Pharmacokinetics of buprenorphine after intravenous administration of clinical doses to dogs |
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Authors: | Andaluz Anna Moll Xavier Abellán Rosario Ventura Rosa Carbó Marcellí Fresno Laura García Félix |
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Affiliation: | aDepartment of Animal Medicine and Surgery, Faculty of Veterinary Medicine, Autonomous University of Barcelona (U.A.B), 08193 Bellaterra, Barcelona, Spain;bPharmacology Research Unit, Institut Municipal d’Investigació Mèdica (IMIM), Doctor Aiguader 80, 08003 Barcelona, Spain;cDepartment of Experimental and Health Research, Universitat Pompeu Fabra (UPF), Doctor Aiguader 80, 08003 Barcelona, Spain |
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Abstract: | The purpose of this study was to evaluate plasma concentrations and pharmacokinetic parameters of buprenorphine in dogs following intravenous (IV) administration of clinical doses of the opioid. An IV bolus of 0.02 mg/kg buprenorphine was administered to six healthy Beagles and blood samples were collected through a jugular catheter before and at 1, 5, 10, 15, 20, 30 and 45 min, and 1, 2, 4, 6, 8 and 12 h after administration. Plasma buprenorphine concentrations, measured using a commercial radioimmunoassay (RIA), decreased following a three-exponential curve. The two distribution and the elimination half-lives were 2.9 ± 1.8 min, 16.5 ± 3.7 min, and 266.6 ± 82.0 min, respectively; the clearance was 329.6 ± 62.2 mL/min, and the steady state volume of distribution was 83.7 ± 26.5 L.The results demonstrated the feasibility of the RIA assay to analyse buprenorphine in dog plasma samples. Following IV administration buprenorphine showed a three-compartment kinetic profile, as has been described previously in humans, rabbits and cats. The relationship between plasma concentrations and dynamic effects in dogs remains to be established. |
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Keywords: | Buprenorphine Dogs Pharmacokinetics Intravenous Radioimmunoassay |
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