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Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions

5-aminolevulinic acid (5-ALA)-based fluorescence diagnosis is now clinically applied for accurate and ultrarapid diagnosis of malignant lesions such as lymph node metastasis during surgery. 5-ALA-based diagnosis evaluates fluorescence intensity of a fluorescent metabolite of 5-ALA, protoporphyrin IX...

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Autores principales: Minamikawa, Takeo, Matsuo, Hisataka, Kato, Yoshiyuki, Harada, Yoshinori, Otsuji, Eigo, Yanagisawa, Akio, Tanaka, Hideo, Takamatsu, Tetsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857744/
https://www.ncbi.nlm.nih.gov/pubmed/27149301
http://dx.doi.org/10.1038/srep25530
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author Minamikawa, Takeo
Matsuo, Hisataka
Kato, Yoshiyuki
Harada, Yoshinori
Otsuji, Eigo
Yanagisawa, Akio
Tanaka, Hideo
Takamatsu, Tetsuro
author_facet Minamikawa, Takeo
Matsuo, Hisataka
Kato, Yoshiyuki
Harada, Yoshinori
Otsuji, Eigo
Yanagisawa, Akio
Tanaka, Hideo
Takamatsu, Tetsuro
author_sort Minamikawa, Takeo
collection PubMed
description 5-aminolevulinic acid (5-ALA)-based fluorescence diagnosis is now clinically applied for accurate and ultrarapid diagnosis of malignant lesions such as lymph node metastasis during surgery. 5-ALA-based diagnosis evaluates fluorescence intensity of a fluorescent metabolite of 5-ALA, protoporphyrin IX (PPIX); however, the fluorescence of PPIX is often affected by autofluorescence of tissue chromophores, such as collagen and flavins. In this study, we demonstrated PPIX fluorescence estimation with autofluorescence elimination for 5-ALA-based fluorescence diagnosis of malignant lesions by simplified and optimized multispectral imaging. We computationally optimized observation wavelength regions for the estimation of PPIX fluorescence in terms of minimizing prediction error of PPIX fluorescence intensity in the presence of typical chromophores, collagen and flavins. By using the fluorescence intensities of the optimized wavelength regions, we verified quantitative detection of PPIX fluorescence by using chemical mixtures of PPIX, flavins, and collagen. Furthermore, we demonstrated detection capability by using metastatic and non-metastatic lymph nodes of colorectal cancer patients. These results suggest the potential and usefulness of the background-free estimation method of PPIX fluorescence for 5-ALA-based fluorescence diagnosis of malignant lesions, and we expect this method to be beneficial for intraoperative and rapid cancer diagnosis.
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spelling pubmed-48577442016-05-19 Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions Minamikawa, Takeo Matsuo, Hisataka Kato, Yoshiyuki Harada, Yoshinori Otsuji, Eigo Yanagisawa, Akio Tanaka, Hideo Takamatsu, Tetsuro Sci Rep Article 5-aminolevulinic acid (5-ALA)-based fluorescence diagnosis is now clinically applied for accurate and ultrarapid diagnosis of malignant lesions such as lymph node metastasis during surgery. 5-ALA-based diagnosis evaluates fluorescence intensity of a fluorescent metabolite of 5-ALA, protoporphyrin IX (PPIX); however, the fluorescence of PPIX is often affected by autofluorescence of tissue chromophores, such as collagen and flavins. In this study, we demonstrated PPIX fluorescence estimation with autofluorescence elimination for 5-ALA-based fluorescence diagnosis of malignant lesions by simplified and optimized multispectral imaging. We computationally optimized observation wavelength regions for the estimation of PPIX fluorescence in terms of minimizing prediction error of PPIX fluorescence intensity in the presence of typical chromophores, collagen and flavins. By using the fluorescence intensities of the optimized wavelength regions, we verified quantitative detection of PPIX fluorescence by using chemical mixtures of PPIX, flavins, and collagen. Furthermore, we demonstrated detection capability by using metastatic and non-metastatic lymph nodes of colorectal cancer patients. These results suggest the potential and usefulness of the background-free estimation method of PPIX fluorescence for 5-ALA-based fluorescence diagnosis of malignant lesions, and we expect this method to be beneficial for intraoperative and rapid cancer diagnosis. Nature Publishing Group 2016-05-05 /pmc/articles/PMC4857744/ /pubmed/27149301 http://dx.doi.org/10.1038/srep25530 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Minamikawa, Takeo
Matsuo, Hisataka
Kato, Yoshiyuki
Harada, Yoshinori
Otsuji, Eigo
Yanagisawa, Akio
Tanaka, Hideo
Takamatsu, Tetsuro
Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title_full Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title_fullStr Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title_full_unstemmed Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title_short Simplified and optimized multispectral imaging for 5-ALA-based fluorescence diagnosis of malignant lesions
title_sort simplified and optimized multispectral imaging for 5-ala-based fluorescence diagnosis of malignant lesions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857744/
https://www.ncbi.nlm.nih.gov/pubmed/27149301
http://dx.doi.org/10.1038/srep25530
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