职业与健康 ›› 2025, Vol. 41 ›› Issue (3): 336-340.

• 论著 • 上一篇    下一篇

电子烟的体外染色体畸变遗传毒性试验研究

卜志超1, 王振屹2, 许赫雷3, 贾玉玲1, 周冬华1, 韦娜1   

  1. 1.国科赛赋(深圳)新药研发科技有限公司,广东 深圳 518110;
    2.人大附中西山学校,北京 100193;
    3.国科赛赋河北医药技术有限公司,河北 廊坊 065500
  • 收稿日期:2024-04-19 修回日期:2024-04-29 出版日期:2025-02-01 发布日期:2025-12-17
  • 通信作者: 韦娜,副研究员,E-mail:weina@safeglp.com
  • 作者简介:卜志超,男,助理研究员,主要从事毒理安全评价工作。

Study on genotoxicity of chromosomal aberrations in vitro of electronic cigarettes

BU Zhichao1, WANG Zhenyi2, XU Helei3, JIA Yuling1, ZHOU Donghua1, WEI Na1   

  1. 1. Guoke SAFE(Shenzhen) New Drug Research Technology Co.,Ltd.,Shenzhen,Guangdong 518110,China;
    2. Xishan School,High School Affiliated to Renmin University of China,Beijing 100193,China;
    3. Guoke SAFE Hebei Pharmaceutical Technology Co.,Ltd,Langfang,Hebei 065500,China
  • Received:2024-04-19 Revised:2024-04-29 Online:2025-02-01 Published:2025-12-17
  • Contact: WEI Na,Associate research fellow,E-mail:weina@safeglp.com

摘要: 目的 在良好实验室规范(good laboratory practice,GLP)条件下检测电子烟体外染色体畸变遗传毒性。方法 参考国际人用药品注册技术协调会(International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use,ICH)S2(R1)、经济合作与发展组织(Organization for Economic Co-operation and Development,OECD)测试指南473染色体畸变试验要求,使用中国仓鼠肺成纤维细胞(Chinese hamster fibroblast cell line,CHL),将悦刻幻影电子烟液最终暴露浓度设置为409.4、136.5、45.5和15.2 μg/mL,另设溶媒对照组、环磷酰胺和丝裂霉素阳性组,暴露约4 h(有或无代谢活化系统,S9)和暴露约24 h(无S9)后收集细胞,台盼蓝染色计数,低渗、固定、滴片、姬姆萨染色后观察1 000个中期相细胞和至少300个中期分裂相下细胞畸变类型,采用Fisher确切概率法比较统计学差异。结果 在各暴露条件下,收集细胞时未见受试物沉淀;在有或无S9代谢活化系统暴露约4 h及无S9代谢活化系统暴露约24 h,各暴露条件下相对细胞群倍增数(%)均>50%,且细胞分裂指数、分裂指数抑制率均在正常值范围内,未见明显细胞毒性;CHL细胞染色体畸变率均未见有意义的升高。结论 在本试验条件下,电子烟未引起CHL细胞染色体结构畸变率有统计学意义的升高,试验结果为阴性。

关键词: 电子烟, 良好实验室规范, 染色体畸变, 遗传毒性

Abstract: Objective To study the genotoxicity of chromosomal aberration in vitro of electronic cigarette under good laboratory practices(GLP). Methods In accordance with the requirements of International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use(ICH)S2(R1) and Organization for Economic Co-operation and Development(OECD) Test Guideline 473 chromosomal aberration test,the Chinese hamster fibroblast cell line(CHL) were used,the final exposure concentrations of Yuekehuanying e-cigarette liquid were set at 409.4,136.5,45.5 and 15.2 μg/mL,while a solvent control group,cyclophosphamide and mitomycin-positive group were set up. The cells were harvested after exposure for approximately 4 hours(with or without metabolic activation system,S9) and approximately 24 hours(without S9). The cells were counted by Trypan blue staining. After hypotonic,fixed,droplet,and Giemsa staining,1 000 metaphase phase cells and at least 300 metaphase division phase cells were observed to analyze the aberration types. Fisher's exact probability method was used to compare statistical differences. Results Under each exposure condition,no test articles were deposited when cells were collected. The relative cell population multiplication(%) was >50% under each exposure condition for approximately 4 hours with or without S9 metabolic activation system and for approximately 24 hours with or without S9,and the cell division index and the inhibition rate of the division index were within the normal range,and no apparent cytotoxicity was observed. There was no significant increase in the chromosome aberration rate of CHL cells. Conclusion Under the conditions of this study,the electronic cigarettes do not cause a significant increase in the chromosome structural aberration rate of CHL cells,so the results of this experiment are negative.

Key words: Electronic cigarettes, Good laboratory practice, Chromosomal aberration, Genotoxicity

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