1994
DOI: 10.1079/pns19940041
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The use of stable isotopes and mass spectrometry in studying lipid metabolism

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Cited by 8 publications
(3 citation statements)
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“…Independent of these purification procedures, all modern applications utilize isotope dilution for quantification (De Bievre, 1993; Beylot, 1994; Thienpont, Stockl, & de Leenheer, 1995). Stable‐isotope labeled internal standards offer five advantages: As these internal standards are chemically identical and physically similar to the target analytes, maximized correction for errors introduced during sample preparation, storage and detection steps can be achieved. Distinct and parallel detection of unlabeled, endogenous analytes and labeled administered/injected analytes becomes feasible, resulting in minimized uncontrolled, endogenous interferences (e.g., absorption of the studied compound from unknown sources). The fate of different forms of the same compound (free, acetylated, glucuronidated, sulfated) can be specifically monitored provided they are labeled to different degrees. It is possible to study the effect of food structure on the absorption if the compared food types (e.g., solid food or drink) contain the nutrient in differently labeled forms. The fate of nutrients introduced in different modes to the human body (e.g., absorption via lumen or injected into circulation) can be followed distinctly. …”
Section: Technology Reviewmentioning
confidence: 99%
“…Independent of these purification procedures, all modern applications utilize isotope dilution for quantification (De Bievre, 1993; Beylot, 1994; Thienpont, Stockl, & de Leenheer, 1995). Stable‐isotope labeled internal standards offer five advantages: As these internal standards are chemically identical and physically similar to the target analytes, maximized correction for errors introduced during sample preparation, storage and detection steps can be achieved. Distinct and parallel detection of unlabeled, endogenous analytes and labeled administered/injected analytes becomes feasible, resulting in minimized uncontrolled, endogenous interferences (e.g., absorption of the studied compound from unknown sources). The fate of different forms of the same compound (free, acetylated, glucuronidated, sulfated) can be specifically monitored provided they are labeled to different degrees. It is possible to study the effect of food structure on the absorption if the compared food types (e.g., solid food or drink) contain the nutrient in differently labeled forms. The fate of nutrients introduced in different modes to the human body (e.g., absorption via lumen or injected into circulation) can be followed distinctly. …”
Section: Technology Reviewmentioning
confidence: 99%
“…This seems to be a reasonable point at which we might now turn to the more contemporary scene of isotopes in metabolic and nutrition research, a topic that has been the subject of extensive reviews (Halliday & Rennie, 1982;Janghorbani & Young, 1982;Matthews & Bier, 1983;Janghorbani, 1984;Bier, 1987;Wolfe, 1992;Abrams, 1994;Crews et al 1994;Aggett, 1997;Demmelmair et aE. 1997;Patterson, 1997), including presentations at past Nutrition Society meetings (Garlick & Millward, 1972;Halliday & Read, 1981;Buckley, 1988;Beylot, 1994). The focus, for various reasons, will largely be concerned with stable isotopes as tracers, using, where appropriate, some examples taken from the research carried out in our laboratories at the Massachusetts Institute of Technology.…”
Section: Isotopes In Today's Nutrition Researchmentioning
confidence: 99%
“…1997;Patterson, 1997), including presentations at past Nutrition Society meetings (Garlick & Millward, 1972;Halliday & Read, 1981;Buckley, 1988;Beylot, 1994). The focus, for various reasons, will largely be concerned with stable isotopes as tracers, using, where appropriate, some examples taken from the research carried out in our laboratories at the Massachusetts Institute of Technology.…”
Section: Isotopes In Today's Nutrition Researchmentioning
confidence: 99%