Trebše, Polonca

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orcid::0000-0003-4979-1336
  • Trebše, Polonca (7)
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Author's Bibliography

Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles

Malev, Olga; Trebše, Polonca; Piecha, Malgorzata; Novak, Sara; Budic, Bojan; Dramićanin, Miroslav; Drobne, Damjana

(2017)

TY  - JOUR
AU  - Malev, Olga
AU  - Trebše, Polonca
AU  - Piecha, Malgorzata
AU  - Novak, Sara
AU  - Budic, Bojan
AU  - Dramićanin, Miroslav
AU  - Drobne, Damjana
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1474
AB  - Nano-sized cerium dioxide (CeO2) particles are emerging as an environmental issue due to their extensive use in automobile industries as fuel additives. Limited information is available on the potential toxicity of CeO2 nanoparticles (NPs) on terrestrial invertebrates through dietary exposure. In the present study, the toxic effects of CeO2 NPs on the model soil organism Porcellio scaber were evaluated. Nanotoxicity was assessed by monitoring the lipid peroxidation (LP) level and feeding rate after 14-days exposure to food amended with nano CeO2. The exposure concentration of 1000 lg of CeO2 NPs g(-1) dry weight food for 14 days significantly increased both the feeding rate and LP. Thus, this exposure dose is considered the lowest observed effect dose. At higher exposure doses of 2000 and 5000 lg of CeO2 NPs g(-1) dry weight food, NPs significantly decreased the feeding rate and increased the LP level. Comparative studies showed that CeO2 NPs are more biologically potent than TiO2 NPs, ZnO NPs, CuO NPs, CoFe2O4 NPs, and Ag NPs based on feeding rate using the same model organism and experimental setup. Based on comparative metal oxide NPs toxicities, the present results contribute to the knowledge related to the ecotoxicological effects of CeO2 NPs in terrestrial invertebrates exposed through feeding.
T2  - Archives of Environmental Contamination and Toxicology
T1  - Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles
VL  - 72
IS  - 2
SP  - 303
EP  - 311
DO  - 10.1007/s00244-017-0363-3
ER  - 
@article{
author = "Malev, Olga and Trebše, Polonca and Piecha, Malgorzata and Novak, Sara and Budic, Bojan and Dramićanin, Miroslav and Drobne, Damjana",
year = "2017",
abstract = "Nano-sized cerium dioxide (CeO2) particles are emerging as an environmental issue due to their extensive use in automobile industries as fuel additives. Limited information is available on the potential toxicity of CeO2 nanoparticles (NPs) on terrestrial invertebrates through dietary exposure. In the present study, the toxic effects of CeO2 NPs on the model soil organism Porcellio scaber were evaluated. Nanotoxicity was assessed by monitoring the lipid peroxidation (LP) level and feeding rate after 14-days exposure to food amended with nano CeO2. The exposure concentration of 1000 lg of CeO2 NPs g(-1) dry weight food for 14 days significantly increased both the feeding rate and LP. Thus, this exposure dose is considered the lowest observed effect dose. At higher exposure doses of 2000 and 5000 lg of CeO2 NPs g(-1) dry weight food, NPs significantly decreased the feeding rate and increased the LP level. Comparative studies showed that CeO2 NPs are more biologically potent than TiO2 NPs, ZnO NPs, CuO NPs, CoFe2O4 NPs, and Ag NPs based on feeding rate using the same model organism and experimental setup. Based on comparative metal oxide NPs toxicities, the present results contribute to the knowledge related to the ecotoxicological effects of CeO2 NPs in terrestrial invertebrates exposed through feeding.",
journal = "Archives of Environmental Contamination and Toxicology",
title = "Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles",
volume = "72",
number = "2",
pages = "303-311",
doi = "10.1007/s00244-017-0363-3"
}
Malev, O., Trebše, P., Piecha, M., Novak, S., Budic, B., Dramićanin, M.,& Drobne, D.. (2017). Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles. in Archives of Environmental Contamination and Toxicology, 72(2), 303-311.
https://doi.org/10.1007/s00244-017-0363-3
Malev O, Trebše P, Piecha M, Novak S, Budic B, Dramićanin M, Drobne D. Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles. in Archives of Environmental Contamination and Toxicology. 2017;72(2):303-311.
doi:10.1007/s00244-017-0363-3 .
Malev, Olga, Trebše, Polonca, Piecha, Malgorzata, Novak, Sara, Budic, Bojan, Dramićanin, Miroslav, Drobne, Damjana, "Effects of CeO2 Nanoparticles on Terrestrial Isopod Porcellio scaber: Comparison of CeO2 Biological Potential with Other Nanoparticles" in Archives of Environmental Contamination and Toxicology, 72, no. 2 (2017):303-311,
https://doi.org/10.1007/s00244-017-0363-3 . .
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Toxic effects of diazinon and its photodegradation products

Čolović, Mirjana B.; Krstić, Danijela Z.; Petrović, Sandra; Leskovac, Andreja; Joksić, Gordana; Savić, Jasmina; Franko, Mladen; Trebše, Polonca; Vasić, Vesna M.

(2010)

TY  - JOUR
AU  - Čolović, Mirjana B.
AU  - Krstić, Danijela Z.
AU  - Petrović, Sandra
AU  - Leskovac, Andreja
AU  - Joksić, Gordana
AU  - Savić, Jasmina
AU  - Franko, Mladen
AU  - Trebše, Polonca
AU  - Vasić, Vesna M.
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3931
AB  - The toxic effects of diazinon and its irradiated Solutions were investigated using cultivated human blood cells (lymphocytes and erythrocytes) and skin fibroblasts. Ultra Performance Liquid Chromatography (UPLC)-UV/VIS system was used to monitor the disappearance of starting diazinon during 115-min photodegradation and formation of its by-products (diazoxon and 2-isopropyl-6-methyl-4-pyrimidinol (IMP)) as a function of time Dose-dependent AChE and Na+/K+-ATPase inhibition by diazinon was obtained for all investigated cells Calculated IC50 (72 h) values, in M, were 7 5 x 10(-6)/3 4 x 10(-5), 8.7 x 10(-5)/6.6 x 10(-5), and 3 0 x 10(-5)/4 6 x 10(-5) for fibroblast, erythrocyte and lymphocyte AChE/Na+/K+-ATPase, respectively. Results obtained for reference commercially purified target enzymes indicate similar sensitivity of AChE towards diazinon (IC50 (20 min)-7.8 x 10(-5) M). while diazinon concentrations below 10 mM did not noticeably affect Na+/K+-ATPase activity Besides, diazinon and IMP induced increasing incidence of micronuclei (via clastogenic mode of action) in a dose-dependent manner up to 2 x 10(-6) M and significant inhibition of cell proliferation and increased level of malondialdehyde at all investigated concentrations Although after 15-min diazinon irradiation formed products do not affect purified commercial enzymes activities, inhibitory effect of irradiated solutions on cell enzymes increased as a function of time exposure to UV light and resulted in significant reduction of AChE (LIP to 28-45%) and Na+/K+-ATPase (up to 35-40%) at the end of irradiation period Moreover, photodegradation treatment strengthened prooxidative properties of diazinon as well as its potency to induce cytogenetic damage (C) 2009 Elsevier Ireland Ltd All rights reserved.
T2  - Toxicology Letters
T1  - Toxic effects of diazinon and its photodegradation products
VL  - 193
IS  - 1
SP  - 9
EP  - 18
DO  - 10.1016/j.toxlet.2009.11.022
ER  - 
@article{
author = "Čolović, Mirjana B. and Krstić, Danijela Z. and Petrović, Sandra and Leskovac, Andreja and Joksić, Gordana and Savić, Jasmina and Franko, Mladen and Trebše, Polonca and Vasić, Vesna M.",
year = "2010",
abstract = "The toxic effects of diazinon and its irradiated Solutions were investigated using cultivated human blood cells (lymphocytes and erythrocytes) and skin fibroblasts. Ultra Performance Liquid Chromatography (UPLC)-UV/VIS system was used to monitor the disappearance of starting diazinon during 115-min photodegradation and formation of its by-products (diazoxon and 2-isopropyl-6-methyl-4-pyrimidinol (IMP)) as a function of time Dose-dependent AChE and Na+/K+-ATPase inhibition by diazinon was obtained for all investigated cells Calculated IC50 (72 h) values, in M, were 7 5 x 10(-6)/3 4 x 10(-5), 8.7 x 10(-5)/6.6 x 10(-5), and 3 0 x 10(-5)/4 6 x 10(-5) for fibroblast, erythrocyte and lymphocyte AChE/Na+/K+-ATPase, respectively. Results obtained for reference commercially purified target enzymes indicate similar sensitivity of AChE towards diazinon (IC50 (20 min)-7.8 x 10(-5) M). while diazinon concentrations below 10 mM did not noticeably affect Na+/K+-ATPase activity Besides, diazinon and IMP induced increasing incidence of micronuclei (via clastogenic mode of action) in a dose-dependent manner up to 2 x 10(-6) M and significant inhibition of cell proliferation and increased level of malondialdehyde at all investigated concentrations Although after 15-min diazinon irradiation formed products do not affect purified commercial enzymes activities, inhibitory effect of irradiated solutions on cell enzymes increased as a function of time exposure to UV light and resulted in significant reduction of AChE (LIP to 28-45%) and Na+/K+-ATPase (up to 35-40%) at the end of irradiation period Moreover, photodegradation treatment strengthened prooxidative properties of diazinon as well as its potency to induce cytogenetic damage (C) 2009 Elsevier Ireland Ltd All rights reserved.",
journal = "Toxicology Letters",
title = "Toxic effects of diazinon and its photodegradation products",
volume = "193",
number = "1",
pages = "9-18",
doi = "10.1016/j.toxlet.2009.11.022"
}
Čolović, M. B., Krstić, D. Z., Petrović, S., Leskovac, A., Joksić, G., Savić, J., Franko, M., Trebše, P.,& Vasić, V. M.. (2010). Toxic effects of diazinon and its photodegradation products. in Toxicology Letters, 193(1), 9-18.
https://doi.org/10.1016/j.toxlet.2009.11.022
Čolović MB, Krstić DZ, Petrović S, Leskovac A, Joksić G, Savić J, Franko M, Trebše P, Vasić VM. Toxic effects of diazinon and its photodegradation products. in Toxicology Letters. 2010;193(1):9-18.
doi:10.1016/j.toxlet.2009.11.022 .
Čolović, Mirjana B., Krstić, Danijela Z., Petrović, Sandra, Leskovac, Andreja, Joksić, Gordana, Savić, Jasmina, Franko, Mladen, Trebše, Polonca, Vasić, Vesna M., "Toxic effects of diazinon and its photodegradation products" in Toxicology Letters, 193, no. 1 (2010):9-18,
https://doi.org/10.1016/j.toxlet.2009.11.022 . .
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Inhibition of AChE by malathion and some structurally similar compounds

Krstić, Danijela Z.; Čolović, Mirjana B.; Kralj, Mojca Bavcon; Franko, Mladen; Krinulović, Katarina; Trebše, Polonca; Vasić, Vesna M.

(2008)

TY  - JOUR
AU  - Krstić, Danijela Z.
AU  - Čolović, Mirjana B.
AU  - Kralj, Mojca Bavcon
AU  - Franko, Mladen
AU  - Krinulović, Katarina
AU  - Trebše, Polonca
AU  - Vasić, Vesna M.
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3499
AB  - Inhibition of bovine erythrocyte acetylcholinesterase (free and immobilized on controlled pore glass) by separate and simultaneous exposure to malathion and malathion transformation products which are generally formed during storage or through natural or photochemical degradation was investigated. Increasing concentrations of malathion, its oxidation product malaoxon, and its isomerisation product isomalathion inhibited free and immobilized AChE in a concentration-dependent manner. K-I, the dissociation constant for the initial reversible enzyme inhibitor-complex, and k(3), the first order rate constant for the conversion of the reversible complex into the irreversibly inhibited enzyme, were determined from the progressive development of inhibition produced by reaction of native AChE with malathion, malaoxon and isomalathion. KI values of 1.3 x 10(-4) M-1, 5.6 x 10(-6) M-1 and 7.2 x 10(-6) M-1 were obtained for malathion, malaoxon and isomalathion, respectively. The IC50 values for free/immobilized AChE, (3.7 +/- 0.2)10(-4) M/(1.6 +/- 0.1)10(-4), (2.4 +/- 0.3)10(-6)/(3.4 +/- 0.1)10(-6) M and (3.2 +/- 0.3)10(-6) M/(2.7 +/- 0.2)10(-6) M, were obtained from the inhibition curves induced by malathion, malaoxon and isomalathion, respectively. However, the products formed due to photoinduced degradation, phosphorodithioic O,O,S-trimethyl ester and O,O-dimethyl thiophosphate, did not noticeably affect enzymatic activity, while diethyl maleate inhibited AChE activity at concentrations GT 10 mM. Inhibition of acetylcholinesterase increased with the time of exposure to malathion and its inhibiting by-products within the interval from 0 to 5 minutes. Through simultaneous exposure of the enzyme to malaoxon and isomalathion, an additive effect was achieved for lower concentrations of the inhibitors (in the presence of malaoxon/isomalathion at concentrations 2 x 10(-7) M/2 x 10(-7) M, 2 x 10(-7) M/3 x 10(-7) M and 2 x 10(-7) M/4.5 x 10(-7)M), while an antagonistic effect was obtained for all higher concentrations of inhibitors. The presence of a non-inhibitory degradation product (phosphorodithioic O,O,S-trimethyl ester) did not affect the inhibition efficiencies of the malathion by-products, malaoxon and isomalathion.
T2  - Journal of Enzyme Inhibition and Medicinal Chemistry
T1  - Inhibition of AChE by malathion and some structurally similar compounds
VL  - 23
IS  - 4
SP  - 562
EP  - 573
DO  - 10.1080/14756360701632031
ER  - 
@article{
author = "Krstić, Danijela Z. and Čolović, Mirjana B. and Kralj, Mojca Bavcon and Franko, Mladen and Krinulović, Katarina and Trebše, Polonca and Vasić, Vesna M.",
year = "2008",
abstract = "Inhibition of bovine erythrocyte acetylcholinesterase (free and immobilized on controlled pore glass) by separate and simultaneous exposure to malathion and malathion transformation products which are generally formed during storage or through natural or photochemical degradation was investigated. Increasing concentrations of malathion, its oxidation product malaoxon, and its isomerisation product isomalathion inhibited free and immobilized AChE in a concentration-dependent manner. K-I, the dissociation constant for the initial reversible enzyme inhibitor-complex, and k(3), the first order rate constant for the conversion of the reversible complex into the irreversibly inhibited enzyme, were determined from the progressive development of inhibition produced by reaction of native AChE with malathion, malaoxon and isomalathion. KI values of 1.3 x 10(-4) M-1, 5.6 x 10(-6) M-1 and 7.2 x 10(-6) M-1 were obtained for malathion, malaoxon and isomalathion, respectively. The IC50 values for free/immobilized AChE, (3.7 +/- 0.2)10(-4) M/(1.6 +/- 0.1)10(-4), (2.4 +/- 0.3)10(-6)/(3.4 +/- 0.1)10(-6) M and (3.2 +/- 0.3)10(-6) M/(2.7 +/- 0.2)10(-6) M, were obtained from the inhibition curves induced by malathion, malaoxon and isomalathion, respectively. However, the products formed due to photoinduced degradation, phosphorodithioic O,O,S-trimethyl ester and O,O-dimethyl thiophosphate, did not noticeably affect enzymatic activity, while diethyl maleate inhibited AChE activity at concentrations GT 10 mM. Inhibition of acetylcholinesterase increased with the time of exposure to malathion and its inhibiting by-products within the interval from 0 to 5 minutes. Through simultaneous exposure of the enzyme to malaoxon and isomalathion, an additive effect was achieved for lower concentrations of the inhibitors (in the presence of malaoxon/isomalathion at concentrations 2 x 10(-7) M/2 x 10(-7) M, 2 x 10(-7) M/3 x 10(-7) M and 2 x 10(-7) M/4.5 x 10(-7)M), while an antagonistic effect was obtained for all higher concentrations of inhibitors. The presence of a non-inhibitory degradation product (phosphorodithioic O,O,S-trimethyl ester) did not affect the inhibition efficiencies of the malathion by-products, malaoxon and isomalathion.",
journal = "Journal of Enzyme Inhibition and Medicinal Chemistry",
title = "Inhibition of AChE by malathion and some structurally similar compounds",
volume = "23",
number = "4",
pages = "562-573",
doi = "10.1080/14756360701632031"
}
Krstić, D. Z., Čolović, M. B., Kralj, M. B., Franko, M., Krinulović, K., Trebše, P.,& Vasić, V. M.. (2008). Inhibition of AChE by malathion and some structurally similar compounds. in Journal of Enzyme Inhibition and Medicinal Chemistry, 23(4), 562-573.
https://doi.org/10.1080/14756360701632031
Krstić DZ, Čolović MB, Kralj MB, Franko M, Krinulović K, Trebše P, Vasić VM. Inhibition of AChE by malathion and some structurally similar compounds. in Journal of Enzyme Inhibition and Medicinal Chemistry. 2008;23(4):562-573.
doi:10.1080/14756360701632031 .
Krstić, Danijela Z., Čolović, Mirjana B., Kralj, Mojca Bavcon, Franko, Mladen, Krinulović, Katarina, Trebše, Polonca, Vasić, Vesna M., "Inhibition of AChE by malathion and some structurally similar compounds" in Journal of Enzyme Inhibition and Medicinal Chemistry, 23, no. 4 (2008):562-573,
https://doi.org/10.1080/14756360701632031 . .
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The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase

Krstić, Danijela Z.; Čolović, Mirjana B.; Kralj, M. B.; Trebše, Polonca; Krinulović, Katarina; Vasić, Vesna M.

(2008)

TY  - JOUR
AU  - Krstić, Danijela Z.
AU  - Čolović, Mirjana B.
AU  - Kralj, M. B.
AU  - Trebše, Polonca
AU  - Krinulović, Katarina
AU  - Vasić, Vesna M.
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3421
AB  - The influence of malathion and its four main degradation products found in irradiated solutions (malaoxon, isomalathion, diethyl maleate and O,O-dimethyl phosphate) on acetylcholinesterase (AChE) of free and immobilized bovine erythrocytes was investigated. The concentration-dependent responses to malathion and related organophosphates, malaoxon and isomalathion, of both AChE bioassays used were obtained. The IC (50) values for free and immobilized AChE (3.7 +/- 0.2) x 10(-4) M/(1.6 +/- 0.1) x 10(-4), (2.4 +/- 0.3) x 10(-6)/(3.4 +/- 0.1) x 10(-6) M, and (3.2 +/- 0.3) x 10(-6) M/(2.7 +/- 0.2) x 10(-6) M were obtained in the presence of malathion, malaoxon and isomalathion, respectively. However, diethyl maleate inhibited AChE activity at concentrations GT = 10 mM, while O,O-dimethyl phosphate did not noticeably affect enzyme activity at all investigated concentrations. The relation between the structure of the compounds and their ability to inhibit enzyme activity was discussed.
T2  - Russian Journal of Physical Chemistry A
T1  - The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase
VL  - 82
IS  - 4
SP  - 663
EP  - 668
DO  - 10.1134/S0036024408040274
ER  - 
@article{
author = "Krstić, Danijela Z. and Čolović, Mirjana B. and Kralj, M. B. and Trebše, Polonca and Krinulović, Katarina and Vasić, Vesna M.",
year = "2008",
abstract = "The influence of malathion and its four main degradation products found in irradiated solutions (malaoxon, isomalathion, diethyl maleate and O,O-dimethyl phosphate) on acetylcholinesterase (AChE) of free and immobilized bovine erythrocytes was investigated. The concentration-dependent responses to malathion and related organophosphates, malaoxon and isomalathion, of both AChE bioassays used were obtained. The IC (50) values for free and immobilized AChE (3.7 +/- 0.2) x 10(-4) M/(1.6 +/- 0.1) x 10(-4), (2.4 +/- 0.3) x 10(-6)/(3.4 +/- 0.1) x 10(-6) M, and (3.2 +/- 0.3) x 10(-6) M/(2.7 +/- 0.2) x 10(-6) M were obtained in the presence of malathion, malaoxon and isomalathion, respectively. However, diethyl maleate inhibited AChE activity at concentrations GT = 10 mM, while O,O-dimethyl phosphate did not noticeably affect enzyme activity at all investigated concentrations. The relation between the structure of the compounds and their ability to inhibit enzyme activity was discussed.",
journal = "Russian Journal of Physical Chemistry A",
title = "The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase",
volume = "82",
number = "4",
pages = "663-668",
doi = "10.1134/S0036024408040274"
}
Krstić, D. Z., Čolović, M. B., Kralj, M. B., Trebše, P., Krinulović, K.,& Vasić, V. M.. (2008). The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase. in Russian Journal of Physical Chemistry A, 82(4), 663-668.
https://doi.org/10.1134/S0036024408040274
Krstić DZ, Čolović MB, Kralj MB, Trebše P, Krinulović K, Vasić VM. The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase. in Russian Journal of Physical Chemistry A. 2008;82(4):663-668.
doi:10.1134/S0036024408040274 .
Krstić, Danijela Z., Čolović, Mirjana B., Kralj, M. B., Trebše, Polonca, Krinulović, Katarina, Vasić, Vesna M., "The influence of malathion and its decomposition products on free and immobilized acetylcholinesterase" in Russian Journal of Physical Chemistry A, 82, no. 4 (2008):663-668,
https://doi.org/10.1134/S0036024408040274 . .
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6

Protolytic equilibria and photodegradation of quercetin in aqueous solution

Momić, Tatjana; Savić, Jasmina; Černigoj, Urh; Trebše, Polonca; Vasić, Vesna M.

(2007)

TY  - JOUR
AU  - Momić, Tatjana
AU  - Savić, Jasmina
AU  - Černigoj, Urh
AU  - Trebše, Polonca
AU  - Vasić, Vesna M.
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3355
AB  - Studies of protolytic equilibria and investigations of stability of flavonoids at different acidities are necessary to better understand their antioxidant efficiencies and autoxidation characteristics. The protonation constant of carbonyl group and dissociation constants of OH groups of quercetin in aqueous solutions were determined spectrophotometrically. The distribution diagram of ionic species in aqueous solutions of various acidities was calculated. Study of the effects of UV irradiation on quercetin at pH 5.00, 7.50 and 10.00 indicated that UV irradiation accelerated quercetin autoxidation via the formation of the oxidation product. The stability of quercetin and oxidation product was investigated as a function of irradiation time by using spectrophotometric and HPLC techniques. The apparent pseudo-first-order rate constants for quercetin degradation and oxidation product formation were calculated and discussed.
T2  - Collection of Czechoslovak Chemical Communications
T1  - Protolytic equilibria and photodegradation of quercetin in aqueous solution
VL  - 72
IS  - 11
SP  - 1447
EP  - 1460
DO  - 10.1135/cccc20071447
ER  - 
@article{
author = "Momić, Tatjana and Savić, Jasmina and Černigoj, Urh and Trebše, Polonca and Vasić, Vesna M.",
year = "2007",
abstract = "Studies of protolytic equilibria and investigations of stability of flavonoids at different acidities are necessary to better understand their antioxidant efficiencies and autoxidation characteristics. The protonation constant of carbonyl group and dissociation constants of OH groups of quercetin in aqueous solutions were determined spectrophotometrically. The distribution diagram of ionic species in aqueous solutions of various acidities was calculated. Study of the effects of UV irradiation on quercetin at pH 5.00, 7.50 and 10.00 indicated that UV irradiation accelerated quercetin autoxidation via the formation of the oxidation product. The stability of quercetin and oxidation product was investigated as a function of irradiation time by using spectrophotometric and HPLC techniques. The apparent pseudo-first-order rate constants for quercetin degradation and oxidation product formation were calculated and discussed.",
journal = "Collection of Czechoslovak Chemical Communications",
title = "Protolytic equilibria and photodegradation of quercetin in aqueous solution",
volume = "72",
number = "11",
pages = "1447-1460",
doi = "10.1135/cccc20071447"
}
Momić, T., Savić, J., Černigoj, U., Trebše, P.,& Vasić, V. M.. (2007). Protolytic equilibria and photodegradation of quercetin in aqueous solution. in Collection of Czechoslovak Chemical Communications, 72(11), 1447-1460.
https://doi.org/10.1135/cccc20071447
Momić T, Savić J, Černigoj U, Trebše P, Vasić VM. Protolytic equilibria and photodegradation of quercetin in aqueous solution. in Collection of Czechoslovak Chemical Communications. 2007;72(11):1447-1460.
doi:10.1135/cccc20071447 .
Momić, Tatjana, Savić, Jasmina, Černigoj, Urh, Trebše, Polonca, Vasić, Vesna M., "Protolytic equilibria and photodegradation of quercetin in aqueous solution" in Collection of Czechoslovak Chemical Communications, 72, no. 11 (2007):1447-1460,
https://doi.org/10.1135/cccc20071447 . .
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Inhibition of ache by malathion and some structuraly similar compounds

Krstić, Danijela Z.; Bavcon Kralj, Mojca; Trebše, Polonca; Čolović, Mirjana B.; Krinulović, Katarina; Vasić, Vesna M.

(Society of Physical Chemists of Serbia, 2006)

TY  - CONF
AU  - Krstić, Danijela Z.
AU  - Bavcon Kralj, Mojca
AU  - Trebše, Polonca
AU  - Čolović, Mirjana B.
AU  - Krinulović, Katarina
AU  - Vasić, Vesna M.
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9429
AB  - Inhibition of bovine serum acetylcholinesterase by in vitro exposure to malathion, malaoxon, isomalathion and diethyl maleate was investigated to elucidate the mechanism of the enzyme interaction with structurally similar organophosphorus compounds. IC50 (half maximum inhibitory concentrations) were determined by Hill analysis of experimentally obtained inhibition curves. The values (2.87 ± 0.24)x10-6 M, (2.65±0.61)x10-6M, (3.01±0.36)x10-4 M and (5.69 ±0.7)x10-2 M were obtained for malaoxon, isomalathion, malathion and their hydrolysis product diethyl maleate, respectively. The relationship between the structure of the compounds and their potency to inhibit the enzyme activity was discussed.
PB  - Society of Physical Chemists of Serbia
C3  - Physical chemistry 2006: 8th international conference on fundemental and applied aspract of physical chemistry
T1  - Inhibition of ache by malathion and some structuraly similar compounds
SP  - 401
EP  - 413
UR  - https://hdl.handle.net/21.15107/rcub_vinar_9429
ER  - 
@conference{
author = "Krstić, Danijela Z. and Bavcon Kralj, Mojca and Trebše, Polonca and Čolović, Mirjana B. and Krinulović, Katarina and Vasić, Vesna M.",
year = "2006",
abstract = "Inhibition of bovine serum acetylcholinesterase by in vitro exposure to malathion, malaoxon, isomalathion and diethyl maleate was investigated to elucidate the mechanism of the enzyme interaction with structurally similar organophosphorus compounds. IC50 (half maximum inhibitory concentrations) were determined by Hill analysis of experimentally obtained inhibition curves. The values (2.87 ± 0.24)x10-6 M, (2.65±0.61)x10-6M, (3.01±0.36)x10-4 M and (5.69 ±0.7)x10-2 M were obtained for malaoxon, isomalathion, malathion and their hydrolysis product diethyl maleate, respectively. The relationship between the structure of the compounds and their potency to inhibit the enzyme activity was discussed.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Physical chemistry 2006: 8th international conference on fundemental and applied aspract of physical chemistry",
title = "Inhibition of ache by malathion and some structuraly similar compounds",
pages = "401-413",
url = "https://hdl.handle.net/21.15107/rcub_vinar_9429"
}
Krstić, D. Z., Bavcon Kralj, M., Trebše, P., Čolović, M. B., Krinulović, K.,& Vasić, V. M.. (2006). Inhibition of ache by malathion and some structuraly similar compounds. in Physical chemistry 2006: 8th international conference on fundemental and applied aspract of physical chemistry
Society of Physical Chemists of Serbia., 401-413.
https://hdl.handle.net/21.15107/rcub_vinar_9429
Krstić DZ, Bavcon Kralj M, Trebše P, Čolović MB, Krinulović K, Vasić VM. Inhibition of ache by malathion and some structuraly similar compounds. in Physical chemistry 2006: 8th international conference on fundemental and applied aspract of physical chemistry. 2006;:401-413.
https://hdl.handle.net/21.15107/rcub_vinar_9429 .
Krstić, Danijela Z., Bavcon Kralj, Mojca, Trebše, Polonca, Čolović, Mirjana B., Krinulović, Katarina, Vasić, Vesna M., "Inhibition of ache by malathion and some structuraly similar compounds" in Physical chemistry 2006: 8th international conference on fundemental and applied aspract of physical chemistry (2006):401-413,
https://hdl.handle.net/21.15107/rcub_vinar_9429 .

Insight in the toxicity of malathion photodegradation product

Kralj, Mojca Bavcon; Trebše, Polonca; Vasić, Vesna M.

(2006)

TY  - CONF
AU  - Kralj, Mojca Bavcon
AU  - Trebše, Polonca
AU  - Vasić, Vesna M.
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3082
C3  - Toxicology Letters
T1  - Insight in the toxicity of malathion photodegradation product
VL  - 164
IS  - SI
SP  - S249
EP  - S249
DO  - 10.1016/j.toxlet.2006.07.179
ER  - 
@conference{
author = "Kralj, Mojca Bavcon and Trebše, Polonca and Vasić, Vesna M.",
year = "2006",
journal = "Toxicology Letters",
title = "Insight in the toxicity of malathion photodegradation product",
volume = "164",
number = "SI",
pages = "S249-S249",
doi = "10.1016/j.toxlet.2006.07.179"
}
Kralj, M. B., Trebše, P.,& Vasić, V. M.. (2006). Insight in the toxicity of malathion photodegradation product. in Toxicology Letters, 164(SI), S249-S249.
https://doi.org/10.1016/j.toxlet.2006.07.179
Kralj MB, Trebše P, Vasić VM. Insight in the toxicity of malathion photodegradation product. in Toxicology Letters. 2006;164(SI):S249-S249.
doi:10.1016/j.toxlet.2006.07.179 .
Kralj, Mojca Bavcon, Trebše, Polonca, Vasić, Vesna M., "Insight in the toxicity of malathion photodegradation product" in Toxicology Letters, 164, no. SI (2006):S249-S249,
https://doi.org/10.1016/j.toxlet.2006.07.179 . .