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dc.contributor.authorFathiazad, F
dc.contributor.authorAfshar, J
dc.date.accessioned2018-08-26T08:34:04Z
dc.date.available2018-08-26T08:34:04Z
dc.date.issued2004
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52505
dc.description.abstractSince hesperidin is a poor water soluble compound, in pharmaceutical formulations its methylated derivatives (hesperidin methyl chalcone, HMC) are used. The aim of this study was to establish an efficient methylation method for preparation of hesperidin methyl derivatives. For this purpose hesperidin was isolated from tangerine peel, purified and its methyl derivatives were prepared using three different techniques, i.e. diazomethane, methyl iodide-sodium hydride and dimethylsulfate. The efficiency of the methods was evaluated in terms of the percentage of unchanged and intact hesperidin in the final methylated products the and amount of unchanged hesperidin was an indication of the better efficiency of the method. A reversed phase HPLC method was also developed for determination and quantification of hesperidin in the final methylated products. The method involved the use of a Shim pack CLC-ODS column, a mixture of methanol-phosphate buffer (37:63, v/v) of pH = 2.6 as a mobile phase in an isocratic mode at a flow rate of 1 ml/min and UV detection at 280 nm. The results showed that methylation with methyl iodide-sodium hydride have the highest efficiency among different methylation methods.
dc.language.isoEnglish
dc.relation.ispartofDaru
dc.subjectdiazomethane
dc.subjectdimethyl sulfate
dc.subjecthesperidin
dc.subjecthesperidin methylchalcone
dc.subjectmethyl iodide
dc.subjectunclassified drug
dc.subjectanalytic method
dc.subjectarticle
dc.subjectdrug determination
dc.subjectdrug formulation
dc.subjectdrug research
dc.subjectdrug solubility
dc.subjectflow rate
dc.subjectintermethod comparison
dc.subjectmethylation
dc.subjectnonhuman
dc.subjectprocess optimization
dc.subjectprotein purification
dc.subjectquantitative diagnosis
dc.subjecttangerine
dc.titleAn investigation on methylation methods of hesperidin
dc.typeArticle
dc.citation.volume12
dc.citation.issue2
dc.citation.spage67
dc.citation.epage70
dc.citation.indexScopus


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