Pharmacokinetics of intravenous and oral meloxicam in ruminant calves.

Veterinary Therapeutics Pub Date : 2009-01-01
Johann F Coetzee, Butch KuKanich, Ruby Mosher, Portia S Allen
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Abstract

The purpose of this study was to investigate the pharmacokinetics and oral bioavailability of meloxicam in ruminant calves. Six Holstein calves (145 to 170 kg) received meloxicam at 0.5 mg/kg IV or 1 mg/kg PO in a randomized crossover design with a 10-day washout period. Plasma samples collected up to 96 hours after administration were analyzed by liquid chromatography/mass spectrometry followed by noncompartmental pharmacokinetic analysis. A mean peak plasma concentration of 3.10 microg/ml (range, 2.64 to 3.79 microg/ml) was recorded at 11.64 hours (range, 10 to 12 hours) with a half-life of 27.54 hours (range, 19.97 to 43.29 hours) after oral meloxicam administration. The bioavailability of oral meloxicam corrected for dose was 1.00 (range, 0.64 to 1.66). These findings indicate that oral meloxicam administration might be an effective and convenient means of providing long-lasting analgesia to ruminant calves.

静脉注射和口服美洛昔康在反刍动物犊牛体内的药代动力学。
本研究的目的是研究美洛昔康在反刍动物犊牛体内的药代动力学和口服生物利用度。在为期10天的随机交叉设计中,6头荷斯坦犊牛(145 - 170公斤)接受了0.5 mg/kg IV或1 mg/kg PO剂量的美洛昔康治疗。使用液相色谱/质谱法分析给药后96小时内收集的血浆样本,然后进行非室间药代动力学分析。口服美洛昔康后11.64小时(10 ~ 12小时),血药浓度平均峰值为3.10 μ g/ml(范围2.64 ~ 3.79 μ g/ml),半衰期27.54小时(范围19.97 ~ 43.29小时)。口服美洛昔康经剂量校正后的生物利用度为1.00(范围0.64 ~ 1.66)。这些结果表明,口服美洛昔康可能是一种有效和方便的方法,为反刍动物犊牛提供持久的镇痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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