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Voltammetric determination of the trace amounts of bromate in drinking water after pre-concentration on hydrous γ-Al2O3

100%
Kościelna H., Ren M.
Open Chemistry
|
2004
|
vol. 2
|
issue 3
491-499
EN
A differential pulse voltammetric (DPV) method for the determination of bromate in drinking water, after pre-concentration on γ-Al2O3, is proposed. The reduction peak of bromate has been observed at the potential Ep-−1.6 V in an ammonia buffer as a supporting electrolyte. The method has been successfully applied to determine a bromate concentration of 2.5 μg·l−1 in drinking water (RSD=6.1%, n=7). A sample pre-treatment with a column filled with mixed cation-exchange resin in Ag, Ba and H forms was needed before pre-concentration of bromate on alumina.
2
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Method validation in quantitative electrochemical analysis of colchicine using glassy carbon electrode

88%
Bodoki E., Săndulescu R., Roman L.
Open Chemistry
|
2007
|
vol. 5
|
issue 3
766-778
EN
A cathodic differential pulse voltammetric determination of colchicine was validated using a glassy carbon electrode in HClO4/H3PO4 0.01 M. Colchicine gives an irreversible, diffusion-controlled peak at −862 mV vs. Ag/AgCl reference electrode. The cathodic peak is strongly influenced by a more alkaline environment with a shift towards more negative potentials. Method optimization was carried out in parallel for three types of electrodes (glassy carbon, mercury film and bismuth film coated glassy carbon). The cathodic peak current is higher using film-coated electrodes, but shows poorer intra-day reproducibility and a longer analysis time due to film renewal. Thus, a bare glassy carbon electrode was used to determine colchicine in the concentration range of 2.4 − 50 μg mL−1 (R 2 = 0.9998, n = 5), with a calculated detection limit of 0.80 μg mL−1. The proposed method was characterized according to ICH Harmonized Tripartite Guidance Q2(R1) by validation parameters (selectivity, linearity, accuracy, fidelity, limit of detection, limit of quantification) and it was successfully applied for the determination of colchicine from tablets, without the interference of the excipients. The method’s performances were evaluated and compared with both a known polarographic method and the official quantitative spectrophotometric determination from the Romanian Pharmacopoeia, Xth edition, respectively. [...]
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