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A validated thin-layer chromatographic method for analysis of bupropion hydrochloride in a pharmaceutical dosage form

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dc.contributor.authorYeniceli, Duygu
dc.contributor.authorAK, DİLEK
dc.contributor.orcid0000-0001-6986-3638
dc.date.accessioned2025-11-13T11:18:16Z
dc.date.issued2010-06-01
dc.identifier.doihttps://doi.org/10.1556/jpc.23.2010.3.9
dc.identifier.endpage218
dc.identifier.issn0933-4173
dc.identifier.issue3
dc.identifier.openalexW2102117380
dc.identifier.startpage212
dc.identifier.urihttps://hdl.handle.net/11421/6362
dc.identifier.urihttps://doi.org/10.1556/jpc.23.2010.3.9
dc.identifier.volume23
dc.language.isoen
dc.relation.ispartofJournal of Planar Chromatography – Modern TLC
dc.rightsrestrictedAccess
dc.subjectChromatography
dc.subjectChemistry
dc.subjectRepeatability
dc.subjectPharmaceutical formulation
dc.subjectDosage form
dc.subjectPhotodegradation
dc.subjectSilica gel
dc.subjectCiprofloxacin Hydrochloride
dc.subjectOrganic chemistry
dc.subject.sdg6
dc.titleA validated thin-layer chromatographic method for analysis of bupropion hydrochloride in a pharmaceutical dosage form
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5109338275
local.authorid.openalexA5075665999

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