PAAm hydrogels were found to exhibit excellent biocompatibility as well as effective wound healing ability, as proven by the in vitro and in vivo tests. In this regard, XG-CCS/PAAm hydrogels can act as promising multifunctional wound dressings.
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