Electrospray ionization/mass spectrometry compatible reversed-phase separation of phospholipids: piperidine as a post column modifier for negative ion detection

被引:32
作者
Lytle, CA
Gan, YD
White, DC
机构
[1] Univ Tennessee, Ctr Environm Biotechnol, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Environm Sci, Oak Ridge, TN 37983 USA
基金
美国国家科学基金会;
关键词
electrospray ionization; phospholipids; phosphatidylglycerol; phospatidylethanolamine; phosphatidylcholine; high-performance liquid chromatography/electrospray ionization/mass spectrometry;
D O I
10.1016/S0167-7012(00)00156-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An electrospray ionization (ESI) compatible separation of phospholipids (PL), phosphatidylglycerol (PG), phosphatidyl ethanolamine (PE), and phosphatidylcholine (PC), was performed on a C18 column by reversed phase High Performance Liquid Chromatography (HPLC) with minimal ESI suppression. The mobile phase,used isocratically, consisted of methanol and water. ESI was used to efficiently transfer the ions present in solution to the gas phase for mass spectrometric (MS) detection. Formation of negative ions was reinforced by incorporating piperidine post column. Limits of detection (LOD) and limits of quantitation (LOQ) were experimentally determined to be 20 and 60 fmol/mu l, respectively, when acquiring data in the selected ion monitoring (SIM) mode monitoring three ions with a single quadrupole MS. When acquiring data from m/z 110-900 in the scanning mode, the LOD and LOQ were experimentally determined to be 1 pmol/mu l and 3 pmol/mu l. When acquiring product ion spectra for m/z 747, the LOD and LOQ were experimentally determined to be 446 attomol/mu l and 1.3 fmol/mu l, respectively. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:227 / 234
页数:8
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