Simultaneous lipidomic analysis of three families of bioactive lipid mediators leukotrienes, resolvins, protectins and related hydroxy-fatty acids by liquid chromatography/electrospray tandem mass spectrometry.
Publication date
2008Keyword
Hydroxy fatty acidsEicosanoids
Arachidonic Acid
Eicosapentaenoic Acid
Resolvins
Protectin
Docosahexaenoic acid
Polyunsaturated fatty acids (PUFA)
Liquid Chromatograpy Electrospray Ionisation Tandem Mass Spectrometry (LC/ESI-MS/MS)
Lipid mediators
Peer-Reviewed
YesOpen Access status
closedAccess
Metadata
Show full item recordAbstract
Bioactive lipid mediators derived from polyunsaturated fatty acids (PUFA) and exhibit a range of tissue and cell-specific activities in many physiological and pathological processes. Electrospray tandem mass spectrometry coupled to liquid chromatography (LC/ESI-MS/MS) is a sensitive, versatile analytical methodology for the qualitative and quantitative analysis of lipid mediators. Here we present an LC/ESI-MS/MS assay for the simultaneous analysis of twenty mono- and poly-hydroxy fatty acid derivatives of linoleic, arachidonic, eicosapentaenoic and docosahexaenoic acids. The assay was linear over the concentration range 1-100 pg/¿L, whilst the limits of detection and quantitation were 10-20 and 20-50 pg respectively. The recovery of the extraction methodology varied from 76-122% depending on the metabolite. This system is useful for profiling a range of biochemically-related potent mediators including the newly discovered resolvins and protectins, and their precursor hydroxy-eicosapentaenoic and hydroxy-docosahexaenoic acids, and, consequently, advance our understanding of the role of PUFA in health and disease.Version
No full-text in the repositoryCitation
Masoodi, M., Mir, A. A., Petasis, N. A., Serhan, C. N. and Nicolaou, A. (2008). Simultaneous lipidomic analysis of three families of bioactive lipid mediators leukotrienes, resolvins, protectins and related hydroxy-fatty acids by liquid chromatography/electrospray ionisation tandem mass spectrometry. Rapid Communications in Mass Spectrometry, Vol. 22, No 2., pp.75¿83.Link to Version of Record
https://doi.org/10.1002/rcm.3331Type
Articleae974a485f413a2113503eed53cd6c53
https://doi.org/10.1002/rcm.3331