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dc.contributor.authorDoğan, Hatice Neşe
dc.date.accessioned2016-04-21T06:58:35Z
dc.date.available2016-04-21T06:58:35Z
dc.date.issued2014
dc.identifier.issn18723128
dc.identifier.urihttp://tinyurl.com/jbm4mtz
dc.identifier.urihttp://hdl.handle.net/11424/4452
dc.description.abstractIn the present study, two new methods were developed for the quantitative determination of active components of Seretide®, commercially available pharmaceutical preparation in the diskus form. One of these methods was based on derivative spectrophotometry and used a zero-crossing technique. The determinations of fluticasone propionate and salmeterol xinafoate were performed by first order derivatisation at 216.5 nm and second order derivatisation at 250 nm, respectively. The concentration ranges were 5.0-32.5 μg/mL for fluticasone propionate and 2-12 μg/mL for salmeterol xinafoate. The second method developed also included high performance liquid chromatography. In this method, a methanol-water mobile phase mixture (95:5, v/v) and a C18 chromasil column as a stationary phase were used. The wavelength of the diode array UV detector was 260 nm; the flow rate was 1 mL/min. The concentration ranges were 2-16 μg/mL for fluticasone propionate and 1-8 μg/mL for salmeterol xinafoate. The results for both methods from diskus are in the pharmacopea limits. For the statistical determination of these results, these two methods were compared with t-test for the means and with F-test for the standard deviations. © 2014 Bentham Science Publishers.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_US
dc.subjectDerivative spectrophotometry; Fluticasone propionate; HPLC; Quantitative determination; Salmeterol xinafoateen_US
dc.titleSimultaneous quantitative determinations of fluticasone propionate and salmeterol xinafote in diskus inhalersen_US
dc.typearticleen_US
dc.relation.journalDrug Metabolism Lettersen_US
dc.contributor.departmentDepartment of Pharmaceutical Chemistry, Marmara Universityen_US
dc.identifier.volume8en_US
dc.identifier.issue1en_US
dc.identifier.startpage31en_US
dc.identifier.endpage35en_US


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