[HTML][HTML] Interaction of luteolin, naringenin, and their sulfate and glucuronide conjugates with human serum albumin, cytochrome P450 (CYP2C9, CYP2C19, and …

H Kaci, S Bodnárová, E Fliszár-Nyúl, B Lemli… - Biomedicine & …, 2023 - Elsevier
Luteolin and naringenin are flavonoids found in various foods/beverages and present in
certain dietary supplements. After a high intake of these flavonoids, their sulfate and …

Importance of hepatic transporters in clinical disposition of drugs and their metabolites

M Patel, KS Taskar… - The Journal of Clinical …, 2016 - Wiley Online Library
This review provides a practical clinical perspective on the relevance of hepatic transporters
in pharmacokinetics and drug‐drug interactions (DDIs). Special emphasis is placed on …

Meeting the challenge of predicting hepatic clearance of compounds slowly metabolized by cytochrome P450 using a novel hepatocyte model, HepatoPac

TS Chan, H Yu, A Moore, SR Khetani… - Drug metabolism and …, 2013 - ASPET
Generating accurate in vitro intrinsic clearance data is an important aspect of predicting in
vivo human clearance. Primary hepatocytes in suspension are routinely used to predict in …

Setting Clinical Exposure Levels of Concern for Drug-Induced Liver Injury (DILI) Using Mechanistic in vitro Assays

F Shah, L Leung, HA Barton, Y Will… - Toxicological …, 2015 - academic.oup.com
Severe drug-induced liver injury (DILI) remains a major safety issue due to its frequency of
occurrence, idiosyncratic nature, poor prognosis, and diverse underlying mechanisms …

Interindividual and interethnic variability in drug disposition: polymorphisms in organic anion transporting polypeptide 1B1 (OATP1B1; SLCO1B1)

HH Lee, RH Ho - British journal of clinical pharmacology, 2017 - Wiley Online Library
OATP1B1 (SLCO1B1) is predominantly expressed at the basolateral membrane of
hepatocytes and is critically important for the hepatic uptake and clearance of numerous …

Evaluation of pharmacokinetic drug–drug interactions: a review of the mechanisms, in vitro and in silico approaches

Y Peng, Z Cheng, F Xie - Metabolites, 2021 - mdpi.com
Pharmacokinetic drug–drug interactions (DDIs) occur when a drug alters the absorption,
transport, distribution, metabolism or excretion of a co-administered agent. The occurrence …

Coproporphyrins I and III as functional markers of OATP1B activity: in vitro and in vivo evaluation in preclinical species

H Shen, J Dai, T Liu, Y Cheng, W Chen… - … of Pharmacology and …, 2016 - ASPET
Inhibition of organic anion-transporting polypeptide (OATP) 1B function can lead to serious
clinical drug-drug interactions, thus a thorough evaluation of the potential for this type of …

Metabolism and interactions of Ivermectin with human cytochrome P450 enzymes and drug transporters, possible adverse and toxic effects

SP Rendic - Archives of Toxicology, 2021 - Springer
The review presents metabolic properties of Ivermectin (IVM) as substrate and inhibitor of
human P450 (P450, CYP) enzymes and drug transporters. IVM is metabolized, both in vivo …

Prediction of organic anion-transporting polypeptide 1B1-and 1B3-mediated hepatic uptake of statins based on transporter protein expression and activity data

A Kunze, J Huwyler, G Camenisch, B Poller - Drug Metabolism and …, 2014 - ASPET
Organic anion-transporting polypeptides (OATP) 1B1 and OATP1B3 are drug transporters
mediating the active hepatic uptake of their substrates. Because they exhibit overlapping …

Hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions

A Vildhede, M Karlgren, EK Svedberg… - Drug metabolism and …, 2014 - ASPET
Differences in the expression and function of the organic anion transporting polypeptide
(OATP) transporters contribute to interindividual variability in atorvastatin clearance …