Abstract
The objective of the study was to assess the pharmacokinetics of terbinafine administered orally to horses and Greyhound dogs. A secondary objective was to assess terbinafine metabolites. Six healthy horses and six healthy Greyhound dogs were included in the pharmacokinetic data. The targeted dose of terbinafine was 20 and 30mg/kg for horses and dogs, respectively. Blood was collected at predetermined intervals for the quantification of terbinafine concentrations with liquid chromatography and mass spectrometry. The half-life (geometric mean) was 8.1 and 8.6h for horses and Greyhounds, respectively. The mean maximum plasma concentration was 0.31 and 4.01μg/mL for horses and Greyhounds, respectively. The area under the curve (to infinity) was 1.793h·μg/mL for horses and 17.253h·μg/mL for Greyhounds. Adverse effects observed in one study horse included pawing at the ground, curling lips, head shaking, anxiety and circling, but these resolved spontaneously within 30min of onset. No adverse effects were noted in the dogs. Ions consistent with carboxyterbinafine, n-desmethylterbinafine, hydroxyterbinafine and desmethylhydroxyterbinafine were identified in horse and Greyhound plasma after terbinafine administration. Further studies are needed assessing the safety and efficacy of terbinafine in horses and dogs. © 2010 Blackwell Publishing Ltd.
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CITATION STYLE
Williams, M. M., Davis, E. G., & KuKanich, B. (2011). Pharmacokinetics of oral terbinafine in horses and Greyhound dogs. Journal of Veterinary Pharmacology and Therapeutics, 34(3), 232–237. https://doi.org/10.1111/j.1365-2885.2010.01213.x
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