Comparison of full factorial design, central composite design, and box-behnken design in chromatographic method development for the determination of fluconazole and its impurities T Rakić, I Kasagić-Vujanović, M Jovanović, B Jančić-Stojanović, ... Analytical Letters 47 (8), 1334-1347, 2014 | 231 | 2014 |
Application of Analytical Quality by Design concept for bilastine and its degradation impurities determination by hydrophilic interaction liquid chromatographic method J Terzić, I Popović, A Stajić, A Tumpa, B Jančić-Stojanović Journal of pharmaceutical and biomedical analysis 125, 385-393, 2016 | 77 | 2016 |
Retention modelling in liquid chromatographic separation of simvastatin and six impurities using a microemulsion as eluent A Malenovic, D Ivanovic, M Medenica, B Jancic, S Markovic Journal of separation science 27 (13), 1087-1092, 2004 | 73 | 2004 |
Desirability-based optimization and its sensitivity analysis for the perindopril and its impurities analysis in a microemulsion LC system A Malenović, Y Dotsikas, M Mašković, B Jančić–Stojanović, D Ivanović, ... Microchemical Journal 99 (2), 454-460, 2011 | 63 | 2011 |
Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities D Ivanovic, M Medenica, B Jancic, N Knezevic, A Malenovic, J Milic Acta chromatographica 18, 143, 2007 | 59 | 2007 |
Development of liquid chromatographic method for fosinoprilat determination in human plasma using microemulsion as eluent B Jancic, D Ivanovic, M Medenica, A Malenovic, N Dimkovic Journal of Chromatography a 1088 (1-2), 187-192, 2005 | 56 | 2005 |
Evaluation of impurities level of perindopril tert-butylamine in tablets M Medenica, D Ivanović, M Mašković, B Jančić, A Malenović Journal of pharmaceutical and biomedical analysis 44 (5), 1087-1094, 2007 | 53 | 2007 |
Development and validation of RP–HPLC method for cetrimonium bromide and lidocaine determination A Malenovic, M Medenica, D Ivanovic, B Jancic, S Markovic Il Farmaco 60 (2), 157-161, 2005 | 52 | 2005 |
Experimental design in reversed-phase high-performance liquid chromatographic analysis of imatinib mesylate and its impurity M Medenica, B Jancic, D Ivanovic, A Malenovic Journal of Chromatography A 1031 (1-2), 243-248, 2004 | 51 | 2004 |
Reversed-phase liquid chromatography analysis of imatinib mesylate and impurity product in Glivec® capsules D Ivanovic, M Medenica, B Jancic, A Malenovic Journal of Chromatography B 800 (1-2), 253-258, 2004 | 51 | 2004 |
Quality by design in the development of hydrophilic interaction liquid chromatography method with gradient elution for the analysis of olanzapine A Tumpa, A Stajić, B Jančić-Stojanović, M Medenica Journal of pharmaceutical and biomedical analysis 134, 18-26, 2017 | 46 | 2017 |
Chemometrical evaluation of ropinirole and its impurity's chromatographic behavior B Jancic-Stojanovic, A Malenovic, D Ivanovic, T Rakic, M Medenica Journal of chromatography A 1216 (8), 1263-1269, 2009 | 46 | 2009 |
FDA licences imatinib mesylate for CML M Habeck The Lancet Oncology 3 (1), 6, 2002 | 44 | 2002 |
Influence of structural and interfacial properties of microemulsion eluent on chromatographic separation of simvastatin and its impurities M Anđelija, I Darko, M Mirjana, J Biljana, M Slavko Journal of chromatography A 1131 (1-2), 67-73, 2006 | 41 | 2006 |
Synthesis and deposition of ZnO based particles by aerosol spray pyrolysis O Milošević, V Gagić, J Vodnik, A Mitrović, L Karanović, B Stojanović Thin Solid Films 296 (1-2), 44-48, 1997 | 41 | 1997 |
Monitoring of simvastatin impurities by HPLC with microemulsion eluents A Malenović, M Medenica, D Ivanović, B Jančić Chromatographia 63, S95-S100, 2006 | 40 | 2006 |
Validation of the RP–HPLC method for analysis of hydrochlorothiazide and captopril in tablets D Ivanovic, M Medenica, A Malenovic, B Jancic Accreditation and quality assurance 9, 76-81, 2004 | 40 | 2004 |
Determination of higenamine in dietary supplements by UHPLC/MS/MS method A Stajić, M Anđelković, N Dikić, J Rašić, M Vukašinović-Vesić, D Ivanović, ... Journal of Pharmaceutical and Biomedical Analysis 146, 48-52, 2017 | 37 | 2017 |
Chaotropic agents in liquid chromatographic method development for the simultaneous analysis of levodopa, carbidopa, entacapone and their impurities A Vemić, BJ Stojanović, I Stamenković, A Malenović Journal of pharmaceutical and biomedical analysis 77, 9-15, 2013 | 37 | 2013 |
LC determination of lercanidipine and its impurities using DryLab software and experimental design procedures I Popovic, D Ivanovic, M Medenica, A Malenovic, B Jancic-Stojanovic Chromatographia 67, 449-454, 2008 | 37 | 2008 |