CHROMATOGRAPHIC DETERMINATION OF DIURETICS IN URINE SAMPLES USING HYBRID MICELLAR MOBILE PHASES WITH FLUOROMETRIC DETECTION

Citation
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
Citations number
20
Categorie Soggetti
Chemistry Analytical
Journal title
ISSN journal
00032670
Volume
375
Issue
1-2
Year of publication
1998
Pages
143 - 154
Database
ISI
SICI code
0003-2670(1998)375:1-2<143:CDODIU>2.0.ZU;2-J
Abstract
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 98 Elsevier Science B.V. All rights reserved.