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Eicosanoids reversed-phase

Analysis of individual lipid species of a class in the Lipid MAPS protocols was largely developed based on reversed-phase LC-MS. For example, in the protocol for eicosanoid analysis, a C18 column (250 X 2.1 mm) was employed and a specific gradient from mobile phase A (water-acetonitrile-formic acid, 63 37 0.02, v/v/v) to B (acetonitrile-isopropanol, 50 50, v/v) was applied [71]. Individual eicosanoid species were detected by using the MRM approach and quantified in comparison to the relevant internal standard. [Pg.70]

Yue, H., Strauss, K.L, Borenstein, M.R., Barbe, M.F., Rossi, L.J. and Jansen, S.A. (2004) Determination of bioactive eicosanoids in brain tissue by a sensitive reversed-phase liquid chromatographic method with fluorescence detection. J. Chromatogr. B 803, 267-277. Puppolo, M., Varma, D. and Jansen, S.A. (2014) A review of analytical methods for eicosanoids in brain tissue. J. Chromatogr. B 964,50-64. [Pg.242]

Another major asset in the routine purification and analysis of the eicosanoids is high-performance liquid chromatography (HPLC). In particular, reversed-phase HPLC has proven to be extremely effective, especially when combined with radioactive, spectroscopic or immunochemical detection methods.For example, the combination of reversed-phase HPLC with ultraviolet absorbance spectroscopy was instrumental to the discovery of leukotrienes and lipoxins, and it is still widely used to detect these compounds as well as other ultraviolet-absorbing eicosanoids. ... [Pg.83]


See other pages where Eicosanoids reversed-phase is mentioned: [Pg.678]    [Pg.678]    [Pg.147]    [Pg.647]    [Pg.190]    [Pg.234]    [Pg.83]    [Pg.80]   
See also in sourсe #XX -- [ Pg.70 ]




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Eicosanoids

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