Pharmacokinetics, dosage regimen and in vitro plasma protein binding of intramuscular levofloxacin in buffalo calves

The pharmacokinetics of levofloxacin following its single intramuscular administration (3 mg/kg) wasinvestigated in six male buffalo calves. Peak plasma level of 2.95 ± 0.13 μg/ml was observed at 1 h and thedrug level above MIC90 in plasma was detected up to 12 h of administration. The bioavailability was 68.1 ±5.4% and levofloxacin was bound to the plasma proteins to the extent of 19.1 ± 1.5%. High values of AUC(8.81 ± 0.37 μg.h/ml) and Vdarea (1.06 ± 0.04 L/kg) reflected a vast area of body covered by drugconcentration and appropriate penetration of levofloxacin into various body fluids and tissues. Theelimination half-life and mean residence time were 3.27 ± 0.31 h and 5.4 ± 0.59 h, respectively. The totalbody clearance was 343.2 ± 14.1 ml/kg/h. An appropriate intramuscular dosage regimen for levofloxacin inbuffalo calves would be 1.7 mg/kg repeated at 12-h intervals.