Avramov-Ivić, M

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  • Avramov-Ivić, M (2)
  • Avramov-Ivić, M. (1)
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Author's Bibliography

Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode

Vajdle, O; Guzsvány, V; Škorić, D; Csanádi, J; Petković, Miloš; Avramov-Ivić, M; Kónya, Z; Petrović, Slobodan D.; Bobrowski, A

(Elsevier Ltd, 2017)

TY  - JOUR
AU  - Vajdle, O
AU  - Guzsvány, V
AU  - Škorić, D
AU  - Csanádi, J
AU  - Petković, Miloš
AU  - Avramov-Ivić, M
AU  - Kónya, Z
AU  - Petrović, Slobodan D.
AU  - Bobrowski, A
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2970
AB  - The renewable silver-amalgam film electrode (Hg(Ag)FE) was applied for voltammetric characterization and determination of semi-synthetic macrolide antibiotics azithromycin (AZI), clarithromycin (CLA) and roxithromycin (ROX) in the Britton-Robinson buffer as supporting electrolyte ranging the pH from 4.0 to 11.9. All three macrolides showed reduction signals in fairly negative potential range. During direct cathodic square wave voltammetric (SWV) investigations conducted over the potential range from −0.75 V to −2.00 V vs SCE, either one or two reduction peaks were obtained in the potential range from −1.5 to −1.9 V. The shapes and intensities of the signals depend on the applied pH values in wider pH ranges. For analytical purposes concerning the development of direct cathodic SWV and adsorptive stripping SWV (SW-AdSV) methods the neutral and slightly alkaline media were suitable as pH 7.2, pH 7.4 and pH 7.0 for AZI, CLA and ROX, respectively. Based on the cyclic voltammograms recorded at these pH values, adsorption-controlled electrode kinetics process can be proposed for all three macrolides. Furthermore, the water suppressed 1H NMR measurements in the pH range between 6.0 and 10.5 indicated that the macrolide molecules at the optimal analytical conditions are predominantly in protonated form via their tertiary amino groups which supported in all three cases their adsorption on the appropriately polarized Hg(Ag)FE electrode. The optimized direct cathodic SWV methods showed good linearity in concentration ranges 4.81–23.3 μg mL−1, 1.96–28.6 μg mL−1 and 1.48–25.9 μg mL−1 for AZI, CLA and ROX, respectively. The development of the SW-AdSV methods resulted in the linear responses at lower concentration ranges as 1.0–2.46 μg mL−1, 0.05–0.99 μg mL−1 and 0.10–0.99 μg mL−1, for AZI, CLA and ROX, respectively. The relative standard deviation for all developed methods was not higher than 1.0% except the SWV method for AZI with 4.7%. In the case of all three investigated macrolide antibiotics the protonated form of the tertiary amino group(s) at appropriate accumulation potential and time favored the adsorption of the ionic form of the target molecules offering the opportunity for the development of SW-AdSV methods for their trace level analysis on Hg(Ag)FE. Optimized SW-AdSV method was applied for determination of ROX in pharmaceutical preparation Runac®.
PB  - Elsevier Ltd
T2  - Electrochimica Acta
T1  - Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode
VL  - 229
SP  - 334
EP  - 344
DO  - 10.1016/j.electacta.2017.01.146
ER  - 
@article{
author = "Vajdle, O and Guzsvány, V and Škorić, D and Csanádi, J and Petković, Miloš and Avramov-Ivić, M and Kónya, Z and Petrović, Slobodan D. and Bobrowski, A",
year = "2017",
abstract = "The renewable silver-amalgam film electrode (Hg(Ag)FE) was applied for voltammetric characterization and determination of semi-synthetic macrolide antibiotics azithromycin (AZI), clarithromycin (CLA) and roxithromycin (ROX) in the Britton-Robinson buffer as supporting electrolyte ranging the pH from 4.0 to 11.9. All three macrolides showed reduction signals in fairly negative potential range. During direct cathodic square wave voltammetric (SWV) investigations conducted over the potential range from −0.75 V to −2.00 V vs SCE, either one or two reduction peaks were obtained in the potential range from −1.5 to −1.9 V. The shapes and intensities of the signals depend on the applied pH values in wider pH ranges. For analytical purposes concerning the development of direct cathodic SWV and adsorptive stripping SWV (SW-AdSV) methods the neutral and slightly alkaline media were suitable as pH 7.2, pH 7.4 and pH 7.0 for AZI, CLA and ROX, respectively. Based on the cyclic voltammograms recorded at these pH values, adsorption-controlled electrode kinetics process can be proposed for all three macrolides. Furthermore, the water suppressed 1H NMR measurements in the pH range between 6.0 and 10.5 indicated that the macrolide molecules at the optimal analytical conditions are predominantly in protonated form via their tertiary amino groups which supported in all three cases their adsorption on the appropriately polarized Hg(Ag)FE electrode. The optimized direct cathodic SWV methods showed good linearity in concentration ranges 4.81–23.3 μg mL−1, 1.96–28.6 μg mL−1 and 1.48–25.9 μg mL−1 for AZI, CLA and ROX, respectively. The development of the SW-AdSV methods resulted in the linear responses at lower concentration ranges as 1.0–2.46 μg mL−1, 0.05–0.99 μg mL−1 and 0.10–0.99 μg mL−1, for AZI, CLA and ROX, respectively. The relative standard deviation for all developed methods was not higher than 1.0% except the SWV method for AZI with 4.7%. In the case of all three investigated macrolide antibiotics the protonated form of the tertiary amino group(s) at appropriate accumulation potential and time favored the adsorption of the ionic form of the target molecules offering the opportunity for the development of SW-AdSV methods for their trace level analysis on Hg(Ag)FE. Optimized SW-AdSV method was applied for determination of ROX in pharmaceutical preparation Runac®.",
publisher = "Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode",
volume = "229",
pages = "334-344",
doi = "10.1016/j.electacta.2017.01.146"
}
Vajdle, O., Guzsvány, V., Škorić, D., Csanádi, J., Petković, M., Avramov-Ivić, M., Kónya, Z., Petrović, S. D.,& Bobrowski, A.. (2017). Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode. in Electrochimica Acta
Elsevier Ltd., 229, 334-344.
https://doi.org/10.1016/j.electacta.2017.01.146
Vajdle O, Guzsvány V, Škorić D, Csanádi J, Petković M, Avramov-Ivić M, Kónya Z, Petrović SD, Bobrowski A. Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode. in Electrochimica Acta. 2017;229:334-344.
doi:10.1016/j.electacta.2017.01.146 .
Vajdle, O, Guzsvány, V, Škorić, D, Csanádi, J, Petković, Miloš, Avramov-Ivić, M, Kónya, Z, Petrović, Slobodan D., Bobrowski, A, "Voltammetric behavior and determination of the macrolide antibiotics azithromycin, clarithromycin and roxithromycin at a renewable silver – amalgam film electrode" in Electrochimica Acta, 229 (2017):334-344,
https://doi.org/10.1016/j.electacta.2017.01.146 . .
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Electroreduction of cefetamet on mercury, platinum and gold electrodes

Avramov-Ivić, M.; Kapetanović, Vera; Aleksić, Mara; Zuman, P.

(Srpsko hemijsko društvo, Beograd, 2000)

TY  - JOUR
AU  - Avramov-Ivić, M.
AU  - Kapetanović, Vera
AU  - Aleksić, Mara
AU  - Zuman, P.
PY  - 2000
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/272
AB  - The electroreduction of cefetamet (CEF) using gold and platinum electrodes has been investigated in slightly alkaline medium (pH 8.40) where adsorption, previously observed at mercury electrode, was pronounced. This investigation was performed in order to determine whether the adsorption interferes with the reduction process even at solid electrodes and to compare with a mercury electrode.
AB  - Redukcija cefetameta na elektrodama od zlata i platine je proučavana u slabo alkalnoj sredini (pH 8,40) gde je u prethodnim ispitivanjima na živinoj elektrodi u toku reakcije uočena adsorpcija antibiotika. Ovaj rad je posvećen ispitivanju uticaja adsorpcije na elektroredukciju cefetameta na čvrstim elektrodama i poređenju sa živom.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Electroreduction of cefetamet on mercury, platinum and gold electrodes
T1  - Elektroredukcija cefetameta na elektrodama od žive, platine i zlata
VL  - 65
IS  - 1
SP  - 47
EP  - 53
UR  - https://hdl.handle.net/21.15107/rcub_farfar_272
ER  - 
@article{
author = "Avramov-Ivić, M. and Kapetanović, Vera and Aleksić, Mara and Zuman, P.",
year = "2000",
abstract = "The electroreduction of cefetamet (CEF) using gold and platinum electrodes has been investigated in slightly alkaline medium (pH 8.40) where adsorption, previously observed at mercury electrode, was pronounced. This investigation was performed in order to determine whether the adsorption interferes with the reduction process even at solid electrodes and to compare with a mercury electrode., Redukcija cefetameta na elektrodama od zlata i platine je proučavana u slabo alkalnoj sredini (pH 8,40) gde je u prethodnim ispitivanjima na živinoj elektrodi u toku reakcije uočena adsorpcija antibiotika. Ovaj rad je posvećen ispitivanju uticaja adsorpcije na elektroredukciju cefetameta na čvrstim elektrodama i poređenju sa živom.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Electroreduction of cefetamet on mercury, platinum and gold electrodes, Elektroredukcija cefetameta na elektrodama od žive, platine i zlata",
volume = "65",
number = "1",
pages = "47-53",
url = "https://hdl.handle.net/21.15107/rcub_farfar_272"
}
Avramov-Ivić, M., Kapetanović, V., Aleksić, M.,& Zuman, P.. (2000). Electroreduction of cefetamet on mercury, platinum and gold electrodes. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 65(1), 47-53.
https://hdl.handle.net/21.15107/rcub_farfar_272
Avramov-Ivić M, Kapetanović V, Aleksić M, Zuman P. Electroreduction of cefetamet on mercury, platinum and gold electrodes. in Journal of the Serbian Chemical Society. 2000;65(1):47-53.
https://hdl.handle.net/21.15107/rcub_farfar_272 .
Avramov-Ivić, M., Kapetanović, Vera, Aleksić, Mara, Zuman, P., "Electroreduction of cefetamet on mercury, platinum and gold electrodes" in Journal of the Serbian Chemical Society, 65, no. 1 (2000):47-53,
https://hdl.handle.net/21.15107/rcub_farfar_272 .
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Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators

Čakar, Mira; Vasić, Vesna; Petkovska, LT; Stojić, DL; Avramov-Ivić, M; Milovanović, GA

(Pergamon-Elsevier Science Ltd, Oxford, 1999)

TY  - JOUR
AU  - Čakar, Mira
AU  - Vasić, Vesna
AU  - Petkovska, LT
AU  - Stojić, DL
AU  - Avramov-Ivić, M
AU  - Milovanović, GA
PY  - 1999
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/218
AB  - Newly synthesized oximes, mono and bis imidazole derivatives, which promise to be more effective acetylcholinesterase reactivators than standard antidotes used, were investigated by spectrophotometric and electrochemical methods. The electrochemical investigations confirmed the existence of overlapping equilibria, obtained by spectrophotometric methods. Dissociation constants of those oximes were also obtained by numerical treatment of overlapping equilibria, using the Lavendberg-Marquardt least square method, and when compared with the same for some similar compounds, were found to be very effective acetylcholinesterase reactivators. The distribution of ionic forms of the investigated oximes, as a dependence of pH values, was calculated from the obtained values of dissociation constants. The results indicated that many oxime anions will be available at physiological pH 7.4 and a relative increased ability to reactivate inhibited acetylcholinesterase could be expected.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators
VL  - 20
IS  - 4
SP  - 655
EP  - 662
DO  - 10.1016/S0731-7085(99)00056-4
ER  - 
@article{
author = "Čakar, Mira and Vasić, Vesna and Petkovska, LT and Stojić, DL and Avramov-Ivić, M and Milovanović, GA",
year = "1999",
abstract = "Newly synthesized oximes, mono and bis imidazole derivatives, which promise to be more effective acetylcholinesterase reactivators than standard antidotes used, were investigated by spectrophotometric and electrochemical methods. The electrochemical investigations confirmed the existence of overlapping equilibria, obtained by spectrophotometric methods. Dissociation constants of those oximes were also obtained by numerical treatment of overlapping equilibria, using the Lavendberg-Marquardt least square method, and when compared with the same for some similar compounds, were found to be very effective acetylcholinesterase reactivators. The distribution of ionic forms of the investigated oximes, as a dependence of pH values, was calculated from the obtained values of dissociation constants. The results indicated that many oxime anions will be available at physiological pH 7.4 and a relative increased ability to reactivate inhibited acetylcholinesterase could be expected.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators",
volume = "20",
number = "4",
pages = "655-662",
doi = "10.1016/S0731-7085(99)00056-4"
}
Čakar, M., Vasić, V., Petkovska, L., Stojić, D., Avramov-Ivić, M.,& Milovanović, G.. (1999). Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators. in Journal of Pharmaceutical and Biomedical Analysis
Pergamon-Elsevier Science Ltd, Oxford., 20(4), 655-662.
https://doi.org/10.1016/S0731-7085(99)00056-4
Čakar M, Vasić V, Petkovska L, Stojić D, Avramov-Ivić M, Milovanović G. Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators. in Journal of Pharmaceutical and Biomedical Analysis. 1999;20(4):655-662.
doi:10.1016/S0731-7085(99)00056-4 .
Čakar, Mira, Vasić, Vesna, Petkovska, LT, Stojić, DL, Avramov-Ivić, M, Milovanović, GA, "Spectrophotometric and electrochemical study of protolytic equilibria of some oximes-acetylcholinesterase reactivators" in Journal of Pharmaceutical and Biomedical Analysis, 20, no. 4 (1999):655-662,
https://doi.org/10.1016/S0731-7085(99)00056-4 . .
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