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Rapid liquid chromatography-tandem mass spectrometry method for determination of 24,25(OH) 2 D and 25OHD with efficient separation of 3-epi analogs.
Journal of Steroid Biochemistry and Molecular Biology 2018 November 24
This study establishes and validates a rapid method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) without derivatization steps to simultaneously measure of 24,25(OH)2 D2 , 24,25(OH)2 D3 , 25OHD2 , and 25OHD3 , while efficiently separating the 3-epi analogs. Samples were prepared by precipitation and liquid-liquid extraction. The linearity, precision, accuracy, recovery and matrix of the method were thoroughly evaluated according to the Clinical & Laboratory Standards Institute guidelines. Additionally, the four vitamin D metabolites in the serum of 38 apparently healthy Chinese volunteers were evaluated. The total analysis time was 8.0 min, with efficient separation of 3-epi 24,25(OH)2 D3 and 3-epi 25OHD3 , without interference from isomers such as 23,25(OH)2 D3 or 1,25(OH)2 D2 , 1,25(OH)2 D3 . Good reproducibility was obtained for all four metabolites with within-run coefficient variations (CVs) of 4.07%-6.55%, 4.26%-7.84%, 2.46%-7.21%, and 4.90%-6.87% for 25OHD3 , 25OHD2 , 24,25(OH)2 D3 , and 24,25(OH)2 D2 , respectively, and the total CVs were 4.29%-6.64%, 6.14%-7.84%, 4.33%-7.21%, 5.82%-9.90%, respectively. The limit of quantification was 0.625 ng/mL for 25OHD3 and 25OHD2 , and 0.5 ng/mL for 24,25(OH)2 D3 and 24,25(OH)2 D2 . The relative bias of the LC-MS/MS method compared to the certified results of SRM 972a for 25OHD3 , 25OHD2 and 24,25(OH)2 D3 was -2.21% to 1.01%, 3.38% to 6.73%, and -7.72% to -3.9%, respectively. The mean ± SD values for 25OHD, 24,25(OH)2 D and 25OHD/24,25(OH)2 D in the volunteers were 13.5 ± 4.4 ng/mL(range:7.6-27.5 ng/mL), 0.84 ± 0.42 ng/mL (range:0.26-2.1 ng/mL), and 18 ± 7( range:8-37), respectively. Thus, a simple, precise LC-MS/MS method for appropriate retention and separation of vitamin D metabolites and their epi analogs was developed.
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