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Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?

The primary aim of in vitro testing of chemicals delivered via the percutaneous route is to predict the absorption that would ensue if exposure occurred in live animals. While there is mounting evidence that in vitro diffusion studies in mammalian skin can provide valid information regarding likely...

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Autores principales: Llewelyn, Victoria K., Berger, Lee, Glass, Beverley D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390353/
https://www.ncbi.nlm.nih.gov/pubmed/32726322
http://dx.doi.org/10.1371/journal.pone.0235737
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author Llewelyn, Victoria K.
Berger, Lee
Glass, Beverley D.
author_facet Llewelyn, Victoria K.
Berger, Lee
Glass, Beverley D.
author_sort Llewelyn, Victoria K.
collection PubMed
description The primary aim of in vitro testing of chemicals delivered via the percutaneous route is to predict the absorption that would ensue if exposure occurred in live animals. While there is mounting evidence that in vitro diffusion studies in mammalian skin can provide valid information regarding likely in vivo absorption, little is known whether such a correlation exists between in vitro diffusion testing and in vivo blood levels in amphibians. The current study used previously-reported in vitro absorption data for caffeine, benzoic acid, and ibuprofen across isolated skin from the cane toad (Rhinella marina) to produce a series of linear mixed-effect models of the absorption parameters flux and permeability coefficient (K(p)). Models investigated the relative impacts of animal weight, physicochemical characteristics of the applied chemical (logP or molecular weight), and site of application. The top models were then used to predict the flux, K(p) and serum concentrations of the same three model chemicals. Finally, the absorption of these chemicals was determined in live cane toads, and results compared to the model predictions. LogP and site of application were included in all top models. In vivo absorption rates were lower than predicted for all chemicals, however, the models provided reasonable predictions of serum concentration, with factors of difference (FOD) ranging from 2.5–10.5. Ibuprofen, the chemical with the highest relative lipophilicity, had the poorest predictive performance, consistently having the highest FOD for all predictions. This report presents the first models of percutaneous absorption in an amphibian. These models provide a basic method to establish the approximate in vivo absorption of hydrophilic and moderately-lipophilic chemicals through frog skin, and could therefore be used to predict absorption when formulating such chemicals for treatment of disease in frogs, or for risk-assessments regarding chemical pollutants in frog habitats.
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spelling pubmed-73903532020-08-05 Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption? Llewelyn, Victoria K. Berger, Lee Glass, Beverley D. PLoS One Research Article The primary aim of in vitro testing of chemicals delivered via the percutaneous route is to predict the absorption that would ensue if exposure occurred in live animals. While there is mounting evidence that in vitro diffusion studies in mammalian skin can provide valid information regarding likely in vivo absorption, little is known whether such a correlation exists between in vitro diffusion testing and in vivo blood levels in amphibians. The current study used previously-reported in vitro absorption data for caffeine, benzoic acid, and ibuprofen across isolated skin from the cane toad (Rhinella marina) to produce a series of linear mixed-effect models of the absorption parameters flux and permeability coefficient (K(p)). Models investigated the relative impacts of animal weight, physicochemical characteristics of the applied chemical (logP or molecular weight), and site of application. The top models were then used to predict the flux, K(p) and serum concentrations of the same three model chemicals. Finally, the absorption of these chemicals was determined in live cane toads, and results compared to the model predictions. LogP and site of application were included in all top models. In vivo absorption rates were lower than predicted for all chemicals, however, the models provided reasonable predictions of serum concentration, with factors of difference (FOD) ranging from 2.5–10.5. Ibuprofen, the chemical with the highest relative lipophilicity, had the poorest predictive performance, consistently having the highest FOD for all predictions. This report presents the first models of percutaneous absorption in an amphibian. These models provide a basic method to establish the approximate in vivo absorption of hydrophilic and moderately-lipophilic chemicals through frog skin, and could therefore be used to predict absorption when formulating such chemicals for treatment of disease in frogs, or for risk-assessments regarding chemical pollutants in frog habitats. Public Library of Science 2020-07-29 /pmc/articles/PMC7390353/ /pubmed/32726322 http://dx.doi.org/10.1371/journal.pone.0235737 Text en © 2020 Llewelyn et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Llewelyn, Victoria K.
Berger, Lee
Glass, Beverley D.
Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title_full Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title_fullStr Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title_full_unstemmed Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title_short Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
title_sort can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390353/
https://www.ncbi.nlm.nih.gov/pubmed/32726322
http://dx.doi.org/10.1371/journal.pone.0235737
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