• Media type: E-Article
  • Title: Population Pharmacokinetics and Penetration into Prostatic, Seminal, and Vaginal Fluid for Ciprofloxacin, Levofloxacin, and Their Combination
  • Contributor: Bulitta, Jurgen B.; Kinzig, Martina; Naber, Christoph K.; Wagenlehner, Florian M.E.; Sauber, Christian; Landersdorfer, Cornelia B.; Sörgel, Fritz; Naber, Kurt G.
  • imprint: S. Karger AG, 2011
  • Published in: Chemotherapy
  • Language: English
  • DOI: 10.1159/000329520
  • ISSN: 0009-3157; 1421-9794
  • Keywords: Infectious Diseases ; Pharmacology (medical) ; Drug Discovery ; Pharmacology ; Oncology ; General Medicine
  • Origination:
  • Footnote:
  • Description: <jats:p>&lt;i&gt;Background:&lt;/i&gt; Our objectives were to assess the pharmacokinetic interaction and body fluid penetration of ciprofloxacin and levofloxacin. &lt;i&gt;Methods:&lt;/i&gt; This study was a single-dose open randomized three-way crossover in 15 healthy volunteers receiving 500 mg oral levofloxacin, 500 mg oral ciprofloxacin, or 250 mg levofloxacin and 250 mg ciprofloxacin co-administered. Serum, urine, and body fluid concentrations were determined by high-performance liquid chromatography and analyzed via population pharmacokinetic modeling. &lt;i&gt;Results:&lt;/i&gt; Modeling indicated that ciprofloxacin inhibited the renal reabsorption of levofloxacin. Ciprofloxacin increased the net renal clearance of levofloxacin by 13%, as its estimated affinity for a putative tubular reabsorption transporter was 12-fold higher (Km: 568 µ&lt;i&gt;M&lt;/i&gt;) compared to levofloxacin (Km: 6,830 µ&lt;i&gt;M&lt;/i&gt;). Levofloxacin increased the bioavailability of ciprofloxacin by 12% and achieved significantly (p &lt; 0.05) higher concentrations at 3 h in ejaculate, prostatic, seminal, and vaginal fluid compared to ciprofloxacin. &lt;i&gt;Conclusion:&lt;/i&gt; Modeling suggested that ciprofloxacin inhibited the tubular reabsorption of levofloxacin due to a 12-fold higher affinity for a putative tubular reabsorption transporter compared to levofloxacin. This pharmacokinetic interaction was not clinically relevant.</jats:p>