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Isotope-dilution mass spectrometry synthesis

There are two main types of internal standards. The first ones are stable isotope labeled (SIL) internal standards. They are compounds in which several atoms in the analytes are replaced by their respective stable isotopes, such as deuterium (2H, D or d), 13C, 15N, or 170. Labeling with the first three isotopes are most common, particularly labeling with deuterium (due to less difficulty in synthesis and therefore less expensive). For examples, raloxifene-d4-6-glucuronide was used as the internal standard for the determination of raloxifene-6-glucuronide [5] and 1, 2, 3, 4-13C4 estrone (PCJEl) was used as the internal standard for estrone (El) [6], The usage of stable isotope labeled internal standards in quantitative LC-MS or GC-MS analysis is often termed as isotope dilution mass spectrometry (IDMS) [7],... [Pg.3]

Dehennin, L., Reiffsteck, A., and Scholler, R. (1980). Simple methods for the synthesis of twenty different, highly enriched deuterium labelled steroids, suitable as internal standards for isotope dilution mass spectrometry. Biomed. Mass Spectrom. 7, 493-499. [Pg.154]

Fig. 2. Trideuterated methoxypyrazines, used as internal standards in quantitative wine analysis by isotope-dilution mass spectrometry, and the corresponding chloropyrazines used in their synthesis... Fig. 2. Trideuterated methoxypyrazines, used as internal standards in quantitative wine analysis by isotope-dilution mass spectrometry, and the corresponding chloropyrazines used in their synthesis...
Rodrlguez-Gonziles, R, Ruiz-Encinar, J., Garcla-Alonso, J. I., and Sanz-Medel, A. (2004) Development of a triple spike methodology for validation of butyltin compounds speciation analysis by isotope dilution mass spectrometry, Part I Synthesis of the spike, characterisation and development of the mathematical equations. J. Anal. At. Spectrom., 19, 685-91. [Pg.315]

Escherichia coli Adenine and adenosine are inhibitory74 and the synthesis of thiamine can be derepressed by culture in their presence.13,75 adth- Mutants are known.76 [l4C]Formate incorporates at C-2 of pyramine without dilution of molar activity. Glycine labeled with stable isotopes was fed to E. coli and the pyramine was analyzed by mass spectrometry. The two carbon atoms of glycine separated during the biosynthesis. The carboxyl was found12 at C-4, and the C-N fragment was the precursor of C-6-N-1. In conclusion, it is beyond doubt that pyramine synthesis follows the AIR pathway in E. coli. [Pg.305]

In the past decade, eight inherited disorders have been linked to specific enzyme defects in the isoprenoid/cholesterol biosynthetic pathway after the finding of abnormally increased levels of intermediate metabolites in tissues and/or body fluids of patients (Table 5.1.1) [7, 9, 10]. Two of these disorders are due to a defect of the enzyme mevalonate kinase, and in principle affect the synthesis of all isoprenoids (Fig. 5.1.1) [5]. The hallmark of these two disorders is the accumulation of mevalonic acid in body fluids and tissues, which can be detected by organic acid analysis, or preferably, by stable-isotope dilution gas chromatography (GC)-mass spectrometry (GC-MS) [2]. Confirmative diagnostic possibilities include direct measurement of mevalonate kinase activities in white blood cells or primary skin fibroblasts [3] from patients, and/or molecular analysis of the MVK gene [8]. [Pg.485]


See other pages where Isotope-dilution mass spectrometry synthesis is mentioned: [Pg.677]    [Pg.23]    [Pg.15]   
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