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首页> 外文期刊>Analytical Letters >Quantification of Levosulpiride in Human Plasma by High-Performance Liquid Chromatography
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Quantification of Levosulpiride in Human Plasma by High-Performance Liquid Chromatography

机译:高效液相色谱法定量测定人血浆中的左硫磺必利

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摘要

An analytical procedure was developed and validated for the quantification of levosulpiride in human plasma.After subjecting a plasma sample to a two-step extraction procedure,an aliquot of the aqueous phase was injected onto an high-performance liquid chromatography system equipped with a fluorescence detector.The detector response was linear for levosulpiride concentrations in the range of 2.5 to 500 ng/ml.The intra- and inter-day precision was below 15.4 and 10.1%,and the accuracy was in a range from 89.7 to 109.4%.The method is applicable for use in the pharmacokinetic characterization of levosulpiride after a 75-mg oral dose in humans.
机译:开发了一种分析程序并验证了人血浆中左旋硫脲的定量。将血浆样品经过两步萃取程序后,将等分试样的水相注入配备了荧光检测器的高效液相色谱系统中左旋磺酰脲浓度在2.5至500 ng / ml范围内,检测器响应呈线性关系。日内和日间精密度分别低于15.4和10.1%,准确度介于89.7至109.4%之间。可用于人类口服75毫克后左旋磺必利的药代动力学表征。

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