Imidazoles and Quaternary Ammonium Compounds as Effective Therapies against (Multidrug-Resistant) Bacterial Wound Infections.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Lauren Van de Vliet, Thijs Vackier, Karin Thevissen, David Decoster, Hans P Steenackers
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Abstract

Background/objectives: The rise and spread of antimicrobial resistance complicates the treatment of bacterial wound pathogens, further increasing the need for newer, effective therapies. Azoles such as miconazole have shown promise as antibacterial compounds; however, they are currently only used as antifungals. Previous research has shown that combining azoles with quaternary ammonium compounds yields synergistic activity against fungal pathogens, but the effect on bacterial pathogens has not been studied yet.

Methods: In this study, the focus was on finding active synergistic combinations of imidazoles and quaternary ammonium compounds against (multidrug-resistant) bacterial pathogens through checkerboard assays. Experimental evolution in liquid culture was used to evaluate the possible emergence of resistance against the most active synergistic combination.

Results: Several promising synergistic combinations were identified against an array of Gram-positive pathogens: miconazole/domiphen bromide, ketoconazole/domiphen bromide, clotrimazole/domiphen bromide, fluconazole/domiphen bromide and miconazole/benzalkonium chloride. Especially, miconazole with domiphen bromide exhibits potential, as it has activity at a low concentration against a broad range of pathogens and shows an absence of strong resistance development over 11 cycles of evolution.

Conclusions: This study provides valuable insight into the possible combinations of imidazoles and quaternary ammonium compounds that could be repurposed for (topical) wound treatment. Miconazole with domiphen bromide shows the highest application potential as a possible future wound therapy. However, further research is needed into the mode of action of these compounds and their efficacy and toxicity in vivo.

咪唑类和季铵盐化合物是治疗(耐多药)细菌性伤口感染的有效药物。
背景/目的:抗菌药耐药性的增加和蔓延使细菌性伤口病原体的治疗变得更加复杂,从而进一步增加了对更新、更有效疗法的需求。咪康唑等偶氮类化合物有望成为抗菌化合物,但目前只用作抗真菌药。以前的研究表明,将唑类与季铵盐化合物结合可产生抗真菌病原体的协同活性,但对细菌病原体的影响尚未研究:本研究的重点是通过棋盘试验找到咪唑类和季铵化合物对(耐多药)细菌病原体的活性协同组合。液体培养中的实验演化被用来评估对最有效的协同组合可能产生的抗药性:结果:针对一系列革兰氏阳性病原体确定了几种有前景的增效组合:咪康唑/溴化多咪唑、酮康唑/溴化多咪唑、克霉唑/溴化多咪唑、氟康唑/溴化多咪唑和咪康唑/苯扎氯铵。特别是咪康唑与多米酚溴化物的组合具有潜力,因为它在低浓度下对多种病原体具有活性,而且在 11 个进化周期中没有出现强烈的抗药性:这项研究对咪唑类与季铵盐化合物的可能组合提供了宝贵的见解,这些组合可重新用于(局部)伤口治疗。咪康唑与多米酚溴化物在未来伤口治疗中的应用潜力最大。不过,还需要进一步研究这些化合物的作用模式及其在体内的疗效和毒性。
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
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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