文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

高效抗菌纳米颗粒对抗致病菌。

Potent antibacterial nanoparticles for pathogenic bacteria.

机构信息

Department of Applied Chemistry, National Chiao Tung University , Hsinchu 300, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2015 Jan 28;7(3):2046-54. doi: 10.1021/am507919m. Epub 2015 Jan 13.


DOI:10.1021/am507919m
PMID:25584802
Abstract

Antibiotic-resistant bacteria have emerged because of the prevalent use of antibacterial agents. Thus, new antibacterial agents and therapeutics that can treat bacterial infections are necessary. Vancomycin is a potent antibiotic. Unfortunately, some bacterial strains have developed their resistance toward vancomycin. Nevertheless, it has been demonstrated that vancomycin-immobilized nanoparticles (NPs) are capable to be used in inhibition of the cell growth of vancomycin-resistant bacterial strains through multivalent interactions. However, multistep syntheses are usually necessary to generate vancomycin-immobilized NPs. Thus, maintaining the antibiotic activity of vancomycin when the drug is immobilized on the surface of NPs is challenging. In this study, a facile approach to generate vancomycin immobilized gold (Van-Au) NPs through one-pot stirring of vancomycin with aqueous tetrachloroauric acid at pH 12 and 25 °C for 24 h was demonstrated. Van-Au NPs (8.4 ± 1.3 nm in size) were readily generated. The generated Van-Au NPs maintained their antibiotic activities and inhibited the cell growth of pathogens, which included Gram-positive and Gram-negative bacteria as well as antibiotic-resistant bacterial strains. Furthermore, the minimum inhibitory concentration of the Van-Au NPs against bacteria was lower than that of free-form vancomycin. Staphylococcus aureus-infected macrophages were used as the model samples to examine the antibacterial activity of the Van-Au NPs. Macrophages have the tendency to engulf Van-Au NPs through endocytosis. The results showed that the cell growth of S. aureus in the macrophages was effectively inhibited, suggesting the potential of using the generated Van-Au NPs as antibacterial agents for bacterial infectious diseases.

摘要

由于抗菌剂的普遍使用,出现了耐药菌。因此,有必要开发新的抗菌药物和疗法来治疗细菌感染。万古霉素是一种强效抗生素。不幸的是,一些细菌株已经对万古霉素产生了耐药性。然而,已经证明万古霉素固定化纳米颗粒(NPs)通过多价相互作用能够用于抑制万古霉素耐药菌株的细胞生长。然而,通常需要多步合成来生成万古霉素固定化 NPs。因此,当药物固定在 NPs 表面时,保持万古霉素的抗生素活性是具有挑战性的。在这项研究中,通过在 pH 12 和 25°C 下将万古霉素与四氯金酸的水溶液一锅搅拌 24 小时,展示了一种简便的方法来生成万古霉素固定化金(Van-Au)NPs。容易生成了 Van-Au NPs(尺寸为 8.4±1.3nm)。生成的 Van-Au NPs 保持了它们的抗生素活性,并抑制了病原体的细胞生长,包括革兰氏阳性和革兰氏阴性细菌以及耐药菌株。此外,Van-Au NPs 对细菌的最低抑菌浓度低于游离形式的万古霉素。金黄色葡萄球菌感染的巨噬细胞被用作模型样品来检测 Van-Au NPs 的抗菌活性。巨噬细胞通过内吞作用有吞噬 Van-Au NPs 的趋势。结果表明,巨噬细胞中金黄色葡萄球菌的细胞生长得到了有效抑制,表明所生成的 Van-Au NPs 有潜力作为治疗细菌感染性疾病的抗菌剂。

相似文献

[1]
Potent antibacterial nanoparticles for pathogenic bacteria.

ACS Appl Mater Interfaces. 2015-1-13

[2]
Nanotechnology as a therapeutic tool to combat microbial resistance.

Adv Drug Deliv Rev. 2013-7-24

[3]
Vancomycin-modified mesoporous silica nanoparticles for selective recognition and killing of pathogenic gram-positive bacteria over macrophage-like cells.

ACS Appl Mater Interfaces. 2013-10-30

[4]
pH-Responsive Lipid-Dendrimer Hybrid Nanoparticles: An Approach To Target and Eliminate Intracellular Pathogens.

Mol Pharm. 2019-10-16

[5]
Functional gold nanoparticle-based antibacterial agents for nosocomial and antibiotic-resistant bacteria.

Nanomedicine (Lond). 2016-9-13

[6]
Antibacterial gold nanoparticle-based photothermal killing of vancomycin-resistant bacteria.

Nanomedicine (Lond). 2018-7-4

[7]
Bacteriolysis by vancomycin-conjugated acryl nanoparticles and morphological component analysis.

Drug Dev Ind Pharm. 2013-4-17

[8]
[Synthesis of antibiotic loaded polylactic acid nanoparticles and their antibacterial activity against Escherichia coli O157:H7 and methicillin-resistant Staphylococcus aureus].

Biomedica. 2017-1-24

[9]
Enhancing the Thermo-Stability and Anti-Bacterium Activity of Lysozyme by Immobilization on Chitosan Nanoparticles.

Int J Mol Sci. 2020-2-27

[10]
Potent Antibacterial Nanoparticles against Biofilm and Intracellular Bacteria.

Sci Rep. 2016-1-5

引用本文的文献

[1]
Metal-Based Approaches for the Fight against Antimicrobial Resistance: Mechanisms, Opportunities, and Challenges.

J Am Chem Soc. 2025-4-16

[2]
Antibacterial Activity of Zinc-Doped Hydroxyapatite and Vancomycin-Loaded Gelatin Nanoparticles against Intracellular in Human THP-1 Derived Macrophages.

ACS Appl Nano Mater. 2024-9-11

[3]
Multidrug-Resistant Remains Susceptible to Metal Ions and Graphene-Based Compounds.

Antibiotics (Basel). 2024-4-24

[4]
Biosynthesis of Zinc Nanoparticles From Actinobacterium Streptomyces Species and Their Biological Potential.

Cureus. 2024-2-13

[5]
Alternative mechanisms of action of metallic nanoparticles to mitigate the global spread of antibiotic-resistant bacteria.

Cell Surf. 2023-10-20

[6]
as a Prediction Platform for Nanotechnology-Based Strategies: Insights on Analytical Challenges.

Toxics. 2023-3-1

[7]
Nanotechnology in combating biofilm: A smart and promising therapeutic strategy.

Front Microbiol. 2023-3-3

[8]
Antibiotic resistant bacteria: A bibliometric review of literature.

Front Public Health. 2022

[9]
Combination of vancomycin and guanidinium-functionalized helical polymers for synergistic antibacterial activity and biofilm ablation.

Chem Sci. 2022-8-9

[10]
Multidrug-Resistant Bacteria: Their Mechanism of Action and Prophylaxis.

Biomed Res Int. 2022

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索