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Progress of liquid chromatography-mass spectrometry in measurement of vitamin D metabolites and analogues
Authors:Joe M El-Khoury  Edmunds Z Reineks  Sihe Wang
Institution:aDepartment of Clinical Pathology, Cleveland Clinic, Cleveland, OH, USA;bDepartment of Chemistry, Cleveland State University, Cleveland, OH, USA
Abstract:

Objective

Clinical testing for vitamin D nutritional status has experienced tremendous growth in the past several years, driven by research results linking various diseases with low serum 25-hydroxyvitamin D 25(OH)D] levels. Meanwhile, interest in the pathophysiological mechanism elucidation and pharmaceutical applications requires measurement of vitamin D metabolites and analogues. Liquid chromatography-mass spectrometry (LC-MS) has been increasingly utilized in these applications. In this work, our objective was to critically review the progress of LC-MS application in measuring vitamin D metabolites and analogues in biological fluids.

Methods

The LC-MS methods included were selected from those searchable in PubMed up to January 2010.

Results and Conclusion

LC-MS has unique advantages in measuring various vitamin D metabolites and analogues due to its flexibility, sensitivity, and specificity. Despite some controversies over serum 25(OH)D tests, LC-MS will be used for standardizing serum 25(OH)D assays using reference materials available from the National Institute of Standards and Technology.
Keywords:Abbreviations: 25(OH)D  25-hydroxyvitamin D  1  25(OH)2D    25-dihydroxyvitamin D  DBP  Vitamin D binding protein  VDR  Vitamin D receptor  t1/2  half-life time  1OHD  1α-hydroxyvitamin D  24  25(OH)2D  24R  25-dihydroxyvitamin D  OCT  22-oxacalcitriol  ASMS  American Society for Mass Spectrometry  IS  Internal standard  SRM  Standardized reference materials  NIST  National Institute of Standards and Technology  DBS  Dried blood spots  CSF  Cerebrospinal fluid  LLOQ  Lower limit of quantification  SPE  Solid phase extraction  LLE  Liquid-liquid extraction  PPE  Protein precipitation extraction  DMEQTAD  4-[2-(6  7-dimethoxy-4-methyl-3-oxo-3  4-dihydroquinoxalyl)ethyl]-1  2  4-triazoline-3  5-dione  PTAD  4-phenyl-1  2  4-triazoline-3  5-dione  UVB  Ultraviolet B radiation  LC-MS  liquid chromatography-mass spectrometry  LC-SMS  liquid chromatography-single mass spectrometry  LC-TMS  liquid chromatography-tandem mass spectrometry  APCI  atmospheric pressure chemical ionization  ESI  electrospray ionization
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