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Analytical and Bioanalytical Chemistry

, Volume 396, Issue 8, pp 2987–2995 | Cite as

Evaluation of potential breath biomarkers for active smoking: assessment of smoking habits

  • Monica Alonso
  • Mar Castellanos
  • Juan M. Sanchez
Original Paper

Abstract

Different compounds have been reported as biomarkers of a smoking habit, but, to date, there is no appropriate biomarker for tobacco-related exposure because the proposed chemicals seem to be nonspecific or they are only appropriate for short-term exposure. Moreover, conventional sampling methodologies require an invasive method because blood or urine samples are required. The use of a microtrap system coupled to gas chromatography–mass spectrometry analysis has been found to be very effective for the noninvasive analysis of volatile organic compounds in breath samples. The levels of benzene, 2,5-dimethylfuran, toluene, o-xylene, and m- p-xylene have been analyzed in breath samples obtained from 204 volunteers (100 smokers, 104 nonsmokers; 147 females, 57 males; ages 16 to 53 years). 2,5-Dimethylfuran was always below the limit of detection (0.005 ppbv) in the nonsmoker population and always detected in smokers independently of the smoking habits. Benzene was only an effective biomarker for medium and heavy smokers, and its level was affected by smoking habits. Regarding the levels of xylenes and toluene, they were only different in heavy smokers and after short-term exposure. The results obtained suggest that 2,5-dimethylfuran is a specific breath biomarker of smoking status independently of the smoking habits (e.g., short- and long-term exposure, light and heavy consumption), and so this compound might be useful as a biomarker of smoking exposure.

Figure

Extracted GC-MS chromatograms (m/z=78, 91, and 96) from a smoker and a healthy nonsmoker person.

Keywords

Breath biomarkers Smoking 2,5-Dimethylfuran Benzene 

Notes

Acknowledgements

We gratefully acknowledge the financial support of the University of Girona (project # 003798, R+D grants within the framework of IdIBGi 2006) and MICINN (project # CTM2008-06847-C02-02/TECNO). M. Alonso acknowledges the Spanish Ministry of Education for her research grant (AP2008-01628). We would like to thank the staff and students who have participated in the study.

Supplementary material

216_2010_3524_MOESM1_ESM.pdf (437 kb)
ESM 1 (PDF 437 kb)

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Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Monica Alonso
    • 1
  • Mar Castellanos
    • 2
    • 3
  • Juan M. Sanchez
    • 1
    • 3
  1. 1.Department of ChemistryUniversity of GironaGeronaSpain
  2. 2.Department of NeurologyDr. Josep Trueta University HospitalGeronaSpain
  3. 3.Girona Biomedical Research Institute (IdIBGi)GeronaSpain

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