S. Cardabroch et al., CHROMATOGRAPHIC DETERMINATION OF DIURETICS IN URINE SAMPLES USING HYBRID MICELLAR MOBILE PHASES WITH FLUOROMETRIC DETECTION, Analytica chimica acta, 375(1-2), 1998, pp. 143-154
A rapid and simple chromatographic procedure, that uses hybrid micella
r mobile phases of sodium dodecyl sulphate (SDS), propanol and phospha
te buffer at pH 3, and fluorimetric detection (lambda(exc)=270nm, lamb
da(em)=430nm), is reported for the determination of mixtures of seven
diuretics of diverse efficacy (amiloride, bendroflumethiazide, bumetan
ide, furosemide, hydroflumethiazide, piretanide and triamterene), in u
rine samples. The application of a sequential optimization procedure f
or the resolution of the mixtures of the diuretics was problematic. Ho
wever, their separation was achieved through the use of an interpretiv
e optimization procedure based on the accurate description of the rete
ntion. The optimum mobile phase contained 0.055 M SDS-8% propanol. The
limits of detection (ng/ml) and inter-day reproducibilities (%) in th
e urine samples were: amiloride (9.7, 5.7), bendroflumethiazide (10, 8
.8), bumetanide (1.4, 3.6), hydroflumethiazide (7.1, 5.6), piretanide
(54, 4.1), and triamterene (1.7, 1.4). Detection of urinary excretion
of the diuretics was possible at least up to 24-72 h after their inges
tion. Injection of furosemide standards originated four chromatographi
c peaks, which corresponded to the drug and diverse impurities. (C) 19
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