TY  - JOUR
AU  - Lović, Jelena
AU  - Lađarević, Jelena
AU  - Trišović, Nemanja
AU  - Andrić, Filip
AU  - Mladenović, Aleksandar R.
AU  - Mijin, Dušan
AU  - Vuković, Dragan
AU  - Petrović, Slobodan D.
AU  - Avramov Ivić, Milka
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4246
AB  - The electrochemical characterization of sertraline at gold electrode was examined by cyclic voltammetry measurements (CV) in pH 8.4 bicarbonate buffer. Then Au electrode was evaluated for the quantitative determination of sertraline using square wave voltammetry (SWV). To enhance the sensitivity during the drug determination, (2-hydroxypropyl)-β-cyclodextrin
(HPβCD) and β-cyclodextrin (βCD) inclusion complexes were employed. Using the proposed SWV technique, the anodic current peak was linear within a concentration range of 0.1–0.5 μM with a limit of detection (LOD) of 2.0 × 10–8 M and a limit of quantification (LOQ) of 6.7 × 10–8 M. In the case of inclusion complex of the sertraline with HPβCD, a good linearity range of 0.1–0.9 μM was obtained with a LOD of 2.6 × 10–8 M and a LOQ of 8.8 × 10–8 M. The gold electrode
revealed the same linearity range for inclusion complex of the sertraline with βCD with a LOD and a LOQ being 2.6 × 10–8 and 8.6 × 10–8 M, respectively. Comparing the regression equations, it can be concluded that the sensitivity in the presence of inclusion complex can be up to 5 times higher. The applicability of the developed method was confirmed by the analysis of this drug in pharmaceutical formulation and in human serum spiked with sertraline standard. The comparison to HPLC method was successfully performed.
PB  - Springer
T2  - Monatshefte für Chemie - Chemical Monthly
T1  - Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution
SP  - 185
EP  - 192
DO  - 10.1007/s00706-021-02745-3
ER  - 

@article{
author = "Lović, Jelena and Lađarević, Jelena and Trišović, Nemanja and Andrić, Filip and Mladenović, Aleksandar R. and Mijin, Dušan and Vuković, Dragan and Petrović, Slobodan D. and Avramov Ivić, Milka",
year = "2021",
abstract = "The electrochemical characterization of sertraline at gold electrode was examined by cyclic voltammetry measurements (CV) in pH 8.4 bicarbonate buffer. Then Au electrode was evaluated for the quantitative determination of sertraline using square wave voltammetry (SWV). To enhance the sensitivity during the drug determination, (2-hydroxypropyl)-β-cyclodextrin
(HPβCD) and β-cyclodextrin (βCD) inclusion complexes were employed. Using the proposed SWV technique, the anodic current peak was linear within a concentration range of 0.1–0.5 μM with a limit of detection (LOD) of 2.0 × 10–8 M and a limit of quantification (LOQ) of 6.7 × 10–8 M. In the case of inclusion complex of the sertraline with HPβCD, a good linearity range of 0.1–0.9 μM was obtained with a LOD of 2.6 × 10–8 M and a LOQ of 8.8 × 10–8 M. The gold electrode
revealed the same linearity range for inclusion complex of the sertraline with βCD with a LOD and a LOQ being 2.6 × 10–8 and 8.6 × 10–8 M, respectively. Comparing the regression equations, it can be concluded that the sensitivity in the presence of inclusion complex can be up to 5 times higher. The applicability of the developed method was confirmed by the analysis of this drug in pharmaceutical formulation and in human serum spiked with sertraline standard. The comparison to HPLC method was successfully performed.",
publisher = "Springer",
journal = "Monatshefte für Chemie - Chemical Monthly",
title = "Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution",
pages = "185-192",
doi = "10.1007/s00706-021-02745-3"
}

Lović, J., Lađarević, J., Trišović, N., Andrić, F., Mladenović, A. R., Mijin, D., Vuković, D., Petrović, S. D.,& Avramov Ivić, M.. (2021). Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution. in Monatshefte für Chemie - Chemical Monthly
Springer., 185-192.
https://doi.org/10.1007/s00706-021-02745-3

Lović J, Lađarević J, Trišović N, Andrić F, Mladenović AR, Mijin D, Vuković D, Petrović SD, Avramov Ivić M. Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution. in Monatshefte für Chemie - Chemical Monthly. 2021;:185-192.
doi:10.1007/s00706-021-02745-3 .

Lović, Jelena, Lađarević, Jelena, Trišović, Nemanja, Andrić, Filip, Mladenović, Aleksandar R., Mijin, Dušan, Vuković, Dragan, Petrović, Slobodan D., Avramov Ivić, Milka, "Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution" in Monatshefte für Chemie - Chemical Monthly (2021):185-192,
https://doi.org/10.1007/s00706-021-02745-3 . .

TY  - JOUR
AU  - Avramov Ivić, Milka
AU  - Lović, Jelena
AU  - Stevanović, Sanja
AU  - Nikolić, Nebojša D.
AU  - Trišović, Nemanja
AU  - Lađarević, Jelena
AU  - Vuković, Dragan
AU  - Drmanić, Saša Ž.
AU  - Mladenović, Aleksandar R.
AU  - Jadranin, Milka
AU  - Petrović, Slobodan D.
AU  - Mijin, Dušan
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3062
AB  - Esomeprazole is the most effective of the proton-pump inhibitors for the acid-related diseases and at first was examined for the electroanalytical purposes. The drug standard and as a content of injection powder was investigated by cyclic voltammetry (CV) and quantitatively determined using square wave voltammetry (SWV) via its electrooxidation at Au electrode in 0.05 M NaHCO3. SWV showed a linear dependency of the anodic peak currents vs. esomeprazole standard concentrations in the range from 3.0 to 500 μg mL−1 with the values of limit of detection (LOD) and limit of quantification (LOQ): 1.4 and 4.6 μg mL−1, respectively. Using the constructed and validated calibration curve, the values of unknown esomeprazole concentrations in injection powder and in human serum spiked with standard were determined. Before the electrochemical oxidation, it was shown by atomic force microscopy (AFM) that the small esomeprazole islands formed inside holes were visible and their diameter was about 200 nm attributed to physico-chemical characteristics of esomeprazole. After the electrochemical oxidation, the morphology of esomeprazole standard on Au surface was completely changed and composed of spherical particles in a diameter between 200 and 600 nm. With esomeprazole suspended in human serum, the process of crystallization partly occurred in the form of spherical grains with the average size of these grains was about 4 μm. The analysis at the macro level done by the optical microscopy (OM) confirmed this opinion. The study of esomeprazole degradation showed that at Au electrode, after 3 h of cycling, a neglectable amount of the esomeprazole was changed. Using IrOx electrode under directed stress conditions, its almost complete degradation was realized after 3 h confirmed by high performance liquid chromatography (HPLC). Total organic carbon (TOC) analysis showed that 95% of esomeprazole was mineralized. The HPLC and Liquid chromatography-mass spectrometry (LC-MS) study revealed the formation of 4-hydroxy omeprazole sulphide, 4-hydroxy omeprazole sulphone, esomeprazole sulphone and methylated esomeprazole.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Electrochemical behavior of esomeprazole: Its determination at Au electrode as standard and in injection powder combined with the study of its degradation
VL  - 848
SP  - 113303
DO  - 10.1016/j.jelechem.2019.113303
ER  - 

@article{
author = "Avramov Ivić, Milka and Lović, Jelena and Stevanović, Sanja and Nikolić, Nebojša D. and Trišović, Nemanja and Lađarević, Jelena and Vuković, Dragan and Drmanić, Saša Ž. and Mladenović, Aleksandar R. and Jadranin, Milka and Petrović, Slobodan D. and Mijin, Dušan",
year = "2019",
abstract = "Esomeprazole is the most effective of the proton-pump inhibitors for the acid-related diseases and at first was examined for the electroanalytical purposes. The drug standard and as a content of injection powder was investigated by cyclic voltammetry (CV) and quantitatively determined using square wave voltammetry (SWV) via its electrooxidation at Au electrode in 0.05 M NaHCO3. SWV showed a linear dependency of the anodic peak currents vs. esomeprazole standard concentrations in the range from 3.0 to 500 μg mL−1 with the values of limit of detection (LOD) and limit of quantification (LOQ): 1.4 and 4.6 μg mL−1, respectively. Using the constructed and validated calibration curve, the values of unknown esomeprazole concentrations in injection powder and in human serum spiked with standard were determined. Before the electrochemical oxidation, it was shown by atomic force microscopy (AFM) that the small esomeprazole islands formed inside holes were visible and their diameter was about 200 nm attributed to physico-chemical characteristics of esomeprazole. After the electrochemical oxidation, the morphology of esomeprazole standard on Au surface was completely changed and composed of spherical particles in a diameter between 200 and 600 nm. With esomeprazole suspended in human serum, the process of crystallization partly occurred in the form of spherical grains with the average size of these grains was about 4 μm. The analysis at the macro level done by the optical microscopy (OM) confirmed this opinion. The study of esomeprazole degradation showed that at Au electrode, after 3 h of cycling, a neglectable amount of the esomeprazole was changed. Using IrOx electrode under directed stress conditions, its almost complete degradation was realized after 3 h confirmed by high performance liquid chromatography (HPLC). Total organic carbon (TOC) analysis showed that 95% of esomeprazole was mineralized. The HPLC and Liquid chromatography-mass spectrometry (LC-MS) study revealed the formation of 4-hydroxy omeprazole sulphide, 4-hydroxy omeprazole sulphone, esomeprazole sulphone and methylated esomeprazole.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrochemical behavior of esomeprazole: Its determination at Au electrode as standard and in injection powder combined with the study of its degradation",
volume = "848",
pages = "113303",
doi = "10.1016/j.jelechem.2019.113303"
}

Avramov Ivić, M., Lović, J., Stevanović, S., Nikolić, N. D., Trišović, N., Lađarević, J., Vuković, D., Drmanić, S. Ž., Mladenović, A. R., Jadranin, M., Petrović, S. D.,& Mijin, D.. (2019). Electrochemical behavior of esomeprazole: Its determination at Au electrode as standard and in injection powder combined with the study of its degradation. in Journal of Electroanalytical Chemistry
Elsevier., 848, 113303.
https://doi.org/10.1016/j.jelechem.2019.113303

Avramov Ivić M, Lović J, Stevanović S, Nikolić ND, Trišović N, Lađarević J, Vuković D, Drmanić SŽ, Mladenović AR, Jadranin M, Petrović SD, Mijin D. Electrochemical behavior of esomeprazole: Its determination at Au electrode as standard and in injection powder combined with the study of its degradation. in Journal of Electroanalytical Chemistry. 2019;848:113303.
doi:10.1016/j.jelechem.2019.113303 .

Avramov Ivić, Milka, Lović, Jelena, Stevanović, Sanja, Nikolić, Nebojša D., Trišović, Nemanja, Lađarević, Jelena, Vuković, Dragan, Drmanić, Saša Ž., Mladenović, Aleksandar R., Jadranin, Milka, Petrović, Slobodan D., Mijin, Dušan, "Electrochemical behavior of esomeprazole: Its determination at Au electrode as standard and in injection powder combined with the study of its degradation" in Journal of Electroanalytical Chemistry, 848 (2019):113303,
https://doi.org/10.1016/j.jelechem.2019.113303 . .

TY  - CONF
AU  - Avramov -  Ivić, Milka
AU  - Lović, Jelena
AU  - Trišović, Nemanja
AU  - Lađarević, Jelena
AU  - Mladenović, Aleksandar R.
AU  - Jadranin, Milka
AU  - Petrović, Slobodan
AU  - Mijin, Dušan
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5656
AB  - The electrochemical activity of esomeprazole at the gold electrode was investigated by CV and the development of an electroanalytical procedure for its quantitative determination was established with the aid of SWV measurements. The study of the electrochemical degradation of the drug was
performed at Au and IrOx electrodes.
PB  - International Association of Physical Chemists
C3  - Book of abstracts - 7th Regional Symposium on Electrochemistry – South East Europe & 8th Kurt Schwabe Symposium, May 27 – 30, 2019, Split, Croatia
T1  - The SWV determination of esomeprazole at Au and its degradation at IrOx followed by HPLC and LC-MS
SP  - EAS-P-11
UR  - https://hdl.handle.net/21.15107/rcub_cer_5656
ER  - 

@conference{
author = "Avramov -  Ivić, Milka and Lović, Jelena and Trišović, Nemanja and Lađarević, Jelena and Mladenović, Aleksandar R. and Jadranin, Milka and Petrović, Slobodan and Mijin, Dušan",
year = "2019",
abstract = "The electrochemical activity of esomeprazole at the gold electrode was investigated by CV and the development of an electroanalytical procedure for its quantitative determination was established with the aid of SWV measurements. The study of the electrochemical degradation of the drug was
performed at Au and IrOx electrodes.",
publisher = "International Association of Physical Chemists",
journal = "Book of abstracts - 7th Regional Symposium on Electrochemistry – South East Europe & 8th Kurt Schwabe Symposium, May 27 – 30, 2019, Split, Croatia",
title = "The SWV determination of esomeprazole at Au and its degradation at IrOx followed by HPLC and LC-MS",
pages = "EAS-P-11",
url = "https://hdl.handle.net/21.15107/rcub_cer_5656"
}

Avramov -  Ivić, M., Lović, J., Trišović, N., Lađarević, J., Mladenović, A. R., Jadranin, M., Petrović, S.,& Mijin, D.. (2019). The SWV determination of esomeprazole at Au and its degradation at IrOx followed by HPLC and LC-MS. in Book of abstracts - 7th Regional Symposium on Electrochemistry – South East Europe & 8th Kurt Schwabe Symposium, May 27 – 30, 2019, Split, Croatia
International Association of Physical Chemists., EAS-P-11.
https://hdl.handle.net/21.15107/rcub_cer_5656

Avramov -  Ivić M, Lović J, Trišović N, Lađarević J, Mladenović AR, Jadranin M, Petrović S, Mijin D. The SWV determination of esomeprazole at Au and its degradation at IrOx followed by HPLC and LC-MS. in Book of abstracts - 7th Regional Symposium on Electrochemistry – South East Europe & 8th Kurt Schwabe Symposium, May 27 – 30, 2019, Split, Croatia. 2019;:EAS-P-11.
https://hdl.handle.net/21.15107/rcub_cer_5656 .

Avramov -  Ivić, Milka, Lović, Jelena, Trišović, Nemanja, Lađarević, Jelena, Mladenović, Aleksandar R., Jadranin, Milka, Petrović, Slobodan, Mijin, Dušan, "The SWV determination of esomeprazole at Au and its degradation at IrOx followed by HPLC and LC-MS" in Book of abstracts - 7th Regional Symposium on Electrochemistry – South East Europe & 8th Kurt Schwabe Symposium, May 27 – 30, 2019, Split, Croatia (2019):EAS-P-11,
https://hdl.handle.net/21.15107/rcub_cer_5656 .

TY  - JOUR
AU  - Radosavljevic, Kristina D.
AU  - Lović, Jelena
AU  - Mijin, Dušan
AU  - Petrović, Slobodan D.
AU  - Jadranin, Milka
AU  - Mladenović, Aleksandar R.
AU  - Avramov Ivić, Milka
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2233
AB  - The electrodegradation of azithromycin was studied by its indirect oxidation using dimensionally stable Ti/RuO2 anode as catalyst in the electrolyte containing methanol, 0.05 M NaHCO3, sodium chloride and deionized water. The optimal conditions for galvanostatic electrodegradation for the azithromycin concentration of 0.472 mg cm(-3) were found to be NaCl concentration of 7 mg cm(-3) and the applied current of 300 mA. The differential pulse voltammetry using glassy carbon electrode was performed for the first time in the above-mentioned content of electrolyte for the nine concentration of azithromycin (0.075-0.675 mg cm(-3)) giving the limits of azithromycin detection and of quantification as: LOD 0.044 mg cm(-3) and LOQ 0.145 mg cm(-3). The calibration curve was constructed enabling the electrolyte analysis during its electrodegradation process. The electrolyte was analyzed by high-performance liquid chromatography and electrospray ionization time-of-flight mass spectrometry. The electrooxidation products were identified and after 180 min there was no azithromycin in the electrolyte while TOC analysis showed that 79% of azithromycin was mineralized. The proposed degradation scheme is presented.
PB  - Versita, Warsaw
T2  - Chemical Papers
T1  - Degradation of azithromycin using Ti/RuO2 anode as catalyst followed by DPV, HPLC-UV and MS analysis
VL  - 71
IS  - 7
SP  - 1217
EP  - 1224
DO  - 10.1007/s11696-016-0115-2
ER  - 

@article{
author = "Radosavljevic, Kristina D. and Lović, Jelena and Mijin, Dušan and Petrović, Slobodan D. and Jadranin, Milka and Mladenović, Aleksandar R. and Avramov Ivić, Milka",
year = "2017",
abstract = "The electrodegradation of azithromycin was studied by its indirect oxidation using dimensionally stable Ti/RuO2 anode as catalyst in the electrolyte containing methanol, 0.05 M NaHCO3, sodium chloride and deionized water. The optimal conditions for galvanostatic electrodegradation for the azithromycin concentration of 0.472 mg cm(-3) were found to be NaCl concentration of 7 mg cm(-3) and the applied current of 300 mA. The differential pulse voltammetry using glassy carbon electrode was performed for the first time in the above-mentioned content of electrolyte for the nine concentration of azithromycin (0.075-0.675 mg cm(-3)) giving the limits of azithromycin detection and of quantification as: LOD 0.044 mg cm(-3) and LOQ 0.145 mg cm(-3). The calibration curve was constructed enabling the electrolyte analysis during its electrodegradation process. The electrolyte was analyzed by high-performance liquid chromatography and electrospray ionization time-of-flight mass spectrometry. The electrooxidation products were identified and after 180 min there was no azithromycin in the electrolyte while TOC analysis showed that 79% of azithromycin was mineralized. The proposed degradation scheme is presented.",
publisher = "Versita, Warsaw",
journal = "Chemical Papers",
title = "Degradation of azithromycin using Ti/RuO2 anode as catalyst followed by DPV, HPLC-UV and MS analysis",
volume = "71",
number = "7",
pages = "1217-1224",
doi = "10.1007/s11696-016-0115-2"
}

Radosavljevic, K. D., Lović, J., Mijin, D., Petrović, S. D., Jadranin, M., Mladenović, A. R.,& Avramov Ivić, M.. (2017). Degradation of azithromycin using Ti/RuO2 anode as catalyst followed by DPV, HPLC-UV and MS analysis. in Chemical Papers
Versita, Warsaw., 71(7), 1217-1224.
https://doi.org/10.1007/s11696-016-0115-2

Radosavljevic KD, Lović J, Mijin D, Petrović SD, Jadranin M, Mladenović AR, Avramov Ivić M. Degradation of azithromycin using Ti/RuO2 anode as catalyst followed by DPV, HPLC-UV and MS analysis. in Chemical Papers. 2017;71(7):1217-1224.
doi:10.1007/s11696-016-0115-2 .

Radosavljevic, Kristina D., Lović, Jelena, Mijin, Dušan, Petrović, Slobodan D., Jadranin, Milka, Mladenović, Aleksandar R., Avramov Ivić, Milka, "Degradation of azithromycin using Ti/RuO2 anode as catalyst followed by DPV, HPLC-UV and MS analysis" in Chemical Papers, 71, no. 7 (2017):1217-1224,
https://doi.org/10.1007/s11696-016-0115-2 . .

TY  - JOUR
AU  - Lović, Jelena
AU  - Trišović, Nemanja
AU  - Antanasijevic, Jelena
AU  - Nikolić, Nebojša D.
AU  - Stevanović, Sanja
AU  - Mijin, Dušan
AU  - Vukovic, Dragan
AU  - Mladenović, Aleksandar R.
AU  - Petrović, Slobodan D.
AU  - Avramov Ivić, Milka
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4310
AB  - Nonmedical use of sildenafil citrate (SC) requires new methods for drug determination in human serum and in tablets. SC as standard and in Sildena (R) tablets is determined by square wave voltammetry (SWV) in 0.1 M H2SO4 (harmful for human serum) at gold electrode in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.5,1) mu M and on cysteine (Cys) modified gold electrode (Au/Cys) in a range: (1 x 10(-3),1 x 10(-2), 0.05, 0.1) mu M. The presence of Cys causes two times larger peak currents and shifting of the incipient potential of the SC oxidation to 0.1 V in negative direction. A safe procedure for SC determination as standard and in Sildena (R) tablets spiked with human serum is developed by SWV at gold electrode in 0.05 M NaHCO3 (suitable for human liquids) in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.2, 03) mu M. Microscopic characterization of the surfaces morphology was also performed. The SC concentrations were checked by high performance liquid chromatography-ultraviolet spectroscopy (HPLC-UV) showing that electrochemical method is more sensitive and can be used for the measurements of very low concentrations of the analyte.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode
VL  - 782
SP  - 103
EP  - 107
DO  - 10.1016/j.jelechem.2016.10.022
ER  - 

@article{
author = "Lović, Jelena and Trišović, Nemanja and Antanasijevic, Jelena and Nikolić, Nebojša D. and Stevanović, Sanja and Mijin, Dušan and Vukovic, Dragan and Mladenović, Aleksandar R. and Petrović, Slobodan D. and Avramov Ivić, Milka",
year = "2016",
abstract = "Nonmedical use of sildenafil citrate (SC) requires new methods for drug determination in human serum and in tablets. SC as standard and in Sildena (R) tablets is determined by square wave voltammetry (SWV) in 0.1 M H2SO4 (harmful for human serum) at gold electrode in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.5,1) mu M and on cysteine (Cys) modified gold electrode (Au/Cys) in a range: (1 x 10(-3),1 x 10(-2), 0.05, 0.1) mu M. The presence of Cys causes two times larger peak currents and shifting of the incipient potential of the SC oxidation to 0.1 V in negative direction. A safe procedure for SC determination as standard and in Sildena (R) tablets spiked with human serum is developed by SWV at gold electrode in 0.05 M NaHCO3 (suitable for human liquids) in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.2, 03) mu M. Microscopic characterization of the surfaces morphology was also performed. The SC concentrations were checked by high performance liquid chromatography-ultraviolet spectroscopy (HPLC-UV) showing that electrochemical method is more sensitive and can be used for the measurements of very low concentrations of the analyte.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode",
volume = "782",
pages = "103-107",
doi = "10.1016/j.jelechem.2016.10.022"
}

Lović, J., Trišović, N., Antanasijevic, J., Nikolić, N. D., Stevanović, S., Mijin, D., Vukovic, D., Mladenović, A. R., Petrović, S. D.,& Avramov Ivić, M.. (2016). Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode. in Journal of Electroanalytical Chemistry
Elsevier., 782, 103-107.
https://doi.org/10.1016/j.jelechem.2016.10.022

Lović J, Trišović N, Antanasijevic J, Nikolić ND, Stevanović S, Mijin D, Vukovic D, Mladenović AR, Petrović SD, Avramov Ivić M. Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode. in Journal of Electroanalytical Chemistry. 2016;782:103-107.
doi:10.1016/j.jelechem.2016.10.022 .

Lović, Jelena, Trišović, Nemanja, Antanasijevic, Jelena, Nikolić, Nebojša D., Stevanović, Sanja, Mijin, Dušan, Vukovic, Dragan, Mladenović, Aleksandar R., Petrović, Slobodan D., Avramov Ivić, Milka, "Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode" in Journal of Electroanalytical Chemistry, 782 (2016):103-107,
https://doi.org/10.1016/j.jelechem.2016.10.022 . .

TY  - JOUR
AU  - Lović, Jelena
AU  - Trišović, Nemanja
AU  - Antanasijevic, Jelena
AU  - Nikolić, Nebojša D.
AU  - Stevanović, Sanja
AU  - Mijin, Dušan
AU  - Vukovic, Dragan
AU  - Mladenović, Aleksandar R.
AU  - Petrović, Slobodan D.
AU  - Avramov Ivić, Milka
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1902
AB  - Nonmedical use of sildenafil citrate (SC) requires new methods for drug determination in human serum and in tablets. SC as standard and in Sildena (R) tablets is determined by square wave voltammetry (SWV) in 0.1 M H2SO4 (harmful for human serum) at gold electrode in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.5,1) mu M and on cysteine (Cys) modified gold electrode (Au/Cys) in a range: (1 x 10(-3),1 x 10(-2), 0.05, 0.1) mu M. The presence of Cys causes two times larger peak currents and shifting of the incipient potential of the SC oxidation to 0.1 V in negative direction. A safe procedure for SC determination as standard and in Sildena (R) tablets spiked with human serum is developed by SWV at gold electrode in 0.05 M NaHCO3 (suitable for human liquids) in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.2, 03) mu M. Microscopic characterization of the surfaces morphology was also performed. The SC concentrations were checked by high performance liquid chromatography-ultraviolet spectroscopy (HPLC-UV) showing that electrochemical method is more sensitive and can be used for the measurements of very low concentrations of the analyte.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode
VL  - 782
SP  - 103
EP  - 107
DO  - 10.1016/j.jelechem.2016.10.022
ER  - 

@article{
author = "Lović, Jelena and Trišović, Nemanja and Antanasijevic, Jelena and Nikolić, Nebojša D. and Stevanović, Sanja and Mijin, Dušan and Vukovic, Dragan and Mladenović, Aleksandar R. and Petrović, Slobodan D. and Avramov Ivić, Milka",
year = "2016",
abstract = "Nonmedical use of sildenafil citrate (SC) requires new methods for drug determination in human serum and in tablets. SC as standard and in Sildena (R) tablets is determined by square wave voltammetry (SWV) in 0.1 M H2SO4 (harmful for human serum) at gold electrode in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.5,1) mu M and on cysteine (Cys) modified gold electrode (Au/Cys) in a range: (1 x 10(-3),1 x 10(-2), 0.05, 0.1) mu M. The presence of Cys causes two times larger peak currents and shifting of the incipient potential of the SC oxidation to 0.1 V in negative direction. A safe procedure for SC determination as standard and in Sildena (R) tablets spiked with human serum is developed by SWV at gold electrode in 0.05 M NaHCO3 (suitable for human liquids) in a range: (1 x 10(-3),1 x 10(-2), 0.1, 0.2, 03) mu M. Microscopic characterization of the surfaces morphology was also performed. The SC concentrations were checked by high performance liquid chromatography-ultraviolet spectroscopy (HPLC-UV) showing that electrochemical method is more sensitive and can be used for the measurements of very low concentrations of the analyte.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode",
volume = "782",
pages = "103-107",
doi = "10.1016/j.jelechem.2016.10.022"
}

Lović, J., Trišović, N., Antanasijevic, J., Nikolić, N. D., Stevanović, S., Mijin, D., Vukovic, D., Mladenović, A. R., Petrović, S. D.,& Avramov Ivić, M.. (2016). Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode. in Journal of Electroanalytical Chemistry
Elsevier., 782, 103-107.
https://doi.org/10.1016/j.jelechem.2016.10.022

Lović J, Trišović N, Antanasijevic J, Nikolić ND, Stevanović S, Mijin D, Vukovic D, Mladenović AR, Petrović SD, Avramov Ivić M. Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode. in Journal of Electroanalytical Chemistry. 2016;782:103-107.
doi:10.1016/j.jelechem.2016.10.022 .

Lović, Jelena, Trišović, Nemanja, Antanasijevic, Jelena, Nikolić, Nebojša D., Stevanović, Sanja, Mijin, Dušan, Vukovic, Dragan, Mladenović, Aleksandar R., Petrović, Slobodan D., Avramov Ivić, Milka, "Electrochemical determination of sildenafil citrate as standard, in tablets and spiked with human serum at gold and cystein modified gold electrode" in Journal of Electroanalytical Chemistry, 782 (2016):103-107,
https://doi.org/10.1016/j.jelechem.2016.10.022 . .

TY  - JOUR
AU  - Mladenović, Aleksandar R.
AU  - Jadranin, Milka
AU  - Pavlović, Aleksandar D.
AU  - Petrović, Slobodan D.
AU  - Drmanić, Saša Ž.
AU  - Avramov Ivić, Milka
AU  - Mijin, Dušan
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1731
AB  - This study describes the investigation of degradation products of donepezil (DP) using a stability-indicating RP-HPLC method for determination of donepezil, which is a centrally acting reversible acetyl cholinesterase inhibitor. In order to investigate the stability of the drug and formed degradation products, a forced degradation study of the drug sample and finished product under different forced degradation conditions was conducted. Donepezil hydrochloride and donepezil tablets were subjected to stress degradation conditions recommended by the International Conference on Harmonization (ICH). Donepezil hydrochloride solutions were subjected to acid and alkali hydrolysis, chemical oxidation and thermal degradation. Significant degradation was observed under alkali hydrolysis and oxidative degradation conditions. Additional degradation products were observed under the conditions of oxidative degradation. The degradation products observed during forced degradation studies were monitored using the developed high performance liquid chromatography (HPLC) method. The parent method was modified in order to obtain LC-MS compatible method, which was used to identify the degradation products from forced degradation samples using high resolution mass spectrometry. The mass spectrum provided the precise mass from which the molecular formula of the drug substance and formed degradation products was derived, and proved the specificity of the method unambiguously.
AB  - Proučavanje degradacionih proizvoda donepezila je izvršeno korišćenjem RP-HPLC metode za određivanje stabilnosti donepezila, leka koji pripada grupi reverzibilnih inhibitora acetilholinesteraze. U cilju ispitivanja stabilnosti leka i njegovih degradacionih proizvoda sprovedena je studija forsirane degradacije čiste supstance kao i farmaceutskog proizvoda pod različitim uslovima. Donepezil-hidrohlorid i donepezil tablete su podvrgnuti različitim uslovima degradacije prema preporukama Internacionalne konferencije za harmonizaciju. Rastvori donepezil-hidrohlorida su podvrgnuti kiseloj i baznoj hidrolizi, hemijskoj oksidaciji i termalnoj degradaciji. Pri baznoj hidrolizi i hemijskoj oksidaciji uočena je značajna degradacija polaznog molekula. Oksidativnom degradacijom nastaju i proizvodi koji nisu uočeni kod ostalih postupaka forsirane degradacije. Nastali proizvodi analizirani su novorazvijenom HPLC metodom. Osnovna metoda je modifikovana u cilju dobijanja LC-MS kompatibilne metode kako bi se identifikovali nastali degradacioni proizvodi. Na osnovu resultata dobijenih masenom spektrometrijom dobijene su tačne mase proizvoda degradacije, čime je omogućeno određivanje njihovih molekulskih formula.
PB  - Association of the Chemical Engineers of Serbia
T2  - Chemical Industry and Chemical Engineering Quarterly / CICEQ
T1  - Liquid chromatography and liquid chromatography-mass spectrometry analysis of donepezil degradation products
T1  - Analiza degradacionih proizvoda donepezila primenom tečne hromatografije i tečne hromatografije-masene spektrometrije
VL  - 21
IS  - 3
SP  - 447
EP  - 455
DO  - 10.2298/CICEQ141023047M
ER  - 

@article{
author = "Mladenović, Aleksandar R. and Jadranin, Milka and Pavlović, Aleksandar D. and Petrović, Slobodan D. and Drmanić, Saša Ž. and Avramov Ivić, Milka and Mijin, Dušan",
year = "2015",
abstract = "This study describes the investigation of degradation products of donepezil (DP) using a stability-indicating RP-HPLC method for determination of donepezil, which is a centrally acting reversible acetyl cholinesterase inhibitor. In order to investigate the stability of the drug and formed degradation products, a forced degradation study of the drug sample and finished product under different forced degradation conditions was conducted. Donepezil hydrochloride and donepezil tablets were subjected to stress degradation conditions recommended by the International Conference on Harmonization (ICH). Donepezil hydrochloride solutions were subjected to acid and alkali hydrolysis, chemical oxidation and thermal degradation. Significant degradation was observed under alkali hydrolysis and oxidative degradation conditions. Additional degradation products were observed under the conditions of oxidative degradation. The degradation products observed during forced degradation studies were monitored using the developed high performance liquid chromatography (HPLC) method. The parent method was modified in order to obtain LC-MS compatible method, which was used to identify the degradation products from forced degradation samples using high resolution mass spectrometry. The mass spectrum provided the precise mass from which the molecular formula of the drug substance and formed degradation products was derived, and proved the specificity of the method unambiguously., Proučavanje degradacionih proizvoda donepezila je izvršeno korišćenjem RP-HPLC metode za određivanje stabilnosti donepezila, leka koji pripada grupi reverzibilnih inhibitora acetilholinesteraze. U cilju ispitivanja stabilnosti leka i njegovih degradacionih proizvoda sprovedena je studija forsirane degradacije čiste supstance kao i farmaceutskog proizvoda pod različitim uslovima. Donepezil-hidrohlorid i donepezil tablete su podvrgnuti različitim uslovima degradacije prema preporukama Internacionalne konferencije za harmonizaciju. Rastvori donepezil-hidrohlorida su podvrgnuti kiseloj i baznoj hidrolizi, hemijskoj oksidaciji i termalnoj degradaciji. Pri baznoj hidrolizi i hemijskoj oksidaciji uočena je značajna degradacija polaznog molekula. Oksidativnom degradacijom nastaju i proizvodi koji nisu uočeni kod ostalih postupaka forsirane degradacije. Nastali proizvodi analizirani su novorazvijenom HPLC metodom. Osnovna metoda je modifikovana u cilju dobijanja LC-MS kompatibilne metode kako bi se identifikovali nastali degradacioni proizvodi. Na osnovu resultata dobijenih masenom spektrometrijom dobijene su tačne mase proizvoda degradacije, čime je omogućeno određivanje njihovih molekulskih formula.",
publisher = "Association of the Chemical Engineers of Serbia",
journal = "Chemical Industry and Chemical Engineering Quarterly / CICEQ",
title = "Liquid chromatography and liquid chromatography-mass spectrometry analysis of donepezil degradation products, Analiza degradacionih proizvoda donepezila primenom tečne hromatografije i tečne hromatografije-masene spektrometrije",
volume = "21",
number = "3",
pages = "447-455",
doi = "10.2298/CICEQ141023047M"
}

Mladenović, A. R., Jadranin, M., Pavlović, A. D., Petrović, S. D., Drmanić, S. Ž., Avramov Ivić, M.,& Mijin, D.. (2015). Liquid chromatography and liquid chromatography-mass spectrometry analysis of donepezil degradation products. in Chemical Industry and Chemical Engineering Quarterly / CICEQ
Association of the Chemical Engineers of Serbia., 21(3), 447-455.
https://doi.org/10.2298/CICEQ141023047M

Mladenović AR, Jadranin M, Pavlović AD, Petrović SD, Drmanić SŽ, Avramov Ivić M, Mijin D. Liquid chromatography and liquid chromatography-mass spectrometry analysis of donepezil degradation products. in Chemical Industry and Chemical Engineering Quarterly / CICEQ. 2015;21(3):447-455.
doi:10.2298/CICEQ141023047M .

Mladenović, Aleksandar R., Jadranin, Milka, Pavlović, Aleksandar D., Petrović, Slobodan D., Drmanić, Saša Ž., Avramov Ivić, Milka, Mijin, Dušan, "Liquid chromatography and liquid chromatography-mass spectrometry analysis of donepezil degradation products" in Chemical Industry and Chemical Engineering Quarterly / CICEQ, 21, no. 3 (2015):447-455,
https://doi.org/10.2298/CICEQ141023047M . .

TY  - JOUR
AU  - Mladenović, Aleksandar R.
AU  - Mijin, Dušan
AU  - Drmanić, Saša Ž.
AU  - Vajs, Vlatka
AU  - Jovanović, Vladislava M.
AU  - Petrović, Slobodan D.
AU  - Avramov Ivić, Milka
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1577
AB  - The oxidative ability of donepezil, a frequently prescribed drug for the treatment of Alzheimer's disease is reported for the first time at a gold electrode. It was oxidized by cyclic voltammetry and determined by square wave voltammetry in phosphate buffer electrolyte. Electrochemical degradation of donepezil was carried out by long term potential cycling. The identification and characterization of the major product, isolated by preparative high performance liquid chromatography, was performed by high resolution mass spectrometry and 1D and 2D nuclear magnetic resonance spectroscopy. Donepezil hydroxy derivative was identified as the major electrochemical oxidation product from donepezil.
PB  - Wiley-Blackwell, Malden
T2  - Electroanalysis
T1  - Electrochemical Oxidation of Donepezil and Its Voltammetric Determination at Gold Electrode
VL  - 26
IS  - 5
SP  - 893
EP  - 897
DO  - 10.1002/elan.201400034
ER  - 

@article{
author = "Mladenović, Aleksandar R. and Mijin, Dušan and Drmanić, Saša Ž. and Vajs, Vlatka and Jovanović, Vladislava M. and Petrović, Slobodan D. and Avramov Ivić, Milka",
year = "2014",
abstract = "The oxidative ability of donepezil, a frequently prescribed drug for the treatment of Alzheimer's disease is reported for the first time at a gold electrode. It was oxidized by cyclic voltammetry and determined by square wave voltammetry in phosphate buffer electrolyte. Electrochemical degradation of donepezil was carried out by long term potential cycling. The identification and characterization of the major product, isolated by preparative high performance liquid chromatography, was performed by high resolution mass spectrometry and 1D and 2D nuclear magnetic resonance spectroscopy. Donepezil hydroxy derivative was identified as the major electrochemical oxidation product from donepezil.",
publisher = "Wiley-Blackwell, Malden",
journal = "Electroanalysis",
title = "Electrochemical Oxidation of Donepezil and Its Voltammetric Determination at Gold Electrode",
volume = "26",
number = "5",
pages = "893-897",
doi = "10.1002/elan.201400034"
}

Mladenović, A. R., Mijin, D., Drmanić, S. Ž., Vajs, V., Jovanović, V. M., Petrović, S. D.,& Avramov Ivić, M.. (2014). Electrochemical Oxidation of Donepezil and Its Voltammetric Determination at Gold Electrode. in Electroanalysis
Wiley-Blackwell, Malden., 26(5), 893-897.
https://doi.org/10.1002/elan.201400034

Mladenović AR, Mijin D, Drmanić SŽ, Vajs V, Jovanović VM, Petrović SD, Avramov Ivić M. Electrochemical Oxidation of Donepezil and Its Voltammetric Determination at Gold Electrode. in Electroanalysis. 2014;26(5):893-897.
doi:10.1002/elan.201400034 .

Mladenović, Aleksandar R., Mijin, Dušan, Drmanić, Saša Ž., Vajs, Vlatka, Jovanović, Vladislava M., Petrović, Slobodan D., Avramov Ivić, Milka, "Electrochemical Oxidation of Donepezil and Its Voltammetric Determination at Gold Electrode" in Electroanalysis, 26, no. 5 (2014):893-897,
https://doi.org/10.1002/elan.201400034 . .

TY  - JOUR
AU  - Mladenović, Aleksandar R.
AU  - Jovanović, Vladislava M.
AU  - Petrović, Slobodan D.
AU  - Mijin, Dušan
AU  - Drmanić, Saša Ž.
AU  - Avramov Ivić, Milka
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1230
AB  - The determination of clopidogrel, an antiplatelet agent, was performed at a gold electrode in pH 3.7 acetate buffer using cyclic voltammetry (CV) and square wave voltammetry (SWV). Each voltammogram was characterized by the well defined peak at approximately 1.0 V. The current of anodic stripping peak exhibited a linear dependence on the clopidogrel concentration in the range from 317.89 to 935.16 μg cm-3. The obtained linearity was applied to determine clopidogrel in the tablet form of the pharmaceutical preparation (Plavix®). The results were compared to the UV spectrophotometric and HPLC methods. .
AB  - Klopidogrel je antitrombotski agens iz tijenopiridinske klase, koji se koristi za inhibiranje formiranja krvnih ugrušaka pri lečenju koronarne arterijske bolesti, periferne vaskularne bolesti, i cerebrovaskularne bolesti. Elektrohemijsko ponašanje klopidogrel standarda i kao sastojka tablete Plavix® je definisano cikličnom voltametrijom. Njihovo kvantitativno određivanje na elektrodi od zlata u acetatnom puferu, pH 3,7, urađeno je voltametrijom sa pravougaonim impulsima (SWV). Pokazano je obema tehnikama da je svaki voltamogram okarakterisan dobro definisanim strujnim vrhom na 1,0 V. Na osnovu linearne zavisnosti anodnih struja od koncentracije klopidogrel standarda određena je masa klopidogrela u Plavix® tableti. Dobijeni rezultati pokazuju da SWV tehnika može biti korišćena direktno, brzo i jednostavno za određivanje klopidogrela u tabletama. Rezultati dobijeni SWV voltametrijskom tehnikom su poređeni sa rezultatima analize klopidogrela UV spektrofotometrijom i tečnom hromatografijom sa visokim performansama. Analitički rezultati pokazuju da je masa aktivne supstance u tabletama Plavix® u okviru limita specifikovanog farmakopejom. To ukazuje da voltametrija sa pravougaonim impulsima može biti uspešna alternativa hromatografskim i spektrofotometrijskim metodama. .
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Determination of clopidogrel using square wave voltammetry at a gold electrode
T1  - Određivanje klopidogrela voltametrijom sa pravouglim impulsima na elektrodi od zlata
VL  - 78
IS  - 12
SP  - 2131
EP  - 2140
DO  - 10.2298/JSC130913116M
ER  - 

@article{
author = "Mladenović, Aleksandar R. and Jovanović, Vladislava M. and Petrović, Slobodan D. and Mijin, Dušan and Drmanić, Saša Ž. and Avramov Ivić, Milka",
year = "2013",
abstract = "The determination of clopidogrel, an antiplatelet agent, was performed at a gold electrode in pH 3.7 acetate buffer using cyclic voltammetry (CV) and square wave voltammetry (SWV). Each voltammogram was characterized by the well defined peak at approximately 1.0 V. The current of anodic stripping peak exhibited a linear dependence on the clopidogrel concentration in the range from 317.89 to 935.16 μg cm-3. The obtained linearity was applied to determine clopidogrel in the tablet form of the pharmaceutical preparation (Plavix®). The results were compared to the UV spectrophotometric and HPLC methods. ., Klopidogrel je antitrombotski agens iz tijenopiridinske klase, koji se koristi za inhibiranje formiranja krvnih ugrušaka pri lečenju koronarne arterijske bolesti, periferne vaskularne bolesti, i cerebrovaskularne bolesti. Elektrohemijsko ponašanje klopidogrel standarda i kao sastojka tablete Plavix® je definisano cikličnom voltametrijom. Njihovo kvantitativno određivanje na elektrodi od zlata u acetatnom puferu, pH 3,7, urađeno je voltametrijom sa pravougaonim impulsima (SWV). Pokazano je obema tehnikama da je svaki voltamogram okarakterisan dobro definisanim strujnim vrhom na 1,0 V. Na osnovu linearne zavisnosti anodnih struja od koncentracije klopidogrel standarda određena je masa klopidogrela u Plavix® tableti. Dobijeni rezultati pokazuju da SWV tehnika može biti korišćena direktno, brzo i jednostavno za određivanje klopidogrela u tabletama. Rezultati dobijeni SWV voltametrijskom tehnikom su poređeni sa rezultatima analize klopidogrela UV spektrofotometrijom i tečnom hromatografijom sa visokim performansama. Analitički rezultati pokazuju da je masa aktivne supstance u tabletama Plavix® u okviru limita specifikovanog farmakopejom. To ukazuje da voltametrija sa pravougaonim impulsima može biti uspešna alternativa hromatografskim i spektrofotometrijskim metodama. .",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Determination of clopidogrel using square wave voltammetry at a gold electrode, Određivanje klopidogrela voltametrijom sa pravouglim impulsima na elektrodi od zlata",
volume = "78",
number = "12",
pages = "2131-2140",
doi = "10.2298/JSC130913116M"
}

Mladenović, A. R., Jovanović, V. M., Petrović, S. D., Mijin, D., Drmanić, S. Ž.,& Avramov Ivić, M.. (2013). Determination of clopidogrel using square wave voltammetry at a gold electrode. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 78(12), 2131-2140.
https://doi.org/10.2298/JSC130913116M

Mladenović AR, Jovanović VM, Petrović SD, Mijin D, Drmanić SŽ, Avramov Ivić M. Determination of clopidogrel using square wave voltammetry at a gold electrode. in Journal of the Serbian Chemical Society. 2013;78(12):2131-2140.
doi:10.2298/JSC130913116M .

Mladenović, Aleksandar R., Jovanović, Vladislava M., Petrović, Slobodan D., Mijin, Dušan, Drmanić, Saša Ž., Avramov Ivić, Milka, "Determination of clopidogrel using square wave voltammetry at a gold electrode" in Journal of the Serbian Chemical Society, 78, no. 12 (2013):2131-2140,
https://doi.org/10.2298/JSC130913116M . .