Experiment 67506

Details

PropertyValue
Pharmacology
Administration routeINTRAGASTRIC
OrganismAndrographis paniculata (ACANTHACEAE)
CitationPANOSSIAN,A: HOVHANNISYAN,A: MAMIKONYAN,G: ABRAHAMIAN,H: HAMBARDZUMYAN,E: GABRIELIAN,E: GOUKASOVA,G: WIKMAN,G: WAGNER,H:. (2000). PHARMACOKINETIC AND ORAL BIOAVAILABILITY OF ANDROGRAPHOLIDE FROM ANDROGARPHIS PANICULATA FIXED COMBINATION KAN JANG IN RATS AND HUMAN.. 7(5)
Amount utilized
Compound isolated
DiseaseANDROGRAPHOLIDE WAS QUICKLY AND ALMOST COMPLETELY ABSORBED INTO THE BLOOD FOLLOWING THE ORAL ADMINISTRATION OF APE AT A DOSE OF 20 MG/KG BODY WT. IN RATS. ITS BIO-AVAILITY, HOWEVER, DECREASED FOUR-FOLD WHEN A 10-TIMES-HIGHER DOSE WAS USED. SINCE A LARGE PART (55%) OF AND IS BOUND TO PLASMA PROTEINS AND ONLY A LIMITED AMOUNT CAN ENTER THE CELL, THE PHARMACOKINETICS OF AND ARE DESCRIBED WELL BY A ONE-COMPARTMENT MODEL. RENAL EXCRETION IS NOT THE MAIN ROUTE FOR ELIMINATING AND. IT IS MOST LIKELY INTENSELY AND DOSE DEPENDENTLY METABOLIZED.
Dose amount20.0 MG
Number1
Qualitative resultACTIVE
AnimalRAT
Per unitKG
Dose expressionDOSE
ExtractETOH(60%)EXT
GenderMALE