Items

Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate, and their impurities on three different HILIC columns (2018-10)

I. Kasagić-Vujanović, B. Jančić-Stojanović, D. Ivanović, Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate, and their impurities on three different HILIC columns, JOURNAL OF LIQUID CHROMATOGRAPHY AND RELATED TECHNOLOGIES, Vol. 41, No. 9, pp. 523 - 531, Oct, 2018
Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns (2018-10)

I. Kasagić-Vujanović, B. Jančić-Stojanović, D. Knežević, D. Ivanović, Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns, pp. 401 - 402, Oct, 2018
Hemometrijska analiza hromatografskog ponašanja amlodipin-besilata i bisoprolol-fumarata u tečnoj hromatografiji hidrofilnih interakcija (2016)
Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna (2012-02)

I. Kasagić-Vujanović, M. Jovanović, T. Rakić, B. Jančić Stojanović, D. Ivanović, Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna, Arhiv za farmaciju, Vol. 62, No. 5, pp. 475 - 488, Feb, 2012
Chemometrically assissted optimization and validation of RP–HPLC method for the analysis of itraconazole and its impurities (2013-06)

I. Kasagić-Vujanović, A. Malenović, M. Jovanović, T. Rakić, B. Stojanović, D. Ivanović, Chemometrically assissted optimization and validation of RP–HPLC method for the analysis of itraconazole and its impurities, ACTA PHARMACEUTICA, Vol. 63, No. 2, pp. 159 - 173, Jun, 2013
Studije forsirane degradacije amlodipin-besilata i bisoprolol-fumarata primjenom tečne hromatografije hidrofilnih interakcija (2014)

I. Kasagić-Vujanović, B. Jančić Stojanović, D. Ivanović, Studije forsirane degradacije amlodipin-besilata i bisoprolol-fumarata primjenom tečne hromatografije hidrofilnih interakcija, Arhiv za farmaciju, Vol. 64, No. 3, pp. 230 - 246, 2014
Stability study of amlodipine besylate and bisoprolol fumarate in aqueous solutions (2014)

I. Vujanović-Kasagić, D. Jelić, V. Antunović, B. Jančić-Stojanović, D. Ivanović, Stability study of amlodipine besylate and bisoprolol fumarate in aqueous solutions, CONTEMPORARY MATERIALS, Vol. 5, No. 2, pp. 212 - 221, 2014
Comparison of full factorial desing, central composite desing and Box Behenken desing in cromatographic method development for the analysis of fluconazole and its impurities (2014-02)

T. Rakić, I. Kasagić-Vujanović, M. Jovanović, B. Jančić Stojanović, D. Ivanović, Comparison of full factorial desing, central composite desing and Box Behenken desing in cromatographic method development for the analysis of fluconazole and its impurities, ANALYTICAL LETTERS: AN INTERNATIONAL JOURNAL FOR RAPID COMMUNICATION, Vol. 47, No. 8, pp. 1334 - 1347, Feb, 2014
Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipin besylate and bisoprolol fumarate (2015-02)

I. Kasagić-Vujanović, B. Jančić-Stojanović, T. Rakić, D. Ivanović, Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipin besylate and bisoprolol fumarate, Journal of Liquid Chromatography & Related Technologies, Vol. 38, No. 8, pp. 919 - 928, Feb, 2015
QbD principles in validation of LC method for raloxifen and its impurities determination (2011-11)

B. Stojanović, T. Rakić, M. Šober, I. Kasagić-Vujanović, D. Ivanović, QbD principles in validation of LC method for raloxifen and its impurities determination, Zbornik radova - proceedings II Kongresa farmaceuta Bosne i Hercegovine, pp. 102 - 104, Nov, 2011
Ispitivanje uticaja promjene pH vrijednosti mobilne faze, sadržaja acetonitrila i trietilamina na retencione parametre nimesulida iz tableta primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom (2013-11)

I. Kasagić-Vujanović, I. Grabovac, M. Gajić, V. Vujanović, D. Ivanović, Ispitivanje uticaja promjene pH vrijednosti mobilne faze, sadržaja acetonitrila i trietilamina na retencione parametre nimesulida iz tableta primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom, Zbornik radova - proceedings, pp. 23 - 34, Nov, 2013
Application of chemical kinetics to predict/test the stability of amlodipine-besilate and bisoprolol-fumarate individualy and in mixture (2014)

I. Kasagić-Vujanović, D. Jelić, V. Antunović, B. Jančić-Stojanović, D. Ivanović, Application of chemical kinetics to predict/test the stability of amlodipine-besilate and bisoprolol-fumarate individualy and in mixture, ABSTRACT BOOK, pp. 185 - 186, 2014
Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and bisoprolol fumarate (2014-09)

I. Kasagić-Vujanović, B. Jančić Stojanović, D. Ivanović, Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and bisoprolol fumarate, Communicating Separation Science for the Future, pp. 107 - 108, Sep, 2014
Stability testing of bisoprolol fumarate in the presence of stress agents using hidrophilic interactions liquid chromatography and UPLC–MS/MS methods (2015-05)

I. Kasagić-Vujanović, B. Stojanović, D. Ivanović, Stability testing of bisoprolol fumarate in the presence of stress agents using hidrophilic interactions liquid chromatography and UPLC–MS/MS methods, Pharmacia 2015; Vol. 18(1), pp. 182 - 183, May, 2015
Poređenje punog faktorskog dizajna, centralnog kompozicionog dizajna i Box–Behenken dizajna u razvoju hromatografske metode za analizu flukonazola i njegovih nečistoća (2015-05)

T. Rakić, I. Kasagić-Vujanović, M. Jovanović, B. Jančić Stojanović, D. Ivanović, Poređenje punog faktorskog dizajna, centralnog kompozicionog dizajna i Box–Behenken dizajna u razvoju hromatografske metode za analizu flukonazola i njegovih nečistoća, Zbornik sažetaka II Kongresa farmaceuta Crne Gore sa međunarodnim učešćem, pp. 192 - 193, May, 2015
Praćenje stabilnosti amlodipin-besilata stres testom primjenom tečne hromatografije hidrofilnih interakcija i tečnom hromatografijom sa masenim detektorom (2015-05)

I. Kasagić-Vujanović, B. Jančić Stojanović, D. Ivanović, Praćenje stabilnosti amlodipin-besilata stres testom primjenom tečne hromatografije hidrofilnih interakcija i tečnom hromatografijom sa masenim detektorom, Zbornik sažetaka II Kongresa farmaceuta Crne Gore sa međunarodnim učešćem, pp. 194 - 195, May, 2015
The stage of termal degradation of amlodipine besylate estimated by simultaneous TG/DTA analysis (2015-05)

I. Kasagić-Vujanović, D. Jelić, S. Mentus, B. Jančić Stojanović, D. Ivanović, The stage of termal degradation of amlodipine besylate estimated by simultaneous TG/DTA analysis, Pharmacia 2015; Vol. 18 (1), pp. 163 - 164, May, 2015
Experimental desing in the optimization and validation of RP–HPLC mrthod for the determination of itraconazole and its impurities (2015-05)

I. Kasagić-Vujanović, M. Jovanović, B. Stojanović, D. Ivanović, Experimental desing in the optimization and validation of RP–HPLC mrthod for the determination of itraconazole and its impurities, Pharmacia 2015; Vol 18(1), pp. 178 - 179, May, 2015
Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns (2018)

I. Kasagić-Vujanović, B. Jančić-Stojanović, D. Knežević, D. Ivanović, Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns, pp. 401 - 402, 2018
Testing of the effect of change pH value of mobile phase and the content of acetonitril and triethylamine on retention parameters of nimesulide in tablet form using reversed–phase high–pressure liquid chromatography (2013-11)

I. Kasagić-Vujanović, I. Grabovac, M. Gajić, V. Vujanović, D. Ivanović, Testing of the effect of change pH value of mobile phase and the content of acetonitril and triethylamine on retention parameters of nimesulide in tablet form using reversed–phase high–pressure liquid chromatography, Zbornik radova, pp. 23 - 34, Nov, 2013

Items

Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate, and their impurities on three different HILIC columns (2018-10)

Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns (2018-10)

Hemometrijska analiza hromatografskog ponašanja amlodipin-besilata i bisoprolol-fumarata u tečnoj hromatografiji hidrofilnih interakcija (2016)

Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna (2012-02)

Chemometrically assissted optimization and validation of RP–HPLC method for the analysis of itraconazole and its impurities (2013-06)

Studije forsirane degradacije amlodipin-besilata i bisoprolol-fumarata primjenom tečne hromatografije hidrofilnih interakcija (2014)

Stability study of amlodipine besylate and bisoprolol fumarate in aqueous solutions (2014)

Comparison of full factorial desing, central composite desing and Box Behenken desing in cromatographic method development for the analysis of fluconazole and its impurities (2014-02)

Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipin besylate and bisoprolol fumarate (2015-02)

QbD principles in validation of LC method for raloxifen and its impurities determination (2011-11)

Ispitivanje uticaja promjene pH vrijednosti mobilne faze, sadržaja acetonitrila i trietilamina na retencione parametre nimesulida iz tableta primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom (2013-11)

Application of chemical kinetics to predict/test the stability of amlodipine-besilate and bisoprolol-fumarate individualy and in mixture (2014)

Desing of experiments in optimization and validation of a hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and bisoprolol fumarate (2014-09)

Stability testing of bisoprolol fumarate in the presence of stress agents using hidrophilic interactions liquid chromatography and UPLC–MS/MS methods (2015-05)

Poređenje punog faktorskog dizajna, centralnog kompozicionog dizajna i Box–Behenken dizajna u razvoju hromatografske metode za analizu flukonazola i njegovih nečistoća (2015-05)

Praćenje stabilnosti amlodipin-besilata stres testom primjenom tečne hromatografije hidrofilnih interakcija i tečnom hromatografijom sa masenim detektorom (2015-05)

The stage of termal degradation of amlodipine besylate estimated by simultaneous TG/DTA analysis (2015-05)

Experimental desing in the optimization and validation of RP–HPLC mrthod for the determination of itraconazole and its impurities (2015-05)

Investigation of the retention mechanisms of amlodipine besylate, bisoprolol fumarate and their impurities on three different HILIC columns (2018)

Testing of the effect of change pH value of mobile phase and the content of acetonitril and triethylamine on retention parameters of nimesulide in tablet form using reversed–phase high–pressure liquid chromatography (2013-11)