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喹诺酮类药物对鸟分枝杆菌的活性:体外活性

Anti-Mycobacterium avium activity of quinolones: in vitro activities.

作者信息

Klopman G, Wang S, Jacobs M R, Bajaksouzian S, Edmonds K, Ellner J J

机构信息

Chemistry Department, Case Western Reserve University, Cleveland, Ohio 44106.

出版信息

Antimicrob Agents Chemother. 1993 Sep;37(9):1799-806. doi: 10.1128/AAC.37.9.1799.

Abstract

The MICs of 88 quinolones against 14 selected reference and clinical strains of Mycobacterium avium-M. intracellular complex were determined. Agents tested included ciprofloxacin, sparfloxacin (PD 131501), and 86 other experimental quinolones. Test strains were selected to represent various susceptibilities to ciprofloxacin and other drug resistance profiles. MICs were determined by the microdilution method in 7HSF broth, with incubation for 14 days at 35 degrees C. The results showed 25 of the quinolones to be active against the strains, with MICs for 90% of the strains (MIC90s) of 2 to 32 micrograms/ml. Ten of these compounds had activities equivalent to or greater than that of ciprofloxacin. The most active compound was PD 125354, with an MIC50 of 0.5 micrograms/ml and an MIC90 of 2 micrograms/ml; comparable values for ciprofloxacin were 4 and 8 micrograms/ml, respectively. The next most active compounds, with MIC90s of 4 micrograms/ml, were sparfloxacin (PD 131501), PD 123982, PD 135144, and PD 119421. MIC90s of PD 131575, PD 126889, PD 122642, PD 139586, and PD 143289 were 8 micrograms/ml. Further evaluation of the most active agents is warranted, as is assessment of structure-activity relationships of active and inactive agents to elucidate the active portions of the compounds and to lead to the development of compounds with enhanced activity.

摘要

测定了88种喹诺酮类药物对14株鸟分枝杆菌-胞内分枝杆菌复合群参考菌株和临床菌株的最低抑菌浓度(MIC)。所测试的药物包括环丙沙星、司帕沙星(PD 131501)以及其他86种实验性喹诺酮类药物。选择测试菌株以代表对环丙沙星的不同敏感性和其他耐药谱。采用微量稀释法在7HSF肉汤中测定MIC,于35℃孵育14天。结果显示,25种喹诺酮类药物对这些菌株有活性,90%菌株的MIC(MIC90)为2至32微克/毫升。其中10种化合物的活性等同于或高于环丙沙星。活性最高的化合物是PD 125354,MIC50为0.5微克/毫升,MIC90为2微克/毫升;环丙沙星的相应值分别为4和8微克/毫升。其次活性最高的化合物,MIC90为4微克/毫升,是司帕沙星(PD 131501)、PD 123982、PD 135144和PD 119421。PD 131575、PD 126889、PD 122642、PD 139586和PD 143289的MIC90为8微克/毫升。有必要对活性最高的药物进行进一步评估,同时也需要评估活性和非活性药物的构效关系,以阐明化合物的活性部分,并推动开发活性增强的化合物。

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