Prediction of Human Distribution Volumes of Compounds in Various Elimination Phases Using Physiologically Based Pharmacokinetic Modeling and Experimental Pharmacokinetics in Animals

Drug Metabolism and Disposition - United States
doi 10.1124/dmd.118.083642
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Related search

Prediction of Human CNS Pharmacokinetics Using a Physiologically-Based Pharmacokinetic Modeling Approach

European Journal of Pharmaceutical Sciences
Pharmaceutical Science
2018English

Application of Physiologically Based Pharmacokinetic Modeling to the Understanding of Bosutinib Pharmacokinetics: Prediction of Drug–Drug and Drug–Disease Interactions

Drug Metabolism and Disposition
PharmacologyPharmaceutical Science
2017English

Prediction of Renal Transporter Mediated Drug-Drug Interactions for Pemetrexed Using Physiologically Based Pharmacokinetic Modeling

Drug Metabolism and Disposition
PharmacologyPharmaceutical Science
2014English

Prediction of Olanzapine Exposure in Individual Patients Using Physiologically-Based Pharmacokinetic Modelling and Simulation

British Journal of Clinical Pharmacology
Pharmacology
2018English

Prediction of Drug–Drug Interactions Between Opioids and Overdosed Benzodiazepines Using Physiologically Based Pharmacokinetic (PBPK) Modeling and Simulation

Drugs in R and D
Pharmacology
2019English

Prediction of the Pharmacokinetics of Cefodizime and Cefotetan in Humans From Pharmacokinetic Parameters in Animals.

Journal of Pharmacobio-Dynamics
1990English

Physiologically Based Pharmacokinetic Modeling of Chloroethane Disposition in Mice, Rats, and Women

Toxicological Sciences
Toxicology
2008English

Reverse Dosimetry: Interpreting Trihalomethanes Biomonitoring Data Using Physiologically Based Pharmacokinetic Modeling

Journal of Exposure Science and Environmental Epidemiology
EpidemiologyPublic HealthEnvironmentalToxicologyPollutionOccupational Health
2006English

Prediction of Serum Concentration Time Course of Quinidine in Human Using a Physiologically Based Pharmacokinetic Model Developed From the Rat.

Journal of Pharmacobio-Dynamics
1986English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy