Efficacy Evaluation and Mechanism Study of Nonantibiotic Nanoplatform for Clearing MRSA.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Xiangjun Chen, Xinzhong Zhang, Qing Fan, Menglin Cao, Sai Zhang, Wenting Li, Rui Ma, Xiuping Zhang, Wei Hong
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引用次数: 0

Abstract

The effective treatment of infections induced by biofilms has remained a substantial challenge in clinical practice. Presently, there is an imperative demand for innovative antimicrobial strategies that can not only eliminate biofilms but also incorporate controlled delivery and intelligent release mechanisms. In this research, the charge-reversible nonantibiotic nanodelivery system (MPDA/AuNCs/ICG@Lip NPs) is synthesized. Initially, AuNCs and indocyanine green (ICG) were introduced onto MPDA NPs via adsorption and mesoporous loading, followed by the modification of the phospholipids on the exterior surface. Within the biofilm microenvironment, the surface charge was reversed, thereby improving its affinity for methicillin-resistant Staphylococcus aureus (MRSA) and facilitating enhanced biofilm permeability. Owing to the ultrasmall AuNCs, they were internalized by the bacteria and, in conjunction with ICG, contributed to the elevation of local ROS concentrations under the 808 nm laser. As anticipated, the in vitro findings confirmed that MPDA/AuNCs/ICG@Lip NPs demonstrated superior biofilm-clearing capabilities and antibacterial effect. In vivo experiments corroborated that MPDA/AuNCs/ICG@Lip NPs successfully targeted the cyst site and remained localized for an extended period, resulting in excellent therapeutic efficacy. This discovery offers a novel perspective for the development of nonantibiotic nanoplatform for clearing MRSA.

非抗生素纳米平台清除MRSA的疗效评价及机制研究。
生物膜感染的有效治疗在临床实践中仍然是一个重大挑战。目前,迫切需要创新的抗菌策略,既能消除生物膜,又能结合控制递送和智能释放机制。在本研究中,合成了电荷可逆的非抗生素纳米递送系统(MPDA/AuNCs/ICG@Lip NPs)。首先,通过吸附和介孔负载将AuNCs和吲哚菁绿(ICG)引入MPDA NPs,然后对外表面的磷脂进行修饰。在生物膜微环境中,表面电荷被逆转,从而提高了其对耐甲氧西林金黄色葡萄球菌(MRSA)的亲和力,促进了生物膜的渗透性增强。由于超小的aunc,它们被细菌内化,并与ICG一起,促进了808 nm激光下局部ROS浓度的升高。正如预期的那样,体外研究结果证实MPDA/AuNCs/ICG@Lip NPs具有优越的生物膜清除能力和抗菌效果。体内实验证实MPDA/ aunc /ICG@Lip NPs成功靶向囊肿部位,并在较长时间内保持定位,具有良好的治疗效果。这一发现为开发清除MRSA的非抗生素纳米平台提供了一个新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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