首页> 外文期刊>Journal of clinical laboratory analysis. >A simple, rapid atmospheric pressure chemical ionization liquid chromatography tandem mass spectrometry method for the determination of 25-hydroxyvitamin D2 and D3
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A simple, rapid atmospheric pressure chemical ionization liquid chromatography tandem mass spectrometry method for the determination of 25-hydroxyvitamin D2 and D3

机译:一种简单快速的常压化学电离液相色谱串联质谱法测定25-羟基维生素D2和D3

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摘要

Vitamin D plays a vital role not only in bone health but also in pathophysiology of many other body functions. In recent years, there has been significant increase in testing of 25-hydroxyvitamin D (25-OH vitamin D), a marker of vitamin D deficiency. The most commonly used methods for the measurement of 25-OH vitamin D are immunoassays and liquid chromatography tandem mass spectrometry (LC-MS-MS). Since immunoassays suffer from inaccuracies and interferences, LC-MS-MS is a preferred method. In LC-MS-MS methods, 25-OH vitamin D is extracted from serum or plasma by solid-phase or liquid-phase extraction. Because these extraction methods are time consuming, we developed an easy method that uses simple protein precipitation followed by injection of the supernatant to LC-MS-MS. Several mass-to-charge (m/z) ratio transitions, including commonly used transitions based on water loss, were evaluated and several tube types were tested. The optimal transitions for 25-OH vitamin D2 and D3 were 395.5 > 269.5 and 383.4 > 257.3, respectively. The reportable range of the method was 1-100 ng/mL, and repeatability (within-run) and within-laboratory imprecision were <4% and <6%, respectively. The method agreed well with the solid-phase extraction methods.
机译:维生素D不仅在骨骼健康中而且在许多其他身体机能的病理生理中都起着至关重要的作用。近年来,对25-羟基维生素D(25-OH维生素D)(维生素D缺乏症的标志)的检测已显着增加。测量25-OH维生素D的最常用方法是免疫测定和液相色谱串联质谱(LC-MS-MS)。由于免疫测定存在误差和干扰,因此LC-MS-MS是首选方法。在LC-MS-MS方法中,通过固相或液相提取从血清或血浆中提取25-OH维生素D。由于这些提取方法耗时,因此我们开发了一种简单的方法,该方法使用简单的蛋白质沉淀,然后将上清液注入LC-MS-MS。评估了几个质荷比(m / z)转换,包括基于失水量的常用转换,并测试了几种管子类型。 25-OH维生素D2和D3的最佳过渡分别为395.5> 269.5和383.4> 257.3。该方法的报告范围为1-100 ng / mL,重复性(运行内)和实验室内不精密度分别为<4%和<6%。该方法与固相萃取方法吻合良好。

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