Приказ основних података о документу

dc.creatorAgbaba, Danica
dc.creatorNovović, D
dc.creatorKarljiković-Rajić, Katarina
dc.creatorMarinković, Valentina
dc.date.accessioned2019-09-02T10:59:15Z
dc.date.available2019-09-02T10:59:15Z
dc.date.issued2004
dc.identifier.issn0933-4173
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/525
dc.description.abstractA method has been developed for separation of omeprazole and pantoprazole, and their impurities omeprazole sulfone and N-methylpantoprazole, by HPTLC. The mobile phase chloroform-2-propanol-25% ammonia-acetonitrile, 10.8 + 1.2 + 0.3 + 4 (v/v), enables good resolution of large excesses of the drugs from the possible impurities. Regression coefficients (r > 0.998), recovery (90.7-120.0%), and detection limit (0.025-0.05%) were validated and found to be satisfactory. The methods is convenient for quantitative analysis and purity control of the compounds.en
dc.publisherResearch Inst Medicinal Plants, Budakalasz
dc.rightsrestrictedAccess
dc.sourceJournal of Planar Chromatography - Modern TLC
dc.subjectplanar chromatographyen
dc.subjectomeprazoleen
dc.subjectpantoprazoleen
dc.subjectimpuritiesen
dc.subjectpharmaceutical preparationsen
dc.titleDensitometric determination of omeprazole, pantoprazole, and their impurities in pharmaceuticalsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractНововић, Д; Карљиковић-Рајић, Катарина; Маринковић, Валентина; Aгбаба, Даница;
dc.citation.volume17
dc.citation.issue3
dc.citation.spage169
dc.citation.epage172
dc.citation.other17(3): 169-172
dc.citation.rankM23
dc.identifier.wos000222956100002
dc.identifier.doi10.1556/JPC.17.2004.3.2
dc.identifier.scopus2-s2.0-4043090664
dc.type.versionpublishedVersion


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Приказ основних података о документу