Successful prediction of human hepatic concentrations of transported drugs using the proteomics‐informed relative expression factor approach

M Yin, A Balhara, S Marie, N Tournier… - Clinical …, 2024 - Wiley Online Library
Tissue drug concentrations determine the efficacy and toxicity of drugs. When a drug is the
substrate of transporters that are present at the blood: tissue barrier, the steady‐state …

[HTML][HTML] Screening of chemicals for human bioaccumulative potential with a physiologically based toxicokinetic model

A Tonnelier, S Coecke, JM Zaldívar - Archives of toxicology, 2012 - Springer
Human bioaccumulative potential is an important element in the risk assessment of
chemicals. Due to the high number of synthetic chemicals, there exists the need to develop …

Human intestinal transporter database: QSAR modeling and virtual profiling of drug uptake, efflux and interactions

A Sedykh, D Fourches, J Duan, O Hucke… - Pharmaceutical …, 2013 - Springer
Purpose Membrane transporters mediate many biological effects of chemicals and play a
major role in pharmacokinetics and drug resistance. The selection of viable drug candidates …

[HTML][HTML] The importance of drug transporter characterization to precision medicine

P Fisel, AT Nies, E Schaeffeler… - Expert opinion on drug …, 2017 - Taylor & Francis
The aim of precision medicine is to improve health care by tailoring drug treatment to
patientsL individual characteristics through the integration of knowledge explaining …

Interindividual and regional variability in drug transporter abundance at the human blood–brain barrier measured by quantitative targeted proteomics

S Billington, L Salphati, CECA Hop… - Clinical …, 2019 - Wiley Online Library
For in vitro to in vivo extrapolation (IVIVE) of brain distribution of drugs that are transported at
the human blood–brain barrier (BBB), it is important to quantify the interindividual and …

RNA-Seq reveals different mRNA abundance of transporters and their alternative transcript isoforms during liver development

JY Cui, SS Gunewardena, B Yoo, J Liu… - Toxicological …, 2012 - academic.oup.com
During development, the maturation of liver transporters is essential for chemical elimination
in newborns and children. One cannot compare the real abundance of transcripts by …

[HTML][HTML] An open source physiologically based kinetic model for the chicken (Gallus gallus domesticus): Calibration and validation for the prediction residues in tissues …

LS Lautz, C Nebbia, S Hoeks, R Oldenkamp… - Environment …, 2020 - Elsevier
Xenobiotics from anthropogenic and natural origin enter animal feed and human food as
regulated compounds, environmental contaminants or as part of components of the diet …

Incorporating population-level genetic variability within laboratory models in toxicology: from the individual to the population

P Dornbos, JJ LaPres - Toxicology, 2018 - Elsevier
Humans respond to chemical exposures differently due to many factors, such as previous
and concurrent stressors, age, sex, and genetic background. The vast majority of laboratory …

Involvement of drug transporters in organ toxicity: the fundamental basis of drug discovery and development

Y Cheng, A El-Kattan, Y Zhang, AS Ray… - Chemical research in …, 2016 - ACS Publications
Membrane transporters play a pivotal role in many organs to maintain their normal
physiological functions and contribute significantly to drug absorption, distribution, and …

Comparison of the predictability of human hepatic clearance for organic anion transporting polypeptide substrate drugs between different in vitro–in vivo extrapolation …

S Izumi, Y Nozaki, T Komori, O Takenaka… - Journal of …, 2017 - Elsevier
Prediction of human pharmacokinetic profiles of drug candidates is an essential step toward
first-in-human studies. However, it remains difficult to quantitatively predict hepatic …