Уноси

Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach (2022-06)

Н. Мандић-Ковачевић, I. Kasagić-Vujanović, A. Popović Bijelić, Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach, JOURNAL OF CHROMATOGRAPHIC SCIENCE, Vol. bmac044, pp. 1 - 13, Jun, 2022
Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach (2022-08)

Н. Мандић-Ковачевић, I. Kasagić-Vujanović, A. Popović Bijelić, Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach, Journal of Chromatographic Science, Vol. 1, No. 1, pp. 1 - 13, Aug, 2022
Design of experiments and Derringer’s desirability function in optimisation and validation of RP-HPLC method for the analysis of enrofloxacin and its impurities (2023-01)

J. Dokmanović, I. Kasagić-Vujanović, Ж. Гагић, K. Nikolić, M. Čarapić, D. Agbaba, Design of experiments and Derringer’s desirability function in optimisation and validation of RP-HPLC method for the analysis of enrofloxacin and its impurities, Acta Chromatographica , Vol. 1, No. 1, pp. 1 - 11, Jan, 2023
Ispitivanje efikasnosti inkapsulacije ketoprofena u poli(e–kaprolakton) nanočestice primjenom RP–HPLC metode (2011)

V. Topić, S. Vučen, L. Mendes, I. Vujanović-Kasagić, Ž. Gagić, Ispitivanje efikasnosti inkapsulacije ketoprofena u poli(e–kaprolakton) nanočestice primjenom RP–HPLC metode, Zbornik radova, pp. 120 - 122, 2011
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
Испитивање утицаја промјене pH вриједности мобилне фазе на степен дисоцијације и могућност детекције јонизованог нимесулида из таблета примјеном реверзно–фазне течне хроматографије под високим притиском (2013)

I. Grabovac, I. Kasagić-Vujanović, Испитивање утицаја промјене pH вриједности мобилне фазе на степен дисоцијације и могућност детекције јонизованог нимесулида из таблета примјеном реверзно–фазне течне хроматографије под високим притиском, 2013
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
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, И. Грабовац, М. Гајић, В. Вујановић, Д. Ивановић, 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, Зборник радова, pp. 23 - 34, Nov, 2013
Spectrophotometric determination of water content in some liquid pharmaceutical products (2014)

D. Jelić, V. Antunović, I. Kasagić-Vujanović, M. Đermanović, A. Đukić-Drvar, Spectrophotometric determination of water content in some liquid pharmaceutical products, ABSTRACT BOOK, pp. 213 - 214, 2014
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
The use of anhidrous cobalt chloride for water content determination in some pharmaceutical products by means of spectrophotometry (2015)

D. Jelić, V. Antunović, I. Kasagić-Vujanović, M. Đermanović, A Đukić-Drvar, The use of anhidrous cobalt chloride for water content determination in some pharmaceutical products by means of spectrophotometry, КЊИГА XXI, pp. 643 - 653, 2015
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
Stability study of ambroxol hydrochloride in water medium by high pressure liquid chromatography (2016)

I. Kasagić-Vujanović, Д. Јелић, В. Антуновић, С. Фазлагић, Stability study of ambroxol hydrochloride in water medium by high pressure liquid chromatography, IX Међународни научни скуп Contemorary Мaterials - Зборник радова, 2016
Testing of the influence of media's pH value on the solubility and partition coefficient of the acetylsalicylic acid (2017)

D. Knežević, I. Kasagić-Vujanović, Testing of the influence of media's pH value on the solubility and partition coefficient of the acetylsalicylic acid, Springer Nature Singapore Pte Ltd. 2017, pp. 368 - 371, 2017
Monitoring of bisoprolol fumarate stability under different stress conditions (2017-03)

I. Kasagić-Vujanović, Б. Јанчић Стојановић, Д. Ивановић, Monitoring of bisoprolol fumarate stability under different stress conditions, Springer Nature Singapore Pte Ltd. 2017, pp. 415 - 424, Mar, 2017

Уноси

Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach (2022-06)

Analysis of Fixed-Dose Combination of Three Antihypertensive Drugs by a Green and Quality by Design Approach (2022-08)

Design of experiments and Derringer’s desirability function in optimisation and validation of RP-HPLC method for the analysis of enrofloxacin and its impurities (2023-01)

Ispitivanje efikasnosti inkapsulacije ketoprofena u poli(e–kaprolakton) nanočestice primjenom RP–HPLC metode (2011)

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)

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)

Spectrophotometric determination of water content in some liquid pharmaceutical products (2014)

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)

The use of anhidrous cobalt chloride for water content determination in some pharmaceutical products by means of spectrophotometry (2015)

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)

Stability study of ambroxol hydrochloride in water medium by high pressure liquid chromatography (2016)

Testing of the influence of media's pH value on the solubility and partition coefficient of the acetylsalicylic acid (2017)

Monitoring of bisoprolol fumarate stability under different stress conditions (2017-03)