Clarke C R, Burrows G E, MacAllister C G, Spillers D K, Ewing P, Lauer A K
Department of Physiological Sciences, College of Veterinary Medicine, Oklahoma State University, Stillwater 74078.
Am J Vet Res. 1992 Dec;53(12):2292-5.
Single-dose pharmacokinetic variables of pyrimethamine were studied in horses. Pyrimethamine (1 mg/kg of body weight) was administered IV and orally to 6 adult horses, and plasma samples were obtained at frequent intervals thereafter. Plasma pyrimethamine concentration was assayed by gas chromatography, and concentration-time data were analyzed, using a pharmacokinetic computer program. The IV and oral administration data were best described by 3-compartment and 1-compartment models, respectively. The median volume of distribution at steady state after IV administration was 1,521 ml/kg and the median elimination half-time was 12.06 hours. Mean plasma concentration after oral administration fluctuated between a maximal concentration of 0.18 microgram/ml and 0.09 microgram/ml (24 hours after dosing). Bioavailability after oral administration was 56%.
在马匹中研究了乙胺嘧啶的单剂量药代动力学变量。给6匹成年马静脉注射和口服乙胺嘧啶(1毫克/千克体重),此后定期采集血样。采用气相色谱法测定血浆乙胺嘧啶浓度,并使用药代动力学计算机程序分析浓度-时间数据。静脉注射和口服给药数据分别用三室模型和一室模型能得到最佳描述。静脉注射后稳态分布容积中位数为1521毫升/千克,消除半衰期中位数为12.06小时。口服给药后平均血浆浓度在最大浓度0.18微克/毫升和0.09微克/毫升(给药后24小时)之间波动。口服给药后的生物利用度为56%。