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Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms

The development of improved, innovative models for the detection of toxicity of drugs, chemicals, or chemicals in cosmetics is crucial to efficiently bring new products safely to market in a cost-effective and timely manner. In addition, improvement in models to detect toxicity may reduce the incide...

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Autores principales: Pridgeon, Chris S., Schlott, Constanze, Wong, Min Wei, Heringa, Minne B., Heckel, Tobias, Leedale, Joe, Launay, Laurence, Gryshkova, Vitalina, Przyborski, Stefan, Bearon, Rachel N., Wilkinson, Emma L., Ansari, Tahera, Greenman, John, Hendriks, Delilah F. G., Gibbs, Sue, Sidaway, James, Sison-Young, Rowena L., Walker, Paul, Cross, Mike J., Park, B. Kevin, Goldring, Chris E. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818581/
https://www.ncbi.nlm.nih.gov/pubmed/29362863
http://dx.doi.org/10.1007/s00204-018-2152-9
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author Pridgeon, Chris S.
Schlott, Constanze
Wong, Min Wei
Heringa, Minne B.
Heckel, Tobias
Leedale, Joe
Launay, Laurence
Gryshkova, Vitalina
Przyborski, Stefan
Bearon, Rachel N.
Wilkinson, Emma L.
Ansari, Tahera
Greenman, John
Hendriks, Delilah F. G.
Gibbs, Sue
Sidaway, James
Sison-Young, Rowena L.
Walker, Paul
Cross, Mike J.
Park, B. Kevin
Goldring, Chris E. P.
author_facet Pridgeon, Chris S.
Schlott, Constanze
Wong, Min Wei
Heringa, Minne B.
Heckel, Tobias
Leedale, Joe
Launay, Laurence
Gryshkova, Vitalina
Przyborski, Stefan
Bearon, Rachel N.
Wilkinson, Emma L.
Ansari, Tahera
Greenman, John
Hendriks, Delilah F. G.
Gibbs, Sue
Sidaway, James
Sison-Young, Rowena L.
Walker, Paul
Cross, Mike J.
Park, B. Kevin
Goldring, Chris E. P.
author_sort Pridgeon, Chris S.
collection PubMed
description The development of improved, innovative models for the detection of toxicity of drugs, chemicals, or chemicals in cosmetics is crucial to efficiently bring new products safely to market in a cost-effective and timely manner. In addition, improvement in models to detect toxicity may reduce the incidence of unexpected post-marketing toxicity and reduce or eliminate the need for animal testing. The safety of novel products of the pharmaceutical, chemical, or cosmetics industry must be assured; therefore, toxicological properties need to be assessed. Accepted methods for gathering the information required by law for approval of substances are often animal methods. To reduce, refine, and replace animal testing, innovative organotypic in vitro models have emerged. Such models appear at different levels of complexity ranging from simpler, self-organized three-dimensional (3D) cell cultures up to more advanced scaffold-based co-cultures consisting of multiple cell types. This review provides an overview of recent developments in the field of toxicity testing with in vitro models for three major organ types: heart, skin, and liver. This review also examines regulatory aspects of such models in Europe and the UK, and summarizes best practices to facilitate the acceptance and appropriate use of advanced in vitro models.
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spelling pubmed-58185812018-02-27 Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms Pridgeon, Chris S. Schlott, Constanze Wong, Min Wei Heringa, Minne B. Heckel, Tobias Leedale, Joe Launay, Laurence Gryshkova, Vitalina Przyborski, Stefan Bearon, Rachel N. Wilkinson, Emma L. Ansari, Tahera Greenman, John Hendriks, Delilah F. G. Gibbs, Sue Sidaway, James Sison-Young, Rowena L. Walker, Paul Cross, Mike J. Park, B. Kevin Goldring, Chris E. P. Arch Toxicol Review Article The development of improved, innovative models for the detection of toxicity of drugs, chemicals, or chemicals in cosmetics is crucial to efficiently bring new products safely to market in a cost-effective and timely manner. In addition, improvement in models to detect toxicity may reduce the incidence of unexpected post-marketing toxicity and reduce or eliminate the need for animal testing. The safety of novel products of the pharmaceutical, chemical, or cosmetics industry must be assured; therefore, toxicological properties need to be assessed. Accepted methods for gathering the information required by law for approval of substances are often animal methods. To reduce, refine, and replace animal testing, innovative organotypic in vitro models have emerged. Such models appear at different levels of complexity ranging from simpler, self-organized three-dimensional (3D) cell cultures up to more advanced scaffold-based co-cultures consisting of multiple cell types. This review provides an overview of recent developments in the field of toxicity testing with in vitro models for three major organ types: heart, skin, and liver. This review also examines regulatory aspects of such models in Europe and the UK, and summarizes best practices to facilitate the acceptance and appropriate use of advanced in vitro models. Springer Berlin Heidelberg 2018-01-23 2018 /pmc/articles/PMC5818581/ /pubmed/29362863 http://dx.doi.org/10.1007/s00204-018-2152-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review Article
Pridgeon, Chris S.
Schlott, Constanze
Wong, Min Wei
Heringa, Minne B.
Heckel, Tobias
Leedale, Joe
Launay, Laurence
Gryshkova, Vitalina
Przyborski, Stefan
Bearon, Rachel N.
Wilkinson, Emma L.
Ansari, Tahera
Greenman, John
Hendriks, Delilah F. G.
Gibbs, Sue
Sidaway, James
Sison-Young, Rowena L.
Walker, Paul
Cross, Mike J.
Park, B. Kevin
Goldring, Chris E. P.
Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title_full Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title_fullStr Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title_full_unstemmed Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title_short Innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
title_sort innovative organotypic in vitro models for safety assessment: aligning with regulatory requirements and understanding models of the heart, skin, and liver as paradigms
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818581/
https://www.ncbi.nlm.nih.gov/pubmed/29362863
http://dx.doi.org/10.1007/s00204-018-2152-9
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