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Clinical Chemistry, Vol 41, 1028-1032, Copyright © 1995 by American Association for Clinical Chemistry
Y Lin, SR Dueker, AD Jones, SE Ebeler and AJ Clifford
Department of Nutrition, University of California, Davis 95616, USA.
This noninvasive method for collection and analysis of a wide range of aldehydes and ketones in human breath may enable assessment of lipid peroxidation and metabolic status in vivo. Breath samples are drawn through silica cartridges impregnated with 2,4-dinitrophenylhydrazine, which traps carbonyls as their hydrazone derivatives. The hydrazone derivatives are eluted from the cartridges with acetonitrile, separated by reversed-phase HPLC, and quantified spectrophotometrically. Using this method, we have measured formaldehyde, acetaldehyde, acetone, propanal, 2-butanone, butanal, pentanal, and hexanal. Recoveries of carbonyls added to Douglas bags were > 90%, except for 2-butanone, which was 86.2%. The overall CVs for sampling plus analyzing duplicate aliquots of breath were < 11%. The results indicate that this protocol can be used to monitor changes of carbonyl production by analyzing expired air, which may, with further study, indicate physiological and pathological status.
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D. Smith, P. Spanel, and S. Davies Trace gases in breath of healthy volunteers when fasting and after a protein-calorie meal: a preliminary study J Appl Physiol, November 1, 1999; 87(5): 1584 - 1588. [Abstract] [Full Text] [PDF] |
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