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Authordc.contributor.authorMorales, A. 
Authordc.contributor.authorRichter Duk, Pablo es_CL
Authordc.contributor.authorToral Ponce, María es_CL
Admission datedc.date.accessioned2011-06-03T14:16:59Z
Available datedc.date.available2011-06-03T14:16:59Z
Publication datedc.date.issued1987
Cita de ítemdc.identifier.citationAnalyst 112: 971-973es_CL
Identifierdc.identifier.issn0003-2654
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121246
Abstractdc.description.abstractIn pyridine - formic acid buffer and tetramethylammonium chloride solution over the pH range 0-8.5, nitrofurazone, furazolidone and other nitrofuran derivatives are reduced in a six-electron process, giving rise to a well defined polarographic reduction wave at a dropping mercury electrode. The current is difussion controlled and proportional to the concentration from about 5.88 x 10-3M to the limit of detection of 1.24 x10-6M. The proposed method permits these drugs to be determined, without any prior separation or extraction, in pharmaceutical formulations and in urine at levels at which the unchanged drugs are excreted. Other drugs commonly used as therapeutic agents, such as nitro derivatives of 1,4-benzodiazepines,chloramphenicol, metronidazole and tinidazole, are reduced in a single four-electron process at more negative potentials, which makes simultaneous determinations possible.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherRoyal Society of Chemistryes_CL
Keywordsdc.subjectNitrofurazonees_CL
Títulodc.titlePolarographic determination of nitrofurazone and furazolidone in pharmaceutical formulations and urinees_CL
Document typedc.typeArtículo de revista


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