Publications by authors named "Sergei Alekseev"

In the present manuscript, we highlight the contradictions in the thermally activated processes theory which treats a system's activated state as a state of the phonon subsystem. We offer an alternative model, in which the activated state is treated as an electron subsystem state. The mechanism of the activated state formation is as follows: thermal fluctuations excite electrons of some particles within the activation zone.

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Background: Biodiversity conservation is an important goal of most ecosystem management efforts. Therefore, proper monitoring of biodiversity requires constant attention. Coleoptera should be monitored as an essential part of the overall biodiversity.

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Carbon dots (CDs) are easy-obtained nanoparticles with wide range of biological activity; however, their toxicity after prolonged exposure is poorly investigated. So, in vitro and in vivo toxicity of CDs with the surfaces enriched with hydroxylated hydrocarbon chains and methylene groups (CD_GE), carboxyl and phenol groups accompanied with nitrogen (CD_3011), trifluoromethyl (CDF19) or toluidine and aniline groups (CDN19) were aimed to be discovered. CDs' in vitro toxicity was assessed on A549 cells (real-time cell analysis of impedance, fluorescence microscopy) after 24 h of incubation, and we observed no changes in cell viability and morphology.

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Carbon-based nanomaterials are promising for a wide range of biomedical applications, i.e. drug delivery, therapy, and imaging including photoacoustic tomography, where they can serve as contrast agents, biocompatibility and biodistribution of which should be assessed before clinical setting.

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X-ray photoelectron spectroscopy (XPS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) were employed to study the isothermal decomposition of MnCO under ultrahigh vacuum and N environmental conditions, respectively. High-resolution core-level XP spectra, X-ray-induced Auger spectra, and infrared spectra were obtained as a function of annealing time. In XPS studies, the time-dependent thermal decomposition characteristics were elucidated by analyzing surface composition, chemical shifts, satellites in the Mn 2p and Mn LMV bands, and Auger parameters for Mn and O.

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Cytotoxicity of fluorescent carbon fluoroxide (CFO) nanoparticles (NPs) was studied in a label-free manner on several cancer and non-cancer cell lines. A direct cytotoxic effect of the CFO NPs was clearly observed by a suppression of cell proliferation. The real-time measurement of cell activities allowed to quantify the impact of the uptaken NPs on cell proliferation and after washout of the NPs from the cell culture medium.

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Hydrogen generation rate is one of the most important parameters which must be considered for the development of engineering solutions in the field of hydrogen energy applications. In this paper, the kinetics of hydrogen generation from oxidation of hydrogenated porous silicon nanopowders in water are analyzed in detail. The splitting of the Si-H bonds of the nanopowders and water molecules during the oxidation reaction results in powerful hydrogen generation.

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Nanocrystallite-liquid phase transitions are studied for 1-octadecene confined in the pores of chemically functionalized silica gels. These silica gels possess similar fractal geometries of the pore system but differ in chemical termination of the surface, specific surface area (F) and pore volume (V). Linear dependencies of the melting temperature and specific melting heat on the F/V ratio are found for a series of silica gels with identical surface termination.

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Article Synopsis
  • Researchers studied the chemical transformations of 3C-SiC nanoparticles using FTIR, XPS, and temperature-programmed desorption mass spectrometry methods.
  • Thermal oxidation created a hydroxylated SiO surface layer and allowed for size adjustment of SiC nanoparticles from 17 nm to 9 nm via specific treatments.
  • The modified SiC nanoparticles, with hydroxyl, carboxyl, and amino groups, can form stable aqueous solutions, making them suitable for further chemical functionalization.
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The porous silicon (PS) surface modification diagnostics due to functionalization and water adsorption/desorption processes were provided by the self-action effects of picosecond range pulsed laser radiation at 1064 nm. It was shown that the PS surface functionalization-oxide removal, alkylation, and oxidation-resulted in a refractive nonlinear optical (NLO) response sign turn to self-focusing (Δn>0) versus the self-defocusing (Δn<0) observed in the aged PS. The sensitivity of the proposed technique was revealed to water adsorption/desorption from the chemically oxidized PS interface.

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The m-aminophenylarsonic acid (m-APAA) was immobilized onto the silica gel surface with covalently grafted quaternary ammonium groups via ion exchange. The diazotization of ion-bonded m-APAA resulted in a new solid-phase spectrophotometric reagent for detection of 1-naphtol in environmental water samples. The procedure of solid-phase spectrophotometric analysis is characterized by 20 μg L(-1) limit of detection (LOD) of 1-naphtol, up to 2000 concentration factor, and insensitivity to the presence of natural water components as well as to 30-fold excess of phenol, resorcinol, and catechol.

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Trypsin is often used to detach adhered cell subculture from a substrate. However, the proteolytic activity of trypsin may harm cells by cleaving the cell membrane proteins. The present study shows that cellular uptake of fluorescent nanoparticles is remarkably increased within 24 h after trypsinization.

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A comparative photoluminescence analysis of as-prepared and chemically modified (by alkyl chains -C18H37) silicon and carbon nanoparticles dispersed in low-polar liquids is reported. Influence of the low-polar liquid nature and ambient temperature on photoluminescence of the nanoparticles has been investigated from the point of view of their possible application as thermal nanoprobes.

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The amount of hydrogen present in porous silicon (PS) nanostructures is analyzed in detail. Concentration of atomic hydrogen chemically bound to the specific surface of PS is quantitatively evaluated by means of attenuated total reflection infrared (ATR-IR) spectroscopy and temperature-programmed desorption (TPD) spectroscopy. The concentration values are correlated to the PS nanoscale morphology.

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Previous studies point to the XPC-hHR23B complex as the principal initiator of global genome nucleotide excision repair (NER) pathway, responsible for the repair of UV-induced cyclobutane pyrimidine dimers (CPD) and 6-4 photoproducts (6-4PP) in human cells. However, the UV-damaged DNA binding protein (UV-DDB) has also been proposed as a damage recognition factor involved in repair of UV-photoproducts, especially CPD. Here, we show in human XP-E cells (UV-DDB deficient) that the incision complex formation at UV-induced lesions was severely diminished in locally damaged nuclear spots.

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