Kaitlyn G Forrest, Jennifer L Halleran, Ronald E Baynes, Danielle A Mzyk
{"title":"Pharmacokinetics of Intravenous and Transdermal Flunixin Meglumine in Wool and Hair Sheep (Ovis aries).","authors":"Kaitlyn G Forrest, Jennifer L Halleran, Ronald E Baynes, Danielle A Mzyk","doi":"10.1111/jvp.70015","DOIUrl":null,"url":null,"abstract":"<p><p>The objective of the study was to evaluate the pharmacokinetics of flunixin meglumine of intravenous (IV) and transdermal (TD) flunixin meglumine administration on different coat types (wool vs. hair) in 12 healthy sheep. Polled dorset (wool) sheep (n = 6) and katahdin (hair) sheep (n = 6) received 2.2 mg/kg IV and 3.3 mg/kg TD with a 10-day washout period between treatments. Plasma samples were obtained for 96 h following both IV and TD administration, respectively. Flunixin concentrations were quantified by use of high-performance liquid chromatography with mass spectrometry, and PK parameters were derived using different modeling techniques. A population non-linear mixed effect model showed that coat type has a significant effect on the absorption rate following TD administration. The mean bioavailability of TD flunixin was not significantly different (48.76% ± 17.49% and 36.61% ± 4.33%; p = 0.093) in wool and hair sheep, respectively. Maximum plasma concentrations following TD administration were higher in wool sheep (1.57 μg/mL; range, 0.6-3.41 μg/mL) compared to hair sheep (0.57 μg/mL; range, 0.36-0.83 μg/mL). The PK results provide further support for clinical studies to examine the efficacy of TD flunixin in different breeds of sheep.</p>","PeriodicalId":17596,"journal":{"name":"Journal of veterinary pharmacology and therapeutics","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of veterinary pharmacology and therapeutics","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/jvp.70015","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
The objective of the study was to evaluate the pharmacokinetics of flunixin meglumine of intravenous (IV) and transdermal (TD) flunixin meglumine administration on different coat types (wool vs. hair) in 12 healthy sheep. Polled dorset (wool) sheep (n = 6) and katahdin (hair) sheep (n = 6) received 2.2 mg/kg IV and 3.3 mg/kg TD with a 10-day washout period between treatments. Plasma samples were obtained for 96 h following both IV and TD administration, respectively. Flunixin concentrations were quantified by use of high-performance liquid chromatography with mass spectrometry, and PK parameters were derived using different modeling techniques. A population non-linear mixed effect model showed that coat type has a significant effect on the absorption rate following TD administration. The mean bioavailability of TD flunixin was not significantly different (48.76% ± 17.49% and 36.61% ± 4.33%; p = 0.093) in wool and hair sheep, respectively. Maximum plasma concentrations following TD administration were higher in wool sheep (1.57 μg/mL; range, 0.6-3.41 μg/mL) compared to hair sheep (0.57 μg/mL; range, 0.36-0.83 μg/mL). The PK results provide further support for clinical studies to examine the efficacy of TD flunixin in different breeds of sheep.
期刊介绍:
The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.