Centre for Analytical Research and Technologies (CART), University of Liege, Belgium.
Research and Development, British American Tobacco, Southampton, UK.
J Chromatogr A. 2018 Dec 21;1581-1582:105-115. doi: 10.1016/j.chroma.2018.10.035. Epub 2018 Oct 19.
A simple direct sample collection/dilution and introduction method was developed using quartz wool and Tenax/sulficarb sorbents for thermal desorption and comprehensive two-dimensional gas chromatography (TD-GC × GC) analyses of volatile organic compounds from vapour phase (VP) fractions of aerosol produced by tobacco heating products (THP1.0) and 3R4F mainstream tobacco smoke (MTS). Analyses were carried out using flame ionisation detection (FID) for semi-quantification and both low and high resolution time-of-flight mass spectrometry (LR/HR-TOFMS) for qualitative comparison and peak assignment. Qualitative analysis was carried out by combining identification data based on linear retention indices (LRIs) with a match window of ±10 index units, mass spectral forward and reverse library searches (from LR and HRTOFMS spectra) with a match factor threshold of >700 (both forward and reverse), and accurate mass values of ± 3 ppm for increased confidence in peak identification. Using this comprehensive approach of data mining, a total of 79 out of 85 compounds and a total of 198 out of 202 compounds were identified in THP1.0 aerosol and in 3R4F MTS, respectively. Among the identified analytes, a set of 35 compounds was found in both VP sample types. Semi-quantitative analyses were carried out using a chemical class-based external calibration method. Acyclic, alicyclic, aromatic hydrocarbons and ketones appeared to be prominent in 3R4F MTS VP, whereas larger amounts of aldehydes, ketones, heterocyclic hydrocarbons and esters were present in THP1.0 aerosol VP. The results demontsrate the capability and versatility of the method for the characterization and comparison of complex aerosol samples and highlighted the relative chemical simplicity of THP1.0 aerosol in comparison to MTS.
开发了一种简单的直接样品采集/稀释方法,使用石英棉和 Tenax/sulficarb 吸附剂进行热解吸和全面二维气相色谱(TD-GC×GC)分析,分析物来自烟草加热产品(THP1.0)和 3R4F 主流烟气(MTS)气溶胶蒸气相(VP)馏分中的挥发性有机化合物。使用火焰离子化检测(FID)进行半定量分析,以及低分辨率和高分辨率飞行时间质谱(LR/HR-TOFMS)进行定性比较和峰归属。定性分析通过结合基于线性保留指数(LRIs)的鉴定数据,在±10 索引单位的匹配窗口内,质量光谱正向和反向库搜索(来自 LR 和 HRTOFMS 光谱),匹配因子阈值>700(正向和反向),以及精确质量值为±3ppm,以提高峰识别的可信度。使用这种综合的数据挖掘方法,总共在 THP1.0 气溶胶和 3R4F MTS 中鉴定出了 79 种化合物中的 85 种和 198 种化合物中的 202 种。在所鉴定的分析物中,有一组 35 种化合物存在于两种 VP 样品类型中。使用基于化学类别的外部校准方法进行半定量分析。无环、脂环、芳烃和酮似乎在 3R4F MTS VP 中较为突出,而醛、酮、杂环烃和酯在 THP1.0 气溶胶 VP 中含量更高。结果表明该方法能够用于复杂气溶胶样品的表征和比较,并突出了 THP1.0 气溶胶相对简单的化学性质,与 MTS 相比。