4.6 Article

Determination of vitamin D metabolites in various biological samples through an improved chemical derivatization assisted liquid chromatography-tandem mass spectrometry approach

Journal

ANALYTICAL METHODS
Volume 15, Issue 44, Pages 6009-6014

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ay01769a

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A chemical derivatization assisted LC-MS/MS method was developed for the detection and quantification of vitamin D metabolites. The method significantly increased the sensitivities of the metabolites and allowed for accurate quantification in various biological samples. This method provides a promising tool for studying vitamin D metabolism.
Vitamin D (VD) metabolites are involved in a variety of important metabolic processes and physiological effects in organisms. Profiling of VD metabolites favors a deep understanding of the physiological role of VD. However, VD metabolites are difficult to detect due to their high chemical structural rigidity, structural similarity, and low sensitivities under liquid chromatography-tandem mass spectrometry (LC-MS). Herein, we present a chemical derivatization assisted LC-MS/MS strategy for the detection of VDs, in which 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) is employed to derivatize the conjugated diene of VD metabolites and provides sensitizing reporters for MS detection. After PTAD derivatization, the sensitivities of seven VD metabolites increased by 24-276 folds, with the limits of detection ranging from 3 to 20 pg mL-1. Using this method, we achieved a sensitive and accurate quantification of 7 VD metabolites (vitamin D2, vitamin D3, 25-hydroxyvitamin D2, 25-hydroxyvitamin D3, 1,25-dihydroxyvitamin D2, 1,25-dihydroxyvitamin D3, and 1,24,25-trihydroxyvitamin D3) of the VD metabolic pathway in different trace biological samples, including human serum, mouse tissues (namely liver, kidney, lung, and spleen), and cells. We believe that the present method can provide a promising tool for an in-depth analysis of VD metabolism. A PTAD derivatization assisted LC-MS/MS method for the simultaneous determination of seven vitamin D metabolites was established, enabling the quantification of the vitamin D metabolism pathway in various biological samples.

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