4.6 Article

Predicting nonlinear relationships between external and internal concentrations with physiologically based pharmacokinetic modeling

期刊

TOXICOLOGY AND APPLIED PHARMACOLOGY
卷 440, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.taap.2022.115922

关键词

Physiologically Based Pharmacokinetic (PBPK); Animal Study Design; Internal Concentrations; Nonlinear Pharmacokinetics; Saturation of Absorption; Saturation of Clearance

资金

  1. Health and Environmental Sciences Institute PBPK Committee

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The internal concentration of environmental chemicals has a closer relationship with toxicological response than the external concentration. The methods of absorption, distribution, metabolism, and excretion determine the quantitative relationship between the two concentrations, and these processes can be saturated at high concentrations, resulting in non-linear changes. By using PBPK models, researchers can explore the influence of saturation on the relationship between internal and external concentrations, and also investigate the impact of different factors on this relationship.
Although external concentrations are more readily quantified and often used as the metric for regulating and mitigating exposures to environmental chemicals, the toxicological response to an environmental chemical is more directly related to its internal concentrations than the external concentration. The processes of absorption, distribution, metabolism, and excretion (ADME) determine the quantitative relationship between the external and internal concentrations, and these processes are often susceptible to saturation at high concentrations, which can lead to nonlinear changes in internal concentrations that deviate from proportionality. Using generic physiologically-based pharmacokinetic (PBPK) models, we explored how saturable absorption or clearance influence the shape of the internal to external concentration (IEC) relationship. We used the models for hypothetical chemicals to show how differences in kinetic parameters can impact the shape of an IEC relationship; and models for styrene and caffeine to explore how exposure route, frequency, and duration impact the IEC relationships in rat and human exposures. We also analyzed available plasma concentration data for 2,4-dichlorophenoxyacetic acid to demonstrate how a PBPK modeling approach can be an alternative to common statistical methods for analyzing dose proportionality. A PBPK modeling approach can be a valuable tool used in the early stages of a chemical safety assessment program to optimize the design of longer-term animal toxicity studies or to interpret study results.

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