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首页> 外文期刊>Infection and Drug Resistance >In vitro Antibacterial Activity of Isopropoxy Benzene Guanidine Against Multidrug-Resistant Enterococci
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In vitro Antibacterial Activity of Isopropoxy Benzene Guanidine Against Multidrug-Resistant Enterococci

机译:异丙氧基苯胍对多药抗肠癌的体外抗菌活性

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Background: Bacterial infections cause a serious public health crisis due to the emergence of resistance towards multiple conventional antibacterial drugs. In particular, multidrug-resistant (MDR) Enterococcus faecium which belongs to “ESKAPE” organisms is causing significant problems worldwide. Hence, there is an urgent need to find alternative therapies. Recently, substituted benzene guanidine compounds have been used as lead structures to discover new promising drugs in both synthetic and medicinal chemistry. Purpose: Here we investigated the antimicrobial activity of a new substituted benzene guanidine analog, isopropoxy benzene guanidine, against Enterococci . Material and methods: The isopropoxy benzene guanidine was synthesized by Guangzhou Insighter Biotechnology Co., Ltd and tested on both reference bacterial strain and 32 clinical MDR Enterococci strains. The in vitro antibacterial activity was evaluated by microdilution method and kill kinetic assays. The potential antibacterial mechanism was measured by fluorescence spectrometry using fluorescent membrane potential probe 3, 3-diethyloxacarbocyanine iodide (DiOCsub2/sub (3)). Results: Isopropoxy benzene guanidine exhibited potent bactericidal activity against both reference strain and MDR Enterococci isolates. The minimum inhibitory concentration (MIC) range for isopropoxy benzene guanidine was 1–4 μg/mL. Minimum bactericidal concentration (MBC) was about 2-8-fold of its MIC values. Time-kill studies showed that isopropoxy benzene guanidine provided superior bactericidal effect against reference and MDR strains within 12 hrs at 2×MIC. Furthermore, isopropoxy benzene guanidine could cause a large reduction in the magnitude of the generated membrane potential compared to that of the untreated cells. Conclusion: The present study highlights the potent bactericidal activity of isopropoxy benzene guanidine on Enterococci by disrupting the cell membrane potential. These findings demonstrate that isopropoxy benzene guanidine may be a good chemical lead for further medicinal chemistry and pharmaceutical development and could be used as a therapeutic agent for infectious diseases caused by MDR Enterococci.
机译:背景:由于对多种常规抗菌药物的抗性出现,细菌感染导致严重的公共卫生危机。特别是,属于“Eskape”生物的多药抗性(MDR)肠球菌粪便在全世界造成重大问题。因此,迫切需要寻找替代疗法。最近,取代的苯胍化合物已被用作铅结构,以发现合成和药用化学的新有希望的药物。目的:在这里,我们研究了新的取代苯胍基类似物,异丙氧基苯胍的抗菌活性,对抗肠球菌。材料和方法:广州罕见的生物技术有限公司合成异丙氧基苯胍,并在辅学细菌菌株和32例临床MDR肠球菌菌株上进行测试。通过微稀释方法评估体外抗菌活性并杀死动力学测定。通过使用荧光膜电位探针3,3-二乙基丙碳碳碳糖苷碘化物(DIOC 2 (3))通过荧光光谱法测量潜在的抗菌机理。结果:异丙氧基苯胍对参考菌株和MDR肠球菌分离株表现出有效的杀菌活性。异丙氧基苯胍的最小抑制浓度(MIC)范围为1-4μg/ ml。最小杀菌浓度(MBC)为其MIC值的约2-8倍。时间杀死研究表明,异丙氧基苯胍在2×MIC的12小时内为参考和MDR菌株提供了优异的杀菌效果。此外,与未处理的细胞相比,异丙氧基苯胍可以引起产生的膜电位的大小的大小。结论:本研究突出了通过破坏细胞膜电位来突出异丙氧基苯胍的有效杀菌活性。这些研究结果表明,异丙氧基苯胍可以是进一步药物化学和药物发育的良好化学铅,可用作由MDR肠球菌引起的传染病的治疗剂。

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