Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21040
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dc.contributor.authorŞentürk, Zühre-
dc.contributor.authorErk, Nevin-
dc.contributor.authorÖzkan, Sibel A.-
dc.contributor.authorAkay, Cemal-
dc.date.accessioned2021-07-05T07:29:53Z-
dc.date.available2021-07-05T07:29:53Z-
dc.date.issued2002-06-20-
dc.identifier.citationŞentürk, Z. vd. (2002). "Determination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LC". Journal of Pharmaceutical And Biomedical Analysis, 29(1-2), 291-298.tr_TR
dc.identifier.issn0731-7085-
dc.identifier.urihttps://doi.org/10.1016/S0731-7085(02)00065-1-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0731708502000651?via%3Dihub-
dc.identifier.urihttp://hdl.handle.net/11452/21040-
dc.description.abstractTwo methods are described for the determination of theophylline (THP) and ephedrine hydrochloride (EPH) in combined pharmaceutical tablet forms. The first method depends on the use of the first derivative of the ratio-spectra obtained by dividing the absorption spectrum of binary mixtures by a standard spectrum of one of the compounds. The first derivative amplitudes at 231.8 and 250.3 nm were selected for the assay of THP and EPH, respectively. Calibration graphs were established for 20-180 mug ml(-1) for THP and 10-50 mug ml(-1) for EPH. The second method is based on high-performance liquid chromatography on a reversed-phase column using a mobile phase of methanol-water (40 + 60,v/v) (pH 3) with detection at 217 nm. Linearity was obtained in the concentration range of 5-150 mug ml(-1) for THP and 15-75 mug ml(-1) for EPH. The detection limits for THP and EPH were 0.73 and 0.92 mug ml(-1) by ratio-spectra derivative spectrophotometry and 0.59 and 0.86 mug ml(-1) by HPLC, respectively. The proposed methods were successfully applied to the determination of these drugs in laboratory-prepared mixtures and in tablets. The relative standard deviations were found to be less than 1.5%, indicating reasonable repeatibility of both methods.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHigh-performance liquid chromatographyen_US
dc.subjectTheophylline and ephedrine hydrochloride determinationen_US
dc.subjectRatio-spectra derivative spectrophotometryen_US
dc.subjectPharmaceutical formulationen_US
dc.subjectTrimethoprimen_US
dc.subjectPerformance liquid-chromatographyen_US
dc.subjectPharmaceutical formulationsen_US
dc.subjectChlorpheniramine maleateen_US
dc.subjectHydrochlorideen_US
dc.subjectMixturesen_US
dc.subjectHydrochlorothiazideen_US
dc.subjectResolutionen_US
dc.subjectElectrodeen_US
dc.subjectAssayen_US
dc.subjectChemistryen_US
dc.subjectPharmacology & pharmacyen_US
dc.titleDetermination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LCen_US
dc.typeArticleen_US
dc.identifier.wos000176493900031tr_TR
dc.identifier.scopus2-s2.0-0037142353tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.identifier.startpage291tr_TR
dc.identifier.endpage298tr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue1-2tr_TR
dc.relation.journalJournal of Pharmaceutical and Biomedical Analysisen_US
dc.contributor.buuauthorCevheroğlu, Şemsettin-
dc.identifier.pubmed12062689tr_TR
dc.subject.wosChemistry, analyticalen_US
dc.subject.wosPharmacology & pharmacyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2 (Chemistry, analytical)en_US
dc.wos.quartileQ3 (Pharmacology & pharmacy)en_US
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