Ion selective membrane electrodes for determination of Citalopram Hydrobromide in drug product and in presence of its degradation products

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dc.contributor.author Nebsen M.
dc.contributor.author El-Maraghy C.M.
dc.contributor.author Salem H.
dc.contributor.author Amer S.M.
dc.contributor.other Analytical Chemistry department
dc.contributor.other Cairo University
dc.contributor.other Kasr-El Aini Street
dc.contributor.other Cairo
dc.contributor.other 11562
dc.contributor.other Egypt; Pharmaceutical Analytical Chemistry department
dc.contributor.other Heliopolis University
dc.contributor.other 3 Cairo Belbeis desert road
dc.contributor.other El-Horria
dc.contributor.other Cairo
dc.contributor.other 2834
dc.contributor.other Egypt; Analytical Chemistry department
dc.contributor.other October University for Modern Sciences and Arts (MSA)
dc.contributor.other 6th October city
dc.contributor.other 11787
dc.contributor.other Egypt; Pharmaceutical Analytical Chemistry department
dc.contributor.other Deraya University
dc.contributor.other Minia
dc.contributor.other Egypt
dc.date.accessioned 2020-01-09T20:41:47Z
dc.date.available 2020-01-09T20:41:47Z
dc.date.issued 2015
dc.identifier.issn 20084226
dc.identifier.other https://doi.org/
dc.identifier.uri https://t.ly/5x6eY
dc.description Scopus
dc.description.abstract This paper presents a comparative study between three sensors developed to determine Citalopram Hydrobromide (CT) in the presence of its alkaline hydrolysis and oxidation induced degradation products using different ion association complexes. Sensor 1 was fabricated using phosphomolybdic acid, Sensor 2 used phosphotungestic acid and sensor 3 used the sodium tetraphenyl borate. Linear responses of CT were obtained within the concentration ranges of 1�10?6 to 1�10?2 mol L-1 for sensor 1 and 2 and 1�10?5 to 1�10?2 mol L-1 for sensor 3 over the pH range of 3.0�6.0. The selectivity coefficients of the developed sensors indicated excellent selectivity for CT. The proposed sensors displayed useful analytical characteristics for the determination of CT in bulk powder, pharmaceutical formulation, and in the presence of its degradation products and thus could be used for stability-indicating methods. The method was validated according to ICH guidelines. Statistical comparison between the results from the proposed method and the results from the reference HPLC method showed no significant difference regarding accuracy and precision. � 2015 by CEE (Center of Excellence in Electrochemistry). en_US
dc.description.uri https://www.scimagojr.com/journalsearch.php?q=21100224440&tip=sid&clean=0
dc.language.iso English en_US
dc.publisher Center of Excellence in Electrochemistry, Univ. of Tehran en_US
dc.relation.ispartofseries Analytical and Bioanalytical Electrochemistry
dc.relation.ispartofseries 7
dc.subject Cation exchanger en_US
dc.subject Citalopram Hydrobromide en_US
dc.subject Degradation products en_US
dc.subject Ion selective electrode en_US
dc.subject PVC en_US
dc.title Ion selective membrane electrodes for determination of Citalopram Hydrobromide in drug product and in presence of its degradation products en_US
dc.type Article en_US
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dcterms.source Scopus
dc.identifier.doi https://doi.org/
dc.Affiliation October University for modern sciences and Arts (MSA)


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