Altered pharmacokinetics of enrofloxacin in experimental models of hepatic and renal impairment

Vet Res Commun. 2009 Jun;33(5):481-7. doi: 10.1007/s11259-008-9195-y. Epub 2008 Dec 16.

Abstract

We investigated the effects of hepatic and renal impairment on the pharmacokinetics of enrofloxacin in Sprague-Dawley rats. Experimental hepatic and renal failure were induced by carbon tetrachloride (CCL(4)) and 5/6 nephrectomy, respectively. After intravenous dosing of enrofloxacin (10 mg/kg), plasma concentrations of enrofloxacin were measured using liquid chromatograph/mass spectrometry. There was no significant effect of hepatic impairment on enrofloxacin pharmacokinetics. However, renal impairment markedly prolonged elimination half life (t(1/2lambdaz)) of enrofloxacin (P < 0.05), comparing with respective control. Total body clearance (Cl(b)) and volume of distribution at steady state (V(ss)) were significantly decreased (P < 0.05) by renal impairment. In conclusion, these results suggested that renal impairment could affect the pharmacokinetics of enrofloxacin.

MeSH terms

  • Animals
  • Antineoplastic Agents / blood
  • Antineoplastic Agents / pharmacokinetics*
  • Carbon Tetrachloride Poisoning / pathology
  • Enrofloxacin
  • Fluoroquinolones / blood
  • Fluoroquinolones / pharmacokinetics*
  • Liver Failure / chemically induced*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Renal Insufficiency / chemically induced*

Substances

  • Antineoplastic Agents
  • Fluoroquinolones
  • Enrofloxacin