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The ascendance of microphysiological systems to solve the drug testing dilemma
The development of drugs is a process obstructed with manifold security and efficacy concerns. Although animal models are still widely used to meet the diligence required, they are regarded as outdated tools with limited predictability. Novel microphysiological systems intend to create systemic mode...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481853/ https://www.ncbi.nlm.nih.gov/pubmed/28670475 http://dx.doi.org/10.4155/fsoa-2017-0002 |
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author | Dehne, Eva-Maria Hasenberg, Tobias Marx, Uwe |
author_facet | Dehne, Eva-Maria Hasenberg, Tobias Marx, Uwe |
author_sort | Dehne, Eva-Maria |
collection | PubMed |
description | The development of drugs is a process obstructed with manifold security and efficacy concerns. Although animal models are still widely used to meet the diligence required, they are regarded as outdated tools with limited predictability. Novel microphysiological systems intend to create systemic models of human biology. Their ability to host 3D organoid constructs in a controlled microenvironment with mechanical and electrophysiological stimuli enables them to create and maintain homeostasis. These platforms are, thus, envisioned to be superior tools for testing and developing substances such as drugs, cosmetics and chemicals. We will present reasons why microphysiological systems are required for the emerging demands, highlight current technological and regulatory obstacles, and depict possible solutions from state-of-the-art platforms from major contributors. |
format | Online Article Text |
id | pubmed-5481853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54818532017-06-30 The ascendance of microphysiological systems to solve the drug testing dilemma Dehne, Eva-Maria Hasenberg, Tobias Marx, Uwe Future Sci OA Review The development of drugs is a process obstructed with manifold security and efficacy concerns. Although animal models are still widely used to meet the diligence required, they are regarded as outdated tools with limited predictability. Novel microphysiological systems intend to create systemic models of human biology. Their ability to host 3D organoid constructs in a controlled microenvironment with mechanical and electrophysiological stimuli enables them to create and maintain homeostasis. These platforms are, thus, envisioned to be superior tools for testing and developing substances such as drugs, cosmetics and chemicals. We will present reasons why microphysiological systems are required for the emerging demands, highlight current technological and regulatory obstacles, and depict possible solutions from state-of-the-art platforms from major contributors. Future Science Ltd 2017-03-31 /pmc/articles/PMC5481853/ /pubmed/28670475 http://dx.doi.org/10.4155/fsoa-2017-0002 Text en © Eva-Maria Dehne This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Review Dehne, Eva-Maria Hasenberg, Tobias Marx, Uwe The ascendance of microphysiological systems to solve the drug testing dilemma |
title | The ascendance of microphysiological systems to solve the drug testing dilemma |
title_full | The ascendance of microphysiological systems to solve the drug testing dilemma |
title_fullStr | The ascendance of microphysiological systems to solve the drug testing dilemma |
title_full_unstemmed | The ascendance of microphysiological systems to solve the drug testing dilemma |
title_short | The ascendance of microphysiological systems to solve the drug testing dilemma |
title_sort | ascendance of microphysiological systems to solve the drug testing dilemma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481853/ https://www.ncbi.nlm.nih.gov/pubmed/28670475 http://dx.doi.org/10.4155/fsoa-2017-0002 |
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