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Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry

Three-dimensional (3D) cell cultures, including organ-on-a-chip (OOC) devices, offer the possibility to mimic human physiology conditions better than 2D models. The organ-on-a-chip devices have a wide range of applications, including mechanical studies, functional validation, and toxicology investig...

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Autores principales: Hadavi, Darya, Tosheva, Ilona, Siegel, Tiffany Porta, Cuypers, Eva, Honing, Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239923/
https://www.ncbi.nlm.nih.gov/pubmed/37284240
http://dx.doi.org/10.3389/fbioe.2023.1197760
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author Hadavi, Darya
Tosheva, Ilona
Siegel, Tiffany Porta
Cuypers, Eva
Honing, Maarten
author_facet Hadavi, Darya
Tosheva, Ilona
Siegel, Tiffany Porta
Cuypers, Eva
Honing, Maarten
author_sort Hadavi, Darya
collection PubMed
description Three-dimensional (3D) cell cultures, including organ-on-a-chip (OOC) devices, offer the possibility to mimic human physiology conditions better than 2D models. The organ-on-a-chip devices have a wide range of applications, including mechanical studies, functional validation, and toxicology investigations. Despite many advances in this field, the major challenge with the use of organ-on-a-chips relies on the lack of online analysis methods preventing the real-time observation of cultured cells. Mass spectrometry is a promising analytical technique for real-time analysis of cell excretes from organ-on-a-chip models. This is due to its high sensitivity, selectivity, and ability to tentatively identify a large variety of unknown compounds, ranging from metabolites, lipids, and peptides to proteins. However, the hyphenation of organ-on-a-chip with MS is largely hampered by the nature of the media used, and the presence of nonvolatile buffers. This in turn stalls the straightforward and online connection of organ-on-a-chip outlet to MS. To overcome this challenge, multiple advances have been made to pre-treat samples right after organ-on-a-chip and just before MS. In this review, we summarised these technological advances and exhaustively evaluated their benefits and shortcomings for successful hyphenation of organ-on-a-chip with MS.
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spelling pubmed-102399232023-06-06 Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry Hadavi, Darya Tosheva, Ilona Siegel, Tiffany Porta Cuypers, Eva Honing, Maarten Front Bioeng Biotechnol Bioengineering and Biotechnology Three-dimensional (3D) cell cultures, including organ-on-a-chip (OOC) devices, offer the possibility to mimic human physiology conditions better than 2D models. The organ-on-a-chip devices have a wide range of applications, including mechanical studies, functional validation, and toxicology investigations. Despite many advances in this field, the major challenge with the use of organ-on-a-chips relies on the lack of online analysis methods preventing the real-time observation of cultured cells. Mass spectrometry is a promising analytical technique for real-time analysis of cell excretes from organ-on-a-chip models. This is due to its high sensitivity, selectivity, and ability to tentatively identify a large variety of unknown compounds, ranging from metabolites, lipids, and peptides to proteins. However, the hyphenation of organ-on-a-chip with MS is largely hampered by the nature of the media used, and the presence of nonvolatile buffers. This in turn stalls the straightforward and online connection of organ-on-a-chip outlet to MS. To overcome this challenge, multiple advances have been made to pre-treat samples right after organ-on-a-chip and just before MS. In this review, we summarised these technological advances and exhaustively evaluated their benefits and shortcomings for successful hyphenation of organ-on-a-chip with MS. Frontiers Media S.A. 2023-05-22 /pmc/articles/PMC10239923/ /pubmed/37284240 http://dx.doi.org/10.3389/fbioe.2023.1197760 Text en Copyright © 2023 Hadavi, Tosheva, Siegel, Cuypers and Honing. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Hadavi, Darya
Tosheva, Ilona
Siegel, Tiffany Porta
Cuypers, Eva
Honing, Maarten
Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title_full Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title_fullStr Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title_full_unstemmed Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title_short Technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
title_sort technological advances for analyzing the content of organ-on-a-chip by mass spectrometry
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239923/
https://www.ncbi.nlm.nih.gov/pubmed/37284240
http://dx.doi.org/10.3389/fbioe.2023.1197760
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