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Subscriber access provided by ZHEJIANG UNIV OF TECH Analytical Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Article Acylic Sugar Derivatives for GC/MS Analysis of 13 C-Enrichment during Carbohydrate Metabolism Neil P. J. Price Anal. Chem., 2004, 76 (22), 6566-6574 ? DOI: 10.1021/ac049198m Downloaded from on November 26, 2008 More About This Article Additional resources and features associated with this article are available within the HTML version: ? Supporting Information ? Links to the 1 articles that cite this article, as of the time of this article download ? Access to high resolution figures ? Links to articles and content related to this article ? Copyright permission to reproduce figures and/or text from this article Acylic Sugar Derivatives for GC/MS Analysis of 13C-Enrichment during Carbohydrate Metabolism Neil P. J. Price* Departments of Pharmacology and Physiology, and Anesthesiology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Rochester, New York 14642-8711 Metabolic profiling with stable-isotope tracers in combina- tion with gas chromatography/mass spectrometry (GC/ MS) is a well-established technique for measuring sub- strate redistribution within metabolic pathways. This analysis relies on the ability to localize and quantify the fractional incorporation of 13C isotope into each carbon atom of precursor-derived metabolites. In this paper, several carbohydrate derivatization procedures (peracety- lation, deuterioalditol acetates, and aldononitrile acetates) are evaluated for the positional isotopic information obtained by gas chromatography/electron impact mass spectrometry (GC/EI-MS). These derivatives have been compared for the quantitative evaluation of 13C distribu- tion into isotopomers of 13C-labeled aldoses and ketoses, and the fragmentation pathways for 15 hexoses, pentoses, and amino sugars of biological origin have been assessed. In addition, a new
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