Exploring Tafamidis Effects Through PBPK-QSP Modelling. [PDF]
Ulaszek S +3 more
europepmc +1 more source
Bridging the life-course exposome approach with a life-cycle perspective in safe and sustainable by design (SSbD) for chemical risk. [PDF]
Sarigiannis D +4 more
europepmc +1 more source
Accelerating Subcutaneous Drug Development: A Mechanistic Absorption Model for the Open Systems Pharmacology Framework. [PDF]
Pellowe M, Dubbelboer I, Sjögren E.
europepmc +1 more source
Predicting Pharmacokinetic Variability and Drug Interaction Risk Using Omics-Based Biomarkers. [PDF]
Prasad B.
europepmc +1 more source
Dose optimization of inhaled tigecycline in humans to overcome inherent adverse events and maximize bacterial clearance using a physiologically-based pharmacokinetic modeling approach. [PDF]
Park H +12 more
europepmc +1 more source
Utility of a physiologically-based pharmacokinetic model for investigating time-dependent variability in the fetal-to-maternal plasma concentration ratio of digoxin. [PDF]
Okuba K, Ikeda K.
europepmc +1 more source
Assessing transporter-mediated rifampin-linezolid interaction using physiologically-based pharmacokinetic modelling. [PDF]
Nguyen HD +4 more
europepmc +1 more source
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QSARs for PBPK modelling of environmental contaminants
SAR and QSAR in Environmental Research, 2011Physiologically-based pharmacokinetic (PBPK) models are increasingly finding use in risk assessment applications of data-rich compounds. However, it is a challenge to determine the chemical-specific parameters for these models, particularly in time- and resource-limiting situations.
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PBPK in Preterm and Term Neonates: A Review
Current Pharmaceutical Design, 2018The neonatal population remains one of the populations in which appropriate dosing regimens are still lacking, resulting in a large off-label or unlicensed use. Clinical research in these small infants remains a challenge, which sparks the need for modeling and simulation as an additional tool for neonatal drug research.The use of physiologically based
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