Publications by authors named "Yury Zolotov"

Microfluidic paper-based analytical devices (µPADs) represent one of the promising green analytical strategies for low-cost and simple determination of various analytes. The actual task is the development of such devices for quantitation of antioxidants, e.g.

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Optical sensors based on silver triangular nanoplates (AgTNPs) are insufficiently studied as probes for the spectrophotometric determination of biologically active compounds. In the present article, an interaction between label-free AgTNPs and bioflavonoids in the presence of silver(I) ions was assessed to outline the possibilities of AgTNPs as a colorimetric probe for the fast and sensitive determination of bioflavonoids. It is shown that the interaction was accompanied by a bathochromic shift of the local surface plasmon resonance band of nanoparticles and an increase in its intensity.

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A modern level of nanotechnology allows us to create conceptually new test systems for chemical analyses and to develop sensitive and compact sensors for various types of substances. However, at present, there are very few commercially available compact sensors for the determination of toxic and carcinogenic substances, such as organic solvents that are used in some construction materials. This article contains an overview of how 3D photonic crystals are used for the creation of a new test system for nonpolar organic solvents.

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A novel method towards spectrophotometric determination of catecholamines and their metabolites differing in their functional groups has been developed. This method is based on a change in morphology of silver triangular nanoplates upon the action of cateсholamines and their metabolites, which is manifested by the decrease of the nanoparticle local surface plasmon resonance (LSPR) band intensity or its shift to the short-wavelength region of the spectrum. The shift value of the LSPR band or the change of its intensity increases with increasing concentration of catecholamines or their metabolites, which is proposed for their spectrophotometric determination.

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An improved step-by-step colorimetric method for determination of halides has been developed. The method is based on successive selective oxidation of iodide, bromide and chloride into corresponding free halogens, their extraction by airflow and colorimetric detection with different paper test-strips. This procedure can be performed in a single analyzed solution and possesses high selectivity and good sensitivity due to the extraction step.

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The creation of gas chromatography is traditionally associated with the names of Nobel Prize winner Archer Martin and his colleagues Richard Synge and Anthony James. However, sometimes references to their predecessors can be found. An investigation conducted by the authors of this article not only confirmed the reliability of these references; but in fact led to the conclusion that by 1952, which is commonly believed to be the year when gas chromatography was born, many research papers had already been devoted to this method, mainly, in its gas-solid version.

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The article describes a novel approach towards improving selectivity of volatile compounds detection using metal nanoparticles. It is based on combination of sensitive optical detection using convenient nanoparticle-modified paper test strips and dynamic gas extraction improving selectivity to volatile compounds. A simple and inexpensive setup allowing for realization of this combination is described.

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In this paper, we report on a novel type of nanocomposites based on gold nanoparticles (AuNPs) and polyurethane foam (PUF), which represents an ability of AuNP aggregation on solid polymer matrix with the strongly different selectivity in comparison with aggregation of the same AuNPs in solution. This may indicate that a new type of aggregation takes place, which can be called solid-phase aggregation. A systematic study using diffuse reflectance spectroscopy revealed features of the solid-phase aggregation.

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A comparison of the efficiency of sorbents obtained by different methods of non-covalent immobilization of β-diketones on some low-polar matrices with respect to extraction of rare earth elements (REEs) was carried out. It was shown that sorbents containing reagent amounts of 1-8mmol/g can be obtained by sorption of reagents on low-polar matrices from aqueous and aqueous-organic solutions, and the value for the maximum capacity of the sorbent correlates with the specific surface of the matrix. Similar sorbents were also prepared by impregnating the matrix with reagent.

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In this study, a novel magnetic solid-phase extraction (MSPE) sorbent, magnetic hypercrosslinked polystyrene (HCP/Fe3O4), was prepared and used for preconcentration of four sulfonamides (sulfamethoxypyridazine, sulfamethazine, sulfamethoxazole and sulfachloropyridazine) from natural water and milk samples. This material was prepared by sorption of pre-synthesized Fe3O4 nanoparticles (NPs) onto HCP. A number of sorbents with varying Fe3O4NPs content were prepared, and their structural, magnetic and sorption properties were studied.

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A simple screening method for isolation and determination of the total content of some sulfonamides in milk using solid-phase extraction and a color reaction is described. This procedure is based on SPE of sulfonamides on hypercrosslinked polystyrene, elution with acetonitrile and off-line derivatization with p-dimethylaminocinnamaldehyde in acetonitrile followed by spectrophotometric determination. The reaction produces intense violet-red color and can be easily used both for quantitation of sulfonamides using spectrophotometry and for naked-eye semi-quantitative estimation.

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Sulfonamides (SAs) have been the most widely used antimicrobial drugs for more than 70 years, and their residues in foodstuffs and environmental samples pose serious health hazards. For this reason, sensitive and specific methods for the quantification of these compounds in numerous matrices have been developed. This review intends to provide an updated overview of the recent trends over the past five years in sample preparation techniques and methods for detecting SAs.

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A new spectrophotometric method for the determination of neomycin has been developed. The method is based on aggregation of label-free gold nanoparticles leading to change in absorption spectra and color of the solution. Influence of different factors (the concentration of ethylenediaminetetraacetate (EDTA), pH, the concentrations of neomycin and the nanoparticles) on the aggregation and analytical performance of the method was investigated.

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We propose a novel approach for assessment of total antioxidant activity by monitoring kinetics of hydrogen peroxide (H(2)O(2)) scavenging after its injection into liquid sample under study. H(2)O(2) is known to be the strongest oxidant, really presented in human body in contrast to the majority of the model oxidative systems used for evaluation of antioxidant activity. In addition, kinetic approach, being more informative than the commonly used determination of the final product, obviously provides better discrimination of potential antioxidants.

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Naphthalene, biphenyl, acenaphtene, anthracene and pyrene were extracted from water samples using inner walls of polytetrafluoroethylene capillary. Optimum conditions for sorption, desorption and heart-cutting of the analyte zone were found. Combined on-line solid-phase extraction and HPLC method for determination of these compounds was proposed.

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Cellulose films containing entrapped analytical reagents suitable for metal-ion detection are produced by joint dissolution of cellulose and the reagents in ionic liquids then precipitation with water. The conditions of preparation of these test materials have been optimized and their properties have been studied. The film obtained by use of the ionic liquid 1-butyl-3-methylimidazolium chloride and 1-(2-pyridylazo)-2-naphthol has been used for colorimetric determination of divalent zinc, manganese, and nickel with detection limits at the 10(-6) mol L-1 level.

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