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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Determination of penciclovir in human plasma by liquid chromatography-electrospray ionization tandem mass spectrometry: application to a clinical pharmacokinetic study.
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Determination of penciclovir in human plasma by liquid chromatography-electrospray ionization tandem mass spectrometry: application to a clinical pharmacokinetic study.

机译:液相色谱-电喷雾串联质谱法测定人血浆中的喷昔洛韦:在临床药代动力学研究中的应用。

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摘要

A rapid, specific and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed for the determination of penciclovir in human plasma. The method involved simple, one-step SPE procedure coupled with a C(18) , 75 x 4.mm, 3microm column with a flow-rate of 0.5 mL/min, and acyclovir was used as the internal standard. The Quattro Micro mass spectrometry was operated under the multiple reaction-monitoring mode using the electrospray ionization technique. Using 250 microL plasma, the methods were validated over the concentration range 52.555-6626.181 ng/mL, with a lower limit of quantification of 52.55 ng/mL. The intra- and inter-day precision and accuracy values were found to be within the assay variability limits as per the FDA guidelines. The developed assay method was applied to a clinical pharmacokinetic study in human volunteers. Copyright (c) 2010 John Wiley & Sons, Ltd.
机译:建立了一种快速,灵敏,灵敏的液相色谱串联质谱法(LC-MS / MS),用于测定人血浆中的喷昔洛韦。该方法涉及简单的一步式SPE程序,并采用流速为0.5 mL / min的C(18),75 x 4.mm,3微米色谱柱,并使用阿昔洛韦作为内标。 Quattro Micro质谱仪使用电喷雾电离技术在多反应监测模式下运行。使用250微升血浆,在52.555-6626.181 ng / mL的浓度范围内对方法进行了验证,定量下限为52.55 ng / mL。根据FDA准则,发现日内和日间精度和准确度值均在测定变异性范围内。所开发的测定方法已应用于人类志愿者的临床药代动力学研究。版权所有(c)2010 John Wiley&Sons,Ltd.

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