Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Igor L. Kanev is active.

Publication


Featured researches published by Igor L. Kanev.


Analytical Chemistry | 2014

Are Reactive Oxygen Species Generated in Electrospray at Low Currents

Igor L. Kanev; Andrei Y. Mikheev; Yuri M. Shlyapnikov; Elena A. Shlyapnikova; Tamara Ya. Morozova; Victor N. Morozov

It was demonstrated that electrospraying (ES) of solvents from a glass capillary proceeds without emission of light provided that the current is kept below a certain critical level (<100 nA at positive potential and <25 nA at negative potential for 96% ethanol; < 40 nA at positive potential for water). Though the onset of corona, as detected by the appearance of light, was always accompanied by a break in the current-voltage slope, such breaks also happened before the onset of corona, so they cannot be used as an adequate indicator of corona ignition. Of four ROS studied (hydrogen peroxide, ozone, hydroxyl radicals, and superoxide anions), only H2O2 and ozone were found to be generated at a current of 150-200 nA in detectable quantities: with a yield of 0.5-1 H2O2 molecules per electron at positive potential and 1.5-3 at negative potential. Despite the low yield of the ROS, jack bean urease was shown to be inactivated when the enzyme solution with a concentration below 20 μg/mL was electrosprayed at a current of 200 nA. Addition of 0.1 mM EDTA totally protected the activity of the electrosprayed urease.


Journal of Physical Chemistry B | 2012

Computer Simulation of Gas-Phase Neutralization of Electrospray-Generated Protein Macroions

Igor L. Kanev; N. K. Balabaev; Anna V. Glyakina; Victor N. Morozov

The process of neutralizing hydrated multicharged gas-phase protein ions with small counterions was simulated using a molecular dynamics (MD) technique. Hen egg white lysozyme (HEWL) molecules with different numbers of positive charges, both dry and solvated by up to 1500 water molecules, were first equilibrated. Simulations revealed that the hydration layer over a highly charged protein surface adapted a spiny structure with water protrusions composed of oriented water dipoles. MD simulations of the neutralization process showed that the impact of a small dehydrated single-charged counterion with a dehydrated HEWL ion bearing eight uncompensated charges resulted in a short local increase in temperature by 600-1000 K, which quickly (in 3-5 ps) dissipated over the whole protein molecule, increasing its average temperature by 20-25 K. When the protein ion was solvated, no drastic local increase in the temperature of the protein atoms was observed, because the impact energy was dissipated among the water molecules near the collision site.


Lung | 2015

Dry Lung as a Physical Model in Studies of Aerosol Deposition.

Victor N. Morozov; Igor L. Kanev

A new physical model was developed to evaluate the deposition of micro- and nanoaerosol particles (NAPs) into the lungs as a function of size and charges. The model was manufactured of a dry, inflated swine lung produced by Nasco company (Fort Atkinson, WI). The dry lung was cut into two lobes and a conductive tube was glued into the bronchial tube. The upper 1–2-mm-thick layer of the lung lobe was removed with a razor blade to expose the alveoli. The lobe was further enclosed into a plastic bag and placed within a metalized plastic box. The probability of aerosol deposition was calculated by comparing the size distribution of NAPs passed through the lung with that of control, where aerosol passed through a box bypassing the lung. Using this new lung model, it was demonstrated that charged NAPs are deposited inside the lung substantially more efficiently than neutral ones. It was also demonstrated that deposition of neutral NAPs well fits prediction of the Multiple-Path Particle Dosimetry (MPPD) model developed by the Applied Research Associates, Inc. (ARA).


Langmuir | 2017

Ballistic Penetration of Highly Charged Nanoaerosol Particles through a Lipid Monolayer

Victor N. Morozov; Yuri M. Shlyapnikov; Igor L. Kanev; Elena A. Shlyapnikova

To be used as a drug, inhaled nanoaerosol particles (NAPs) must first penetrate the lipid layer on top of the lung fluid before they will be able to reach the lung epithelium. We investigated how the penetration of NAPs through a model lipid monolayer (LM) depends upon their charging level and size. It was shown that deposition of NAPs 20-200 nm in diameter and charged to the Rayleigh limit gradually increased the surface tension of a dipalmitoylphosphatidylcholine monolayer (DPPC), indicating a loss of lipid molecules from the monolayer. This phenomenon was reproduced with a variety of NAPs produced from glucose, proteins, and polymers. Transfer of the lipid material into the subphase was documented by direct visualization of lipid nanoparticles in the subphase with atomic force microscopy after deposition of glucose NAPs on a DPPC monolayer, followed by collection of the lipid nanoparticles on a mica surface. Partial restoration of tension upon storage indicates that some of the lipid may return to the monolayer. Experiments with the deposition of highly charged calibrated polystyrene nanoparticles showed that the amount of lipid removed from the surface was roughly proportional to the overall surface area of the deposited NAPs. When the number of charges on the NAPs was reduced from their Rayleigh level of 103-104 units to 1-10 units, no notable changes in monolayer surface tension were observed even with prolonged deposition of such NAPs. It was therefore concluded that only highly charged NAPs of a certain size acquire sufficient speed from their attraction by mirror charges to enable ballistic penetration through a lipid monolayer.


European Journal of Nanomedicine | 2016

Exposure to bleomycin nanoaerosol does not induce fibrosis in mice

Elena A. Shlyapnikova; Igor L. Kanev; Nadezhda N. Novikova; Elena G. Litvinova; Yuri M. Shlyapnikov; Victor N. Morozov

Abstract Bleomycin (BLM), a cytostatic drug widely used in the treatment of cancer, often induces lung fibrosis as a side effect. This phenomenon has been exploited in biomedical studies to create a fibrosis model. Inhalation of BLM nanoaerosol particles (NAPs) was expected to induce severe fibrosis in mice. Instead, inhalation of BLM NAPs for 13 days with a total inhaled dose of ~1 mg/kg did not cause pneumofibrosis in CD-1 mice; only marked pneumonitis with infiltration of macrophages in all parts of the lungs was observed in all eight mice exposed. These changes were notably reversible within 2 weeks of cessation of exposure. Despite the limited number of animals it was confidently concluded that slow administration of BLM in the form of NAPs did not cause fibrosis as the bolus instillation of similar doses does.


Journal of Membrane Science | 2013

Water-soluble filters from ultra-thin polyvinylpirrolidone nanofibers

Andrei Y. Mikheev; Igor L. Kanev; Tamara Ya. Morozova; Victor N. Morozov


Journal of Aerosol Science | 2014

Generation and delivery of nanoaerosols from biological and biologically active substances

Victor N. Morozov; Igor L. Kanev; Andrei Y. Mikheev; Elena A. Shlyapnikova; Yuri M. Shlyapnikov; Maxim P. Nikitin; Petr I. Nikitin; Albert O. Nwabueze; Monique L. van Hoek


European Polymer Journal | 2016

Filtering and optical properties of free standing electrospun nanomats from nylon-4,6

Andrei Y. Mikheev; Yuri M. Shlyapnikov; Igor L. Kanev; Andrei V. Avseenko; Victor N. Morozov


Journal of Nanobiotechnology | 2016

Nanoaerosols reduce required effective dose of liposomal levofloxacin against pulmonary murine Francisella tularensis subsp. novicida infection

Crystal N. Propst; Albert O. Nwabueze; Igor L. Kanev; Rachel E. Pepin; Bradford W. Gutting; Victor N. Morozov; Monique L. van Hoek


Environmental Science & Technology | 2015

Knockdown of Fruit Flies by Imidacloprid Nanoaerosol.

Victor N. Morozov; Igor L. Kanev

Collaboration


Dive into the Igor L. Kanev's collaboration.

Top Co-Authors

Avatar

Victor N. Morozov

Russian Academy of Sciences

View shared research outputs
Top Co-Authors

Avatar

Andrei Y. Mikheev

Russian Academy of Sciences

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Andrei V. Avseenko

Moscow Institute of Physics and Technology

View shared research outputs
Top Co-Authors

Avatar

Anna V. Glyakina

Russian Academy of Sciences

View shared research outputs
Top Co-Authors

Avatar

Maxim P. Nikitin

Moscow Institute of Physics and Technology

View shared research outputs
Researchain Logo
Decentralizing Knowledge