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NMR microsystem for label-free characterization of 3D nanoliter microtissues
Performing chemical analysis at the nanoliter (nL) scale is of paramount importance for medicine, drug development, toxicology, and research. Despite the numerous methodologies available, a tool for obtaining chemical information non-invasively is still missing at this scale. Observer effects, sampl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758329/ https://www.ncbi.nlm.nih.gov/pubmed/33110145 http://dx.doi.org/10.1038/s41598-020-75480-0 |
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author | Grisi, Marco Conley, Gaurasundar M. Rodriguez, Kyle J. Riva, Erika Egli, Lukas Moritz, Wolfgang Lichtenberg, Jan Brugger, Jürgen Boero, Giovanni |
author_facet | Grisi, Marco Conley, Gaurasundar M. Rodriguez, Kyle J. Riva, Erika Egli, Lukas Moritz, Wolfgang Lichtenberg, Jan Brugger, Jürgen Boero, Giovanni |
author_sort | Grisi, Marco |
collection | PubMed |
description | Performing chemical analysis at the nanoliter (nL) scale is of paramount importance for medicine, drug development, toxicology, and research. Despite the numerous methodologies available, a tool for obtaining chemical information non-invasively is still missing at this scale. Observer effects, sample destruction and complex preparatory procedures remain a necessary compromise. Among non-invasive spectroscopic techniques, one able to provide holistic and highly resolved chemical information in-vivo is nuclear magnetic resonance (NMR). For its renowned informative power and ability to foster discoveries and life-saving applications, efficient NMR at microscopic scales is highly sought after, but so far technical limitations could not match the stringent necessities of microbiology, such as biocompatible handling, ease of use, and high throughput. Here we introduce a novel microsystem, which combines CMOS technology with 3D microfabrication, enabling nL NMR as a platform tool for non-invasive spectroscopy of organoids, 3D cell cultures, and early stage embryos. In this study we show its application to microlivers models simulating non-alcoholic fatty liver disease, demonstrating detection of lipid metabolism dynamics in a time frame of 14 days based on 117 measurements of single 3D human liver microtissues. |
format | Online Article Text |
id | pubmed-7758329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77583292020-12-30 NMR microsystem for label-free characterization of 3D nanoliter microtissues Grisi, Marco Conley, Gaurasundar M. Rodriguez, Kyle J. Riva, Erika Egli, Lukas Moritz, Wolfgang Lichtenberg, Jan Brugger, Jürgen Boero, Giovanni Sci Rep Article Performing chemical analysis at the nanoliter (nL) scale is of paramount importance for medicine, drug development, toxicology, and research. Despite the numerous methodologies available, a tool for obtaining chemical information non-invasively is still missing at this scale. Observer effects, sample destruction and complex preparatory procedures remain a necessary compromise. Among non-invasive spectroscopic techniques, one able to provide holistic and highly resolved chemical information in-vivo is nuclear magnetic resonance (NMR). For its renowned informative power and ability to foster discoveries and life-saving applications, efficient NMR at microscopic scales is highly sought after, but so far technical limitations could not match the stringent necessities of microbiology, such as biocompatible handling, ease of use, and high throughput. Here we introduce a novel microsystem, which combines CMOS technology with 3D microfabrication, enabling nL NMR as a platform tool for non-invasive spectroscopy of organoids, 3D cell cultures, and early stage embryos. In this study we show its application to microlivers models simulating non-alcoholic fatty liver disease, demonstrating detection of lipid metabolism dynamics in a time frame of 14 days based on 117 measurements of single 3D human liver microtissues. Nature Publishing Group UK 2020-12-22 /pmc/articles/PMC7758329/ /pubmed/33110145 http://dx.doi.org/10.1038/s41598-020-75480-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Grisi, Marco Conley, Gaurasundar M. Rodriguez, Kyle J. Riva, Erika Egli, Lukas Moritz, Wolfgang Lichtenberg, Jan Brugger, Jürgen Boero, Giovanni NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title | NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title_full | NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title_fullStr | NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title_full_unstemmed | NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title_short | NMR microsystem for label-free characterization of 3D nanoliter microtissues |
title_sort | nmr microsystem for label-free characterization of 3d nanoliter microtissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758329/ https://www.ncbi.nlm.nih.gov/pubmed/33110145 http://dx.doi.org/10.1038/s41598-020-75480-0 |
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