Differential pulse voltammetry and chronoamperometry as analytical tools for epinephrine detection using a tyrosinase-based electrochemical biosensor

The main goal of the presented study was to design a biosensor-based system for epinephrine (EP) detection using a poly-thiophene derivative and tyrosinase as a biorecognition element. We compared two different electroanalytical techniques to select the most prominent technique for analyzing the neurotransmitter. The prepared biosensor system exhibited good parameters; the differential pulse (DPV) technique presented a wide linear range (1-20 mu M and 30-200 mu M), with a low detection limit (0.18 nM and 1.03 nM). In the case of chronoamperometry (CA), a high signal-to-noise ratio and lower reproducibility were observed, causing a less broad linear range (10-200 mu M) and a higher detection limit (125 nM). Therefore, the DPV technique was used for the calculation of sensitivity (0.0011 mu A mM(-1) cm(-2)), stability (49 days), and total surface coverage (4.18 x 10(-12) mol cm(-2)). The biosensor also showed very high selectivity in the presence of common interfering species (i.e. ascorbic acid, uric acid, norepinephrine, dopamine) and was successfully applied for EP determination in a pharmaceutical sample.

Automated summary

The study aims to develop a biosensor-based system for detecting epinephrine using a poly-thiophene derivative and tyrosinase as the recognition element. Comparison of two electroanalytical techniques showed that differential pulse voltammetry (DPV) exhibited a wider linear range and lower detection limit compared to chronoamperometry (CA). The prepared biosensor system demonstrated good parameters and high selectivity for epinephrine detection, making it suitable for pharmaceutical applications.