A novel high performance liquid chromatography method is presented for the
separation and identification of intact molecular species of phosphatidylet
hanolamine (PE), After isocratic separation, detection of species can be ac
hieved by measurement of UV absorbance as well as by the quantitative metho
d of light scattering detection. A mathematical relationship exists between
i) the relative retention time of a PE molecular species and ii) the numbe
r of carbon atoms and double bonds in the aliphatic groups of the species.
This relationship can aid in the identification of the species. Furthermore
, the absence of non-volatile components in the solvent allows the use of e
lectrospray mass spectrometry to identify the eluting components and to est
ablish the position of the individual radyl groups at the glycerol backbone
, Using this method, samples of bovine heart PE (rich in plasmalogens) and
rat liver PE (rich in diacyl species) have been analyzed.