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一种新型利福霉素衍生物对麻风分枝杆菌的体外活性

In vitro activity of a new rifamycin derivative against Mycobacterium leprae.

作者信息

Dhople A M, Dimova V

机构信息

Florida Institute of Technology, Melbourne, USA.

出版信息

Arzneimittelforschung. 1996 Feb;46(2):210-2.

PMID:8720317
Abstract

The antimicrobial effects of T9 (3-(4-cinamyl-1-piperazinyl)iminomethyl rifamycin SV) alone and in combination with ofloxacin, against strains of M. leprae were evaluated, using an in vitro cell-free culture system. The minimum inhibitory concentrations (MICs) of T9 against rifampin-sensitive and rifampin-resistant strains of M. leprae were 0.1 microgram/ml and 0.4 microgram/ml, respectively. Furthermore, in common with rifabutin, but not with rifamycin, T9 demonstrated synergy with ofloxacin against both rifampin-sensitive rifampin-resistant strains of M. leprae. The results suggest that T9, in combination with ofloxacin as part of multidrug regimens, warrants further evaluation as treatment for patients with leprosy.

摘要

使用体外无细胞培养系统评估了T9(3-(4-肉桂基-1-哌嗪基)亚氨基甲基利福霉素SV)单独以及与氧氟沙星联合对麻风杆菌菌株的抗菌作用。T9对利福平敏感和利福平耐药的麻风杆菌菌株的最低抑菌浓度(MIC)分别为0.1微克/毫升和0.4微克/毫升。此外,与利福布汀相同,但与利福霉素不同,T9与氧氟沙星联合对利福平敏感和利福平耐药的麻风杆菌菌株均显示出协同作用。结果表明,T9与氧氟沙星联合作为多药治疗方案的一部分,作为麻风病患者的治疗方法值得进一步评估。

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