期刊
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
卷 187, 期 -, 页码 146-151出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jsbmb.2018.11.012
关键词
Vitamin D; Liquid chromatography/tandem mass spectrometry; Interference; Matrix effect; Metabolite
资金
- National Natural Science Foundation of China [81702060, 81201337]
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)D-2, 24,25(OH)(2)D-3, 250HD(2), and 25OHD(3), while efficiently separating the 3-epi analogs. Samples were prepared by precipitation and liquid liquid extraction. The linearity, precision, accuracy, recovery and matrix effect 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)D-3 and 3-epi 250HD(3), without interference from isomers such as 23,25(OH)(2)D-3 or 1,25(OH)(2)D-2, 1,25(OH)(2)D-3. 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 250HD(3), 25OHD(2), 24,25(OH)(2)D-3, and 24,25(OH)(2)D-2, 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 250HD(3) and 250HD(2), and 0.5 ng/mL for 24,25(OH)(2)D-3 and 24,25(OH)(2)D-2. The relative bias of the LC-MS/MS method compared to the certified results of SRM 972a for 25OHD(3), 25OHD(2) and 24,25(OH)(2)D-3 was -2.21% to 1.01%, 3.38% to 6.73%, and-7.72% to-19%, respectively. The mean SD values for 250HD, 24,25(OH)(2)D and 250HD/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 LCMS/MS method for appropriate retention and separation of vitamin D metabolites and their epi analogs was developed.
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