Jović, Žarko

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  • Jović, Žarko (9)
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Author's Bibliography

Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods

Malesević, M.; Živanović, Ljiljana; Protić, Ana; Radisić, Marina; Lausević, M.; Jović, Žarko; Zečević, Mira

(Akademiai Kiado Zrt, Budapest, 2014)

TY  - JOUR
AU  - Malesević, M.
AU  - Živanović, Ljiljana
AU  - Protić, Ana
AU  - Radisić, Marina
AU  - Lausević, M.
AU  - Jović, Žarko
AU  - Zečević, Mira
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2150
AB  - The present study was designed to characterize the possible degradation products of zolpidem tartrate under various stress conditions according to International Conference on Harmonization (ICH) guidelines Q1A(R2). After exposure to light, heat, hydrolysis, and oxidation, the drug significantly degraded under photolytic and acid/base hydrolytic conditions. Degradation resulted in the formation of four key degradants. Degradation products were resolved from each other and the drug by employing an isocratic elution method on Luna C-18 column with mobile phase consisting of methanol-10 mM ammonium acetate (68.4: 31.6, v/v), wherein pH was adjusted to 5.4 with glacial acetic acid. To characterize the degradation products, a method was extended to LC-MS and a mass fragmentation pattern was established using single quad-rupole. The degradants were identified as zolpacid, oxozolpidem, zolpaldehyde, and zolpyridine. Finally, the most possible degradation mechanism of zolpidem tartrate in different environments was proposed.
PB  - Akademiai Kiado Zrt, Budapest
T2  - Acta Chromatographica
T1  - Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods
VL  - 26
IS  - 1
SP  - 81
EP  - 96
DO  - 10.1556/AChrom.26.2014.1.8
ER  - 
@article{
author = "Malesević, M. and Živanović, Ljiljana and Protić, Ana and Radisić, Marina and Lausević, M. and Jović, Žarko and Zečević, Mira",
year = "2014",
abstract = "The present study was designed to characterize the possible degradation products of zolpidem tartrate under various stress conditions according to International Conference on Harmonization (ICH) guidelines Q1A(R2). After exposure to light, heat, hydrolysis, and oxidation, the drug significantly degraded under photolytic and acid/base hydrolytic conditions. Degradation resulted in the formation of four key degradants. Degradation products were resolved from each other and the drug by employing an isocratic elution method on Luna C-18 column with mobile phase consisting of methanol-10 mM ammonium acetate (68.4: 31.6, v/v), wherein pH was adjusted to 5.4 with glacial acetic acid. To characterize the degradation products, a method was extended to LC-MS and a mass fragmentation pattern was established using single quad-rupole. The degradants were identified as zolpacid, oxozolpidem, zolpaldehyde, and zolpyridine. Finally, the most possible degradation mechanism of zolpidem tartrate in different environments was proposed.",
publisher = "Akademiai Kiado Zrt, Budapest",
journal = "Acta Chromatographica",
title = "Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods",
volume = "26",
number = "1",
pages = "81-96",
doi = "10.1556/AChrom.26.2014.1.8"
}
Malesević, M., Živanović, L., Protić, A., Radisić, M., Lausević, M., Jović, Ž.,& Zečević, M.. (2014). Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods. in Acta Chromatographica
Akademiai Kiado Zrt, Budapest., 26(1), 81-96.
https://doi.org/10.1556/AChrom.26.2014.1.8
Malesević M, Živanović L, Protić A, Radisić M, Lausević M, Jović Ž, Zečević M. Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods. in Acta Chromatographica. 2014;26(1):81-96.
doi:10.1556/AChrom.26.2014.1.8 .
Malesević, M., Živanović, Ljiljana, Protić, Ana, Radisić, Marina, Lausević, M., Jović, Žarko, Zečević, Mira, "Stress Degradation Studies on Zolpidem Tartrate Using LC-DAD and LC-MS Methods" in Acta Chromatographica, 26, no. 1 (2014):81-96,
https://doi.org/10.1556/AChrom.26.2014.1.8 . .
6
4
5

Forced degradation study of torasemide: Characterization of its degradation products

Jović, Žarko; Živanović, Ljiljana; Protić, Ana; Radisić, Marina; Lausević, Mila; Malešević, Marija; Zečević, Mira

(Taylor & Francis Inc, Philadelphia, 2013)

TY  - JOUR
AU  - Jović, Žarko
AU  - Živanović, Ljiljana
AU  - Protić, Ana
AU  - Radisić, Marina
AU  - Lausević, Mila
AU  - Malešević, Marija
AU  - Zečević, Mira
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1961
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3431
AB  - Torasemide was subjected to forced degradation studies. Stress conditions were varied concerning hydrolysis (acid, base, and neutral), oxidation, photolysis, and thermal degradation in order to identify the potential degradation products and consequently establish the possible degradation pathways and intrinsic stability of the drug. The study was performed according to ICH guidelines and drug was found to be relatively stable in the solid form. It showed that torasemide degraded significantly under acidic, neutral and alkaline conditions and resulted in formation of degradation product R2. When temperature was increased the degradation was accelerated. Also, the drug showed slight instability under extreme oxidative stress conditions which resulted in formation of two degradation products in total. The drug and degradation products have been separated employing gradient elution method on Zorbax SB C-18 analytical column. To characterize the degradation products LC-MSn was applied. The mass fragmentation pattern was established using single quadrupole and ion trap mass analyzers. Finally, the most possible degradation mechanism of torasemide in different experimental conditions was proposed.
PB  - Taylor & Francis Inc, Philadelphia
T2  - Journal of Liquid Chromatography & Related Technologies
T1  - Forced degradation study of torasemide: Characterization of its degradation products
VL  - 36
IS  - 15
SP  - 2082
EP  - 2094
DO  - 10.1080/10826076.2012.712932
ER  - 
@article{
author = "Jović, Žarko and Živanović, Ljiljana and Protić, Ana and Radisić, Marina and Lausević, Mila and Malešević, Marija and Zečević, Mira",
year = "2013",
abstract = "Torasemide was subjected to forced degradation studies. Stress conditions were varied concerning hydrolysis (acid, base, and neutral), oxidation, photolysis, and thermal degradation in order to identify the potential degradation products and consequently establish the possible degradation pathways and intrinsic stability of the drug. The study was performed according to ICH guidelines and drug was found to be relatively stable in the solid form. It showed that torasemide degraded significantly under acidic, neutral and alkaline conditions and resulted in formation of degradation product R2. When temperature was increased the degradation was accelerated. Also, the drug showed slight instability under extreme oxidative stress conditions which resulted in formation of two degradation products in total. The drug and degradation products have been separated employing gradient elution method on Zorbax SB C-18 analytical column. To characterize the degradation products LC-MSn was applied. The mass fragmentation pattern was established using single quadrupole and ion trap mass analyzers. Finally, the most possible degradation mechanism of torasemide in different experimental conditions was proposed.",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Journal of Liquid Chromatography & Related Technologies",
title = "Forced degradation study of torasemide: Characterization of its degradation products",
volume = "36",
number = "15",
pages = "2082-2094",
doi = "10.1080/10826076.2012.712932"
}
Jović, Ž., Živanović, L., Protić, A., Radisić, M., Lausević, M., Malešević, M.,& Zečević, M.. (2013). Forced degradation study of torasemide: Characterization of its degradation products. in Journal of Liquid Chromatography & Related Technologies
Taylor & Francis Inc, Philadelphia., 36(15), 2082-2094.
https://doi.org/10.1080/10826076.2012.712932
Jović Ž, Živanović L, Protić A, Radisić M, Lausević M, Malešević M, Zečević M. Forced degradation study of torasemide: Characterization of its degradation products. in Journal of Liquid Chromatography & Related Technologies. 2013;36(15):2082-2094.
doi:10.1080/10826076.2012.712932 .
Jović, Žarko, Živanović, Ljiljana, Protić, Ana, Radisić, Marina, Lausević, Mila, Malešević, Marija, Zečević, Mira, "Forced degradation study of torasemide: Characterization of its degradation products" in Journal of Liquid Chromatography & Related Technologies, 36, no. 15 (2013):2082-2094,
https://doi.org/10.1080/10826076.2012.712932 . .
5
5
6

Forced degradation study of torasemide: Characterization of its degradation products

Jović, Žarko; Živanović, Ljiljana; Protić, Ana; Radisić, Marina; Lausević, Mila; Malešević, Marija; Zečević, Mira

(Taylor & Francis Inc, Philadelphia, 2013)

TY  - JOUR
AU  - Jović, Žarko
AU  - Živanović, Ljiljana
AU  - Protić, Ana
AU  - Radisić, Marina
AU  - Lausević, Mila
AU  - Malešević, Marija
AU  - Zečević, Mira
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1961
AB  - Torasemide was subjected to forced degradation studies. Stress conditions were varied concerning hydrolysis (acid, base, and neutral), oxidation, photolysis, and thermal degradation in order to identify the potential degradation products and consequently establish the possible degradation pathways and intrinsic stability of the drug. The study was performed according to ICH guidelines and drug was found to be relatively stable in the solid form. It showed that torasemide degraded significantly under acidic, neutral and alkaline conditions and resulted in formation of degradation product R2. When temperature was increased the degradation was accelerated. Also, the drug showed slight instability under extreme oxidative stress conditions which resulted in formation of two degradation products in total. The drug and degradation products have been separated employing gradient elution method on Zorbax SB C-18 analytical column. To characterize the degradation products LC-MSn was applied. The mass fragmentation pattern was established using single quadrupole and ion trap mass analyzers. Finally, the most possible degradation mechanism of torasemide in different experimental conditions was proposed.
PB  - Taylor & Francis Inc, Philadelphia
T2  - Journal of Liquid Chromatography & Related Technologies
T1  - Forced degradation study of torasemide: Characterization of its degradation products
VL  - 36
IS  - 15
SP  - 2082
EP  - 2094
DO  - 10.1080/10826076.2012.712932
ER  - 
@article{
author = "Jović, Žarko and Živanović, Ljiljana and Protić, Ana and Radisić, Marina and Lausević, Mila and Malešević, Marija and Zečević, Mira",
year = "2013",
abstract = "Torasemide was subjected to forced degradation studies. Stress conditions were varied concerning hydrolysis (acid, base, and neutral), oxidation, photolysis, and thermal degradation in order to identify the potential degradation products and consequently establish the possible degradation pathways and intrinsic stability of the drug. The study was performed according to ICH guidelines and drug was found to be relatively stable in the solid form. It showed that torasemide degraded significantly under acidic, neutral and alkaline conditions and resulted in formation of degradation product R2. When temperature was increased the degradation was accelerated. Also, the drug showed slight instability under extreme oxidative stress conditions which resulted in formation of two degradation products in total. The drug and degradation products have been separated employing gradient elution method on Zorbax SB C-18 analytical column. To characterize the degradation products LC-MSn was applied. The mass fragmentation pattern was established using single quadrupole and ion trap mass analyzers. Finally, the most possible degradation mechanism of torasemide in different experimental conditions was proposed.",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Journal of Liquid Chromatography & Related Technologies",
title = "Forced degradation study of torasemide: Characterization of its degradation products",
volume = "36",
number = "15",
pages = "2082-2094",
doi = "10.1080/10826076.2012.712932"
}
Jović, Ž., Živanović, L., Protić, A., Radisić, M., Lausević, M., Malešević, M.,& Zečević, M.. (2013). Forced degradation study of torasemide: Characterization of its degradation products. in Journal of Liquid Chromatography & Related Technologies
Taylor & Francis Inc, Philadelphia., 36(15), 2082-2094.
https://doi.org/10.1080/10826076.2012.712932
Jović Ž, Živanović L, Protić A, Radisić M, Lausević M, Malešević M, Zečević M. Forced degradation study of torasemide: Characterization of its degradation products. in Journal of Liquid Chromatography & Related Technologies. 2013;36(15):2082-2094.
doi:10.1080/10826076.2012.712932 .
Jović, Žarko, Živanović, Ljiljana, Protić, Ana, Radisić, Marina, Lausević, Mila, Malešević, Marija, Zečević, Mira, "Forced degradation study of torasemide: Characterization of its degradation products" in Journal of Liquid Chromatography & Related Technologies, 36, no. 15 (2013):2082-2094,
https://doi.org/10.1080/10826076.2012.712932 . .
5
5
6

Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities

Jović, Žarko; Živanović, Ljiljana; Radisić, Marina; Protić, Ana; Malesevic, Marija

(Oxford Univ Press Inc, Cary, 2012)

TY  - JOUR
AU  - Jović, Žarko
AU  - Živanović, Ljiljana
AU  - Radisić, Marina
AU  - Protić, Ana
AU  - Malesevic, Marija
PY  - 2012
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1700
PB  - Oxford Univ Press Inc, Cary
T2  - Journal of Chromatographic Science
T1  - Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities
VL  - 50
IS  - 4
SP  - 324
EP  - 334
DO  - 10.1093/chromsci/bms033
ER  - 
@article{
author = "Jović, Žarko and Živanović, Ljiljana and Radisić, Marina and Protić, Ana and Malesevic, Marija",
year = "2012",
publisher = "Oxford Univ Press Inc, Cary",
journal = "Journal of Chromatographic Science",
title = "Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities",
volume = "50",
number = "4",
pages = "324-334",
doi = "10.1093/chromsci/bms033"
}
Jović, Ž., Živanović, L., Radisić, M., Protić, A.,& Malesevic, M.. (2012). Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities. in Journal of Chromatographic Science
Oxford Univ Press Inc, Cary., 50(4), 324-334.
https://doi.org/10.1093/chromsci/bms033
Jović Ž, Živanović L, Radisić M, Protić A, Malesevic M. Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities. in Journal of Chromatographic Science. 2012;50(4):324-334.
doi:10.1093/chromsci/bms033 .
Jović, Žarko, Živanović, Ljiljana, Radisić, Marina, Protić, Ana, Malesevic, Marija, "Chemometrically Assisted Development and Validation of LC-UV and LC-MS Methods for Simultaneous Determination of Torasemide and its Impurities" in Journal of Chromatographic Science, 50, no. 4 (2012):324-334,
https://doi.org/10.1093/chromsci/bms033 . .
5
2
5

Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products

Malesevic, Marija; Živanović, Ljiljana; Protić, Ana; Jović, Žarko

(Springer Heidelberg, Heidelberg, 2011)

TY  - JOUR
AU  - Malesevic, Marija
AU  - Živanović, Ljiljana
AU  - Protić, Ana
AU  - Jović, Žarko
PY  - 2011
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1485
AB  - Multiresponse optimization methodology in combination with experimental design was employed as a powerful technique for simultaneous optimization of input variables significant for evaluation of chromatographic behaviour of zolpidem tartrate, zolpacid, oxozolpidem, zolpyridine and zolpaldehyde towards various responses. In the first stage of the investigation fractional factorial design was used to decrease the number of variables that should be studied in detail. Among examined variables, pH of the mobile phase, percentage of organic modifier and buffer concentration showed to be statistically important and were consequently optimized with central composite design and Derringer's desirability function. Four responses were considered, the retention factors of zolpacid and zolpaldehyde (the first and last peak) and the resolutions between critical peaks. Optimal conditions included Luna C-18(2) analytical column (250 mm x 4.6 mm, 5 mu m particle size), mobile phase consisted of methanol-10 mM ammonium acetate (68.4:31.6, v/v, pH 5.4) and column temperature of 35 degrees C. The flow rate of the mobile phase was 1 mL min(-1) and the detection was performed at 254 nm. At the end, the method was successfully validated in accordance with ICH guideline and subsequently applied to the analysis of commercially available zolpidem tartrate tablets.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products
VL  - 74
IS  - 3-4
SP  - 197
EP  - 208
DO  - 10.1007/s10337-011-2064-9
ER  - 
@article{
author = "Malesevic, Marija and Živanović, Ljiljana and Protić, Ana and Jović, Žarko",
year = "2011",
abstract = "Multiresponse optimization methodology in combination with experimental design was employed as a powerful technique for simultaneous optimization of input variables significant for evaluation of chromatographic behaviour of zolpidem tartrate, zolpacid, oxozolpidem, zolpyridine and zolpaldehyde towards various responses. In the first stage of the investigation fractional factorial design was used to decrease the number of variables that should be studied in detail. Among examined variables, pH of the mobile phase, percentage of organic modifier and buffer concentration showed to be statistically important and were consequently optimized with central composite design and Derringer's desirability function. Four responses were considered, the retention factors of zolpacid and zolpaldehyde (the first and last peak) and the resolutions between critical peaks. Optimal conditions included Luna C-18(2) analytical column (250 mm x 4.6 mm, 5 mu m particle size), mobile phase consisted of methanol-10 mM ammonium acetate (68.4:31.6, v/v, pH 5.4) and column temperature of 35 degrees C. The flow rate of the mobile phase was 1 mL min(-1) and the detection was performed at 254 nm. At the end, the method was successfully validated in accordance with ICH guideline and subsequently applied to the analysis of commercially available zolpidem tartrate tablets.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products",
volume = "74",
number = "3-4",
pages = "197-208",
doi = "10.1007/s10337-011-2064-9"
}
Malesevic, M., Živanović, L., Protić, A.,& Jović, Ž.. (2011). Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products. in Chromatographia
Springer Heidelberg, Heidelberg., 74(3-4), 197-208.
https://doi.org/10.1007/s10337-011-2064-9
Malesevic M, Živanović L, Protić A, Jović Ž. Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products. in Chromatographia. 2011;74(3-4):197-208.
doi:10.1007/s10337-011-2064-9 .
Malesevic, Marija, Živanović, Ljiljana, Protić, Ana, Jović, Žarko, "Multiobjective Optimization Approach in Evaluation of Chromatographic Behaviour of Zolpidem Tartrate and Its Degradation Products" in Chromatographia, 74, no. 3-4 (2011):197-208,
https://doi.org/10.1007/s10337-011-2064-9 . .
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6
8

Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles

Cekić, Nebojša; Milić, Jela; Savić, Snežana; Savić, Miroslav; Jović, Žarko; Daniels, Rolf

(Taylor & Francis Ltd, Abingdon, 2009)

TY  - JOUR
AU  - Cekić, Nebojša
AU  - Milić, Jela
AU  - Savić, Snežana
AU  - Savić, Miroslav
AU  - Jović, Žarko
AU  - Daniels, Rolf
PY  - 2009
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1261
AB  - Background: The potential for use of chitosan-treated alginate microparticles as a vehicle for oral phenytoin delivery has not been thoroughly exploited. Aim: We studied the influence of preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles. Method: The total number of 24 microparticles formulations prepared by varying contents of calcium gelling ions and varying contents and type of chitosan was examined. As an additional variable, two different hardening times (1 and 24 hours) were employed. Possible interactions of components, surface morphology of microparticles as well as release profile of phenytoin were studied. Results: Both series of formulations with regard to hardening times, irrespective of the chitosan type and/or concentration employed appeared to be highly loaded with the model drug (above 90%). The drug release studies showed that the kinetics of phenytoin cannot be straightforwardly predicted based on the molecular weight of chitosan alone. On the other hand, prolonging the hardening time from 1 to 24 hours had significantly improved phenytoin kinetics, and gave rise to a formulation with the liberation half-time of about 2.5 hours. Conclusion: This study showed that the latter formulation is eligible for further modifications aimed at improving the regularity of phenytoin absorption.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Drug Development and Industrial Pharmacy
T1  - Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles
VL  - 35
IS  - 9
SP  - 1092
EP  - 1102
DO  - 10.1080/03639040902774164
ER  - 
@article{
author = "Cekić, Nebojša and Milić, Jela and Savić, Snežana and Savić, Miroslav and Jović, Žarko and Daniels, Rolf",
year = "2009",
abstract = "Background: The potential for use of chitosan-treated alginate microparticles as a vehicle for oral phenytoin delivery has not been thoroughly exploited. Aim: We studied the influence of preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles. Method: The total number of 24 microparticles formulations prepared by varying contents of calcium gelling ions and varying contents and type of chitosan was examined. As an additional variable, two different hardening times (1 and 24 hours) were employed. Possible interactions of components, surface morphology of microparticles as well as release profile of phenytoin were studied. Results: Both series of formulations with regard to hardening times, irrespective of the chitosan type and/or concentration employed appeared to be highly loaded with the model drug (above 90%). The drug release studies showed that the kinetics of phenytoin cannot be straightforwardly predicted based on the molecular weight of chitosan alone. On the other hand, prolonging the hardening time from 1 to 24 hours had significantly improved phenytoin kinetics, and gave rise to a formulation with the liberation half-time of about 2.5 hours. Conclusion: This study showed that the latter formulation is eligible for further modifications aimed at improving the regularity of phenytoin absorption.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Drug Development and Industrial Pharmacy",
title = "Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles",
volume = "35",
number = "9",
pages = "1092-1102",
doi = "10.1080/03639040902774164"
}
Cekić, N., Milić, J., Savić, S., Savić, M., Jović, Ž.,& Daniels, R.. (2009). Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles. in Drug Development and Industrial Pharmacy
Taylor & Francis Ltd, Abingdon., 35(9), 1092-1102.
https://doi.org/10.1080/03639040902774164
Cekić N, Milić J, Savić S, Savić M, Jović Ž, Daniels R. Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles. in Drug Development and Industrial Pharmacy. 2009;35(9):1092-1102.
doi:10.1080/03639040902774164 .
Cekić, Nebojša, Milić, Jela, Savić, Snežana, Savić, Miroslav, Jović, Žarko, Daniels, Rolf, "Influence of the preparation procedure and chitosan type on physicochemical properties and release behavior of alginate-chitosan microparticles" in Drug Development and Industrial Pharmacy, 35, no. 9 (2009):1092-1102,
https://doi.org/10.1080/03639040902774164 . .
3
20
16
16

Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles

Cekić, Nebojša; Savić, Snežana; Milić, Jela; Savić, Miroslav; Jović, Žarko; Malesević, Marjia

(Taylor & Francis Inc, Philadelphia, 2007)

TY  - JOUR
AU  - Cekić, Nebojša
AU  - Savić, Snežana
AU  - Milić, Jela
AU  - Savić, Miroslav
AU  - Jović, Žarko
AU  - Malesević, Marjia
PY  - 2007
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/890
AB  - We aimed to prepare and investigate microparticles with the varying contents of calcium gelling ion, loaded with phenytoin, a standard antiepileptic agent, in its acidic form. Two different methods of alginate-based microparticles preparation were used: with and without treatment with chitosan. Furthermore, two standard procedures, the one-stage and the two-stage, were applied. Microparticle size of 12 one-stage formulations ranged from 466 to 636 m. Both types of formulations, chitosan-treated and nontreated, appeared to be highly loaded with the model drug ( 91-96%). The chitosan-coated alginate-based microparticles prepared by the one-stage procedure exhibited kinetics of phenytoin liberation comparable to a similar sustained release system that had been tested at pH 6.8, as published earlier. As the gel erosion of alginate-based microparticles should be potentiated by the higher pH ( used in the present study at pH 7.4), the most favorable of 12 formulations, with the liberation half-time of about 2 hr, seemed to be eligible for further modifications. Counterintuitively, the applied two-stage procedure did not appear to beneficially affect the dissolution behavior of phenytoin when tested in two formulations, which makes further modifications necessary.
PB  - Taylor & Francis Inc, Philadelphia
T2  - Drug Delivery
T1  - Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles
VL  - 14
IS  - 8
SP  - 483
EP  - 490
DO  - 10.1080/10717540701604769
ER  - 
@article{
author = "Cekić, Nebojša and Savić, Snežana and Milić, Jela and Savić, Miroslav and Jović, Žarko and Malesević, Marjia",
year = "2007",
abstract = "We aimed to prepare and investigate microparticles with the varying contents of calcium gelling ion, loaded with phenytoin, a standard antiepileptic agent, in its acidic form. Two different methods of alginate-based microparticles preparation were used: with and without treatment with chitosan. Furthermore, two standard procedures, the one-stage and the two-stage, were applied. Microparticle size of 12 one-stage formulations ranged from 466 to 636 m. Both types of formulations, chitosan-treated and nontreated, appeared to be highly loaded with the model drug ( 91-96%). The chitosan-coated alginate-based microparticles prepared by the one-stage procedure exhibited kinetics of phenytoin liberation comparable to a similar sustained release system that had been tested at pH 6.8, as published earlier. As the gel erosion of alginate-based microparticles should be potentiated by the higher pH ( used in the present study at pH 7.4), the most favorable of 12 formulations, with the liberation half-time of about 2 hr, seemed to be eligible for further modifications. Counterintuitively, the applied two-stage procedure did not appear to beneficially affect the dissolution behavior of phenytoin when tested in two formulations, which makes further modifications necessary.",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Drug Delivery",
title = "Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles",
volume = "14",
number = "8",
pages = "483-490",
doi = "10.1080/10717540701604769"
}
Cekić, N., Savić, S., Milić, J., Savić, M., Jović, Ž.,& Malesević, M.. (2007). Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles. in Drug Delivery
Taylor & Francis Inc, Philadelphia., 14(8), 483-490.
https://doi.org/10.1080/10717540701604769
Cekić N, Savić S, Milić J, Savić M, Jović Ž, Malesević M. Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles. in Drug Delivery. 2007;14(8):483-490.
doi:10.1080/10717540701604769 .
Cekić, Nebojša, Savić, Snežana, Milić, Jela, Savić, Miroslav, Jović, Žarko, Malesević, Marjia, "Preparation and characterisation of phenytoin-loaded alginate and alginate-chitosan microparticles" in Drug Delivery, 14, no. 8 (2007):483-490,
https://doi.org/10.1080/10717540701604769 . .
6
14
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18

Formulation and characterization of alginate-based microparticles

Cekić, Nebojša; Savić, Snežana; Savić, Miroslav; Jović, Žarko; Malešević, M.; Milić, Jela

(Savez farmaceutskih udruženja Srbije, Beograd, 2006)

TY  - CONF
AU  - Cekić, Nebojša
AU  - Savić, Snežana
AU  - Savić, Miroslav
AU  - Jović, Žarko
AU  - Malešević, M.
AU  - Milić, Jela
PY  - 2006
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/831
PB  - Savez farmaceutskih udruženja Srbije, Beograd
C3  - Arhiv za farmaciju
T1  - Formulation and characterization of alginate-based microparticles
T1  - Formulacija i karakterizacija mikročestica na bazi alginata
VL  - 56
IS  - 4
SP  - 444
EP  - 445
UR  - https://hdl.handle.net/21.15107/rcub_farfar_831
ER  - 
@conference{
author = "Cekić, Nebojša and Savić, Snežana and Savić, Miroslav and Jović, Žarko and Malešević, M. and Milić, Jela",
year = "2006",
publisher = "Savez farmaceutskih udruženja Srbije, Beograd",
journal = "Arhiv za farmaciju",
title = "Formulation and characterization of alginate-based microparticles, Formulacija i karakterizacija mikročestica na bazi alginata",
volume = "56",
number = "4",
pages = "444-445",
url = "https://hdl.handle.net/21.15107/rcub_farfar_831"
}
Cekić, N., Savić, S., Savić, M., Jović, Ž., Malešević, M.,& Milić, J.. (2006). Formulation and characterization of alginate-based microparticles. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije, Beograd., 56(4), 444-445.
https://hdl.handle.net/21.15107/rcub_farfar_831
Cekić N, Savić S, Savić M, Jović Ž, Malešević M, Milić J. Formulation and characterization of alginate-based microparticles. in Arhiv za farmaciju. 2006;56(4):444-445.
https://hdl.handle.net/21.15107/rcub_farfar_831 .
Cekić, Nebojša, Savić, Snežana, Savić, Miroslav, Jović, Žarko, Malešević, M., Milić, Jela, "Formulation and characterization of alginate-based microparticles" in Arhiv za farmaciju, 56, no. 4 (2006):444-445,
https://hdl.handle.net/21.15107/rcub_farfar_831 .

Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products

Đukić-Ćosić, Danijela; Plamenac-Bulat, Zorica; Jović, Žarko; Vuleta, Gordana; Matović, Vesna

(Savez farmaceutskih udruženja Srbije, Beograd, 2006)

TY  - CONF
AU  - Đukić-Ćosić, Danijela
AU  - Plamenac-Bulat, Zorica
AU  - Jović, Žarko
AU  - Vuleta, Gordana
AU  - Matović, Vesna
PY  - 2006
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/795
PB  - Savez farmaceutskih udruženja Srbije, Beograd
C3  - Arhiv za farmaciju
T1  - Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products
T1  - Određivanje sadržaja toksičnih metala (Pb, Cd, Cr, As, Hg i Ni) u kozmetičkim proizvodima za negu kože lica
VL  - 56
IS  - 4
SP  - 612
EP  - 613
UR  - https://hdl.handle.net/21.15107/rcub_farfar_795
ER  - 
@conference{
author = "Đukić-Ćosić, Danijela and Plamenac-Bulat, Zorica and Jović, Žarko and Vuleta, Gordana and Matović, Vesna",
year = "2006",
publisher = "Savez farmaceutskih udruženja Srbije, Beograd",
journal = "Arhiv za farmaciju",
title = "Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products, Određivanje sadržaja toksičnih metala (Pb, Cd, Cr, As, Hg i Ni) u kozmetičkim proizvodima za negu kože lica",
volume = "56",
number = "4",
pages = "612-613",
url = "https://hdl.handle.net/21.15107/rcub_farfar_795"
}
Đukić-Ćosić, D., Plamenac-Bulat, Z., Jović, Ž., Vuleta, G.,& Matović, V.. (2006). Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije, Beograd., 56(4), 612-613.
https://hdl.handle.net/21.15107/rcub_farfar_795
Đukić-Ćosić D, Plamenac-Bulat Z, Jović Ž, Vuleta G, Matović V. Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products. in Arhiv za farmaciju. 2006;56(4):612-613.
https://hdl.handle.net/21.15107/rcub_farfar_795 .
Đukić-Ćosić, Danijela, Plamenac-Bulat, Zorica, Jović, Žarko, Vuleta, Gordana, Matović, Vesna, "Determination of toxic metals (Pb, Cd, Cr, As, Hg and Ni) in face care cosmetic products" in Arhiv za farmaciju, 56, no. 4 (2006):612-613,
https://hdl.handle.net/21.15107/rcub_farfar_795 .