To protect consumers from risks related to overexposure to sulfadiazine, total residues of this antibacterial agent in animal-origin foodstuffs not exceed international regulations. To this end, a new electrochemical sensor based on a molecularly imprinted polymer nanocomposite using overoxidized polypyrrole and copper nanoparticles for the detection of sulfadiazine is elaborated. After optimization of the preparation of the electrochemical sensors, their differential pulse voltammetric signal exhibits an excellent stability and reproducibility at 1.05 V, with a large linear range between 10⁻⁹ and 10⁻⁵ mol L⁻¹ and a low detection limit of 3.1 × 10⁻¹⁰ mol L⁻¹. The produced sulfadiazine sensor was successfully tested in real milk samples. The combination of the properties of the electrical conduction of copper nanoparticles with the properties of the preconcentration of the molecularly imprinted overoxidized polypyrrole allows for the highly sensitive detection of sulfadiazine, even in real milk samples. This strategy is new and leads to the lowest detection limit yet achieved, compared to those of the previously published sulfadiazine electrochemical sensors.

The key solution to combat trace metal pollution and keep the environment, ecosystem, animals, and humans safe is earlier and rapid trace metal detection. For all these reasons, we propose in this work the design of a simple electrochemical sensor functionalized with green nanoparticles for electrochemical detection of the fourth most dangerous heavy metal ions namely copper, zinc, lead, and mercury. The green nanoparticles are fabricated by a one-step, consisting of reducing platinum nanoparticles by a natural gum Arabic polymer. To guarantee the success of these nanoparticles' design, the nanoparticles have been characterized by Fourier-transform infrared spectroscopy FTIR, and thermogravimetric TGA techniques. While, for the electrochemical characterization, we have adopted cyclic voltammetry CV and electrochemical impedance spectroscopy EIS to control different steps of surface modification, and the differential pulse anodic stripping DPAS was monitored to follow up the electrochemical detection of different heavy metals. have confirmed the good chemical and physical properties of the elaborated nanoparticles. As, the developed sensor showed a specific electrochemical response toward the heavy metal ions separately, with a lower limit of detection lower LOD than that recommended by the World Health Organization, in order of 9.6 ppb for Cu²⁺, 1.9 ppb for Zn²⁺, 0.9 ppb for Hg²⁺, and 4.2 ppb for Pb²⁺. Impressively, the elaborated sensor has demonstrated also high stability, outstanding sensitivity, and excellent analytical performance. In addition, the elaborated analytical tool has been successfully applied to the determination of various heavy metal ions in real samples, reflecting then its promising prospect in practical application.

Ochratoxin A (OTA) is considered the most toxic member of the ochratoxin group. Herein, a novel label-free electrochemical sensor based on the horseradish peroxidase (HRP) enzyme is developed for OTA detection. The HRP enzyme was covalently immobilized on the working electrode of a planar boron-doped diamond (BDD) electrochemical microcell previously covered with diazonium film and grafted with single-walled carbon nanotubes (SWCNTs). Each surface modification step was evaluated by cyclic voltammetry and scanning electron microscopy. Square wave voltammetry was used for the detection of OTA. The linear working range of the biosensors ranged between 10⁻¹⁴ and 0.1 M, with a limit of detection (LOD) of 10 fM, an RSD equal to 5%, and a sensitivity of 0.8 µA per decade. In addition, the sensor showed good selectivity in the presence of OTA analogs; it was validated in samples such as corn, feed, and wheat. The metrological performance of the present sensor makes it a good alternative for OTA detection.

Study presents a comparative analytical investigation into the green synthesis of monometallic and bimetallic nanoparticles using Punica granatum (pomegranate) extract, aimed at developing high-performance electrochemical sensors for the detection of ciprofloxacin (CIP) as a representative pharmaceutical pollutant. Three nanoparticle systems were successfully synthesized: monometallic Au@NPs and TiO₂@NPs, as well as the bimetallic AuTiO₂@NPs. Their structural and physicochemical characteristics were comprehensively analyzed using UV–Vis spectroscopy, FTIR, SEM, TEM, and XRD techniques. The obtained nanoparticles exhibited predominantly spherical morphologies with average particle sizes of approximately 40 ± 5 nm for Au@NPs, 50 ± 7 nm for TiO₂@NPs, and 60 ± 6 nm for AuTiO₂@NPs. These nanomaterials were subsequently employed to modify electrode surfaces for electrochemical sensing applications. Their analytical performance was evaluated using cyclic voltammetry (CV) and square-wave voltammetry (SWV). The sensors displayed excellent sensitivity, with limits of detection of 0.8 ppb for TiO₂@NPs, 0.8 ppb for Au@NPs, and 0.2 ppb for the AuTiO₂@NP-based sensor. The bimetallic platform demonstrated superior electrochemical behavior, enhanced signal intensity, and strong selectivity, achieving recovery rates of 98% in tap water and 103% in wastewater. Overall, the results confirm the effectiveness of green-synthesized bimetallic nanoparticles as efficient, low-cost materials for environmental monitoring of emerging pharmaceutical contaminants.