Data di Pubblicazione:
2010
Abstract:
A simple and sensitive liquid chromatography-tandem mass spectrometry (negative ion-electrospray
ionization) methodology to determine sphingosine 1-phosphate (S1P) and sphinganine 1-phosphate
(DH-S1P) in biological samples is described. The method has been validated over the linearity range
of 2-100 ng/ml (r > 0.999) using synthetic C17-sphingosine 1-phosphate (C17-S1P) as an internal standard.
In multiple reaction monitoring analysis (378.2 > 79.2), the lower limit of quantification for S1P
was 5.0 ng/ml but the detection limit for the bioactive lipid was below 5 pg (12 fmol). Chromatographic
separation was achieved on a UPLC BEH Hilic column with a binary mobile phase consisting of 30mM
ammonium acetate (pH 4.0) and acetonitrile/MeOH/30mM ammonium acetate buffer (pH 4.0). The
methodology detected 176.7±54.0 ng/ml of S1P and 81.2±23.3 ng/ml of DH-S1P in human plasma, as
well as 201.0±72.0 ng/ml of S1P and 96.5±20.1 ng/ml of DH-S1P in mice plasma.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Phosphosphingolipid; UPLC column; Tandem mass spectrometry; Multiple reaction monitoring; Electrospray negative mode
Elenco autori:
Vella, FILOMENA MONICA; Fontana, Angelo; Cutignano, Adele
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