首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous quantitation of folates, flavins and B-6 metabolites in human plasma by LC-MS/MS assay: Applications in colorectal cancer
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Simultaneous quantitation of folates, flavins and B-6 metabolites in human plasma by LC-MS/MS assay: Applications in colorectal cancer

机译:通过LC-MS / MS测定同时定量人血浆中人血浆中的叶酸,黄曲生物和B-6代谢物:结直肠癌中的应用

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摘要

An analytical method using electrospray ionization and high- performance liquid chromatography/tandem mass spectrometry (LC/ESI-MS/MS) was developed to quantify the vitamin B metabolites found in the folate one-carbon metabolism, using 50 mu L of human plasma. Analytes in plasma were extracted using protein precipitation after being stabilized in 1% ascorbic acid. The analytes were separated using a Kinetex 2.6 mu m Pentafluorophenyl (2.1 x 30 mm) column utilizing a gradient mobile phase system of 0.1% formic acid in water and 100% acetonitrile in a 13.2 min run. The MS detector run using a positive multiple reaction monitoring with parameters optimized for each analyte's ion pair. The assay was selective and linear for all analytes at defined dynamic ranges. The recoveries were generally above 80% except for the folate metabolites whose recoveries dipped possibly due to the drying process. The inter-day precision (%coefficient of variation) and accuracy (%calculated concentration of the nominal concentrations) for six replicates of all quality control samples were = 14% and within 12.2%, respectively. The lower limit of quantification ranged from 0.2 to 3.9 nM. No significant instability was observed after repeated freezing and thawing or in processed samples.
机译:使用50μL人血浆来制定使用电喷雾电离和高效液相色谱/串联质谱/串联质谱(LC / ESI-MS / MS)的分析方法以量化叶酸单碳代谢中的维生素B代谢物。在1%抗坏血酸稳定后,使用蛋白质沉淀提取血浆中的分析物。利用水在水中的梯度流动相系统和100%乙腈中使用0.1%甲酸的梯度流动相系统,在13.2分钟中使用0.1%甲酸的梯度流动相系统分离分析物。 MS检测器使用正多反应监测运行,对于针对每个分析物的离子对进行优化的参数运行。测定对于定义的动态范围的所有分析物是选择性和线性。除了由于干燥过程中,回收率通常高于80%以上,除了可能是由于干燥过程浸渍的叶酸代谢物。所有质量对照样品的六种重复的日常精度(%变化系数)和精度(名称浓度的%计算的浓度)分别为12.2%。量化的下限范围为0.2至3.9nm。在重复冻结和解冻或在加工样品中没有观察到明显不稳定性。

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