AstraZeneca India Pvt Ltd, Hebbal, Bangalore, India.
Antimicrob Agents Chemother. 2012 Jun;56(6):3054-7. doi: 10.1128/AAC.06383-11. Epub 2012 Apr 2.
Coadministration of moxifloxacin and rifampin was evaluated in a murine model of Mycobacterium tuberculosis pulmonary infection to determine whether the finding of antagonism documented in a hollow-fiber infection model could be recapitulated in vivo. Colony counts were followed in a no-treatment control group, groups administered moxifloxacin or rifampin monotherapy, and a group administered a combination of the two agents. Following 18 days of once-daily oral administration to mice infected with M. tuberculosis, there was a reduction in the plasma exposure to rifampin that decreased further when rifampin was coadministered with moxifloxacin. Pharmacodynamic analysis demonstrated a mild antagonistic interaction between moxifloxacin and rifampin with respect to cell kill in the mouse model for tuberculosis (TB). No emergence of resistance was noted over 28 days of therapy, even with monotherapy. This was true even though one of the agents in the combination (moxifloxacin) induces error-prone replication. The previously noted antagonism with respect to cell kill shown in the hollow-fiber infection model was recapitulated in the murine TB lung model, although to a lesser extent.
莫西沙星与利福平联合用药在结核分枝杆菌肺部感染的小鼠模型中进行了评价,以确定在中空纤维感染模型中记录的拮抗作用是否可以在体内重现。在未治疗对照组、莫西沙星或利福平单药治疗组和联合使用两种药物的组中,对菌落计数进行了随访。在感染结核分枝杆菌的小鼠每日口服给药 18 天后,利福平的血浆暴露减少,当与莫西沙星联合使用时,利福平的暴露进一步减少。药效学分析表明,莫西沙星和利福平在结核(TB)小鼠模型中对细胞杀伤具有轻度拮抗作用。即使在 28 天的治疗期间,也没有出现耐药性,即使是单药治疗。即使联合用药中的一种药物(莫西沙星)诱导易错复制,这也是如此。在中空纤维感染模型中观察到的细胞杀伤方面的先前报道的拮抗作用在鼠结核肺部模型中得到了重现,尽管程度较小。