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Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics
Multiphoton imaging based on two-photon excitation is making its way into the clinics, particularly for skin cancer diagnostics. It has been suggested that endogenously formed protoporphyrin IX (PpIX) induced by aminolevulinic acid or methylaminolevulinate can be applied to improve tumor contrast, i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732385/ https://www.ncbi.nlm.nih.gov/pubmed/22997024 http://dx.doi.org/10.1002/jbio.201200119 |
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author | Kantere, Despina Guldbrand, Stina Paoli, John Goksör, Mattias Hanstorp, Dag Wennberg, Ann-Marie Smedh, Maria Ericson, Marica B |
author_facet | Kantere, Despina Guldbrand, Stina Paoli, John Goksör, Mattias Hanstorp, Dag Wennberg, Ann-Marie Smedh, Maria Ericson, Marica B |
author_sort | Kantere, Despina |
collection | PubMed |
description | Multiphoton imaging based on two-photon excitation is making its way into the clinics, particularly for skin cancer diagnostics. It has been suggested that endogenously formed protoporphyrin IX (PpIX) induced by aminolevulinic acid or methylaminolevulinate can be applied to improve tumor contrast, in connection to imaging of tissue autofluorescence. However, previous reports are limited to cell studies and data from tissue are scarce. No report shows conclusive evidence that endogenously formed PpIX increases tumor contrast when performing multiphoton imaging in the clinical situation. We here demonstrate by spectral analysis that two-photon excitation of endogenously formed PpIX does not provide additional contrast in superficial basal cell carcinomas. In fact, the PpIX signal is overshadowed by the autofluorescent background. The results show that PpIX should be excited at a wavelength giving rise to one-photon anti-Stokes fluorescence, to overcome the autofluorescent background. Thus, this study reports on a plausible method, which can be implemented for clinical investigations on endogenously formed PpIX using multiphoton microscopy. [Image: see text] Three-dimensional multiphoton microscopy images obtained from a superficial basal cell carcinoma illustrating higher porphyrin contrast when anti-stokes excitation (710 nm) is used compared to two-photon excitation (810 nm). |
format | Online Article Text |
id | pubmed-3732385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-37323852013-08-05 Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics Kantere, Despina Guldbrand, Stina Paoli, John Goksör, Mattias Hanstorp, Dag Wennberg, Ann-Marie Smedh, Maria Ericson, Marica B J Biophotonics Full Articles Multiphoton imaging based on two-photon excitation is making its way into the clinics, particularly for skin cancer diagnostics. It has been suggested that endogenously formed protoporphyrin IX (PpIX) induced by aminolevulinic acid or methylaminolevulinate can be applied to improve tumor contrast, in connection to imaging of tissue autofluorescence. However, previous reports are limited to cell studies and data from tissue are scarce. No report shows conclusive evidence that endogenously formed PpIX increases tumor contrast when performing multiphoton imaging in the clinical situation. We here demonstrate by spectral analysis that two-photon excitation of endogenously formed PpIX does not provide additional contrast in superficial basal cell carcinomas. In fact, the PpIX signal is overshadowed by the autofluorescent background. The results show that PpIX should be excited at a wavelength giving rise to one-photon anti-Stokes fluorescence, to overcome the autofluorescent background. Thus, this study reports on a plausible method, which can be implemented for clinical investigations on endogenously formed PpIX using multiphoton microscopy. [Image: see text] Three-dimensional multiphoton microscopy images obtained from a superficial basal cell carcinoma illustrating higher porphyrin contrast when anti-stokes excitation (710 nm) is used compared to two-photon excitation (810 nm). WILEY-VCH Verlag 2013-05 2012-09-18 /pmc/articles/PMC3732385/ /pubmed/22997024 http://dx.doi.org/10.1002/jbio.201200119 Text en © 2013 The Authors. J. Biophotonics published by WILEY-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Full Articles Kantere, Despina Guldbrand, Stina Paoli, John Goksör, Mattias Hanstorp, Dag Wennberg, Ann-Marie Smedh, Maria Ericson, Marica B Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title | Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title_full | Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title_fullStr | Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title_full_unstemmed | Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title_short | Anti-Stokes fluorescence from endogenously formed protoporphyrin IX – Implications for clinical multiphoton diagnostics |
title_sort | anti-stokes fluorescence from endogenously formed protoporphyrin ix – implications for clinical multiphoton diagnostics |
topic | Full Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3732385/ https://www.ncbi.nlm.nih.gov/pubmed/22997024 http://dx.doi.org/10.1002/jbio.201200119 |
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