In-vitro physiologically based extraction of solid materials: Do we have reliable analytical methods for bioaccessibility studies of emerging organic contaminants?

C Rodríguez-Navas, M Rosende, M Miró - TrAC Trends in Analytical …, 2017 - Elsevier
In-vitro oral bioaccessibility tests do remain alluring as viable tools for fast assessment of
potential human exposure to environmental contaminants to comply with the ethical …

Development of novel, 384-well high-throughput assay panels for human drug transporters: drug interaction and safety assessment in support of discovery research

H Tang, DR Shen, YH Han, Y Kong… - Journal of …, 2013 - journals.sagepub.com
Transporter proteins are known to play a critical role in affecting the overall absorption,
distribution, metabolism, and excretion characteristics of drug candidates. In addition to …

Quantitative targeted absolute proteomics for 28 human transporters in plasma membrane of Caco-2 cell monolayer cultured for 2, 3, and 4 weeks

Y Uchida, S Ohtsuki, J Kamiie, K Ohmine… - Drug metabolism and …, 2015 - Elsevier
The purpose of the present study was to evaluate and compare the absolute protein
expression levels of 28 drug-related transporters in Caco-2 cell monolayers cultured for 2, 3 …

Consumer product in vitro digestion model: bioaccessibility of contaminants and its application in risk assessment

EFA Brandon, AG Oomen, CJM Rompelberg… - Regulatory Toxicology …, 2006 - Elsevier
This paper describes the applicability of in vitro digestion models as a tool for consumer
products in (ad hoc) risk assessment. In current risk assessment, oral bioavailability from a …

Transporter biology in drug approval: regulatory aspects

K Maeda, Y Sugiyama - Molecular aspects of medicine, 2013 - Elsevier
Previous in vitro and clinical research have indicated that a wide variety of drug transporters
as well as metabolic enzymes dominate the pharmacokinetics of drugs and that some drugs …

[HTML][HTML] Using Ex Vivo Porcine Jejunum to Identify Membrane Transporter Substrates: A Screening Tool for Early—Stage Drug Development

YE Arnold, YN Kalia - Biomedicines, 2020 - mdpi.com
Robust, predictive ex vivo/in vitro models to study intestinal drug absorption by passive and
active transport mechanisms are scarce. Membrane transporters can significantly impact …

Physiologically based pharmacokinetic modeling of intestinal first-pass metabolism of CYP3A substrates with high intestinal extraction

M Gertz, JB Houston, A Galetin - Drug metabolism and disposition, 2011 - ASPET
Prediction of intestinal availability (FG), in conjunction with hepatic metabolism, is of
considerable importance in drug disposition to assess oral clearance and liability to drug …

Predicting the oral uptake efficiency of chemicals in mammals: Combining the hydrophilic and lipophilic range

IA O'connor, MAJ Huijbregts, AMJ Ragas… - Toxicology and applied …, 2013 - Elsevier
Environmental risk assessment requires models for estimating the bioaccumulation of
untested compounds. So far, bioaccumulation models have focused on lipophilic …

Principles and experimental considerations for in vitro transporter interaction assays

S Bhoopathy, C Bode, V Naageshwaran… - Enzyme Kinetics in Drug …, 2014 - Springer
Drug transporters are now universally acknowledged as important determinants of the
absorption, distribution, metabolism and excretion of both endogenous and exogenous …

Physicochemical property space of hepatobiliary transport and computational models for predicting rat biliary excretion

MVS Varma, G Chang, Y Lai, B Feng… - Drug Metabolism and …, 2012 - ASPET
Biliary excretion (BE) is a major elimination pathway, and its prediction is particularly
important for optimization of systemic and/or target-site exposure of new molecular entities …