An injectable double network hydrogel with hemostasis and antibacterial activity for promoting multidrug-resistant bacteria infected wound healing

伤口愈合 自愈水凝胶 止血 微生物学 化学 抗菌剂 细菌 生物膜 抗生素 体内 抗菌肽 多重耐药 医学 生物 免疫学 外科 生物技术 有机化学 遗传学
作者
Zibo Zhang,Jiadong Guo,Yuxiang He,Jinzhi Han,Mingmao Chen,Yunquan Zheng,Shenghang Zhang,Shaobin Guo,Xianai Shi,Jianming Yang
出处
期刊:Biomaterials Science [Royal Society of Chemistry]
卷期号:10 (12): 3268-3281 被引量:20
标识
DOI:10.1039/d2bm00347c
摘要

Multidrug-resistant bacteria infections frequently occur in wound care due to the excessive use of antibiotics. It can cause scar formation, wound closure delay, multiple organ failure, and high mortality. Here, a double network hydrogel with injectability, hemostasis, and antibacterial activity was developed to prompt multidrug-resistant bacteria infected wound healing. The double network hydrogel is composed of gelatin methacryloyl (GelMA), oxidized dextran (ODex), ε-polylysine (EPL), and bacitracin, and formed through the Schiff-base and UV-initiated crosslinking reaction. The injectable hydrogel with an adhesion effect could adapt to the irregular shape of the wound and possesses good hemostatic ability. The hydrogel presents good flexibility and rapid resilience due to its double network structure, and it can prompt cell proliferation and migration. In particular, the hydrogel has broad-spectrum in vitro antimicrobial activities against S. aureus, E. coli, and methicillin-resistant S. aureus (MRSA), and disrupts E. coli and MRSA biofilms. In vivo results demonstrated that the hydrogel can completely heal MRSA-infected wound in rats within 15 days, through inhibiting the growth of bacteria, accelerating skin tissue reepithelialization, collagen deposition, and angiogenesis, as well as adjusting the expression of CD31, α-SMA, and TNF-α. The findings of this study suggest that the presented hydrogel could enhance multidrug-resistant bacteria infected wound healing and mitigate antimicrobial resistance.
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