Clinical implications of altered drug transporter abundance/function and PBPK modeling in specific populations: an ITC perspective
The role of membrane transporters on pharmacokinetics (PKs), drug–drug interactions
(DDIs), pharmacodynamics (PDs), and toxicity of drugs has been broadly recognized …
(DDIs), pharmacodynamics (PDs), and toxicity of drugs has been broadly recognized …
ITC recommendations for transporter kinetic parameter estimation and translational modeling of transport‐mediated PK and DDIs in humans
MJ Zamek‐Gliszczynski, CA Lee… - Clinical …, 2013 - Wiley Online Library
This white paper provides a critical analysis of methods for estimating transporter kinetics
and recommendations on proper parameter calculation in various experimental systems …
and recommendations on proper parameter calculation in various experimental systems …
Species differences in drug transporters and implications for translating preclinical findings to humans
X Chu, K Bleasby, R Evers - Expert opinion on drug metabolism & …, 2013 - Taylor & Francis
Introduction: Drug transporters play an important role in the absorption, distribution, and
excretion (ADE) of many drugs. In the last several years it has become increasingly clear …
excretion (ADE) of many drugs. In the last several years it has become increasingly clear …
In vitro and in vivo approaches to characterize transporter-mediated disposition in drug discovery
Introduction: It is becoming increasingly evident that transporters play an important role in
the absorption, distribution and elimination of many drugs. Different approaches have been …
the absorption, distribution and elimination of many drugs. Different approaches have been …
The application of physiologically based pharmacokinetic modeling to predict the role of drug transporters: scientific and regulatory perspectives
Transporters play an important role in drug absorption, disposition, and drug action. The
evaluation of drug transporters requires a comprehensive understanding of transporter …
evaluation of drug transporters requires a comprehensive understanding of transporter …
Physiologically‐based pharmacokinetic models for evaluating membrane transporter mediated drug–drug interactions: current capabilities, case studies, future …
KS Taskar, V Pilla Reddy, H Burt… - Clinical …, 2020 - Wiley Online Library
Physiologically‐based pharmacokinetic (PBPK) modeling has been extensively used to
quantitatively translate in vitro data and evaluate temporal effects from drug–drug …
quantitatively translate in vitro data and evaluate temporal effects from drug–drug …
[HTML][HTML] Endogenous biomarkers for SLC transporter-mediated drug-drug interaction evaluation
Membrane transporters play an important role in the absorption, distribution, metabolism,
and excretion of xenobiotic substrates, as well as endogenous compounds. The evaluation …
and excretion of xenobiotic substrates, as well as endogenous compounds. The evaluation …
Regulation of drug transport proteins—From mechanisms to clinical impact: A white paper on behalf of the international transporter consortium
Membrane transport proteins are involved in the absorption, disposition, efficacy, and/or
toxicity of many drugs. Numerous mechanisms (eg, nuclear receptors, epigenetic gene …
toxicity of many drugs. Numerous mechanisms (eg, nuclear receptors, epigenetic gene …
Disease‐associated changes in drug transporters may impact the pharmacokinetics and/or toxicity of drugs: a white paper from the International Transporter …
R Evers, M Piquette‐Miller, JW Polli… - Clinical …, 2018 - Wiley Online Library
Drug transporters are critically important for the absorption, distribution, metabolism, and
excretion (ADME) of many drugs and endogenous compounds. Therefore, disruption of …
excretion (ADME) of many drugs and endogenous compounds. Therefore, disruption of …
The next frontier in ADME science: Predicting transporter-based drug disposition, tissue concentrations and drug-drug interactions in humans
Predicting transporter-based drug clearance (CL) and tissue concentrations (TC) in humans
is important to reduce the risk of failure during drug development. In addition, when …
is important to reduce the risk of failure during drug development. In addition, when …
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