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Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid

Neurochemical dysregulation underlies many pathologies and can be monitored by measuring the composition of brain interstitial fluid (ISF). Existing in vivo tools for sampling ISF do not enable measuring large rare molecules, such as proteins and neuropeptides, and thus cannot generate a complete pi...

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Autores principales: Raman, Ritu, Rousseau, Erin B., Wade, Michael, Tong, Allison, Cotler, Max J., Kuang, Jenevieve, Lugo, Alejandro Aponte, Zhang, Elizabeth, Graybiel, Ann M., White, Forest M., Langer, Robert, Cima, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518871/
https://www.ncbi.nlm.nih.gov/pubmed/32978160
http://dx.doi.org/10.1126/sciadv.abb0657
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author Raman, Ritu
Rousseau, Erin B.
Wade, Michael
Tong, Allison
Cotler, Max J.
Kuang, Jenevieve
Lugo, Alejandro Aponte
Zhang, Elizabeth
Graybiel, Ann M.
White, Forest M.
Langer, Robert
Cima, Michael J.
author_facet Raman, Ritu
Rousseau, Erin B.
Wade, Michael
Tong, Allison
Cotler, Max J.
Kuang, Jenevieve
Lugo, Alejandro Aponte
Zhang, Elizabeth
Graybiel, Ann M.
White, Forest M.
Langer, Robert
Cima, Michael J.
author_sort Raman, Ritu
collection PubMed
description Neurochemical dysregulation underlies many pathologies and can be monitored by measuring the composition of brain interstitial fluid (ISF). Existing in vivo tools for sampling ISF do not enable measuring large rare molecules, such as proteins and neuropeptides, and thus cannot generate a complete picture of the neurochemical connectome. Our micro-invasive platform, composed of a nanofluidic pump coupled to a membrane-free probe, enables sampling multiple neural biomarkers in parallel. This platform outperforms the state of the art in low-flow pumps by offering low volume control (single stroke volumes, <3 nl) and bidirectional fluid flow (<100 nl/min) with negligible dead volume (<30 nl) and has been validated in vitro, ex vivo, and in vivo in rodents. ISF samples (<1.5 μL) can be processed via liquid chromatography–tandem mass spectrometry. These label-free liquid biopsies of the brain could yield a deeper understanding of the onset, mechanism, and progression of diverse neural pathologies.
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spelling pubmed-75188712020-10-02 Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid Raman, Ritu Rousseau, Erin B. Wade, Michael Tong, Allison Cotler, Max J. Kuang, Jenevieve Lugo, Alejandro Aponte Zhang, Elizabeth Graybiel, Ann M. White, Forest M. Langer, Robert Cima, Michael J. Sci Adv Research Articles Neurochemical dysregulation underlies many pathologies and can be monitored by measuring the composition of brain interstitial fluid (ISF). Existing in vivo tools for sampling ISF do not enable measuring large rare molecules, such as proteins and neuropeptides, and thus cannot generate a complete picture of the neurochemical connectome. Our micro-invasive platform, composed of a nanofluidic pump coupled to a membrane-free probe, enables sampling multiple neural biomarkers in parallel. This platform outperforms the state of the art in low-flow pumps by offering low volume control (single stroke volumes, <3 nl) and bidirectional fluid flow (<100 nl/min) with negligible dead volume (<30 nl) and has been validated in vitro, ex vivo, and in vivo in rodents. ISF samples (<1.5 μL) can be processed via liquid chromatography–tandem mass spectrometry. These label-free liquid biopsies of the brain could yield a deeper understanding of the onset, mechanism, and progression of diverse neural pathologies. American Association for the Advancement of Science 2020-09-25 /pmc/articles/PMC7518871/ /pubmed/32978160 http://dx.doi.org/10.1126/sciadv.abb0657 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Raman, Ritu
Rousseau, Erin B.
Wade, Michael
Tong, Allison
Cotler, Max J.
Kuang, Jenevieve
Lugo, Alejandro Aponte
Zhang, Elizabeth
Graybiel, Ann M.
White, Forest M.
Langer, Robert
Cima, Michael J.
Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title_full Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title_fullStr Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title_full_unstemmed Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title_short Platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
title_sort platform for micro-invasive membrane-free biochemical sampling of brain interstitial fluid
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518871/
https://www.ncbi.nlm.nih.gov/pubmed/32978160
http://dx.doi.org/10.1126/sciadv.abb0657
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