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Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans
A key challenge of central nervous system tumor surgery is to discriminate between brain regions infiltrated by tumor cells and surrounding healthy tissue. Although monitoring of autofluorescence could potentially be an efficient way to provide reliable information for these regions, we found little...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656602/ https://www.ncbi.nlm.nih.gov/pubmed/29070870 http://dx.doi.org/10.1038/s41598-017-14381-1 |
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author | Poulon, F. Mehidine, H. Juchaux, M. Varlet, P. Devaux, B. Pallud, J. Abi Haidar, D. |
author_facet | Poulon, F. Mehidine, H. Juchaux, M. Varlet, P. Devaux, B. Pallud, J. Abi Haidar, D. |
author_sort | Poulon, F. |
collection | PubMed |
description | A key challenge of central nervous system tumor surgery is to discriminate between brain regions infiltrated by tumor cells and surrounding healthy tissue. Although monitoring of autofluorescence could potentially be an efficient way to provide reliable information for these regions, we found little information on this subject, and thus we conducted studies of brain tissue optical properties. This particular study focuses on the different optical quantitative responses of human central nervous system tumors and their corresponding controls. Measurements were performed on different fixed human tumoral and healthy brain samples. Four groups of central nervous system tumors (glioblastoma, diffuse glioma, meningioma and metastasis) were discriminated from healthy brain and meninx control tissues. A threshold value was found for the scattering and absorption coefficient between tumoral and healthy groups. Emission Spectra of healthy tissue had a significant higher intensity than tumoral groups. The redox and optical index ratio were thenn calculated and these also showed significant discrimination. Two fluorescent molecules, NADH and porphyrins, showed distinct lifetim values among the different groups of samples. This study defines several optical indexes that can act as combinated indicators to discriminate healthy from tumoral tissues. |
format | Online Article Text |
id | pubmed-5656602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56566022017-10-31 Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans Poulon, F. Mehidine, H. Juchaux, M. Varlet, P. Devaux, B. Pallud, J. Abi Haidar, D. Sci Rep Article A key challenge of central nervous system tumor surgery is to discriminate between brain regions infiltrated by tumor cells and surrounding healthy tissue. Although monitoring of autofluorescence could potentially be an efficient way to provide reliable information for these regions, we found little information on this subject, and thus we conducted studies of brain tissue optical properties. This particular study focuses on the different optical quantitative responses of human central nervous system tumors and their corresponding controls. Measurements were performed on different fixed human tumoral and healthy brain samples. Four groups of central nervous system tumors (glioblastoma, diffuse glioma, meningioma and metastasis) were discriminated from healthy brain and meninx control tissues. A threshold value was found for the scattering and absorption coefficient between tumoral and healthy groups. Emission Spectra of healthy tissue had a significant higher intensity than tumoral groups. The redox and optical index ratio were thenn calculated and these also showed significant discrimination. Two fluorescent molecules, NADH and porphyrins, showed distinct lifetim values among the different groups of samples. This study defines several optical indexes that can act as combinated indicators to discriminate healthy from tumoral tissues. Nature Publishing Group UK 2017-10-25 /pmc/articles/PMC5656602/ /pubmed/29070870 http://dx.doi.org/10.1038/s41598-017-14381-1 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Poulon, F. Mehidine, H. Juchaux, M. Varlet, P. Devaux, B. Pallud, J. Abi Haidar, D. Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title | Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title_full | Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title_fullStr | Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title_full_unstemmed | Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title_short | Optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
title_sort | optical properties, spectral, and lifetime measurements of central nervous system tumors in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656602/ https://www.ncbi.nlm.nih.gov/pubmed/29070870 http://dx.doi.org/10.1038/s41598-017-14381-1 |
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