Приказ основних података о документу

dc.creatorMaksić, Jelena
dc.creatorTumpa, Anja
dc.creatorStajić, Ana
dc.creatorJovanović, Marko
dc.creatorRakić, Tijana
dc.creatorJančić-Stojanović, Biljana
dc.date.accessioned2019-09-02T11:52:25Z
dc.date.available2019-09-02T11:52:25Z
dc.date.issued2016
dc.identifier.issn0731-7085
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/2604
dc.description.abstractIn this paper separation of granisetron and its two related substances in HILIC mode is presented. Separation was done on silica column derivatized with sulfoalkylbetaine groups (ZIC-HILIC). Firstly, retention mechanisms were assessed whereby retention factors of substances were followed in wide range of acetonitrile content (80-97%), at constant concentration of aqueous buffer (10 mM) as well as at constant pH value of 3.0. Further, in order to developed optimal HILIC method, Design of Experiments (DoE) methodology was applied. For optimization full factorial design 32 was employed. Influence of acetonitrile content and ammonium acetate concentration were investigated while pH of the water phase was kept at 3.3. Adequacy of obtained mathematical models was confirmed by ANOVA. Optimization goals (alpha > 1.15 and minimal run time) were accomplished with 94.7% of acetonitrile in mobile phase and 70 mM of ammonium acetate in water phase. Optimal point was in the middle of defined Design Space. In the next phase, robustness was experimetally tested by Rechtschaffen design. The investigated factors and their levels were: acetonitrile content (+/- 1%), ammonium acetate molarity in water phase (+/- 2 mM), pH value of water phase (+/- 0.2) and column temperature (+/- 4 degrees C). The validation scope included selectivity, linearity, accuracy and precision as well as determination of limit of detection (LOD) and limit of quantification (LOQ) for the related substances. Additionally, the validation acceptance criteria were met in all cases. Finally, the proposed method could be successfully utilized for estimation of granisetron HCl and its related substances in tablets and parenteral dosage forms, as well as for monitoring degradation under various stress conditions.en
dc.publisherElsevier Science BV, Amsterdam
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172052/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Pharmaceutical and Biomedical Analysis
dc.titleHydrophilic interaction liquid chromatography in analysis of granisetron HCl and its related substances. Retention mechanisms and method developmenten
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСтајић, Aна; Ракић, Тијана; Тумпа, Aња; Јанчић-Стојановић, Биљана; Максић, Јелена; Јовановић, Марко;
dc.citation.volume123
dc.citation.spage93
dc.citation.epage103
dc.citation.other123: 93-103
dc.citation.rankM21
dc.identifier.wos000372769700012
dc.identifier.doi10.1016/j.jpba.2016.02.010
dc.identifier.pmid26895494
dc.identifier.scopus2-s2.0-84958206586
dc.type.versionpublishedVersion


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Приказ основних података о документу