Cristiane L. Jost

Simultaneous determination of Al(III) and Fe(III) in post-hemodialysis fluids by spectrophotometry and multivariate calibration

A multivariate calibration model (PLS) was developed for the simultaneous spectrophotometric determination of Al(III) and Fe(III) in post-hemodialysis fluids with pyrocathecol violet (PCV) as chromogenic reagent. The analytes build stable complexes with PCV in presence of hexamine buffered medium at pH 6.1. The complexes show overlapped absorption bands in the spectral range of 220-800nm so that absorptions of 580 wavelengths were necessary for the calibrations. Determinations of Al(III) and Fe(III) were done without masking agents. The best calibration model was obtained by using PLS-1 regression with three components after data mean centering. The spectrophotometric method applied to assay the analytes in real post-hemodialysis samples containing no desferrioxamine B presented good agreement with voltammetric measurements used as reference. Concentrations ranging from 0.20 to 0.60mgL(-1) for Al(III) and for Fe(III) were determined in real samples. The multivariate detection limits for Al(III) and Fe(III) were 0.044 and 0.052mgL(-1), respectively, and the calculated values of sensitivity were 6.33 for Al(III) and 3.44 for Fe(III). The proposed method showed to be straightforward and useful to follow the hemodialysis progress for patients under treatment. Interferents were also investigated.

Voltammetric determination of Se(IV) and Se(VI) in saline samples--studies with seawater, hydrothermal and hemodialysis fluids.

Determination of Se(IV) and Se(VI) in high saline media was investigated by cathodic stripping voltammetry (CSV). The voltammetric method was applied to assay selenium in seawater, hydrothermal and hemodialysis fluids. The influence of ionic strength on selenium determination is discussed. The CSV method was based on the co-electrodeposition of Se(IV) with Cu(II) ions and Se(VI) determined by difference after sample UV-irradiation for photolytic selenium reduction. UV-irradiation was also used as sample pre-treatment for organic matter decomposition. Detection limit of 0.030 microg L(-1) (240 s deposition time) and relative standard deviation (RSD) of 6.19% (n=5) for 5.0 microg L(-1) of Se(IV) were calculated. Linear calibration range for selenium was observed from 1.0 to 100.0 microg L(-1). Concerning the pre-treatment step, best results were obtained by using 60 min UV-irradiation interval in H(2)O(2)/HCl medium. Se(VI) was reduced to the Se(IV) electroactive species with recoveries between 91.7% and 112.9%. Interferents were also investigated.

Sequential voltammetric determination of chromium, thallium, cadmium, lead, copper and antimony in saline hemodialysis concentrates using electrolyte pH gradient

The sequential voltammetric determination of chromium, thallium, cadmium, lead, copper and antimony in dialysate concentrates (DCs), is presented herein. Chromium was quantified by adsorptive cathodic stripping voltammetry and thallium, cadmium, lead, copper and antimony were assayed by anodic stripping voltammetry. The novel method developed to test these samples exploits the effect of electrolyte pH gradient on voltammetric response. The limits of detection (LOD) ranged from 0.03 µg L-1 for cadmium to 0.27 µg L-1 for copper. Recoveries from spiked samples were 92.0-117.5%. This method was applied to the analysis of commercial DCs, where the investigated metals were found in some samples at concentrations between 0.16 µg L-1 for antimony and 140.00 µg L-1 for copper. Interferences and the reference method are discussed

Simultaneous determination of aluminoxamine and ferrioxamine in post-hemodialysis fluids by spectrophotometry and multivariate calibration

A spectrophotometric method for simultaneous determination of Al(III) and Fe(III) using the chelator Desferal® (desferrioxamine B) was developed. Partial least squares (PLS) regression was performed to resolve the overlapped signals obtained from Al(III) and Fe(III) complexes. The parameters controlling behavior of the system were investigated and optimum conditions were selected. PLS was the choice for the analysis of binary mixtures of Fe(III) and Al(III) over the range of 0.1 to 0.8 mg L−1 by using the data of first derivative spectra. Absorbance data were taken between 200 and 600 nm. The calculated sensitivity values for the multivariate method were 4.88 and 5.64 for Al(III) and Fe(III), respectively. Multivariate detection limits were 0.075 and 0.064 mg L−1 for Al(III) and Fe(III), respectively. The method was applied to real post-hemodialysis samples, and sample digestion by UV irradiation was discussed.