Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Frédérique Fenneteau"'
Publikováno v:
Chaos (Woodbury, N.Y.). 31(2)
Quantitative systems pharmacology (QSP) proved to be a powerful tool to elucidate the underlying pathophysiological complexity that is intensified by the biological variability and overlapped by the level of sophistication of drug dosing regimens. Th
Publikováno v:
Pharmacology & Pharmacy. :42-52
Noncompliance to therapeutic regimen is a real public health problem with tremendous socioeconomic consequences. Instead of direct intervention to patients, which can add extra burden to the already overloaded health system, alternative strategies or
Publikováno v:
Journal of pharmaceutical sciences. 99(1)
The first objective of the present study was to predict the pharmacokinetics of selected CYP3A substrates administered at a single oral dose to human. The second objective was to predict pharmacokinetics of the selected drugs in presence of inhibitor
Autor:
Lucie Couture, Veronique Michaud, Frédérique Fenneteau, Jacques Turgeon, Fahima Nekka, Jun Li
Publikováno v:
Theoretical Biology and Medical Modelling, Vol 6, Iss 1, p 2 (2009)
Theoretical Biology & Medical Modelling
Theoretical Biology & Medical Modelling
Background The expression and activity of P-glycoproteins due to genetic or environmental factors may have a significant impact on drug disposition, drug effectiveness or drug toxicity. Hence, characterization of drug disposition over a wide range of
Publikováno v:
Journal of pharmacokinetics and pharmacodynamics. 36(6)
The structural complexity of a PBPK model is usually accompanied with significant uncertainty in estimating its input parameters. In the last decade, the global sensitivity analysis, which accounts for the variability of all model input parameters si
Publikováno v:
PAMM. 7:1121905-1121906
In order to improve understanding and prediction of drug disposition prior to in vivo experiments, we aimed to develop a PBPK model that accounts for the involvement of P-glycoprotein activity and expression in mouse brain, liver, kidney and heart ti
Publikováno v:
Clinical Pharmacology & Therapeutics. 79:P49-P49