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Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles

The use of 5-aminolaevulinic acid (ALA) is gaining increasing attention for photosensitization in photodynamic therapy of superficially localized tumours. The aim of this work was to determine the kinetics of porphyrin generation in tissues after topical application of ALA delivered in different veh...

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Autores principales: Casas, A, Fukuda, H, Batlle, A M del C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374280/
https://www.ncbi.nlm.nih.gov/pubmed/10487606
http://dx.doi.org/10.1038/sj.bjc.6690644
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author Casas, A
Fukuda, H
Batlle, A M del C
author_facet Casas, A
Fukuda, H
Batlle, A M del C
author_sort Casas, A
collection PubMed
description The use of 5-aminolaevulinic acid (ALA) is gaining increasing attention for photosensitization in photodynamic therapy of superficially localized tumours. The aim of this work was to determine the kinetics of porphyrin generation in tissues after topical application of ALA delivered in different vehicles on the skin overlying the tumour and normal skin of mice. Maximal accumulation was found in tumour 3 h after ALA application in both cream and lotion preparations. Normal and overlying tumour skin tissues showed different kinetic patterns, reflecting histological changes when the latter is invaded by tumour cells. Liver, kidney, spleen and blood porphyrins also raised from basal levels, showing that ALA and/or ALA-induced porphyrins reach all tissues after topical application. During the first 24 h of ALA topical application, precursors and porphyrins are excreted by both urine and faeces. ALA lotion applied on the skin overlying the tumour induced higher accumulation of tumoural porphyrins than cream, and lotion applied on normal skin appeared to be the most efficient upon inducing total body porphyrins. This work has demonstrated the great influence of the formulation of ALA vehicle on penetration through the skin. Knowledge of the kinetics of porphyrin generation after different conditions of ALA application is needed for the optimization of diagnosis and phototherapy in human tumours. © 1999 Cancer Research Campaign
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spelling pubmed-23742802009-09-10 Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles Casas, A Fukuda, H Batlle, A M del C Br J Cancer Regular Article The use of 5-aminolaevulinic acid (ALA) is gaining increasing attention for photosensitization in photodynamic therapy of superficially localized tumours. The aim of this work was to determine the kinetics of porphyrin generation in tissues after topical application of ALA delivered in different vehicles on the skin overlying the tumour and normal skin of mice. Maximal accumulation was found in tumour 3 h after ALA application in both cream and lotion preparations. Normal and overlying tumour skin tissues showed different kinetic patterns, reflecting histological changes when the latter is invaded by tumour cells. Liver, kidney, spleen and blood porphyrins also raised from basal levels, showing that ALA and/or ALA-induced porphyrins reach all tissues after topical application. During the first 24 h of ALA topical application, precursors and porphyrins are excreted by both urine and faeces. ALA lotion applied on the skin overlying the tumour induced higher accumulation of tumoural porphyrins than cream, and lotion applied on normal skin appeared to be the most efficient upon inducing total body porphyrins. This work has demonstrated the great influence of the formulation of ALA vehicle on penetration through the skin. Knowledge of the kinetics of porphyrin generation after different conditions of ALA application is needed for the optimization of diagnosis and phototherapy in human tumours. © 1999 Cancer Research Campaign Nature Publishing Group 1999-09 /pmc/articles/PMC2374280/ /pubmed/10487606 http://dx.doi.org/10.1038/sj.bjc.6690644 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Casas, A
Fukuda, H
Batlle, A M del C
Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title_full Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title_fullStr Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title_full_unstemmed Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title_short Tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ALA in different vehicles
title_sort tissue distribution and kinetics of endogenous porphyrins synthesized after topical application of ala in different vehicles
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374280/
https://www.ncbi.nlm.nih.gov/pubmed/10487606
http://dx.doi.org/10.1038/sj.bjc.6690644
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