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ε-聚赖氨酸纳米共轭物:用于耐药细菌的增值抗菌剂。

ε-Polylysine Nanoconjugates: Value-Added Antimicrobials for Drug-Resistant Bacteria.

作者信息

Prasad Puja, Singh Rohini, Kamaraju Saipriya, Sritharan Venkataraman, Gupta Shalini

机构信息

Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi 110016, India.

Molecular Diagnostics and Biomarkers Lab, Gleneagles Global Hospitals, Lakdi ka pul, Hyderabad 500004, India.

出版信息

ACS Appl Bio Mater. 2020 Oct 19;3(10):6688-6696. doi: 10.1021/acsabm.0c00569. Epub 2020 Sep 30.

Abstract

Antimicrobial resistance poses a serious threat to human health and is evidently not restricted to any one part of the globe. Over the last few decades, no new antibiotics have been discovered, and many antibiotics currently available are failing against several critical pathogenic strains due to emerging drug resistance. We have designed a strategy to combat deadly drug-resistant bacteria by using nanocargos that consist of gold nanoparticles (AuNPs) conjugated to ε-polylysine (PLL) and octadecanethiol (C18) either alone or in combination. These nanocargos when tested against reference strains of carbapenem-resistant (CRAB) and methicillin-resistant (MRSA) showed 15-20-fold higher antibacterial activity compared to free PLL. The minimum inhibitory concentration (MIC) of the nanoconjugates was found to lie between 8 and 15 μg/mL for both these bacteria, and they were also found to be nonhemolytic and nontoxic to mammalian cells. The mechanistic evaluation of antibacterial action showed alternate pathways of uptake for free PLL and the nanoconjugates. Further, the nanocargos were successfully used and found to be superior to free PLL in preventing biofilm formation in MRSA and CRAB. The PLL nanoconjugates may find applications in prevention of bacterial biofilm formation on surfaces such as surgical instruments and indwelling devices like stents, catheters, cannulas, orthopedic implants, and pacemakers.

摘要

抗菌耐药性对人类健康构成严重威胁,而且显然并不局限于全球的任何一个地区。在过去几十年里,没有发现新的抗生素,由于新出现的耐药性,目前可用的许多抗生素对几种关键致病菌株已经失效。我们设计了一种策略,通过使用由金纳米颗粒(AuNPs)与ε-聚赖氨酸(PLL)和十八烷硫醇(C18)单独或组合缀合而成的纳米载体来对抗致命的耐药细菌。这些纳米载体在针对耐碳青霉烯类(CRAB)和耐甲氧西林(MRSA)参考菌株进行测试时,与游离PLL相比,显示出高15至20倍的抗菌活性。发现这些纳米缀合物对这两种细菌的最低抑菌浓度(MIC)在8至15μg/mL之间,并且还发现它们对哺乳动物细胞无溶血和无毒作用。抗菌作用的机制评估显示,游离PLL和纳米缀合物的摄取途径不同。此外,纳米载体已成功使用,并且在预防MRSA和CRAB生物膜形成方面优于游离PLL。PLL纳米缀合物可能在预防手术器械和诸如支架、导管、套管、骨科植入物和起搏器等植入装置等表面的细菌生物膜形成中找到应用。

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