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新型烟草加热产品 THP1.0 的评估。第 6 部分:使用当代筛选方法的体外比较研究。

Assessment of novel tobacco heating product THP1.0. Part 6: A comparative in vitro study using contemporary screening approaches.

机构信息

British American Tobacco, Research and Development Centre, Southampton, Hampshire, SO15 8TL, United Kingdom.

British American Tobacco, Research and Development Centre, Southampton, Hampshire, SO15 8TL, United Kingdom.

出版信息

Regul Toxicol Pharmacol. 2018 Mar;93:62-70. doi: 10.1016/j.yrtph.2017.08.016. Epub 2017 Oct 25.

DOI:10.1016/j.yrtph.2017.08.016
PMID:29080849
Abstract

Cigarette smoking is a major risk factor for many adverse health conditions. Novel tobacco heating products (THPs) heat tobacco, reducing exposure to many of the harmful combustion toxicants in conventional cigarette emissions. In vitro studies have been employed to support the toxicological evaluation of chemicals and complex mixtures, including cigarette smoke. The use of automated robotics platforms for in vitro toxicological screening complements traditional testing approaches. Multiparametric toxicity and oxidative stress endpoints were used to assess in vitro biological responses elicited after exposure to total particulate matter (TPM) from two commercially available THPs, and the reference tobacco product 3R4F, in human bronchial epithelial cells. A luciferase-based reporter gene assay was used to assess antioxidant response element (ARE) transcriptional activation in stably transfected H292 cells after 6 and 24 h exposures. High-content screening was used to assess 10 endpoints normal human bronchial epithelial cells after 4 or 24 h exposures. 3R4F TPM stimulated significant increases in ARE activation (p < 0.005) and moderate activity in HCS cell-based assays compared to THP at comparable doses. THPs showed little or no activity in all assays. HCS techniques can extend safety assessments providing information quickly in the early stages of product innovation and development.

摘要

吸烟是许多不良健康状况的主要危险因素。新型烟草加热产品(THP)加热烟草,减少了传统卷烟烟雾中许多有害燃烧毒物的暴露。体外研究已被用于支持化学物质和复杂混合物的毒理学评估,包括卷烟烟雾。自动化机器人平台用于体外毒理学筛选,补充了传统的测试方法。多参数毒性和氧化应激终点用于评估暴露于两种市售 THP 和参考烟草产品 3R4F 的总颗粒物(TPM)后,人支气管上皮细胞中引发的体外生物学反应。荧光素酶报告基因测定用于评估稳定转染的 H292 细胞中抗氧化反应元件(ARE)转录激活在 6 和 24 小时暴露后的情况。高内涵筛选用于评估暴露 4 或 24 小时后 10 个正常人类支气管上皮细胞的终点。与 THP 相比,3R4F TPM 在可比剂量下刺激 ARE 激活显著增加(p<0.005),并且在基于 HCS 的细胞测定中具有中等活性。THP 在所有测定中几乎没有或没有活性。HCS 技术可以扩展安全性评估,在产品创新和开发的早期阶段快速提供信息。

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