An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System
Red blood cells are constantly exposed to reactive species under physiological or pathological conditions or during administration of xenobiotics. Regardless of the source, its accurate quantification is paramount in the area of theragnostics, which had been elusive up until now. Even if there are a...
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doaj-6b0f37b31b3e45cfbc687369b2e4383f2020-11-25T02:36:29ZengMDPI AGMetabolites2218-19892020-04-011017517510.3390/metabo10050175An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood SystemIoannis Tsamesidis0Chinedu O. Egwu1Pierre Pério2Jean-Michel Augereau3Françoise Benoit-Vical4Karine Reybier5Pharmadev, UMR 152, Université de Toulouse, IRD, UPS, 31400 Toulouse, FrancePharmadev, UMR 152, Université de Toulouse, IRD, UPS, 31400 Toulouse, FrancePharmadev, UMR 152, Université de Toulouse, IRD, UPS, 31400 Toulouse, FranceCNRS, LCC, Laboratoire de Chimie de Coordination, Université de Toulouse, 31077 Toulouse CEDEX 4, FranceCNRS, LCC, Laboratoire de Chimie de Coordination, Université de Toulouse, 31077 Toulouse CEDEX 4, FrancePharmadev, UMR 152, Université de Toulouse, IRD, UPS, 31400 Toulouse, FranceRed blood cells are constantly exposed to reactive species under physiological or pathological conditions or during administration of xenobiotics. Regardless of the source, its accurate quantification is paramount in the area of theragnostics, which had been elusive up until now. Even if there are a lot of approaches to evaluate the oxidative stress, very sensitive methods are missing for the blood system. We therefore sought to apply a highly sensitive approach, by liquid chromatography coupled to mass spectrometry (UPLC–MS), for the quantification of reactive species such as superoxide radical and hydrogen peroxide using dihydroethidium (DHE) and coumarin boronic acid (CBA) probes respectively through the detection of 2-hydroxyethidium (2OH-E<sup>+</sup>) and 7-hydroxycoumarin (COH). The use of the high-resolution mass spectrometry associated to UPLC ensured a selective detection of superoxide and hydrogen peroxide in the blood system under diverse conditions such as oxidized red blood cells (RBCs), untreated and treated parasitized RBCs. Moreover, this technique allowed the determination of reactive species in human plasma. This protocol provides a huge opportunity for in-depth study of several pathological conditions vis-a-vis their treatment in modern medicine.https://www.mdpi.com/2218-1989/10/5/175liquid-chromatographymass spectrometrysuperoxide radicalshydrogen peroxide speciesred blood cellshuman plasma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ioannis Tsamesidis Chinedu O. Egwu Pierre Pério Jean-Michel Augereau Françoise Benoit-Vical Karine Reybier |
spellingShingle |
Ioannis Tsamesidis Chinedu O. Egwu Pierre Pério Jean-Michel Augereau Françoise Benoit-Vical Karine Reybier An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System Metabolites liquid-chromatography mass spectrometry superoxide radicals hydrogen peroxide species red blood cells human plasma |
author_facet |
Ioannis Tsamesidis Chinedu O. Egwu Pierre Pério Jean-Michel Augereau Françoise Benoit-Vical Karine Reybier |
author_sort |
Ioannis Tsamesidis |
title |
An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System |
title_short |
An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System |
title_full |
An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System |
title_fullStr |
An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System |
title_full_unstemmed |
An LC–MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System |
title_sort |
lc–ms assay to measure superoxide radicals and hydrogen peroxide in the blood system |
publisher |
MDPI AG |
series |
Metabolites |
issn |
2218-1989 |
publishDate |
2020-04-01 |
description |
Red blood cells are constantly exposed to reactive species under physiological or pathological conditions or during administration of xenobiotics. Regardless of the source, its accurate quantification is paramount in the area of theragnostics, which had been elusive up until now. Even if there are a lot of approaches to evaluate the oxidative stress, very sensitive methods are missing for the blood system. We therefore sought to apply a highly sensitive approach, by liquid chromatography coupled to mass spectrometry (UPLC–MS), for the quantification of reactive species such as superoxide radical and hydrogen peroxide using dihydroethidium (DHE) and coumarin boronic acid (CBA) probes respectively through the detection of 2-hydroxyethidium (2OH-E<sup>+</sup>) and 7-hydroxycoumarin (COH). The use of the high-resolution mass spectrometry associated to UPLC ensured a selective detection of superoxide and hydrogen peroxide in the blood system under diverse conditions such as oxidized red blood cells (RBCs), untreated and treated parasitized RBCs. Moreover, this technique allowed the determination of reactive species in human plasma. This protocol provides a huge opportunity for in-depth study of several pathological conditions vis-a-vis their treatment in modern medicine. |
topic |
liquid-chromatography mass spectrometry superoxide radicals hydrogen peroxide species red blood cells human plasma |
url |
https://www.mdpi.com/2218-1989/10/5/175 |
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