| Literature DB >> 33618358 |
Madeleine Werneth1, Jutta Pani1, Ludwig Hofbauer1, Stefan Pummer1, Maria-Theres Weber1, Georg Pour1, Hanspeter Kählig2, Bernhard Mayer-Helm1, Herwig Stepan1.
Abstract
The carcinogenic compound N-nitrososarcosine (NSAR) is found in foods and tobacco products, and its quantification is of great interest. Although the presence of two stereoisomers, E- and Z-NSAR, is well-known, individual investigation of the isomers has not been reported so far. The present study by liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) reveals that (i) the mass spectrometric responses of the isomers differ by a factor of approximately two and (ii) the isomer ratio is unstable in freshly prepared standard solutions. As a consequence, NSAR concentrations determined by LC-ESI-MS/MS are biased if those facts are not taken into account. The method described here overcomes the difficulty of stereospecific response by adjusting the isomer ratio and was applied to 100 tobacco products and fully validated for moist and dry snuff reference materials showing expanded measurement uncertainties of ~20% and limits of quantification of ~20 ng/g.Entities:
Year: 2021 PMID: 33618358 DOI: 10.1093/chromsci/bmab013
Source DB: PubMed Journal: J Chromatogr Sci ISSN: 0021-9665 Impact factor: 1.618