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一种用3-巯基丙酸衍生化后测定人血浆中维生素K3的新型液相色谱-串联质谱法。

A novel liquid chromatography-tandem mass spectrometry method for determination of menadione in human plasma after derivatization with 3-mercaptopropionic acid.

作者信息

Liu Ruijuan, Wang Mengmeng, Ding Li

机构信息

Department of Pharmaceutical Analysis, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.

Department of Pharmaceutical Analysis, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.

出版信息

Talanta. 2014 Oct;128:51-7. doi: 10.1016/j.talanta.2014.04.039. Epub 2014 Apr 30.

Abstract

Menadione (VK3), an essential fat-soluble naphthoquinone, takes very important physiological and pathological roles, but its detection and quantification is challenging. Herein, a new method was developed for quantification of VK3 in human plasma by liquid chromatography-tandem mass spectrometry (LC-MS/MS) after derivatization with 3-mercaptopropionic acid via Michael addition reaction. The derivative had been identified by the mass spectra and the derivatization conditions were optimized by considering different parameters. The method was demonstrated with high sensitivity and a low limit of quantification of 0.03 ng mL(-1) for VK3, which is about 33-fold better than that for the direct analysis of the underivatized compound. The method also had good precision and reproducibility. It was applied in the determination of basal VK3 in human plasma and a clinical pharmacokinetic study of menadiol sodium diphosphate. Furthermore, the method for the quantification of VK3 using LC-MS/MS was reported in this paper for the first time, and it will provide an important strategy for the further research on VK3 and menadione analogs.

摘要

甲萘醌(VK3)是一种必需的脂溶性萘醌,具有非常重要的生理和病理作用,但其检测和定量具有挑战性。在此,通过3-巯基丙酸经迈克尔加成反应衍生化后,开发了一种用液相色谱-串联质谱(LC-MS/MS)定量人血浆中甲萘醌的新方法。通过质谱鉴定了衍生物,并通过考虑不同参数优化了衍生化条件。该方法具有高灵敏度,甲萘醌的定量下限为0.03 ng mL(-1),比直接分析未衍生化化合物的灵敏度约高33倍。该方法还具有良好的精密度和重现性。它被应用于人血浆中基础甲萘醌的测定以及维生素K4二磷酸酯钠的临床药代动力学研究。此外,本文首次报道了使用LC-MS/MS定量甲萘醌的方法,它将为进一步研究甲萘醌和甲萘醌类似物提供重要策略。

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