Franko, Mladen

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orcid::0000-0002-8799-5914
  • Franko, Mladen (5)
Projects

Author's Bibliography

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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Low-cost, portable photoacoustic setup for solid samples

Rabasović, Mihailo D.; Nikolić, Marko G.; Dramićanin, Miroslav; Franko, Mladen; Markushev, Dragan D.

(2009)

TY  - JOUR
AU  - Rabasović, Mihailo D.
AU  - Nikolić, Marko G.
AU  - Dramićanin, Miroslav
AU  - Franko, Mladen
AU  - Markushev, Dragan D.
PY  - 2009
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3774
AB  - We have developed a low-cost, portable photoacoustic instrument. The device consists of a detection unit comprising a photoacoustic cell with an embedded laser diode or a light-emitting diode, a photodiode, an electret microphone (60 x 40 x 40 mm(3)), and a signal processing and power supply unit in a box containing batteries and electronics (160 x 140 x 60 mm(3)). A PC or portable computer is required to operate the device and for data processing. The weight of the instrument without the computer is 1.70 kg. The computer, or more precisely, its sound card is the essential part of the apparatus because it generates the signal for the laser diode or light-emitting diode modulation and processes signals from the microphone and photodiode. The computer sound card is used as a dual-phase lock-in amplifier. The software used for the control of the setup was also developed in course of this work. The photoacoustic instrument presented here allows measurements and quantitative analysis of numerous solid-state samples. It is simple in design and use, having a reasonable weight and portability.
T2  - Measurement Science and Technology
T1  - Low-cost, portable photoacoustic setup for solid samples
VL  - 20
IS  - 9
DO  - 10.1088/0957-0233/20/9/095902
ER  - 
@article{
author = "Rabasović, Mihailo D. and Nikolić, Marko G. and Dramićanin, Miroslav and Franko, Mladen and Markushev, Dragan D.",
year = "2009",
abstract = "We have developed a low-cost, portable photoacoustic instrument. The device consists of a detection unit comprising a photoacoustic cell with an embedded laser diode or a light-emitting diode, a photodiode, an electret microphone (60 x 40 x 40 mm(3)), and a signal processing and power supply unit in a box containing batteries and electronics (160 x 140 x 60 mm(3)). A PC or portable computer is required to operate the device and for data processing. The weight of the instrument without the computer is 1.70 kg. The computer, or more precisely, its sound card is the essential part of the apparatus because it generates the signal for the laser diode or light-emitting diode modulation and processes signals from the microphone and photodiode. The computer sound card is used as a dual-phase lock-in amplifier. The software used for the control of the setup was also developed in course of this work. The photoacoustic instrument presented here allows measurements and quantitative analysis of numerous solid-state samples. It is simple in design and use, having a reasonable weight and portability.",
journal = "Measurement Science and Technology",
title = "Low-cost, portable photoacoustic setup for solid samples",
volume = "20",
number = "9",
doi = "10.1088/0957-0233/20/9/095902"
}
Rabasović, M. D., Nikolić, M. G., Dramićanin, M., Franko, M.,& Markushev, D. D.. (2009). Low-cost, portable photoacoustic setup for solid samples. in Measurement Science and Technology, 20(9).
https://doi.org/10.1088/0957-0233/20/9/095902
Rabasović MD, Nikolić MG, Dramićanin M, Franko M, Markushev DD. Low-cost, portable photoacoustic setup for solid samples. in Measurement Science and Technology. 2009;20(9).
doi:10.1088/0957-0233/20/9/095902 .
Rabasović, Mihailo D., Nikolić, Marko G., Dramićanin, Miroslav, Franko, Mladen, Markushev, Dragan D., "Low-cost, portable photoacoustic setup for solid samples" in Measurement Science and Technology, 20, no. 9 (2009),
https://doi.org/10.1088/0957-0233/20/9/095902 . .
47
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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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37
44

Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay

Vasić, Vesna M.; Černigoj, Urh; Krinulović, Katarina; Joksić, Gordana; Franko, Mladen

(2006)

TY  - JOUR
AU  - Vasić, Vesna M.
AU  - Černigoj, Urh
AU  - Krinulović, Katarina
AU  - Joksić, Gordana
AU  - Franko, Mladen
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2972
AB  - A simple Na,K-ATPase assay is described as a suitable method for testing of digoxin photodegradation. The exposure of Na,K-ATPase to the photodegraded samples exhibited reduced inhibition of the enzyme, compared to the unirradiated samples containing equal initial concentrations of drug. The degree of inhibition was dependent on the irradiation time. The concentrations of digoxin in irradiated samples were evaluated by HPLC analysis. Excellent agreement of the results obtained by both methods was observed. The investigation of the influence of irradiated samples on Na,K-ATPase inhibition revealed no side products acting as Na,K-ATPase inhibitors. The cytokinesis block micronucleus test (CBMN) was applied in order to investigate the cytotoxicity of the possible degradation products after exposure to UV irradiation. The results confirmed that the photochemical treatment did not induce the cytotoxic side products. Zero order kinetics, which was observed for digoxin photodegradation and the associated reaction mechanism are also discussed. (c) 2005 Elsevier B.V. All rights reserved.
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay
VL  - 40
IS  - 2
SP  - 404
EP  - 409
DO  - 10.1016/j.jpba.2005.05.018
ER  - 
@article{
author = "Vasić, Vesna M. and Černigoj, Urh and Krinulović, Katarina and Joksić, Gordana and Franko, Mladen",
year = "2006",
abstract = "A simple Na,K-ATPase assay is described as a suitable method for testing of digoxin photodegradation. The exposure of Na,K-ATPase to the photodegraded samples exhibited reduced inhibition of the enzyme, compared to the unirradiated samples containing equal initial concentrations of drug. The degree of inhibition was dependent on the irradiation time. The concentrations of digoxin in irradiated samples were evaluated by HPLC analysis. Excellent agreement of the results obtained by both methods was observed. The investigation of the influence of irradiated samples on Na,K-ATPase inhibition revealed no side products acting as Na,K-ATPase inhibitors. The cytokinesis block micronucleus test (CBMN) was applied in order to investigate the cytotoxicity of the possible degradation products after exposure to UV irradiation. The results confirmed that the photochemical treatment did not induce the cytotoxic side products. Zero order kinetics, which was observed for digoxin photodegradation and the associated reaction mechanism are also discussed. (c) 2005 Elsevier B.V. All rights reserved.",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay",
volume = "40",
number = "2",
pages = "404-409",
doi = "10.1016/j.jpba.2005.05.018"
}
Vasić, V. M., Černigoj, U., Krinulović, K., Joksić, G.,& Franko, M.. (2006). Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay. in Journal of Pharmaceutical and Biomedical Analysis, 40(2), 404-409.
https://doi.org/10.1016/j.jpba.2005.05.018
Vasić VM, Černigoj U, Krinulović K, Joksić G, Franko M. Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay. in Journal of Pharmaceutical and Biomedical Analysis. 2006;40(2):404-409.
doi:10.1016/j.jpba.2005.05.018 .
Vasić, Vesna M., Černigoj, Urh, Krinulović, Katarina, Joksić, Gordana, Franko, Mladen, "Evaluation of photochemical degradation of digoxin by Na,K-ATPase assay" in Journal of Pharmaceutical and Biomedical Analysis, 40, no. 2 (2006):404-409,
https://doi.org/10.1016/j.jpba.2005.05.018 . .
3
5
5

Photochemical degradation of digoxin tested by Na,K-ATPase activity

Krinulović, Katarina; Vasić, Vesna M.; Černigoj, Urh; Franko, Mladen

(Society of Physical Chemists of Serbia, 2004)

TY  - CONF
AU  - Krinulović, Katarina
AU  - Vasić, Vesna M.
AU  - Černigoj, Urh
AU  - Franko, Mladen
PY  - 2004
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9584
AB  - The photochemical degradation of digoxin aqueous solution was obtained by Xelamp irradiation. The concentrations of digoxin in irradiated solutions were detected by measurements of Na,K-ATPase activity and by HPLC analysis. The excellent agreement using two independent methods for determination of digoxin concentration in the irradiated samples was achieved.
PB  - Society of Physical Chemists of Serbia
C3  - Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry
T1  - Photochemical degradation of digoxin tested by Na,K-ATPase activity
VL  - 2
SP  - 694
EP  - 696
UR  - https://hdl.handle.net/21.15107/rcub_vinar_9584
ER  - 
@conference{
author = "Krinulović, Katarina and Vasić, Vesna M. and Černigoj, Urh and Franko, Mladen",
year = "2004",
abstract = "The photochemical degradation of digoxin aqueous solution was obtained by Xelamp irradiation. The concentrations of digoxin in irradiated solutions were detected by measurements of Na,K-ATPase activity and by HPLC analysis. The excellent agreement using two independent methods for determination of digoxin concentration in the irradiated samples was achieved.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry",
title = "Photochemical degradation of digoxin tested by Na,K-ATPase activity",
volume = "2",
pages = "694-696",
url = "https://hdl.handle.net/21.15107/rcub_vinar_9584"
}
Krinulović, K., Vasić, V. M., Černigoj, U.,& Franko, M.. (2004). Photochemical degradation of digoxin tested by Na,K-ATPase activity. in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry
Society of Physical Chemists of Serbia., 2, 694-696.
https://hdl.handle.net/21.15107/rcub_vinar_9584
Krinulović K, Vasić VM, Černigoj U, Franko M. Photochemical degradation of digoxin tested by Na,K-ATPase activity. in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry. 2004;2:694-696.
https://hdl.handle.net/21.15107/rcub_vinar_9584 .
Krinulović, Katarina, Vasić, Vesna M., Černigoj, Urh, Franko, Mladen, "Photochemical degradation of digoxin tested by Na,K-ATPase activity" in Physical chemistry 2004: 7th international conference on fundemental and applied aspract of physical chemistry, 2 (2004):694-696,
https://hdl.handle.net/21.15107/rcub_vinar_9584 .