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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/7549
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dc.contributor.authorBruschi, M. L.-
dc.contributor.authorFranco, S. L.-
dc.contributor.authorGremiao, MPD-
dc.date.accessioned2014-05-20T13:24:24Z-
dc.date.accessioned2016-10-25T16:45:06Z-
dc.date.available2014-05-20T13:24:24Z-
dc.date.available2016-10-25T16:45:06Z-
dc.date.issued2003-01-01-
dc.identifierhttp://dx.doi.org/10.1081/JLC-120023254-
dc.identifier.citationJournal of Liquid Chromatography & Related Technologies. New York: Marcel Dekker Inc., v. 26, n. 14, p. 2399-2409, 2003.-
dc.identifier.issn1082-6076-
dc.identifier.urihttp://hdl.handle.net/11449/7549-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/7549-
dc.description.abstractPropolis obtained from honeybee hives has been widely used in medicine, cosmetics, and industry due to its versatile biological activities (antioxidant, antimicrobial, fungicidal, antiviral, antiulcer, immunostimulating, and cytostatic). These activities are mainly attributed to the presence of flavonoids in propolis, which points out the interest in quantifying these constituents in propolis preparations, as well as validation of analytical methodologies. High-performance liquid chromatography (HPLC) methods have been reported to quantify isolated flavonoids or these compounds in complex biological matrices, such as herbal raw materials and extractive preparations. An efficient, precise, and reliable method was developed for quantification of propolis extractive solution using HPLC with UV detection. The chromatograms were obtained from various gradient elution systems (GES) tested in order to establish the ideal conditions for the analysis of propolis extractive solution, using methanol and water: acetonitrile (97.5 : 2.5, v/v) as mobile phase. Gradient reversed phase chromatography was performed using a stainless steel column (250 x 4.6 mm i.d., 5 mum) filled with Chromsep RP 18 (Varian), column temperature at 30.0 +/- 0.1degreesC and detection at 310 nm. The main validation parameters of the method were also determined. The method showed linearity for chrysin in the range 0.24-2.4 mug mL(-1) with good correlation coefficients (0.9975). Precision and accuracy were determined. The obtained results demonstrate the efficiency of the proposed method. The analytical procedure is reliable and offers advantages in terms of speed and cost of reagents.en
dc.format.extent2399-2409-
dc.language.isoeng-
dc.publisherMarcel Dekker Inc-
dc.sourceWeb of Science-
dc.subjectpropolispt
dc.subjecthigh-performance liquid chromatography (HPLC)pt
dc.subjectchrysinpt
dc.subjectphytochemicalspt
dc.subjectflavonoidspt
dc.titleApplication of an HPLC method for analysis of propolis extracten
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP, Programa Posgraduacao Ciências Farmaceut, BR-14802902 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, Programa Posgraduacao Ciências Farmaceut, BR-14802902 Araraquara, SP, Brazil-
dc.identifier.doi10.1081/JLC-120023254-
dc.identifier.wosWOS:000184983400012-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Liquid Chromatography & Related Technologies-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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