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根据欧盟烟草制品指令(2014/40/EU)的要求评估优先烟草添加剂:第 2 部分:烟雾化学和体外毒理学。

Assessment of priority tobacco additives per the requirements in the EU Tobacco Products Directive (2014/40/EU): Part 2: Smoke chemistry and in vitro toxicology.

机构信息

Philip Morris International, Philip Morris Products SA, Rue des Usines 90, 2000, Neuchâtel, Switzerland.

Philip Morris International, Philip Morris International Management SA, Avenue de Rhodanie 50, 1001, Lausanne, Switzerland.

出版信息

Regul Toxicol Pharmacol. 2019 Jun;104:163-199. doi: 10.1016/j.yrtph.2019.03.002. Epub 2019 Mar 8.

DOI:10.1016/j.yrtph.2019.03.002
PMID:30858113
Abstract

This publication is part of a series of three publications and describes the non-clinical assessment performed to fulfill the regulatory requirement per Art. 6 (2) of the EU Tobacco Products Directive 2014/40/EU under which Member States shall require manufacturers and importers of cigarettes and Roll Your Own tobacco containing an additive that is included in the priority list established by Commission Implementing Decision (EU) 2016/787 to carry out comprehensive studies (European Comission, 2016). This publication contains the results of a literature search, comprehensive smoke chemistry, additive transfer, and in vitro toxicity studies for the 13 priority additives (carob bean extract, cocoa powder, fenugreek extract, fig juice concentrate, geraniol, glycerol, guaiacol, guar gum, liquorice extract powder, maltol, l-menthol (synthetic), propylene glycol, and sorbitol) commissioned by the members of the Priority Additives Tobacco Consortium to independent Contract Research Organizations. Comparisons of the 39 World Health Organisation smoke emissions in smoke from cigarettes with and without priority additives identified some differences that, with few exceptions, were minor and well within the inherent variability of the analytical method observed for the 3R4F monitor cigarette. Most differences were not statistically significant and did not show consistent additive-related increases or decreases. However, test cigarettes with guar gum showed a statistically significant, additive-related increase in formaldehyde and cadmium; test cigarettes with sorbitol showed a statistically significant, additive-related increase in formaldehyde and acrolein; test cigarettes with glycerol showed a statistically significant, additive-related decrease in phenols, benzo[a]pyrene and N-nitrosoanabasine; and test cigarettes with propylene glycol showed a statistically significant, additive-related decrease in phenol and m + p-cresols. These changes were not observed when the additives were tested as a mixture. None of the increases or decreases in smoke chemistry translated into changes in the in vitro toxicity. Comparisons of the in vitro toxicity of smoke from cigarettes with and without priority additives gave some differences that were minor, well within the inherent variability of the assays, not statistically significant, and did not show consistent additive-related increases or decreases. Thus, it can be concluded that the addition of priority additives had no effect on the in vitro toxicity of the cigarette smoke. The results obtained in our studies are consistent with those in scientific literature.

摘要

本出版物是三部分系列出版物之一,描述了为履行欧盟 2014/40/EU 烟草制品指令第 6(2)条的监管要求而进行的非临床评估,根据该指令,成员国应要求卷烟和含有列入欧盟委员会实施决定(EU)2016/787 建立的优先清单中的添加剂的卷制烟草的制造商和进口商进行全面研究(欧洲委员会,2016 年)。本出版物包含了为独立合同研究组织委托的优先添加剂烟草联盟成员进行的文献检索、全面的烟雾化学、添加剂转移和体外毒性研究的结果,涉及 13 种优先添加剂(角豆提取物、可可粉、葫芦巴提取物、无花果汁浓缩物、香叶醇、甘油、愈创木酚、瓜尔胶、甘草提取物粉、麦芽醇、l-薄荷醇(合成)、丙二醇和山梨糖醇)。在含有和不含有优先添加剂的香烟烟雾中进行的 39 项世界卫生组织烟雾排放物的比较发现了一些差异,除了少数情况外,这些差异都很小,并且在观察到的 3R4F 监测香烟的分析方法的固有可变性范围内。大多数差异没有统计学意义,并且没有显示出一致的与添加剂相关的增加或减少。然而,含有瓜尔胶的测试香烟显示出甲醛和镉的与添加剂相关的、具有统计学意义的增加;含有山梨糖醇的测试香烟显示出甲醛和丙烯醛的与添加剂相关的、具有统计学意义的增加;含有甘油的测试香烟显示出苯酚、苯并[a]芘和 N-亚硝胺的与添加剂相关的、具有统计学意义的减少;含有丙二醇的测试香烟显示出苯酚和间甲酚的与添加剂相关的、具有统计学意义的减少。当添加剂作为混合物进行测试时,没有观察到这些变化。烟雾化学成分的变化并没有转化为体外毒性的变化。在含有和不含有优先添加剂的香烟烟雾的体外毒性比较中,发现了一些差异,这些差异很小,在测定方法的固有可变性范围内,没有统计学意义,并且没有显示出一致的与添加剂相关的增加或减少。因此,可以得出结论,优先添加剂的添加对香烟烟雾的体外毒性没有影响。我们的研究结果与科学文献中的结果一致。

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