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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/37317
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dc.contributor.authorPereira, F. C.-
dc.contributor.authorFogg, A. G.-
dc.contributor.authorUgo, P.-
dc.contributor.authorBergamo, E. P.-
dc.contributor.authorStradiotto, Nelson Ramos-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.date.accessioned2014-05-20T15:27:18Z-
dc.date.accessioned2016-10-25T18:02:06Z-
dc.date.available2014-05-20T15:27:18Z-
dc.date.available2016-10-25T18:02:06Z-
dc.date.issued2005-07-01-
dc.identifierhttp://dx.doi.org/10.1002/elan.200403247-
dc.identifier.citationElectroanalysis. Weinheim: Wiley-v C H Verlag Gmbh, v. 17, n. 14, p. 1309-1316, 2005.-
dc.identifier.issn1040-0397-
dc.identifier.urihttp://hdl.handle.net/11449/37317-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/37317-
dc.description.abstractThe detection limit (about 0.017 mu g mL(-1)) for voltammetric determination of iodide (peak at +0.87 V vs. Ag/AgCl at pH 2) at a glutaraldehyde-cross-linked poly-L-lysine modified glassy carbon electrode involving oxidation to iodine was found to be several orders of magnitude lower than that for the voltammetric determination on a bare glassy carbon electrode. This method was applied successfully to the determination of iodide in two medicinal formulations. Idoxuridine was determined indirectly at the same electrode by accumulating it first at -0.8 V vs. Ag/AgCl. At this potential the C-I bond in the adsorbed idoxuridine is reduced giving iodide, which is then determined at the modified electrode. The method was successfully applied to the determination of idoxuridine in a urine sample.en
dc.format.extent1309-1316-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectglutaraldehyde-cross-linked poly-L-lysine modified glassy carbon electrodept
dc.subjectiodide determinationpt
dc.subjectidoxuridine determinationpt
dc.subjectmodified electrodept
dc.titleDetermination of iodide and idoxuridine at a glutaraldehyde-cross-linked poly-L-lysine modified glassy carbon electrodeen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv Luton-
dc.contributor.institutionUniv Loughborough-
dc.contributor.institutionUniv Ca Foscari Venezia-
dc.description.affiliationUniv Estadual Paulista, Inst Quim, Dept Quim Analit, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUniv Luton, Luton Inst, Luton LU1 5DU, Beds, England-
dc.description.affiliationUniv Loughborough, Loughborough LE11 3TU, Leics, England-
dc.description.affiliationUniv Ca Foscari Venezia, Dipartimento Chim Fis, Venice, Italy-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, Dept Quim Analit, BR-14801970 Araraquara, SP, Brazil-
dc.identifier.doi10.1002/elan.200403247-
dc.identifier.wosWOS:000230874700010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofElectroanalysis-
dc.identifier.orcid0000-0002-2296-1393-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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