Natalia Tomasovicova

Dr. Natalia Tomasovicova

Institute of Experimental Physics, Slovak Academy of Sciences, Watsonova 47, 040 01 Košice, Slovakia
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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 July 2008 in Physical Review E
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Journal Article
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PKPeter Kopcansky
Peter Kopcansky
NTNatalia Tomasovicova
Natalia Tomasovicova
MKMartina Koneracka
Martina Koneracka
VZVlasta Zavisova
Vlasta Zavisova
MTMilan Timko
Milan Timko
JJJan Jadzyn
Jan Jadzyn
In this work the 4-(trans-4′−n-hexylcyclohexyl)-isothiocyanatobenzene (6CHBT) liquid crystal was doped with differently shaped magnetite nanoparticles. The structural changes were observed by capacitance measurements and showed significant influence of the shape and size of the magnetic particles on the magnetic Fréedericksz transition. For the volume concentration ϕ=2×10−4 of the magnetic particles, the critical magnetic field was established for the pure liquid crystal, and for liquid crystals doped with spherical, chainlike, and rodlike magnetic particles. The influence of the magnetic field depends on the type of anchoring, which is characterized by the density of anchoring energy and by the initial orientation between the liquid crystal molecules and the magnetic moment of the magnetic particles. The experimental results indicated soft anchoring in the case of spherical magnetic particles and rigid anchoring in the case of rodlike and chainlike magnetic particles, with parallel initial orientation between the magnetic moments of the magnetic particles and director.

11 January 2010 in Nanotechnology
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ABAndrea Bellova
Andrea Bellova
EBEva Bystrenova
Eva Bystrenova
MKMartina Koneracka
Martina Koneracka
PKPeter Kopcansky
Peter Kopcansky
FVFrancesco Valle
Francesco Valle
ZGZuzana Gazova
Zuzana Gazova
Peptide amyloid aggregation is a hallmark of several human pathologies termed amyloid diseases. We have investigated the effect of electrostatically stabilized magnetic nanoparticles of Fe(3)O(4) on the amyloid aggregation of lysozyme, as a prototypical amyloidogenic protein. Thioflavin T fluorescence assay and atomic force microscopy were used for monitoring the inhibiting and disassembly activity of magnetic nanoparticles of Fe(3)O(4). We have found that magnetic Fe(3)O(4) nanoparticles are able to interact with lysozyme amyloids in vitro leading to a reduction of the amyloid aggregates, thus promoting depolymerization; the studied nanoparticles also inhibit lysozyme amyloid aggregation. The ability to inhibit lysozyme amyloid formation and promote lysozyme amyloid disassembly exhibit concentration-dependent characteristics with IC50 = 0.65 mg ml(-1) and DC50 = 0.16 mg ml(-1) indicating that nanoparticles interfere with lysozyme aggregation already at stoichiometric concentrations. These features make Fe(3)O(4) nanoparticles of potential interest as therapeutic agents against amyloid diseases and their non-risk exploitation in nanomedicine and nanodiagnostics.

3 January 2013 in Physical Review E
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Journal Article
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NTNatalia Tomasovicova
Natalia Tomasovicova
MTMilan Timko
Milan Timko
ZMZuzana Mitróová
Zuzana Mitróová
MKMartina Koneracka
Martina Koneracka
MRMichal Rajňak
Michal Rajňak
PKPeter Kopcansky
Peter Kopcansky
The response in capacitance to low external magnetic fields (up to 0.1 T) of suspensions of spherical magnetic nanoparticles, single-wall carbon nanotubes (SWCNT), SWCNT functionalized with carboxyl group (SWCNT-COOH), and SWCNT functionalized with Fe3O4 nanoparticles in a nematic liquid crystal has been studied experimentally. The volume concentration of nanoparticles was $\phi${}1=10$-${}4 and $\phi${}2=10$-${}3. Independent of the type and the volume concentration of the nanoparticles, a linear response to low magnetic fields (far below the magnetic Fr\'eederiksz transition threshold) has been observed, which is not present in the undoped nematic.

1 May 2009 in Journal of Magnetism and Magnetic Materials
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MTMilan Timko
Milan Timko
ADAnezka Dzarova
Anezka Dzarova
JKJozef Kovac
Jozef Kovac
ASAndrzej Skumiel
Andrzej Skumiel
Arkadiusz JózefczakArkadiusz Józefczak
Arkadiusz Józefczak
NTNatalia Tomasovicova
Natalia Tomasovicova

26 September 2014 in Physical Review E
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MRMichal Rajnak
Michal Rajnak
JKJuraj Kurimský
Juraj Kurimský
Bystrík DolníkBystrík Dolník
Bystrík Dolník
PKPeter Kopcansky
Peter Kopcansky
NTNatalia Tomasovicova
Natalia Tomasovicova
MTMilan Timko
Milan Timko
An experimental study of magnetic colloidal particles cluster formation induced by an external electric field in a ferrofluid based on transformer oil is presented. Using frequency domain isothermal dielectric spectroscopy, we study the influence of a test cell electrode separation distance on a low-frequency relaxation process. We consider the relaxation process to be associated with an electric double layer polarization taking place on the particle surface. It has been found that the relaxation maximum considerably shifts towards lower frequencies when conducting the measurements in the test cells with greater electrode separation distances. As the electric field intensity was always kept at a constant value, we propose that the particle cluster formation induced by the external ac electric field accounts for that phenomenon. The increase in the relaxation time is in accordance with the Schwarz theory of electric double layer polarization. In addition, we analyze the influence of a static electric field generated by dc bias voltage on a similar shift in the relaxation maximum position. The variation of the dc electric field for the hysteresis measurements purpose provides understanding of the development of the particle clusters and their decay. Following our results, we emphasize the utility of dielectric spectroscopy as a simple, complementary method for detection and study of clusters of colloidal particles induced by external electric field.

19 August 2010 in Journal of Applied Crystallography
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Mikhail AvdeevMikhail Avdeev
Mikhail Avdeev
AFArtem V. Feoktystov
Artem V. Feoktystov
PKPeter Kopcansky
Peter Kopcansky
GLGabor Lancz
Gabor Lancz
VGVasil M. Garamus
Vasil M. Garamus
LBLeonid Bulavin
Leonid Bulavin