Analysis of endogenous aldehydes in human urine by static headspace gas chromatography–mass spectrometry

•HS–GC–MS method to determine 12 relevant endogenous aldehydes in human urine.•Simple, automatic and environmentally friendly method.•LODs (ng/L) at least one order of magnitude lower than those of recent alternatives.•Aldehydes are detected with good accuracy in un-diluted real urine samples.•Urine...

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Published inJournal of Chromatography A Vol. 1437; pp. 241 - 246
Main Authors Serrano, María, Gallego, Mercedes, Silva, Manuel
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 11.03.2016
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Abstract •HS–GC–MS method to determine 12 relevant endogenous aldehydes in human urine.•Simple, automatic and environmentally friendly method.•LODs (ng/L) at least one order of magnitude lower than those of recent alternatives.•Aldehydes are detected with good accuracy in un-diluted real urine samples.•Urine is a suitable matrix for monitoring aldehydes as markers of oxidative stress. Endogenous aldehydes (EAs) generated during oxidative stress and cell processes are associated with many pathogenic and toxicogenic processes. The aim of this research was to develop a solvent-free and automated analytical method for the determination of EAs in human urine using a static headspace generator sampler coupled with gas chromatography–mass spectrometry (HS–GC–MS). Twelve significant EAs used as markers of different biochemical and physiological processes, namely short- and medium-chain alkanals, α,β-unsaturated aldehydes and dicarbonyl aldehydes have been selected as target analytes. Human urine samples (no dilution is required) were derivatized with O-2,3,4,5,6-pentafluorobenzylhydroxylamine in alkaline medium (hydrogen carbonate–carbonate buffer, pH 10.3). The HS–GC–MS method developed renders an efficient tool for the sensitive and precise determination of EAs in human urine with limits of detection from 1 to 15ng/L and relative standard deviations, (RSDs) from 6.0 to 7.9%. Average recoveries by enriching urine samples ranged between 92 and 95%. Aldehydes were readily determined at 0.005–50μg/L levels in human urine from healthy subjects, smokers and diabetic adults.
AbstractList Endogenous aldehydes (EAs) generated during oxidative stress and cell processes are associated with many pathogenic and toxicogenic processes. The aim of this research was to develop a solvent-free and automated analytical method for the determination of EAs in human urine using a static headspace generator sampler coupled with gas chromatography–mass spectrometry (HS–GC–MS). Twelve significant EAs used as markers of different biochemical and physiological processes, namely short- and medium-chain alkanals, α,β-unsaturated aldehydes and dicarbonyl aldehydes have been selected as target analytes. Human urine samples (no dilution is required) were derivatized with O-2,3,4,5,6-pentafluorobenzylhydroxylamine in alkaline medium (hydrogen carbonate–carbonate buffer, pH 10.3). The HS–GC–MS method developed renders an efficient tool for the sensitive and precise determination of EAs in human urine with limits of detection from 1 to 15ng/L and relative standard deviations, (RSDs) from 6.0 to 7.9%. Average recoveries by enriching urine samples ranged between 92 and 95%. Aldehydes were readily determined at 0.005–50μg/L levels in human urine from healthy subjects, smokers and diabetic adults.
Endogenous aldehydes (EAs) generated during oxidative stress and cell processes are associated with many pathogenic and toxicogenic processes. The aim of this research was to develop a solvent-free and automated analytical method for the determination of EAs in human urine using a static headspace generator sampler coupled with gas chromatography-mass spectrometry (HS-GC-MS). Twelve significant EAs used as markers of different biochemical and physiological processes, namely short- and medium-chain alkanals, alpha , beta -unsaturated aldehydes and dicarbonyl aldehydes have been selected as target analytes. Human urine samples (no dilution is required) were derivatized with O-2,3,4,5,6-pentafluorobenzylhydroxylamine in alkaline medium (hydrogen carbonate-carbonate buffer, pH 10.3). The HS-GC-MS method developed renders an efficient tool for the sensitive and precise determination of EAs in human urine with limits of detection from 1 to 15 ng/L and relative standard deviations, (RSDs) from 6.0 to 7.9%. Average recoveries by enriching urine samples ranged between 92 and 95%. Aldehydes were readily determined at 0.005-50 mu g/L levels in human urine from healthy subjects, smokers and diabetic adults.
•HS–GC–MS method to determine 12 relevant endogenous aldehydes in human urine.•Simple, automatic and environmentally friendly method.•LODs (ng/L) at least one order of magnitude lower than those of recent alternatives.•Aldehydes are detected with good accuracy in un-diluted real urine samples.•Urine is a suitable matrix for monitoring aldehydes as markers of oxidative stress. Endogenous aldehydes (EAs) generated during oxidative stress and cell processes are associated with many pathogenic and toxicogenic processes. The aim of this research was to develop a solvent-free and automated analytical method for the determination of EAs in human urine using a static headspace generator sampler coupled with gas chromatography–mass spectrometry (HS–GC–MS). Twelve significant EAs used as markers of different biochemical and physiological processes, namely short- and medium-chain alkanals, α,β-unsaturated aldehydes and dicarbonyl aldehydes have been selected as target analytes. Human urine samples (no dilution is required) were derivatized with O-2,3,4,5,6-pentafluorobenzylhydroxylamine in alkaline medium (hydrogen carbonate–carbonate buffer, pH 10.3). The HS–GC–MS method developed renders an efficient tool for the sensitive and precise determination of EAs in human urine with limits of detection from 1 to 15ng/L and relative standard deviations, (RSDs) from 6.0 to 7.9%. Average recoveries by enriching urine samples ranged between 92 and 95%. Aldehydes were readily determined at 0.005–50μg/L levels in human urine from healthy subjects, smokers and diabetic adults.
Author Silva, Manuel
Serrano, María
Gallego, Mercedes
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Keywords Static headspace technique
Oxidative stress
Human urine
Endogenous aldehydes
Gas chromatography–mass spectrometry
Language English
License Copyright © 2016 Elsevier B.V. All rights reserved.
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Snippet •HS–GC–MS method to determine 12 relevant endogenous aldehydes in human urine.•Simple, automatic and environmentally friendly method.•LODs (ng/L) at least one...
Endogenous aldehydes (EAs) generated during oxidative stress and cell processes are associated with many pathogenic and toxicogenic processes. The aim of this...
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StartPage 241
SubjectTerms Adult
Adults
Aldehydes
Aldehydes - analysis
Automation
buffers
detection limit
Endogenous aldehydes
Enrichment
Gas chromatography
Gas Chromatography-Mass Spectrometry
headspace analysis
Human
Human urine
Humans
hydrogen
Mass spectrometry
Oxidative stress
Sensitivity and Specificity
Solvents - analysis
Static headspace technique
statistical analysis
Urinalysis - instrumentation
Urinalysis - methods
Urine
Title Analysis of endogenous aldehydes in human urine by static headspace gas chromatography–mass spectrometry
URI https://dx.doi.org/10.1016/j.chroma.2016.01.056
https://www.ncbi.nlm.nih.gov/pubmed/26879451
https://www.proquest.com/docview/1816079172
https://www.proquest.com/docview/2000594799
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