6533b85bfe1ef96bd12baae5

RESEARCH PRODUCT

Assessment of oxidative damage to proteins and DNA in urine of newborn infants by a validated UPLC-MS/MS approach

Miguel AsensiMáximo VentoGuillermo QuintásJulia KuligowskiIsabel LlisoIsabel Torres-cuevasAntonio NuñezDenise RookElena CubellsJavier EscobarJohannes B. Van Goudoever

subject

AnalyteScienceUrinary systemUrineResearch and Analysis Methodsmedicine.disease_causeTandem mass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryOxidative DamageTandem Mass SpectrometryDiagnostic MedicineLiquid chromatography–mass spectrometryNucleic AcidsDNA-binding proteinsMedicine and Health SciencesmedicineHumansClinical ChemistryMultidisciplinaryChromatographyBiology and life sciencesbusiness.industryQChromatographic TechniquesRInfant NewbornProteinsDNAClinical Laboratory SciencesClinical trialOxidative StressChemistryBioassays and Physiological AnalysisPhysical SciencesMedicineMedicinal ChemistryBiochemical AnalysisbusinessBiomarkersOxidative stressResearch Article

description

The assessment of oxidative stress is highly relevant in clinical Perinatology as it is associated to adverse outcomes in newborn infants. This study summarizes results from the validation of an Ultra Performance Liquid Chromatography-tandem Mass Spectrometry (UPLC-MS/MS) method for the simultaneous quantification of the urinary concentrations of a set of endogenous biomarkers, capable to provide a valid snapshot of the oxidative stress status applicable in human clinical trials, especially in the field of Perinatology. The set of analytes included are phenylalanine (Phe), para-tyrosine (p-Tyr), ortho-tyrosine (o-Tyr), meta-tyrosine (m-Tyr), 3-NO2-tyrosine (3NO(2)-Tyr), 3-Cl-tyrosine (3Cl-Tyr), 2'-deoxyguanosine (2dG) and 8-hydroxy-2'-deoxyguanosine (8OHdG). Following the FDA-based guidelines, appropriate levels of accuracy and precision, as well as adequate levels of sensitivity with limits of detection (LODs) in the low nanomolar (nmol/L) range were confirmed after method validation. The validity of the proposed UPLC-MS/MS method was assessed by analysing urine samples from a clinical trial in extremely low birth weight (ELBW) infants randomized to be resuscitated with two different initial inspiratory fractions of oxygen.

10.1371/journal.pone.0093703https://doi.org/10.1371/journal.pone.0093703