![]() |
Volumn 22, Issue 1, 2001, Pages 1-14
|
Investigation of 5-FU disposition after oral administration of capecitabine, a triple-prodrug of 5-FU, using a physiologically based pharmacokinetic model in a human cancer xenograft model: Comparison of the simulated 5-FU exposures in the tumour tissue between human and xenograft model
|
Author keywords
[No Author keywords available]
|
Indexed keywords
CAPECITABINE;
DOXIFLURIDINE;
DRUG METABOLITE;
FLUOROURACIL;
PLASMA PROTEIN;
PRODRUG;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
AREA UNDER THE CURVE;
ARTICLE;
CANCER MODEL;
CONTROLLED STUDY;
DIARRHEA;
DOSE RESPONSE;
DOSE TIME EFFECT RELATION;
DRUG ACCUMULATION;
DRUG ACTIVATION;
DRUG BLOOD LEVEL;
DRUG ELIMINATION;
DRUG EXPOSURE;
DRUG METABOLISM;
DRUG PROTEIN BINDING;
DRUG TISSUE LEVEL;
ENZYME KINETICS;
GASTROINTESTINAL TRACT;
HUMAN;
HUMAN TISSUE;
IN VITRO STUDY;
MALE;
MOUSE;
NONHUMAN;
PLASMA PROTEIN BINDING;
SIMULATION;
TUMOR XENOGRAFT;
ADMINISTRATION, ORAL;
ANIMALS;
ANTIMETABOLITES, ANTINEOPLASTIC;
AREA UNDER CURVE;
COLONIC NEOPLASMS;
CYTOSOL;
DEOXYCYTIDINE;
DOSE-RESPONSE RELATIONSHIP, DRUG;
FLUOROURACIL;
HUMANS;
KIDNEY;
MALE;
MICE;
MICE, INBRED BALB C;
MICE, NUDE;
NEOPLASM TRANSPLANTATION;
PRODRUGS;
SUBCELLULAR FRACTIONS;
THERAPEUTIC EQUIVALENCY;
TISSUE DISTRIBUTION;
TUMOR CELLS, CULTURED;
XENOGRAFT MODEL ANTITUMOR ASSAYS;
|
EID: 0035188291
PISSN: 01422782
EISSN: None
Source Type: Journal
DOI: 10.1002/bdd.250 Document Type: Article |
Times cited : (24)
|
References (19)
|