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Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy

Corroles and hexaphyrins are porphyrinoids with great potential for diverse applications. Like porphyrins, many of their applications are based on their unique capability to interact with light, i.e., based on their photophysical properties. Corroles have intense absorptions in the low-energy region...

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Detalles Bibliográficos
Autores principales: Lopes, Susana M. M., Pineiro, Marta, Pinho e Melo, Teresa M. V. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435872/
https://www.ncbi.nlm.nih.gov/pubmed/32751215
http://dx.doi.org/10.3390/molecules25153450
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author Lopes, Susana M. M.
Pineiro, Marta
Pinho e Melo, Teresa M. V. D.
author_facet Lopes, Susana M. M.
Pineiro, Marta
Pinho e Melo, Teresa M. V. D.
author_sort Lopes, Susana M. M.
collection PubMed
description Corroles and hexaphyrins are porphyrinoids with great potential for diverse applications. Like porphyrins, many of their applications are based on their unique capability to interact with light, i.e., based on their photophysical properties. Corroles have intense absorptions in the low-energy region of the uv-vis, while hexaphyrins have the capability to absorb light in the near-infrared (NIR) region, presenting photophysical features which are complementary to those of porphyrins. Despite the increasing interest in corroles and hexaphyrins in recent years, the full potential of both classes of compounds, regarding biological applications, has been hampered by their challenging synthesis. Herein, recent developments in the synthesis of corroles and hexaphyrins are reviewed, highlighting their potential application in photodynamic therapy.
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spelling pubmed-74358722020-08-25 Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy Lopes, Susana M. M. Pineiro, Marta Pinho e Melo, Teresa M. V. D. Molecules Review Corroles and hexaphyrins are porphyrinoids with great potential for diverse applications. Like porphyrins, many of their applications are based on their unique capability to interact with light, i.e., based on their photophysical properties. Corroles have intense absorptions in the low-energy region of the uv-vis, while hexaphyrins have the capability to absorb light in the near-infrared (NIR) region, presenting photophysical features which are complementary to those of porphyrins. Despite the increasing interest in corroles and hexaphyrins in recent years, the full potential of both classes of compounds, regarding biological applications, has been hampered by their challenging synthesis. Herein, recent developments in the synthesis of corroles and hexaphyrins are reviewed, highlighting their potential application in photodynamic therapy. MDPI 2020-07-29 /pmc/articles/PMC7435872/ /pubmed/32751215 http://dx.doi.org/10.3390/molecules25153450 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lopes, Susana M. M.
Pineiro, Marta
Pinho e Melo, Teresa M. V. D.
Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title_full Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title_fullStr Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title_full_unstemmed Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title_short Corroles and Hexaphyrins: Synthesis and Application in Cancer Photodynamic Therapy
title_sort corroles and hexaphyrins: synthesis and application in cancer photodynamic therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435872/
https://www.ncbi.nlm.nih.gov/pubmed/32751215
http://dx.doi.org/10.3390/molecules25153450
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