利用互补统计模型评估表面稳定的零价铁纳米颗粒对不同细菌物种的影响。

IF 5 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Brittany J Carnathan, Dinny Stevens, Swarna Shikha, Carson Slater, Nathen Byford, Rodney X Sturdivant, Kuzy Zarzosa, W Evan Braswell, Christie M Sayes
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引用次数: 0

摘要

纳米颗粒被提议作为传统抗菌剂的替代品。通过操纵纳米粒子的核心和表面涂层,可以定制针对各种微生物种群的抗菌效果,这被称为“设计师效应”。然而,纳米颗粒核心-涂层组合的抗菌性能尚未得到充分研究;关于它们对不同细菌的影响的研究很少。由于其在水中的稳定性和铁磁性,表面稳定的零价铁纳米颗粒(FeNPs)的抗菌效果特别有趣。本研究探讨了三种表面涂层的FeNPs对六种不同细菌的影响。用l -抗坏血酸(AA)、十六烷基三甲基溴化铵(CTAB)或聚乙烯吡咯烷酮(PVP)盖层合成FeNPs。抑菌区(Zone of inhibition, ZOI)结果表明,AA-FeNPs和CTAB-FeNPs的抑菌活性最强。抑菌效果从最敏感到最不敏感依次为:nealsonii芽孢杆菌>大肠杆菌>金黄色葡萄球菌> Delftia acidovorans >黄杆菌> multivorsphingobacterium。使用有序回归和广义线性混合模型进行比较,发现细菌对不同涂层和纳米颗粒浓度的反应存在显著差异。统计模型的结果是一致的,从而增加了这些结论的可信度。这项研究支持了“设计纳米粒子”概念的可行性,并为未来的研究提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the Effects of Surface-Stabilized Zero-Valent Iron Nanoparticles on Diverse Bacteria Species Using Complementary Statistical Models.

Nanoparticles are proposed as alternatives to traditional antimicrobial agents. By manipulating a nanoparticle's core and surface coating, antimicrobial effects against various microbial populations can be customized, known as the "designer effect". However, the antimicrobial properties of nanoparticle core-coating combinations are understudied; little research exists on their effects on diverse bacteria. The antimicrobial effects of surface-stabilized zero-valent iron nanoparticles (FeNPs) are particularly interesting due to their stability in water and ferromagnetic properties. This study explores the impact of FeNPs coated with three surface coatings on six diverse bacterial species. The FeNPs were synthesized and capped with L-ascorbic acid (AA), cetyltrimethylammonium bromide (CTAB), or polyvinylpyrrolidone (PVP) using a bottom-up approach. Zone of inhibition (ZOI) values, assessed through the disc diffusion assay, indicated that AA-FeNPs and CTAB-FeNPs displayed the most potent antibacterial activity. Bacteria inhibition results ranked from most sensitive to least sensitive are the following: Bacillus nealsonii > Escherichia coli > Staphylococcus aureus > Delftia acidovorans > Chryseobacterium sp. > Sphingobacterium multivorum. Comparisons using ordinal regression and generalized linear mixed models revealed significant differences in bacterial responses to the different coatings and nanoparticle concentrations. The statistical model results are in agreement, thus increasing confidence in these conclusions. This study supports the feasibility of the "designer nanoparticle" concept and offers a framework for future research.

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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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