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HPLC determination of Vitamin D(3) and its metabolite in human plasma with on-line sample cleanup
Authors:Brunetto M R  Obando M A  Gallignani M  Alarcón O M  Nieto E  Salinas R  Burguera J L  Burguera M
Institution:

a IVAIQUIM, Venezuelan Andean Institute for Chemical Research, Faculty of Sciences, Los Andes University, Ipostel La Hechicera, P.O. Box 3, Mérida 5101-A, Venezuela

b Metabolic Bone Research Group, Faculty of Medicine, Los Andes University, Mérida 5101-A, Venezuela

Abstract:A HPLC method with automated column switching and UV-diode array detection is described for the simultaneous determination of Vitamin D3 and 25-hydroxyvitamin D3 (25-OH-D3) in a sample of human plasma. The system uses a BioTrap precolumn for the on-line sample cleanup. A sample of 1 ml of human plasma was treated with 2 ml of a mixture of ethanol–acetonitrile (2:1 (v/v)). Following centrifugation, the supernatant was evaporated to dryness under a stream of dry and pure nitrogen. The residue was reconstituted in 250 μL of a solution of methanol 5 mmol l?1 phosphate buffer, pH 6.5 (4:1 (v/v)), and a 200 μl aliquot of this solution was injected onto the BioTrap precolumn. After washing during 5 min with a mobile phase constituted by a solution of 6% acetonitrile in 5 mmol l?1 phosphate buffer, pH 6.5 (extraction mobile phase), the retained analytes were then transferred to the analytical column in the backflush mode. The analytical separation was then performed by reverse-phase chromatography in the gradient elution mode with the solvents A and B (Solvent A: acetonitrile–phosphate buffer 5 mmol l?1, pH 6.5; 20:80 (v/v); solvent B: methanol–acetonitrile–tetrahydrofuran, 65:20:15 (v/v)). The compounds of interest were detected at 265 nm. The method was linear in the range 3.0–32.0 ng ml?1 with a limit of quantification of 3.0 ng ml?1. Quantitative recoveries from spiked plasma samples were between 91.0 and 98.0%. In all cases, the coefficient of variation (CV) of the intra-day and inter-day-assay precision was ≤2.80%. The proposed method permitted the simultaneous determination of Vitamin D3 and 25-OH-D3 in 16 min, with an adequate precision and sensitivity. However, the overlap of the sample cleanup step with the analysis increases the sampling frequency to five samples h?1. The method was successfully applied for the determination of Vitamin D3 and 25-OH-D3 in plasma from 46 female volunteers, ranging from 50 to 94 years old. Vitamin D3 and 25-OH-D3 concentrations in plasma were found from 4.30–40.70 ng ml?1 (19.74 ± 9.48 ng ml?1) and 3.1–36.52 ng ml?1 (7.13 ± 7.80 ng ml?1), respectively. These results were in good agreement with data published by other authors.
Keywords:Vitamin D3  25-OH-D3  Plasma samples  HPLC  Solid-phase extraction  Column switching  On-line sample cleanup
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