Determination of selenosugars in crude human urine using high‐performance liquid chromatography/atmospheric pressure chemical ionization tandem mass spectrometry

Abstract The narrow gap between essentiality and toxicity of selenium requires detailed investigations on selenium metabolism in order to find suitable indicators for the selenium status in the human body. Current methods for quantitative selenium speciation in human urine are based on separation by high‐performance liquid chromatography (HPLC) coupled online with elemental mass spectrometry (MS), and the potential of molecular MS detection techniques for the reliable identification and quantification of selenosugars in crude human urine has not been utilized. Now we report the development of an HPLC tandem mass spectrometric (MS/MS) method for the reliable determination in crude human urine of three significant selenium urinary metabolites, collectively termed selenosugars, namely methyl 2‐acetamido‐2‐deoxy‐1‐seleno‐ β ‐D‐galactopyranoside (SeGalNAc), methyl 2‐acetamido‐2‐deoxy‐1‐seleno‐ β ‐D‐glucopyranoside (SeGluNAc) and methyl 2‐amino‐2‐deoxy‐1‐seleno‐ β ‐D‐galactopyranoside (SeGalNH 2 ). Reversed‐phase HPLC, with and without cation‐exchange guard columns, was applied for the separation of the selenosugars, and atmospheric pressure chemical ionization (APCI) and selected reaction monitoring (SRM) were used for selective and sensitive detection. The collision‐induced dissociation behaviour of the selenosugars was studied in detail using APCI triple quadrupole MS/MS and electrospray ion trap MS. The developed method was applied to urine samples collected prior to and after selenium supplementation for the quantification of SeGalNAc using both external calibration and the method of standard additions. Additionally, SeGalNH 2 was detected in urine samples after Se supplementation. Finally, neutral loss scanning was explored as a possible method for the detection of unknown methyl‐selenosugars. Copyright © 2007 John Wiley & Sons, Ltd.