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在高级氧化工艺降解 N-亚硝胺过程中致突变性的发展。

Development of mutagenicity during degradation of N-nitrosamines by advanced oxidation processes.

机构信息

Eawag, Swiss Federal Institute of Aquatic Science and Technology, Überlandstrasse 133, P.O. Box 611, CH-8600 Dübendorf, Switzerland.

Eawag, Swiss Federal Institute of Aquatic Science and Technology, Überlandstrasse 133, P.O. Box 611, CH-8600 Dübendorf, Switzerland; School of Architecture, Civil and Environmental Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), GR A1 465, Station 2, CH-1015 Lausanne, Switzerland; Institute of Biogeochemistry and Pollutant Dynamics, ETH Zürich Universitätstrasse 16, CH-8092 Zürich, Switzerland.

出版信息

Water Res. 2014 Dec 1;66:399-410. doi: 10.1016/j.watres.2014.08.012. Epub 2014 Aug 21.

Abstract

Development of mutagenicity of five N-nitrosamines (N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA), N-nitrosodi-n-propylamine (NDPA), N-nitrosopyrrolidine (NPYR) and N-nitrosodiphenylamine (NDPhA)) was investigated during oxidative processes involving UV-photolysis, ozone and OH radicals. The mutagenicity was detected by the Ames test with 3 different strains, TA98, TAMix and YG7108, a strain which is sensitive for N-nitrosamines, in presence and absence of metabolic activation (S9). UV photolysis of mutagenic N-nitrosamines (NDMA, NDEA, NDPA and NPYR) leads to the removal of their specific mutagenic activity as detected in YG7108 in the presence of S9. A formation of mutagens during UV photolysis was detected only in case of NDPhA in the strain TA98. Oxidation products of NDMA, NDEA and NDPhA did not show any significant mutagenicity in the strains used, whereas oxidation of NDPA and NPYR by hydroxyl radicals seems to lead to the formation of direct mutagens (mutagenic in the absence of S9) in YG7108 and TAMix. Oxidation by hydroxyl radicals of N-nitrosamines with chains longer than ethyl can mimic metabolic activation of N-nitrosamines in vivo.

摘要

研究了五种 N-亚硝胺(N-亚硝二甲胺(NDMA)、N-亚硝二乙胺(NDEA)、N-亚硝二正丙胺(NDPA)、N-亚硝吡咯烷(NPYR)和 N-亚硝二苯胺(NDPhA))在涉及 UV 光解、臭氧和 OH 自由基的氧化过程中的致突变性发展。使用 Ames 试验检测致突变性,该试验使用了 3 种不同的菌株 TA98、TAMix 和 YG7108,其中 YG7108 对 N-亚硝胺敏感,存在和不存在代谢激活(S9)的情况下进行检测。具有致突变性的 N-亚硝胺(NDMA、NDEA、NDPA 和 NPYR)的 UV 光解导致其在 S9 存在下 YG7108 中检测到的特定致突变活性丧失。仅在 TA98 菌株中检测到 NDPhA 在 UV 光解过程中形成致突变剂。NDMA、NDEA 和 NDPhA 的氧化产物在所用菌株中没有显示出任何显著的致突变性,而羟基自由基对 NDPA 和 NPYR 的氧化似乎导致 YG7108 和 TAMix 中形成直接致突变剂(无需 S9 即可致突变)。长链 N-亚硝胺(乙基以上)的羟基自由基氧化可以模拟体内 N-亚硝胺的代谢激活。

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