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关于将一种使用质谱法分析电子烟液中尼古丁、甘油和丙二醇的标准操作规程的使用范围进行扩展。

On the extension of the use of a standard operating procedure for nicotine, glycerol and propylene glycol analysis in e-liquids using mass spectrometry.

作者信息

Turina Alessia, Passoni Alice, Gallus Silvano, Lugo Alessandra, Klerx Walther, Talhout Reinskje, Fayokun Ranti, Vardavas Constantine, Davoli Enrico

机构信息

Laboratory of Mass Spectrometry, Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milan, Italy.

Department of Medical Epidemiology, Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), Milan, Italy.

出版信息

Tob Induc Dis. 2024 Sep 11;22. doi: 10.18332/tid/191823. eCollection 2024.

Abstract

INTRODUCTION

Standard operating procedures (SOP), accessible to several laboratories, are essential for product verification. EU-JATC (European-Joint Action on Tobacco Control) SOP and the WHO TobLabNet (World Health Organization Tobacco Laboratories Network) SOP (SOP11) are available standard methodologies to measure nicotine, glycerol, and propylene glycol, and propose mass spectrometer (MS) as an alternative method to flame ionization detector (FID). This study conducted a comparison between FID and MS concentration results, following the MS method described in SOP11.

METHODS

In May 2020, five test e-liquids in replicates (A-E) were prepared at the Istituto di Ricerche Farmacologiche Mario Negri and sent, with SOP 11, validation document and results datasheet to 32 different laboratories all over the world from WHO TobLabNet and EU-JATC (18 from JATC, ten from WHO TobLabNet and four academic laboratories). Among thirty-two independent laboratories that participated in the study, results were received from 30 laboratories.

RESULTS

The e-liquids analyses, using the two approaches, were compared. Of the 30 laboratories surveyed, 21 utilized the FID approach exclusively, 7 opted for MS detection, and 2 employed both methods. The findings demonstrated that the gas chromatography-mass spectrometry (GC-MS) method offers comparable analytical capabilities regarding accuracy and precision for nicotine, glycerol, and propylene glycol to the FID approach. Through Pearson's correlation test with r≃1 showing a positive correlation between GC-FID and GC-MS data, and the Student's t-test, no significant differences between the two approaches were revealed, showing p>0.005 for almost all three analytes in all samples.

CONCLUSIONS

This study indicates that it is possible to apply the available EU-JATC SOP and the WHO TobLabNet SOP11 even in laboratories that do not have access to an FID, for example, to analyze flavors, trace compounds or carcinogenic, mutagenic, or toxic for reproduction (CMR) in electronic cigarette liquids.

摘要

引言

可供多个实验室使用的标准操作规程(SOP)对于产品验证至关重要。欧盟烟草控制联合行动(EU-JATC)的SOP和世界卫生组织烟草实验室网络(WHO TobLabNet)的SOP(SOP11)是用于测量尼古丁、甘油和丙二醇的可用标准方法,并提议将质谱仪(MS)作为火焰离子化检测器(FID)的替代方法。本研究按照SOP11中描述的MS方法,对FID和MS的浓度结果进行了比较。

方法

2020年5月,在马里奥·内格里药理研究所制备了五份重复的测试电子烟液(A-E),并将其与SOP 11、验证文件和结果数据表一起发送给来自WHO TobLabNet和EU-JATC的全球32个不同实验室(18个来自JATC,10个来自WHO TobLabNet,4个学术实验室)。在参与该研究的32个独立实验室中,收到了30个实验室的结果。

结果

对使用两种方法的电子烟液分析进行了比较。在接受调查的30个实验室中,21个仅采用FID方法,7个选择MS检测,2个同时使用两种方法。研究结果表明,气相色谱-质谱联用(GC-MS)方法在尼古丁、甘油和丙二醇的准确性和精密度方面,与FID方法具有相当的分析能力。通过Pearson相关检验(r≃1表明GC-FID和GC-MS数据之间呈正相关)以及Student's t检验,未发现两种方法之间存在显著差异,所有样品中几乎所有三种分析物的p值均>0.005。

结论

本研究表明,即使在没有FID的实验室中,也可以应用现有的欧盟烟草控制联合行动SOP和世界卫生组织烟草实验室网络SOP11来分析电子烟液中的香料、痕量化合物或致癌、致突变或生殖毒性(CMR)物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b5/11389164/b97742e76cfa/TID-22-157-g001.jpg

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