Pharmacokinetic and Pharmacodynamic Profiles of Danofloxacin Administered by Two Dosing Regimens in Calves Infected with Mannheimia ( Pasteurella ) haemolytica

Author:

Sarasola Patxi1,Lees Peter2,AliAbadi Fariborz Shojaee3,McKellar Quintin A.4,Donachie William4,Marr Kate A.5,Sunderland Simon J.5,Rowan Tim G.5

Affiliation:

1. Ondax Scientific, 20280 Hondarribia, Gipuzkoa, Spain

2. The Royal Veterinary College, Hawkshead Campus, North Mymms, Hatfield, Hertfordshire

3. Ministry of Jahad-e-Keshavarzi, Veterinary Organisation of I. R. Iran, Tehran, Iran

4. The Moredun Foundation, Pentlands Science Park, Bush Loan, Penicuik, Midlothian

5. Pfizer Global Research and Development, Sandwich, Kent, United Kingdom

Abstract

ABSTRACT The pharmacokinetics and pharmacodynamics of danofloxacin in calves with induced Mannheimia ( Pasteurella ) haemolytica pneumonia were evaluated. Calves received either saline as an intravenous (IV) bolus or danofloxacin (0.738 mg/kg of body weight) administered as either a single IV bolus or a 36-h continuous IV infusion. Blood samples and bronchial secretions were collected before and at predetermined times over 48 h following the start of treatment. Calves were assessed clinically throughout, and lung consolidation was assessed at necropsy. Bronchial secretions and lung tissue were cultured for M. haemolytica . Bolus administration of danofloxacin produced a high maximum drug concentration-to-MIC ratio ( C max :MIC) of 14.5 and a time period of 9.1 h when plasma danofloxacin concentrations exceeded the MIC ( T >MIC). Following danofloxacin infusion, the C max :MIC was low (2.3), with a long T >MIC (33.3 h). The area under the curve-to-MIC ratios were 43.3 and 49.1 for the bolus and infusion administrations, respectively. The single bolus of danofloxacin was more effective than the same dose administered by continuous infusion, as indicated by a significantly lower ( P < 0.05) number of animals with M. haemolytica in bronchial secretions after treatment and lower rectal temperatures in the 24 h after the start of treatment. Thus, danofloxacin exhibited concentration-dependent antimicrobial activity in cattle with respiratory disease caused by M. haemolytica.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference20 articles.

1. Apley, M. D., and D. W. Upson. 1993. Lung tissue concentrations and plasma pharmacokinetics of danofloxacin in calves with acute pneumonia. Am. J. Vet. Res.54:937-943.

2. Apley, M. D., and D. W. Upson. 1993. Regional danofloxacin lung tissue concentrations and their relationship to regional pulmonary blood flow in consolidated and nonconsolidated bovine lung. Am. J. Vet. Res.54:944-951.

3. Craig, W. 1993. Pharmacodynamics of antimicrobial agents as a basis for determining dosage regimens. Eur. J. Clin. Microbiol. Infect. Dis.12(Suppl.):S6-S8.

4. Pharmacodynamics of a fluoroquinolone antimicrobial agent in a neutropenic rat model of Pseudomonas sepsis

5. European Union Committee for Veterinary Medicinal Products. 1994. Good clinical practice for the conduct of clinical trials for veterinary medicinal products (GCPV): the EU note for guidance. FEDESA Brussels Belgium.

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