Stable quantification

This reaction has been also described for low chlorinated dibenzodioxins. Assuming an identical MS response factor for monoBrDD and monobromohydroxy-biphenyl ether (monoBrDPE) a quantification study shows that monoBrDPE is much more stable towards photolysis compared to monoBrDD, because it accumulates in the mixture of the reaction products. For the dibrominated dibenzodioxins the same reaction (ether fission) is observed but to a minor extent. With triBrDD and higher brominated BrDD no diaryl-ether products are observed at all. 

Chromosome aberrations were detected in lymphocytes of individuals acutely intoxicated by methyl parathion by the inhalation route (Van Bao et al. 1974). Blood samples were taken 3-6 days after exposure and again at 30 and 380 days. A temporary but significant (p<0.05) increase was noted in the frequency of stable chromosomal aberrations in the exposed individuals. The study limitations include small sample size, absence of a control group, lack of quantification of exposure levels, and a possible concomitant exposure to other substances via the dermal route. 

McCann MT, Thompson MM, Gueron IC et al. (1996) Methyl malonic acid quantification by stable isotope dilution gas chromatography-mass spectrometry from filter paper urine samples. Clin Chem 42 9io-9i4. 

Grosch, W., Sen, A., Guth, H., and Zeiler-Hilgart, G. (1990). Quantification of aroma compounds using a stable isotope dUution assay. In "Flavour Science and Technology", (Y. Bressiere and A. F. Thomas, Eds), pp. 191-194. John Wiley Sons, Chichester, England. 

The quantification of gross root production, rhizodeposition, microbial assimilation, and the production of organic materials in soil has made increasing progress ever since stable ( C) and radioactive ( C) carbon isotopes have been used (see Chap. 12). Measurements of soil organic matter dynamics without these isotopes are difficult due to the large amount present as compared to the smaller rates of input. 

The development of new fiber coatings in the near future should further improve the specificity of SPME and overcome some of the observed matrix effects. Quantification by stable isotope dilution gas chromatography/mass spectrometry (GC/MS) may assist in improving analytical performance. Along with the possible application of micro LC and capillary LC columns to in-tube SPME, the development of novel derivatization methods and the potential for the analysis of fumigant pesticides, SPME appears to be a technique with a future in the analysis of pesticide residues in food. 

TI is a very precise and accurate method in stable isotope ratio measurements and quantification of inorganic elements, for example, by isotope dilution mass spectrometry [8]. Because TI is a continuous ion source, it could be coupled to any analyzer that is suitable for such sources. However, because the strength of TI lies in the quantitative precision and accuracy, sector analyzers are preferred to ensure maximum quality. 

For a quantification an addition of stable isotope-labelled analytes, which exhibit the same chromatographic and ionisation behaviour as their unlabelled analogues present in the sample, and which can be... 

The significant relative mass difference (c. 16%) between the two stable isotopes of Li (approximately Li 7.5%, Li 92.5%), coupled with broad elemental dispersion in Earth and planetary materials, makes this a system of considerable interest in fingerprinting geochemical processes, determining mass balances, and in thermometry. Natural mass fractionation in this system is responsible for c. 6% variation among materials examined to date (Fig. 1). Although the modem era of Li isotope quantification has begun, there are still many questions about the Li isotopic compositions of fundamental materials and the nature of fractionation by important mechanisms that are unanswered (e.g., Hoefs 1997). 

Murphey LJ, Hachey DL, Vaughan DE, Brown NJ, Morrow JD. 2001. Quantification of BKl-5, the stable bradykinin plasma metabolite in humans, by a highly accurate liquid chromatographic tandem mass spectrometric assay. Anal Biochem 292 87. 

Wolfe has presented an excellent description of the systematic application of stable and radioactive isotope tracers in determining the kinetics of substrate oxidation, carbon dioxide formation (including C02 breath tests), glucose oxidation, and fat oxidation in normal and diseased states. Quantification of the rate and extent of substrate oxidation can be achieved by using a specific or C-substrate which upon oxidation releases radioactive carbon dioxide. 

Quantification of the separated amino acids is usually performed by using external calibration or the internal standard method. Due to the large differences in chemical structure exhibited by the various amino acids, there is not a single ideal standard for the overall amino acid profile. Nevertheless, a suitable internal standard must be stable to hydrolysis and offer chromatographic resolution. The most popular choices comprise norleucine, norvaline, and a-amino-n-butanoic acid (AABA) [196]. 

Besides C, also other stable isotopes, such as H, or have been applied. An example for the use of is the quantification of the flux partitioning... 

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