Publication | Open Access
Pharmacokinetics of phenylbutazone in neonatal foals
36
Citations
3
References
1993
Year
EducationPbz DispositionPharmacotherapyPhysiologically-based Pharmacokinetic ModelingPharmacodynamic ModelingPre-clinical PharmacologySummary Single DosesToxicologyAnimal PhysiologyVeterinary PhysiologyPharmacokinetic ModelingMedian Terminal Half-lifePharmacologyAnimal SciencePhysiologyVeterinary ScienceClinical PharmacologyMetabolismMedicinePharmacokineticsNeonatal Foals
Summary Single doses (2.2 mg/kg of body weight) of phenylbutazone ( pbz ) were administered iv to 6 neonatal horses (5 to 17 hours old at time of dosing). Plasma concentrations of pbz and its metabolite oxyphenbutazone were monitored serially for 120 hours after drug administration. Pharmacokinetic variables were calculated, using 1- and 2-compartment open models. Descriptive equations from the best model for each foal were then used to derive model-independent variables describing pbz disposition. Median volume of distribution at steady-state was 0.274 L/ kg (range, 0.190 to 0.401 L/kg). Median terminal half-life was 7.4 (6.4 to 22.1) hours, and median total plasma clearance of pbz for foals in this study was 0.018 L/kg/h (range, 0.013 to 0.038 L/kg/h). Volume of distribution was larger, half-life was longer, and total clearance was lower, compared with similar values reported for administration of pbz to adult horses.
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