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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 >Development and validation of automated SPE-LC-MS/MS method for determination of indapamide in human whole blood and its application to real study samples
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Development and validation of automated SPE-LC-MS/MS method for determination of indapamide in human whole blood and its application to real study samples

机译:用于测定人全血中吲达帕胺的自动SPE-LC-MS / MS方法的开发和验证及其在实际研究样品中的应用

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摘要

A fast and simple liquid chromatography-electrospray ionization tandem mass spectrometry method for determination of indapamide in human whole blood was developed and validated. The sample extraction of indapamide from human whole blood was achieved using automated solid-phase extraction. Chromatographic separation was performed on Kinetex C18 column (100×2.1mm, 1.7μm particle size) using acetonitrile and 2mm ammonium formate in ratio 90:10 (v/v) as a mobile phase. The mass spectrometer was operated in the multiple reaction monitoring mode using positive electrospray ionization for indapamide and the internal standard (zolpidem tartarate). The total run time was 2.5min. The present method was found to be linear in the concentration range of 1-50ng/mL with the coefficient of determination 0.9987. The absolute recoveries of indapamide were 90.51-93.90%. The method was validated according the recommendations for validation of bioanalytical methods of European Medicines Agency guideline and was successfully used to analyze human whole blood samples for application in a pharmacokinetic study.
机译:建立并验证了一种快速简便的液相色谱-电喷雾串联质谱法测定人全血中吲达帕胺的方法。使用自动固相萃取技术从人全血中提取吲达帕胺。色谱分离在Kinetex C18色谱柱(100×2.1mm,粒径1.7μm)上进行,使用乙腈和2mm甲酸铵(比率为90:10(v / v))作为流动相。质谱仪使用吲达帕胺和内标物(酒石酸左乙哌啶)的正电喷雾电离,在多反应监测模式下运行。总运行时间为2.5分钟。发现本方法在1-50ng / mL的浓度范围内呈线性,测定系数为0.9987。吲达帕胺的绝对回收率为90.51-93.90%。该方法已根据欧洲药品管理局指南的生物分析方法验证建议进行了验证,并成功用于分析人全血样品,以用于药代动力学研究。

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