Population pharmacokinetics of buprenorphine following a two-stage intravenous infusion in healthy volunteers

ML Jensen, DJR Foster, RN Upton… - European journal of …, 2007 - Springer
Objective The aim of this investigation was to characterize the pharmacokinetics of
buprenorphine following administration of an intravenous (iv) infusion. To date, the …

Pharmacokinetics of intravenous, oral transmucosal, and intranasal buprenorphine in healthy male dogs

H Enomoto, L Love, M Madsen… - Journal of Veterinary …, 2022 - Wiley Online Library
Effective management of pain in animals is of critical importance but options are limited for
treating acute pain in dogs on an outpatient basis. The objective of this study was to …

[PDF][PDF] Pharmacokinetics of buprenorphine following intravenous and oral transmucosal administration in dogs

LA Abbo, JCH Ko, LK Maxwell… - Veterinary …, 2008 - assets.prod.vetlearn.com.s3 …
■ MATERIALS AND METHODS The Purdue Animal Care and Use Committee approved
this study. Eight healthy 2-yearold purpose-bred mixed-breed research dogs weighing …

[HTML][HTML] Central nervous system distribution of buprenorphine in pregnant sheep, fetuses and newborn lambs after continuous transdermal and single subcutaneous …

H Hakomäki, S Eskola, H Kokki, M Lehtonen… - European Journal of …, 2022 - Elsevier
Buprenorphine is used during pregnancy for the treatment of opioid use disorder. Limited
data exist on the central nervous system (CNS) permeation and distribution, and on the fetal …

The pharmacokinetics and analgesic effects of extended‐release buprenorphine administered subcutaneously in healthy dogs

M Barletta, SM Ostenkamp, AC Taylor… - Journal of veterinary …, 2018 - Wiley Online Library
Buprenorphine is a partial μ agonist opioid used for analgesia in dogs. An extended‐release
formulation (ER‐buprenorphine) has been shown to provide effective analgesia for 72 hr in …

Intranasal bioavailability of buprenorphine in rabbit correlated to sheep and man

K Lindhardt, M Bagger, KH Andreasen… - International journal of …, 2001 - Elsevier
The purpose of the present study of buprenorphine is to add information about the
correlation between various animal models and nasal bioavailabilities in man. PEG 300 was …

Safety and efficacy of buprenorphine for analgesia in laboratory mice and rats

M Guarnieri, C Brayton, L DeTolla, N Forbes-McBean… - Lab animal, 2012 - nature.com
Buprenorphine is a long-acting opiate with a high therapeutic index. The authors review the
pharmacology, toxicity, analgesic effects and delivery of buprenorphine for use in laboratory …

A comparison of buprenorphine, sustained release buprenorphine, and high concentration buprenorphine in male New Zealand white rabbits

DD Andrews, VR Fajt, KC Baker… - Journal of the …, 2020 - ingentaconnect.com
Pain management in rabbits can be difficult because they are adept at hiding pain and can
be stressed by handling and restraint for injection. The use of opioid analgesics with …

[引用][C] Update on the general pharmacology of buprenorphine

A Cowan - Buprenorphine: combatting drug abuse with a …, 1995 - Wiley-Liss New York

Pharmacokinetic and pharmacodynamic properties of buprenorphine after a single intravenous administration in healthy volunteers: a randomized, double-blind …

M Escher, Y Daali, J Chabert, G Hopfgartner, P Dayer… - Clinical …, 2007 - Elsevier
Background: Buprenorphine is used as an analgesic for postoperative and chronic pain. The
usual sublingual dose is 0.2 to 0.8 mg, and the usual parenteral dose is 0.3 mg for acute …