Transporters and drug-drug interactions: important determinants of drug disposition and effects

J König, F Müller, MF Fromm - Pharmacological reviews, 2013 - ASPET
Uptake and efflux transporters determine plasma and tissue concentrations of a broad
variety of drugs. They are localized in organs such as small intestine, liver, and kidney …

Organic anion transporting polypeptide 1B1: a genetically polymorphic transporter of major importance for hepatic drug uptake

M Niemi, MK Pasanen, PJ Neuvonen - Pharmacological reviews, 2011 - ASPET
The importance of membrane transporters for drug pharmacokinetics has been increasingly
recognized during the last decade. Organic anion transporting polypeptide 1B1 (OATP1B1) …

Clinical significance of organic anion transporting polypeptides (OATPs) in drug disposition: their roles in hepatic clearance and intestinal absorption

Y Shitara, K Maeda, K Ikejiri, K Yoshida… - … & drug disposition, 2013 - Wiley Online Library
Organic anion transporting polypeptide (OATP) family transporters accept a number of drugs
and are increasingly being recognized as important factors in governing drug and …

The role of BCS (biopharmaceutics classification system) and BDDCS (biopharmaceutics drug disposition classification system) in drug development

LZ Benet - Journal of pharmaceutical sciences, 2013 - Elsevier
ABSTRACT Biopharmaceutics Classification System and Biopharmaceutics Drug
Distribution Classification System are complimentary, not competing, classification systems …

Clinical probes and endogenous biomarkers as substrates for transporter drug‐drug interaction evaluation: perspectives from the international transporter consortium

X Chu, M Liao, H Shen, K Yoshida… - Clinical …, 2018 - Wiley Online Library
Drug transporters can govern the absorption, distribution, metabolism, and excretion of
substrate drugs and endogenous substances. Investigations to examine their potential …

Predicting clearance mechanism in drug discovery: extended clearance classification system (ECCS)

MV Varma, SJ Steyn, C Allerton, AF El-Kattan - Pharmaceutical research, 2015 - Springer
Early prediction of clearance mechanisms allows for the rapid progression of drug discovery
and development programs, and facilitates risk assessment of the pharmacokinetic …

Drug–drug–gene interactions and adverse drug reactions

MA Malki, ER Pearson - The pharmacogenomics journal, 2020 - nature.com
The economic and health burden caused by adverse drug reactions has increased
dramatically in the last few years. This is likely to be mediated by increasing polypharmacy …

Drug–drug interaction studies: regulatory guidance and an industry perspective

T Prueksaritanont, X Chu, C Gibson, D Cui, KL Yee… - The AAPS journal, 2013 - Springer
Recently, the US Food and Drug Administration and European Medicines Agency have
issued new guidance for industry on drug interaction studies, which outline comprehensive …

Transporter-mediated drug-drug interactions and their significance

X Liu - Drug Transporters in Drug Disposition, Effects and …, 2019 - Springer
Drug transporters are considered to be determinants of drug disposition and effects/toxicities
by affecting the absorption, distribution, and excretion of drugs. Drug transporters are …

Investigation of the rate-determining process in the hepatic elimination of HMG-CoA reductase inhibitors in rats and humans

T Watanabe, H Kusuhara, K Maeda, H Kanamaru… - Drug Metabolism and …, 2010 - ASPET
Elucidation of the rate-determining process in the overall hepatic elimination of drugs is
critical for predicting their intrinsic hepatic clearance and the impact of variation of …