Louie Arnold, Liu Weiguo, VanGuilder Michael, Neely Michael N, Schumitzky Alan, Jelliffe Roger, Fikes Steven, Kurhanewicz Stephanie, Robbins Nichole, Brown David, Baluya Dodge, Drusano George L
Institute for Therapeutic Innovation, University of Florida, Lake Nona.
Laboratory of Applied Pharmacokinetics, University of Southern California, Los Angeles.
J Infect Dis. 2015 Apr 15;211(8):1326-33. doi: 10.1093/infdis/jiu603. Epub 2014 Oct 31.
Meropenem plus levofloxacin treatment was shown to be a promising combination in our in vitro hollow fiber infection model. We strove to validate this finding in a murine Pseudomonas pneumonia model.
A dose-ranging study with meropenem and levofloxacin alone and in combination against Pseudomonas aeruginosa was performed in a granulocytopenic murine pneumonia model. Meropenem and levofloxacin were administered to partially humanize their pharmacokinetic profiles in mouse serum. Total and resistant bacterial populations were estimated after 24 hours of therapy. Pharmacokinetic profiling of both drugs was performed in plasma and epithelial lining fluid, using a population model.
Meropenem and levofloxacin penetrations into epithelial lining fluid were 39.3% and 64.3%, respectively. Both monotherapies demonstrated good exposure responses. An innovative combination-therapy analytic approach demonstrated that the combination was statistically significantly synergistic (α = 2.475), as was shown in the hollow fiber infection model. Bacterial resistant to levofloxacin and meropenem was seen in the control arm. Levofloxacin monotherapy selected for resistance to itself. No resistant subpopulations were observed in any combination therapy arm.
The combination of meropenem plus levofloxacin was synergistic, producing good bacterial kill and resistance suppression. Given the track record of safety of each agent, this combination may be worthy of clinical trial.
在我们的体外中空纤维感染模型中,美罗培南联合左氧氟沙星治疗显示出有前景的联合效果。我们努力在小鼠铜绿假单胞菌肺炎模型中验证这一发现。
在粒细胞减少的小鼠肺炎模型中,进行了美罗培南和左氧氟沙星单独及联合应用对铜绿假单胞菌的剂量范围研究。给予美罗培南和左氧氟沙星以使其在小鼠血清中的药代动力学特征部分人源化。治疗24小时后估计总细菌和耐药细菌群体。使用群体模型在血浆和上皮衬液中进行两种药物的药代动力学分析。
美罗培南和左氧氟沙星在上皮衬液中的穿透率分别为39.3%和64.3%。两种单一疗法均显示出良好的暴露反应。一种创新的联合治疗分析方法表明,联合治疗在统计学上具有显著的协同作用(α = 2.475),如在中空纤维感染模型中所示。在对照臂中观察到对左氧氟沙星和美罗培南耐药的细菌。左氧氟沙星单一疗法导致对其自身产生耐药性。在任何联合治疗组中均未观察到耐药亚群。
美罗培南联合左氧氟沙星具有协同作用,能有效杀灭细菌并抑制耐药性。鉴于每种药物的安全记录,这种联合可能值得进行临床试验。