Back to Search Start Over

Temperature‐programmed capillary high‐performance liquid chromatography with atmospheric pressure chemical ionization mass spectrometry for analysis of fatty acid methyl esters.

Authors :
Vrkoslav, Vladimír
Rumlová, Barbora
Strmeň, Timotej
Cvačka, Josef
Source :
Journal of Separation Science; Jul2020, Vol. 43 Issue 13, p2579-2588, 10p
Publication Year :
2020

Abstract

A new capillary high‐performance liquid chromatography method with atmospheric pressure chemical ionization mass spectrometry was developed for the analysis of fatty acid methyl esters and long‐chain alcohols. The chromatographic separation was achieved using a Zorbax SB‐C18 HPLC column (0.3 × 150 mm, 3.5 μm) with a mobile phase composed of acetonitrile and formic acid and delivered isocratically at a flow rate of 10 μL/min. The column temperature was programmed simply, using a common column oven. Good reproducibility of the temperature profile and retention times were achieved. The temperature programming during the isocratic high‐performance liquid chromatography run had a similar effect as a solvent gradient; it reduced retention times of later eluting analytes and improved their detection limits. Two atmospheric pressure chemical ionization sources of the mass spectrometry detector were compared: an enclosed conventional ion source and an in‐house made ion source with a glass microchip nebulizer. The enclosed source provided better detectability of saturated fatty acid methyl esters and made it possible to determine the double bond positions using acetonitrile‐related adducts, while the open chip‐based source provided better analytical figures of merit for unsaturated fatty acid methyl esters. Temperature‐programmed capillary high‐performance liquid chromatography is a promising method for analyzing neutral lipids in lipidomics and other applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16159306
Volume :
43
Issue :
13
Database :
Complementary Index
Journal :
Journal of Separation Science
Publication Type :
Academic Journal
Accession number :
144406146
Full Text :
https://doi.org/10.1002/jssc.201901235