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Sheep are often subjected to painful procedures and thus they need to be treated with analgesics. Nevertheless, knowledges about pharmacokinetic features of these drugs in this species are poor. The aim of this study was to evaluate plasma behaviour of cimicoxib in sheep after a single oral administration at two different dose rates (4 and 6 mg/kg). Maximum plasma concentrations of cimicoxib were equal to 273.78 (median value; range 189.00-567.32) and 565.01 (range 308.27-822.59) ng/mL after treatment with 4 and 6 mg/kg, respectively. The time of maximum concentration (Tmax) was achieved between 4 and 10 hours following treatment at the lower dose, and between 6 and 10 hours after the administration of the higher dose, with one sheep achieving the concentration peak at 0.75 hours. The slow absorption and the great individual variability in plasma concentration, probably due to ruminal effects, suggest that cimicoxib is not suitable for oral treatment in sheep.
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p.535-538,fig.,ref.
Twórcy
autor
- Department of Veterinary Medicine, University of Perugia, Perugia, Italy
autor
- Department of Veterinary Medicine, University of Pisa, Pisa, Italy
autor
- Pharmacology and Toxicology, College of Veterinary Medicine, Chungnam University, Daejon, South Korea
autor
- Department of Veterinary Sciences, University of Torino, Grugliasco, Torino, Italy
autor
- Department of Veterinary Medicine, University of Perugia, Perugia, Italy
autor
autor
- Department of Veterinary Medicine, University of Perugia, Perugia, Italy
Bibliografia
- Baggot JD, Brown SA (1998) Basis for selection of the dosage form. In: Hardee GE, Baggot JD (eds) Development and Formulation of Veterinary Dosage Forms, 2nd ed., Marcel Dekker Inc, New York, pp 7-143.
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- EMA, (2011). European Medicine Agency. Cimalgex: EPAR – Public assessment report. EMA/CVMP/513842/ 2011.
- Giorgi M, Kim TW, Saba A, Rouini M-R, Yun H, Ryschanova R, Owen H (2013) Detection and quantification of cimicoxib, a novel COX-2 inhibitor, in canine plasma by HPLC with spectrofluorimetric detection: development and validation of a new methodology. J Pharm Biomed Anal 83: 28-33.
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- Kim TW, Della Rocca G, Di Salvo A, Ryschanova R, Sgorbini M, Giorgi M (2015) Evaluation of pharmacokinetic and pharmacodynamic properties of cimicoxib in fasted and fed horses. N Z Vet J 63: 92-97.
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- Stock ML, Coetzee JF, KuKanich B, Smith BI (2013) Pharmacokinetics of intravenously and orally administered meloxicam in sheep. Am J Vet Res 74: 779-783.
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- Welsh EM, Nolan AM (1995) Effect of flunixin meglumine on the thresholds to mechanical stimulation in healthy and lame sheep. Res Vet Sci 58: 61-66.
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Bibliografia
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