Abstract
A precise and specific method for measuring 25-hydroxyvitamin D3 in 1 ml of human serum is described. Extraction with chloroform/methanol followed by chromatography on a 0.5 x 2-cm silica gel column yields a sample that is sufficiently free of extraneous material for high-performance liquid chromatography on a column of microporous silica gel (10 μm average particle diameter). The measurement is not influenced by vitamins D2 or D3, 25-hydroxyvitamin D2, or any of the more hydroxylated metabolites of the vitamin D group. Results by this method correlate well with a competitive protein-binding assay (r = 0.961), but with a negative bias of 6.9 ± 3.3 μg/liter. We measured concentrations of 25-hydroxyvitamin D3 in serum drawn during February from 24 persons who were judged normal by physical examinations. The range was 5.5-23.8 μg/liter (mean, 15.0 ± 5.2 μg/liter). The day-to-day CV for the assay was 5.46%.
Cite
CITATION STYLE
Gilbertson, T. J., & Stryd, R. P. (1977). High-performance liquid chromatographic assay for 25-hydroxyvitamin D3 in serum. Clinical Chemistry, 23(9), 1700–1704. https://doi.org/10.1093/clinchem/23.9.1700
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