烟草和烟雾的HPHC测试以检验香烟的时间变异性

Rana Tayyarah, M. Morton, J. Flora
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摘要

分析了商业卷烟中烟草和烟雾中的有害和潜在有害成分(HPHCs),以调查一周、一年和三年的时间产品变异性独立于分析变异性。在3年的时间里,从全球市场收集具有各种设计特征的卷烟,储存并同时检测HPHCs,以尽量减少分析差异;参考卷烟3R4F的重复检测作为研究设计的分析对照。发现物理参数是相对一致的。没有注意到基于混合类型、烟雾分析物基质或HPHC产量大小的变异性趋势。与燃烧相关的HPHCs总体变化不大。发现烟草相关化合物的长期批次变异性高于短期变异性,后者可能因天气和农艺做法而随时间变化。“焦油”、尼古丁和一氧化碳在多个实验室进行了测试,在所有阶段,实验室与实验室之间的差异比批次与批次之间的差异更大。根据本研究的结果,商业香烟产品似乎具有相对较低的产品变异性。本研究中在非常规控制的分析条件下测试的产品的低分析物可变性表明,随着时间的推移和实验室间研究,分析可变性可能是一般产品测试的总体可变性的重要贡献者。实验室对照和在研究之间和实验室之间使用匹配的参考产品对于评估检测差异和可变性非常重要。
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HPHC Testing of Tobacco and Smoke to Examine Cigarette Temporal Variability
Summary Commercial cigarettes were analyzed for harmful and potentially harmful constituents (HPHCs) in tobacco and smoke to investigate temporal product variability independent of analytical variability over one week, one year, and three years. Cigarettes from the worldwide market with various design features were collected over a 3-year period, stored, and tested concurrently for HPHCs to minimize analytical variability; repeat testing of reference cigarette 3R4F was included as an analytical control for the study design. Physical parameters were found to be relatively consistent. No trends in variability were noted based on blend type, smoke analyte matrix, or magnitude of an HPHC's yield. Combustion-related HPHCs generally showed low variation. Long-term batch-to-batch variability was found to be higher than short-term variability for tobacco-related compounds that have the potential to vary over time due to weather and agronomic practices. “Tar”, nicotine, and carbon monoxide were tested in multiple labs and showed greater lab-to-lab variability than batch-to-batch variability across all phases. Based on the results of this study, commercial cigarette products appear to have relatively low product variability. The low analyte variability noted in this study with products tested under unconventionally controlled analytical conditions serves to indicate that analytical variability may be a significant contributor to overall variability for general product testing over time and in interlaboratory studies. Laboratory controls and using a matched reference product across studies and between laboratories are important to assess testing differences and variability.
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