A sensitive method for the determination of propylene glycol esters of
fatty acids (PGEs) in foods by HPLC was developed. The PGEs were extr
acted from foods and purified by silica gel column chromatography. The
isolated PGEs were derivatized with 3,5-dinitrobenzoyl chloride and t
he reaction products were dissolved in a mixture of tetrahydrofuran an
d acetonitrile (1:1) for HPLC. A portion of this solution was injected
onto an Inertsil 5C8 column, and eluted with a mixture of acetonitril
e and water (90:10) as the mobile phase. Detection was done with a UV
detector set at 230 nm. PGEs in various foods could be selectively det
ected without interference. Peaks of PGE having fatty acids of C16:0 a
nd C18:0 could be well separated. The recoveries of PGEs added to marg
arine, shortening and cake powder at the level of 0.5% or 1.0% were mo
re than 93%. The detection limits were 10 mu g/g for total PGE. The pr
oposed method for determination of the content and fatty acids composi
tion of PGE in foods is suitable for routine work.