Unosi

• Farmakopejske metode u kontroli kvaliteta lijekova (2021)

  I. Kasagić-Vujanović, Farmakopejske metode u kontroli kvaliteta lijekova, Medicinski fakultet Univerziteta u Banjoj Luci, 2021

• 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

• Ispitivanje sadržaja aktivne supstance i degradacionih proizvoda/nečistoća u tabletama nimesulida primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom (2013)

  B. Tubić, I. Vujanović-Kasagić, N. Mihajlica, Ž. Gagić, N. Bubić Pajić, Ispitivanje sadržaja aktivne supstance i degradacionih proizvoda/nečistoća u tabletama nimesulida primjenom reverzno-fazne tečne hromatografije pod visokim pritiskom, Arhiv za farmaciju, Vol. 63, No. 1, pp. 1 - 19, 2013

• 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

• STRESS DEGRADATION OF LISINOPRIL DIHYDRATE IN DIFFERENT AQUEOUS MEDIA (2017-02)

  I. Kasagić-Vujanović, D. Knežević, N. Vukićević, STRESS DEGRADATION OF LISINOPRIL DIHYDRATE IN DIFFERENT AQUEOUS MEDIA, Contemporary Materials, Vol. 2, No. 8, pp. 164 - 171, Feb, 2017

• 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

• Quality control of distilled water used for reconstitution of powders for oral suspension in pharmacies on the territory of Bosnia and Herzegovina (2019)

  I. Kasagić-Vujanović, Ž. Gagić, N. Okuka, D. Knežević, Quality control of distilled water used for reconstitution of powders for oral suspension in pharmacies on the territory of Bosnia and Herzegovina, CONTEMPORARY MATERIALS, Vol. X, No. 1, pp. 47 - 55, 2019

• Quality by Design oriented development of hydrophilic interaction liquid chromatography method for the analysis of amitriptyline and its impurities (2019-05)

  I. Kasagić-Vujanović, B. Jančić-Stojanović, Quality by Design oriented development of hydrophilic interaction liquid chromatography method for the analysis of amitriptyline and its impurities, JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, Vol. 173, pp. 86 - 95, May, 2019

• Design of experiments in optimization and validation of hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and its impurities (2020)

  I. Kasagić-Vujanović, D. Knežević, Design of experiments in optimization and validation of hydrophilic interaction liquid chromatography method for determination of amlodipine besylate and its impurities, Acta Chromatographica , Vol. AChrom 2021;, pp. 1 - 12, 2020

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

  N. Mandić-Kovačević, 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)

  N. Mandić-Kovačević, 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, Ž. Gagić, 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

• Ispitivanje uticaja promjene pH vrijednosti mobilne faze na stepen disocijacije i mogućnost detekcije jonizovanog nimesulida iz tableta primjenom reverzno–fazne tečne hromatografije pod visokim pritiskom (2013)

  I. Grabovac, I. Kasagić-Vujanović, Ispitivanje uticaja promjene pH vrijednosti mobilne faze na stepen disocijacije i mogućnost detekcije jonizovanog nimesulida iz tableta primjenom reverzno–fazne tečne hromatografije pod visokim pritiskom, 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