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The Colorimetric Detection of the Hydroxyl Radical

An aromatic substrate for hydroxylation by hydroxyl radicals ((•)OH) was investigated. The probe, N,N’-(5-nitro-1,3-phenylene)-bis-glutaramide, and its hydroxylated product do not bind either iron(III) or iron(II), and so they do not interfere with the Fenton reaction. A spectrophotometric assay bas...

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Detalles Bibliográficos
Autores principales: Ran, Yandong, Moursy, Mohammed, Hider, Robert C., Cilibrizzi, Agostino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964436/
https://www.ncbi.nlm.nih.gov/pubmed/36835574
http://dx.doi.org/10.3390/ijms24044162
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author Ran, Yandong
Moursy, Mohammed
Hider, Robert C.
Cilibrizzi, Agostino
author_facet Ran, Yandong
Moursy, Mohammed
Hider, Robert C.
Cilibrizzi, Agostino
author_sort Ran, Yandong
collection PubMed
description An aromatic substrate for hydroxylation by hydroxyl radicals ((•)OH) was investigated. The probe, N,N’-(5-nitro-1,3-phenylene)-bis-glutaramide, and its hydroxylated product do not bind either iron(III) or iron(II), and so they do not interfere with the Fenton reaction. A spectrophotometric assay based on the hydroxylation of the substrate was developed. The synthesis and purification methods of this probe from previously published methodologies were improved upon, as well as the analytical procedure for monitoring the Fenton reaction through its use, enabling univocal and sensitive (•)OH detection. The assay was utilised to demonstrate that the iron(III) complexes of long-chain fatty acids lack Fenton activity under biological conditions.
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spelling pubmed-99644362023-02-26 The Colorimetric Detection of the Hydroxyl Radical Ran, Yandong Moursy, Mohammed Hider, Robert C. Cilibrizzi, Agostino Int J Mol Sci Communication An aromatic substrate for hydroxylation by hydroxyl radicals ((•)OH) was investigated. The probe, N,N’-(5-nitro-1,3-phenylene)-bis-glutaramide, and its hydroxylated product do not bind either iron(III) or iron(II), and so they do not interfere with the Fenton reaction. A spectrophotometric assay based on the hydroxylation of the substrate was developed. The synthesis and purification methods of this probe from previously published methodologies were improved upon, as well as the analytical procedure for monitoring the Fenton reaction through its use, enabling univocal and sensitive (•)OH detection. The assay was utilised to demonstrate that the iron(III) complexes of long-chain fatty acids lack Fenton activity under biological conditions. MDPI 2023-02-19 /pmc/articles/PMC9964436/ /pubmed/36835574 http://dx.doi.org/10.3390/ijms24044162 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Ran, Yandong
Moursy, Mohammed
Hider, Robert C.
Cilibrizzi, Agostino
The Colorimetric Detection of the Hydroxyl Radical
title The Colorimetric Detection of the Hydroxyl Radical
title_full The Colorimetric Detection of the Hydroxyl Radical
title_fullStr The Colorimetric Detection of the Hydroxyl Radical
title_full_unstemmed The Colorimetric Detection of the Hydroxyl Radical
title_short The Colorimetric Detection of the Hydroxyl Radical
title_sort colorimetric detection of the hydroxyl radical
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964436/
https://www.ncbi.nlm.nih.gov/pubmed/36835574
http://dx.doi.org/10.3390/ijms24044162
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