Disposition of Nifurtimox and Metabolite Activity Against Trypanosoma cruzi using Rat Isolated Perfused Liver
Author
dc.contributor.author
GONZÁLEZ‐MARTIN, GUILLERMO
Author
dc.contributor.author
PAULOS, CLAUDÍO
Author
dc.contributor.author
GUEVARA, ALFREDO
Author
dc.contributor.author
PONCE, GRACIELA
Admission date
dc.date.accessioned
2018-12-20T14:34:25Z
Available date
dc.date.available
2018-12-20T14:34:25Z
Publication date
dc.date.issued
1994
Cita de ítem
dc.identifier.citation
Journal of Pharmacy and Pharmacology, Volumen 46, Issue 5, 2018, Pages 356-359
Identifier
dc.identifier.issn
20427158
Identifier
dc.identifier.issn
00223573
Identifier
dc.identifier.other
10.1111/j.2042-7158.1994.tb03812.x
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/156542
Abstract
dc.description.abstract
Abstract— 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