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采用微量分析技术研究大鼠体内伪麻黄碱的药代动力学。

Pseudoephedrine pharmacokinetics in the rat using a microanalysis technique.

作者信息

Till A E, Benet L Z

出版信息

Pharmacology. 1979;18(6):306-10. doi: 10.1159/000137270.

Abstract

A microanalytical procedure was developed using a gas chromatographic-electron capture technique which is capable of detecting 2 ng pseudoephedrine in 20 microliter plasma samples. Standard curves for pseudoephedrine are linear over the concentration range 0.1--1.6 microgram/ml. Plasma and urine concentrations of pseudoephedrine were followed in 3 rats after intravenous dosing. Derived pharmacokinetics parameters exhibited little inter-animal variation. Average plasma clearance was 67.6 ml/min/kg, with renal clearance averaging 30.3 ml/min/kg. This latter value is approximately 4X the glomerular filtration rate in the rat.

摘要

开发了一种微量分析方法,该方法采用气相色谱 - 电子捕获技术,能够在20微升血浆样本中检测到2纳克伪麻黄碱。伪麻黄碱的标准曲线在0.1 - 1.6微克/毫升的浓度范围内呈线性。对3只大鼠静脉给药后,跟踪测定了伪麻黄碱的血浆和尿液浓度。推导得到的药代动力学参数在动物个体间差异很小。平均血浆清除率为67.6毫升/分钟/千克,肾脏清除率平均为30.3毫升/分钟/千克。后一数值约为大鼠肾小球滤过率的4倍。

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