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Pharmacokinetics of tapentadol in laying hens and its residues in eggs after multiple oral dose administration
Authors:V De Vito  H Owen  M Marzoni  TW Kim  A Poapolathep  M Giorgi
Institution:1. Department of Veterinary Sciences, University of Sassari, Sassari, Italyvirgidevit@libero.it;3. School of Veterinary Science, The University of Queensland, Gatton, Australia;4. Department of Veterinary Sciences, University of Pisa, Pisa, Italy;5. Colleage of Veterinary Medicine, Chungnam National University, Daejeon, South Korea;6. Department of Pharmacology, Faculty of Veterinary Medicine, Kasetsart University, Bangkok, Thailand
Abstract:1. The aim of the study was to evaluate the pharmacokinetics (PKs) of tapentadol (TAP), a novel opioid analgesic, in laying hens after intravenous (IV) and oral (PO) administration and to quantify the concentrations of TAP residues in eggs.

2. Twenty healthy laying hens were divided into three groups: A (n = 6), B (n = 6) and C (n = 8). The study was conducted in two phases. Groups A and B received TAP by IV and PO routes at the dose of 1 and 5 mg/kg, respectively.

3. No visible adverse effects were observed after administration of the drug. TAP plasma concentrations were detectable up to 4 h following administration. Following IV administration, TAP plasma concentrations were only higher than the minimal effective concentration (148 ng/ml) reported for humans for 1 h. After single PO administration, plasma concentrations of TAP would not conform to software algorithms and the PK parameters were not calculated. TAP concentration following multiple PO doses at 5 mg/kg for 5 d was found to be higher and more persistent (12 h vs. 7 h) in yolk compared with albumen.

4. This is the first PK study on the novel atypical opioid TAP in laying hens. Further studies are required to investigate the analgesic efficacy and actual effective plasma concentration of TAP in this species.
Keywords:Eggs residues  intravenous and oral administrations  laying hens  pharmacokinetics  tapentadol
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