The influence of organization of LbL films containing a silsesquioxane polymer on the electrochemical response of dopamine

This paper describes the construction, evaluation, and application of an electrochemical sensor for the determination of dopamine (DA) in the presence of ascorbic acid (AA) and uric acid (UA). Satisfactory results were achieved for the simultaneous determination of DA and UA, it was verified that it is possible to detect AA in the presence of DA, but high concentrations of AA interfere in detection of DA. The sensor was constructed using the layer-by-layer (LbL) technique with the modification of the surface of indium tin oxide coated glass (ITO) substrate with nanostructured films comprising a 3-n-propylpyridinium silsesquioxane polymer (SiPy⁺Cl^?) and nickel(II) tetrasulfophthalocyanine (NiTsPc). Using the square wave voltammetry technique (SWV), the LbL modified electrodes produced at different pHs (pH 2 and 8) were used to determine DA in the presence UA, and the electrochemical responses of the electrodes were compared. It was observed that the electrodes with the highest concentration of monomeric species showed the highest current intensity and the lowest peak potential for the DA and UA analytes in analysis of DA and UA, individually and simultaneously, with peak potential separation of 460 mV versus Ag/AgCl. Applying SWV, a linear dynamic range of 10–99 μmol L^?1 and 100–900 μmol L^?1 with detection limit of 16.8 μmol L^?1 and 58.3 μmol L^?1 was obtained for DA and UA, respectively. The method has good selectivity and sensitivity, and it was successfully applied to the simultaneous determination of DA and UA in spiked human urine sample.