Development of a physiologically based pharmacokinetic/pharmacodynamic model to identify mechanisms contributing to entacapone low bioavailability.
Alqahtani, Saeed
Development of a physiologically based pharmacokinetic/pharmacodynamic model to identify mechanisms contributing to entacapone low bioavailability. [electronic resource] - Biopharmaceutics & drug disposition Dec 2015 - 587-602 p. digital
Publication Type: Journal Article
1099-081X
10.1002/bdd.1986 doi
Adult
Animals
Antiparkinson Agents--blood
Biological Availability
Biotransformation
Caco-2 Cells
Catechol O-Methyltransferase Inhibitors--blood
Catechols--blood
Computational Biology
Enterocytes--metabolism
Expert Systems
Humans
Intestinal Absorption
Liver--metabolism
Male
Metabolic Clearance Rate
Models, Biological
Nitriles--blood
Phosphorylation
Prodrugs--analysis
Rats
Solubility
Tissue Distribution
Development of a physiologically based pharmacokinetic/pharmacodynamic model to identify mechanisms contributing to entacapone low bioavailability. [electronic resource] - Biopharmaceutics & drug disposition Dec 2015 - 587-602 p. digital
Publication Type: Journal Article
1099-081X
10.1002/bdd.1986 doi
Adult
Animals
Antiparkinson Agents--blood
Biological Availability
Biotransformation
Caco-2 Cells
Catechol O-Methyltransferase Inhibitors--blood
Catechols--blood
Computational Biology
Enterocytes--metabolism
Expert Systems
Humans
Intestinal Absorption
Liver--metabolism
Male
Metabolic Clearance Rate
Models, Biological
Nitriles--blood
Phosphorylation
Prodrugs--analysis
Rats
Solubility
Tissue Distribution