Caco-2/TC7 cell line characterization for intestinal absorption: How reliable is this in vitro model for the prediction of the oral dose fraction absorbed in human?
- 28 February 2011
- journal article
- Published by Elsevier BV in Toxicology in Vitro
- Vol. 25 (1), 13-20
- https://doi.org/10.1016/j.tiv.2010.08.009
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Prediction of drug bioavailability in humans using immobilized artificial membrane phosphatidylcholine column chromatography and in vitro hepatic metabolic clearanceBiomedical Chromatography, 2009
- Effects of dietary flavonoids on the transport of cimetidine via P-glycoprotein and cationic transporters in Caco-2 and LLC-PK1 cell modelsXenobiotica, 2008
- Seromucosal Transport of Intravenously Administered Carbamazepine Is Not Enhanced by Oral Doses of Activated Charcoal in RatsBasic & Clinical Pharmacology & Toxicology, 2008
- Development of an in silico model for predicting efflux substrates in Caco-2 cellsInternational Journal of Pharmaceutics, 2007
- Prediction of human pharmacokinetics —gastrointestinal absorptionJournal of Pharmacy and Pharmacology, 2007
- Human Hepatic Cytochrome P450-Specific Metabolism of Parathion and ChlorpyrifosDrug Metabolism and Disposition, 2006
- Ultraviolet absorbance detection of colchicine and related alkaloids on a capillary electrophoresis microchipAnalytica Chimica Acta, 2006
- THE HUMAN INTESTINAL CYTOCHROME P450 “PIE”Drug Metabolism and Disposition, 2006
- Self‐Association of Dexverapamil in Aqueous SolutionJournal of Pharmaceutical Sciences, 1995
- Identification and Quantification of Tricyclic Antidepressants by Uv-Photodiode Array Detection with Multicomponent AnalysisJournal of Liquid Chromatography, 1993