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.
UPLC-MS/MS method for analysis of sphingosine 1-phosphate in biological samples
Cutignano A;Vella FM;Fontana A
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
