建立了不补充维生素K个体血清中维生素K1、甲基萘醌-4、甲基萘醌-7和维生素K1-2、3环氧化物的液相色谱-质谱测定方法

A. Meinitzer, D. Enko, S. Zelzer, F. Prüller, N. Alonso, E. Fritz-Petrin, M. Herrmann
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引用次数: 3

摘要

【摘要】目的维生素K及其代谢产物在血液凝固、骨代谢和生长中具有有益作用。然而,在饮食中含有天然维生素K的患者血液中维生素K浓度的测定目前具有挑战性。我们的目标是开发一种具有成本效益和快速的方法来测量维生素K代谢物,具有潜在的应用于临床和研究。方法建立了一种简单的液相色谱-串联质谱(LC-MS/MS)测定人血清中维生素K1、甲基萘醌-4 (MK-4)、甲基萘醌-7 (MK-7)和维生素K1-2、3环氧化物的方法,并在162例碳水化合物吸收不良患者和20例口服phenprocoumon患者中进行了验证。结果在规定的工作范围内(除MK-7为0.04 ~ 6.16 nmol/L外,其余分析物的总精密度为0.06 ~ 9.0 nmol/L), CVs值在4.8 ~ 17.7%之间。在吸收不良队列样本中,除维生素k1 -2,3环氧化物外,获得了所有不同维生素K代谢物的测量值。该代谢物仅在摄入苯丙酚的患者中检测到。该方法的良好性能是通过三个因素的相互作用实现的:在样品制备中使用脂肪酶,使用非典型氟化反相柱,以及对数甲醇梯度。结论本方法可快速、简便、经济地测定四种维生素K代谢物的浓度。它既适用于常规诊所,也适用于研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a liquid chromatography mass spectrometry method for the determination of vitamin K1, menaquinone-4, menaquinone-7 and vitamin K1-2,3 epoxide in serum of individuals without vitamin K supplements
Abstract Objectives Vitamin K and metabolites have a beneficial role in blood coagulation, bone metabolism and growth. However, the determination of vitamin K concentrations in the blood in patients consuming a diet with naturally occurring vitamin K is currently challenging. We aim to develop a cost-effective and rapid method to measure vitamin K metabolites with potential application for clinics and research. Methods We developed a simple liquid chromatography-tandem mass spectrometric (LC-MS/MS) method for the determination of vitamin K1, menaquinone-4 (MK-4), menaquinone-7 (MK-7) and vitamin K1-2,3 epoxide in human serum and validated the method in a study cohort of 162 patients tested for carbohydrate malabsorption and in 20 patients with oral phenprocoumon intake. Results The overall precision (CVs) ranged between 4.8 and 17.7% in the specified working range (0.06–9.0 nmol/L for all analytes except for MK-7 with 0.04–6.16 nmol/L). In the malabsorption cohort samples, measured values were obtained for all different vitamin K metabolites except for vitamin K1-2,3 epoxide. This metabolite could be detected only in patients with phenprocoumon intake. The good performance of the method is especially achieved by the interaction of three factors: the use of lipase in the sample preparation, the use of an atypical fluorinated reversed phase column, and a logarithmic methanol gradient. Conclusions The described method is able to determine the concentration of four vitamin K metabolites in a time-efficient, simple and cost-effective manner. It can be suitable for both routine clinics and research.
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