Hermsen Elizabeth D, Hovde Laurie B, Sprandel Kelly A, Rodvold Keith A, Rotschafer John C
Department of Experimental and Clinical Pharmacology, University of Minnesota College of Pharmacy, 9-157 Weaver-Densford Hall, 308 Harvard St. SE, Minneapolis, MN 55455, USA.
Antimicrob Agents Chemother. 2005 Feb;49(2):685-9. doi: 10.1128/AAC.49.2.685-689.2005.
Moxifloxacin has been suggested as an option for monotherapy of intra-abdominal infections. Recent data support the use of a once-daily metronidazole regimen. The purpose of this study was to investigate the activity of levofloxacin (750 mg every 24 h [q24h]) plus metronidazole (1,500 mg q24h) compared with that of moxifloxacin (400 mg q24h) monotherapy in a mixed-infection model. By using an in vitro pharmacodynamic model in duplicate, Escherichia coli and Bacteroides fragilis were exposed to peak concentrations of 8.5 mg of levofloxacin/liter q24h, 32 mg of metronidazole/liter q24h, and 2 mg for moxifloxacin/liter q24h for 24 h. The activities of levofloxacin, metronidazole, moxifloxacin, and levofloxacin plus metronidazole were evaluated against E. coli, B. fragilis, and E. coli plus B. fragilis. The targeted half-lives of levofloxacin, metronidazole, and moxifloxacin were 8, 8, and 12 h, respectively. Time-kill curves were analyzed for time to 3-log killing, slope, and regrowth. Pre- and postexposure MICs were determined. The preexposure levofloxacin, metronidazole, and moxifloxacin MICs for E. coli and B. fragilis were 0.5 and 1, >64 and 0.5, and 1 and 0.25 mg/liter, respectively. Levofloxacin and moxifloxacin achieved a 3-log killing against E. coli and B. fragilis in all experiments, as did metronidazole against B. fragilis. Metronidazole did not decrease the starting inoculum of E. coli. The area under the concentration-time curve/MIC ratios for E. coli and B. fragilis were 171.7 and 85.9, respectively, for levofloxacin and 26 and 103.9, respectively, for moxifloxacin. Levofloxacin plus metronidazole exhibited the fastest rates of killing. The levofloxacin and moxifloxacin MICs for B. fragilis increased 8- to 16-fold after the organism was exposed to moxifloxacin. No other changes in the postexposure MICs were found. Levofloxacin plus metronidazole administered once daily exhibited activity similar to that of moxifloxacin against the mixed E. coli and B. fragilis infection. A once-daily regimen of levofloxacin plus metronidazole looks promising for the treatment of intra-abdominal infections.
莫西沙星已被提议作为腹腔内感染单一疗法的一种选择。近期数据支持使用每日一次的甲硝唑治疗方案。本研究的目的是在混合感染模型中,研究左氧氟沙星(每24小时750毫克[q24h])加甲硝唑(每24小时1500毫克q24h)与莫西沙星(每24小时400毫克q24h)单一疗法相比的活性。通过使用一式两份的体外药效学模型,将大肠埃希菌和脆弱拟杆菌暴露于每24小时8.5毫克左氧氟沙星/升、每24小时32毫克甲硝唑/升和每24小时2毫克莫西沙星/升的峰值浓度下24小时。评估了左氧氟沙星、甲硝唑、莫西沙星以及左氧氟沙星加甲硝唑对大肠埃希菌、脆弱拟杆菌以及大肠埃希菌加脆弱拟杆菌的活性。左氧氟沙星、甲硝唑和莫西沙星的目标半衰期分别为8、8和12小时。分析了时间-杀菌曲线的3对数杀菌时间、斜率和再生长情况。测定了暴露前和暴露后的最低抑菌浓度(MIC)。大肠埃希菌和脆弱拟杆菌暴露前的左氧氟沙星、甲硝唑和莫西沙星MIC分别为0.5和1、>64和0.5以及1和0.25毫克/升。在所有实验中,左氧氟沙星和莫西沙星对大肠埃希菌和脆弱拟杆菌均实现了3对数杀菌,甲硝唑对脆弱拟杆菌也实现了3对数杀菌。甲硝唑并未降低大肠埃希菌的起始接种量。左氧氟沙星对大肠埃希菌和脆弱拟杆菌的浓度-时间曲线下面积/MIC比值分别为171.7和85.9,莫西沙星分别为26和103.9。左氧氟沙星加甲硝唑表现出最快的杀菌速率。脆弱拟杆菌暴露于莫西沙星后,其左氧氟沙星和莫西沙星MIC增加了8至16倍。暴露后的MIC未发现其他变化。每日一次给予左氧氟沙星加甲硝唑对大肠埃希菌和脆弱拟杆菌混合感染的活性与莫西沙星相似。每日一次的左氧氟沙星加甲硝唑治疗方案在治疗腹腔内感染方面看起来很有前景。