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Electron. j. biotechnol ; 10(2): 271-278, Apr. 15, 2007. ilus, graf, tab
Artículo en Inglés | LILACS | ID: lil-499174

RESUMEN

The pharmacokinetic behaviour of the non-glycosylated, bacterially-derived recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) and the glycosylated mammalian product was studied after intra and extra vascular administration of a single dose in rodents. Each route of administration gave a different rhGM-CSF concentration-time profile. After extra vascular administration of equivalent doses, a higher peak concentration and faster elimination were observed in the group treated with the E. coli-derived cytokine. The faster elimination resulted in a return to pre-treatment plasma levels after 12 hrs, versus 48 hrs following the administration of glycosylated rhGM-CSF. After intravascular administration, clearance of rhGM-CSF was significantly decreased by the presence of carbohydrates. Non-significant differences in the terminal phase of the biphasic kinetics were found, but the distribution phase was significantly longer for the glycosylated form


Asunto(s)
Animales , Femenino , Ratones , Ratas , Factor Estimulante de Colonias de Granulocitos/farmacocinética , Células Cultivadas , Relación Dosis-Respuesta a Droga , Factor Estimulante de Colonias de Granulocitos/administración & dosificación , Factor Estimulante de Colonias de Granulocitos/aislamiento & purificación , Factor Estimulante de Colonias de Granulocitos/sangre , Glicosilación , Inyecciones Intraperitoneales , Inyecciones Intravenosas , Ratones Endogámicos BALB C , Estándares de Referencia , Proteínas Recombinantes/farmacocinética , Ratas Wistar , Factores de Tiempo , Distribución Tisular
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