Metabolic profiling of major vitamin D metabolites using Diels-Alder derivatization and ultra-performance liquid chromatography-tandem mass spectrometry

被引:151
作者
Aronov, Pavel A. [1 ]
Hall, Laura M.
Dettmer, Katja [3 ]
Stephensen, Charles B.
Hammock, Bruce D. [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
[2] Univ Calif Davis, UC Davis Canc Res Ctr, Davis, CA 95616 USA
[3] Univ Regensburg, Inst Funct Genom, Regensburg, Germany
关键词
1; alpha; 25-dihydroxyvitamin D-3; 25-hydroxyvitamin D-3; 24R; UPLC; LC-MS; metabolic profiling; derivatization;
D O I
10.1007/s00216-008-2095-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biologically active forms of vitamin D are important analytical targets in both research and clinical practice. The current technology is such that each of the vitamin D metabolites is usually analyzed by individual assay. However, current LC-MS technologies allow the simultaneous metabolic profiling of entire biochemical pathways. The impediment to the metabolic profiling of vitamin D metabolites is the low level of 1 alpha,25-dihydroxyvitamin D-3 in human serum (15-60 pg/mL). Here, we demonstrate that liquid-liquid or solid-phase extraction of vitamin D metabolites in combination with Diels-Alder derivatization with the commercially available reagent 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) followed by ultra-performance liquid chromatography (UPLC)-electrospray/tandem mass spectrometry analysis provides rapid and simultaneous quantification of 1 alpha,25-dihydroxyvitamin D-3, 1 alpha,25-dihydroxyvitamin D-2, 24R,25-dihydroxyvitamin D-3, 25-hydroxyvitamin D-3 and 25-hydroxyvitamin D-2 in 0.5 mL human serum at a lower limit of quantification of 25 pg/mL. Precision ranged from 1.6-4.8 % and 5-16 % for 25-hydroxyvitamin D-3 and 1 alpha,25-dihydroxyvitamin D-3, respectively, using solid-phase extraction.
引用
收藏
页码:1917 / 1930
页数:14
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