Feasibility of capillary liquid chromatography/microchip atmospheric pressure photoionization mass spectrometry in analyzing anabolic steroids in urine samples | Zendy

Ahonen Linda L. | Zendy; Haapala Markus | Zendy; Saarela Ville | Zendy; Franssila Sami | Zendy; Kotiaho Tapio | Zendy; Kostiainen Risto | Zendy

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Feasibility of capillary liquid chromatography/microchip atmospheric pressure photoionization mass spectrometry in analyzing anabolic steroids in urine samples

Author(s) -

Ahonen Linda L.,

Haapala Markus,

Saarela Ville,

Franssila Sami,

Kotiaho Tapio,

Kostiainen Risto

Publication year - 2010

Publication title -

rapid communications in mass spectrometry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.528

H-Index - 136

eISSN - 1097-0231

pISSN - 0951-4198

DOI - 10.1002/rcm.4468

Subject(s) - chemistry , chromatography , mass spectrometry , repeatability , tandem mass spectrometry , photoionization , atmospheric pressure , analytical chemistry (journal) , liquid chromatography–mass spectrometry , ionization , ion , organic chemistry , oceanography , geology

We examined the feasibility of capillary liquid chromatography/microchip atmospheric pressure photoionization tandem mass spectrometry (capLC/µAPPI‐MS/MS) for the analysis of anabolic steroids in human urine. The urine samples were pretreated by enzymatic hydrolysis (with β ‐glucuronidase from Helix pomatia ), and the compounds were liquid‐liquid extracted with diethyl ether. After separation the compounds were vaporized by microchip APPI, photoionized by a 10 eV krypton discharge lamp, and detected by selected reaction monitoring. The capLC/µAPPI‐MS/MS method showed good sensitivity with detection limits at the level of 1.0 ng mL −1 , good linearity with correlation coefficients between 0.9954 and 0.9990, and good repeatability with relative standard deviations below 10%. These results demonstrate that microchip APPI combined with capLC/MS/MS provides a new potential method for analyzing non‐polar and neutral compounds in biological samples. Copyright © 2010 John Wiley & Sons, Ltd.

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