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dc.creatorRanković, Katarina
dc.creatorFilipić, Slavica
dc.creatorNikolić, Katarina
dc.creatorAgbaba, Danica
dc.date.accessioned2019-09-02T11:29:41Z
dc.date.available2019-09-02T11:29:41Z
dc.date.issued2012
dc.identifier.issn1082-6076
dc.identifier.urihttp://farfar.pharmacy.bg.ac.rs/handle/123456789/1732
dc.description.abstractA simple and sensitive HPTLC method for separation and determination of tiapride hydrochloride and its degradation products has been developed and evaluated. Analysis of tiapride hydrochloride and impurities III, VII, and VIII, was performed on silica gel 60F(254) HPTLC plates using methylene chloride-methanol-concentrated ammonia, 9:1.6:0.1 (v/v) as mobile phase. Detection was performed at 240 nm. All validation requirements, specificity, linearity (r >= 0.997), recovery (95.08-100.39%), limit of quantification (0.1-0.2%), and robustness were examined and fulfilled, and the proposed method can be successfully applied for the quality control analysis of commercially available tablets and injections.en
dc.publisherTaylor & Francis Inc, Philadelphia
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172033/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Liquid Chromatography & Related Technologies
dc.subjectdosage formsen
dc.subjectHPTLCen
dc.subjectimpuritiesen
dc.subjectpharmaceutical preparationsen
dc.subjectquantificationen
dc.subjecttiapride hydrochlorideen
dc.titleTLC determination of tiapride hydrochloride and its impurities in pharmaceuticalsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractФилипић, Славица; Aгбаба, Даница; Ранковић, Катарина; Николић, Катарина;
dc.citation.volume35
dc.citation.issue10
dc.citation.spage1336
dc.citation.epage1345
dc.citation.other35(10): 1336-1345
dc.citation.rankM23
dc.identifier.wos000305566500007
dc.identifier.doi10.1080/10826076.2012.675870
dc.identifier.scopus2-s2.0-84862980565
dc.identifier.rcubconv_2653
dc.type.versionpublishedVersion


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