Determination of nine volatile N‐nitrosamines in tobacco and smokeless tobacco products by dispersive solid‐phase extraction with gas chromatography and tandem mass spectrometry. Issue 11 (28th April 2016)

• Record Type: Journal Article
• Authors: Lv, Fang; Guo, Junwei; Yu, Fei; Zhang, Tingting; Zhang, Shimin; Cui, Huapeng; Liu, Xianjun; Chen, Li; Liu, Leiyu; Liu, Shaofeng; Xie, Fuwei
• Is Part Of: Journal of separation science. Volume 39:Issue 11(2016)
• Page Start: 2123
• Page End: 2128
• Publication Date: 2016-04-28
• Subjects: Dispersive solid‐phase extraction -- Gas chromatography with tandem mass spectrometry -- N‐nitrosamines -- Tobacco; Separation (Technology) -- Periodicals; Chromatographic analysis -- Periodicals; 543.089
• DOI: 10.1002/jssc.201600037
• Languages: English
• ISSNs: 1615-9306

Abstract

Abstract : A method was developed for the determination of nine volatile N‐nitrosamines in tobacco and smokeless tobacco products. The targets are N ‐nitrosodimethylamine, N ‐nitrosopyrrolidine, N ‐nitrosopiperidine, N ‐nitrosomorpholine, N ‐nitrosoethylmethylamine, N ‐nitrosodiethylamine, N ‐nitrosodipropylamine, N ‐nitrosobuylmethylmine, and N ‐nitrosodibutylamine. The samples were treated by dispersive solid‐phase extraction using 1 g of primary secondary amine and 0.5 g of carbon and then analyzed by gas chromatography with tandem mass spectrometry with an electron impact ion source. The recoveries for the targets ranged from 84 to 118%, with <16% relative standard deviations at three spiking levels of 0.5, 1.25, and 2.5 ng/g. The limits of detection ranged from 0.03 to 0.15 ng/g. With the use of the proposed method, we detected the presence of six nitrosamines in the range of 0.4–30.7 ng/g. The study demonstrated that the method could be used as a rapid, convenient, and high‐throughput method for N‐nitrosamines analysis in tobacco matrix.