Literature DB >> 23561158

A method for determining regioisomer abundances of polyunsaturated triacylglycerols in omega-3 enriched fish oils using reversed-phase liquid chromatography and triple-stage mass spectrometry.

Lisandra Cubero Herrera1, Louis Ramaley, Michael A Potvin, Jeremy E Melanson.   

Abstract

Reversed-phase high performance liquid chromatography (RP-HPLC), followed by post-column addition of lithium salts and electrospray ionisation triple-stage mass spectrometry (ESI-MS(3)) of lithiated TAG adducts, is shown to provide a useful method for the positional analysis of triacylglycerols (TAGs) in fish oils containing eicosapentaenoic (EPA, 20:5) and docosahexaenoic acids (DHA, 22:6). One prominent fragmentation pathway in the ESI-MS(3) of these adduct ions involves the loss of a fatty acid from the sn-1/3 position in the first step followed by the loss of an α,β-unsaturated fatty acid from the sn-2 position in the second. Regioisomeric TAGs of the type ABA and AAB produced abundant product ions - [ABA+Li-RACOOH-R'BCHCHCOOH](+) and [AAB+Li-RACOOH-R'ACHCHCOOH](+) - the relative intensities of which were dependent on the position of acyl substituents. Standard solutions of TAGs containing different ratios of the regioisomeric pairs MME/MEM, PPE/PEP, PPD/PDP, EEP/EPE and DDP/DPD (M=14:0, P=16:0, E=20:5, D=22:6) were analysed by ESI-MS(3) with a quadrupole linear ion trap instrument. Methodology developed on the standards was applied to quantifying the relative isomeric abundances of EPA and DHA in several fish oil samples. DHA was preferentially located at the sn-2 position in both DHA-containing TAGs studied, while EPA was either observed at near equal levels in all positions, or predominantly at the sn-1 and -3 positions in some cases. The analysis protocol allows for quantification of the designated regioisomers in one simple, rapid chromatographic procedure using a single column and has the advantage of specificity over other methods for the positional analysis of TAGs, since it eliminates interferences associated with co-eluting TAGs of the same molecular weight that yield isobaric diacylglycerol-like product ions. Crown
Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23561158     DOI: 10.1016/j.foodchem.2012.12.059

Source DB:  PubMed          Journal:  Food Chem        ISSN: 0308-8146            Impact factor:   7.514


  5 in total

1.  Studying the chemistry of cationized triacylglycerols using electrospray ionization mass spectrometry and density functional theory computations.

Authors:  J Stuart Grossert; Lisandra Cubero Herrera; Louis Ramaley; Jeremy E Melanson
Journal:  J Am Soc Mass Spectrom       Date:  2014-05-28       Impact factor: 3.109

2.  The Simulacrum System as a Construct for Mass Spectrometry of Triacylglycerols and Others.

Authors:  William Craig Byrdwell
Journal:  Lipids       Date:  2015-12-11       Impact factor: 1.880

3.  Characterization of Positional Distribution of Fatty Acids and Triacylglycerol Molecular Compositions of Marine Fish Oils Rich in Omega-3 Polyunsaturated Fatty Acids.

Authors:  Huijun Zhang; Hui Zhao; Youwei Zhang; Yingbin Shen; Hang Su; Jun Jin; Qingzhe Jin; Xingguo Wang
Journal:  Biomed Res Int       Date:  2018-07-10       Impact factor: 3.411

4.  Comparison of the Fatty Acid and Triglyceride Profiles of Big Eye Tuna (Thunnus obesus), Atlantic salmon (Salmo salar) and Bighead Carp (Aristichthysnobilis) Heads.

Authors:  Jing Zhang; Ningping Tao; Yueliang Zhao; Xichang Wang; Mingfu Wang
Journal:  Molecules       Date:  2019-11-04       Impact factor: 4.411

5.  Bovine Milk Triacylglycerol Regioisomer Ratio Shows Remarkable Inter-Breed and Inter-Cow Variation.

Authors:  Zhiqian Liu; Simone Rochfort
Journal:  Molecules       Date:  2021-06-28       Impact factor: 4.411

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.