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Authordc.contributor.authorGONZÁLEZ‐MARTIN, GUILLERMO 
Authordc.contributor.authorPAULOS, CLAUDÍO 
Authordc.contributor.authorGUEVARA, ALFREDO 
Authordc.contributor.authorPONCE, GRACIELA 
Admission datedc.date.accessioned2018-12-20T14:34:25Z
Available datedc.date.available2018-12-20T14:34:25Z
Publication datedc.date.issued1994
Cita de ítemdc.identifier.citationJournal of Pharmacy and Pharmacology, Volumen 46, Issue 5, 2018, Pages 356-359
Identifierdc.identifier.issn20427158
Identifierdc.identifier.issn00223573
Identifierdc.identifier.other10.1111/j.2042-7158.1994.tb03812.x
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/156542
Abstractdc.description.abstractAbstract— Nifurtimox disposition was investigated using the rat isolated perfused‐liver method after administration of 25 μg mL−1 nifurtimox, and its disappearance was monitored by analysing the perfusate sample at various times. Biliary excretion was also measured. The drug concentration profile underwent a biexponential decline over the 2‐h study period, with a terminal half‐life of 62·76 ± 17·56 min. Nifurtimox is a high clearance compound (15·23±5·53 mL min−1). The extraction ratio was 0·621 ±0·159. Biliary excretion accounted for 0·05% of the dose, the remainder consisting of highly polar metabolites. By 2 h, a minimal fraction of unchanged nifurtimox was recovered from the perfusate. Nifurtimox activity against Trypanosoma cruzi (clone CA‐1) during the perfusion was also determined. Epimastigotes isolated from continuous culture were exposed to the samples of perfusate at different perfusion times in a microtitre plate. After an incubation time of 72 h at 27°C, the parasite numbe
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceJournal of Pharmacy and Pharmacology
Keywordsdc.subjectPharmacology
Keywordsdc.subjectPharmaceutical Science
Títulodc.titleDisposition of Nifurtimox and Metabolite Activity Against Trypanosoma cruzi using Rat Isolated Perfused Liver
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile