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dc.contributor.authorTuerkoez, Ebru
dc.contributor.authorOnar, A. Nur
dc.date.accessioned2020-06-21T15:24:10Z
dc.date.available2020-06-21T15:24:10Z
dc.date.issued2007
dc.identifier.issn0003-2719
dc.identifier.issn1532-236X
dc.identifier.urihttps://doi.org/10.1080/00032710701566651
dc.identifier.urihttps://hdl.handle.net/20.500.12712/20186
dc.descriptionAcar, Ebru Turkoz/0000-0002-8164-6617en_US
dc.descriptionWOS: 000250834700014en_US
dc.description.abstractThe voltammetric behaviour of ticlopidine-HCl was studied using square-wave, sampled direct current and cyclic voltammetry. The drug showed a cathodic peak at -0.01V versus Ag/AgCl with hanging mercury drop electrode. The current was investigated using cyclic voltammetry and characterized as diffusion controlled. The calibration plot was linear over the concentration range of 1.96 x 10(-6) -1.13 x 10(-4) M in 0.5 M phosphate buffer of pH 5.0. Limit of detection and limit of quantification were achieved as 5.17 x 10(-7), 1.72 x 10(-6) M, respectively. Precision and accuracy of the developed method was checked by recovery studies. The proposed procedure was successfully applied for assay of ticlopidine in its pharmaceutical formulation as tablet without the necessity for sample pretreatment prior to assay of the drug.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.isversionof10.1080/00032710701566651en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectticlopidine-HClen_US
dc.subjectdrug determinationen_US
dc.subjectvoltammetryen_US
dc.subjectelectrochemical analysisen_US
dc.titleDetermination of ticlopidine in pharmaceutical productsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume40en_US
dc.identifier.issue11en_US
dc.identifier.startpage2231en_US
dc.identifier.endpage2240en_US
dc.relation.journalAnalytical Lettersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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