Pharmacokinetic‐pharmacodynamic integration of moxifloxacin in rabbits after intravenous, intramuscular and oral administration

The pharmacokinetics of moxifloxacin was studied following intravenous (i.v.), intramuscular (i.m.) and oral dose of 5 mg/kg to healthy white New Zealand rabbits (n = 6). Moxifloxacin concentrations were determined by HPLC assay with fluorescence detection. The moxifloxacin plasma concentration vs. time data after i.v. administration could best be described by a two-compartment open model. The disposition of i.m. and orally administered moxifloxacin was best described by a one-compartment model. The plasma moxifloxacin clearance (CI) for the i.v route was (mean ′ SD) 0.80 ′ 0.02 L/h.kg. The steady-state volume of distribution (V s s ) was 1.95 ′ 0.18 L/kg. The terminal half-life (t 1 / 2 λ z ) was (mean ′ SD) 1.84 ′ 0.12, 2.09 ′ 0.05 and 2.15 ′ 0.07 h after i.v., i.m. and oral, respectively. Minimal inhibitory concentration (MIC) assays of moxifloxacin against different strains of S. aureus were performed in order to compute pharmacodynamic surrogate markers. Prom these data, it is concluded that a 5 mg/kg dose moxifloxacin would be effective by i.m. and oral routes in rabbits against bacterial isolates with MJC < 0.06 μg/mL and possibly for MIC ≤ 0.12 μg/mL, but in the latter case a higher dose would be required.