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新型咪唑衍生物的抑菌潜力评估——时间杀菌和脱氢酶活性研究。

Inhibitory potential of a novel imidazole derivative as evaluated by time-kill and dehydrogenase activity.

机构信息

Department of Biology-Ecology, Faculty of Natural Sciences and Agricultural Sciences, Ovidius University of Constanta, 1, University Street, 900470, Constanta, Romania.

出版信息

Curr Microbiol. 2013 Feb;66(2):162-8. doi: 10.1007/s00284-012-0252-y. Epub 2012 Oct 25.

Abstract

Antibacterial activity of 1,1'-methandiylbis(2-methyl-1H-imidazole) (AIM) has been estimated both qualitatively and quantitatively against reference and clinical strains of Gram-positive and Gram-negative bacteria. MICs showed little variability among strains tested, ranging from 360 to 450 μg/ml and indicating rather a moderate antibacterial activity. Inhibition of dehydrogenase activity was significant in Escherichia coli ATCC 25922 and followed closely time-kill dynamics. Although moderate, AIM proved also to be useful on the ability to successfully inhibit the growth of antibiotic resistant clinical strains.

摘要

1,1'-亚甲基双(2-甲基-1H-咪唑)(AIM) 的抗菌活性已经针对革兰氏阳性和革兰氏阴性参考菌株和临床分离株进行了定性和定量评估。MIC 在测试的菌株之间变化不大,范围为 360 至 450μg/ml,表明抗菌活性中等。在大肠杆菌 ATCC 25922 中,脱氢酶活性的抑制作用非常显著,并且与时间杀灭动力学密切相关。尽管活性中等,但 AIM 也被证明在成功抑制抗生素耐药临床分离株的生长方面非常有用。

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