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Identification and Quantification of Flavonoids in Human Urine Samples by Column-Switching Liquid Chromatography Coupled to Atmospheric Pressure Chemical Ionization Mass Spectrometry

机译:柱切换液相色谱-常压化学电离质谱联用技术鉴定和定量人类尿液样品中的类黄酮

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摘要

A rapid and sensitive high-performance liquid chromatographic mass spectrometric (HPLC-MS) method is described for the determination and quantification of 12 dietary flavonoid glycosides and aglycons in human urine samples. Chromatographic separation of the analytes of interest was achieved by column-switching, using the first column (a Zorbax 300SB C-3 column) for sample cleanup and eluting the heart-cut flavonoid fraction onto the second column (a Zorbax SB C-18 column) for separation and detection by ultraviolet and atmospheric pressure chemical ionization MS using single ion monitoring in negative mode. The fragmentor voltage was optimized with regard to maximum abundance of the mollecular ion and qualifier ions of the analytes. Calibration graphs were prepared for urine, and good linearity was achieved over a dynamic range of 205-1000 ng/mL. The inter- and intraassay coefficients of variation for the analysis of the 12 different flavonoids in quality control urine samples were 12.3% on average (range 11.0-13.7%, n = 24, reproducibility) and the repeatability of the assay were 5.0% (mean, range 0.1-14.8%, n = 12). A subset of 10 urine samples from a human dietary intervention study with high and low flavonoid content was analyzed, and the results are reported.
机译:描述了一种快速灵敏的高效液相色谱质谱(HPLC-MS)方法,用于测定和定量人尿液样品中的12种膳食类黄酮苷和糖苷配基。感兴趣的分析物的色谱分离是通过使用第一根色谱柱(Zorbax 300SB C-3色谱柱)进行色谱柱切换以及将心切的类黄酮馏分洗脱到第二根色谱柱(Zorbax SB C-18色谱柱)上实现的)的分离和检测,采用负离子模式的单离子监测,通过紫外和大气压化学电离MS进行检测。关于分析物的分子离子和定性离子的最大丰度,优化了碎裂电压。准备了尿液的校准图,并且在205-1000 ng / mL的动态范围内实现了良好的线性。用于分析质控尿液样品中12种不同类黄酮的测定间和测定内变异系数平均为12.3%(范围11.0-13.7%,n = 24,可重复性),测定的重复性为5.0%(平均值,范围为0.1-14.8%,n = 12)。分析了一项来自人类饮食干预研究的10份尿液样品的子集,这些样品具有高和低的类黄酮含量,并报告了结果。

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