Strengthening of the MagBioVin Research and Innovation Team for Development of Novel Approaches for Tumour Therapy based on Nanostructured Materials

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Strengthening of the MagBioVin Research and Innovation Team for Development of Novel Approaches for Tumour Therapy based on Nanostructured Materials (en)
Authors

Publications

Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye

Ognjanović, Miloš; Stanković, Dalibor M.; Fabian, Martin; Vranješ-Đurić, Sanja; Antić, Bratislav; Dojčinović, Biljana P.

(2020)

TY  - JOUR
AU  - Ognjanović, Miloš
AU  - Stanković, Dalibor M.
AU  - Fabian, Martin
AU  - Vranješ-Đurić, Sanja
AU  - Antić, Bratislav
AU  - Dojčinović, Biljana P.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8810
AB  - Iron oxide nanoparticles (IONP) with different distinctive morphologies (spherical, cubic, flower-like and needles) were utilized for modification of screen-printed carbon electrodes (SPCE) to be used for synthetic organic dye degradation by an electrochemical approach. This platform was implemented for removal of the synthetic organic dye, Reactive Black 5 (RB5) in aqueous solution. Modified SPCE with spherically shaped IONP (IONS) had the highest dye removal efficiency. Thus, IONS were then used for surface decoration of the most common carbon-based materials (graphene, graphene oxide, carboxylated graphene, graphene nanoribbons, graphene nanoplatelets, single- and multi-wall carbon nanotubes), and the nanocomposites formed were deposited on the electrode surfaces. Using IONS/graphene composite (IONS@GN) for electrode modification resulted in the best effect. Removal of RB5 with this electrode was 51% better in comparison with bare SPCE, reducing the time required for complete dye degradation from 61 to 30 min Using IONS-modified SPCE, total RB5 removal occurred in 51 min, improving the performance by 16% over that of bare SPCE. The effects determined, i.e., the best IONP morphology and best type of carbon-based material for nanocomposite formation to enhance RB5 removal will provide guidelines for further modifications of SPCE with nanomaterials and nanocomposites, for application of this electrochemical approach in the degradation of organic pollutants. © 2020 The Author(s). Published by IOP Publishing Ltd.
T2  - Materials Research Express
T1  - Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye
VL  - 7
IS  - 1
SP  - 015509
DO  - 10.1088/2053-1591/ab6490
ER  - 
@article{
author = "Ognjanović, Miloš and Stanković, Dalibor M. and Fabian, Martin and Vranješ-Đurić, Sanja and Antić, Bratislav and Dojčinović, Biljana P.",
year = "2020",
url = "https://vinar.vin.bg.ac.rs/handle/123456789/8810",
abstract = "Iron oxide nanoparticles (IONP) with different distinctive morphologies (spherical, cubic, flower-like and needles) were utilized for modification of screen-printed carbon electrodes (SPCE) to be used for synthetic organic dye degradation by an electrochemical approach. This platform was implemented for removal of the synthetic organic dye, Reactive Black 5 (RB5) in aqueous solution. Modified SPCE with spherically shaped IONP (IONS) had the highest dye removal efficiency. Thus, IONS were then used for surface decoration of the most common carbon-based materials (graphene, graphene oxide, carboxylated graphene, graphene nanoribbons, graphene nanoplatelets, single- and multi-wall carbon nanotubes), and the nanocomposites formed were deposited on the electrode surfaces. Using IONS/graphene composite (IONS@GN) for electrode modification resulted in the best effect. Removal of RB5 with this electrode was 51% better in comparison with bare SPCE, reducing the time required for complete dye degradation from 61 to 30 min Using IONS-modified SPCE, total RB5 removal occurred in 51 min, improving the performance by 16% over that of bare SPCE. The effects determined, i.e., the best IONP morphology and best type of carbon-based material for nanocomposite formation to enhance RB5 removal will provide guidelines for further modifications of SPCE with nanomaterials and nanocomposites, for application of this electrochemical approach in the degradation of organic pollutants. © 2020 The Author(s). Published by IOP Publishing Ltd.",
journal = "Materials Research Express",
title = "Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye",
volume = "7",
number = "1",
pages = "015509",
doi = "10.1088/2053-1591/ab6490"
}
Ognjanović, M., Stanković, D. M., Fabian, M., Vranješ-Đurić, S., Antić, B.,& Dojčinović, B. P. (2020). Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye.
Materials Research Express, 7(1), 015509.
https://doi.org/10.1088/2053-1591/ab6490
Ognjanović M, Stanković DM, Fabian M, Vranješ-Đurić S, Antić B, Dojčinović BP. Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye. Materials Research Express. 2020;7(1):015509
Ognjanović Miloš, Stanković Dalibor M., Fabian Martin, Vranješ-Đurić Sanja, Antić Bratislav, Dojčinović Biljana P., "Tailoring IONP shape and designing nanocomposite IONS@GN toward modification of SPCE to enhance electrochemical degradation of organic dye" Materials Research Express, 7, no. 1 (2020):015509,
https://doi.org/10.1088/2053-1591/ab6490 .

Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co

Mariano, Jose F. M. L.; Bessergenev, Valentim G; Lourenço, João P; Hantusch, Martin; Burkel, Eberhard; do Rego, Ana M Botelho; Rajňák, Michal; Timko, Milan; Kopčanský, Peter

(2020)

TY  - JOUR
AU  - Mariano, Jose F. M. L.
AU  - Bessergenev, Valentim G
AU  - Lourenço, João P
AU  - Hantusch, Martin
AU  - Burkel, Eberhard
AU  - do Rego, Ana M Botelho
AU  - Rajňák, Michal
AU  - Timko, Milan
AU  - Kopčanský, Peter
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8802
AB  - The present work reports on the structural and magnetic properties of TiO2 P25 Degussa powder doped with cobalt. Dissolution of cobalt in TiO2 matrix was achieved by precipitation of tris(diethyldithiocarbamato) cobalt(III) (CoDtc - Co[S2CN(C2H5)2]3 in chloroform (CHCl3) and consequent thermal treatment. Five different Co atomic percentage contents were chosen, e.g., 0.5%, 1%, 2%, 5% and 10%. It was shown that cobalt atoms are uniformly distributed across TiO2 matrix and exhibit antiferromagnetic interactions at low temperatures. © 2020 Elsevier B.V.
T2  - Journal of Magnetism and Magnetic Materials
T1  - Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co
VL  - 501
SP  - 166442
DO  - 10.1016/j.jmmm.2020.166442
ER  - 
@article{
author = "Mariano, Jose F. M. L. and Bessergenev, Valentim G and Lourenço, João P and Hantusch, Martin and Burkel, Eberhard and do Rego, Ana M Botelho and Rajňák, Michal and Timko, Milan and Kopčanský, Peter",
year = "2020",
url = "https://vinar.vin.bg.ac.rs/handle/123456789/8802",
abstract = "The present work reports on the structural and magnetic properties of TiO2 P25 Degussa powder doped with cobalt. Dissolution of cobalt in TiO2 matrix was achieved by precipitation of tris(diethyldithiocarbamato) cobalt(III) (CoDtc - Co[S2CN(C2H5)2]3 in chloroform (CHCl3) and consequent thermal treatment. Five different Co atomic percentage contents were chosen, e.g., 0.5%, 1%, 2%, 5% and 10%. It was shown that cobalt atoms are uniformly distributed across TiO2 matrix and exhibit antiferromagnetic interactions at low temperatures. © 2020 Elsevier B.V.",
journal = "Journal of Magnetism and Magnetic Materials",
title = "Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co",
volume = "501",
pages = "166442",
doi = "10.1016/j.jmmm.2020.166442"
}
Mariano, J. F. M. L., Bessergenev, V. G., Lourenço, J. P., Hantusch, M., Burkel, E., do Rego, A. M. B., Rajňák, M., Timko, M.,& Kopčanský, P. (2020). Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co.
Journal of Magnetism and Magnetic Materials, 501, 166442.
https://doi.org/10.1016/j.jmmm.2020.166442
Mariano JFML, Bessergenev VG, Lourenço JP, Hantusch M, Burkel E, do Rego AMB, Rajňák M, Timko M, Kopčanský P. Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co. Journal of Magnetism and Magnetic Materials. 2020;501:166442
Mariano Jose F. M. L., Bessergenev Valentim G, Lourenço João P, Hantusch Martin, Burkel Eberhard, do Rego Ana M Botelho, Rajňák Michal, Timko Milan, Kopčanský Peter, "Structural and magnetic properties of P25 TiO2 nanoparticles doped by Co" Journal of Magnetism and Magnetic Materials, 501 (2020):166442,
https://doi.org/10.1016/j.jmmm.2020.166442 .
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Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity

Vasić, Vesna M.; Gašić, Uroš M.; Stanković, Dalibor M.; Lušić, Dražen; Vukić-Lušić, Darija; Milojković-Opsenica, Dušanka M.; Tešić, Živoslav; Trifković, Jelena Đ.

(2019)

TY  - JOUR
AU  - Vasić, Vesna M.
AU  - Gašić, Uroš M.
AU  - Stanković, Dalibor M.
AU  - Lušić, Dražen
AU  - Vukić-Lušić, Darija
AU  - Milojković-Opsenica, Dušanka M.
AU  - Tešić, Živoslav
AU  - Trifković, Jelena Đ.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0308814618316169
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7868
AB  - Concerning the particular nutritive value of honeydew honey compared to blossom honey, and small number of studies defining botanical origin of honeydew honey, comprehensive analysis of phenolic profile of 64 honeydew honey samples of specific botanical origin was performed. Two advanced techniques of liquid chromatography hyphenated with mass spectrometry were used for identification of a total of 52 compounds and quantification of 25 of them. Pattern recognition analysis applied on data on phenolic compounds content confirmed that quercetin, naringenin, caffeoylquinic acid, hydroxyphenylacetic acid, apigenin and genistein, could be considered as potential markers of botanical origin of honeydew honey. Spectroscopic and electrochemical approaches were applied for the evaluation of the antioxidant capacity. Quercus sps. samples, Quercus frainetto and Quercus ilex, showed high biological activity and specific chemical composition. Additionally, cyclic voltammetry profiles were used for characterization and natural clustering of honeydew honey for the first time. © 2018 Elsevier Ltd
T2  - Food Chemistry
T1  - Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity
VL  - 274
SP  - 629
EP  - 641
DO  - 10.1016/j.foodchem.2018.09.045
ER  - 
@article{
author = "Vasić, Vesna M. and Gašić, Uroš M. and Stanković, Dalibor M. and Lušić, Dražen and Vukić-Lušić, Darija and Milojković-Opsenica, Dušanka M. and Tešić, Živoslav and Trifković, Jelena Đ.",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0308814618316169, http://vinar.vin.bg.ac.rs/handle/123456789/7868",
abstract = "Concerning the particular nutritive value of honeydew honey compared to blossom honey, and small number of studies defining botanical origin of honeydew honey, comprehensive analysis of phenolic profile of 64 honeydew honey samples of specific botanical origin was performed. Two advanced techniques of liquid chromatography hyphenated with mass spectrometry were used for identification of a total of 52 compounds and quantification of 25 of them. Pattern recognition analysis applied on data on phenolic compounds content confirmed that quercetin, naringenin, caffeoylquinic acid, hydroxyphenylacetic acid, apigenin and genistein, could be considered as potential markers of botanical origin of honeydew honey. Spectroscopic and electrochemical approaches were applied for the evaluation of the antioxidant capacity. Quercus sps. samples, Quercus frainetto and Quercus ilex, showed high biological activity and specific chemical composition. Additionally, cyclic voltammetry profiles were used for characterization and natural clustering of honeydew honey for the first time. © 2018 Elsevier Ltd",
journal = "Food Chemistry",
title = "Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity",
volume = "274",
pages = "629-641",
doi = "10.1016/j.foodchem.2018.09.045"
}
Vasić, V. M., Gašić, U. M., Stanković, D. M., Lušić, D., Vukić-Lušić, D., Milojković-Opsenica, D. M., Tešić, Ž.,& Trifković, J. Đ. (2019). Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity.
Food Chemistry, 274, 629-641.
https://doi.org/10.1016/j.foodchem.2018.09.045
Vasić VM, Gašić UM, Stanković DM, Lušić D, Vukić-Lušić D, Milojković-Opsenica DM, Tešić Ž, Trifković JĐ. Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity. Food Chemistry. 2019;274:629-641
Vasić Vesna M., Gašić Uroš M., Stanković Dalibor M., Lušić Dražen, Vukić-Lušić Darija, Milojković-Opsenica Dušanka M., Tešić Živoslav, Trifković Jelena Đ., "Towards better quality criteria of European honeydew honey: Phenolic profile and antioxidant capacity" Food Chemistry, 274 (2019):629-641,
https://doi.org/10.1016/j.foodchem.2018.09.045 .
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Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand

Perić, Marko R.; Kyne, Sara H.; Gruden, Maja; Rodić, Marko V.; Jeremić, Dejan; Stanković, Dalibor M.; Brčeski, Ilija

(2019)

TY  - JOUR
AU  - Perić, Marko R.
AU  - Kyne, Sara H.
AU  - Gruden, Maja
AU  - Rodić, Marko V.
AU  - Jeremić, Dejan
AU  - Stanković, Dalibor M.
AU  - Brčeski, Ilija
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8381
AB  - In this work we present the synthesis, and experimental and theoretical analysis of a binuclear nickel(II) complex coordinated to a new phthalazine dihydrazone-based ligand. Single-crystal X-ray diffraction analysis of the metal complex shows that the coordination geometry around each nickel(II) atom is distorted octahedral. DFT calculations predict that the magnetic exchange coupling constant of the binuclear nickel(II) complex is predominantly anti-ferromagnetic.
T2  - Monatshefte fur Chemie
T1  - Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand
VL  - 150
IS  - 7
SP  - 1241
EP  - 1248
DO  - 10.1007/s00706-019-02405-7
ER  - 
@article{
author = "Perić, Marko R. and Kyne, Sara H. and Gruden, Maja and Rodić, Marko V. and Jeremić, Dejan and Stanković, Dalibor M. and Brčeski, Ilija",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8381",
abstract = "In this work we present the synthesis, and experimental and theoretical analysis of a binuclear nickel(II) complex coordinated to a new phthalazine dihydrazone-based ligand. Single-crystal X-ray diffraction analysis of the metal complex shows that the coordination geometry around each nickel(II) atom is distorted octahedral. DFT calculations predict that the magnetic exchange coupling constant of the binuclear nickel(II) complex is predominantly anti-ferromagnetic.",
journal = "Monatshefte fur Chemie",
title = "Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand",
volume = "150",
number = "7",
pages = "1241-1248",
doi = "10.1007/s00706-019-02405-7"
}
Perić, M. R., Kyne, S. H., Gruden, M., Rodić, M. V., Jeremić, D., Stanković, D. M.,& Brčeski, I. (2019). Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand.
Monatshefte fur Chemie, 150(7), 1241-1248.
https://doi.org/10.1007/s00706-019-02405-7
Perić MR, Kyne SH, Gruden M, Rodić MV, Jeremić D, Stanković DM, Brčeski I. Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand. Monatshefte fur Chemie. 2019;150(7):1241-1248
Perić Marko R., Kyne Sara H., Gruden Maja, Rodić Marko V., Jeremić Dejan, Stanković Dalibor M., Brčeski Ilija, "Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand" Monatshefte fur Chemie, 150, no. 7 (2019):1241-1248,
https://doi.org/10.1007/s00706-019-02405-7 .
1

Biliverdin-copper complex at physiological pH

Dimitrijević, Milena S.; Bogdanović-Pristov, Jelena; Žižić, Milan; Stanković, Dalibor M.; Bajuk-Bogdanović, Danica V.; Stanić, Marina; Spasić, Snežana D.; Hagen, Wilfred; Spasojević, Ivan

(2019)

TY  - JOUR
AU  - Dimitrijević, Milena S.
AU  - Bogdanović-Pristov, Jelena
AU  - Žižić, Milan
AU  - Stanković, Dalibor M.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Stanić, Marina
AU  - Spasić, Snežana D.
AU  - Hagen, Wilfred
AU  - Spasojević, Ivan
PY  - 2019
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/3066
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8200
AB  - Biliverdin (BV), a product of heme catabolism, is known to interact with transition metals, but the details of such interactions under physiological conditions are scarce. Herein, we examined coordinate/redox interactions of BV with Cu2+ in phosphate buffer at pH 7.4, using spectrophotometry, HESI-MS, Raman spectroscopy, 1 H NMR, EPR, fluorimetry, and electrochemical methods. BV formed a stable coordination complex with copper in 1 : 1 stoichiometry. The structure of BV was more planar and energetically stable in the complex. The complex showed strong paramagnetic effects that were attributed to an unpaired delocalized e−. The delocalized electron may come from BV or Cu2+, so the complex is formally composed either of BV radical cation and Cu1+ or of BV radical anion and Cu3+. The complex underwent oxidation only in the presence of both O2 and an excess of Cu2+, or a strong oxidizing agent, and it was resistant to reducing agents. The biological effects of the stable BV metallocomplex containing a delocalized unpaired electron should be further examined, and may provide an answer to the long-standing question of high energy investment in the catabolism of BV, which represents a relatively harmless molecule per se.
T2  - Dalton Transactions
T1  - Biliverdin-copper complex at physiological pH
VL  - 48
IS  - 18
SP  - 6061
EP  - 6070
DO  - 10.1039/c8dt04724c
ER  - 
@article{
author = "Dimitrijević, Milena S. and Bogdanović-Pristov, Jelena and Žižić, Milan and Stanković, Dalibor M. and Bajuk-Bogdanović, Danica V. and Stanić, Marina and Spasić, Snežana D. and Hagen, Wilfred and Spasojević, Ivan",
year = "2019",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3066, http://vinar.vin.bg.ac.rs/handle/123456789/8200",
abstract = "Biliverdin (BV), a product of heme catabolism, is known to interact with transition metals, but the details of such interactions under physiological conditions are scarce. Herein, we examined coordinate/redox interactions of BV with Cu2+ in phosphate buffer at pH 7.4, using spectrophotometry, HESI-MS, Raman spectroscopy, 1 H NMR, EPR, fluorimetry, and electrochemical methods. BV formed a stable coordination complex with copper in 1 : 1 stoichiometry. The structure of BV was more planar and energetically stable in the complex. The complex showed strong paramagnetic effects that were attributed to an unpaired delocalized e−. The delocalized electron may come from BV or Cu2+, so the complex is formally composed either of BV radical cation and Cu1+ or of BV radical anion and Cu3+. The complex underwent oxidation only in the presence of both O2 and an excess of Cu2+, or a strong oxidizing agent, and it was resistant to reducing agents. The biological effects of the stable BV metallocomplex containing a delocalized unpaired electron should be further examined, and may provide an answer to the long-standing question of high energy investment in the catabolism of BV, which represents a relatively harmless molecule per se.",
journal = "Dalton Transactions",
title = "Biliverdin-copper complex at physiological pH",
volume = "48",
number = "18",
pages = "6061-6070",
doi = "10.1039/c8dt04724c"
}
Dimitrijević, M. S., Bogdanović-Pristov, J., Žižić, M., Stanković, D. M., Bajuk-Bogdanović, D. V., Stanić, M., Spasić, S. D., Hagen, W.,& Spasojević, I. (2019). Biliverdin-copper complex at physiological pH.
Dalton Transactions, 48(18), 6061-6070.
https://doi.org/10.1039/c8dt04724c
Dimitrijević MS, Bogdanović-Pristov J, Žižić M, Stanković DM, Bajuk-Bogdanović DV, Stanić M, Spasić SD, Hagen W, Spasojević I. Biliverdin-copper complex at physiological pH. Dalton Transactions. 2019;48(18):6061-6070
Dimitrijević Milena S., Bogdanović-Pristov Jelena, Žižić Milan, Stanković Dalibor M., Bajuk-Bogdanović Danica V., Stanić Marina, Spasić Snežana D., Hagen Wilfred, Spasojević Ivan, "Biliverdin-copper complex at physiological pH" Dalton Transactions, 48, no. 18 (2019):6061-6070,
https://doi.org/10.1039/c8dt04724c .
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Biliverdin-copper complex at physiological pH

Dimitrijević, Milena S.; Bogdanović-Pristov, Jelena; Žižić, Milan; Stanković, Dalibor M.; Bajuk-Bogdanović, Danica V.; Stanić, Marina; Spasić, Snežana D.; Hagen, Wilfred; Spasojević, Ivan

(2019)

TY  - JOUR
AU  - Dimitrijević, Milena S.
AU  - Bogdanović-Pristov, Jelena
AU  - Žižić, Milan
AU  - Stanković, Dalibor M.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Stanić, Marina
AU  - Spasić, Snežana D.
AU  - Hagen, Wilfred
AU  - Spasojević, Ivan
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8258
AB  - Biliverdin (BV), a product of heme catabolism, is known to interact with transition metals, but the details of such interactions under physiological conditions are scarce. Herein, we examined coordinate/redox interactions of BV with Cu2+ in phosphate buffer at pH 7.4, using spectrophotometry, HESI-MS, Raman spectroscopy, 1 H NMR, EPR, fluorimetry, and electrochemical methods. BV formed a stable coordination complex with copper in 1 : 1 stoichiometry. The structure of BV was more planar and energetically stable in the complex. The complex showed strong paramagnetic effects that were attributed to an unpaired delocalized e−. The delocalized electron may come from BV or Cu2+, so the complex is formally composed either of BV radical cation and Cu1+ or of BV radical anion and Cu3+. The complex underwent oxidation only in the presence of both O2 and an excess of Cu2+, or a strong oxidizing agent, and it was resistant to reducing agents. The biological effects of the stable BV metallocomplex containing a delocalized unpaired electron should be further examined, and may provide an answer to the long-standing question of high energy investment in the catabolism of BV, which represents a relatively harmless molecule per se.
T2  - Dalton Transactions
T1  - Biliverdin-copper complex at physiological pH
VL  - 48
IS  - 18
SP  - 6061
EP  - 6070
DO  - 10.1039/c8dt04724c
ER  - 
@article{
author = "Dimitrijević, Milena S. and Bogdanović-Pristov, Jelena and Žižić, Milan and Stanković, Dalibor M. and Bajuk-Bogdanović, Danica V. and Stanić, Marina and Spasić, Snežana D. and Hagen, Wilfred and Spasojević, Ivan",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8258",
abstract = "Biliverdin (BV), a product of heme catabolism, is known to interact with transition metals, but the details of such interactions under physiological conditions are scarce. Herein, we examined coordinate/redox interactions of BV with Cu2+ in phosphate buffer at pH 7.4, using spectrophotometry, HESI-MS, Raman spectroscopy, 1 H NMR, EPR, fluorimetry, and electrochemical methods. BV formed a stable coordination complex with copper in 1 : 1 stoichiometry. The structure of BV was more planar and energetically stable in the complex. The complex showed strong paramagnetic effects that were attributed to an unpaired delocalized e−. The delocalized electron may come from BV or Cu2+, so the complex is formally composed either of BV radical cation and Cu1+ or of BV radical anion and Cu3+. The complex underwent oxidation only in the presence of both O2 and an excess of Cu2+, or a strong oxidizing agent, and it was resistant to reducing agents. The biological effects of the stable BV metallocomplex containing a delocalized unpaired electron should be further examined, and may provide an answer to the long-standing question of high energy investment in the catabolism of BV, which represents a relatively harmless molecule per se.",
journal = "Dalton Transactions",
title = "Biliverdin-copper complex at physiological pH",
volume = "48",
number = "18",
pages = "6061-6070",
doi = "10.1039/c8dt04724c"
}
Dimitrijević, M. S., Bogdanović-Pristov, J., Žižić, M., Stanković, D. M., Bajuk-Bogdanović, D. V., Stanić, M., Spasić, S. D., Hagen, W.,& Spasojević, I. (2019). Biliverdin-copper complex at physiological pH.
Dalton Transactions, 48(18), 6061-6070.
https://doi.org/10.1039/c8dt04724c
Dimitrijević MS, Bogdanović-Pristov J, Žižić M, Stanković DM, Bajuk-Bogdanović DV, Stanić M, Spasić SD, Hagen W, Spasojević I. Biliverdin-copper complex at physiological pH. Dalton Transactions. 2019;48(18):6061-6070
Dimitrijević Milena S., Bogdanović-Pristov Jelena, Žižić Milan, Stanković Dalibor M., Bajuk-Bogdanović Danica V., Stanić Marina, Spasić Snežana D., Hagen Wilfred, Spasojević Ivan, "Biliverdin-copper complex at physiological pH" Dalton Transactions, 48, no. 18 (2019):6061-6070,
https://doi.org/10.1039/c8dt04724c .
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99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent

Mirković, Marija D.; Radović, Magdalena; Stanković, Dragana; Milanović, Zorana; Janković, Drina; Matović, Milovan D.; Jeremić, Marija; Antić, Bratislav; Vranješ-Đurić, Sanja

(2019)

TY  - JOUR
AU  - Mirković, Marija D.
AU  - Radović, Magdalena
AU  - Stanković, Dragana
AU  - Milanović, Zorana
AU  - Janković, Drina
AU  - Matović, Milovan D.
AU  - Jeremić, Marija
AU  - Antić, Bratislav
AU  - Vranješ-Đurić, Sanja
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8156
AB  - Novel theranostic nanoplatform is expected to integrate imaging for guiding and monitoring of the tumor therapy with great therapeutic efficacy and fewer side effects. Here we describe the preparation of a multifunctional 99mTc–bisphosphonate–coated magnetic nanoparticles (MNPs) based on Fe3O4 and coated with two hydrophilic bisphosphonate ligands, i.e., methylene diphosphonate (MDP) and 1–hydroxyethane-1,1- diphosphonate (HEDP). The presence of the bisphosphonates on the MNPs surface, enabled their biocompatibility, colloidal stability and successful binding of the radionuclide. The morphology, size, structure, surface charge and magnetic properties of obtained bisphosphonate–coated Fe3O4 MNPs were characterized by transmission electron microscopy, X–ray powder diffraction, dynamic light scattering, laser Doppler electrophoresis, Fourier transform infrared spectroscopy and vibrating sample magnetometer. The specific power absorption values for Fe3O4–MDP and Fe3O4–HEDP were 113 W/g and 141 W/g, respectively, indicated their heating ability under applied magnetic field. Coated MNPs were radiolabeled with 99mTc using stannous chloride as the reducing agent in a reproducible high yield (95% for Fe3O4–MDP and 97% for Fe3O4–HEDP MNPs) and were remained stable in saline and human serum for 24 h. Ex vivo biodistribution studies presented significant liver and spleen uptake in healthy Wistar rats after intravenous administration at all examined time points due to the colloidal nature of both 99mTc–MNPs. Results of scintigraphy studies are in accordance with ex vivo biodistribution studies, demonstrating high in vivo stability of radiolabeled MNPs and therefore results of both methods were proved as accurate information on the biodistribution profile of investigated MNPs. Overall, in vitro and in vivo stability as well as heating ability, indicate that biocompatible radiolabeled bisphosphonate magnetic nanoparticles exhibit promising potential as a theranostic nanoagent. © 2019 Elsevier B.V.
T2  - Materials Science and Engineering: C
T1  - 99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent
VL  - 102
SP  - 124
EP  - 133
DO  - 10.1016/j.msec.2019.04.034
ER  - 
@article{
author = "Mirković, Marija D. and Radović, Magdalena and Stanković, Dragana and Milanović, Zorana and Janković, Drina and Matović, Milovan D. and Jeremić, Marija and Antić, Bratislav and Vranješ-Đurić, Sanja",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8156",
abstract = "Novel theranostic nanoplatform is expected to integrate imaging for guiding and monitoring of the tumor therapy with great therapeutic efficacy and fewer side effects. Here we describe the preparation of a multifunctional 99mTc–bisphosphonate–coated magnetic nanoparticles (MNPs) based on Fe3O4 and coated with two hydrophilic bisphosphonate ligands, i.e., methylene diphosphonate (MDP) and 1–hydroxyethane-1,1- diphosphonate (HEDP). The presence of the bisphosphonates on the MNPs surface, enabled their biocompatibility, colloidal stability and successful binding of the radionuclide. The morphology, size, structure, surface charge and magnetic properties of obtained bisphosphonate–coated Fe3O4 MNPs were characterized by transmission electron microscopy, X–ray powder diffraction, dynamic light scattering, laser Doppler electrophoresis, Fourier transform infrared spectroscopy and vibrating sample magnetometer. The specific power absorption values for Fe3O4–MDP and Fe3O4–HEDP were 113 W/g and 141 W/g, respectively, indicated their heating ability under applied magnetic field. Coated MNPs were radiolabeled with 99mTc using stannous chloride as the reducing agent in a reproducible high yield (95% for Fe3O4–MDP and 97% for Fe3O4–HEDP MNPs) and were remained stable in saline and human serum for 24 h. Ex vivo biodistribution studies presented significant liver and spleen uptake in healthy Wistar rats after intravenous administration at all examined time points due to the colloidal nature of both 99mTc–MNPs. Results of scintigraphy studies are in accordance with ex vivo biodistribution studies, demonstrating high in vivo stability of radiolabeled MNPs and therefore results of both methods were proved as accurate information on the biodistribution profile of investigated MNPs. Overall, in vitro and in vivo stability as well as heating ability, indicate that biocompatible radiolabeled bisphosphonate magnetic nanoparticles exhibit promising potential as a theranostic nanoagent. © 2019 Elsevier B.V.",
journal = "Materials Science and Engineering: C",
title = "99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent",
volume = "102",
pages = "124-133",
doi = "10.1016/j.msec.2019.04.034"
}
Mirković, M. D., Radović, M., Stanković, D., Milanović, Z., Janković, D., Matović, M. D., Jeremić, M., Antić, B.,& Vranješ-Đurić, S. (2019). 99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent.
Materials Science and Engineering: C, 102, 124-133.
https://doi.org/10.1016/j.msec.2019.04.034
Mirković MD, Radović M, Stanković D, Milanović Z, Janković D, Matović MD, Jeremić M, Antić B, Vranješ-Đurić S. 99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent. Materials Science and Engineering: C. 2019;102:124-133
Mirković Marija D., Radović Magdalena, Stanković Dragana, Milanović Zorana, Janković Drina, Matović Milovan D., Jeremić Marija, Antić Bratislav, Vranješ-Đurić Sanja, "99mTc–bisphosphonate–coated magnetic nanoparticles as potential theranostic nanoagent" Materials Science and Engineering: C, 102 (2019):124-133,
https://doi.org/10.1016/j.msec.2019.04.034 .
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10

99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis

Ognjanović, Miloš; Radović, Magdalena; Mirković, Marija D.; Prijović, Željko; Puerto Morales, Maria del; Čeh, Miran; Vranješ-Đurić, Sanja; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Ognjanović, Miloš
AU  - Radović, Magdalena
AU  - Mirković, Marija D.
AU  - Prijović, Željko
AU  - Puerto Morales, Maria del
AU  - Čeh, Miran
AU  - Vranješ-Đurić, Sanja
AU  - Antić, Bratislav
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8622
AB  - Development of a complex based on iron oxide nanoparticles (IONPs) for diagnosis and dual magnetic hyperthermia/radionuclide cancer therapy accomplishing high yields of radiolabeling and great magnetic heat induction is still a challenge. We report here the synthesis of citric acid, poly(acrylic acid) (PAA) and poly(ethylene glycol) coated IONPs and their labeling with three radionuclides, namely, technetium (99mTc), yttrium (90Y), and lutetium (177Lu), aiming at potential use in cancer diagnosis and therapy. Polyol-synthesized IONPs are a flowerlike structure with 13.5 nm spherically shaped cores and 24.8 nm diameter. PAA-coated nanoparticles (PAA@IONP) showed the best characteristics such as easy radiolabeling with very high yields (>97.5%) with all three radionuclides, and excellent in vitro stabilities with less than 10% of radionuclides detaching after 24 h. Heating ability of PAA@IONP in an alternating external magnetic field showed intrinsic loss power value of 7.3 nH m2/kg, which is one of higher reported values. Additionally, PAA@IONP itself presented no significant cytotoxicity to the CT-26 cancer cells, reaching IC50 at 60 μg/mL. However, under the external magnetic field, they show hyperthermia-mediated cells killing, which correlated with the magnetic field strength and time of exposure. Since PAA@IONP are easy to prepare, biocompatible, and with excellent magnetic heat induction, these nanoparticles radiolabeled with high-energy beta emitters 90Y and 177Lu have valuable potential as agent for dual magnetic hyperthermia/radionuclide therapy, while radiolabeled with 99mTc could be used in diagnostic imaging. Copyright © 2019 American Chemical Society.
T2  - ACS Applied Materials & Interfaces
T1  - 99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis
VL  - 11
IS  - 44
SP  - 41109
EP  - 41117
DO  - 10.1021/acsami.9b16428
ER  - 
@article{
author = "Ognjanović, Miloš and Radović, Magdalena and Mirković, Marija D. and Prijović, Željko and Puerto Morales, Maria del and Čeh, Miran and Vranješ-Đurić, Sanja and Antić, Bratislav",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8622",
abstract = "Development of a complex based on iron oxide nanoparticles (IONPs) for diagnosis and dual magnetic hyperthermia/radionuclide cancer therapy accomplishing high yields of radiolabeling and great magnetic heat induction is still a challenge. We report here the synthesis of citric acid, poly(acrylic acid) (PAA) and poly(ethylene glycol) coated IONPs and their labeling with three radionuclides, namely, technetium (99mTc), yttrium (90Y), and lutetium (177Lu), aiming at potential use in cancer diagnosis and therapy. Polyol-synthesized IONPs are a flowerlike structure with 13.5 nm spherically shaped cores and 24.8 nm diameter. PAA-coated nanoparticles (PAA@IONP) showed the best characteristics such as easy radiolabeling with very high yields (>97.5%) with all three radionuclides, and excellent in vitro stabilities with less than 10% of radionuclides detaching after 24 h. Heating ability of PAA@IONP in an alternating external magnetic field showed intrinsic loss power value of 7.3 nH m2/kg, which is one of higher reported values. Additionally, PAA@IONP itself presented no significant cytotoxicity to the CT-26 cancer cells, reaching IC50 at 60 μg/mL. However, under the external magnetic field, they show hyperthermia-mediated cells killing, which correlated with the magnetic field strength and time of exposure. Since PAA@IONP are easy to prepare, biocompatible, and with excellent magnetic heat induction, these nanoparticles radiolabeled with high-energy beta emitters 90Y and 177Lu have valuable potential as agent for dual magnetic hyperthermia/radionuclide therapy, while radiolabeled with 99mTc could be used in diagnostic imaging. Copyright © 2019 American Chemical Society.",
journal = "ACS Applied Materials & Interfaces",
title = "99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis",
volume = "11",
number = "44",
pages = "41109-41117",
doi = "10.1021/acsami.9b16428"
}
Ognjanović, M., Radović, M., Mirković, M. D., Prijović, Ž., Puerto Morales, M. d., Čeh, M., Vranješ-Đurić, S.,& Antić, B. (2019). 99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis.
ACS Applied Materials & Interfaces, 11(44), 41109-41117.
https://doi.org/10.1021/acsami.9b16428
Ognjanović M, Radović M, Mirković MD, Prijović Ž, Puerto Morales MD, Čeh M, Vranješ-Đurić S, Antić B. 99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis. ACS Applied Materials & Interfaces. 2019;11(44):41109-41117
Ognjanović Miloš, Radović Magdalena, Mirković Marija D., Prijović Željko, Puerto Morales Maria del, Čeh Miran, Vranješ-Đurić Sanja, Antić Bratislav, "99m Tc-, 90 Y-, and 177 Lu-Labeled Iron Oxide Nanoflowers Designed for Potential Use in Dual Magnetic Hyperthermia/Radionuclide Cancer Therapy and Diagnosis" ACS Applied Materials & Interfaces, 11, no. 44 (2019):41109-41117,
https://doi.org/10.1021/acsami.9b16428 .
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Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay

Jović-Jovičić, Nataša P.; Mojović, Miloš D.; Stanković, Dalibor M.; Vasiljević-Nedić, Bojana; Milutinović-Nikolić, Aleksandra D.; Banković, Predrag T.; Mojović, Zorica D.

(2019)

TY  - JOUR
AU  - Jović-Jovičić, Nataša P.
AU  - Mojović, Miloš D.
AU  - Stanković, Dalibor M.
AU  - Vasiljević-Nedić, Bojana
AU  - Milutinović-Nikolić, Aleksandra D.
AU  - Banković, Predrag T.
AU  - Mojović, Zorica D.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618325039
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7979
AB  - Series of alkylammonium modified smectites with different alkylammoinum/clay ratios was synthesized (H series). The obtained organoclays were used as precursors for carbon-clay composite materials (C series). Both set of materials were characterized by X-ray diffraction (XRD), point of zero charge (pHPZC), N2 adsorption-desorption isotherms, Raman spectroscopy and electron paramagnetic resonance (EPR) analysis. XRD analysis of organomodified clays confirmed incorporation of HDTMA+ into interlamellar space of smectite. Series of carbonized clays showed constant d001 value of 1.4 nm. The pHPZC of two series differed indicating that carbonization changed the profile of pH dependent sites on the clay surface. Textural properties of the H series decreased throughout the series, while in the C series the most developed porous structure was obtained for sample where HDTMA+ loading was equal to cation exchange capacity. Raman spectroscopy showed that amorphous carbon was formed during carbonization process. The obtained materials were used as modifiers of carbon paste electrode and investigated using electrochemical impedance spectroscopy, cyclic voltammetry and square wave voltammetry. The comparison of electrochemical behavior of H series and C series showed the importance of interlamellar species for charge transfer process. The investigation of influence of composition of carbon paste and form of added carbon showed that performance of carbon-clay based electrodes depended on synergy of different factors. © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay
VL  - 296
SP  - 387
EP  - 396
DO  - 10.1016/j.electacta.2018.11.031
ER  - 
@article{
author = "Jović-Jovičić, Nataša P. and Mojović, Miloš D. and Stanković, Dalibor M. and Vasiljević-Nedić, Bojana and Milutinović-Nikolić, Aleksandra D. and Banković, Predrag T. and Mojović, Zorica D.",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0013468618325039, http://vinar.vin.bg.ac.rs/handle/123456789/7979",
abstract = "Series of alkylammonium modified smectites with different alkylammoinum/clay ratios was synthesized (H series). The obtained organoclays were used as precursors for carbon-clay composite materials (C series). Both set of materials were characterized by X-ray diffraction (XRD), point of zero charge (pHPZC), N2 adsorption-desorption isotherms, Raman spectroscopy and electron paramagnetic resonance (EPR) analysis. XRD analysis of organomodified clays confirmed incorporation of HDTMA+ into interlamellar space of smectite. Series of carbonized clays showed constant d001 value of 1.4 nm. The pHPZC of two series differed indicating that carbonization changed the profile of pH dependent sites on the clay surface. Textural properties of the H series decreased throughout the series, while in the C series the most developed porous structure was obtained for sample where HDTMA+ loading was equal to cation exchange capacity. Raman spectroscopy showed that amorphous carbon was formed during carbonization process. The obtained materials were used as modifiers of carbon paste electrode and investigated using electrochemical impedance spectroscopy, cyclic voltammetry and square wave voltammetry. The comparison of electrochemical behavior of H series and C series showed the importance of interlamellar species for charge transfer process. The investigation of influence of composition of carbon paste and form of added carbon showed that performance of carbon-clay based electrodes depended on synergy of different factors. © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay",
volume = "296",
pages = "387-396",
doi = "10.1016/j.electacta.2018.11.031"
}
Jović-Jovičić, N. P., Mojović, M. D., Stanković, D. M., Vasiljević-Nedić, B., Milutinović-Nikolić, A. D., Banković, P. T.,& Mojović, Z. D. (2019). Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay.
Electrochimica Acta, 296, 387-396.
https://doi.org/10.1016/j.electacta.2018.11.031
Jović-Jovičić NP, Mojović MD, Stanković DM, Vasiljević-Nedić B, Milutinović-Nikolić AD, Banković PT, Mojović ZD. Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay. Electrochimica Acta. 2019;296:387-396
Jović-Jovičić Nataša P., Mojović Miloš D., Stanković Dalibor M., Vasiljević-Nedić Bojana, Milutinović-Nikolić Aleksandra D., Banković Predrag T., Mojović Zorica D., "Characterization and electrochemical properties of organomodified and corresponding derived carbonized clay" Electrochimica Acta, 296 (2019):387-396,
https://doi.org/10.1016/j.electacta.2018.11.031 .
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3

CCDC 1879001: Experimental Crystal Structure Determination

Pavić, Aleksandar B.; Savić, Nada D.; Glišić, Biljana Đ.; Crochet, Aurélien; Vojnović, Sandra; Kurutos, Atanas; Stanković, Dalibor M.; Fromm, Katharina M.; Nikodinović-Runić, Jasmina; Đuran, Miloš I.

(2019)

TY  - BOOK
AU  - Pavić, Aleksandar B.
AU  - Savić, Nada D.
AU  - Glišić, Biljana Đ.
AU  - Crochet, Aurélien
AU  - Vojnović, Sandra
AU  - Kurutos, Atanas
AU  - Stanković, Dalibor M.
AU  - Fromm, Katharina M.
AU  - Nikodinović-Runić, Jasmina
AU  - Đuran, Miloš I.
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8130
AB  - Data associated with the article "Pavic, A., Savić, N. D., Glišić, B. Đ., Crochet, A., Vojnovic, S., Kurutos, A., ... & Djuran, M. I. (2019). Silver (I) complexes with 4, 7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection. Journal of Inorganic Biochemistry."
T2  - The Cambridge Crystallographic Data Centre (CCDC)
T1  - CCDC 1879001: Experimental Crystal Structure Determination
DO  - 10.5517/ccdc.csd.cc2127yb
ER  - 
@book{
author = "Pavić, Aleksandar B. and Savić, Nada D. and Glišić, Biljana Đ. and Crochet, Aurélien and Vojnović, Sandra and Kurutos, Atanas and Stanković, Dalibor M. and Fromm, Katharina M. and Nikodinović-Runić, Jasmina and Đuran, Miloš I.",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8130",
abstract = "Data associated with the article "Pavic, A., Savić, N. D., Glišić, B. Đ., Crochet, A., Vojnovic, S., Kurutos, A., ... & Djuran, M. I. (2019). Silver (I) complexes with 4, 7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection. Journal of Inorganic Biochemistry."",
journal = "The Cambridge Crystallographic Data Centre (CCDC)",
title = "CCDC 1879001: Experimental Crystal Structure Determination",
doi = "10.5517/ccdc.csd.cc2127yb"
}
Pavić, A. B., Savić, N. D., Glišić, B. Đ., Crochet, A., Vojnović, S., Kurutos, A., Stanković, D. M., Fromm, K. M., Nikodinović-Runić, J.,& Đuran, M. I. (2019). CCDC 1879001: Experimental Crystal Structure Determination.
The Cambridge Crystallographic Data Centre (CCDC).
https://doi.org/10.5517/ccdc.csd.cc2127yb
Pavić AB, Savić ND, Glišić BĐ, Crochet A, Vojnović S, Kurutos A, Stanković DM, Fromm KM, Nikodinović-Runić J, Đuran MI. CCDC 1879001: Experimental Crystal Structure Determination. The Cambridge Crystallographic Data Centre (CCDC). 2019;
Pavić Aleksandar B., Savić Nada D., Glišić Biljana Đ., Crochet Aurélien, Vojnović Sandra, Kurutos Atanas, Stanković Dalibor M., Fromm Katharina M., Nikodinović-Runić Jasmina, Đuran Miloš I., "CCDC 1879001: Experimental Crystal Structure Determination" The Cambridge Crystallographic Data Centre (CCDC) (2019),
https://doi.org/10.5517/ccdc.csd.cc2127yb .

Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection

Pavić, Aleksandar B.; Savić, Nada D.; Glišić, Biljana Đ.; Crochet, Aurélien; Vojnović, Sandra; Kurutos, Atanas; Stanković, Dalibor M.; Fromm, Katharina M.; Nikodinović-Runić, Jasmina; Đuran, Miloš I.

(2019)

TY  - JOUR
AU  - Pavić, Aleksandar B.
AU  - Savić, Nada D.
AU  - Glišić, Biljana Đ.
AU  - Crochet, Aurélien
AU  - Vojnović, Sandra
AU  - Kurutos, Atanas
AU  - Stanković, Dalibor M.
AU  - Fromm, Katharina M.
AU  - Nikodinović-Runić, Jasmina
AU  - Đuran, Miloš I.
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8127
AB  - Five novel silver(I) complexes with 4,7-phenanthroline (4,7-phen), [Ag(NO 3 -O)(4,7-phen-μ-N4,N7)] n (1), [Ag(ClO 4 -О)(4,7-phen-μ-N4,N7)] n (2), [Ag(CF 3 COO-O)(4,7-phen-μ-N4,N7)] n (3), [Ag 2 (H 2 O) 0.58 (4,7-phen) 3 ](SbF 6 ) 2 (4) and {[Ag 2 (H 2 O)(4,7-phen-μ-N4,N7) 2 ](BF 4 ) 2 } n (5) were synthesized, structurally elucidated and biologically evaluated. These complexes showed selectivity towards Candida spp. in comparison to the tested bacteria and effectively inhibited the growth of four different Candida species, particularly of C. albicans strains, with minimal inhibitory concentrations (MICs) in the range of 2.0–10.0 μM. In order to evaluate the therapeutic potential of 1–5, in vivo toxicity studies were conducted in the zebrafish model. Based on the favorable therapeutic profiles, complexes 1, 3 and 5 were selected for the evaluation of their antifungal efficacy in vivo using the zebrafish model of lethal disseminated candidiasis. Complexes 1 and 3 efficiently controlled and prevented fungal filamentation even at sub-MIC doses, while drastically increased the survival of the infected embryos. Moreover, at the MIC doses, both complexes totally prevented C. albicans filamentation and rescued almost all infected fish of the fatal infection outcome. On the other side, complex 5, which demonstrated the highest antifungal activity in vitro, affected the neutrophils occurrence of the infected host, failed to inhibit the C. albicans cells filamentation and showed a poor potential to cure candidal infection, highlighting the importance of the in vivo activity evaluation early in the therapeutic design and development process. The mechanism of action of the investigated silver(I) complexes was related to the induction of reactive oxygen species (ROS) response in C. albicans, with DNA being one of the possible target biomolecules. © 2019 Elsevier Inc.
T2  - Journal of Inorganic Biochemistry
T1  - Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection
VL  - 195
SP  - 149
EP  - 163
DO  - 10.1016/j.jinorgbio.2019.03.017
ER  - 
@article{
author = "Pavić, Aleksandar B. and Savić, Nada D. and Glišić, Biljana Đ. and Crochet, Aurélien and Vojnović, Sandra and Kurutos, Atanas and Stanković, Dalibor M. and Fromm, Katharina M. and Nikodinović-Runić, Jasmina and Đuran, Miloš I.",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8127",
abstract = "Five novel silver(I) complexes with 4,7-phenanthroline (4,7-phen), [Ag(NO 3 -O)(4,7-phen-μ-N4,N7)] n (1), [Ag(ClO 4 -О)(4,7-phen-μ-N4,N7)] n (2), [Ag(CF 3 COO-O)(4,7-phen-μ-N4,N7)] n (3), [Ag 2 (H 2 O) 0.58 (4,7-phen) 3 ](SbF 6 ) 2 (4) and {[Ag 2 (H 2 O)(4,7-phen-μ-N4,N7) 2 ](BF 4 ) 2 } n (5) were synthesized, structurally elucidated and biologically evaluated. These complexes showed selectivity towards Candida spp. in comparison to the tested bacteria and effectively inhibited the growth of four different Candida species, particularly of C. albicans strains, with minimal inhibitory concentrations (MICs) in the range of 2.0–10.0 μM. In order to evaluate the therapeutic potential of 1–5, in vivo toxicity studies were conducted in the zebrafish model. Based on the favorable therapeutic profiles, complexes 1, 3 and 5 were selected for the evaluation of their antifungal efficacy in vivo using the zebrafish model of lethal disseminated candidiasis. Complexes 1 and 3 efficiently controlled and prevented fungal filamentation even at sub-MIC doses, while drastically increased the survival of the infected embryos. Moreover, at the MIC doses, both complexes totally prevented C. albicans filamentation and rescued almost all infected fish of the fatal infection outcome. On the other side, complex 5, which demonstrated the highest antifungal activity in vitro, affected the neutrophils occurrence of the infected host, failed to inhibit the C. albicans cells filamentation and showed a poor potential to cure candidal infection, highlighting the importance of the in vivo activity evaluation early in the therapeutic design and development process. The mechanism of action of the investigated silver(I) complexes was related to the induction of reactive oxygen species (ROS) response in C. albicans, with DNA being one of the possible target biomolecules. © 2019 Elsevier Inc.",
journal = "Journal of Inorganic Biochemistry",
title = "Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection",
volume = "195",
pages = "149-163",
doi = "10.1016/j.jinorgbio.2019.03.017"
}
Pavić, A. B., Savić, N. D., Glišić, B. Đ., Crochet, A., Vojnović, S., Kurutos, A., Stanković, D. M., Fromm, K. M., Nikodinović-Runić, J.,& Đuran, M. I. (2019). Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection.
Journal of Inorganic Biochemistry, 195, 149-163.
https://doi.org/10.1016/j.jinorgbio.2019.03.017
Pavić AB, Savić ND, Glišić BĐ, Crochet A, Vojnović S, Kurutos A, Stanković DM, Fromm KM, Nikodinović-Runić J, Đuran MI. Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection. Journal of Inorganic Biochemistry. 2019;195:149-163
Pavić Aleksandar B., Savić Nada D., Glišić Biljana Đ., Crochet Aurélien, Vojnović Sandra, Kurutos Atanas, Stanković Dalibor M., Fromm Katharina M., Nikodinović-Runić Jasmina, Đuran Miloš I., "Silver(I) complexes with 4,7-phenanthroline efficient in rescuing the zebrafish embryos of lethal Candida albicans infection" Journal of Inorganic Biochemistry, 195 (2019):149-163,
https://doi.org/10.1016/j.jinorgbio.2019.03.017 .
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Effect of magnetic nanoparticles coating on cell proliferation and uptake

Zavišova, Vlasta; Koneracka, Martina; Gabelova, Alena; Svitkova, Barbora; Ursinyova, Monika; Kubovčikova, Martina; Antal, Iryna; Khmara, Iryna; Jurikova, Alena; Molčan, Matuš; Ognjanović, Miloš; Antić, Bratislav; Kopčansky, Peter

(2019)

TY  - JOUR
AU  - Zavišova, Vlasta
AU  - Koneracka, Martina
AU  - Gabelova, Alena
AU  - Svitkova, Barbora
AU  - Ursinyova, Monika
AU  - Kubovčikova, Martina
AU  - Antal, Iryna
AU  - Khmara, Iryna
AU  - Jurikova, Alena
AU  - Molčan, Matuš
AU  - Ognjanović, Miloš
AU  - Antić, Bratislav
AU  - Kopčansky, Peter
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0304885318320183
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7906
AB  - Magnetic iron oxide nanoparticles (MNPs) are one of the most promising types of nanoparticles for biomedical applications, primarily in the context of nanomedicine-based diagnostics and therapy. They are used as contrast agents in magnetic resonance imaging and magnetite cell labelling. Furthermore, they are promising heating mediator in magnetic hyperthermia-based therapy, and can serve as nanocarriers in targeted gene and drug delivery as well. In biomedical applications, coating plays an important role in nanoparticle dispersion stability and biocompatibility. However, the impact of nanoparticle surface chemistry on cell uptake and proliferation has not been sufficiently investigated. The objective of this study is to prepare magnetic nanoparticles with inner magnetite core and hydrophilic outer shell of surfactant, protein and polymers that are commonly used in biomedical research. MNPs were characterized in-depth by various physicochemical methods. Magnetic hyperthermia, applied to find out the influence of MNPs coating on heating characteristics of the samples, did not show any correlation between layer thickness and specific adsorption rate. To evaluate the impact of surface chemistry on cell proliferation and internalization, the human lung adenocarcinoma epithelial (A549) cells were utilized. Substantial differences were determined in the amount of internalized MNPs and cell viability in dependence on surface coating. Our results indicate that the surface chemistry not only protects particles from agglomeration but also affect the interaction between cell and MNPs. © 2018 Elsevier B.V.
T2  - Journal of Magnetism and Magnetic Materials
T1  - Effect of magnetic nanoparticles coating on cell proliferation and uptake
VL  - 472
SP  - 66
EP  - 73
DO  - 10.1016/j.jmmm.2018.09.116
ER  - 
@article{
author = "Zavišova, Vlasta and Koneracka, Martina and Gabelova, Alena and Svitkova, Barbora and Ursinyova, Monika and Kubovčikova, Martina and Antal, Iryna and Khmara, Iryna and Jurikova, Alena and Molčan, Matuš and Ognjanović, Miloš and Antić, Bratislav and Kopčansky, Peter",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0304885318320183, http://vinar.vin.bg.ac.rs/handle/123456789/7906",
abstract = "Magnetic iron oxide nanoparticles (MNPs) are one of the most promising types of nanoparticles for biomedical applications, primarily in the context of nanomedicine-based diagnostics and therapy. They are used as contrast agents in magnetic resonance imaging and magnetite cell labelling. Furthermore, they are promising heating mediator in magnetic hyperthermia-based therapy, and can serve as nanocarriers in targeted gene and drug delivery as well. In biomedical applications, coating plays an important role in nanoparticle dispersion stability and biocompatibility. However, the impact of nanoparticle surface chemistry on cell uptake and proliferation has not been sufficiently investigated. The objective of this study is to prepare magnetic nanoparticles with inner magnetite core and hydrophilic outer shell of surfactant, protein and polymers that are commonly used in biomedical research. MNPs were characterized in-depth by various physicochemical methods. Magnetic hyperthermia, applied to find out the influence of MNPs coating on heating characteristics of the samples, did not show any correlation between layer thickness and specific adsorption rate. To evaluate the impact of surface chemistry on cell proliferation and internalization, the human lung adenocarcinoma epithelial (A549) cells were utilized. Substantial differences were determined in the amount of internalized MNPs and cell viability in dependence on surface coating. Our results indicate that the surface chemistry not only protects particles from agglomeration but also affect the interaction between cell and MNPs. © 2018 Elsevier B.V.",
journal = "Journal of Magnetism and Magnetic Materials",
title = "Effect of magnetic nanoparticles coating on cell proliferation and uptake",
volume = "472",
pages = "66-73",
doi = "10.1016/j.jmmm.2018.09.116"
}
Zavišova, V., Koneracka, M., Gabelova, A., Svitkova, B., Ursinyova, M., Kubovčikova, M., Antal, I., Khmara, I., Jurikova, A., Molčan, M., Ognjanović, M., Antić, B.,& Kopčansky, P. (2019). Effect of magnetic nanoparticles coating on cell proliferation and uptake.
Journal of Magnetism and Magnetic Materials, 472, 66-73.
https://doi.org/10.1016/j.jmmm.2018.09.116
Zavišova V, Koneracka M, Gabelova A, Svitkova B, Ursinyova M, Kubovčikova M, Antal I, Khmara I, Jurikova A, Molčan M, Ognjanović M, Antić B, Kopčansky P. Effect of magnetic nanoparticles coating on cell proliferation and uptake. Journal of Magnetism and Magnetic Materials. 2019;472:66-73
Zavišova Vlasta, Koneracka Martina, Gabelova Alena, Svitkova Barbora, Ursinyova Monika, Kubovčikova Martina, Antal Iryna, Khmara Iryna, Jurikova Alena, Molčan Matuš, Ognjanović Miloš, Antić Bratislav, Kopčansky Peter, "Effect of magnetic nanoparticles coating on cell proliferation and uptake" Journal of Magnetism and Magnetic Materials, 472 (2019):66-73,
https://doi.org/10.1016/j.jmmm.2018.09.116 .
21
14
19

Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia

Ognjanović, Miloš; Stanković, Dalibor M.; Ming, Yue; Zhang, Hongguo; Jančar, Boštjan; Dojčinović, Biljana P.; Prijović, Željko; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Ognjanović, Miloš
AU  - Stanković, Dalibor M.
AU  - Ming, Yue
AU  - Zhang, Hongguo
AU  - Jančar, Boštjan
AU  - Dojčinović, Biljana P.
AU  - Prijović, Željko
AU  - Antić, Bratislav
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0925838818340684
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7942
AB  - In a new approach based on a two-step procedure, co-precipitation method followed by hydrothermal treatment in a microwave field, Zn-substituted Fe3O4 nanoparticles (ZnxFe3-xO4) were synthesized. Results of XRD, FT–IR and TEM analysis clearly demonstrate that nanoparticles were single phase, crystallizing in the spinel structure type (S.G. Fd3¯m) with crystallite size in the range of 2–20 nm, which strongly depends on Zn concentration. The produced nanoparticles were used for fabrication of modified carbon paste electrodes as a novel system for electrochemical non-enzymatic glucose detection. It was found that the increase of zinc concentration up to the value of x = 0.56 (Zn0.56Fe2.44O4) of as-prepared nanoparticles was followed with an increase of a performance of the modified carbon paste electrode toward glucose detection. Linear working range from 0.1 to 2 mM was obtained with detection limit of 0.03 mM, and with fast response time (<3 s). Proposed sensor was successfully applied for the determination of glucose level in real samples with satisfactory recovery. The synthesized zinc-ferrite samples were also tested as potential heating agents in magnetic hyperthermia. The heating ability (SAR value) increases with x value, reaching maximum for x = 0.37. This is correlated with changes of particle size and magnetic characteristics which strongly depend on Zn concentration. © 2018 Elsevier B.V.
T2  - Journal of Alloys and Compounds
T1  - Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia
VL  - 777
SP  - 454
EP  - 462
DO  - 10.1016/j.jallcom.2018.10.369
ER  - 
@article{
author = "Ognjanović, Miloš and Stanković, Dalibor M. and Ming, Yue and Zhang, Hongguo and Jančar, Boštjan and Dojčinović, Biljana P. and Prijović, Željko and Antić, Bratislav",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0925838818340684, http://vinar.vin.bg.ac.rs/handle/123456789/7942",
abstract = "In a new approach based on a two-step procedure, co-precipitation method followed by hydrothermal treatment in a microwave field, Zn-substituted Fe3O4 nanoparticles (ZnxFe3-xO4) were synthesized. Results of XRD, FT–IR and TEM analysis clearly demonstrate that nanoparticles were single phase, crystallizing in the spinel structure type (S.G. Fd3¯m) with crystallite size in the range of 2–20 nm, which strongly depends on Zn concentration. The produced nanoparticles were used for fabrication of modified carbon paste electrodes as a novel system for electrochemical non-enzymatic glucose detection. It was found that the increase of zinc concentration up to the value of x = 0.56 (Zn0.56Fe2.44O4) of as-prepared nanoparticles was followed with an increase of a performance of the modified carbon paste electrode toward glucose detection. Linear working range from 0.1 to 2 mM was obtained with detection limit of 0.03 mM, and with fast response time (<3 s). Proposed sensor was successfully applied for the determination of glucose level in real samples with satisfactory recovery. The synthesized zinc-ferrite samples were also tested as potential heating agents in magnetic hyperthermia. The heating ability (SAR value) increases with x value, reaching maximum for x = 0.37. This is correlated with changes of particle size and magnetic characteristics which strongly depend on Zn concentration. © 2018 Elsevier B.V.",
journal = "Journal of Alloys and Compounds",
title = "Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia",
volume = "777",
pages = "454-462",
doi = "10.1016/j.jallcom.2018.10.369"
}
Ognjanović, M., Stanković, D. M., Ming, Y., Zhang, H., Jančar, B., Dojčinović, B. P., Prijović, Ž.,& Antić, B. (2019). Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia.
Journal of Alloys and Compounds, 777, 454-462.
https://doi.org/10.1016/j.jallcom.2018.10.369
Ognjanović M, Stanković DM, Ming Y, Zhang H, Jančar B, Dojčinović BP, Prijović Ž, Antić B. Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia. Journal of Alloys and Compounds. 2019;777:454-462
Ognjanović Miloš, Stanković Dalibor M., Ming Yue, Zhang Hongguo, Jančar Boštjan, Dojčinović Biljana P., Prijović Željko, Antić Bratislav, "Bifunctional (Zn,Fe)3O4 nanoparticles: Tuning their efficiency for potential application in reagentless glucose biosensors and magnetic hyperthermia" Journal of Alloys and Compounds, 777 (2019):454-462,
https://doi.org/10.1016/j.jallcom.2018.10.369 .
11
6
9

Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method

Kusigerski, Vladan; Illés, Erzsébet; Blanuša, Jovan; Gyergyek, Sašo; Bošković, Marko; Perović, Marija M.; Spasojević, Vojislav

(2019)

TY  - JOUR
AU  - Kusigerski, Vladan
AU  - Illés, Erzsébet
AU  - Blanuša, Jovan
AU  - Gyergyek, Sašo
AU  - Bošković, Marko
AU  - Perović, Marija M.
AU  - Spasojević, Vojislav
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7983
AB  - Ferrofluids based on magnesium substituted magnetite nanoparticles MgxFe3−xO4 (x = 0.1; 0.2; 0.4) were synthesised by a chemical co-precipitation method. Their physical properties have been compared with those of the magnetite based ferrofluid obtained by the same synthesis route. Both XRD and TEM studies showed particle size decrease with the increased Mg content while DLS experiments pointed to the more prominent aggregation of Mg-containing nanoparticles. Magnetic properties investigation conducted on the powder (i.e. dried) specimens showed decrease of magnetization values with increased Mg content except for the lowest concentration of x = 0.1 where substantial saturation magnetization rise of about 40% was recorded at room temperature. Heating abilities of the studied ferrofluids under the applied AC fields (SAR values) also showed decreasing trend with the increased Mg content even for x = 0.1 sample despite its elevated magnetization value. This trend has been understood as a consequence of the changed intrinsic nanoparticle properties such as size and magnetic anisotropy, as well as contribution of a collective behaviour due to an increased nanoparticle aggregation in Mg-doped systems.
T2  - Journal of Magnetism and Magnetic Materials
T1  - Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method
VL  - 475
SP  - 470
EP  - 478
DO  - 10.1016/j.jmmm.2018.11.127
ER  - 
@article{
author = "Kusigerski, Vladan and Illés, Erzsébet and Blanuša, Jovan and Gyergyek, Sašo and Bošković, Marko and Perović, Marija M. and Spasojević, Vojislav",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/7983",
abstract = "Ferrofluids based on magnesium substituted magnetite nanoparticles MgxFe3−xO4 (x = 0.1; 0.2; 0.4) were synthesised by a chemical co-precipitation method. Their physical properties have been compared with those of the magnetite based ferrofluid obtained by the same synthesis route. Both XRD and TEM studies showed particle size decrease with the increased Mg content while DLS experiments pointed to the more prominent aggregation of Mg-containing nanoparticles. Magnetic properties investigation conducted on the powder (i.e. dried) specimens showed decrease of magnetization values with increased Mg content except for the lowest concentration of x = 0.1 where substantial saturation magnetization rise of about 40% was recorded at room temperature. Heating abilities of the studied ferrofluids under the applied AC fields (SAR values) also showed decreasing trend with the increased Mg content even for x = 0.1 sample despite its elevated magnetization value. This trend has been understood as a consequence of the changed intrinsic nanoparticle properties such as size and magnetic anisotropy, as well as contribution of a collective behaviour due to an increased nanoparticle aggregation in Mg-doped systems.",
journal = "Journal of Magnetism and Magnetic Materials",
title = "Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method",
volume = "475",
pages = "470-478",
doi = "10.1016/j.jmmm.2018.11.127"
}
Kusigerski, V., Illés, E., Blanuša, J., Gyergyek, S., Bošković, M., Perović, M. M.,& Spasojević, V. (2019). Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method.
Journal of Magnetism and Magnetic Materials, 475, 470-478.
https://doi.org/10.1016/j.jmmm.2018.11.127
Kusigerski V, Illés E, Blanuša J, Gyergyek S, Bošković M, Perović MM, Spasojević V. Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method. Journal of Magnetism and Magnetic Materials. 2019;475:470-478
Kusigerski Vladan, Illés Erzsébet, Blanuša Jovan, Gyergyek Sašo, Bošković Marko, Perović Marija M., Spasojević Vojislav, "Magnetic properties and heating efficacy of magnesium doped magnetite nanoparticles obtained by co-precipitation method" Journal of Magnetism and Magnetic Materials, 475 (2019):470-478,
https://doi.org/10.1016/j.jmmm.2018.11.127 .
15
10
14

Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles

Ognjanović, Miloš; Spasojević, Irena; Stanković, Dalibor M.; Ming, Yue; Jančar, Boštjan; Dojčinović, Biljana P.; Spasojević, Vojislav; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Ognjanović, Miloš
AU  - Spasojević, Irena
AU  - Stanković, Dalibor M.
AU  - Ming, Yue
AU  - Jančar, Boštjan
AU  - Dojčinović, Biljana P.
AU  - Spasojević, Vojislav
AU  - Antić, Bratislav
PY  - 2019
UR  - https://www.ingentaconnect.com/content/10.1166/jnn.2019.16284
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8074
AB  - A series of MgxFe3-xO₄ (x ═ 0-1) nanoparticles was synthesized in order to prepare novel MgxFe3-xO₄/glassy carbon modified electrodes. Effects of magnesium content (x) on the analytical performance of the modified electrodes in the detection of gallic acid were evaluated. It was found that magnesium concentration and crystallite/particle size of the prepared nanoparticles play significant roles in the sensing properties of modified electrodes. The increase of magnesium concentration up to the value of x ═ 0.4 in MgxFe3-xO₄/glassy carbon paste was accompanied by an increase of the corresponding oxidation current of gallic acid. However, further growth of x value caused decline of the obtained oxidation current. An electroanalytical procedure was established, and the analytical performance of the proposed Mg0.4Fe2.6O₄/glassy carbon paste electrode was monitored using previously optimized experimental conditions. A working linear range from 1-39 µM gallic acid was obtained with detection limit of 0.29 µM. According to these results, the developed procedure can be applied for detection of low concentrations of gallic acid with satisfactory selectivity in the presence of some common naturally occurring compounds. Experimental results indicate that the developed procedure could be a novel approach in the detection of antioxidant, overcoming some known disadvantages such as passivation, and could be a promising replacement for sophisticated chromatographic methods.
T2  - Journal of Nanoscience and Nanotechnology
T1  - Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles
VL  - 19
IS  - 7
SP  - 4205
EP  - 4213
DO  - 10.1166/jnn.2019.16284
ER  - 
@article{
author = "Ognjanović, Miloš and Spasojević, Irena and Stanković, Dalibor M. and Ming, Yue and Jančar, Boštjan and Dojčinović, Biljana P. and Spasojević, Vojislav and Antić, Bratislav",
year = "2019",
url = "https://www.ingentaconnect.com/content/10.1166/jnn.2019.16284, http://vinar.vin.bg.ac.rs/handle/123456789/8074",
abstract = "A series of MgxFe3-xO₄ (x ═ 0-1) nanoparticles was synthesized in order to prepare novel MgxFe3-xO₄/glassy carbon modified electrodes. Effects of magnesium content (x) on the analytical performance of the modified electrodes in the detection of gallic acid were evaluated. It was found that magnesium concentration and crystallite/particle size of the prepared nanoparticles play significant roles in the sensing properties of modified electrodes. The increase of magnesium concentration up to the value of x ═ 0.4 in MgxFe3-xO₄/glassy carbon paste was accompanied by an increase of the corresponding oxidation current of gallic acid. However, further growth of x value caused decline of the obtained oxidation current. An electroanalytical procedure was established, and the analytical performance of the proposed Mg0.4Fe2.6O₄/glassy carbon paste electrode was monitored using previously optimized experimental conditions. A working linear range from 1-39 µM gallic acid was obtained with detection limit of 0.29 µM. According to these results, the developed procedure can be applied for detection of low concentrations of gallic acid with satisfactory selectivity in the presence of some common naturally occurring compounds. Experimental results indicate that the developed procedure could be a novel approach in the detection of antioxidant, overcoming some known disadvantages such as passivation, and could be a promising replacement for sophisticated chromatographic methods.",
journal = "Journal of Nanoscience and Nanotechnology",
title = "Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles",
volume = "19",
number = "7",
pages = "4205-4213",
doi = "10.1166/jnn.2019.16284"
}
Ognjanović, M., Spasojević, I., Stanković, D. M., Ming, Y., Jančar, B., Dojčinović, B. P., Spasojević, V.,& Antić, B. (2019). Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles.
Journal of Nanoscience and Nanotechnology, 19(7), 4205-4213.
https://doi.org/10.1166/jnn.2019.16284
Ognjanović M, Spasojević I, Stanković DM, Ming Y, Jančar B, Dojčinović BP, Spasojević V, Antić B. Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles. Journal of Nanoscience and Nanotechnology. 2019;19(7):4205-4213
Ognjanović Miloš, Spasojević Irena, Stanković Dalibor M., Ming Yue, Jančar Boštjan, Dojčinović Biljana P., Spasojević Vojislav, Antić Bratislav, "Enhancing Analytical Performance of (Mg,Fe)3O4/Glassy Carbon Electrodes by Tailoring Chemical Composition of (Mg,Fe)3O4 Nanoparticles" Journal of Nanoscience and Nanotechnology, 19, no. 7 (2019):4205-4213,
https://doi.org/10.1166/jnn.2019.16284 .

Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications

Stanković, Dalibor M.; Ognjanović, Miloš; Jović, Milica; Cuplić, Valentina; Lesch, Andreas; Girault, Hubert H.; Gavrović-Jankulović, Marija; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Stanković, Dalibor M.
AU  - Ognjanović, Miloš
AU  - Jović, Milica
AU  - Cuplić, Valentina
AU  - Lesch, Andreas
AU  - Girault, Hubert H.
AU  - Gavrović-Jankulović, Marija
AU  - Antić, Bratislav
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8342
AB  - A disposable acetaminophen biosensor based on inkjet-printed CNT electrodes (IJPCNT) modified with amidase/cerium dioxide@graphene nanoribbons composite was developed (ACeO2@GNR/IJPCNT). The enzyme amidase A was used for the first time as a recognition element. Inkjet-printed CNT electrodes served as a basis for the construction of a biosensor that enables droplet detection using 5 μL sample volume. The biosensor showed high selectivity, sensitivity, a low detection limit of 0.18 μM and a wide working linear range from 1 to 100 μM. The proposed approach allows fast and reliable detection of acetaminophen in biological fluids with negligible matrix effect and remarkable reproducibility. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
T2  - Electroanalysis
T1  - Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications
VL  - 31
IS  - 8
SP  - 1517
EP  - 1525
DO  - 10.1002/elan.201900129
ER  - 
@article{
author = "Stanković, Dalibor M. and Ognjanović, Miloš and Jović, Milica and Cuplić, Valentina and Lesch, Andreas and Girault, Hubert H. and Gavrović-Jankulović, Marija and Antić, Bratislav",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8342",
abstract = "A disposable acetaminophen biosensor based on inkjet-printed CNT electrodes (IJPCNT) modified with amidase/cerium dioxide@graphene nanoribbons composite was developed (ACeO2@GNR/IJPCNT). The enzyme amidase A was used for the first time as a recognition element. Inkjet-printed CNT electrodes served as a basis for the construction of a biosensor that enables droplet detection using 5 μL sample volume. The biosensor showed high selectivity, sensitivity, a low detection limit of 0.18 μM and a wide working linear range from 1 to 100 μM. The proposed approach allows fast and reliable detection of acetaminophen in biological fluids with negligible matrix effect and remarkable reproducibility. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim",
journal = "Electroanalysis",
title = "Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications",
volume = "31",
number = "8",
pages = "1517-1525",
doi = "10.1002/elan.201900129"
}
Stanković, D. M., Ognjanović, M., Jović, M., Cuplić, V., Lesch, A., Girault, H. H., Gavrović-Jankulović, M.,& Antić, B. (2019). Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications.
Electroanalysis, 31(8), 1517-1525.
https://doi.org/10.1002/elan.201900129
Stanković DM, Ognjanović M, Jović M, Cuplić V, Lesch A, Girault HH, Gavrović-Jankulović M, Antić B. Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications. Electroanalysis. 2019;31(8):1517-1525
Stanković Dalibor M., Ognjanović Miloš, Jović Milica, Cuplić Valentina, Lesch Andreas, Girault Hubert H., Gavrović-Jankulović Marija, Antić Bratislav, "Disposable Biosensor Based on Amidase/CeO2/GNR Modified Inkjet‐printed CNT Electrodes‐droplet Based Paracetamol Detection in Biological Fluids for “Point‐of‐care” Applications" Electroanalysis, 31, no. 8 (2019):1517-1525,
https://doi.org/10.1002/elan.201900129 .
6
4
6

Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species

Dojčinović, Biljana P.; Jančar, Boštjan; Bessais, Lotfi; Kremenović, Aleksandar S.; Jović-Jovičić, Nataša P.; Banković, Predrag T.; Stanković, Dalibor M.; Ognjanović, Miloš; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Dojčinović, Biljana P.
AU  - Jančar, Boštjan
AU  - Bessais, Lotfi
AU  - Kremenović, Aleksandar S.
AU  - Jović-Jovičić, Nataša P.
AU  - Banković, Predrag T.
AU  - Stanković, Dalibor M.
AU  - Ognjanović, Miloš
AU  - Antić, Bratislav
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8612
AB  - Herein we report effects of partial substitution of Fe3+ by Y3+ in magnetite (Fe3O4) on morphology and inorganic arsenic species adsorption efficiency of the Fe3-xYxO4 nanoparticles formed. The series of Fe3-xYxO4 (x = 0.00, 0.042 and 0.084, labeled as Y00, Y05 and Y10, respectively) was synthesized using co-precipitation followed by microwave-hydrothermal treatment (MW) at 200 degrees C. With increase of yttrium content (x value), both the morphological inhomogeneity of the samples and the fraction of spinel nanorods as compared to spinel pseudospherical particles increased. By both transmission electron microscopy and x-ray powder diffraction analyses, it was determined that the direction of growth of the spinel nanorods is along the [110] crystallographic direction. The Fe3-xYxO4 affinities of adsorption toward the inorganic arsenic species, As(III) (arsenite, AsO33-) and As(V) (arsenate, AsO43-), were investigated. Increased Y3+ content related to changes in sample morphology was followed by a decrease of As(III) removal efficiency and vice versa for As(V). The increase in Y3+ content, in addition to increasing the adsorption capacity for As(V), significantly expanded the optimum pH range for the maximum removal and decreased the contact time for necessary 50% removal (t(1/2)) of As(V) (Y00: pH 2-3, t(1/2) = 3.12 min; Y05: pH 2-6, t(1/2) = 2.12 min and Y10: pH 2-10, t(1/2) = 1.12 min). The results point to incorporation of Y3+ in the crystal lattice of magnetite, inducing nanorod spinel structure formation with significant changes in sorption properties important for the removal of inorganic arsenic from waters.
T2  - Nanotechnology
T1  - Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species
VL  - 30
IS  - 47
SP  - 475702
DO  - 10.1088/1361-6528/ab3ca2
ER  - 
@article{
author = "Dojčinović, Biljana P. and Jančar, Boštjan and Bessais, Lotfi and Kremenović, Aleksandar S. and Jović-Jovičić, Nataša P. and Banković, Predrag T. and Stanković, Dalibor M. and Ognjanović, Miloš and Antić, Bratislav",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8612",
abstract = "Herein we report effects of partial substitution of Fe3+ by Y3+ in magnetite (Fe3O4) on morphology and inorganic arsenic species adsorption efficiency of the Fe3-xYxO4 nanoparticles formed. The series of Fe3-xYxO4 (x = 0.00, 0.042 and 0.084, labeled as Y00, Y05 and Y10, respectively) was synthesized using co-precipitation followed by microwave-hydrothermal treatment (MW) at 200 degrees C. With increase of yttrium content (x value), both the morphological inhomogeneity of the samples and the fraction of spinel nanorods as compared to spinel pseudospherical particles increased. By both transmission electron microscopy and x-ray powder diffraction analyses, it was determined that the direction of growth of the spinel nanorods is along the [110] crystallographic direction. The Fe3-xYxO4 affinities of adsorption toward the inorganic arsenic species, As(III) (arsenite, AsO33-) and As(V) (arsenate, AsO43-), were investigated. Increased Y3+ content related to changes in sample morphology was followed by a decrease of As(III) removal efficiency and vice versa for As(V). The increase in Y3+ content, in addition to increasing the adsorption capacity for As(V), significantly expanded the optimum pH range for the maximum removal and decreased the contact time for necessary 50% removal (t(1/2)) of As(V) (Y00: pH 2-3, t(1/2) = 3.12 min; Y05: pH 2-6, t(1/2) = 2.12 min and Y10: pH 2-10, t(1/2) = 1.12 min). The results point to incorporation of Y3+ in the crystal lattice of magnetite, inducing nanorod spinel structure formation with significant changes in sorption properties important for the removal of inorganic arsenic from waters.",
journal = "Nanotechnology",
title = "Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species",
volume = "30",
number = "47",
pages = "475702",
doi = "10.1088/1361-6528/ab3ca2"
}
Dojčinović, B. P., Jančar, B., Bessais, L., Kremenović, A. S., Jović-Jovičić, N. P., Banković, P. T., Stanković, D. M., Ognjanović, M.,& Antić, B. (2019). Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species.
Nanotechnology, 30(47), 475702.
https://doi.org/10.1088/1361-6528/ab3ca2
Dojčinović BP, Jančar B, Bessais L, Kremenović AS, Jović-Jovičić NP, Banković PT, Stanković DM, Ognjanović M, Antić B. Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species. Nanotechnology. 2019;30(47):475702
Dojčinović Biljana P., Jančar Boštjan, Bessais Lotfi, Kremenović Aleksandar S., Jović-Jovičić Nataša P., Banković Predrag T., Stanković Dalibor M., Ognjanović Miloš, Antić Bratislav, "Differently shaped nanocrystalline (Fe, Y)3O4 and its adsorption efficiency toward inorganic arsenic species" Nanotechnology, 30, no. 47 (2019):475702,
https://doi.org/10.1088/1361-6528/ab3ca2 .
2
2
2

Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres

Stanković, Dalibor M.; Jović, Milica; Ognjanović, Miloš; Lesch, Andreas; Fabian, Martin; Girault, Hubert H.; Antić, Bratislav

(2019)

TY  - JOUR
AU  - Stanković, Dalibor M.
AU  - Jović, Milica
AU  - Ognjanović, Miloš
AU  - Lesch, Andreas
AU  - Fabian, Martin
AU  - Girault, Hubert H.
AU  - Antić, Bratislav
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8394
AB  - An electrochemical sensor is described for the determination of L-dopa (levodopa; 3,4-dihydroxyphenylalanine). An inkjet-printed carbon nanotube (IJPCNT) electrode was modified with manganese dioxide microspheres by drop-casting. They coating was characterized by field emission scanning electron microscopy, Fourier-transform infrared spectroscopy and X-ray powder diffraction. The sensor, best operated at a working voltage of 0.3 V, has a linear response in the 0.1 to 10 μM L-dopa concentration range, a 54 nM detection limit, excellent reproducibility, repeatability and selectivity. The amperometric approach was applied to the determination of L-dopa in spiked biological fluids and displayed satisfactory accuracy and precision. [Figure not available: see fulltext.]. © 2019, Springer-Verlag GmbH Austria, part of Springer Nature.
T2  - Microchimica Acta
T1  - Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres
VL  - 186
IS  - 8
SP  - 532
DO  - 10.1007/s00604-019-3644-x
ER  - 
@article{
author = "Stanković, Dalibor M. and Jović, Milica and Ognjanović, Miloš and Lesch, Andreas and Fabian, Martin and Girault, Hubert H. and Antić, Bratislav",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8394",
abstract = "An electrochemical sensor is described for the determination of L-dopa (levodopa; 3,4-dihydroxyphenylalanine). An inkjet-printed carbon nanotube (IJPCNT) electrode was modified with manganese dioxide microspheres by drop-casting. They coating was characterized by field emission scanning electron microscopy, Fourier-transform infrared spectroscopy and X-ray powder diffraction. The sensor, best operated at a working voltage of 0.3 V, has a linear response in the 0.1 to 10 μM L-dopa concentration range, a 54 nM detection limit, excellent reproducibility, repeatability and selectivity. The amperometric approach was applied to the determination of L-dopa in spiked biological fluids and displayed satisfactory accuracy and precision. [Figure not available: see fulltext.]. © 2019, Springer-Verlag GmbH Austria, part of Springer Nature.",
journal = "Microchimica Acta",
title = "Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres",
volume = "186",
number = "8",
pages = "532",
doi = "10.1007/s00604-019-3644-x"
}
Stanković, D. M., Jović, M., Ognjanović, M., Lesch, A., Fabian, M., Girault, H. H.,& Antić, B. (2019). Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres.
Microchimica Acta, 186(8), 532.
https://doi.org/10.1007/s00604-019-3644-x
Stanković DM, Jović M, Ognjanović M, Lesch A, Fabian M, Girault HH, Antić B. Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres. Microchimica Acta. 2019;186(8):532
Stanković Dalibor M., Jović Milica, Ognjanović Miloš, Lesch Andreas, Fabian Martin, Girault Hubert H., Antić Bratislav, "Point-of-care amperometric determination of L-dopa using an inkjet-printed carbon nanotube electrode modified with dandelion-like MnO2 microspheres" Microchimica Acta, 186, no. 8 (2019):532,
https://doi.org/10.1007/s00604-019-3644-x .
15
10
12

First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach

Vukojević, Vesna; Djurdjić, Sladjana; Jevtić, Sonja; Pergal, Marija V.; Marković, Aleksandar; Mutić, Jelena J.; Petković, Branka B.; Stanković, Dalibor M.

(2018)

TY  - JOUR
AU  - Vukojević, Vesna
AU  - Djurdjić, Sladjana
AU  - Jevtić, Sonja
AU  - Pergal, Marija V.
AU  - Marković, Aleksandar
AU  - Mutić, Jelena J.
AU  - Petković, Branka B.
AU  - Stanković, Dalibor M.
PY  - 2018
UR  - https://www.tandfonline.com/doi/full/10.1080/03067319.2018.1537394
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7966
AB  - In this work, the electrochemical behaviour and the subsequent development of an analytical procedure for quantification of pesticide azamethiphos, using boron-doped diamond (BDD) electrode are reported for the first time. It was found that azamethiphos electrochemical behaviour is irreversible oxidation at the potential of around 1.70 V, in 1 M nitric acid (pH 0). Also, it was found that potential of this oxidation was not pH dependent which can be attributed to the no proton involvement in electrochemical reaction on the electrode surface. The square wave voltammetric method was most appropriate for azamethiphos quantification. Under optimised experimental conditions, linear working range from 2 to 100 µM was estimated with the detection limit of 0.45 µM. Negligible effect of the possible interfering compound was observed. The obtained results show that the developed analytical methodology can be an adequate replacement for the, up to date, used methods for detection of organophosphorous pesticide. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
T2  - International Journal of Environmental Analytical Chemistry
T1  - First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach
VL  - 98
IS  - 13
SP  - 1175
EP  - 1185
DO  - 10.1080/03067319.2018.1537394
ER  - 
@article{
author = "Vukojević, Vesna and Djurdjić, Sladjana and Jevtić, Sonja and Pergal, Marija V. and Marković, Aleksandar and Mutić, Jelena J. and Petković, Branka B. and Stanković, Dalibor M.",
year = "2018",
url = "https://www.tandfonline.com/doi/full/10.1080/03067319.2018.1537394, http://vinar.vin.bg.ac.rs/handle/123456789/7966",
abstract = "In this work, the electrochemical behaviour and the subsequent development of an analytical procedure for quantification of pesticide azamethiphos, using boron-doped diamond (BDD) electrode are reported for the first time. It was found that azamethiphos electrochemical behaviour is irreversible oxidation at the potential of around 1.70 V, in 1 M nitric acid (pH 0). Also, it was found that potential of this oxidation was not pH dependent which can be attributed to the no proton involvement in electrochemical reaction on the electrode surface. The square wave voltammetric method was most appropriate for azamethiphos quantification. Under optimised experimental conditions, linear working range from 2 to 100 µM was estimated with the detection limit of 0.45 µM. Negligible effect of the possible interfering compound was observed. The obtained results show that the developed analytical methodology can be an adequate replacement for the, up to date, used methods for detection of organophosphorous pesticide. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.",
journal = "International Journal of Environmental Analytical Chemistry",
title = "First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach",
volume = "98",
number = "13",
pages = "1175-1185",
doi = "10.1080/03067319.2018.1537394"
}
Vukojević, V., Djurdjić, S., Jevtić, S., Pergal, M. V., Marković, A., Mutić, J. J., Petković, B. B.,& Stanković, D. M. (2018). First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach.
International Journal of Environmental Analytical Chemistry, 98(13), 1175-1185.
https://doi.org/10.1080/03067319.2018.1537394
Vukojević V, Djurdjić S, Jevtić S, Pergal MV, Marković A, Mutić JJ, Petković BB, Stanković DM. First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach. International Journal of Environmental Analytical Chemistry. 2018;98(13):1175-1185
Vukojević Vesna, Djurdjić Sladjana, Jevtić Sonja, Pergal Marija V., Marković Aleksandar, Mutić Jelena J., Petković Branka B., Stanković Dalibor M., "First electrochemical investigation of organophosphorus pesticide azametiphos and its quantification using electroanalytical approach" International Journal of Environmental Analytical Chemistry, 98, no. 13 (2018):1175-1185,
https://doi.org/10.1080/03067319.2018.1537394 .
5
3
4

Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide

Pergal, Marija V.; Kodranov, Igor D.; Pergal, Miodrag M.; Dojčinović, Biljana P.; Stanković, Dalibor M.; Petković, Branka B.; Manojlović, Dragan D.

(2018)

TY  - JOUR
AU  - Pergal, Marija V.
AU  - Kodranov, Igor D.
AU  - Pergal, Miodrag M.
AU  - Dojčinović, Biljana P.
AU  - Stanković, Dalibor M.
AU  - Petković, Branka B.
AU  - Manojlović, Dragan D.
PY  - 2018
UR  - http://link.springer.com/10.1007/s11270-018-3947-2
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7847
AB  - The degradation of two sulfonylurea herbicides, nicosulfuron and thifensulfuron methyl in water by chlorine dioxide, was studied for the first time in this paper. In order to examine the optimal parameters for degradation of both herbicides, degradation was investigated under light or dark conditions with different amount of chlorine dioxide, different degradation periods, and at different pH values. Degradation efficiency of herbicides was monitored using high-performance liquid chromatography with photodiode array detection (HPLC-DAD). The degradation products were analyzed by gas chromatography with triple quadrupole mass detector (GC–QQQ). Three products were identified after degradation of nicosulfuron and two products after degradation of thifensulfuron methyl. Total organic analysis (TOC) gave insight into some differences in degradation mechanisms and degrees of mineralization after degradation of the herbicides using chlorine dioxide. A simple mechanism of herbicide degradation was proposed. Acute toxicity tests were performed on the products produced after degradation with chlorine dioxide, and the results showed that the degradation products were less toxic than the parent compounds. The findings of the present study are very useful for the treatment of wastewaters contaminated with herbicides. © 2018, Springer Nature Switzerland AG.
T2  - Water, Air, & Soil Pollution
T1  - Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide
VL  - 229
IS  - 9
SP  - 287
DO  - 10.1007/s11270-018-3947-2
ER  - 
@article{
author = "Pergal, Marija V. and Kodranov, Igor D. and Pergal, Miodrag M. and Dojčinović, Biljana P. and Stanković, Dalibor M. and Petković, Branka B. and Manojlović, Dragan D.",
year = "2018",
url = "http://link.springer.com/10.1007/s11270-018-3947-2, http://vinar.vin.bg.ac.rs/handle/123456789/7847",
abstract = "The degradation of two sulfonylurea herbicides, nicosulfuron and thifensulfuron methyl in water by chlorine dioxide, was studied for the first time in this paper. In order to examine the optimal parameters for degradation of both herbicides, degradation was investigated under light or dark conditions with different amount of chlorine dioxide, different degradation periods, and at different pH values. Degradation efficiency of herbicides was monitored using high-performance liquid chromatography with photodiode array detection (HPLC-DAD). The degradation products were analyzed by gas chromatography with triple quadrupole mass detector (GC–QQQ). Three products were identified after degradation of nicosulfuron and two products after degradation of thifensulfuron methyl. Total organic analysis (TOC) gave insight into some differences in degradation mechanisms and degrees of mineralization after degradation of the herbicides using chlorine dioxide. A simple mechanism of herbicide degradation was proposed. Acute toxicity tests were performed on the products produced after degradation with chlorine dioxide, and the results showed that the degradation products were less toxic than the parent compounds. The findings of the present study are very useful for the treatment of wastewaters contaminated with herbicides. © 2018, Springer Nature Switzerland AG.",
journal = "Water, Air, & Soil Pollution",
title = "Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide",
volume = "229",
number = "9",
pages = "287",
doi = "10.1007/s11270-018-3947-2"
}
Pergal, M. V., Kodranov, I. D., Pergal, M. M., Dojčinović, B. P., Stanković, D. M., Petković, B. B.,& Manojlović, D. D. (2018). Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide.
Water, Air, & Soil Pollution, 229(9), 287.
https://doi.org/10.1007/s11270-018-3947-2
Pergal MV, Kodranov ID, Pergal MM, Dojčinović BP, Stanković DM, Petković BB, Manojlović DD. Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide. Water, Air, & Soil Pollution. 2018;229(9):287
Pergal Marija V., Kodranov Igor D., Pergal Miodrag M., Dojčinović Biljana P., Stanković Dalibor M., Petković Branka B., Manojlović Dragan D., "Assessment of Degradation of Sulfonylurea Herbicides in Water by Chlorine Dioxide" Water, Air, & Soil Pollution, 229, no. 9 (2018):287,
https://doi.org/10.1007/s11270-018-3947-2 .
1
3
4
4

First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product

Jevtić, Sonja; Vukojević, Vesna; Đurđić, Slađana; Pergal, Marija V.; Manojlović, Dragan D.; Petković, Branka B.; Stanković, Dalibor M.

(2018)

TY  - JOUR
AU  - Jevtić, Sonja
AU  - Vukojević, Vesna
AU  - Đurđić, Slađana
AU  - Pergal, Marija V.
AU  - Manojlović, Dragan D.
AU  - Petković, Branka B.
AU  - Stanković, Dalibor M.
PY  - 2018
UR  - http://linkinghub.elsevier.com/retrieve/pii/S0013468618310089
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7689
AB  - This work present a new approach for the detection of relatively new herbicide pethoxamid (POA), a first electrochemical behavior and determination based on its oxidation on boron-doped diamond electrode in Britton-Robinson buffer solution at pH 4. Square wave voltammetric technique was used for quantification of POA at anodic potential of 1.35 V vs reference Ag/AgCl electrode. The proposed electroanalytical method is operational in the linear working range from 3 to 100 μM of POA with a limit of detection of 1.37 μM. The developed analytical procedure was successfully tested for determination of this herbicide in standard/spiked river water samples and commercial herbicide Successor T SE/spiked river water samples, offering a simple, fast and inexpensive alternative way of pesticide determining to chromatographic methods employed for this purpose.
T2  - Electrochimica Acta
T1  - First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product
VL  - 277
SP  - 136
EP  - 142
DO  - 10.1016/j.electacta.2018.05.004
ER  - 
@article{
author = "Jevtić, Sonja and Vukojević, Vesna and Đurđić, Slađana and Pergal, Marija V. and Manojlović, Dragan D. and Petković, Branka B. and Stanković, Dalibor M.",
year = "2018",
url = "http://linkinghub.elsevier.com/retrieve/pii/S0013468618310089, http://vinar.vin.bg.ac.rs/handle/123456789/7689",
abstract = "This work present a new approach for the detection of relatively new herbicide pethoxamid (POA), a first electrochemical behavior and determination based on its oxidation on boron-doped diamond electrode in Britton-Robinson buffer solution at pH 4. Square wave voltammetric technique was used for quantification of POA at anodic potential of 1.35 V vs reference Ag/AgCl electrode. The proposed electroanalytical method is operational in the linear working range from 3 to 100 μM of POA with a limit of detection of 1.37 μM. The developed analytical procedure was successfully tested for determination of this herbicide in standard/spiked river water samples and commercial herbicide Successor T SE/spiked river water samples, offering a simple, fast and inexpensive alternative way of pesticide determining to chromatographic methods employed for this purpose.",
journal = "Electrochimica Acta",
title = "First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product",
volume = "277",
pages = "136-142",
doi = "10.1016/j.electacta.2018.05.004"
}
Jevtić, S., Vukojević, V., Đurđić, S., Pergal, M. V., Manojlović, D. D., Petković, B. B.,& Stanković, D. M. (2018). First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product.
Electrochimica Acta, 277, 136-142.
https://doi.org/10.1016/j.electacta.2018.05.004
Jevtić S, Vukojević V, Đurđić S, Pergal MV, Manojlović DD, Petković BB, Stanković DM. First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product. Electrochimica Acta. 2018;277:136-142
Jevtić Sonja, Vukojević Vesna, Đurđić Slađana, Pergal Marija V., Manojlović Dragan D., Petković Branka B., Stanković Dalibor M., "First electrochemistry of herbicide pethoxamid and its quantification using electroanalytical approach from mixed commercial product" Electrochimica Acta, 277 (2018):136-142,
https://doi.org/10.1016/j.electacta.2018.05.004 .
10
6
9

Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode

Đurđić, Slađana; Vukojević, Vesna; Jevtić, Sonja; Pergal, Marija V.; Petković, Branka B.; Stanković, Dalibor M.

(2018)

TY  - JOUR
AU  - Đurđić, Slađana
AU  - Vukojević, Vesna
AU  - Jevtić, Sonja
AU  - Pergal, Marija V.
AU  - Petković, Branka B.
AU  - Stanković, Dalibor M.
PY  - 2018
UR  - http://www.electrochemsci.org/abstracts/vol13/130302791.pdf
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7661
AB  - In this work, for the first time we proposed electrochemical behavior and development of an analytical procedure for quantification of pesticide clomazone. Electrochemical behavior of clomazone's at boron-doped diamond electrode is characterized with irreversible oxidation at potential of around 1.6 V, in Britton-Robinson buffer solution at pH 2. It was found that potential of this oxidation was not pH dependent excluding presence of proton in the electrochemical reaction. Square wave voltammetry method was the most appropriate for clomazone quantification and proposed procedure was successfully applied for determination of clomazone in river water samples. Obtained parameters, detection limit of 0.21 mu M and working linear range from 1 to 100 mu M and satisfied selectivity can indicate that presented results open new field in research of this group of pesticides and offer possible replacement to the sophisticated and expensive chromatographic methods.
T2  - International Journal of Electrochemical Science
T1  - Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode
VL  - 13
IS  - 3
SP  - 2791
EP  - 2799
DO  - 10.20964/2018.03.39
ER  - 
@article{
author = "Đurđić, Slađana and Vukojević, Vesna and Jevtić, Sonja and Pergal, Marija V. and Petković, Branka B. and Stanković, Dalibor M.",
year = "2018",
url = "http://www.electrochemsci.org/abstracts/vol13/130302791.pdf, http://vinar.vin.bg.ac.rs/handle/123456789/7661",
abstract = "In this work, for the first time we proposed electrochemical behavior and development of an analytical procedure for quantification of pesticide clomazone. Electrochemical behavior of clomazone's at boron-doped diamond electrode is characterized with irreversible oxidation at potential of around 1.6 V, in Britton-Robinson buffer solution at pH 2. It was found that potential of this oxidation was not pH dependent excluding presence of proton in the electrochemical reaction. Square wave voltammetry method was the most appropriate for clomazone quantification and proposed procedure was successfully applied for determination of clomazone in river water samples. Obtained parameters, detection limit of 0.21 mu M and working linear range from 1 to 100 mu M and satisfied selectivity can indicate that presented results open new field in research of this group of pesticides and offer possible replacement to the sophisticated and expensive chromatographic methods.",
journal = "International Journal of Electrochemical Science",
title = "Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode",
volume = "13",
number = "3",
pages = "2791-2799",
doi = "10.20964/2018.03.39"
}
Đurđić, S., Vukojević, V., Jevtić, S., Pergal, M. V., Petković, B. B.,& Stanković, D. M. (2018). Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode.
International Journal of Electrochemical Science, 13(3), 2791-2799.
https://doi.org/10.20964/2018.03.39
Đurđić S, Vukojević V, Jevtić S, Pergal MV, Petković BB, Stanković DM. Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode. International Journal of Electrochemical Science. 2018;13(3):2791-2799
Đurđić Slađana, Vukojević Vesna, Jevtić Sonja, Pergal Marija V., Petković Branka B., Stanković Dalibor M., "Herbicide clomazone detection using electroanalytical approach using boron doped diamond electrode" International Journal of Electrochemical Science, 13, no. 3 (2018):2791-2799,
https://doi.org/10.20964/2018.03.39 .
4
5
6

Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples

Jevtić, Sonja; Stefanović, Anđela; Stanković, Dalibor M.; Pergal, Marija V.; Ivanović, Aleksandra T.; Jokić, Anja; Petković, Branka B.

(2018)

TY  - JOUR
AU  - Jevtić, Sonja
AU  - Stefanović, Anđela
AU  - Stanković, Dalibor M.
AU  - Pergal, Marija V.
AU  - Ivanović, Aleksandra T.
AU  - Jokić, Anja
AU  - Petković, Branka B.
PY  - 2018
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7589
AB  - Bentazone (BZ) is selective contact-past herbicide with suspected reproductive toxicity potential for human due to possible contamination of ground and surface waters. This work presents simple, rapid, sensitive and accurate determination of bentazone at unmodified boron-doped diamond electrode, using differential pulse voltammetry in Britton-Robinson buffer (pH 4, oxidation peak at 1.0 V). Under optimized DPV conditions linear calibration curve was obtained for range of 2 to 100 mu M, with a detection limit of 0.5 mu M. The effect of possible interfering agents is negligible, confirming good selectivity of the method. The method was successfully applied to determination of bentazone in spiked river water samples. This electrochemical determination of bentazone represents a favorable alternative to other used time-consuming and expensive analytical techniques and procedures.
T2  - Diamond and Related Materials
T1  - Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples
VL  - 81
SP  - 133
EP  - 137
DO  - 10.1016/j.diamond.2017.12.009
ER  - 
@article{
author = "Jevtić, Sonja and Stefanović, Anđela and Stanković, Dalibor M. and Pergal, Marija V. and Ivanović, Aleksandra T. and Jokić, Anja and Petković, Branka B.",
year = "2018",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/7589",
abstract = "Bentazone (BZ) is selective contact-past herbicide with suspected reproductive toxicity potential for human due to possible contamination of ground and surface waters. This work presents simple, rapid, sensitive and accurate determination of bentazone at unmodified boron-doped diamond electrode, using differential pulse voltammetry in Britton-Robinson buffer (pH 4, oxidation peak at 1.0 V). Under optimized DPV conditions linear calibration curve was obtained for range of 2 to 100 mu M, with a detection limit of 0.5 mu M. The effect of possible interfering agents is negligible, confirming good selectivity of the method. The method was successfully applied to determination of bentazone in spiked river water samples. This electrochemical determination of bentazone represents a favorable alternative to other used time-consuming and expensive analytical techniques and procedures.",
journal = "Diamond and Related Materials",
title = "Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples",
volume = "81",
pages = "133-137",
doi = "10.1016/j.diamond.2017.12.009"
}
Jevtić, S., Stefanović, A., Stanković, D. M., Pergal, M. V., Ivanović, A. T., Jokić, A.,& Petković, B. B. (2018). Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples.
Diamond and Related Materials, 81, 133-137.
https://doi.org/10.1016/j.diamond.2017.12.009
Jevtić S, Stefanović A, Stanković DM, Pergal MV, Ivanović AT, Jokić A, Petković BB. Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples. Diamond and Related Materials. 2018;81:133-137
Jevtić Sonja, Stefanović Anđela, Stanković Dalibor M., Pergal Marija V., Ivanović Aleksandra T., Jokić Anja, Petković Branka B., "Boron-doped diamond electrode - A prestigious unmodified carbon electrode for simple and fast determination of bentazone in river water samples" Diamond and Related Materials, 81 (2018):133-137,
https://doi.org/10.1016/j.diamond.2017.12.009 .
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A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media

Gavrilov, Nemanja M.; Momčilović, Milan Z.; Dobrota, Ana S.; Stanković, Dalibor M.; Jokić, Bojan M.; Babić, Biljana M.; Skorodumova, Natalia V.; Mentus, Slavko V.; Pašti, Igor A.

(2018)

TY  - JOUR
AU  - Gavrilov, Nemanja M.
AU  - Momčilović, Milan Z.
AU  - Dobrota, Ana S.
AU  - Stanković, Dalibor M.
AU  - Jokić, Bojan M.
AU  - Babić, Biljana M.
AU  - Skorodumova, Natalia V.
AU  - Mentus, Slavko V.
AU  - Pašti, Igor A.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0257897218305838
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7727
AB  - The incorporation of trace amounts (<0.2%) of Co and Ni noticeably enhanced the catalytic activity of nitrogen-free ordered mesoporous carbon (OMC) towards oxygen reduction reaction (ORR). (Co,Ni)-doped OMCs were characterized by N2-adsorption measurements, X-ray powder diffraction, field emission scanning electron microscopy and Raman spectroscopy methods, and their ORR activity was estimated by voltammetry on rotating disk electrode in acidic and alkaline media. (Co,Ni)-doped OMCs show modest activities in acidic media, while the catalytic activity in alkaline media is rather high. The measured activities are compared to the Pt-based and Pt-free ORR catalysts reported in the literature. The number of electrons consumed per O2in metal-doped OMCs was found to vary between 2 and 4, which is advantageous in comparison to metal-free OMC. Also, the mass activities of metal-doped OMCs were found to be up to 2.5 times higher compared to that of metal-free OMC. We suggest that the ORR activity is governed by a balance between (i) textural properties, which determine the electrochemically accessible surface of the catalyst and which are influenced by the addition of a metal precursor, and (ii) novel active sites formed upon the introduction of metals into the carbon structure. In particular, our Density Functional Theory calculations suggest that Co and Ni atoms embedded into the single vacancies of graphene can activate the O2molecule and contribute to the decomposition of peroxide.
T2  - Surface and Coatings Technology
T1  - A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media
VL  - 349
SP  - 511
EP  - 521
DO  - 10.1016/j.surfcoat.2018.06.008
ER  - 
@article{
author = "Gavrilov, Nemanja M. and Momčilović, Milan Z. and Dobrota, Ana S. and Stanković, Dalibor M. and Jokić, Bojan M. and Babić, Biljana M. and Skorodumova, Natalia V. and Mentus, Slavko V. and Pašti, Igor A.",
year = "2018",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0257897218305838, http://vinar.vin.bg.ac.rs/handle/123456789/7727",
abstract = "The incorporation of trace amounts (<0.2%) of Co and Ni noticeably enhanced the catalytic activity of nitrogen-free ordered mesoporous carbon (OMC) towards oxygen reduction reaction (ORR). (Co,Ni)-doped OMCs were characterized by N2-adsorption measurements, X-ray powder diffraction, field emission scanning electron microscopy and Raman spectroscopy methods, and their ORR activity was estimated by voltammetry on rotating disk electrode in acidic and alkaline media. (Co,Ni)-doped OMCs show modest activities in acidic media, while the catalytic activity in alkaline media is rather high. The measured activities are compared to the Pt-based and Pt-free ORR catalysts reported in the literature. The number of electrons consumed per O2in metal-doped OMCs was found to vary between 2 and 4, which is advantageous in comparison to metal-free OMC. Also, the mass activities of metal-doped OMCs were found to be up to 2.5 times higher compared to that of metal-free OMC. We suggest that the ORR activity is governed by a balance between (i) textural properties, which determine the electrochemically accessible surface of the catalyst and which are influenced by the addition of a metal precursor, and (ii) novel active sites formed upon the introduction of metals into the carbon structure. In particular, our Density Functional Theory calculations suggest that Co and Ni atoms embedded into the single vacancies of graphene can activate the O2molecule and contribute to the decomposition of peroxide.",
journal = "Surface and Coatings Technology",
title = "A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media",
volume = "349",
pages = "511-521",
doi = "10.1016/j.surfcoat.2018.06.008"
}
Gavrilov, N. M., Momčilović, M. Z., Dobrota, A. S., Stanković, D. M., Jokić, B. M., Babić, B. M., Skorodumova, N. V., Mentus, S. V.,& Pašti, I. A. (2018). A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media.
Surface and Coatings Technology, 349, 511-521.
https://doi.org/10.1016/j.surfcoat.2018.06.008
Gavrilov NM, Momčilović MZ, Dobrota AS, Stanković DM, Jokić BM, Babić BM, Skorodumova NV, Mentus SV, Pašti IA. A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media. Surface and Coatings Technology. 2018;349:511-521
Gavrilov Nemanja M., Momčilović Milan Z., Dobrota Ana S., Stanković Dalibor M., Jokić Bojan M., Babić Biljana M., Skorodumova Natalia V., Mentus Slavko V., Pašti Igor A., "A study of ordered mesoporous carbon doped with Co and Ni as a catalyst of oxygen reduction reaction in both alkaline and acidic media" Surface and Coatings Technology, 349 (2018):511-521,
https://doi.org/10.1016/j.surfcoat.2018.06.008 .
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Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH

Korać, Jelena; Stanković, Dalibor M.; Stanić, Marina; Bajuk-Bogdanović, Danica V.; Žižić, Milan; Bogdanović-Pristov, Jelena; Grgurić-Šipka, Sanja; Popović-Bijelić, Ana D.; Spasojević, Ivan

(2018)

TY  - JOUR
AU  - Korać, Jelena
AU  - Stanković, Dalibor M.
AU  - Stanić, Marina
AU  - Bajuk-Bogdanović, Danica V.
AU  - Žižić, Milan
AU  - Bogdanović-Pristov, Jelena
AU  - Grgurić-Šipka, Sanja
AU  - Popović-Bijelić, Ana D.
AU  - Spasojević, Ivan
PY  - 2018
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7582
AB  - Coordinate and redox interactions of epinephrine (Epi) with iron at physiological pH are essential for understanding two very different phenomena - the detrimental effects of chronic stress on the cardiovascular system and the cross-linking of catecholamine-rich biopolymers and frameworks. Here we show that Epi and Fe3+ form stable high-spin complexes in the 1:1 or 3:1 stoichiometry, depending on the Epi/Fe3+ concentration ratio (low or high). Oxygen atoms on the catechol ring represent the sites of coordinate bond formation within physiologically relevant bidentate 1:1 complex. Redox properties of Epi are slightly impacted by Fe3+. On the other hand, Epi and Fe2+ form a complex that acts as a strong reducing agent, which leads to the production of hydrogen peroxide via O-2 reduction, and to a facilitated formation of the Epi-Fe3+ complexes. Epi is not oxidized in this process, i.e. Fe2+ is not an electron shuttle, but the electron donor. Epi-catalyzed oxidation of Fe2+ represents a plausible chemical basis of stress-related damage to heart cells. In addition, our results support the previous findings on the interactions of catecholamine moieties in polymers with iron and provide a novel strategy for improving the efficiency of cross-linking.
T2  - Scientific Reports
T1  - Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH
VL  - 8
SP  - 3530
DO  - 10.1038/s41598-018-21940-7
ER  - 
@article{
author = "Korać, Jelena and Stanković, Dalibor M. and Stanić, Marina and Bajuk-Bogdanović, Danica V. and Žižić, Milan and Bogdanović-Pristov, Jelena and Grgurić-Šipka, Sanja and Popović-Bijelić, Ana D. and Spasojević, Ivan",
year = "2018",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/7582",
abstract = "Coordinate and redox interactions of epinephrine (Epi) with iron at physiological pH are essential for understanding two very different phenomena - the detrimental effects of chronic stress on the cardiovascular system and the cross-linking of catecholamine-rich biopolymers and frameworks. Here we show that Epi and Fe3+ form stable high-spin complexes in the 1:1 or 3:1 stoichiometry, depending on the Epi/Fe3+ concentration ratio (low or high). Oxygen atoms on the catechol ring represent the sites of coordinate bond formation within physiologically relevant bidentate 1:1 complex. Redox properties of Epi are slightly impacted by Fe3+. On the other hand, Epi and Fe2+ form a complex that acts as a strong reducing agent, which leads to the production of hydrogen peroxide via O-2 reduction, and to a facilitated formation of the Epi-Fe3+ complexes. Epi is not oxidized in this process, i.e. Fe2+ is not an electron shuttle, but the electron donor. Epi-catalyzed oxidation of Fe2+ represents a plausible chemical basis of stress-related damage to heart cells. In addition, our results support the previous findings on the interactions of catecholamine moieties in polymers with iron and provide a novel strategy for improving the efficiency of cross-linking.",
journal = "Scientific Reports",
title = "Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH",
volume = "8",
pages = "3530",
doi = "10.1038/s41598-018-21940-7"
}
Korać, J., Stanković, D. M., Stanić, M., Bajuk-Bogdanović, D. V., Žižić, M., Bogdanović-Pristov, J., Grgurić-Šipka, S., Popović-Bijelić, A. D.,& Spasojević, I. (2018). Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH.
Scientific Reports, 8, 3530.
https://doi.org/10.1038/s41598-018-21940-7
Korać J, Stanković DM, Stanić M, Bajuk-Bogdanović DV, Žižić M, Bogdanović-Pristov J, Grgurić-Šipka S, Popović-Bijelić AD, Spasojević I. Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH. Scientific Reports. 2018;8:3530
Korać Jelena, Stanković Dalibor M., Stanić Marina, Bajuk-Bogdanović Danica V., Žižić Milan, Bogdanović-Pristov Jelena, Grgurić-Šipka Sanja, Popović-Bijelić Ana D., Spasojević Ivan, "Coordinate and redox interactions of epinephrine with ferric and ferrous iron at physiological pH" Scientific Reports, 8 (2018):3530,
https://doi.org/10.1038/s41598-018-21940-7 .
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