UPLC-MS/MS method for analysis of sphingosine 1-phosphate in biological samples

被引:17
|
作者
Cutignano, Adele [1 ]
Chiuminatto, Ugo [2 ]
Petruzziello, Filomena [1 ]
Vella, Filomena Monica [1 ]
Fontana, Angelo [1 ]
机构
[1] CNR, Inst Biomol Chem, I-80078 Pozzuoli, NA, Italy
[2] AB Sciex, I-20052 Monza, MI, Italy
关键词
Phosphosphingolipid; UPLC column; Tandem mass spectrometry; Multiple reaction monitoring; Electrospray negative mode; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; QUANTITATIVE-ANALYSIS; PLASMA; SPHINGOSINE-1-PHOSPHATE; QUANTIFICATION; SPHINGANINE; PLATELETS;
D O I
10.1016/j.prostaglandins.2010.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 C(17)-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 sepal anon was achieved on a UPLC BEH Hilic column with a binary mobile phase consisting of 30 mM ammonium acetate (pH 4.0) and acetonitrile/MeOH/30 mM ammonium acetate buffer (pH 4 0) The methodology detected 176 7 +/- 540 ng/ml of SIP and 81 2 +/- 233 ng/ml of DH-S1P in human plasma, as well as 2010 +/- 72.0 ng/ml of SIP and 965 +/- 20 1 ng/ml of DH-S1P in mice plasma (C) 2010 Published by Elsevier Inc
引用
收藏
页码:25 / 29
页数:5
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