GCE/poly-4,4′-bBT/tyrosinase biosensor for epinephrine was constructed. Comparison of differential pulse voltammetry (DPV) and chronoamperometry was performed. DPV showed more reproducible results giving high selectivity, sensitivity, stability.

The study of neurotransmitters and stress hormones allows the determination of indicators of the current stress load in the body. These species also create a proper strategy of stress protection. Nowadays, stress is a general factor that affects the population, and it may cause a wide range of serious disorders. Abnormalities in the level of neurohormones, caused by chronic psychological stress, can occur in, for instance, corporate employees, health care workers, shift workers, policemen, or firefighters. Here we present a new nanomaterials-based sensors technology development for the determination of neurohormones. We focus on fluorescent sensors/biosensors that utilize nanomaterials, such as quantum dots or carbon nanomaterials. Nanomaterials, owing to their diversity in size and shape, have been attracting increasing attention in sensing or bioimaging. They possess unique properties, such as fluorescent, electronic, or photoluminescent features. In this Review, we summarize new trends in adopting nanomaterials for applications in fluorescent sensors for neurohormone monitoring.

Enzyme-based amperometric biosensors are proving to be important analytical tools in several fields such as food, environmental and, in recent years, the biomedical one. This work describes the use of 4,7-bis(5-(pyridin-2-yl)thiophen-2-yl)benzo [c][1,2,5]thiadiazole (TBT) in the development of a tyrosinase-based biosensor for epinephrine detection. The modifying agent was obtained as a film by electrochemical oxidation of TBT on a gold disk electrode. Electrochemical characterization and scanning electrode microscopy (SEM) images suggest the formation of a conducting film on the electrode surface. Tyrosinase from mushroom was then immobilized by a mixed technique of adsorption and cross-linking. Glutaraldehyde was used as a coupling agent. The obtained device shows a very good linear response (0.1-50 μM) with a LoD value of 0.06 μM and a LoQ of 0.09 μM. Moreover, good selectivity towards some typical interferents (namely, ascorbic acid, tryptophan, uric acid and L-cysteine) and satisfactory recoveries have been observed.

A heteroleptic [Ru(terpy)2]2+ (terpy = 2,2′:6′,2″-terpyridine) complex was electrochemically polymerized to give the corresponding metal-containing conducting polymer on gold and glassy carbon electrodes. The polymerization of the Ru(II) complex was allowed by a terthiophene functionalization on one of the two terpy coordinating fragments, whereas the presence of -COOH substituents on the second terpy ligand enabled the film to immobilize a tyrosinase enzyme by cross-linking with glutaraldehyde. Then, the Ru(terpy) conducting polymer worked as a transducer as well as an immobilizing agent in the design of amperometric biosensors for the determination of epinephrine. The electrochemical behavior of enzymatic sensors containing Ru(terpy)-based conducting polymers was investigated by differential pulse voltammetry and chronoamperometry. Analytical performances and kinetic parameters were calculated, suggesting a potential application of the reported biosensors in the determination of epinephrine in pharmaceutical products.