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dc.creatorMiguel, Laura de-
dc.creatorBarbas Arribas, Coral.-
dc.date2003-
dc.date.accessioned2011-09-19T15:40:28Z-
dc.date.available2011-09-19T15:40:28Z-
dc.date.issued2003-09-19T15:40:28Z-
dc.identifier000000402246-
dc.identifier.urihttp://hdl.handle.net/10637/782-
dc.descriptionEn: Journal of pharmaceutical and biomedical analysis. 2003. n. 33 (2) : 211-217 p.-
dc.description.abstractA LC method with UV detection for determining azithromycin impurities in tablets as pharmaceutical form has been developed. It is to be employed in routine and stability tests. A linear gradient elution was employed starting with 47% A and 53% B to reach 28% A and 72% B at 48 min. Mobile phase A was KH2PO4 10 mM (H2O) at pH 7.00. B was a mixture methanol:acetonitrile 1:1 (v/v). UV detection was performed at 210 nm. The chromatographic column was Phenomenex Synergi† MAX-RP 4 mm 250 /460 mm kept at 50 8C. Six impurities were separated and identified and it was possible to quantify five out of the six with reasonable accuracy and precision.en-EN
dc.formatapplication/pdf-
dc.language.isoen-
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.es-
dc.subjectAzithromycin.en-EN
dc.subjectImpurities.en-EN
dc.subjectHPLC.en-EN
dc.subjectPharmaceuticals.en-EN
dc.titleLC determination of impurities in azithromycin tablets-
dc.typeArtículo-
europeana.dataProviderUNIVERSIDAD SAN PABLO CEU-
europeana.isShownAthttp://hdl.handle.net/10637/782-
europeana.objecthttp://repositorioinstitucional.ceu.es/visor/libros/402246/thumb_europeana/402246.jpg-
europeana.providerHispana-
europeana.rightshttp://creativecommons.org/publicdomain/zero/1.0/-
europeana.typeTEXT-
dc.centroUniversidad San Pablo-CEU-
Aparece en las colecciones: Facultad de Farmacia




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