Pašti, Igor A.

Link to this page

Authority KeyName Variants
orcid::0000-0002-1000-9784
  • Pašti, Igor A. (6)
Projects
Lithium-ion batteries and fuel cells - research and development Studies of enzyme interactions with toxic and pharmacologically active molecules
Physics and Chemistry with Ion Beams Bilateral cooperation program between the Republic of Serbia and the Federal Republic of Germany (project years 2020−2021, project no. 22), DFG
Development and Application of Methods and Materials for Monitoring New Organic Contaminants, Toxic Compounds and Heavy Metals Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200053 (University of Belgrade, Institute for Multidisciplinary Research)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200135 (University of Belgrade, Faculty of Technology and Metallurgy) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200146 (University of Belgrade, Faculty of Physical Chemistry)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200162 (University of Belgrade, Faculty of Physics) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200168 (University of Belgrade, Faculty of Chemistry)
Advanced technologies for monitoring and environmental protection from chemical pollutants and radiation burden Synthesis, processing and characterization of nanostructured materials for application in the field of energy, mechanical engineering, environmental protection and biomedicine
Fabrication and characterization of nano-photonic functional structrues in biomedicine and informatics RatioCAT - Rational Design of Multifunctional Electrode Interfaces for Efficient Electrocatalytic Hydrogen Production
Operational Program Research, Development and Education (European Regional Development Fund, project no. CZ.02.1.01/0.0/0.0/15_003/0000416 of the Ministry of Education, Youth and Sports of the Czech Republic)

Author's Bibliography

Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance

Krstajić Pajić, Mila N.; Dobrota, Ana S.; Mazare, Anca; Đurđić, Slađana; Hwang, Imgon; Skorodumova, Natalia V.; Manojlović, Dragan; Vasilić, Rastko; Pašti, Igor A.; Schmuki, Patrik; Lačnjevac, Uroš

(American Chemical Society, 2023)

TY  - JOUR
AU  - Krstajić Pajić, Mila N.
AU  - Dobrota, Ana S.
AU  - Mazare, Anca
AU  - Đurđić, Slađana
AU  - Hwang, Imgon
AU  - Skorodumova, Natalia V.
AU  - Manojlović, Dragan
AU  - Vasilić, Rastko
AU  - Pašti, Igor A.
AU  - Schmuki, Patrik
AU  - Lačnjevac, Uroš
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6576
AB  - Efficient cathodes for the hydrogen evolution reaction (HER) in acidic water electrolysis rely on the use of expensive platinum group metals (PGMs). However, to achieve economically viable operation, both the content of PGMs must be reduced and their intrinsically strong H adsorption mitigated. Herein, we show that the surface effects of hydrogenated TiO2 nanotube (TNT) arrays can make osmium, a so far less-explored PGM, a highly active HER electrocatalyst. These defect-rich TiO2 nanostructures provide an interactive scaffold for the galvanic deposition of Os particles with modulated adsorption properties. Through systematic investigations, we identify the synthesis conditions (OsCl3 concentration/temperature/reaction time) that yield a progressive improvement in Os deposition rate and mass loading, thereby decreasing the HER overpotential. At the same time, the Os particles deposited by this procedure remain mainly sub-nanometric and entirely cover the inner tube walls. An optimally balanced Os@TNT composite prepared at 3 mM/55 °C/30 min exhibits a record low overpotential (η) of 61 mV at a current density of 100 mA cm-2, a high mass activity of 20.8 A mgOs-1 at 80 mV, and a stable performance in an acidic medium. Density functional theory calculations indicate the existence of strong interactions between the hydrogenated TiO2 surface and small Os clusters, which may weaken the Os-H* binding strength and thus boost the intrinsic HER activity of Os centers. The results presented in this study offer new directions for the fabrication of cost-effective PGM-based catalysts and a better understanding of the synergistic electronic interactions at the PGM|TiO2 interface.
PB  - American Chemical Society
T1  - Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance
EP  - 31469
IS  - 26
SP  - 31459
VL  - 15
DO  - 10.1021/acsami.3c04498
ER  - 
@article{
author = "Krstajić Pajić, Mila N. and Dobrota, Ana S. and Mazare, Anca and Đurđić, Slađana and Hwang, Imgon and Skorodumova, Natalia V. and Manojlović, Dragan and Vasilić, Rastko and Pašti, Igor A. and Schmuki, Patrik and Lačnjevac, Uroš",
year = "2023",
abstract = "Efficient cathodes for the hydrogen evolution reaction (HER) in acidic water electrolysis rely on the use of expensive platinum group metals (PGMs). However, to achieve economically viable operation, both the content of PGMs must be reduced and their intrinsically strong H adsorption mitigated. Herein, we show that the surface effects of hydrogenated TiO2 nanotube (TNT) arrays can make osmium, a so far less-explored PGM, a highly active HER electrocatalyst. These defect-rich TiO2 nanostructures provide an interactive scaffold for the galvanic deposition of Os particles with modulated adsorption properties. Through systematic investigations, we identify the synthesis conditions (OsCl3 concentration/temperature/reaction time) that yield a progressive improvement in Os deposition rate and mass loading, thereby decreasing the HER overpotential. At the same time, the Os particles deposited by this procedure remain mainly sub-nanometric and entirely cover the inner tube walls. An optimally balanced Os@TNT composite prepared at 3 mM/55 °C/30 min exhibits a record low overpotential (η) of 61 mV at a current density of 100 mA cm-2, a high mass activity of 20.8 A mgOs-1 at 80 mV, and a stable performance in an acidic medium. Density functional theory calculations indicate the existence of strong interactions between the hydrogenated TiO2 surface and small Os clusters, which may weaken the Os-H* binding strength and thus boost the intrinsic HER activity of Os centers. The results presented in this study offer new directions for the fabrication of cost-effective PGM-based catalysts and a better understanding of the synergistic electronic interactions at the PGM|TiO2 interface.",
publisher = "American Chemical Society",
title = "Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance",
pages = "31469-31459",
number = "26",
volume = "15",
doi = "10.1021/acsami.3c04498"
}
Krstajić Pajić, M. N., Dobrota, A. S., Mazare, A., Đurđić, S., Hwang, I., Skorodumova, N. V., Manojlović, D., Vasilić, R., Pašti, I. A., Schmuki, P.,& Lačnjevac, U.. (2023). Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance. 
American Chemical Society., 15(26), 31459-31469.
https://doi.org/10.1021/acsami.3c04498
Krstajić Pajić MN, Dobrota AS, Mazare A, Đurđić S, Hwang I, Skorodumova NV, Manojlović D, Vasilić R, Pašti IA, Schmuki P, Lačnjevac U. Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance. 2023;15(26):31459-31469.
doi:10.1021/acsami.3c04498 .
Krstajić Pajić, Mila N., Dobrota, Ana S., Mazare, Anca, Đurđić, Slađana, Hwang, Imgon, Skorodumova, Natalia V., Manojlović, Dragan, Vasilić, Rastko, Pašti, Igor A., Schmuki, Patrik, Lačnjevac, Uroš, "Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance", 15, no. 26 (2023):31459-31469,
https://doi.org/10.1021/acsami.3c04498 . .
2
2

Composition, structure and potential energy application of nitrogen doped carbon cryogels

Kalijadis, Ana; Gavrilov, Nemanja M.; Jokić, Bojan M.; Gilić, Martina; Krstić, Aleksandar D.; Pašti, Igor A.; Babić, Biljana M.

(2020)

TY  - JOUR
AU  - Kalijadis, Ana
AU  - Gavrilov, Nemanja M.
AU  - Jokić, Bojan M.
AU  - Gilić, Martina
AU  - Krstić, Aleksandar D.
AU  - Pašti, Igor A.
AU  - Babić, Biljana M.
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5887
AB  - Resorcinol–formaldehyde (RF) cryogels were synthesized by sol–gel polycondensation of resorcinol with formaldehyde and freeze-drying was carried out with t-butanol. Carbon cryogel (CC) was obtained by pyrolyzing RF cryogels in an inert atmosphere to 950 °C. Nitrogen doped CCs (CCN) were synthesized by introducing melamine into RF precursor mixture solution to obtain nitrogen concentration 2, 6 and 10 wt.%. Material was characterized by elemental analysis, nitrogen adsorption– desorption measurements, scanning electron microscopy (SEM), Raman spectroscopy, FT-IR Spectroscopy. Cyclic voltammetry (CV) was used to investigate capacitive and electrocatalytic properties. Conductivity measurement was also performed. Elemental analysis results confirmed presence of nitrogen in CCN samples in the range from 0.45 to 1.15 wt.%. Raman spectroscopy of the samples showed increase of D and G peak integrated intensity ratio (ID/IG) with nitrogen doping suggesting that the structural disorder as well as edge plane density increase, but according to similar ID/IG values for CCN samples, their share is not directly related to the amount of incorporated N. Characterization by nitrogen adsorption showed that overall specific surface and maximum mesopores are achieved in CCN sample with medium nitrogen concentration. Results of cyclic voltammetry experiments demonstrated maximum capacitance for CCN sample with smallest N wt.% indicating that narrow pore size distribution and high specific surface area are dominant factors to achieve good capacitive behavior. The relatively low doping level of nitrogen reached in CCN samples may be the reason for the incomplete reduction of oxygen to hydroxide and furthermore it turned out that presence of N in the structure of CC had a negligible effect on the otherwise relatively high conductivity of CC. © 2019 Elsevier B.V.
T2  - Materials Chemistry and Physics
T1  - Composition, structure and potential energy application of nitrogen doped carbon cryogels
SP  - 122120
VL  - 239
DO  - 10.1016/j.matchemphys.2019.122120
ER  - 
@article{
author = "Kalijadis, Ana and Gavrilov, Nemanja M. and Jokić, Bojan M. and Gilić, Martina and Krstić, Aleksandar D. and Pašti, Igor A. and Babić, Biljana M.",
year = "2020",
abstract = "Resorcinol–formaldehyde (RF) cryogels were synthesized by sol–gel polycondensation of resorcinol with formaldehyde and freeze-drying was carried out with t-butanol. Carbon cryogel (CC) was obtained by pyrolyzing RF cryogels in an inert atmosphere to 950 °C. Nitrogen doped CCs (CCN) were synthesized by introducing melamine into RF precursor mixture solution to obtain nitrogen concentration 2, 6 and 10 wt.%. Material was characterized by elemental analysis, nitrogen adsorption– desorption measurements, scanning electron microscopy (SEM), Raman spectroscopy, FT-IR Spectroscopy. Cyclic voltammetry (CV) was used to investigate capacitive and electrocatalytic properties. Conductivity measurement was also performed. Elemental analysis results confirmed presence of nitrogen in CCN samples in the range from 0.45 to 1.15 wt.%. Raman spectroscopy of the samples showed increase of D and G peak integrated intensity ratio (ID/IG) with nitrogen doping suggesting that the structural disorder as well as edge plane density increase, but according to similar ID/IG values for CCN samples, their share is not directly related to the amount of incorporated N. Characterization by nitrogen adsorption showed that overall specific surface and maximum mesopores are achieved in CCN sample with medium nitrogen concentration. Results of cyclic voltammetry experiments demonstrated maximum capacitance for CCN sample with smallest N wt.% indicating that narrow pore size distribution and high specific surface area are dominant factors to achieve good capacitive behavior. The relatively low doping level of nitrogen reached in CCN samples may be the reason for the incomplete reduction of oxygen to hydroxide and furthermore it turned out that presence of N in the structure of CC had a negligible effect on the otherwise relatively high conductivity of CC. © 2019 Elsevier B.V.",
journal = "Materials Chemistry and Physics",
title = "Composition, structure and potential energy application of nitrogen doped carbon cryogels",
pages = "122120",
volume = "239",
doi = "10.1016/j.matchemphys.2019.122120"
}
Kalijadis, A., Gavrilov, N. M., Jokić, B. M., Gilić, M., Krstić, A. D., Pašti, I. A.,& Babić, B. M.. (2020). Composition, structure and potential energy application of nitrogen doped carbon cryogels. in Materials Chemistry and Physics, 239, 122120.
https://doi.org/10.1016/j.matchemphys.2019.122120
Kalijadis A, Gavrilov NM, Jokić BM, Gilić M, Krstić AD, Pašti IA, Babić BM. Composition, structure and potential energy application of nitrogen doped carbon cryogels. in Materials Chemistry and Physics. 2020;239:122120.
doi:10.1016/j.matchemphys.2019.122120 .
Kalijadis, Ana, Gavrilov, Nemanja M., Jokić, Bojan M., Gilić, Martina, Krstić, Aleksandar D., Pašti, Igor A., Babić, Biljana M., "Composition, structure and potential energy application of nitrogen doped carbon cryogels" in Materials Chemistry and Physics, 239 (2020):122120,
https://doi.org/10.1016/j.matchemphys.2019.122120 . .
8
2
9

Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water

Lazarević-Pašti, Tamara; Pašti, Igor A.; Jokić, Bojan M.; Babić, Biljana M.; Vasić, Vesna M.

(Royal Society of Chemistry, 2016)

TY  - JOUR
AU  - Lazarević-Pašti, Tamara
AU  - Pašti, Igor A.
AU  - Jokić, Bojan M.
AU  - Babić, Biljana M.
AU  - Vasić, Vesna M.
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5828
AB  - Extensive use of organophosphate pesticides (OPs) invokes development of efficient procedures for their removal from the environment. By introducing low levels ( LT 1 at%) of B, N or P into the structure of mesoporous carbons, we have produced a series of materials with different surface chemical composition, textural properties and level of structural disorder. These adsorbents were applied for removal of dimethoate and its oxo-analogue omethoate from aqueous solutions under batch adsorption conditions and by filtration using modified nylon membrane filters. Adsorption capacities up to 164 mg g(-1) were measured, with OPs uptake typically above 80% for dimethoate concentration as high as 5 x 10(-3) mol dm(-3). After the adsorption, neurotoxic effects of OP-containing water samples were significantly reduced or completely removed. The level of structural disorder was identified as a key parameter for efficient removal of dimethoate and omethoate while in the filtration experiments surface area of adsorbents also played an important role. While the presented research appeals to new fundamental studies of OP-carbon surface interactions, it also indicates a possible strategy in designing new efficient adsorbents for OPs removal from water.
PB  - Royal Society of Chemistry
T2  - RSC Advances
T1  - Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water
EP  - 62139
IS  - 67
SP  - 62128
VL  - 6
DO  - 10.1039/c6ra06736k
ER  - 
@article{
author = "Lazarević-Pašti, Tamara and Pašti, Igor A. and Jokić, Bojan M. and Babić, Biljana M. and Vasić, Vesna M.",
year = "2016",
abstract = "Extensive use of organophosphate pesticides (OPs) invokes development of efficient procedures for their removal from the environment. By introducing low levels ( LT 1 at%) of B, N or P into the structure of mesoporous carbons, we have produced a series of materials with different surface chemical composition, textural properties and level of structural disorder. These adsorbents were applied for removal of dimethoate and its oxo-analogue omethoate from aqueous solutions under batch adsorption conditions and by filtration using modified nylon membrane filters. Adsorption capacities up to 164 mg g(-1) were measured, with OPs uptake typically above 80% for dimethoate concentration as high as 5 x 10(-3) mol dm(-3). After the adsorption, neurotoxic effects of OP-containing water samples were significantly reduced or completely removed. The level of structural disorder was identified as a key parameter for efficient removal of dimethoate and omethoate while in the filtration experiments surface area of adsorbents also played an important role. While the presented research appeals to new fundamental studies of OP-carbon surface interactions, it also indicates a possible strategy in designing new efficient adsorbents for OPs removal from water.",
publisher = "Royal Society of Chemistry",
journal = "RSC Advances",
title = "Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water",
pages = "62139-62128",
number = "67",
volume = "6",
doi = "10.1039/c6ra06736k"
}
Lazarević-Pašti, T., Pašti, I. A., Jokić, B. M., Babić, B. M.,& Vasić, V. M.. (2016). Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water. in RSC Advances
Royal Society of Chemistry., 6(67), 62128-62139.
https://doi.org/10.1039/c6ra06736k
Lazarević-Pašti T, Pašti IA, Jokić BM, Babić BM, Vasić VM. Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water. in RSC Advances. 2016;6(67):62128-62139.
doi:10.1039/c6ra06736k .
Lazarević-Pašti, Tamara, Pašti, Igor A., Jokić, Bojan M., Babić, Biljana M., Vasić, Vesna M., "Heteroatom-doped mesoporous carbons as efficient adsorbents for removal of dimethoate and omethoate from water" in RSC Advances, 6, no. 67 (2016):62128-62139,
https://doi.org/10.1039/c6ra06736k . .
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Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media

Stojmenović, Marija; Momčilović, Milan Z.; Gavrilov, Nemanja M.; Pašti, Igor A.; Mentus, Slavko V.; Jokić, Bojan M.; Babić, Biljana M.

(2015)

TY  - JOUR
AU  - Stojmenović, Marija
AU  - Momčilović, Milan Z.
AU  - Gavrilov, Nemanja M.
AU  - Pašti, Igor A.
AU  - Mentus, Slavko V.
AU  - Jokić, Bojan M.
AU  - Babić, Biljana M.
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5776
AB  - Ordered mesoporous carbon, volume-doped up to 3w.% with Pt, Ru and Pt-Ru nanoparticles was synthesized by evaporation-induced self-assembly method, under acidic conditions. The content of incorporated metal was determined by EDX analysis. The X-ray diffractometry confirmed the existence of highly dispersed metallic phases in doped samples. Specific surface area was determined by N-2-physisorption measurements to range between 452 and 545m(2) g(-1). Raman spectroscopy of investigated materials indicated highly disordered carbon structure with crystallite sizes around 1.4 nm. In a form of thin-layer electrode on glassy carbon support, in 0.1M KOH solution, the prepared materials displayed high activity toward oxygen reduction reaction (ORR) in alkaline media, with onset potentials more positive than -0.10 V vs. SCE. The kinetics of O-2 reduction was found to be affected by both the specific surface area and the concentration of metal dopants. The ethanol tolerance of (Pt, Ru)-doped OMCs was found to be higher than that of common Pt/C ORR catalysts. Presented study provides a new route for the synthesis of active and selective ORR catalysts in alkaline media, being competitive with, or superior to, the existing ones in terms of performance and price. (C) 2014 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media
EP  - 139
SP  - 130
VL  - 153
DO  - 10.1016/j.electacta.2014.11.080
ER  - 
@article{
author = "Stojmenović, Marija and Momčilović, Milan Z. and Gavrilov, Nemanja M. and Pašti, Igor A. and Mentus, Slavko V. and Jokić, Bojan M. and Babić, Biljana M.",
year = "2015",
abstract = "Ordered mesoporous carbon, volume-doped up to 3w.% with Pt, Ru and Pt-Ru nanoparticles was synthesized by evaporation-induced self-assembly method, under acidic conditions. The content of incorporated metal was determined by EDX analysis. The X-ray diffractometry confirmed the existence of highly dispersed metallic phases in doped samples. Specific surface area was determined by N-2-physisorption measurements to range between 452 and 545m(2) g(-1). Raman spectroscopy of investigated materials indicated highly disordered carbon structure with crystallite sizes around 1.4 nm. In a form of thin-layer electrode on glassy carbon support, in 0.1M KOH solution, the prepared materials displayed high activity toward oxygen reduction reaction (ORR) in alkaline media, with onset potentials more positive than -0.10 V vs. SCE. The kinetics of O-2 reduction was found to be affected by both the specific surface area and the concentration of metal dopants. The ethanol tolerance of (Pt, Ru)-doped OMCs was found to be higher than that of common Pt/C ORR catalysts. Presented study provides a new route for the synthesis of active and selective ORR catalysts in alkaline media, being competitive with, or superior to, the existing ones in terms of performance and price. (C) 2014 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media",
pages = "139-130",
volume = "153",
doi = "10.1016/j.electacta.2014.11.080"
}
Stojmenović, M., Momčilović, M. Z., Gavrilov, N. M., Pašti, I. A., Mentus, S. V., Jokić, B. M.,& Babić, B. M.. (2015). Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media. in Electrochimica Acta, 153, 130-139.
https://doi.org/10.1016/j.electacta.2014.11.080
Stojmenović M, Momčilović MZ, Gavrilov NM, Pašti IA, Mentus SV, Jokić BM, Babić BM. Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media. in Electrochimica Acta. 2015;153:130-139.
doi:10.1016/j.electacta.2014.11.080 .
Stojmenović, Marija, Momčilović, Milan Z., Gavrilov, Nemanja M., Pašti, Igor A., Mentus, Slavko V., Jokić, Bojan M., Babić, Biljana M., "Incorporation of Pt, Ru and Pt-Ru nanoparticles into ordered mesoporous carbons for efficient oxygen reduction reaction in alkaline media" in Electrochimica Acta, 153 (2015):130-139,
https://doi.org/10.1016/j.electacta.2014.11.080 . .
23
22
23

Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts

Nastasijević, Branislav J.; Lazarević-Pašti, Tamara; Dimitrijević-Branković, Suzana; Pašti, Igor A.; Vujačić, Ana V.; Joksić, Gordana; Vasić, Vesna M.

(Elsevier, Amsterdam, 2012)

TY  - JOUR
AU  - Nastasijević, Branislav J.
AU  - Lazarević-Pašti, Tamara
AU  - Dimitrijević-Branković, Suzana
AU  - Pašti, Igor A.
AU  - Vujačić, Ana V.
AU  - Joksić, Gordana
AU  - Vasić, Vesna M.
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2130
AB  - The aim of this study was to investigate the inhibitory activity of Gentiana lutea extracts on the enzyme myeloperoxidase (MPO), as well as the antioxidant activity of these extracts and their correlation with the total polyphenol content. Extracts were prepared using methanol (100%), water and ethanol aqueous solutions (96, 75, 50 and 25% v/v) as solvents for extraction. Also, isovitexin, amarogentin and gentiopicroside, pharmacologically active constituents of G. lutea were tested as potential inhibitors of MPO. Antioxidant activity of extracts was determined using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging test and also using cyclic voltammetry (CV). Among all extracts, the antioxidant capacity of 50% ethanol aqueous extract was the highest, both when measured using the DPPH test, with IC50 = 20.6 mu g/ml, and when using CV. Also, 50% ethanol extract, showed the best inhibition of MPO activity in comparison with other extracts. In the group of the selected G. lutea constituents, gentiopicroside has proved to be the strongest inhibitor of MPO, with IC50 = 0.8 mu g/ml. Also, the concentration of G. lutea constituents were determined in all extracts, using Ultra Performance Liquid Chromatography (UPLC).
PB  - Elsevier, Amsterdam
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts
EP  - 196
SP  - 191
VL  - 66
DO  - 10.1016/j.jpba.2012.03.052
ER  - 
@article{
author = "Nastasijević, Branislav J. and Lazarević-Pašti, Tamara and Dimitrijević-Branković, Suzana and Pašti, Igor A. and Vujačić, Ana V. and Joksić, Gordana and Vasić, Vesna M.",
year = "2012",
abstract = "The aim of this study was to investigate the inhibitory activity of Gentiana lutea extracts on the enzyme myeloperoxidase (MPO), as well as the antioxidant activity of these extracts and their correlation with the total polyphenol content. Extracts were prepared using methanol (100%), water and ethanol aqueous solutions (96, 75, 50 and 25% v/v) as solvents for extraction. Also, isovitexin, amarogentin and gentiopicroside, pharmacologically active constituents of G. lutea were tested as potential inhibitors of MPO. Antioxidant activity of extracts was determined using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging test and also using cyclic voltammetry (CV). Among all extracts, the antioxidant capacity of 50% ethanol aqueous extract was the highest, both when measured using the DPPH test, with IC50 = 20.6 mu g/ml, and when using CV. Also, 50% ethanol extract, showed the best inhibition of MPO activity in comparison with other extracts. In the group of the selected G. lutea constituents, gentiopicroside has proved to be the strongest inhibitor of MPO, with IC50 = 0.8 mu g/ml. Also, the concentration of G. lutea constituents were determined in all extracts, using Ultra Performance Liquid Chromatography (UPLC).",
publisher = "Elsevier, Amsterdam",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts",
pages = "196-191",
volume = "66",
doi = "10.1016/j.jpba.2012.03.052"
}
Nastasijević, B. J., Lazarević-Pašti, T., Dimitrijević-Branković, S., Pašti, I. A., Vujačić, A. V., Joksić, G.,& Vasić, V. M.. (2012). Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts. in Journal of Pharmaceutical and Biomedical Analysis
Elsevier, Amsterdam., 66, 191-196.
https://doi.org/10.1016/j.jpba.2012.03.052
Nastasijević BJ, Lazarević-Pašti T, Dimitrijević-Branković S, Pašti IA, Vujačić AV, Joksić G, Vasić VM. Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts. in Journal of Pharmaceutical and Biomedical Analysis. 2012;66:191-196.
doi:10.1016/j.jpba.2012.03.052 .
Nastasijević, Branislav J., Lazarević-Pašti, Tamara, Dimitrijević-Branković, Suzana, Pašti, Igor A., Vujačić, Ana V., Joksić, Gordana, Vasić, Vesna M., "Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts" in Journal of Pharmaceutical and Biomedical Analysis, 66 (2012):191-196,
https://doi.org/10.1016/j.jpba.2012.03.052 . .
58
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62

Platinum deposition from hydrogen-ion beam irradiated solid precursor

Jovanović, Zoran M.; Pašti, Igor A.; Kalijadis, Ana; Lausevic, Mila; Mentus, Slavko V.; Laušević, Zoran

(2011)

TY  - JOUR
AU  - Jovanović, Zoran M.
AU  - Pašti, Igor A.
AU  - Kalijadis, Ana
AU  - Lausevic, Mila
AU  - Mentus, Slavko V.
AU  - Laušević, Zoran
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5649
AB  - We report a particular method of Pt/glassy carbon (GC) surface formation, based on a 15 key H(+/-) ion beam irradiation of thin H(2)PtCl(6)xnH(2)O layer placed over the GC surface. Hydrogen-ion beam irradiation provided an excellent adherence of Pt deposit, unlike to any other Pt-deposition method. Furthermore, the morphology and electrochemical activity of GC/Pt catalyst obtained at the fluence of 5 x 10(17) cm(-2) was found to be sensitive to the sign of charge of hydrogen ions. The electrochemical activity of such obtained Pt/GC surface toward oxygen reduction and ethanol oxidation was compared with the activity of the Pt deposits obtained by other more common reduction procedures. (C) 2011 Elsevier B.V. All rights reserved.
T2  - Materials Letters
T1  - Platinum deposition from hydrogen-ion beam irradiated solid precursor
EP  - 2657
IS  - 17-18
SP  - 2655
VL  - 65
DO  - 10.1016/j.matlet.2011.05.015
ER  - 
@article{
author = "Jovanović, Zoran M. and Pašti, Igor A. and Kalijadis, Ana and Lausevic, Mila and Mentus, Slavko V. and Laušević, Zoran",
year = "2011",
abstract = "We report a particular method of Pt/glassy carbon (GC) surface formation, based on a 15 key H(+/-) ion beam irradiation of thin H(2)PtCl(6)xnH(2)O layer placed over the GC surface. Hydrogen-ion beam irradiation provided an excellent adherence of Pt deposit, unlike to any other Pt-deposition method. Furthermore, the morphology and electrochemical activity of GC/Pt catalyst obtained at the fluence of 5 x 10(17) cm(-2) was found to be sensitive to the sign of charge of hydrogen ions. The electrochemical activity of such obtained Pt/GC surface toward oxygen reduction and ethanol oxidation was compared with the activity of the Pt deposits obtained by other more common reduction procedures. (C) 2011 Elsevier B.V. All rights reserved.",
journal = "Materials Letters",
title = "Platinum deposition from hydrogen-ion beam irradiated solid precursor",
pages = "2657-2655",
number = "17-18",
volume = "65",
doi = "10.1016/j.matlet.2011.05.015"
}
Jovanović, Z. M., Pašti, I. A., Kalijadis, A., Lausevic, M., Mentus, S. V.,& Laušević, Z.. (2011). Platinum deposition from hydrogen-ion beam irradiated solid precursor. in Materials Letters, 65(17-18), 2655-2657.
https://doi.org/10.1016/j.matlet.2011.05.015
Jovanović ZM, Pašti IA, Kalijadis A, Lausevic M, Mentus SV, Laušević Z. Platinum deposition from hydrogen-ion beam irradiated solid precursor. in Materials Letters. 2011;65(17-18):2655-2657.
doi:10.1016/j.matlet.2011.05.015 .
Jovanović, Zoran M., Pašti, Igor A., Kalijadis, Ana, Lausevic, Mila, Mentus, Slavko V., Laušević, Zoran, "Platinum deposition from hydrogen-ion beam irradiated solid precursor" in Materials Letters, 65, no. 17-18 (2011):2655-2657,
https://doi.org/10.1016/j.matlet.2011.05.015 . .
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