Odenholt Inga, Cars Otto
Infectious Diseases Research Unit, Department of Clinical Sciences, Malmö, Lunds University S-20502 Malmö, Sweden.
J Antimicrob Chemother. 2006 Nov;58(5):960-5. doi: 10.1093/jac/dkl356. Epub 2006 Aug 26.
To compare in an in vitro kinetic model the pharmacodynamics of moxifloxacin and levofloxacin with a concentration-time profile simulating the human free non-protein bound concentrations of 400 mg moxifloxacin intravenous (iv) once daily, 500 mg levofloxacin iv once daily and 750 mg levofloxacin iv once daily against strains of Streptococcus pneumoniae, Staphylococcus aureus, Klebsiella pneumoniae and Escherichia coli with variable susceptibility to fluoroquinolones.
The strains used in the study included S. pneumoniae ATCC 6306 (native strain), S. pneumoniae 19397 (double mutation; gyrA and parC), S. pneumoniae 4241 (single mutation; parC), S. aureus ATCC 13709 (native strain), S. aureus MB5 (single mutation; gyrA), E. coli M12 (single mutation; gyrA), E. coli ATCC 25922 (native strain) and K. pneumoniae ATCC 29655 (native strain). The strains were exposed to moxifloxacin and levofloxacin in an in vitro kinetic model simulating the free human serum concentration-time profile of moxifloxacin 400 mg once daily, levofloxacin 500 mg once daily and 750 mg once daily. Repeated samples were taken regularly during 24 h and viable counts were carried out.
A correlation was seen between both the area under the serum concentration curve and MIC (AUC/MIC) and the peak concentration/MIC (Cmax/MIC) versus area under the bactericidal killing curve (AUBKC) or Deltalog0-24 cfu/mL. Compiling all data, an AUC/MIC of approximately 100 and a Cmax/MIC of 10 gave a maximal bactericidal effect for both levofloxacin and moxifloxacin. In accordance with the results from others, our study indicated that a lower AUC/MIC was needed for S. pneumoniae in comparison with the Gram-negative bacteria studied. Moxifloxacin yielded higher AUC/MIC and Cmax/MIC against the investigated Gram-positive bacteria in comparison with levofloxacin 500 mg once daily and 750 mg once daily.
在体外动力学模型中比较莫西沙星和左氧氟沙星的药效学,其浓度-时间曲线模拟人类游离非蛋白结合浓度,即莫西沙星每日静脉注射(iv)400mg一次、左氧氟沙星每日iv500mg一次和左氧氟沙星每日iv750mg一次,针对对氟喹诺酮类药物敏感性不同的肺炎链球菌、金黄色葡萄球菌、肺炎克雷伯菌和大肠杆菌菌株。
研究中使用的菌株包括肺炎链球菌ATCC 6306(野生株)、肺炎链球菌19397(双突变;gyrA和parC)、肺炎链球菌4241(单突变;parC)、金黄色葡萄球菌ATCC 13709(野生株)、金黄色葡萄球菌MB5(单突变;gyrA)、大肠杆菌M12(单突变;gyrA)、大肠杆菌ATCC 25922(野生株)和肺炎克雷伯菌ATCC 29655(野生株)。在体外动力学模型中,使这些菌株暴露于模拟莫西沙星每日一次400mg、左氧氟沙星每日一次500mg和每日一次750mg的人血清游离浓度-时间曲线的环境中。在24小时内定期采集重复样本并进行活菌计数。
血清浓度曲线下面积与最低抑菌浓度(AUC/MIC)以及峰浓度/MIC(Cmax/MIC)与杀菌曲线下面积(AUBKC)或Deltalog0 - 24 cfu/mL之间均存在相关性。汇总所有数据,左氧氟沙星和莫西沙星的AUC/MIC约为100且Cmax/MIC为10时可产生最大杀菌效果。与其他研究结果一致,我们的研究表明,与所研究的革兰氏阴性菌相比,肺炎链球菌所需的AUC/MIC较低。与每日一次500mg和每日一次750mg的左氧氟沙星相比,莫西沙星对所研究的革兰氏阳性菌产生更高的AUC/MIC和Cmax/MIC。