Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)

Flumequine was administered to halibut ( Hippoglossus hippoglossus ) and turbot ( Scophthalmus maximus ) intravenously (i.v.) and orally (p.o.) at a dose of 10 mg/kg bodyweight, and as a bath‐treatment at a dose of 10 mg/L water for 2 h, using identical experimental designs. The study was performed...

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Published in:Journal of Veterinary Pharmacology and Therapeutics
Main Authors: Hansen, Horsberg
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1999
Subjects:
Online Access:http://dx.doi.org/10.1046/j.1365-2885.1999.00191.x
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spelling crwiley:10.1046/j.1365-2885.1999.00191.x 2024-09-15T18:34:00+00:00 Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus) Hansen Horsberg 1999 http://dx.doi.org/10.1046/j.1365-2885.1999.00191.x https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2885.1999.00191.x https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2885.1999.00191.x en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Veterinary Pharmacology and Therapeutics volume 22, issue 2, page 122-126 ISSN 0140-7783 1365-2885 journal-article 1999 crwiley https://doi.org/10.1046/j.1365-2885.1999.00191.x 2024-08-13T04:14:45Z Flumequine was administered to halibut ( Hippoglossus hippoglossus ) and turbot ( Scophthalmus maximus ) intravenously (i.v.) and orally (p.o.) at a dose of 10 mg/kg bodyweight, and as a bath‐treatment at a dose of 10 mg/L water for 2 h, using identical experimental designs. The study was performed in seawater with a salinity of 3% and a temperature of 10.3 ± 0.4°C (halibut) and 18.0 ± 0.3 °C (turbot). Pharmacokinetic modelling of the data showed that flumequine had quite similar pharmacokinetic properties in halibut and turbot. Following intravenous administration, the volumes of distribution at steady state ( V ss ) were 2.99 L/kg (halibut) and 3.75 L/kg (turbot). Plasma clearances ( Cl ) were 0.12 L/kg (halibut) and 0.17 L/h.kg (turbot) and the elimination half‐lives ( t ½λ z ) were calculated to be 32 h (halibut) and 34 h (turbot). Mean residence times ( MRT ) were 25.1 h (halibut) and 22.2 h (turbot). Following oral administration, the t ½λz were 43 h (halibut) and 42 h (turbot). Maximal plasma concentrations ( t max ) were 1.4 mg/L (halibut) and 1.9 mg/L (turbot), and were observed 7 h post administration in both species. The oral bioavailabilities ( F ) were calculated to 56% (halibut) and 59% (turbot). Following bath administration maximal plasma concentrations were 0.08 mg/L (halibut) and 0.14 mg/L (turbot), and were observed 0 h (halibut) and 3 h (turbot) after the end of the bath. The bioavailability in halibut following a 2‐h bath treatment was 5%. Article in Journal/Newspaper Scophthalmus maximus Turbot Wiley Online Library Journal of Veterinary Pharmacology and Therapeutics 22 2 122 126
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Flumequine was administered to halibut ( Hippoglossus hippoglossus ) and turbot ( Scophthalmus maximus ) intravenously (i.v.) and orally (p.o.) at a dose of 10 mg/kg bodyweight, and as a bath‐treatment at a dose of 10 mg/L water for 2 h, using identical experimental designs. The study was performed in seawater with a salinity of 3% and a temperature of 10.3 ± 0.4°C (halibut) and 18.0 ± 0.3 °C (turbot). Pharmacokinetic modelling of the data showed that flumequine had quite similar pharmacokinetic properties in halibut and turbot. Following intravenous administration, the volumes of distribution at steady state ( V ss ) were 2.99 L/kg (halibut) and 3.75 L/kg (turbot). Plasma clearances ( Cl ) were 0.12 L/kg (halibut) and 0.17 L/h.kg (turbot) and the elimination half‐lives ( t ½λ z ) were calculated to be 32 h (halibut) and 34 h (turbot). Mean residence times ( MRT ) were 25.1 h (halibut) and 22.2 h (turbot). Following oral administration, the t ½λz were 43 h (halibut) and 42 h (turbot). Maximal plasma concentrations ( t max ) were 1.4 mg/L (halibut) and 1.9 mg/L (turbot), and were observed 7 h post administration in both species. The oral bioavailabilities ( F ) were calculated to 56% (halibut) and 59% (turbot). Following bath administration maximal plasma concentrations were 0.08 mg/L (halibut) and 0.14 mg/L (turbot), and were observed 0 h (halibut) and 3 h (turbot) after the end of the bath. The bioavailability in halibut following a 2‐h bath treatment was 5%.
format Article in Journal/Newspaper
author Hansen
Horsberg
spellingShingle Hansen
Horsberg
Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
author_facet Hansen
Horsberg
author_sort Hansen
title Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
title_short Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
title_full Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
title_fullStr Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
title_full_unstemmed Single‐dose pharmacokinetics of flumequine in halibut ( Hippoglossus hippoglossus) and turbot ( Scophthalmus maximus)
title_sort single‐dose pharmacokinetics of flumequine in halibut ( hippoglossus hippoglossus) and turbot ( scophthalmus maximus)
publisher Wiley
publishDate 1999
url http://dx.doi.org/10.1046/j.1365-2885.1999.00191.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2885.1999.00191.x
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2885.1999.00191.x
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
op_source Journal of Veterinary Pharmacology and Therapeutics
volume 22, issue 2, page 122-126
ISSN 0140-7783 1365-2885
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1046/j.1365-2885.1999.00191.x
container_title Journal of Veterinary Pharmacology and Therapeutics
container_volume 22
container_issue 2
container_start_page 122
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