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

ABSTRACT

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


Subject(s)
Animals , Female , Mice , Rats , Granulocyte Colony-Stimulating Factor/pharmacokinetics , Cells, Cultured , Dose-Response Relationship, Drug , Granulocyte Colony-Stimulating Factor/administration & dosage , Granulocyte Colony-Stimulating Factor/isolation & purification , Granulocyte Colony-Stimulating Factor/blood , Glycosylation , Injections, Intraperitoneal , Injections, Intravenous , Mice, Inbred BALB C , Reference Standards , Recombinant Proteins/pharmacokinetics , Rats, Wistar , Time Factors , Tissue Distribution
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