Determination of tobacco alkaloid enantiomers using reversed phase UPLC/MS/MS

被引:18
作者
Ji, Huihua [1 ]
Wu, Ying [1 ]
Fannin, Franklin [2 ]
Bush, Lowell [2 ]
机构
[1] Univ Kentucky, Kentucky Tobacco Res & Dev Ctr, Lexington, KY 40546 USA
[2] Univ Kentucky, Plant & Soil Sci Dept, Lexington, KY 40546 USA
关键词
Agriculture; Analytical chemistry; IN-VIVO; NORNICOTINE; NICOTINE; NITROSONORNICOTINE; SEPARATION; ANABASINE; ANATABINE;
D O I
10.1016/j.heliyon.2019.e01719
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
N'-Nitrosonornicotine (NNN), a carcinogenic tobacco-specific N'-nitrosamine (TSNA), is on the FDA list of harmful and potentially harmful constituents (HPHCs). Nornicotine, a product of the demethylation of nicotine, is the immediate alkaloid precursor for NNN formation. Nicotine, nornicotine and NNN are optically active. The accumulation of the isomers of nicotine, nornicotine, and NNN impacts their biological activity. In this paper, we report the determination of tobacco alkaloid enantiomers (including nicotine, nornicotine, anabasine, and anatabine) in samples of different tobacco lines using a reversed phase ultra-performance liquid chromatography-tandem mass spectrometer (UPLC/MS/MS) method. Current method demonstates excellent detection capability for all alkaloid enantiomers, with correlation coefficients (r(2)) > 0.996 within their linear dynamic ranges. The limit of detection (LOD) and limit of quantitation (LOQ) of all analytes are less than 10 ng/mL and 30 ng/mL, respectively. In addition, their recovery and coefficient of variation (CV%) are within 100-115% and 0.2-3.7%, respectively. The method validated in this paper is simple, fast, and sensitive for the quantification of alkaloid enantiomers in tobacco leaf and has been applied to investigations of tobacco alkaloid enantiomer ratios in different tobacco lines and tobacco products.
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页数:6
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