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Antimicrobial Agents and Chemotherapy, July 2009, p. 3024-3029, Vol. 53, No. 7
0066-4804/09/$08.00+0 doi:10.1128/AAC.01346-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

College of Veterinary Medicine, Kyungpook National University, Daegu 702-701, South Korea,1 School of Veterinary Medicine, Louisiana State University, Baton Rouge, Louisiana 708032
Received 8 October 2008/ Returned for modification 17 January 2009/ Accepted 19 April 2009
The pharmacokinetics (PK) and pharmacodynamics (PD) of orbifloxacin were studied in beagle dogs after intravenous (i.v.) and intramuscular (i.m.) administration at a dose of 2.5 mg/kg body weight. An absolute bioavailability of 100.1% ± 4.76%, a terminal half-life of 4.23 ± 0.2 h and 3.95 ± 0.15 h after i.v. and i.m. administration, a steady-state volume of distribution of 1.61 ± 0.13 liters/kg, and clearance of 0.31 ± 0.03 liters/h/kg were observed. Orbifloxacin showed rapid, concentration-dependent killing against the Escherichia coli, Staphylococcus aureus, Staphylococcus intermedius, and Proteus mirabilis clinical isolates. Computations based on PK-PD analysis indicated that the recommended dose is unlikely to be clinically effective against some strains like S. intermedius. Therefore, a higher dose of orbifloxacin would be worthy of consideration for treatment of certain bacterial infections in dogs.
Published ahead of print on 27 April 2009.
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