TY - JOUR
T1 - Facile determination of sphingolipids under alkali condition using metal-free column by LC-MS/MS
AU - Siddabasave, Siddabasave Gowda
AU - Ikeda, Kazutaka
AU - Arita, Makoto
N1 - Funding Information:
Funding information This work was supported by the Japan Society for the Promotion of Science Grants 15H05898, 15H05897, and 15H04648; the Science and Technology Research Promotion Program for Agriculture, Forestry, Fisheries, and Food Industry; the Japan Agency for Medical Research and Development (JP15gm5910001), and the Japan Science and Technology Agency Core Research for Evolutional Science and Technology.
Publisher Copyright:
© 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Extraction and analysis of sphingolipids from biological samples is a critical step in lipidomics, especially for minor species such as sphingoid bases and sphingosine-1-phosphate. Although several liquid chromatography-mass spectrometry methods enabling the determination of sphingolipid molecular species have been reported, they were limited in analytical sensitivity and reproducibility by causing significant peak tailing, especially by the presence of phosphate groups, and most of the extraction techniques are laborious and do not cover a broad range of sphingolipid metabolites. In this study, we developed a rapid single-phase extraction and highly sensitive analytical method for the detection and quantification of sphingolipids (including phosphates) comprehensively using liquid chromatography-triple quadruple mass spectrometry. After validating the reliability of the method, we analyzed the intestinal tissue sphingolipids of germ-free (GF) and specific pathogen-free (SPF) mice and found significantly higher levels of free sphingoid bases and sphingosine-1-phosphate in the GF condition as compared to the SPF condition. This method enables a rapid extraction and highly sensitive determination of sphingolipids comprehensively at low femtomolar ranges. [Figure not available: see fulltext.].
AB - Extraction and analysis of sphingolipids from biological samples is a critical step in lipidomics, especially for minor species such as sphingoid bases and sphingosine-1-phosphate. Although several liquid chromatography-mass spectrometry methods enabling the determination of sphingolipid molecular species have been reported, they were limited in analytical sensitivity and reproducibility by causing significant peak tailing, especially by the presence of phosphate groups, and most of the extraction techniques are laborious and do not cover a broad range of sphingolipid metabolites. In this study, we developed a rapid single-phase extraction and highly sensitive analytical method for the detection and quantification of sphingolipids (including phosphates) comprehensively using liquid chromatography-triple quadruple mass spectrometry. After validating the reliability of the method, we analyzed the intestinal tissue sphingolipids of germ-free (GF) and specific pathogen-free (SPF) mice and found significantly higher levels of free sphingoid bases and sphingosine-1-phosphate in the GF condition as compared to the SPF condition. This method enables a rapid extraction and highly sensitive determination of sphingolipids comprehensively at low femtomolar ranges. [Figure not available: see fulltext.].
KW - Intestine
KW - Liquid chromatography
KW - Mass spectrometry
KW - Phytosphingosine
KW - Single-phase extraction
KW - Sphingosine-1-phosphate
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U2 - 10.1007/s00216-018-1116-5
DO - 10.1007/s00216-018-1116-5
M3 - Article
C2 - 29740670
AN - SCOPUS:85046680755
SN - 1618-2642
VL - 410
SP - 4793
EP - 4803
JO - Analytical and bioanalytical chemistry
JF - Analytical and bioanalytical chemistry
IS - 20
ER -