Maria De Lara Palmeira de Macedo Arguelho

Electrochemical study of hydroxychloroquine and its determination in plaquenil by differential pulse voltammetry

Hydroxychloroquine (HCQ) is a halogenated aminoquinoline that presents wide biological activity, often being used as an antimalarial drug. The electrochemical reduction of HCQ was investigated by cyclic voltammetry and chronoamperometry using glassy carbon electrodes. By cyclic voltammetry, in acid medium, only the cathodic peak was observed. The electrochemical behavior of this peak is dependent on pH and the electrodic process occurs through an E(r)C(i) mechanism. The electron number (1e) consumed in the reduction of HCQ was obtained by chronoamperometry. A method for the electrochemical determination of HCQ in pharmaceutical tablets was developed using differential pulse voltammetry. The detection limit reached was 11.2 microg ml(-1) of HCQ with a relative standard deviation of 0.46%. A spectrophotometric study of HCQ has been also carried out utilizing a band at 343 nm. The obtained detection limit and the relative standard deviation were 0.1 microg ml(-1) and 0.36%, respectively. The electrochemical methods are sufficiently accurate and precise to be applied for HCQ determination, in laboratorial routine, which can be used to determine the drug at low level.

Electroreduction of the antifouling agent TCMTB and its electroanalytical determination in tannery wastewaters

The electrochemical reduction of antifouling agent 2-thiocyanomethylthiobenzothiazole (TCMTB) was investigated by cyclic and pulse differential voltammetry. The irreversible electrode reduction of TCMTB proceeded by ECEC reaction mechanism by two electrons transfer with one irreversible wave. Upon the basis of electrochemical evidence, the electrodic reaction mechanism was suggested to formation of mercaptobenzothiazole (MTB) in solution. Subsequently, a pulse differential method is described for the formation of TCMTB based on this electroreduction. Having been obtained a detection limit of 1.0 x 10(-7)mol L(-1) and recovery to 98% to concentration of 2.0 x 10(-6)mol L(-1). Therefore, the proposed method in this study is practical, sensitive and accurate for the analysis of TCMTB in tannery wastewater samples.

Electrochemical Oxidation and Voltammetric Determination of the Antimalaria Drug Primaquine

Abstract Primaquine, an antimalarial drug, presents a well‐defined oxidation peak around +0.6 V vs SCE at a glassy carbon electrode that can be used for its determination. Calibration graphs were obtained for primaquine in B‐R buffer pH 4.0 from 3.00×10−5 mol L−1 to 1.00×10−2 mol L−1 using linear‐scan voltammetry and 3.00×10−5 mol L−1 to 1.00×10−4 mol L−1 using differential pulse or square‐wave voltammetry. The correspondent detection limits was 9.4 µg mL−1; 4.2 and 1.8 µg mL−1, respectively. All the voltammetric methods were applied with success in direct determination of the primaquine in commercial tablets without separation or extraction procedures.

Evidence of sewage input to inner shelf sediments in the NE coast of Brazil obtained by molecular markers distribution

Coprostanol (5β-cholestan-3β-ol) and other fecal steroids were used as markers to trace the input of sewage to the shelf along the coast of Sergipe and Alagoas States, in NE Brazil. Surface sediment samples in shallow regions (<50 m depth) on the shelf were collected adjacent to four fluvial systems, whose drainage basins exhibit distinct levels of human influence. Highest coprostanol concentrations were observed in the area under influence of the Sergipe River (58.6 ± 74.6 ng g(-)(1); maximum of 184.1 ng g(-)(1)), whereas in the Vaza-Barris (18.9 ± 23.6 ng g(-)(1)) and the Piaui/Real (12.3 ± 6.7 ng g(-)(1)) rivers the levels of coprostanol were near the methods limit of detection. Nearby the São Francisco River, the largest in the NE Brazil, coprostanol was virtually absent. The findings of the present study, supported by coprostanol-based diagnostic ratios, revealed that, when sanitation is lacking in the coastal region, even a small-sized river like the Sergipe River can effectively contribute to the export of sewage-derived organic matter to the inner continental shelf in the studied region.

Evaluation of the physico-chemical properties of chitosan as a potential carrier for rifampicin, using voltammetric and spectrophotometric techniques.

Rifampicin is an antibiotic which, on a carbon paste electrode, shows an oxidation response of 0.492 V (vs. Ag/AgCl) at pH 7.0, due to the electroactivity of the hydroquinone group. Interaction of rifampicin with chitosan is strongly dependent on pH, species concentrations and contact time between the latter. Compared to the carbon paste electrode, electrodes modified with chitosan showed greater sensitivity, with optimum voltammetric profile obtained at pH 8.0. Spectrophotometric measurements indicate that rifampicin is strongly absorbed by chitosan at pH less than the pKa of the pharmaceutical, such behaviour being favourable for the use of chitosan as a carrier for the controlled release of rifampicin in the intestinal tract.

Electrochemical and theoretical evaluation of the interaction between dna and amodiaquine: evidence of the guanine adduct formation

The electrochemical behavior of the interaction of amodiaquine with DNA on a carbon paste electrode was studied using voltametric techniques. In an acid medium, an electroactive adduct is formed when amodiaquine interacts with DNA. The anodic peak is dependent on pH, scan rate and the concentration of the pharmaceutical. Adduct formation is irreversible in nature, and preferentially occurs by interaction of the amodiaquine with the guanine group. Theoretical calculations for optimization of geometry, and DFT analyses and on the electrostatic potential map (EPM), were used in the investigation of adduct formation between amodiaquine and DNA.

Use of Natural Kaolinite Clay as an Adsorbent to Remove PB(II), CD(II), and CU(II) from Aqueous Solution

Natural kaolinite clay collected in the State of Sergipe (northeast Brazil) was used as an adsorbent for the ions Pb2+, Cd2+, and Cu2+ present in aqueous solution. Adsorption equilibrium was reached rapidly, enabling use of a contact time of 30 minutes, and maximum adsorption was achieved at pH 7.0. For all three metal ions, the adsorption data could be fitted using the Langmuir isotherm and the adsorption process obeyed a pseudo-second order kinetic model.