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dc.creatorAgbaba, Danica
dc.creatorMiljković, Tatjana
dc.creatorMarinković, Valentina
dc.creatorŽivanov-Stakić, Dobrila
dc.creatorVladimirov, Sote
dc.date.accessioned2019-09-02T10:51:21Z
dc.date.available2019-09-02T10:51:21Z
dc.date.issued1999
dc.identifier.issn1060-3271
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/214
dc.description.abstractA simple and reliable thin-layer chromatographic method for determining sulpiride and impurities of 2-aminomethyl-1-ethylpyrrolidine and methyl-5-sulphamoyl-2-methoxybenzoate was developed and validated. A methylene chloride-methanol-ammonia solution (25%; 18 + 2.8 + 0.4, v/v) solvent system is used for separation and quantitative evaluation of chromatograms. The chromatographic plate is first scanned at 240 nm to locate chromatographic zones corresponding to sulpiride and methyl-5-sulphamoyl-2-methoxybenzoate. Then 2-aminomethyl-1-ethylpyrrolidine is derivatized in situ with ninhydrin, and resulting colored spots are measured at 500 nm. The method is reproducible and convenient for quantitative analysis and purity control of sulpiride in its raw material and in its dosage forms.en
dc.publisherAOAC International, Gaithersburg
dc.rightsrestrictedAccess
dc.sourceJournal of AOAC International
dc.titleQuantitative analysis of sulpiride and impurities of 2-aminomethyl-1-ethylpyrrolidine and methyl-5-sulphamoyl-2-methoxybenzoate in pharmaceuticals by high-performance thin-layer chromatography and scanning densitometryen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractAгбаба, Даница; Маринковић, Валентина; Живанов-Стакић, Добрила; Владимиров, С; Миљковић, Т;
dc.citation.volume82
dc.citation.issue4
dc.citation.spage825
dc.citation.epage829
dc.citation.other82(4): 825-829
dc.citation.rankM21
dc.identifier.wos000081600100006
dc.identifier.doi10.1093/jaoac/82.4.825
dc.identifier.pmid10490314
dc.identifier.scopus2-s2.0-0033161548
dc.type.versionpublishedVersion


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