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In this work, a screen-printed carbon electrode (SPCE) modified with Vulcan (V) carbon black on Chitosan (Chi), V@Chi, was developed, followed by electropolymerization of pyrrole (PPy), addition of gold (Au) particles and electropolymerization of cysteine (p-L-Cys). The resulting electrode was named L-Cys/PPy/Au/V@Chi/SPCE and applied for theobromine (TB) detection[1]. The stability, reproducibility and sensitivity of the SPCE were evaluated through cycle voltammetry (CV) using 1.0 mmol L-1 Fe(CN)63−/4− in 0.1 mol L-1 KCl. The SPCE was constructed with a conductive layer composed of 70% graphite ink and showed a significant increase in the electroactive area. The FEG-SEM images by revealed a greater complexity of the surface compared to the unmodified electrode. The analytical curve was established with concentrations ranging from 0.01 to 5.0 μmol L-1 at pH 8.0 (E vs. graphite= 1.25 V), resulting in a limit of detection of 0.00235 μmol L-1. During the interference studies, the platform demonstrated high selectivity for TB over eight interferents compounds. In addition, the L-Cys/PPy/Au/V@Chi/SPCE presented TB recovery percentages ranging from 100.87% to 106.25%, when applied in tap water, green tea, and black tea samples. Thus, the electrochemical platform proved to be a reproducible, selective, and low-cost sensor for the TB detection in different complex matrices. The modifications performed on the SPCE increased the sensitivity of the electrode, making it viable for applications in real samples.
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