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New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo

It is extremely challenging to perform chemical analyses of the brain, particularly in humans, due to the restricted access to this organ. Imaging techniques are the primary approach used in clinical practice, but they only provide limited information about brain chemistry. Solid-phase microextracti...

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Autores principales: Bogusiewicz, Joanna, Burlikowska, Katarzyna, Łuczykowski, Kamil, Jaroch, Karol, Birski, Marcin, Furtak, Jacek, Harat, Marek, Pawliszyn, Janusz, Bojko, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484280/
https://www.ncbi.nlm.nih.gov/pubmed/34593948
http://dx.doi.org/10.1038/s41598-021-98973-y
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author Bogusiewicz, Joanna
Burlikowska, Katarzyna
Łuczykowski, Kamil
Jaroch, Karol
Birski, Marcin
Furtak, Jacek
Harat, Marek
Pawliszyn, Janusz
Bojko, Barbara
author_facet Bogusiewicz, Joanna
Burlikowska, Katarzyna
Łuczykowski, Kamil
Jaroch, Karol
Birski, Marcin
Furtak, Jacek
Harat, Marek
Pawliszyn, Janusz
Bojko, Barbara
author_sort Bogusiewicz, Joanna
collection PubMed
description It is extremely challenging to perform chemical analyses of the brain, particularly in humans, due to the restricted access to this organ. Imaging techniques are the primary approach used in clinical practice, but they only provide limited information about brain chemistry. Solid-phase microextraction (SPME) has been presented recently as a chemical biopsy tool for the study of animal brains. The current work demonstrates for the first time the use of SPME for the spatially resolved sampling of the human brain in vivo. Specially designed multi-probe sampling device was used to simultaneously extract metabolites from the white and grey matter of patients undergoing brain tumor biopsies. Samples were collected by inserting the probes along the planned trajectory of the biopsy needle prior to the procedure, which was followed by metabolomic and lipidomic analyses. The results revealed that studied brain structures were predominantly composed of lipids, while the concentration and diversity of detected metabolites was higher in white than in grey matter. Although the small number of participants in this research precluded conclusions of a biological nature, the results highlight the advantages of the proposed SPME approach, as well as disadvantages that should be addressed in future studies.
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spelling pubmed-84842802021-10-01 New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo Bogusiewicz, Joanna Burlikowska, Katarzyna Łuczykowski, Kamil Jaroch, Karol Birski, Marcin Furtak, Jacek Harat, Marek Pawliszyn, Janusz Bojko, Barbara Sci Rep Article It is extremely challenging to perform chemical analyses of the brain, particularly in humans, due to the restricted access to this organ. Imaging techniques are the primary approach used in clinical practice, but they only provide limited information about brain chemistry. Solid-phase microextraction (SPME) has been presented recently as a chemical biopsy tool for the study of animal brains. The current work demonstrates for the first time the use of SPME for the spatially resolved sampling of the human brain in vivo. Specially designed multi-probe sampling device was used to simultaneously extract metabolites from the white and grey matter of patients undergoing brain tumor biopsies. Samples were collected by inserting the probes along the planned trajectory of the biopsy needle prior to the procedure, which was followed by metabolomic and lipidomic analyses. The results revealed that studied brain structures were predominantly composed of lipids, while the concentration and diversity of detected metabolites was higher in white than in grey matter. Although the small number of participants in this research precluded conclusions of a biological nature, the results highlight the advantages of the proposed SPME approach, as well as disadvantages that should be addressed in future studies. Nature Publishing Group UK 2021-09-30 /pmc/articles/PMC8484280/ /pubmed/34593948 http://dx.doi.org/10.1038/s41598-021-98973-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bogusiewicz, Joanna
Burlikowska, Katarzyna
Łuczykowski, Kamil
Jaroch, Karol
Birski, Marcin
Furtak, Jacek
Harat, Marek
Pawliszyn, Janusz
Bojko, Barbara
New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title_full New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title_fullStr New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title_full_unstemmed New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title_short New chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
title_sort new chemical biopsy tool for spatially resolved profiling of human brain tissue in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484280/
https://www.ncbi.nlm.nih.gov/pubmed/34593948
http://dx.doi.org/10.1038/s41598-021-98973-y
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