F. Traore et al., DETERMINATION OF MALONALDEHYDE BY COUPLED HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY SPECTROFLUOROMETRY AFTER DERIVATIZATION WITH LUMINARIN-3, Journal of chromatography, 648(1), 1993, pp. 111-118
A high-performance liquid chromatographic method with fluorescence det
ection is described for the specific determination of free malonaldehy
de (MDA). Malonaldehyde was labelled with luminarin 3 in acetate buffe
r (pH 4.0) at room temperature in the dark. An aliquot of the reaction
mixture was injected on to an octadecyl-bonded column using acetonitr
ile-imidazole buffer (30:70, v/v) as the mobile phase. The eluate was
monitored with a fluorescence detector at 395 nm (excitation) and 500
nm (emission). A linear calibration graph was established between 7.2
and 90 ng/ml of MDA and the limit of quantification (LOQ) was lower th
an 7 ng/ml of MDA. The precision was characterized by R.S.D.s of 11% a
t 7.2 ng/ml and 2% at 90 ng/ml. The structure of the derivative was co
nfirmed as the 5-hydroxy-2-pyrazoline form. UV absorbance and correcte
d fluorescence spectral data and quantum yields of the luminarin 3 der
ivative of malonaldehyde are presented.