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pubmed-article:3149976pubmed:abstractTextThe fluorescence decay I(t) and time-resolved spectra I(lambda, t) of some porphyrins and chlorins in ethanol and phosphate-buffered aqueous solution were investigated with a time-correlated single-photon-counting apparatus with a mode-locked Ar+ laser (514.5 nm) as the excitation source. The fluorescence of hematoporphyrin, mesoporphyrin and pheophorbide aa is considerably influenced by the conditions of aggregation (these compounds undergo aggregation in phosphate-buffered solution but not in ethanolic solution). The fluorescence decay of chlorin e6 which remains monomeric in both solvents is single exponential in all cases. The fluorescence spectra of hematoporphyrin, mesoporphyrin and pheophorbide a in phosphate-buffered solution are shifted with respect to the spectra obtained in ethanol; moreover, a new emission band (X band) appears, whose intensity increases on increasing the amount of equilibrium aggregates and shows a fast fluorescence decay. For hematoporphyrin and mesoporphyrin the appearance of the X band emission appears to be correlated with irreversible photoprocesses leading to fluorescent photoproducts. Analysis of the reported fluorescence spectra of cancer cells after incubation with hematoporphyrin derivative suggests that the fluorescent photoproducts might be formed also in vivo.lld:pubmed
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pubmed-article:3149976pubmed:pagination103-13lld:pubmed
pubmed-article:3149976pubmed:dateRevised2007-7-23lld:pubmed
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pubmed-article:3149976pubmed:year1987lld:pubmed
pubmed-article:3149976pubmed:articleTitleTime-resolved fluorescence spectroscopy of hematoporphyrin, mesoporphyrin, pheophorbide a and chlorin e6 in ethanol and aqueous solution.lld:pubmed
pubmed-article:3149976pubmed:affiliationHumboldt-University, Dept. of Physics, Berlin, G.D.R.lld:pubmed
pubmed-article:3149976pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3149976pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed