| Literature DB >> 34272712 |
Abstract
Predicting drug-drug interactions (DDIs) from in vitro data is made difficult by not knowing concentrations of substrate and inhibitor at the target site. For in vivo targets, this is understandable, since intracellular concentrations can differ from extracellular concentrations. More vexing is that the concentration of the drug at the target for some in vitro assays can also be unknown. This uncertainty has resulted in standard in vitro practices that cannot accurately predict human pharmacokinetics. This case study highlights the impact of drug distribution, both in vitro and in vivo, with the example of the drug interaction potential of montelukast.Entities:
Keywords: CYP2C8; Cheng-Prusoff equation; Drug-drug interaction; Fraction unbound; Free drug hypothesis; Microsomal proteins; Montelukast; Protein binding
Year: 2021 PMID: 34272712 DOI: 10.1007/978-1-0716-1554-6_24
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745