氟尼辛甲胺在毛羊体内的药动学研究。

IF 1.7 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Kaitlyn G Forrest, Jennifer L Halleran, Ronald E Baynes, Danielle A Mzyk
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引用次数: 0

摘要

本研究的目的是评价氟尼新大明静脉注射(IV)和透皮(TD)给药氟尼新大明在12只健康绵羊不同被毛类型(羊毛和毛)上的药代动力学。试验的多赛特(毛羊)羊(n = 6)和卡塔丁羊(n = 6)分别接受2.2 mg/kg IV和3.3 mg/kg TD治疗,两次治疗之间有10天的洗脱期。分别在静脉注射和TD给药后96小时获得血浆样本。采用高效液相色谱-质谱法定量氟尼辛浓度,并采用不同的建模技术推导出药代动力学参数。种群非线性混合效应模型表明,涂膜类型对TD的吸收率有显著影响。TD氟尼欣的平均生物利用度差异无统计学意义(分别为48.76%±17.49%和36.61%±4.33%);P = 0.093)。给药后毛羊血药浓度较高(1.57 μg/mL;范围为0.6 ~ 3.41 μg/mL),而毛羊为0.57 μg/mL;范围:0.36 ~ 0.83 μg/mL)。PK结果为临床研究TD氟尼辛对不同品种绵羊的疗效提供了进一步的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics of Intravenous and Transdermal Flunixin Meglumine in Wool and Hair Sheep (Ovis aries).

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.

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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
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.
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