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Matching target dose to target organ

In vitro assays have become a mainstay of modern approaches to toxicology with the promise of replacing or reducing the number of in vivo tests required to establish benchmark doses, as well as increasing mechanistic understanding. However, matching target dose to target organ is an often overlooked...

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Autores principales: Bannon, Desmond I., Williams, Marc A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270582/
https://www.ncbi.nlm.nih.gov/pubmed/28163899
http://dx.doi.org/10.12688/f1000research.10055.2
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author Bannon, Desmond I.
Williams, Marc A.
author_facet Bannon, Desmond I.
Williams, Marc A.
author_sort Bannon, Desmond I.
collection PubMed
description In vitro assays have become a mainstay of modern approaches to toxicology with the promise of replacing or reducing the number of in vivo tests required to establish benchmark doses, as well as increasing mechanistic understanding. However, matching target dose to target organ is an often overlooked aspect of in vitro assays, and the calibration of in vitro exposure against in vivo benchmark doses is often ignored, inadvertently or otherwise.  An example of this was recently published in Environmental Health Perspectives by Wagner et al (2016), where neural stems cells were used to model the molecular toxicity of lead.  On closer examination of the in vitro work, the doses used in media reflected in vivo lead doses that would be at the highest end of lead toxicity, perhaps even lethal.  Here we discuss the doses used and suggest more realistic doses for future work with stem cells or other neuronal cell lines.
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spelling pubmed-52705822017-02-03 Matching target dose to target organ Bannon, Desmond I. Williams, Marc A. F1000Res Correspondence In vitro assays have become a mainstay of modern approaches to toxicology with the promise of replacing or reducing the number of in vivo tests required to establish benchmark doses, as well as increasing mechanistic understanding. However, matching target dose to target organ is an often overlooked aspect of in vitro assays, and the calibration of in vitro exposure against in vivo benchmark doses is often ignored, inadvertently or otherwise.  An example of this was recently published in Environmental Health Perspectives by Wagner et al (2016), where neural stems cells were used to model the molecular toxicity of lead.  On closer examination of the in vitro work, the doses used in media reflected in vivo lead doses that would be at the highest end of lead toxicity, perhaps even lethal.  Here we discuss the doses used and suggest more realistic doses for future work with stem cells or other neuronal cell lines. F1000Research 2017-03-30 /pmc/articles/PMC5270582/ /pubmed/28163899 http://dx.doi.org/10.12688/f1000research.10055.2 Text en Copyright: © 2017 Bannon DI and Williams MA http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Correspondence
Bannon, Desmond I.
Williams, Marc A.
Matching target dose to target organ
title Matching target dose to target organ
title_full Matching target dose to target organ
title_fullStr Matching target dose to target organ
title_full_unstemmed Matching target dose to target organ
title_short Matching target dose to target organ
title_sort matching target dose to target organ
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270582/
https://www.ncbi.nlm.nih.gov/pubmed/28163899
http://dx.doi.org/10.12688/f1000research.10055.2
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