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Integration concepts for multi-organ chips: how to maintain flexibility?!
Multi-organ platforms have an enormous potential to lead to a paradigm shift in a multitude of research domains including drug development, toxicological screening, personalized medicine as well as disease modeling. Integrating multiple organ–tissues into one microfluidic circulation merges the adva...
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/PMC5481865/ https://www.ncbi.nlm.nih.gov/pubmed/28670472 http://dx.doi.org/10.4155/fsoa-2016-0092 |
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author | Rogal, Julia Probst, Christopher Loskill, Peter |
author_facet | Rogal, Julia Probst, Christopher Loskill, Peter |
author_sort | Rogal, Julia |
collection | PubMed |
description | Multi-organ platforms have an enormous potential to lead to a paradigm shift in a multitude of research domains including drug development, toxicological screening, personalized medicine as well as disease modeling. Integrating multiple organ–tissues into one microfluidic circulation merges the advantages of cell lines (human genetic background) and animal models (complex physiology) and enables the creation of more in vivo-like in vitro models. In recent years, a variety of design concepts for multi-organ platforms have been introduced, categorizable into static, semistatic and flexible systems. The most promising approach seems to be flexible interconnection of single-organ platforms to application-specific multi-organ systems. This perspective elucidates the concept of ‘mix-and-match’ toolboxes and discusses the numerous advantages compared with static/semistatic platforms as well as remaining challenges. |
format | Online Article Text |
id | pubmed-5481865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54818652017-06-30 Integration concepts for multi-organ chips: how to maintain flexibility?! Rogal, Julia Probst, Christopher Loskill, Peter Future Sci OA Perspective Multi-organ platforms have an enormous potential to lead to a paradigm shift in a multitude of research domains including drug development, toxicological screening, personalized medicine as well as disease modeling. Integrating multiple organ–tissues into one microfluidic circulation merges the advantages of cell lines (human genetic background) and animal models (complex physiology) and enables the creation of more in vivo-like in vitro models. In recent years, a variety of design concepts for multi-organ platforms have been introduced, categorizable into static, semistatic and flexible systems. The most promising approach seems to be flexible interconnection of single-organ platforms to application-specific multi-organ systems. This perspective elucidates the concept of ‘mix-and-match’ toolboxes and discusses the numerous advantages compared with static/semistatic platforms as well as remaining challenges. Future Science Ltd 2017-03-13 /pmc/articles/PMC5481865/ /pubmed/28670472 http://dx.doi.org/10.4155/fsoa-2016-0092 Text en © Peter Loskill This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Perspective Rogal, Julia Probst, Christopher Loskill, Peter Integration concepts for multi-organ chips: how to maintain flexibility?! |
title | Integration concepts for multi-organ chips: how to maintain flexibility?! |
title_full | Integration concepts for multi-organ chips: how to maintain flexibility?! |
title_fullStr | Integration concepts for multi-organ chips: how to maintain flexibility?! |
title_full_unstemmed | Integration concepts for multi-organ chips: how to maintain flexibility?! |
title_short | Integration concepts for multi-organ chips: how to maintain flexibility?! |
title_sort | integration concepts for multi-organ chips: how to maintain flexibility?! |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481865/ https://www.ncbi.nlm.nih.gov/pubmed/28670472 http://dx.doi.org/10.4155/fsoa-2016-0092 |
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