• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

由烯烃与臭氧或二氧化氮通过光化学作用形成诱变化合物。

Photochemical formation of mutagenic compounds from alkenes and ozone or nitrogen dioxide.

作者信息

Victorin K, Ståhlberg M

机构信息

National Institute of Environmental Medicine, Department of Toxicology, Stockholm, Sweden.

出版信息

Environ Mol Mutagen. 1988;11(1):79-90. doi: 10.1002/em.2850110109.

DOI:10.1002/em.2850110109
PMID:3276509
Abstract

In order to investigate the possible formation of mutagenic compounds from alkenes emitted in ambient air, laboratory experiments were performed with Salmonella typhimurium strain TA100 in a small-scale flow-through exposure system. The reaction time for mixtures of alkenes with ozone or nitrogen dioxide was 40 minutes, and the exposure time for bacteria was 6 hours. Ozone gave rise to a small mutagenic effect in combination with 1,3-butadiene or vinyl chloride, with and without ultraviolet (UV) irradiation, but not in combination with ethene or propene. Nitrogen dioxide gave rise to a mutagenic effect in combination with propene, 1,3-butadiene, or vinyl chloride, but only after UV irradiation. The mutagenic activity was highest with butadiene and seemed to be dose-related to the concentration of nitrogen dioxide. Nitrogen dioxide with ethene did not produce a mutagenic effect. A mixture of ethene, propene, and butadiene, tested with ozone or nitrogen dioxide with UV irradiation, did not potentiate each other's mutagenic effect.

摘要

为了研究环境空气中排放的烯烃可能形成诱变化合物的情况,在小型流通式暴露系统中用鼠伤寒沙门氏菌TA100菌株进行了实验室实验。烯烃与臭氧或二氧化氮混合物的反应时间为40分钟,细菌的暴露时间为6小时。臭氧与1,3 - 丁二烯或氯乙烯组合时,无论有无紫外线(UV)照射,都会产生轻微的诱变作用,但与乙烯或丙烯组合时则不会。二氧化氮与丙烯、1,3 - 丁二烯或氯乙烯组合时会产生诱变作用,但仅在紫外线照射后。丁二烯的诱变活性最高,且似乎与二氧化氮浓度呈剂量相关。二氧化氮与乙烯组合不会产生诱变作用。乙烯、丙烯和丁二烯的混合物,在紫外线照射下用臭氧或二氧化氮测试时,不会增强彼此的诱变作用。

相似文献

1
Photochemical formation of mutagenic compounds from alkenes and ozone or nitrogen dioxide.由烯烃与臭氧或二氧化氮通过光化学作用形成诱变化合物。
Environ Mol Mutagen. 1988;11(1):79-90. doi: 10.1002/em.2850110109.
2
Mutagenic activity of ultraviolet-irradiated mixtures of nitrogen dioxide and propene or butadiene.
Environ Res. 1989 Aug;49(2):271-82. doi: 10.1016/s0013-9351(89)80072-6.
3
A method for studying the mutagenicity of some gaseous compounds in Salmonella typhimurium.
Environ Mol Mutagen. 1988;11(1):65-77. doi: 10.1002/em.2850110108.
4
Mutagenic activity of photoreaction products formed from chlorinated ethenes and nitrogen dioxide.由氯乙烯和二氧化氮形成的光反应产物的致突变活性。
Environ Res. 1991 Aug;55(2):178-87. doi: 10.1016/s0013-9351(05)80174-4.
5
Mutagenicity of the reaction products of carbazole in the presence of nitrogen dioxide and nitrocarbazole.
Mutat Res. 1989 May;226(1):55-9. doi: 10.1016/0165-7992(89)90093-6.
6
Mutagenicity of chemicals produced from sodium dodecylbenzenesulfonate by treatment with ozone and ultraviolet irradiation.
Tokushima J Exp Med. 1996 Jun;43(1-2):47-54.
7
Decomposition of linear dodecylbenzenesulfonate by simultaneous treatment with ozone and ultraviolet irradiation: rapid disappearance of formed mutagens.
Chem Pharm Bull (Tokyo). 1992 Jun;40(6):1597-600. doi: 10.1248/cpb.40.1597.
8
Comparison between aqueous-phase and gas-phase exposure protocols for determining the mutagenic potential of nitrogen dioxide and the gas fraction of welding fumes.
Mutat Res. 1987 Jul;188(3):175-84. doi: 10.1016/0165-1218(87)90087-5.
9
Mutagenicity of coal-pyrolyzed products and their photochemical reaction products with nitrogen oxides in Salmonella typhimurium TA98 and TA100.
Mutat Res. 1983 Dec;122(3-4):273-8. doi: 10.1016/0165-7992(83)90006-4.
10
Mutagenicity of the photochemical reaction products of pyrene with nitrogen dioxide.
Mutat Res. 1986 Oct;172(1):19-27. doi: 10.1016/0165-1218(86)90101-1.