| Literature DB >> 33513941 |
Yaru Peng1, Zeneng Cheng1, Feifan Xie1.
Abstract
Pharmacokinetic drug-drug interactions (DDIs) occur when a drug alters the absorption, transport, distribution, metabolism or excretion of a co-administered agent. The occurrence of pharmacokinetic DDIs may result in the increase or the decrease of drug concentrations, which can significantly affect the drug efficacy and safety in patients. Enzyme-mediated DDIs are of primary concern, while the transporter-mediated DDIs are less understood but also important. In this review, we presented an overview of the different mechanisms leading to DDIs, the in vitro experimental tools for capturing the factors affecting DDIs, and in silico methods for quantitative predictions of DDIs. We also emphasized the power and strategy of physiologically based pharmacokinetic (PBPK) models for the assessment of DDIs, which can integrate relevant in vitro data to simulate potential drug interaction in vivo. Lastly, we pointed out the future directions and challenges for the evaluation of pharmacokinetic DDIs.Entities:
Keywords: cytochrome P450; drug–drug interactions; pharmacokinetics; physiologically based pharmacokinetic model; transporter
Year: 2021 PMID: 33513941 DOI: 10.3390/metabo11020075
Source DB: PubMed Journal: Metabolites ISSN: 2218-1989