Tissue pharmacokinetics of levofloxacin in human soft tissue infections

Article date: May 2004

By: Romuald Bellmann, Gerald Kuchling, Pejman Dehghanyar, Markus Zeitlinger, Erich Minar, Bernhard X. Mayer, Markus Müller, Christian Joukhadar, in Volume 57, Issue 5, pages 563-568


The present study addressed the ability of levofloxacin to penetrate into subcutaneous adipose tissues in patients with soft tissue infection.


Tissue concentrations of levofloxacin in inflamed and healthy subcutaneous adipose tissue were measured in six patients by microdialysis after administration of a single intravenous dose of 500 mg. Levofloxacin was assayed by high‐performance liquid chromatography.


The mean concentration vs time profile of free levofloxacin in plasma was identical to that in inflamed and healthy tissues. The ratios of the mean area under the free levofloxacin concentration vs time curve from 0 to 10 h (AUC(0,10 h)) in tissue to that in plasma were 1.2 ± 1.0 for inflamed and 1.1 ± 0.6 for healthy subcutaneous adipose tissue (mean ± SD). The mean difference in the ratio of the AUCtissue : AUCplasma for inflamed and healthy tissue was 0.09 (95% confidence interval −0.58, 0.759, P > 0.05). Interindividual variability in tissue penetration was high, as indicated by a coefficient of variation of approximately 82% for AUCtissue : AUCplasma ratios.


The penetration of levofloxacin into tissue appears to be unaffected by local inflammation. Our plasma and tissue data suggest that an intravenous dose of 500 mg levofloxacin provides effective antibacterial concentrations at the target site. However, in treatment resistant patients, tissue concentrations may be sub‐therapeutic.

DOI: 10.1111/j.1365-2125.2004.02059.x

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