Aggregation susceptibility on phototransformation of hematoporphyrin derivatives

Photosensitizers used in PDT suffer degradation by light. In this work, photobleaching of Photogem® (PG), Photofrin® (PF), and Photosan® (PS), hematoporphyrin derivatives, were induced by light in the presence or absence of 1% Triton X‐100. The degradation efficiency in the absence of 1% Triton X‐10...

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Bibliographic Details
Published inLaser physics letters Vol. 5; no. 3; pp. 227 - 235
Main Authors Menezes, P.F.C., Imasato, H., Ferreira, J., Bagnato, V.S., Sibata, C.H., Perussi, J.R.
Format Journal Article
LanguageEnglish
Published Berlin WILEY-VCH Verlag 01.03.2008
WILEY‐VCH Verlag
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Summary:Photosensitizers used in PDT suffer degradation by light. In this work, photobleaching of Photogem® (PG), Photofrin® (PF), and Photosan® (PS), hematoporphyrin derivatives, were induced by light in the presence or absence of 1% Triton X‐100. The degradation efficiency in the absence of 1% Triton X‐100 follows the sequence: PF > PG > PS, which means that PF presented a greater degradation than PG and PS. However, in the presence of the surfactant the degradation efficiency is different: PG ≅ PS > PF. Besides aggregation susceptibility, studies in cell culture (tumor and non tumor cells) and in animals (depth of necrosis) were performed, trying to correlate the stability of these photosensitizers with their photodynamic effect. The results suggest that PF presents higher light induced photocytotoxicity than PG and PS for both types of cells. For the depth of necrosis studies, more aggregated photosensitizer showed a longer time to accumulate in liver (30 min for PG, 120 h for PF, and 720 h for PS). Then, to establish an ideal dosimetry in PDT, one must consider the intrinsic physical chemistry characteristics of the photosensitizer as well as their ability to undergo photobleaching. (© 2008 by Astro Ltd., Published exclusively by WILEY‐VCH Verlag GmbH & Co. KGaA)
Bibliography:FAPESP
ark:/67375/WNG-HMKGJ4ZP-P
istex:8423C1195A25BEDE861E1E521A14553124B988CA
ArticleID:LAPL200710111
ISSN:1612-2011
1612-202X
DOI:10.1002/lapl.200710111