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评估卷烟烟雾和调味混合物气溶胶的吸入毒性:A/J 小鼠 5 周研究。

Assessment of inhalation toxicity of cigarette smoke and aerosols from flavor mixtures: 5-week study in A/J mice.

机构信息

PMI R&D, Philip Morris International Research Laboratories Pte Ltd, Singapore.

PMI R&D, Philip Morris Products S.A, Neuchâtel, Switzerland.

出版信息

J Appl Toxicol. 2022 Oct;42(10):1701-1722. doi: 10.1002/jat.4338. Epub 2022 Jun 8.

Abstract

Most flavors used in e-liquids are generally recognized as safe for oral consumption, but their potential effects when inhaled are not well characterized. In vivo inhalation studies of flavor ingredients in e-liquids are scarce. A structure-based grouping approach was used to select 38 flavor group representatives (FGR) on the basis of known and in silico-predicted toxicological data. These FGRs were combined to create prototype e-liquid formulations and tested against cigarette smoke (CS) in a 5-week inhalation study. Female A/J mice were whole-body exposed for 6 h/day, 5 days/week, for 5 weeks to air, mainstream CS, or aerosols from (1) test formulations containing propylene glycol (PG), vegetable glycerol (VG), nicotine (N; 2% w/w), and flavor (F) mixtures at low (4.6% w/w), medium (9.3% w/w), or high (18.6% w/w) concentration or (2) base formulation (PG/VG/N). Male A/J mice were exposed to air, PG/VG/N, or PG/VG/N/F-high under the same exposure regimen. There were no significant mortality or in-life clinical findings in the treatment groups, with only transient weight loss during the early exposure adaptation period. While exposure to flavor aerosols did not cause notable lung inflammation, it caused only minimal adaptive changes in the larynx and nasal epithelia. In contrast, exposure to CS resulted in lung inflammation and moderate-to-severe changes in the epithelia of the nose, larynx, and trachea. In summary, the study evaluates an approach for assessing the inhalation toxicity potential of flavor mixtures, thereby informing the selection of flavor exposure concentrations (up to 18.6%) for a future chronic inhalation study.

摘要

大多数用于电子烟液的香精通常被认为可安全用于口服,但它们吸入时的潜在影响尚未得到很好的描述。电子烟液中香精成分的体内吸入研究很少。本研究采用基于结构的分组方法,根据已知和计算机预测的毒理学数据选择 38 种香精代表物(FGR)。这些 FGR 被组合成原型电子烟液配方,并在为期 5 周的吸入研究中与香烟烟雾(CS)进行对比测试。雌性 A/J 小鼠进行全身暴露,每天 6 小时,每周 5 天,分别暴露于空气、主流 CS 或来自以下 3 种气溶胶:(1)含有丙二醇(PG)、蔬菜甘油(VG)、尼古丁(N;2%w/w)和香精(F)混合物的测试配方,低(4.6%w/w)、中(9.3%w/w)或高(18.6%w/w)浓度;或(2)基础配方(PG/VG/N)。雄性 A/J 小鼠在相同的暴露方案下暴露于空气、PG/VG/N 或 PG/VG/N/F-高。治疗组无明显死亡率或生存期中的临床发现,仅在早期暴露适应期间短暂性体重减轻。虽然暴露于香精气溶胶不会引起明显的肺部炎症,但仅会引起喉和鼻腔上皮的轻微适应性变化。相比之下,暴露于 CS 会导致肺部炎症和鼻腔、喉和气管上皮的中度至重度变化。总之,该研究评估了一种评估香精混合物吸入毒性潜力的方法,从而为未来的慢性吸入研究选择香精暴露浓度(高达 18.6%)提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/457a/9545811/0e140baa9b6b/JAT-42-1701-g003.jpg

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