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3D organ models—Revolution in pharmacological research?
3D organ models have gained increasing attention as novel preclinical test systems and alternatives to animal testing. Over the years, many excellent in vitro tissue models have been developed. In parallel, microfluidic organ-on-a-chip tissue cultures have gained increasing interest for their abilit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129286/ https://www.ncbi.nlm.nih.gov/pubmed/30395949 http://dx.doi.org/10.1016/j.phrs.2018.11.002 |
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author | Weinhart, Marie Hocke, Andreas Hippenstiel, Stefan Kurreck, Jens Hedtrich, Sarah |
author_facet | Weinhart, Marie Hocke, Andreas Hippenstiel, Stefan Kurreck, Jens Hedtrich, Sarah |
author_sort | Weinhart, Marie |
collection | PubMed |
description | 3D organ models have gained increasing attention as novel preclinical test systems and alternatives to animal testing. Over the years, many excellent in vitro tissue models have been developed. In parallel, microfluidic organ-on-a-chip tissue cultures have gained increasing interest for their ability to house several organ models on a single device and interlink these within a human-like environment. In contrast to these advancements, the development of human disease models is still in its infancy. Although major advances have recently been made, efforts still need to be intensified. Human disease models have proven valuable for their ability to closely mimic disease patterns in vitro, permitting the study of pathophysiological features and new treatment options. Although animal studies remain the gold standard for preclinical testing, they have major drawbacks such as high cost and ongoing controversy over their predictive value for several human conditions. Moreover, there is growing political and social pressure to develop alternatives to animal models, clearly promoting the search for valid, cost-efficient and easy-to-handle systems lacking interspecies-related differences. In this review, we discuss the current state of the art regarding 3D organ as well as the opportunities, limitations and future implications of their use. |
format | Online Article Text |
id | pubmed-7129286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71292862020-04-08 3D organ models—Revolution in pharmacological research? Weinhart, Marie Hocke, Andreas Hippenstiel, Stefan Kurreck, Jens Hedtrich, Sarah Pharmacol Res Review 3D organ models have gained increasing attention as novel preclinical test systems and alternatives to animal testing. Over the years, many excellent in vitro tissue models have been developed. In parallel, microfluidic organ-on-a-chip tissue cultures have gained increasing interest for their ability to house several organ models on a single device and interlink these within a human-like environment. In contrast to these advancements, the development of human disease models is still in its infancy. Although major advances have recently been made, efforts still need to be intensified. Human disease models have proven valuable for their ability to closely mimic disease patterns in vitro, permitting the study of pathophysiological features and new treatment options. Although animal studies remain the gold standard for preclinical testing, they have major drawbacks such as high cost and ongoing controversy over their predictive value for several human conditions. Moreover, there is growing political and social pressure to develop alternatives to animal models, clearly promoting the search for valid, cost-efficient and easy-to-handle systems lacking interspecies-related differences. In this review, we discuss the current state of the art regarding 3D organ as well as the opportunities, limitations and future implications of their use. Elsevier Ltd. 2019-01 2018-11-03 /pmc/articles/PMC7129286/ /pubmed/30395949 http://dx.doi.org/10.1016/j.phrs.2018.11.002 Text en © 2018 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Weinhart, Marie Hocke, Andreas Hippenstiel, Stefan Kurreck, Jens Hedtrich, Sarah 3D organ models—Revolution in pharmacological research? |
title | 3D organ models—Revolution in pharmacological research? |
title_full | 3D organ models—Revolution in pharmacological research? |
title_fullStr | 3D organ models—Revolution in pharmacological research? |
title_full_unstemmed | 3D organ models—Revolution in pharmacological research? |
title_short | 3D organ models—Revolution in pharmacological research? |
title_sort | 3d organ models—revolution in pharmacological research? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129286/ https://www.ncbi.nlm.nih.gov/pubmed/30395949 http://dx.doi.org/10.1016/j.phrs.2018.11.002 |
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