PBPK Modeling to Simulate the Fate of Compounds in Living Organisms
- PMID: 35188627
- DOI: 10.1007/978-1-0716-1960-5_2
PBPK Modeling to Simulate the Fate of Compounds in Living Organisms
Abstract
Pharmacokinetics study the fate of xenobiotics in a living organism. Physiologically based pharmacokinetic (PBPK) models provide realistic descriptions of xenobiotics' absorption, distribution, metabolism, and excretion processes. They model the body as a set of homogeneous compartments representing organs, and their parameters refer to anatomical, physiological, biochemical, and physicochemical entities. They offer a quantitative mechanistic framework to understand and simulate the time-course of the concentration of a substance in various organs and body fluids. These models are well suited for performing extrapolations inherent to toxicology and pharmacology (e.g., between species or doses) and for integrating data obtained from various sources (e.g., in vitro or in vivo experiments, structure-activity models). In this chapter, we describe the practical development and basic use of a PBPK model from model building to model simulations, through implementation with an easily accessible free software.
Keywords: 1,3-Butadiene; Monte Carlo simulations; Numerical integration; PBPK; R software.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
References
-
- Haggard HW (1924) The absorption, distribution, and elimination of ethyl ether. I. The amount of ether absorbed in relation to the concentration inhaled and its fate in the body. J Biol Chem 59:737–751
-
- Haggard HW (1924) The absorption, distribution, and elimination of ethyl ether. II. Analysis of the mechanism of absorption and elimination of such a gas or vapor as ethyl ether. J Biol Chem 59:753–770
-
- Haggard HW (1924) The absorption, distribution, and elimination of ethyl ether. III. The relation of the concentration of ether, or any similar volatile substance, in the central nervous system to the concentration in the arterial blood, and the buffer action of the body. J Biol Chem 59:771–781
-
- Haggard HW (1924) The absorption, distribution, and elimination of ethyl ether. IV. The anesthetic tension of ether and the physiological response to various concentrations. J Biol Chem 59:783–793
-
- Haggard HW (1924) The absorption, distribution, and elimination of ethyl ether. V. The importance of the volume of breathing during the induction and termination of ether anesthesia. J Biol Chem 59:795–802
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
