Zeitlinger M A, Sauermann R, Traunmüller F, Georgopoulos A, Müller M, Joukhadar C
Department of Clinical Pharmacology, Division of Clinical Pharmacokinetics, Medical University of Vienna, Austria.
J Antimicrob Chemother. 2004 Nov;54(5):876-80. doi: 10.1093/jac/dkh443. Epub 2004 Oct 7.
Plasma protein binding (PPB) is known to impair the antimicrobial activity of beta-lactams, but its impact on the activity of other classes of antimicrobials such as fluoroquinolones is controversial. This study was undertaken to investigate the effect of PPB on bacterial killing by selected antibiotics and moxifloxacin, which served as a model compound for the class of fluoroquinolones.
Bacterial time-killing curves were employed in the absence and presence of physiological albumin concentrations (40 g/L). Moxifloxacin, ampicillin and oxacillin were investigated. Fosfomycin, a non-protein bound antibiotic was used for comparison. Simulations were carried out by employing concentrations of antibiotics of one-fourth of the minimal inhibitory concentration (MIC), equal to the MIC and four-fold the MIC of one select bacterial strain (Staphylococcus aureus ATCC 29213). To correlate bacterial killing to the extent of PPB, bacterial time-killing curves were plotted using the calculated free and the total drug concentration.
Bacterial killing by fosfomycin was not affected by the addition of albumin. The antimicrobial activity of oxacillin and ampicillin was reduced in the presence of albumin as expected by the calculation of the free fraction of these antibiotics. Adding albumin to moxifloxacin resulted in a significant decrease in bacterial killing of more than 1 log10 cfu/mL after a period of 8 h when the moxifloxacin concentration was equal to the respective MIC.
Our data confirm the view that albumin substantially impairs the antimicrobial activity of antibiotics including moxifloxacin, a member of the class of fluoroquinolones.
已知血浆蛋白结合(PPB)会削弱β-内酰胺类抗生素的抗菌活性,但其对其他类抗菌药物如氟喹诺酮类活性的影响存在争议。本研究旨在调查PPB对选定抗生素及莫西沙星(作为氟喹诺酮类的模型化合物)杀菌作用的影响。
在有无生理白蛋白浓度(40 g/L)的情况下绘制细菌时间杀灭曲线。研究了莫西沙星、氨苄西林和苯唑西林。使用未与蛋白结合的抗生素磷霉素作为对照。通过采用一种选定细菌菌株(金黄色葡萄球菌ATCC 29213)的最低抑菌浓度(MIC)的四分之一、等于MIC以及四倍MIC的抗生素浓度进行模拟。为了将细菌杀灭与PPB程度相关联,使用计算得出的游离和总药物浓度绘制细菌时间杀灭曲线。
添加白蛋白对磷霉素的杀菌作用没有影响。正如通过计算这些抗生素的游离分数所预期的那样,在有白蛋白存在的情况下,苯唑西林和氨苄西林的抗菌活性降低。当莫西沙星浓度等于各自的MIC时,在8小时后向莫西沙星中添加白蛋白导致细菌杀灭显著降低超过1 log10 cfu/mL。
我们的数据证实了白蛋白会显著削弱包括莫西沙星(氟喹诺酮类成员之一)在内的抗生素的抗菌活性这一观点。