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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >A simple method for the parallel quantification of nicotine and major solvent components in electronic cigarette liquids and vaped aerosols
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A simple method for the parallel quantification of nicotine and major solvent components in electronic cigarette liquids and vaped aerosols

机译:电子烟液中尼古丁和主要溶剂组分的平行定量简单方法,并吐温气溶胶

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摘要

An analytical method was developed for the parallel quantitation of nicotine (Nic) and two key solvents (propylene glycol (PG) and vegetable glycerin (VG)) in e-cigarette (EC) liquids before vaping and from aerosols after vaping. For analysis of the EC refill solutions, the samples were diluted by a factor of about 100 in methanol. The aerosol samples generated by a modified international puffing protocol were initially collected on Cambridge filter pads and extracted with methanol. Both types of samples were analyzed by a gas chromatography-flame ionization detector (GC-FID) together with the mass change tracking (MCT) procedure introduced in our earlier study. The recovery of all three target components (Nic/PG/VG) in both EC liquid and aerosol samples was assessed after spiking Nic at four different concentrations (2, 5,10, and 20 mg g(-1)) in the e-solutions (prepared in the laboratory at three different PG:VG mass ratios of 10:0, 5:5, and 0:10). The method recoveries of Nic, PG, and VG in the e-liquid samples were 96.0 +/- 1.0, 96.0 +/- 1.2, and 101.4 +/- 6.9%, respectively, while those in the aerosol samples were slightly lower at 94.7 +/- 5.6, 85.5 +/- 3.0, and 91.4 +/- 15.7%, respectively. The amounts of VG and Nic in the e-liquid had a significant influence on the emission factors of PG, VG, and Nic. The detection limit values (ng) were 036 (Nic), 0.72 (PG), and 8.15 (VG) for the liquid samples and 0.51 (Nic), 0.96 (PG), and 3.99 (VG) for the aerosol samples. Overall, this method was reliable enough to determine each target in both liquid and aerosol samples. (C) 2017 Elsevier B.V. All rights reserved.
机译:在Vaping之后,开发了在E形卷烟(EC)液体中的尼古丁(NIC)和两种关键溶剂(丙二醇(PG)和植物甘油(Vg))的分析方法,并在蒸煮后从气溶胶中进行。为了分析EC再填充溶液,将样品稀释在甲醇中约100系列。最初在剑桥过滤焊盘上收集改性国际膨化方案产生的气溶胶样品,并用甲醇提取。通过将气相色谱 - 火焰电离检测器(GC-FID)一起分析两种类型的样品,以及我们之前研究中引入的质量变化跟踪(MCT)程序。在E-在e-以四种不同浓度(2,5,10和20mg(-1))施用NIC后评估EC液体和气溶胶样品中的所有三种靶分组分(NIC / PG / VG)的回收率溶液(在实验室中以三种不同的pg制备:Vg质量比为10:0,5:5和0:10)。 E-液体样品中NIC,Pg和Vg的方法回收率分别为96.0 +/- 1.0,96.0 +/- 1.2和101.4 +/-±6.9%,而气溶胶样品中的那些在94.7略低于94.7 +/- 5.6,85.5 +/- 3.0分别为91.4 +/- 15.7%。 E-液体中Vg和Nic的量对PG,VG和NIC的排放因子产生了显着影响。检测限值(Ng)为036(NIC),0.72(PG)和8.15(Vg),用于气溶胶样品的0.51(NIC),0.96(PG),0.96(PG)和3.99(VG)。总的来说,该方法足以确定液体和气溶胶样品中的每个靶标。 (c)2017 Elsevier B.v.保留所有权利。

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