An LC-MS Assay to Measure Superoxide Radicals and Hydrogen Peroxide in the Blood System.
Ioannis TsamesidisChinedu O EgwuPierre PerioJean-Michel AugereauFrançoise Benoit-VicalKarine ReybierPublished in: Metabolites (2020)
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+) 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.
Keyphrases
- hydrogen peroxide
- liquid chromatography
- mass spectrometry
- red blood cell
- high resolution mass spectrometry
- simultaneous determination
- tandem mass spectrometry
- nitric oxide
- solid phase extraction
- gas chromatography
- ultra high performance liquid chromatography
- oxidative stress
- high performance liquid chromatography
- high resolution
- capillary electrophoresis
- molecularly imprinted
- label free
- small molecule
- loop mediated isothermal amplification
- real time pcr
- fluorescent probe
- ischemia reperfusion injury
- living cells
- high throughput
- fluorescence imaging
- optical coherence tomography
- dna damage
- induced apoptosis
- signaling pathway
- low density lipoprotein
- single molecule
- heat stress
- heat shock