The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.

After 35 years the hunt for improved anthracycline antibiotics is unabated but has yet to achieve the levels of clinical success desired. Electrochemical techniques provide a large amount of kinetic and thermodynamic information, but the use of such procedures is hindered by issues of sensitivity an...

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Main Authors: Batchelor-McAuley, C, Dimov, I, Aldous, L, Compton, R
Format: Journal article
Language:English
Published: 2011
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author Batchelor-McAuley, C
Dimov, I
Aldous, L
Compton, R
author_facet Batchelor-McAuley, C
Dimov, I
Aldous, L
Compton, R
author_sort Batchelor-McAuley, C
collection OXFORD
description After 35 years the hunt for improved anthracycline antibiotics is unabated but has yet to achieve the levels of clinical success desired. Electrochemical techniques provide a large amount of kinetic and thermodynamic information, but the use of such procedures is hindered by issues of sensitivity and selectivity. This work demonstrates how by harnessing the mechanism of catalytic reduction of oxygen by the quinone functionality present within the anthracycline structure it is possible to study the reactive moiety in nanomolar concentration. This methodology allows electrochemical investigation of the intercalation of quinizarin into DNA and, in particular, the quinone oxidation and degradation mechanism. The reversible reduction of the quinizarin, which in the presence of oxygen leads to the formation of reactive oxygen species, is found to occur at -0.535 V (vs. SCE) pH 6.84 and the irreversible oxidation leading to the molecules degradation occurs at +0.386 V (vs. SCE) pH 6.84.
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spelling oxford-uuid:3cea6785-6150-4217-a1ff-58b1941b85452022-03-26T14:16:27ZThe electrochemistry of quinizarin revealed through its mediated reduction of oxygen.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3cea6785-6150-4217-a1ff-58b1941b8545EnglishSymplectic Elements at Oxford2011Batchelor-McAuley, CDimov, IAldous, LCompton, RAfter 35 years the hunt for improved anthracycline antibiotics is unabated but has yet to achieve the levels of clinical success desired. Electrochemical techniques provide a large amount of kinetic and thermodynamic information, but the use of such procedures is hindered by issues of sensitivity and selectivity. This work demonstrates how by harnessing the mechanism of catalytic reduction of oxygen by the quinone functionality present within the anthracycline structure it is possible to study the reactive moiety in nanomolar concentration. This methodology allows electrochemical investigation of the intercalation of quinizarin into DNA and, in particular, the quinone oxidation and degradation mechanism. The reversible reduction of the quinizarin, which in the presence of oxygen leads to the formation of reactive oxygen species, is found to occur at -0.535 V (vs. SCE) pH 6.84 and the irreversible oxidation leading to the molecules degradation occurs at +0.386 V (vs. SCE) pH 6.84.
spellingShingle Batchelor-McAuley, C
Dimov, I
Aldous, L
Compton, R
The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title_full The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title_fullStr The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title_full_unstemmed The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title_short The electrochemistry of quinizarin revealed through its mediated reduction of oxygen.
title_sort electrochemistry of quinizarin revealed through its mediated reduction of oxygen
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