نمایش مختصر رکورد

dc.contributor.authorSzymański, Marcinen_US
dc.contributor.authorMłynarek, Dariaen_US
dc.contributor.authorSzymański, Arkadiuszen_US
dc.contributor.authorMatławska, Irenaen_US
dc.date.accessioned1399-07-09T06:55:10Zfa_IR
dc.date.accessioned2020-09-30T06:55:10Z
dc.date.available1399-07-09T06:55:10Zfa_IR
dc.date.available2020-09-30T06:55:10Z
dc.date.issued2016-02-01en_US
dc.date.issued1394-11-12fa_IR
dc.date.submitted2014-01-02en_US
dc.date.submitted1392-10-12fa_IR
dc.identifier.citationSzymański, Marcin, Młynarek, Daria, Szymański, Arkadiusz, Matławska, Irena. (2016). Simultaneous Determination of Diosmin and Hesperidin in Pharmaceuticals by RPLC using Ionic Liquids as Mobile Phase Modifiers. Iranian Journal of Pharmaceutical Research, 15(1), 141-148. doi: 10.22037/ijpr.2016.1783en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2016.1783
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_1783.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/312011
dc.description.abstractDiosmin and hesperidin are natural flavonoid glycosides found in various plant materials, mainly in citrus fruits in different concentrations. Diosmin for pharmaceutical use is obtained mainly semi-synthetically from hesperidin. Hesperidin often accompanies diosmin as a natural impurity in different pharmaceutical formulations; therefore, a simple, fast and precise method for the simultaneous assay of diosmin and hesperidin in pharmaceutical formulations has been developed to control their contents. Chromatographic resolution was performed using a column with C-18 packing and the following mobile phase: methanol/water (45: 55, v/v) with 0.025% added didecyldimethylammonium lactate, which significantly affects retention, shortening analysis time and having a positive impact on the symmetry of resulting chromatographic peaks. The method shows linearity between 2.5 and 100 μg/mL, high repeatability (0.39 and 0.42% for diosmin and hesperidin, respectively) and accuracy of 96 to 102% for both the assayed compounds. Intraday and interday precision of the new method were less than RSD% 1, 2.  The limit of detection of the assayed compounds is 2.5 and 1.2 μg/mL for diosmin and hesperidin, respectively. The method was tested on several pharmaceutical products available in Poland.en_US
dc.format.extent647
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2016.1783
dc.subjectdiosminen_US
dc.subjecthesperidinen_US
dc.subjectReverse-Phase Liquid Chromatographyen_US
dc.subjectionic liquidsen_US
dc.subjectPharmacognosyen_US
dc.subjectPharmacuticsen_US
dc.subjectPharmacyen_US
dc.subjecttoxicology and Pharmacologyen_US
dc.titleSimultaneous Determination of Diosmin and Hesperidin in Pharmaceuticals by RPLC using Ionic Liquids as Mobile Phase Modifiersen_US
dc.typeTexten_US
dc.typeResearch articleen_US
dc.contributor.departmentDepartment of Pharmacognosy, Poznań University of Medical Sciences, Święcickiego 4, 60-781 Poznań, Polanden_US
dc.contributor.departmentDepartment of Pharmacognosy, Poznań University of Medical Sciences, Święcickiego 4, 60-781 Poznań, Polanden_US
dc.contributor.departmentFaculty of Chemistry, Adam Mickiewicz University, Umultowska 89, 61-614 Poznań, Polanden_US
dc.contributor.departmentDepartment of Pharmacognosy, Poznań University of Medical Sciences, Święcickiego 4, 60-781 Poznań, Polanden_US
dc.citation.volume15
dc.citation.issue1
dc.citation.spage141
dc.citation.epage148


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