Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method

In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tande...

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Veröffentlicht in:Journal of separation science 2020-04, Vol.43 (8), p.1603-1613
Hauptverfasser: Li, Chao, Li, E'xian, Ma, Ming, Liu, Xiuming, You, Junheng, Wu, Yiqin, Jiang, Wei, Liu, Zhihua, Qin, Yunhua
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container_end_page 1613
container_issue 8
container_start_page 1603
container_title Journal of separation science
container_volume 43
creator Li, Chao
Li, E'xian
Ma, Ming
Liu, Xiuming
You, Junheng
Wu, Yiqin
Jiang, Wei
Liu, Zhihua
Qin, Yunhua
description In order to determine six alkaloids (mass fraction) of nicotine, nornicotine, myosmine, anatabine, anabasine, and nicotyrine in tobacco and tobacco products quickly, accurately, and simultaneously, a novel method based on direct analysis of real‐time model in situ ionization technique combined tandem mass spectrometry with a modified sample pretreatment was established, in which experimental parameters such as the type and amount of extraction solvent and injection rate were optimized, respectively. The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. The established method is rapid, reliable, and suitable for the ultrafast determination of six alkaloids in tobacco and tobacco products.
doi_str_mv 10.1002/jssc.201900946
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The samples of five commercial cigarettes and five kinds of tobacco leaves were analyzed by the established method, and the determined values were compared with those obtained using a gas chromatography with mass spectrometry method: (1) Under optimized conditions (30 mL ultrapure water as extraction solvent and with extraction rate of 0.6 mm/s), analysis could be completed within 10 min. (2) The linear range of the method was 0.002–2000 μg/g withR2=0.9957, the recovery ranged from 86.8 to 105.6%, and the limit of detection and the limit of quantification were 0.004–0.835 μg/g and 0.013–2.787 μg/g, respectively. (3) The relative standard deviation between direct analysis of real‐time method and the gas chromatography with mass spectrometry method was 0.34–8.83%. 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subjects Alkaloids
Alkaloids - analysis
Chromatography
Cigarettes
direct analysis
Gas chromatography
Ions
Mass Spectrometry
Nicotine
Parameter modification
Pretreatment
Quadrupoles
Scientific imaging
Solvents
Spectroscopy
Time Factors
Tobacco
Tobacco Products - analysis
ultrapure water
title Simultaneous determination of six alkaloids in tobacco and tobacco products by direct analysis of real‐time triple quadrupole mass spectrometry with a modified pretreatment method
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