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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of enalapril and enalaprilat in human plasma by liquid chromatography-tandem mass spectrometry
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Simultaneous determination of enalapril and enalaprilat in human plasma by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法同时测定人血浆中的依那普利和依那普利拉

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A rapid, sensitive, and highly selective liquid chromatography-tandem mass spectrometry method was developed and validated for simultaneous determination of enalapril and its major active metabolite enalaprilat in human plasma. The analytes were extracted from plasma samples by liquid-liquid extraction, separated on a Zorbax Extend-C-18 column, and detected by tandem mass spectrometry with a Turbo IonSpray ionization interface. The method has a lower limit of quantification (LLOQ) of 0.1 ng/ml for both enalapril and enalaprilat. The chromatographic run time was approximately 3.5 min. The standard calibration curves for both enalapril and enalaprilat were linear in the concentration ranges of 0.10-100.0 ng/ml in human plasma. The intra- and inter-run precisions, expressed as the relative standard deviation (R.S.D.), were less than 7.7 and 7.8%, determined from QC samples for enalapril and enalaprilat, and accuracy was within +/-3.9 and +/-2.7% in terms of relative error, respectively. The method was successfully applied for the evaluation of the pharmacokinetics of enalapril and enalaprilat in 20 volunteers after an oral dose of 10 mg enalapril maleate. (C) 2004 Elsevier B.V. All rights reserved.
机译:建立了一种快速,灵敏,高选择性的液相色谱-串联质谱方法,并验证了该方法可同时测定人血浆中的依那普利及其主要活性代谢物依那普利拉。通过液-液萃取从血浆样品中萃取分析物,在Zorbax Extend-C-18色谱柱上分离,并通过具有Turbo IonSpray电离界面的串联质谱法进行检测。该方法对依那普利和依那普利拉的定量下限(LLOQ)为0.1 ng / ml。色谱运行时间约为3.5分钟。依那普利和依那普利的标准校准曲线在人血浆中的浓度范围为0.10-100.0 ng / ml时均为线性。从依那普利和依那普利的QC样品中确定的运行中和运行间精密度(相对标准偏差(RSD))分别小于7.7和7.8%,准确性在+/- 3.9和+/- 2.7%之内就相对误差而言。该方法已成功用于口服剂量10 mg马来酸依那普利的20名志愿者的依那普利和依那普利拉的药代动力学评估。 (C)2004 Elsevier B.V.保留所有权利。

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