Vol 78, No 4 (2023)

The review covers the specific features of the structure of flavanones and a critical review of methods for their determination in various samples. The data are summarizes according to the methods of analysis: chromatographic, electrophoretic, spectral, and electrochemical. Analytical possibilities of each group of methods and their advantages and disadvantages are discussed. Special attention is paid to the use of chemically modified electrodes based on carbon nanomaterials, 3D nanoporous metal structures, composites of metal oxides and sulfide nanoparticles or dyes with carbon nanomaterials, and also combinations of modifiers of various types in flavanone voltammetry.

Conditions for the formation of a recognition layer of a piezoelectric immunosensor based on magnetic carbon nanocomposites (MCNCs) under the action of an external magnetic field are studied. The effects of the size and number of magnetic nanoparticles (MNPs) in the composite on the analytical characteristics of the gravimetric immunosensor are revealed. Scanning electron microscopy is used to determine the average sizes of Fe3O4 magnetic nanoparticles synthesized by coprecipitation. It is noted that the minimum weight and stability of the recognition layer were observed for the nanocomposite obtained at a ratio of carbon nanotubes and MNPs with an average diameter of 22 nm equal to 3 : 1. The formation of peptide bonds between the MCNCs and a penicillin G conjugate was established by IR spectrometry. It was shown that the use of magnetic carbon nanocomposites in the formation of a recognition layer makes it possible to significantly simplify the procedure for preparing a piezoelectric sensor for analysis and reduce its duration from 24 to 1.5 h. The range of the determined antibiotic concentrations is 1–450 ng/mL, the limit of detection is 0.5 ng/mL.

The article deals with the development of a method for the determination of diflubenzuron in agricultural products using HPLC with a diode array detector. The samples were extracted with acetonitrile, and then purified by solid-phase extraction using C18E and PSA adsorbents and a Diapak C cartridge. The developed method was tested on the green mass of plants, potato tubers, corn grain, soybeans, sunflower seeds, rapeseed, and vegetable oil in the concentration range from 0.025 to 0.25 mg/kg. The average values of recovery were 81–91% with an error of 1.3–2.3%.