dc.contributorLoughborough Univ Technol
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:19:58Z
dc.date.available2014-05-20T15:19:58Z
dc.date.created2014-05-20T15:19:58Z
dc.date.issued1998-07-03
dc.identifierAnalytica Chimica Acta. Amsterdam: Elsevier B.V., v. 367, n. 1-3, p. 255-259, 1998.
dc.identifier0003-2670
dc.identifierhttp://hdl.handle.net/11449/31344
dc.identifier10.1016/S0003-2670(98)00163-9
dc.identifierWOS:000074382600027
dc.identifier0000-0002-2296-1393
dc.description.abstractAt accumulation potentials close to +0.1 V at a hanging mercury drop electrode, ceftazidime is accumulated at pH 9.5, probably in a hydrolysed or otherwise chemically altered form, in an anodic process to give an adsorbed mercury salt. The accumulation of this mercury salt allows the indirect cathodic-stripping voltammetric determination of ceftazidime using the reduction peak of the mercury salt at -0.70 V. The high sensitivity of the method coupled with high sample dilution allows ceftazidime to be determined in milk samples at the 28 mu g ml(-1) level without prior separation. In order to determine lower levels of ceftazidime in milk (ca. 10 ng ml(-1)) a separation process would be required. (C) 1998 Elsevier B.V. B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationAnalytica Chimica Acta
dc.relation5.123
dc.relation1,512
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectceftazidime
dc.subjectcathodic-stripping voltammetry
dc.subjectmilk
dc.subjectmercury salt
dc.titleIndirect cathodic-stripping voltammetric determination of ceftazidime as a mercury salt
dc.typeArtículos de revistas


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