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在脓毒症小鼠模型中,采用全或无死亡率终点指标测定吉米沙星、莫西沙星和左氧氟沙星对携带gyrA和parC点突变肺炎球菌的体内活性。

In vivo activity of gemifloxacin, moxifloxacin and levofloxacin against pneumococci with gyrA and parC point mutations in a sepsis mouse model measured with the all or nothing mortality end-point.

作者信息

Alkorta M, Giménez M J, Vicente D, Aguilar L, Pérez-Trallero E

机构信息

Servicio de Microbiología, Hospital Donostia, Po del Doctor Beguiristain s/n, 20014 San Sebastián, Spain.

出版信息

Int J Antimicrob Agents. 2005 Feb;25(2):163-7. doi: 10.1016/j.ijantimicag.2004.08.017.

Abstract

A dose-decreasing immunocompetent sepsis mouse model was used to evaluate the in vivo effect of levofloxacin, moxifloxacin and gemifloxacin, using a ciprofloxacin/levofloxacin susceptible serotype 6B strain (ciprofloxacin MIC: 1 mg/l) and two resistant serotype 14 and 19F strains with gyrA and parC point mutations (ciprofloxacin MICs of 32 and 64 mg/l, respectively). Significant higher in vivo activity was found for moxifloxacin and gemifloxacin than for levofloxacin against strains 1 and 2, and for gemifloxacin versus moxifloxacin or levofloxacin against strain 3. Gemifloxacin treatment resulted in 100% survival against strains 1 and 2(AUC0-24 h/MIC of 30 and 62) but against strain 3, survival was 60-80% (AUC0-24 h/MIC of 93). Similar AUC0-24 h/MIC values produced different therapeutic results suggesting that in vitro parameters other than the MIC could influence efficacy predictions based on in vitro susceptibility tests (MICs) or pharmacodynamic parameters (AUC0-24 h/MIC).

摘要

使用剂量递减的免疫活性败血症小鼠模型,利用对环丙沙星/左氧氟沙星敏感的6B血清型菌株(环丙沙星MIC:1mg/l)以及两种具有gyrA和parC点突变的耐药14和19F血清型菌株(环丙沙星MIC分别为32mg/l和64mg/l),评估左氧氟沙星、莫西沙星和吉米沙星的体内效果。结果发现,莫西沙星和吉米沙星对菌株1和2的体内活性显著高于左氧氟沙星,而吉米沙星对菌株3的活性高于莫西沙星或左氧氟沙星。吉米沙星治疗对菌株1和2的生存率为100%(AUC0 - 24h/MIC为30和62),但对菌株3的生存率为60 - 80%(AUC0 - 24h/MIC为93)。相似的AUC0 - 24h/MIC值产生了不同的治疗结果,这表明除MIC外的体外参数可能会影响基于体外药敏试验(MIC)或药效学参数(AUC0 - 24h/MIC)的疗效预测。

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