Separation of lipid classes by solid phase extraction.

A rapid and reliable method for the separation of lipid classes is described using aminopropyl disposable columns. This method is a modification to an existing procedure that allows the separation of both neutral and acidic phospholipid fractions and a high recovery of the latter. Acidic phospholipi...

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Main Authors: HY Kim, N Salem, Jr
Format: Article
Language:English
Published: Elsevier 1990-12-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520421169
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spelling doaj-91c5b0f0c3be44f288c4f7b18e1debd42021-04-25T04:21:52ZengElsevierJournal of Lipid Research0022-22751990-12-01311222852289Separation of lipid classes by solid phase extraction.HY Kim0N Salem, Jr1Section of Analytical Chemistry, LCS, DICBR, NIAAA, Bethesda, MD 20892.Section of Analytical Chemistry, LCS, DICBR, NIAAA, Bethesda, MD 20892.A rapid and reliable method for the separation of lipid classes is described using aminopropyl disposable columns. This method is a modification to an existing procedure that allows the separation of both neutral and acidic phospholipid fractions and a high recovery of the latter. Acidic phospholipids were eluted with a mixture of hexane-2-propanol-ethanol-0.1 M ammonium acetate-formic acid 420:350:100:50:0.5 containing 5% phosphoric acid after neutral phospholipids had been eluted with methanol. It was verified that extremely high recoveries of cholesterol (CH), triglycerides (TG), free fatty acids (FFA), phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylinositol (PI), phosphatidylserine (PS), phosphatidic acid (PA), sphingomyelin (SM), and cerebrosides were obtained with this method. In addition, there appeared to be no preferential losses or degradation of any particular molecular species as the fatty acid distribution of bovine brain PS and the molecular species profile of plant PI were unaltered by the procedure. Depending on the tissue, this method may yield fractions containing pure lipid classes and/or simple mixtures of lipid classes of similar polarity. These fractions may then be more easily separated by thin-layer chromatography or high performance liquid chromatography for a complete lipid class analysis.http://www.sciencedirect.com/science/article/pii/S0022227520421169
collection DOAJ
language English
format Article
sources DOAJ
author HY Kim
N Salem, Jr
spellingShingle HY Kim
N Salem, Jr
Separation of lipid classes by solid phase extraction.
Journal of Lipid Research
author_facet HY Kim
N Salem, Jr
author_sort HY Kim
title Separation of lipid classes by solid phase extraction.
title_short Separation of lipid classes by solid phase extraction.
title_full Separation of lipid classes by solid phase extraction.
title_fullStr Separation of lipid classes by solid phase extraction.
title_full_unstemmed Separation of lipid classes by solid phase extraction.
title_sort separation of lipid classes by solid phase extraction.
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1990-12-01
description A rapid and reliable method for the separation of lipid classes is described using aminopropyl disposable columns. This method is a modification to an existing procedure that allows the separation of both neutral and acidic phospholipid fractions and a high recovery of the latter. Acidic phospholipids were eluted with a mixture of hexane-2-propanol-ethanol-0.1 M ammonium acetate-formic acid 420:350:100:50:0.5 containing 5% phosphoric acid after neutral phospholipids had been eluted with methanol. It was verified that extremely high recoveries of cholesterol (CH), triglycerides (TG), free fatty acids (FFA), phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylinositol (PI), phosphatidylserine (PS), phosphatidic acid (PA), sphingomyelin (SM), and cerebrosides were obtained with this method. In addition, there appeared to be no preferential losses or degradation of any particular molecular species as the fatty acid distribution of bovine brain PS and the molecular species profile of plant PI were unaltered by the procedure. Depending on the tissue, this method may yield fractions containing pure lipid classes and/or simple mixtures of lipid classes of similar polarity. These fractions may then be more easily separated by thin-layer chromatography or high performance liquid chromatography for a complete lipid class analysis.
url http://www.sciencedirect.com/science/article/pii/S0022227520421169
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