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Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence
Direct back-face transmission steady-state fluorescence was successfully applied to the study of aggregation of ibuprofen and ibuprofenate anion in solution taking advantage of its own fluorescence. The analysis of the experimental data involves the use of the differential reabsorption model to acco...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166242/ https://www.ncbi.nlm.nih.gov/pubmed/35665917 http://dx.doi.org/10.1007/s43630-022-00247-7 |
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author | Steinberg, Paula Y. Krimer, Nicolás I. Sarmiento, Gabriela P. Rodrigues, Darío Huck-Iriart, Cristián Clemens, Daniel Zelcer, Andrés Mirenda, Martín |
author_facet | Steinberg, Paula Y. Krimer, Nicolás I. Sarmiento, Gabriela P. Rodrigues, Darío Huck-Iriart, Cristián Clemens, Daniel Zelcer, Andrés Mirenda, Martín |
author_sort | Steinberg, Paula Y. |
collection | PubMed |
description | Direct back-face transmission steady-state fluorescence was successfully applied to the study of aggregation of ibuprofen and ibuprofenate anion in solution taking advantage of its own fluorescence. The analysis of the experimental data involves the use of the differential reabsorption model to account for re-absorption phenomenon and the closed association model to describe aggregation. The fluorescence quantum yield of ibuprofenate increases when it aggregates in the presence of sodium, but it markedly decreases when 1-butyl-3-methylimidazolium is used as counterion. The proposed methodology allows the accurate determination of the critical aggregation concentrations and the mean aggregation numbers. Results were supported by complementary techniques such as time-resolved fluorescence, (1)H-NMR and small-angle neutron and X-ray scattering. The developed technique constitutes a promising strategy to characterize the aggregation of poorly fluorescent surfactants that aggregates at high concentrations and hence at high absorbance values, conditions in which the most common right-angle configuration for fluorescence acquisition is troublesome due to re-absorption. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43630-022-00247-7. |
format | Online Article Text |
id | pubmed-9166242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-91662422022-06-07 Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence Steinberg, Paula Y. Krimer, Nicolás I. Sarmiento, Gabriela P. Rodrigues, Darío Huck-Iriart, Cristián Clemens, Daniel Zelcer, Andrés Mirenda, Martín Photochem Photobiol Sci Original Papers Direct back-face transmission steady-state fluorescence was successfully applied to the study of aggregation of ibuprofen and ibuprofenate anion in solution taking advantage of its own fluorescence. The analysis of the experimental data involves the use of the differential reabsorption model to account for re-absorption phenomenon and the closed association model to describe aggregation. The fluorescence quantum yield of ibuprofenate increases when it aggregates in the presence of sodium, but it markedly decreases when 1-butyl-3-methylimidazolium is used as counterion. The proposed methodology allows the accurate determination of the critical aggregation concentrations and the mean aggregation numbers. Results were supported by complementary techniques such as time-resolved fluorescence, (1)H-NMR and small-angle neutron and X-ray scattering. The developed technique constitutes a promising strategy to characterize the aggregation of poorly fluorescent surfactants that aggregates at high concentrations and hence at high absorbance values, conditions in which the most common right-angle configuration for fluorescence acquisition is troublesome due to re-absorption. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43630-022-00247-7. Springer International Publishing 2022-06-04 2022 /pmc/articles/PMC9166242/ /pubmed/35665917 http://dx.doi.org/10.1007/s43630-022-00247-7 Text en © The Author(s), under exclusive licence to European Photochemistry Association, European Society for Photobiology 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Papers Steinberg, Paula Y. Krimer, Nicolás I. Sarmiento, Gabriela P. Rodrigues, Darío Huck-Iriart, Cristián Clemens, Daniel Zelcer, Andrés Mirenda, Martín Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title | Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title_full | Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title_fullStr | Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title_full_unstemmed | Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title_short | Ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
title_sort | ibuprofen molecular aggregation by direct back-face transmission steady-state fluorescence |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166242/ https://www.ncbi.nlm.nih.gov/pubmed/35665917 http://dx.doi.org/10.1007/s43630-022-00247-7 |
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