Exploring the human urine metabolomic potentialities by comprehensive two-dimensional gas chromatography coupled to time of flight mass spectrometry

► HS-SPME/GC×GC-ToFMS was developed for urine metabolite profiling. ► Hundreds of compounds were detected by the developed methodology. ► Relevant SPME and GC×GC parameters were considered. ► Structured GC×GC chromatogram were exploited to simplify the in-depth characterization of urine. Metabolomic...

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Published inJournal of Chromatography A Vol. 1252; pp. 155 - 163
Main Authors Rocha, Sílvia M., Caldeira, Michael, Carrola, Joana, Santos, Magda, Cruz, Nádia, Duarte, Iola F.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 24.08.2012
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Abstract ► HS-SPME/GC×GC-ToFMS was developed for urine metabolite profiling. ► Hundreds of compounds were detected by the developed methodology. ► Relevant SPME and GC×GC parameters were considered. ► Structured GC×GC chromatogram were exploited to simplify the in-depth characterization of urine. Metabolomics represents an emerging issue that can aid in the diagnosis and/or prognosis of different diseases. Metabolomic study of urine is particularly interesting as it can be on the base of the developing of new faster and non-invasive methodologies. In response to this actual trend, comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC×GC-ToFMS) combined with headspace solid phase microextraction (HS-SPME) is applied, for the first time to our knowledge, to the untargeted and comprehensive study of the volatile composition of human urine. From a total of ca. 700 compounds detected per sample, 294 were tentatively identified and distributed over the chemical families of hydrocarbons, amines, amides, esters, ketones, aldehydes, alcohols, carboxylic acids, ethers, nitriles, halides, sulfides, thiols, terpenoids, and heterocyclic compounds. To our knowledge, this is the most complete information available so far about whole human urine volatile composition, which represents a valuable data for future advanced studies in the clinical field based on urine fingerprinting. Relevant SPME and GC×GC parameters were considered. Complex sample characterization of human urine is significantly simplified due to the structured GC×GC chromatogram that produces distinct spaces for metabolite chemical families. Furthermore, the potential of this methodology in health related applications was explored by comparing the urinary volatile profiles between smoker (high-risk population for lung cancer) vs. non-smoker adults, focusing on metabolites related to oxidative stress (aliphatic alkanes and aldehydes). In spite of the small sample numbers considered, the results suggest that the urinary volatile profiles may be useful for differentiating subjects with different physiological conditions, thus making it worth to further explore its diagnostic potential.
AbstractList ► HS-SPME/GC×GC-ToFMS was developed for urine metabolite profiling. ► Hundreds of compounds were detected by the developed methodology. ► Relevant SPME and GC×GC parameters were considered. ► Structured GC×GC chromatogram were exploited to simplify the in-depth characterization of urine. Metabolomics represents an emerging issue that can aid in the diagnosis and/or prognosis of different diseases. Metabolomic study of urine is particularly interesting as it can be on the base of the developing of new faster and non-invasive methodologies. In response to this actual trend, comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC×GC-ToFMS) combined with headspace solid phase microextraction (HS-SPME) is applied, for the first time to our knowledge, to the untargeted and comprehensive study of the volatile composition of human urine. From a total of ca. 700 compounds detected per sample, 294 were tentatively identified and distributed over the chemical families of hydrocarbons, amines, amides, esters, ketones, aldehydes, alcohols, carboxylic acids, ethers, nitriles, halides, sulfides, thiols, terpenoids, and heterocyclic compounds. To our knowledge, this is the most complete information available so far about whole human urine volatile composition, which represents a valuable data for future advanced studies in the clinical field based on urine fingerprinting. Relevant SPME and GC×GC parameters were considered. Complex sample characterization of human urine is significantly simplified due to the structured GC×GC chromatogram that produces distinct spaces for metabolite chemical families. Furthermore, the potential of this methodology in health related applications was explored by comparing the urinary volatile profiles between smoker (high-risk population for lung cancer) vs. non-smoker adults, focusing on metabolites related to oxidative stress (aliphatic alkanes and aldehydes). In spite of the small sample numbers considered, the results suggest that the urinary volatile profiles may be useful for differentiating subjects with different physiological conditions, thus making it worth to further explore its diagnostic potential.
Metabolomics represents an emerging issue that can aid in the diagnosis and/or prognosis of different diseases. Metabolomic study of urine is particularly interesting as it can be on the base of the developing of new faster and non-invasive methodologies. In response to this actual trend, comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC×GC-ToFMS) combined with headspace solid phase microextraction (HS-SPME) is applied, for the first time to our knowledge, to the untargeted and comprehensive study of the volatile composition of human urine. From a total of ca. 700 compounds detected per sample, 294 were tentatively identified and distributed over the chemical families of hydrocarbons, amines, amides, esters, ketones, aldehydes, alcohols, carboxylic acids, ethers, nitriles, halides, sulfides, thiols, terpenoids, and heterocyclic compounds. To our knowledge, this is the most complete information available so far about whole human urine volatile composition, which represents a valuable data for future advanced studies in the clinical field based on urine fingerprinting. Relevant SPME and GC×GC parameters were considered. Complex sample characterization of human urine is significantly simplified due to the structured GC×GC chromatogram that produces distinct spaces for metabolite chemical families. Furthermore, the potential of this methodology in health related applications was explored by comparing the urinary volatile profiles between smoker (high-risk population for lung cancer) vs. non-smoker adults, focusing on metabolites related to oxidative stress (aliphatic alkanes and aldehydes). In spite of the small sample numbers considered, the results suggest that the urinary volatile profiles may be useful for differentiating subjects with different physiological conditions, thus making it worth to further explore its diagnostic potential.
Metabolomics represents an emerging issue that can aid in the diagnosis and/or prognosis of different diseases. Metabolomic study of urine is particularly interesting as it can be on the base of the developing of new faster and non-invasive methodologies. In response to this actual trend, comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC X GC-ToFMS) combined with headspace solid phase microextraction (HS-SPME) is applied, for the first time to our knowledge, to the untargeted and comprehensive study of the volatile composition of human urine. From a total of ca. 700 compounds detected per sample, 294 were tentatively identified and distributed over the chemical families of hydrocarbons, amines, amides, esters, ketones, aldehydes, alcohols, carboxylic acids, ethers, nitriles, halides, sulfides, thiols, terpenoids, and heterocyclic compounds. To our knowledge, this is the most complete information available so far about whole human urine volatile composition, which represents a valuable data for future advanced studies in the clinical field based on urine fingerprinting. Relevant SPME and GC X GC parameters were considered. Complex sample characterization of human urine is significantly simplified due to the structured GC X GC chromatogram that produces distinct spaces for metabolite chemical families. Furthermore, the potential of this methodology in health related applications was explored by comparing the urinary volatile profiles between smoker (high-risk population for lung cancer) vs. non-smoker adults, focusing on metabolites related to oxidative stress (aliphatic alkanes and aldehydes). In spite of the small sample numbers considered, the results suggest that the urinary volatile profiles may be useful for differentiating subjects with different physiological conditions, thus making it worth to further explore its diagnostic potential.
Author Caldeira, Michael
Carrola, Joana
Cruz, Nádia
Rocha, Sílvia M.
Santos, Magda
Duarte, Iola F.
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  surname: Duarte
  fullname: Duarte, Iola F.
  organization: CICECO, Departamento de Química, Universidade de Aveiro, 3810-193 Aveiro, Portugal
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Keywords Solid phase microextraction
Urine
Metabolomics
Comprehensive two-dimensional gas chromatography
Time of flight mass spectrometry
Structurally ordered chromatograms
Language English
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Snippet ► HS-SPME/GC×GC-ToFMS was developed for urine metabolite profiling. ► Hundreds of compounds were detected by the developed methodology. ► Relevant SPME and...
Metabolomics represents an emerging issue that can aid in the diagnosis and/or prognosis of different diseases. Metabolomic study of urine is particularly...
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StartPage 155
SubjectTerms Adult
adults
alcohols
aldehydes
alkanes
amides
amines
carboxylic acids
clinical trials
Comprehensive two-dimensional gas chromatography
esters
ethers
Female
Gas Chromatography-Mass Spectrometry - methods
halides
headspace analysis
heterocyclic compounds
Humans
ketones
lung neoplasms
Male
mass spectrometry
metabolites
Metabolome
Metabolomics
Metabolomics - methods
Middle Aged
Multivariate Analysis
nitriles
Organic Chemicals - chemistry
Organic Chemicals - classification
Organic Chemicals - urine
oxidative stress
prognosis
Solid phase microextraction
Solid Phase Microextraction - methods
Structurally ordered chromatograms
sulfides
terpenoids
thiols
Time of flight mass spectrometry
Urinalysis - methods
Urine
volatile compounds
Title Exploring the human urine metabolomic potentialities by comprehensive two-dimensional gas chromatography coupled to time of flight mass spectrometry
URI https://dx.doi.org/10.1016/j.chroma.2012.06.067
https://www.ncbi.nlm.nih.gov/pubmed/22776727
https://www.proquest.com/docview/1635033237
https://www.proquest.com/docview/1694477046
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