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dc.contributor.authorAtkoşar, Zeki
dc.contributor.authorAltıokka, Göksel
dc.contributor.authorErgün, Bülent
dc.contributor.authorGenç, Lütfi
dc.date.accessioned2019-10-19T14:02:51Z
dc.date.available2019-10-19T14:02:51Z
dc.date.issued2001
dc.identifier.issn1300638X
dc.identifier.urihttps://hdl.handle.net/11421/12416
dc.description.abstractA flow-injection analysis(FIA) of ketorolac tromethamine(KT) using UV detection is described. The best solvent system was found to be 0.1 mol.l-1 acetate buffer at pH 5.2. A flow rate of lml.min-1 was pumped and active material was detected at 323 nm. The calibration equation was linear in the range of 1×10-5 to 5×10-5 mol.l-1. Limit of detection(LOD) and limit of quantitation(LOQ) were calculated to be 2.8×10-6 and 8.2×10-6 mol.l-1 respectively. The proposed method was applied to the determination of KT in pharmaceutical preparations. The results were compared with those obtained by UV-spectrophotometry. The validation studies were realised by the related applications and the results were evaluated statistically and insignificant differences were observed between the methods.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFlow Injection Analysisen_US
dc.subjectKetorolac Tromethamineen_US
dc.subjectPharmaceutical Applicationen_US
dc.titleThe determination of ketorolac tromethamine in pharmaceutical preparations by flow injection analysis using UV detectionen_US
dc.typearticleen_US
dc.relation.journalActa Pharmaceutica Turcicaen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Analitik Kimya Anabilim Dalıen_US
dc.identifier.volume43en_US
dc.identifier.issue2en_US
dc.identifier.startpage143en_US
dc.identifier.endpage146en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorAltıokka, Göksel
dc.contributor.institutionauthorGenç, Lütfi


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