Phospholipids (PLs), the most important class of polar lipids in foods, are ubiquitouscompounds because they are the major components of animal and plant cell membranes. Their technological and biological properties therefore make them importantin human nutrition. The efficient separation and accurate quantification of PLs canbe achieved with high-performance liquid chromatography–evaporative light scatteringdetection (HPLC-ELSD) because ELSD is a quasi-universal detector for liquid,countercurrent, and supercritical fluid chromatography and can detect any analyte less volatile than the mobile phase. In this article, the principles of ELSD operation(i.e., nebulization of the chromatographic effluent, evaporation of the mobile phase, andmeasurement of the scattered light) as well as the application of LC-ELSD to determinethe amount of PLs in different food matrices are reviewed. Food matrices containingPLs include milk and dairy products, meat, fish, eggs, cereals, and oils. Both the technological aspects and analytical parameters affecting the concentration and quantitativedetermination of PLs in food matrices are evaluated. In particular, different extraction,purification, and chromatographic conditions were extensively investigated; moreover,wherever possible, the results obtained are reported and compared with other detection methods.
Determination of phospholipids in food samples
RESTUCCIA, Donatella;SPIZZIRRI U. G;PUOCI, Francesco;CIRILLO G;PICCI, Nevio
2012-01-01
Abstract
Phospholipids (PLs), the most important class of polar lipids in foods, are ubiquitouscompounds because they are the major components of animal and plant cell membranes. Their technological and biological properties therefore make them importantin human nutrition. The efficient separation and accurate quantification of PLs canbe achieved with high-performance liquid chromatography–evaporative light scatteringdetection (HPLC-ELSD) because ELSD is a quasi-universal detector for liquid,countercurrent, and supercritical fluid chromatography and can detect any analyte less volatile than the mobile phase. In this article, the principles of ELSD operation(i.e., nebulization of the chromatographic effluent, evaporation of the mobile phase, andmeasurement of the scattered light) as well as the application of LC-ELSD to determinethe amount of PLs in different food matrices are reviewed. Food matrices containingPLs include milk and dairy products, meat, fish, eggs, cereals, and oils. Both the technological aspects and analytical parameters affecting the concentration and quantitativedetermination of PLs in food matrices are evaluated. In particular, different extraction,purification, and chromatographic conditions were extensively investigated; moreover,wherever possible, the results obtained are reported and compared with other detection methods.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.