Factors influencing fluorescence spectra of free porphyrins

We recorded fluorescence excitation and emission spectra of uro- and coproporphyrin under different experimental conditions, to see how these conditions influence quantification based on measurement of fluorescence intensity. We found that, for bands α and β of the emission spectra and the main peak...

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Autores principales: Polo, C.F., Frisardi, A.L., Resnik, E.R., Schoua, A.E.M., Del Batlle, C.A.M.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00099147_v34_n4_p757_Polo
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spelling todo:paper_00099147_v34_n4_p757_Polo2023-10-03T14:08:52Z Factors influencing fluorescence spectra of free porphyrins Polo, C.F. Frisardi, A.L. Resnik, E.R. Schoua, A.E.M. Del Batlle, C.A.M. porphyrin fluorescence nonhuman Coproporphyrins Hydrogen-Ion Concentration Osmolar Concentration Porphyrins Solvents Spectrometry, Fluorescence Support, Non-U.S. Gov't Uroporphyrins We recorded fluorescence excitation and emission spectra of uro- and coproporphyrin under different experimental conditions, to see how these conditions influence quantification based on measurement of fluorescence intensity. We found that, for bands α and β of the emission spectra and the main peak of the excitation spectra, fluorescence depends on pH and is minimal near pH 5 and near pH 7-7.5 for copro- and uroporphyrin, respectively. For band γ of the emission spectra there was a constant decrease of fluorescence with increasing alkalinity of the solution. The intensity of porphyrin fluorescence also depends on ionic strength, reaching sharp maxima at 0.1 mol/L (for uroporphyrin) and 1 mol/L (for coproporphyrin). The organic mixture ethyl acetate:acetic acid (4:1 by vol), commonly used to extract porphyrins from biological samples, markedly diminishes the fluorescence of both porphyrins as compared with the same concentration of each porphyrin in aqueous acidic solvent. Furthermore, when we measured different ratios of uro:copro mixture at three distinct pHs and buffers, we found that at pH 10.5 (in carbonate buffer) the measured units of fluorescence depend only on total porphyrin concentration and not on the composition of the mixture. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00099147_v34_n4_p757_Polo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic porphyrin
fluorescence
nonhuman
Coproporphyrins
Hydrogen-Ion Concentration
Osmolar Concentration
Porphyrins
Solvents
Spectrometry, Fluorescence
Support, Non-U.S. Gov't
Uroporphyrins
spellingShingle porphyrin
fluorescence
nonhuman
Coproporphyrins
Hydrogen-Ion Concentration
Osmolar Concentration
Porphyrins
Solvents
Spectrometry, Fluorescence
Support, Non-U.S. Gov't
Uroporphyrins
Polo, C.F.
Frisardi, A.L.
Resnik, E.R.
Schoua, A.E.M.
Del Batlle, C.A.M.
Factors influencing fluorescence spectra of free porphyrins
topic_facet porphyrin
fluorescence
nonhuman
Coproporphyrins
Hydrogen-Ion Concentration
Osmolar Concentration
Porphyrins
Solvents
Spectrometry, Fluorescence
Support, Non-U.S. Gov't
Uroporphyrins
description We recorded fluorescence excitation and emission spectra of uro- and coproporphyrin under different experimental conditions, to see how these conditions influence quantification based on measurement of fluorescence intensity. We found that, for bands α and β of the emission spectra and the main peak of the excitation spectra, fluorescence depends on pH and is minimal near pH 5 and near pH 7-7.5 for copro- and uroporphyrin, respectively. For band γ of the emission spectra there was a constant decrease of fluorescence with increasing alkalinity of the solution. The intensity of porphyrin fluorescence also depends on ionic strength, reaching sharp maxima at 0.1 mol/L (for uroporphyrin) and 1 mol/L (for coproporphyrin). The organic mixture ethyl acetate:acetic acid (4:1 by vol), commonly used to extract porphyrins from biological samples, markedly diminishes the fluorescence of both porphyrins as compared with the same concentration of each porphyrin in aqueous acidic solvent. Furthermore, when we measured different ratios of uro:copro mixture at three distinct pHs and buffers, we found that at pH 10.5 (in carbonate buffer) the measured units of fluorescence depend only on total porphyrin concentration and not on the composition of the mixture.
format JOUR
author Polo, C.F.
Frisardi, A.L.
Resnik, E.R.
Schoua, A.E.M.
Del Batlle, C.A.M.
author_facet Polo, C.F.
Frisardi, A.L.
Resnik, E.R.
Schoua, A.E.M.
Del Batlle, C.A.M.
author_sort Polo, C.F.
title Factors influencing fluorescence spectra of free porphyrins
title_short Factors influencing fluorescence spectra of free porphyrins
title_full Factors influencing fluorescence spectra of free porphyrins
title_fullStr Factors influencing fluorescence spectra of free porphyrins
title_full_unstemmed Factors influencing fluorescence spectra of free porphyrins
title_sort factors influencing fluorescence spectra of free porphyrins
url http://hdl.handle.net/20.500.12110/paper_00099147_v34_n4_p757_Polo
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AT resniker factorsinfluencingfluorescencespectraoffreeporphyrins
AT schouaaem factorsinfluencingfluorescencespectraoffreeporphyrins
AT delbatllecam factorsinfluencingfluorescencespectraoffreeporphyrins
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