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Direct Analysis of δ(2)H and δ(18)O in Natural and Enriched Human Urine Using Laser-Based, Off-Axis Integrated Cavity Output Spectroscopy

Authors :
Douglas S. Baer
Peter Thomson
Steven P. Snaith
Edward L. Melanson
Susan L. Fortson
Manish Gupta
John R. Speakman
Isabelle Chery
Stéphane Blanc
Elena S. F. Berman
Los Gatos Research
Département Ecologie, Physiologie et Ethologie (DEPE-IPHC)
Institut Pluridisciplinaire Hubert Curien (IPHC)
Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)
Division of Endocrinology, metabolism and diabetes
University of Colorado Anschutz [Aurora]
Institute of Biological and Environmental Sciences
University of Aberdeen
State Key Laboratory of Molecular and Developmental Biology
Chinese Academy of Sciences [Changchun Branch] (CAS)
NIH SBIR grant n°2R44RR023231-02A1
Source :
Analytical Chemistry, Analytical Chemistry, American Chemical Society, 2012, 84, pp.9768-9773. ⟨10.1021/ac3016642⟩
Publication Year :
2012
Publisher :
HAL CCSD, 2012.

Abstract

International audience; The stable isotopes of hydrogen (δ(2)H) and oxygen (δ(18)O) in human urine are measured during studies of total energy expenditure by the doubly labeled water method, measurement of total body water, and measurement of insulin resistance by glucose disposal among other applications. An ultrasensitive laser absorption spectrometer based on off-axis integrated cavity output spectroscopy was demonstrated for simple and inexpensive measurement of stable isotopes in natural isotopic abundance and isotopically enriched human urine. Preparation of urine for analysis was simple and rapid (approximately 25 samples per hour), requiring no decolorizing or distillation steps. Analysis schemes were demonstrated to address sample-to-sample memory while still allowing analysis of 45 natural or 30 enriched urine samples per day. The instrument was linear over a wide range of water isotopes (δ(2)H = -454 to +1702 ‰ and δ(18)O = -58.3 to +265 ‰). Measurements of human urine were precise to better than 0.65 ‰ 1σ for δ(2)H and 0.09 ‰ 1σ for δ(18)O for natural urines, 1.1 ‰ 1σ for δ(2)H and 0.13 ‰ 1σ for δ(18)O for low enriched urines, and 1.0 ‰ 1σ for δ(2)H and 0.08 ‰ 1σ for δ(18)O for high enriched urines. Furthermore, the accuracy of the isotope measurements of human urines was verified to better than ±0.81 ‰ in δ(2)H and ±0.13 ‰ in δ(18)O (average deviation) against three independent isotope-ratio mass spectrometry laboratories. The ability to immediately and inexpensively measure the stable isotopes of water in human urine is expected to increase the number and variety of experiments which can be undertaken.

Details

Language :
English
ISSN :
00032700 and 15206882
Database :
OpenAIRE
Journal :
Analytical Chemistry, Analytical Chemistry, American Chemical Society, 2012, 84, pp.9768-9773. ⟨10.1021/ac3016642⟩
Accession number :
edsair.doi.dedup.....5f78932180286efe13431d655c35219e
Full Text :
https://doi.org/10.1021/ac3016642⟩