TY - JOUR
T1 - Pharmacokinetics of buprenorphine after intravenous administration of clinical doses to dogs
AU - Andaluz, Anna
AU - Moll, Xavier
AU - Abellán, Rosario
AU - Ventura, Rosa
AU - Carbó, Marcellí
AU - Fresno, Laura
AU - García, Félix
PY - 2009/9/1
Y1 - 2009/9/1
N2 - 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. © 2008 Elsevier Ltd. All rights reserved.
AB - 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. © 2008 Elsevier Ltd. All rights reserved.
KW - Buprenorphine
KW - Dogs
KW - Intravenous
KW - Pharmacokinetics
KW - Radioimmunoassay
UR - https://www.scopus.com/pages/publications/67349218126
U2 - 10.1016/j.tvjl.2008.03.001
DO - 10.1016/j.tvjl.2008.03.001
M3 - Article
SN - 1090-0233
VL - 181
SP - 299
EP - 304
JO - Veterinary Journal
JF - Veterinary Journal
IS - 3
ER -