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A new derivative for oxosteroid analysis by mass spectrometry
Authors:K. Rigdova  Y. Wang  M. Ward  W.J. Griffiths
Affiliation:1. College of Medicine, Swansea University, Singleton Park, Swansea SA2 8PP, UK;2. Proteome Sciences plc, Coveham House, Downside Bridge Road, Cobham, Surrey KT11 3EP, UK
Abstract:Here we report a new method for oxosteroid identification utilizing “tandem mass tag hydrazine” (TMTH) carbonyl-reactive derivatisation reagent. TMTH is a reagent with a chargeable tertiary amino group attached through a linker to a carbonyl-reactive hydrazine group. Thirty oxosteroids were analysed after derivatisation with TMTH by electrospray ionization mass spectrometry (ESI-MS) and were found to give high ion-currents compared to underivatised molecules. ESI-tandem mass spectrometry (MS/MS) analysis of the derivatives yielded characteristic fragmentation patterns with specific mass reporter ions derived from the TMT group. A shotgun ESI-MS method incorporating TMTH derivatisation was applied to a urine sample.
Keywords:API, atmospheric pressure ionization   CID, collision-induced dissociation   ESI, electrospray ionization   GC, gas chromatography   LC, liquid chromatography   MS, mass spectrometry or mass spectrum   MS/MS, tandem mass spectrometry   TMT, tandem mass tag   TMTH, tandem mass tag hydrazine   TOF, time-of-flight   SPE, solid phase extraction
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