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Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo

To improve efficacy of photodynamic therapy (PDT) with intravenously administered 5-aminolaevulinic acid (ALA) fractionating the light dose or reducing the light intensity may be a possibility. Therefore, Syrian Golden hamsters were fitted with dorsal skinfold chambers containing an amelanotic melan...

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Autores principales: Babilas, P, Schacht, V, Liebsch, G, Wolfbeis, O S, Landthaler, M, Szeimies, R-M, Abels, C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741044/
https://www.ncbi.nlm.nih.gov/pubmed/12778078
http://dx.doi.org/10.1038/sj.bjc.6600910
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author Babilas, P
Schacht, V
Liebsch, G
Wolfbeis, O S
Landthaler, M
Szeimies, R-M
Abels, C
author_facet Babilas, P
Schacht, V
Liebsch, G
Wolfbeis, O S
Landthaler, M
Szeimies, R-M
Abels, C
author_sort Babilas, P
collection PubMed
description To improve efficacy of photodynamic therapy (PDT) with intravenously administered 5-aminolaevulinic acid (ALA) fractionating the light dose or reducing the light intensity may be a possibility. Therefore, Syrian Golden hamsters were fitted with dorsal skinfold chambers containing an amelanotic melanoma (n=26). PDT was performed (100 mW cm(−2), 100 J cm(−2), continuously or fractionated, and 25 mW cm(−2), 100 J cm(−2); continuously or fractionated) using an incoherent light source following i.v. application of ALA. Following fractionated irradiation, the light was paused after 20 J cm(−2) for 15 min. Prior to and up to 24 h after PDT tissue, pO(2) was measured using luminescence lifetime imaging. The efficacy was evaluated by measuring the tumour volume of amelanotic melanoma cells grown subcutaneously in the back of Syrian Golden hamsters (n=36). Only high-dose PDT resulted in a significant decrease of pO(2). Irrespective of the mode of irradiation only high-dose PDT induced complete remission of all tumours (13 out of 13). It could be shown that low-dose PDT failed to induce a significant decrease of pO(2). No significant effect of fractionated irradiation was shown regarding the therapeutic efficacy 28 days after PDT. Thus performing a fractionated PDT with ALA or reducing the light intensity seems not to be successful in clinical PDT according to the present data.
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spelling pubmed-27410442009-09-10 Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo Babilas, P Schacht, V Liebsch, G Wolfbeis, O S Landthaler, M Szeimies, R-M Abels, C Br J Cancer Experimental Therapeutics To improve efficacy of photodynamic therapy (PDT) with intravenously administered 5-aminolaevulinic acid (ALA) fractionating the light dose or reducing the light intensity may be a possibility. Therefore, Syrian Golden hamsters were fitted with dorsal skinfold chambers containing an amelanotic melanoma (n=26). PDT was performed (100 mW cm(−2), 100 J cm(−2), continuously or fractionated, and 25 mW cm(−2), 100 J cm(−2); continuously or fractionated) using an incoherent light source following i.v. application of ALA. Following fractionated irradiation, the light was paused after 20 J cm(−2) for 15 min. Prior to and up to 24 h after PDT tissue, pO(2) was measured using luminescence lifetime imaging. The efficacy was evaluated by measuring the tumour volume of amelanotic melanoma cells grown subcutaneously in the back of Syrian Golden hamsters (n=36). Only high-dose PDT resulted in a significant decrease of pO(2). Irrespective of the mode of irradiation only high-dose PDT induced complete remission of all tumours (13 out of 13). It could be shown that low-dose PDT failed to induce a significant decrease of pO(2). No significant effect of fractionated irradiation was shown regarding the therapeutic efficacy 28 days after PDT. Thus performing a fractionated PDT with ALA or reducing the light intensity seems not to be successful in clinical PDT according to the present data. Nature Publishing Group 2003-05-06 2003-04-29 /pmc/articles/PMC2741044/ /pubmed/12778078 http://dx.doi.org/10.1038/sj.bjc.6600910 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Experimental Therapeutics
Babilas, P
Schacht, V
Liebsch, G
Wolfbeis, O S
Landthaler, M
Szeimies, R-M
Abels, C
Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title_full Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title_fullStr Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title_full_unstemmed Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title_short Effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
title_sort effects of light fractionation and different fluence rates on photodynamic therapy with 5-aminolaevulinic acid in vivo
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2741044/
https://www.ncbi.nlm.nih.gov/pubmed/12778078
http://dx.doi.org/10.1038/sj.bjc.6600910
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