Three different spectrophotometric methods exploiting ratio spectra for the selective determination of iohexol in the presence of its acidic degradate

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorEl-Rahman M.K.A.
dc.contributor.authorRiad S.M.
dc.contributor.authorFawaz E.M.
dc.contributor.authorShehata M.A.
dc.contributor.otherAnalytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherKasr-El Aini Street
dc.contributor.otherCairo
dc.contributor.other11562
dc.contributor.otherEgypt; Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherOctober for Modern Sciences and Arts University
dc.contributor.other6th of October city
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:41:06Z
dc.date.available2020-01-09T20:41:06Z
dc.date.issued2018
dc.descriptionScopus
dc.description.abstractBackground: Non-ionic X-ray contrast agents constitute a very important class of pharmaceutical compounds produced in large quantities. Iohexol is an important example of such compounds. Objective: Three simple and selective stability indicating spectrophotometric methods utilizing ratio spectra were proposed for the determination of the widely used X-ray contrast medium, iohexol in the presence of its acidic degradate and in its pharmaceutical formulation. Methods: The first method is the first derivative of ratio spectra method (DD 1 ), the second is the Ratio Difference Method (RD), and the last one is the Mean Centering method (MC). Results: The three proposed methods showed a good linearity over the concentration range of 4-40 ?g.mL -1 . The selectivity of the three developed methods was evaluated by analyzing different laboratory-prepared mixtures and satisfactory results were obtained. Conclusion: Iohexol has been successfully determined in its pure form and pharmaceutical formulation (Omnipaque vials) utilizing the proposed methods with no interference from the present additives. The results obtained by each of the proposed methods were statistically compared to the official United States pharmacopeial method and non-significant difference was obtained regarding accuracy or precision. 2018 Bentham Science Publishers.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=4700152426&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.2174/1573412913666171016163544
dc.identifier.doiPubMed ID :
dc.identifier.issn15734129
dc.identifier.otherhttps://doi.org/10.2174/1573412913666171016163544
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/5XmPb
dc.language.isoEnglishen_US
dc.publisherBentham Science Publishers B.V.en_US
dc.relation.ispartofseriesCurrent Pharmaceutical Analysis
dc.relation.ispartofseries14
dc.subjectAcidic degradateen_US
dc.subjectDerivative ratioen_US
dc.subjectIohexolen_US
dc.subjectMean centeringen_US
dc.subjectRatio differenceen_US
dc.subjectStability indicating methodsen_US
dc.titleThree different spectrophotometric methods exploiting ratio spectra for the selective determination of iohexol in the presence of its acidic degradateen_US
dc.typeArticleen_US
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