Publication:
Determination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LC

dc.contributor.authorŞentürk, Zühre
dc.contributor.authorErk, Nevin
dc.contributor.authorÖzkan, Sibel A.
dc.contributor.authorAkay, Cemal
dc.contributor.buuauthorCevheroğlu, Şemsettin
dc.date.accessioned2021-07-05T07:29:53Z
dc.date.available2021-07-05T07:29:53Z
dc.date.issued2002-06-20
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.
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.
dc.identifier.endpage298
dc.identifier.issn0731-7085
dc.identifier.issue1-2
dc.identifier.pubmed12062689
dc.identifier.scopus2-s2.0-0037142353
dc.identifier.startpage291
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.identifier.volume29
dc.identifier.wos000176493900031
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherPergamon-Elsevier Science
dc.relation.journalJournal of Pharmaceutical and Biomedical Analysis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHigh-performance liquid chromatography
dc.subjectTheophylline and ephedrine hydrochloride determination
dc.subjectRatio-spectra derivative spectrophotometry
dc.subjectPharmaceutical formulation
dc.subjectTrimethoprim
dc.subjectPerformance liquid-chromatography
dc.subjectPharmaceutical formulations
dc.subjectChlorpheniramine maleate
dc.subjectHydrochloride
dc.subjectMixtures
dc.subjectHydrochlorothiazide
dc.subjectResolution
dc.subjectElectrode
dc.subjectAssay
dc.subjectChemistry
dc.subjectPharmacology & pharmacy
dc.subject.wosChemistry, analytical
dc.subject.wosPharmacology & pharmacy
dc.titleDetermination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LC
dc.typeArticle
dc.wos.quartileQ2 (Chemistry, analytical)
dc.wos.quartileQ3 (Pharmacology & pharmacy)
dspace.entity.typePublication
local.indexed.atWOS
local.indexed.atScopus

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