Fluorimetric determination of sulphaguanidine and sulphamethoxazole by host-guest complexation in beta-cyclodextrin and partial least squares calibration.

The host-guest inclusion complexes of sulphamethoxazole (SMTX) and sulphaguanidine (SGN) with beta-cyclodextrin, in aqueous solutions, have been investigated. A 1:1 stoichiometry of the complexes was established, the association constants were calculated by different methods, and the influence of several chemical variables on the complexation processes were established. According to the results obtained, a spectrofluorimetric method for the determination of these sulphonamides has been proposed. The individual and binary mixtures of both sulphonamides have been determined in human urine samples, at representative therapeutic ranges, by application of a first-order multivariate calibration partial least squares (PLS-1) model. The calibration set was designed with 9 samples, containing different concentrations of the two sulphonamides, and 8 blank urine samples, with the aim of modelling the variability of the background. The concentration ranges for the sulphonamides were up to 0.5 microg mL(-1) for SMTX and 1.0 microg mL(-1) for SGN. Figures of merit as selectivity, analytical sensitivity and limit of detection (LOD) were also calculated. The proposed procedure was validated by comparing the obtained results with a HPLC method, with satisfactory results for the assayed method.

Determination of fluoroquinolones in urine and serum by using high performance liquid chromatography and multiemission scan fluorimetric detection.

A high performance liquid chromatography (HPLC) method has been developed for the simultaneous determination of four fluoroquinolones. The studied compounds have been enoxacin (ENO), norfloxacin (NOR), ofloxacin (OFLO) and enrofloxacin (ENRO). An isocratic elution method, using a mixture of tetrahydrofuran (8%) and phosphate buffer (pH 3.00, 30.0mM, 92%) as mobile phase, has been developed. Fluorimetric detection, exciting at 277nm, and multiemission scan (407nm for ENO, 444nm for both NOR and ENRO and 490nm for OFLO) has been used. Detection limits of 500, 14.7, 25.2 and 15.0ngmL(-1) for ENO, NOR, OFLO and ENRO, respectively, have been obtained. The proposed method has been satisfactorily applied to analyze NOR, OFLO and ENRO in human urine and serum samples.

Monitoring of phenylurea and propanil herbicides in river water by solid-phase-extraction high performance liquid chromatography with photoinduced-fluorimetric detection.

The separation and determination of five herbicides, including propanil and the phenylureas diuron, isoproturon, linuron and neburon, has been performed by an HPLC method, using photochemically-induced fluorescence detection. The non-fluorescent herbicides were transformed into fluorescent compounds by post-column photochemical reaction. A 60:40 (v/v) acetonitrile-buffer solution of potassium phosphate dibasic (pH 7, 0.01 M) was used for the chromatographic elution to separate propanil, linuron and neburon. The overlapping of isoproturon and diuron peaks, in the selected conditions, was resolved by changing the initial movil phase composition to 50:50 (v/v) methanol-buffer solution of potassium phosphate dibasic (pH 7, 0.01 M). The procedure was applied with satisfactory results to the analysis of these herbicides in Guadiana river water samples (Badajoz, Spain), allowing the detection of herbicide residues in the order of mug l(-1), by using a solid-phase extraction (SPE) pre-concentration step.