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Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine
Physiologically based pharmacokinetic (PBPK) models for chemicals in food animals are a useful tool in estimating chemical tissue residues and withdrawal intervals. Physiological parameters such as organ weights and blood flows are an important component of a PBPK model. The objective of this study...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540321/ https://www.ncbi.nlm.nih.gov/pubmed/32270548 http://dx.doi.org/10.1111/jvp.12861 |
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author | Lin, Zhoumeng Li, Miao Wang, Yu‐Shin Tell, Lisa A. Baynes, Ronald E. Davis, Jennifer L. Vickroy, Thomas W. Riviere, Jim E. |
author_facet | Lin, Zhoumeng Li, Miao Wang, Yu‐Shin Tell, Lisa A. Baynes, Ronald E. Davis, Jennifer L. Vickroy, Thomas W. Riviere, Jim E. |
author_sort | Lin, Zhoumeng |
collection | PubMed |
description | Physiologically based pharmacokinetic (PBPK) models for chemicals in food animals are a useful tool in estimating chemical tissue residues and withdrawal intervals. Physiological parameters such as organ weights and blood flows are an important component of a PBPK model. The objective of this study was to compile PBPK‐related physiological parameter data in food animals, including cattle and swine. Comprehensive literature searches were performed in PubMed, Google Scholar, ScienceDirect, and ProQuest. Relevant literature was reviewed and tables of relevant parameters such as relative organ weights (% of body weight) and relative blood flows (% of cardiac output) were compiled for different production classes of cattle and swine. The mean and standard deviation of each parameter were calculated to characterize their variability and uncertainty and to allow investigators to conduct population PBPK analysis via Monte Carlo simulations. Regression equations using weight or age were created for parameters having sufficient data. These compiled data provide a comprehensive physiological parameter database for developing PBPK models of chemicals in cattle and swine to support animal‐derived food safety assessment. This work also provides a basis to compile data in other food animal species, including goats, sheep, chickens, and turkeys. |
format | Online Article Text |
id | pubmed-7540321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75403212020-10-09 Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine Lin, Zhoumeng Li, Miao Wang, Yu‐Shin Tell, Lisa A. Baynes, Ronald E. Davis, Jennifer L. Vickroy, Thomas W. Riviere, Jim E. J Vet Pharmacol Ther Review Articles Physiologically based pharmacokinetic (PBPK) models for chemicals in food animals are a useful tool in estimating chemical tissue residues and withdrawal intervals. Physiological parameters such as organ weights and blood flows are an important component of a PBPK model. The objective of this study was to compile PBPK‐related physiological parameter data in food animals, including cattle and swine. Comprehensive literature searches were performed in PubMed, Google Scholar, ScienceDirect, and ProQuest. Relevant literature was reviewed and tables of relevant parameters such as relative organ weights (% of body weight) and relative blood flows (% of cardiac output) were compiled for different production classes of cattle and swine. The mean and standard deviation of each parameter were calculated to characterize their variability and uncertainty and to allow investigators to conduct population PBPK analysis via Monte Carlo simulations. Regression equations using weight or age were created for parameters having sufficient data. These compiled data provide a comprehensive physiological parameter database for developing PBPK models of chemicals in cattle and swine to support animal‐derived food safety assessment. This work also provides a basis to compile data in other food animal species, including goats, sheep, chickens, and turkeys. John Wiley and Sons Inc. 2020-04-08 2020-09 /pmc/articles/PMC7540321/ /pubmed/32270548 http://dx.doi.org/10.1111/jvp.12861 Text en © 2020 The Authors. Journal of Veterinary Pharmacology and Therapeutics published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Articles Lin, Zhoumeng Li, Miao Wang, Yu‐Shin Tell, Lisa A. Baynes, Ronald E. Davis, Jennifer L. Vickroy, Thomas W. Riviere, Jim E. Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title | Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title_full | Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title_fullStr | Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title_full_unstemmed | Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title_short | Physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. Part I: Cattle and swine |
title_sort | physiological parameter values for physiologically based pharmacokinetic models in food‐producing animals. part i: cattle and swine |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540321/ https://www.ncbi.nlm.nih.gov/pubmed/32270548 http://dx.doi.org/10.1111/jvp.12861 |
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