Interlaboratory Comparison for the Determination of 24,25-Dihydroxyvitamin D3 in Human Serum Using Liquid Chromatography with Tandem Mass Spectrometry

Author:

Wise Stephen A1,Tai Susan S-C2,Nelson Michael A2,Burdette Carolyn Q2,Camara Johanna E2,Hoofnagle Andrew N3,Laha Thomas J3,Carter Graham D4,Jones Julia4,Williams Emma L4,Barclay Zoe J4,Jones Glenville5,Kaufmann Martin5,Binkley Neil6,Kapoor Amita6,Ziegler Toni6,Cashman Kevin D7,Dowling Kirsten G7,Sempos Christopher T8

Affiliation:

1. National Institute of Standards and Technology, Chemical Sciences Division, Gaithersburg, MD 20899, USA National Institutes of Health, Office of Dietary Supplements, Bethesda, MD 20892

2. National Institute of Standards and Technology, Chemical Sciences Division, Gaithersburg, MD 20899, USA

3. University of Washington, Department of Laboratory Medicine, Seattle, WA 98195-7110, USA

4. Imperial College Healthcare National Health Service Trust, Charing Cross Hospital, Department of Biochemistry, London, UK

5. Queen's University–Kingston, Kingston, ON, Canada

6. University of Wisconsin–Madison, Madison, WI 53706, USA

7. University College Cork, School of Food and Nutritional Sciences, Cork Centre for Vitamin D and Nutrition Research, Cork, Ireland

8. National Institutes of Health, Office of Dietary Supplements, Bethesda, MD 20892, USA

Abstract

Abstract Six laboratories associated with the Vitamin D Standardization Program (VDSP) participated in an interlaboratory comparison of LC with tandem MS (MS/MS) methods for the determination of 24,25-dihydroxyvitamin D3 [24,25(OH)2D3] in human serum. The laboratories analyzed two different serum-based Standard Reference Materials (SRMs) intended for use in the determination of 25-hydroxyvitamin D and 30 samples from the Vitamin D External Quality Assessment Scheme (DEQAS). All laboratorymethods for 24,25(OH)2D3 were based on isotope dilution LC-MS/MS; three of the methods used derivatization of the vitamin D metabolites before LC-MS/MS. Laboratory results were compared to the National Institute of Standards and Technology (NIST) results, which were obtained using their newly developed candidate reference measurement procedure for 24,25(OH)2D3. Laboratory results for the SRM samples varied in comparability to the NIST results, with one laboratory in excellent agreement (−1.6% mean bias), three laboratories at 10–15% mean bias, and the remaining laboratory at 36% mean bias. For the 30 DEQAS samples, the mean bias for the five laboratories ranged from 6 to 15%; however, the SD of the bias ranged from 8 to 29%. As a result of this intercomparison study, one laboratory discovered and corrected a methodcalculation error and another laboratory modified and improved their LC-MS/MS method.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology,Agronomy and Crop Science,Environmental Chemistry,Food Science,Analytical Chemistry

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