A 2D self-cascade catalytic system based on CoCuFe-LDH nanosheets for accelerated healing of infected wounds

级联 催化作用 自愈 化学 化学工程 材料科学 医学 生物化学 色谱法 工程类 病理 替代医学
作者
Jinyao Zheng,Zongjia Li,Juan Qin,Yuanhao Zhang,Xinyue Guo,Xiue Jiang,Miaomiao Zhang,Jilin Tang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:495: 153298-153298 被引量:18
标识
DOI:10.1016/j.cej.2024.153298
摘要

The emergence of drug-resistant bacteria has rendered traditional antibiotics ineffective, posing a serious threat to human health. There is an urgent need to find alternative antimicrobial agents. Inspired by enzyme immobilization and multi-enzyme biocatalysis, we have designed a tri-metal layered double hydroxide (LDHs)-based cascade catalytic system (CoCuFe-LDH@Gox nanosheets) for treating drug-resistant bacterial infections and promoting wound healing. The synergistic effects of the Co, Cu, and Fe in the tri-metal LDHs structure endow CoCuFe-LDH nanosheets with excellent peroxidase (POD)-like activity. The large specific surface area of CoCuFe-LDH nanosheets render them ideal carriers for glucose oxidase (Gox). CoCuFe-LDH@Gox nanosheets can catalyze glucose to produce gluconic acid and H2O2. The generated gluconic acid decreases the local pH, further enhancing the POD-like activity of CoCuFe-LDH@Gox nanosheets at wound site. CoCuFe-LDH@Gox nanosheets can then catalyze H2O2 generating hydroxyl radicals (•OH) to effectively kill drug-resistant bacteria. This synergistic integration of the catalytic LDHs and the Gox components enables the cascade catalytic system to be highly effective against drug-resistant bacteria. In addition to its remarkable antibacterial properties, this LDHs-based system also exhibits excellent biocompatibility and considerable immunomodulatory capabilities. It can accelerate the healing of drug-resistant bacteria-infected wounds by inhibiting the inflammatory response and regulating macrophage polarization. These multifunctional attributes make the CoCuFe-LDH@Gox nanosheets a highly promising candidate for the treatment of drug-resistant bacterial infections in future clinical applications.
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