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Enantiospecific pharmacokinetics of intravenous dexmedetomidine in beagles

Title: Enantiospecific pharmacokinetics of intravenous dexmedetomidine in beagles
Authors: Levionnois, Olivier Louis; Barbarossa, Andrea; Bardhi, Anisa; Siegenthaler, Joelle; Forss Pleyers, Tekla; Guidi, Monia; Spadavecchia, Claudia; Raillard, Mathieu
Source: Journal of Veterinary Pharmacology and Therapeutics ; volume 45, issue 4, page 366-372 ; ISSN 0140-7783 1365-2885
Publisher Information: Wiley
Publication Year: 2022
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: The goal of this study was to investigate the pharmacokinetic (PK) behaviour of dexmedetomidine in dogs administered as a pure enantiomer versus as part of a racemic mixture. Eight unmedicated intact purpose‐bread beagles were included. Two intravenous treatments of either medetomidine or dexmedetomidine were administered at 10‐ to 14‐day intervals. Atipamezole or saline solution was administered intramuscularly 45 min later. Venous blood samples were collected into EDTA collection tubes, and the quantification of dexmedetomidine and levomedetomidine was performed by chiral LC–MS/MS. All dogs appeared sedated after each treatment without complication. Plasma concentrations of levomedetomidine were measured only in the racemic group and were 51.4% (51.4%–56.1%) lower than dexmedetomidine. Non‐compartmental analysis (NCA) was performed for both drugs, while dexmedetomidine data were further described using a population pharmacokinetic approach. A standard two‐compartment mammillary model with linear elimination with combined additive and multiplicative error model for residual unexplained variability was established for dexmedetomidine. An exponential model was finally retained to describe inter‐individual variability on parameters of clearance (Cl 1 ) and central and peripheral volumes of distribution (V 1 , V 2 ). No effect of occurrence, levomedetomidine or atipamezole could be observed on dexmedetomidine PK parameters. Dexmedetomidine did not undergo significantly different PK when administered alone or as part of the racemic mixture in otherwise unmedicated dogs.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1111/jvp.13063
Availability: http://dx.doi.org/10.1111/jvp.13063; https://onlinelibrary.wiley.com/doi/pdf/10.1111/jvp.13063; https://onlinelibrary.wiley.com/doi/full-xml/10.1111/jvp.13063
Rights: http://creativecommons.org/licenses/by-nc/4.0/
Accession Number: edsbas.A252AAA4
Database: BASE