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Liquid Chromatography–Mass Spectrometric Analysis of Lipids Present in Human Meibomian Gland Secretions
Author(s) -
Butovich Igor A.,
Uchiyama Eduardo,
Pascuale Mario A.,
McCulley James P.
Publication year - 2007
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-007-3080-2
Subject(s) - phosphatidic acid , phosphatidylethanolamine , chromatography , chemistry , sphingomyelin , phosphatidylcholine , phospholipid , phosphatidylserine , high performance liquid chromatography , meibomian gland , phosphatidylinositol , lipidomics , wax , biochemistry , cholesterol , medicine , surgery , kinase , membrane , eyelid
The purpose of the study was to qualitatively characterize the major lipid species present in human meibomian gland secretions (MGS) by means of high‐performance liquid chromatography with atmospheric pressure ionization mass spectrometric detection of the analytes (NP HPLC‐MS). Two different NP HPLC‐MS methods have been developed to analyze lipid species that were expected to be present in MGS. The first method was optimized for the analysis of relatively nonpolar lipids [wax esters (WE), di‐ and triacyl glycerols (DAG and TAG), cholesterol (Chl) and its esters (Chl‐E), and ceramides (Cer)], while the second method was designed to separate and detect phospholipids. The major lipid species in MGS were found to be WE, Chl‐E, and TAG. A minor amount of free Chl (less then 0.5% of the Chl‐E fraction) was detected in MGS. No appreciable amounts of DAG and Cer were found in MGS. The second NP HPLC‐MS method, capable of analyzing model mixtures of authentic phospholipids (e.g. phosphatidylglycerol, phosphatidylethanolamine, phosphatidic acid, phosphatidylinositol, phosphatidylserine, phosphatidylcholine, and sphingomyelin) in submicrogram/mL concentrations, showed little or no presence of these species in the MGS samples. These observations suggest that MGS are a major source of the nonpolar lipids of the WE and Chl‐E families for the tear film lipid layer (TFLL), but not of the previously reported phospholipid components of the TFLL.