CORESTA Meeting, Smoke Science/Product Technology, 2011, Graz, ST 11

Determination of N-nitrososarcosine in tobacco and tobacco products using Isotope Dilution Liquid Chromatography Tandem Mass Spectrometry

Labstat International ULC, Kitchener, Ontario, Canada

A simple, fast, selective, and robust analytical method for the determination of N-nitrososarcosine (NSAR) has been developed based on Supported Liquid-Liquid Extraction (SL-L) coupled with Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS). To our knowledge, this is the first LC-MS/MS method for the analysis of NSAR in tobacco. In the past, NSAR has been determined mainly by gas chromatography with a thermal energy analyzer (GC-TEA), using a variety of sample cleanup and derivatization steps. The LC-MS/MS method described here, using an isotope labeled internal standard, adds greater confidence for the determination of NSAR in complex sample matrices such as tobacco. It also uses a relatively simple extraction (2% formic acid) and cleanup procedure compared to existing methods. The new method has been validated using three different control samples (Kentucky reference KY3R4F, smokeless research tobacco control products 1S2 dry snuff and 2S3 moist snuff), and the method exhibits good linearity (R2 ≥ 0.999) over a wide range of concentration (3-2400ng/g). The limit of detection (LOD) is 27.3 ng/g and the limit of quantification (LOQ) is 91.0 ng/g. While no NSAR was detected in KY3R4F, and only a low amount in 2S3, a relatively larger amount of NSAR (550.5±43.7 ng/g, n=100) was found in the dry snuff reference tobacco 1S2. The precision of the method is good (with a relative standard deviation of 7.94% for 1S2 samples), and the method is robust in a commercial laboratory environment, and can be applied to the determination of NSAR in cigarette tobacco and smokeless tobacco products.