Преглед тема: "impurities"
Приказ резултата 1-20 од 24
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Assessment of Liquid Chromatographic Method Robustness by Use of Plackett-Burman Design
(Akademiai Kiado Zrt, Budapest, 2010) -
Chemical stability of drugs: Influence of light and temperature on montelukast stability in solution / Hemijska stabilnost lekova - uticaj svetlosti i temperature na stabilnost montelukasta u rastvoru
(Savez farmaceutskih udruženja Srbije, Beograd, 2014) -
A chemometrical approach to optimization and validation of an HPLC assay for rizatriptan and its impurities in tablets
(Taylor & Francis Inc, Philadelphia, 2007) -
Chromatographic determination of dissociation constants of pramipexole and its impurities
(Vieweg, Wiesbaden, 2007) -
Densitometric determination of omeprazole, pantoprazole, and their impurities in pharmaceuticals
(Research Inst Medicinal Plants, Budakalasz, 2004) -
Determination of Moxonidine and Its Impurities by Thin-Layer Chromatography
(Taylor & Francis Inc, Philadelphia, 2015) -
Determination of Moxonidine and Its Impurities by Thin-Layer Chromatography
(Taylor & Francis Inc, Philadelphia, 2015) -
Development of a HPTLC method for in-process purity testing of pentoxifylline
(Wiley-VCH Verlag GMBH, Weinheim, 2005) -
Evaluation of impurities level of perindopril tert-butylamine in tablets
(Elsevier Science BV, Amsterdam, 2007) -
First-order UV-derivative spectrophotometry in the analysis of omeprazole and pantoprazole sodium salt and corresponding impurities
(Pergamon-Elsevier Science Ltd, Oxford, 2003) -
LC determination of lercanidipine and its impurities using DryLab software and experimental design procedures
(Vieweg, Wiesbaden, 2008) -
Methylprednisolone and its related substances in freeze-dried powders for injections / Metilprednizolon i njegove srodne supstance u liofilizatu za rastvor za injekcije
(Srpsko hemijsko društvo, Beograd, 2010) -
Monitoring of impurity level of valsartan and hydrochlorothiazide employing an RP-HPLC gradient mode
(Taylor & Francis Inc, Philadelphia, 2007) -
Retention modelling in liquid chromatographic separation of simvastatin and six impurities using a microemulsion as eluent
(Wiley-VCH Verlag GMBH, Weinheim, 2004) -
Robustness testing of liquid chromatographic method for determination of itraconazole and its impurities applying fractional factorial design / Testiranje robusnosti metode tečne hromatografije za određivanje itrakonazola i njegovih nečistoća primenom frakcionog faktorskog dizajna
(Savez farmaceutskih udruženja Srbije, Beograd, 2012) -
Simulataneous determination of nimesulide and its impurities in pharmaceutical formulations by reversed-phase high-performance liquid chromatography
(Slovensko Kemijsko Drustvo, Ljubljana, 2007) -
The stress stability of olanzapine: studies of interactions with excipients in solid state pharmaceutical formulations
(Informa Healthcare, London, 2015)