EGCG金属-多酚框架在mrsa感染伤口治疗中控制一氧化氮释放。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Jia-Xi Chen, , , Xin-Hui Zhou, , , Wei-Qiu Wen, , , Ze-Ting Huang, , , Jie Xuan, , , Ping Gui, , , Wei-Hua Peng*, , , Xi-Ren Wu*, , and , Guan-Hai Wang*, 
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引用次数: 0

摘要

耐药菌已成为医院的主要病原菌。由于它们的耐药性,传统抗生素在治疗耐药细菌方面越来越有限。为了克服这一问题,设计了一种金属-多酚框架(MPN),负载一氧化氮供体(s -亚硝基谷胱甘肽(GSNO)),用于治疗耐甲氧西林金黄色葡萄球菌(MRSA)感染的伤口。MPN通过表没食子儿茶素没食子酸酯(EGCG)和Fe3+之间的螯合形成框架结构,封装GSNO。结果表明,在808 nm激光照射下,光热触发NO释放能够抑制MRSA并消除生物膜。EGCG具有清除ROS和抑制炎症的能力,能有效诱导巨噬细胞从M1向M2极化,促进血管生成和伤口愈合。总之,本工作设计了一种简单有效的给药系统,为控制MRSA感染和促进组织再生提供了一种有前景的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

EGCG Metal–Polyphenol Frameworks for Controlling Nitric Oxide Release in the Treatment of MRSA-Infected Wounds

EGCG Metal–Polyphenol Frameworks for Controlling Nitric Oxide Release in the Treatment of MRSA-Infected Wounds

Drug-resistant bacteria have become the main pathogens in hospitals. Due to their resistance, traditional antibiotics are increasingly limited in treating resistant bacteria. To overcome this problem, a metal–polyphenol framework (MPN) loaded with a nitric oxide donor (S-nitrosoglutathione (GSNO)) was designed for the treatment of methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds. The MPN forms a framework structure through chelation between epigallocatechin gallate (EGCG) and Fe3+, encapsulating the GSNO. The results demonstrated that under 808 nm laser irradiation, the photothermal-triggered release of NO could inhibit MRSA and eliminate biofilms. EGCG has the ability to scavenge ROS and inhibit inflammation, effectively inducing macrophage polarization from M1 to M2, promoting angiogenesis and wound healing. In summary, this work designed a simple and effective drug delivery system, providing a promising therapeutic strategy for controlling MRSA infection and promoting tissue regeneration.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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