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Physiologically-based pharmacokinetic modeling of pyrene in the rat

Environmental Toxicology and Pharmacology, 1998
The objective of the present study was to develop a physiologically-based model to simulate the oral and i.v. pharmacokinetics of pyrene in the rat. The physiologically-based pharmacokinetic (PBPK) model for pyrene consisted of the following tissue compartments: liver, lungs, adipose tissue, slowly perfused tissues, and richly perfused tissues ...
S, Haddad   +4 more
openaire   +2 more sources

Physiologically based pharmacokinetic modelling of cefoperazone in paediatrics

British Journal of Clinical Pharmacology
AimsCefoperazone is commonly used off‐label in the treatment of bacterial meningitis and sepsis in children, and the pharmacokinetic (PK) data are limited in this vulnerable population. The goal of this study was to develop a physiologically based pharmacokinetic (PBPK) model to predict pediatric cefoperazone exposure for rational dosing ...
Qiushi Wang   +4 more
openaire   +2 more sources

A Physiologically Based Pharmacokinetic Model of Inorganic Arsenic

Regulatory Toxicology and Pharmacology, 1999
This study presents a physiologically based pharmacokinetic model of inorganic arsenic disposition in humans. The model focuses on short-term exposures by the oral route. The model considers the four circulating species (AsIII, AsV, and two metabolites, i.e., monomethylarsenic (MMA) and dimethylarsenic (DMA)) in tissue groups.
openaire   +2 more sources

Physiological Parameter Values for Physiologically Based Pharmacokinetic Models

Toxicology and Industrial Health, 1997
R P, Brown   +4 more
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Physiologically Based Pharmacokinetic Models

2007
Thierry Lav   +5 more
openaire   +1 more source

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