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Mass spectrometry radiolabelling

Other methods of sensitive detection of radiotracers have been developed more recently. Eourier transform nmr can be used to detect (nuclear spin 1/2), which has an efficiency of detection - 20% greater than that of H. This technique is useful for ascertaining the position and distribution of tritium in the labeled compound (14). Eield-desorption mass spectrometry (fdms) and other mass spectral techniques can be appHed to detection of nanogram quantities of radiolabeled tracers, and are weU suited for determining the specific activity of these compounds (15). [Pg.439]

Tkn assay using the hard nucleophile cyanide was described in Section 7.5.1.2, where non-radiolabeled KCN was used to detect the presence of cyanide adducts using mass spectrometry. However, by using K CN, it is possible to make this a quantitative assay by assessing the amount of cyanide incorporated into a non-radiolabeled test... [Pg.157]

Zhao, W., Zhang, H., Zhu, M., Warrack, B., Ma, L., Humphreys, W. G., and Sanders, M. (2006). An integrated method for quantification and identification of radiolabeled metabolites Application of chip-based nanoelectrospray and mass defect filter techniques. In Proceedings of the 54th ASMS Conference on Mass Spectrometry and Allied Topics, Seattle, WA. [Pg.251]

Cheng, Z., Winant, R. C., and Gambhir, S. S. (2005). A new strategy to screen molecular imaging probe uptake in cell culture without radiolabeling using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. J. Nucl. Med. 46 878-886. [Pg.379]

From a medicinal chemist s perspective, nuclear magnetic resonance (NMR) was still the analytical tool of choice, whereas mass spectrometry, infrared (IR), and elemental analyses completed the necessary ensemble of analytical structure confirmation. Synthesis routines were capable of generating several milligrams of product, which is more than adequate for proton and carbon NMR experiments. For analyses that involved natural products, metabolites, or synthetic impurities, time-consuming and often painstaking isolation methods were necessary, followed by expensive scale-up procedures, to obtain the necessary amount of material for an NMR experiment. In situations that involved trace-mixture analysis, radiolabeling approaches were often used in conjunction with various formats of chromatographic separation. [Pg.37]

This paper is the only one in the liquid chromatography portion of this symposium which will attempt to deal with chromatography specifically from the viewpoint of the pesticide metabolism chemist. A residue analyst knows what compound he must analyze for, and develops his method with the properties of that substance in mind. On the other hand, the pesticide metabolism chemist has a different problem. At the conclusion of the treatment, exposure, and harvest phases of a radiolabeled metabolism study, he divides his material into appropriate samples, and extracts each sample with selected solvents to obtain the radioactive materials in soluble form. Typically these extracts consist of low levels (ppm) of carbon-14 labeled metabolites in a complicated mixture of normal natural products from the plant, animal, or soil source. The identity of each metabolite is unknown, and each must be isolated from the natural background and from other labeled metabolites in sufficient quantity and in adequate purity for identification studies, usually by mass spectrometry. The situation is rather like looking for the proverbial "needle in the haystack" when one does not know the size, shape,or composition of the needle, or even how many needles there are in the stack. At this point a separation technique must be selected with certain important requirements in mind. [Pg.1]

Radiolabeling Method Associated with Accelerator Mass Spectrometry... [Pg.317]


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See also in sourсe #XX -- [ Pg.85 ]




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