This study reports a new chemical sensor based on ion-imprinted polymer matrix using copper nanoparticles-polyaniline nanocomposite (IIP-Cu-NPs/PANI). This sensor was prepared by electropolymerization using aniline as a functional monomer and nitrate as template onto the copper nanoparticles-modified glassy carbon (GC) electrode surface. Both ion-imprinted (IIP) and nonimprinted (NIP) electrochemical sensor surfaces were evaluated using UV-Visible spectrometry and scanning electron microscopy (SEM). The electrochemical analysis was made via cyclic voltammetry (CV), linear sweep voltammetry (LSV), and impedance spectroscopy (IS). Throughout this study various analytical parameters, such as scan rate, pH value, concentration of monomer and template, and electropolymerization cycles, were optimized. Under the optimum conditions, the peaks current of nitrate was linear to its concentration in the range of 1μM-0.1M with a detection limit of 31μM and 5μM by EIS and LSV. The developed imprinted nitrate sensor was successfully applied for nitrate determination in different real water samples with acceptable recovery rates.

An electrochemical sensor for amoxicillin (AMX) detection based on reduced graphene oxide (RGO), molecular imprinted overoxidized polypyrrole (MIOPPy) modified with gold nanoparticles (AuNPs) is described in this work. The electrochemical behavior of the imprinted and non‐imprinted polymer (NIP) was carried out by cyclic voltammetry (CV) and impedance spectroscopy (IS). The structure and morphology of the prepared MIP sensor were characterized by scanning electron microscopy (SEM), UV‐Visible, Fourier transform infrared spectroscopy (FTIR) and its experimental parameters such as monomer and template concentration, pH buffer solution, incubation time of AMX and AuNPs, scan rate as well as electropolymerization scan cycles were optimized to improve the performance of the sensor. The peak current obtained at the MIP electrode was proportional to the AMX concentration in the range from 10−8 to 10−3 mol L−1 with a detection limit and sensitivity of 1.22 10−6 mol L−1 (Signal to noise ratio=3) and 2.52×10−6 μAmol−1 L, respectively. It was also found that this sensor exhibited reproducibility and excellent selectivity against molecules with similar chemical structures. Besides, the analytical application of the AMX sensor confirms the feasibility of AMX detection in milk and human serum.

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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.

This work was designed to develop an electrochemical sensor based on molecular imprinted polyaniline membranes onto reduced graphene oxide (RGO) and gold nanoparticles (AuNPs) modified glassy carbon (GC) electrode for dapsone (DDS) determination. The prepared RGO/AuNPs/PANI‐MIPs nanocomposite was characterized by Ultra‐Violet‐Visible (UV‐Vis), Fourier transform infrared spectroscopy (FT‐IR) and scanning electronic microscopy (SEM) images. The feature of the imprinted electrode was evaluated by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and impedance spectroscopy (IS). Throughout this study several analytical parameters, such as incubation time, pH value, concentration of monomer/template molecules and electro‐polymerization cycles were investigated. Under the optimized conditions, the experimental results showed best analytical performances for DDS detection with a sensitivity of 0.188 Ω/mol L−1, a linear range from 1.0×10−7 M to 1.0×10−3 M and a detection limit of 6.8×10−7 M. The bioanalytical sensor was applied to the determination of dapsone in real samples with high selectivity and recovery.