Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
Abstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST)....
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doaj-cd856205f3d740beaa251331be29a2942020-11-24T21:27:38ZengWileyAdvanced Science2198-38442019-07-01613n/an/a10.1002/advs.201900294Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In VitroJulia Alicia Boos0Patrick Mark Misun1Astrid Michlmayr2Andreas Hierlemann3Olivier Frey4Bioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandAbstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST). Primary human liver microtissues (hLiMTs) and embryoid bodies (EBs) are combined in the same fluidic network, so that hLiMT‐generated metabolites are directly transported to the EBs. Gravity‐driven flow through the network enables continuous intertissue communication, constant medium turnover, and, most importantly, immediate exchange of metabolites. As a proof of concept, the prodrug cyclophosphamide is investigated and a fourfold lower ID50 concentration (50% inhibition of EB differentiation) is found after biotransformation, which demonstrates the potentially adverse effects of metabolites on embryotoxicity. The metaEST platform provides a promising tool to increase the predictive power of the current EST assay by more comprehensively including and better reflecting physiological processes in in vitro tests.https://doi.org/10.1002/advs.2019002943D microtissuesbody‐on‐a‐chipdevelopmental toxicityembryonic stem cell testsmicrofluidics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Julia Alicia Boos Patrick Mark Misun Astrid Michlmayr Andreas Hierlemann Olivier Frey |
spellingShingle |
Julia Alicia Boos Patrick Mark Misun Astrid Michlmayr Andreas Hierlemann Olivier Frey Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro Advanced Science 3D microtissues body‐on‐a‐chip developmental toxicity embryonic stem cell tests microfluidics |
author_facet |
Julia Alicia Boos Patrick Mark Misun Astrid Michlmayr Andreas Hierlemann Olivier Frey |
author_sort |
Julia Alicia Boos |
title |
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro |
title_short |
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro |
title_full |
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro |
title_fullStr |
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro |
title_full_unstemmed |
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro |
title_sort |
microfluidic multitissue platform for advanced embryotoxicity testing in vitro |
publisher |
Wiley |
series |
Advanced Science |
issn |
2198-3844 |
publishDate |
2019-07-01 |
description |
Abstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST). Primary human liver microtissues (hLiMTs) and embryoid bodies (EBs) are combined in the same fluidic network, so that hLiMT‐generated metabolites are directly transported to the EBs. Gravity‐driven flow through the network enables continuous intertissue communication, constant medium turnover, and, most importantly, immediate exchange of metabolites. As a proof of concept, the prodrug cyclophosphamide is investigated and a fourfold lower ID50 concentration (50% inhibition of EB differentiation) is found after biotransformation, which demonstrates the potentially adverse effects of metabolites on embryotoxicity. The metaEST platform provides a promising tool to increase the predictive power of the current EST assay by more comprehensively including and better reflecting physiological processes in in vitro tests. |
topic |
3D microtissues body‐on‐a‐chip developmental toxicity embryonic stem cell tests microfluidics |
url |
https://doi.org/10.1002/advs.201900294 |
work_keys_str_mv |
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