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  • HPLC method for determination of lipoxygenase positional specific products.

HPLC method for determination of lipoxygenase positional specific products.

Journal of pharmaceutical and biomedical analysis (2013-06-26)
Peter Hoffman, Drahomíra Rauová, Lýdia Bezáková, Marek Obložinský, Peter Mikuš
ABSTRACT

Mammalian lipoxygenases (LOXs) play an important role in physiological and pathological processes through the biosynthesis of lipid mediators-leukotrienes, lipoxins and other arachidonic acid derivatives.There are four major families of LOXs that can be analyzed through the production of hydroxyeicosatetraenoic acids (HETEs). No analytical method to detect 5-, 8-, 12- and 15-HETE in one run has been published to date. The HPLC method combines reversed-phase separative column Nucleosil 120-5 C18 and NP column Zorbax Rx.SIL for identification. This conjunction enables separation of 12-HETE and 15-HETE to the baseline which is essential in 12/15-LOX research and elution of all four HETEs in one run. The method was successfully tested on partially purified LOXs from rat lung cytosol.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Arachidonic acid, >95.0% (GC)
Sigma-Aldrich
Lipoxidase from Glycine max (soybean), Type I-B, lyophilized powder, ≥50,000 units/mg solid
Sigma-Aldrich
Lipoxidase from Glycine max (soybean), Type V, ammonium sulfate suspension, 500,000-1,000,000 units/mg protein
Sigma-Aldrich
Arachidonic acid, from non-animal source, ≥98.5% (GC)