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Original Articles

DEVELOPMENT OF A STABILITY-INDICATING UPLC METHOD FOR DETERMINING ZIPRASIDONE HYDROCHLORIDE AND ITS ASSOCIATED DEGRADATION PRODUCTS PRESENT IN ACTIVE PHARMACEUTICAL INGREDIENTS AND PHARMACEUTICAL DOSAGE FORMS

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Pages 968-982 | Published online: 21 Mar 2013

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Darija Obradović, Slavica Filipić, Katarina Nikolić, Marija Čarapić & Danica Agbaba. (2016) Optimization of TLC method for separation and determination of ziprasidone and its impurities. Journal of Liquid Chromatography & Related Technologies 39:5-6, pages 271-276.
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Articles from other publishers (4)

Jared W. Castle, Danielle M. Butzbach, G. Stewart Walker, Claire E. Lenehan, Frank Reith, Samuel P. Costello & K. Paul Kirkbride. (2022) In vitro degradation of ziprasidone in human whole blood. Drug Testing and Analysis 15:2, pages 220-234.
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Marija Čarapić, Bojan Marković, Milena Pavlovic, Danica Agbaba & Katarina Nikolic. (2022) Comparative study of performances of UHPLC-MS/MS and HPLC/UV methods for analysis of ziprasidone and its main impurities. Acta Chromatographica.
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Marija Čarapić, Katarina Nikolic, Bojan Marković, Miloš Petković, Milena Pavlovic & Danica Agbaba. (2019) Ultra-performance liquid chromatography tandem mass spectrometry for the rapid, simultaneous analysis of ziprasidone and its impurities. Biomedical Chromatography 33:2, pages e4384.
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Mehmet Gumustas, Sevinc Kurbanoglu, Bengi Uslu & Sibel A. Ozkan. (2013) UPLC versus HPLC on Drug Analysis: Advantageous, Applications and Their Validation Parameters. Chromatographia 76:21-22, pages 1365-1427.
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