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通过一种基于新型半胱胺衍生化的超高效液相色谱-串联质谱法对血浆和尿液中的甲萘醌进行定量分析。

Quantification of menadione from plasma and urine by a novel cysteamine-derivatization based UPLC-MS/MS method.

作者信息

Yuan Teng-Fei, Wang Shao-Ting, Li Yan

机构信息

Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.

Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Sep 15;1063:107-111. doi: 10.1016/j.jchromb.2017.08.026. Epub 2017 Aug 24.

Abstract

Menadione, as the crucial component of vitamin Ks, possessed significant nutritional and clinical values. However, there was still lack of favourable quantification strategies for it to date. For improvement, a novel cysteamine derivatization based UPLC-MS/MS method was presented in this work. The derivatizating reaction was proved non-toxic, easy-handling and high-efficient, which realized the MS detection of menadione under positive mode. Benefitting from the excellent sensitivity of the derivatizating product as well as the introduction of the stable isotope dilution technique, the quantification could be achieved in the range of 0.05-50.0ng/mL for plasma and urine matrixes with satisfied accuracy and precision. After analysis of the samples from healthy volunteers after oral administration of menadione sodium bisulfite tablets, the urinary free menadione was quantified for the very first time. We believe the progress in this work could largely promote the exploration of the metabolic mechanism of vitamin K in vivo.

摘要

甲萘醌作为维生素K的关键成分,具有重要的营养和临床价值。然而,迄今为止仍缺乏对其良好的定量策略。为了改进这一情况,本研究提出了一种基于半胱胺衍生化的新型超高效液相色谱-串联质谱(UPLC-MS/MS)方法。该衍生化反应无毒、易于操作且高效,实现了甲萘醌在正模式下的质谱检测。受益于衍生化产物的出色灵敏度以及稳定同位素稀释技术的引入,对于血浆和尿液基质,在0.05-50.0ng/mL范围内可实现定量,准确度和精密度令人满意。在对健康志愿者口服亚硫酸氢钠甲萘醌片后的样品进行分析后,首次对尿中游离甲萘醌进行了定量。我们相信这项工作的进展能够极大地推动体内维生素K代谢机制的探索。

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