Ravnum S, Rundén-Pran E, Fjellsbø L M, Dusinska M
Health Effects Laboratory, Environmental Chemistry Department, NILU, PO Box 100, Instituttveien 18, N-2027 Kjeller, Norway.
Health Effects Laboratory, Environmental Chemistry Department, NILU, PO Box 100, Instituttveien 18, N-2027 Kjeller, Norway.
Regul Toxicol Pharmacol. 2014 Jul;69(2):250-5. doi: 10.1016/j.yrtph.2014.04.002. Epub 2014 Apr 18.
Emission and accumulation of carbon dioxide (CO2) in the atmosphere exert an environmental and climate change challenge. An attempt to deal with this challenge is made at Mongstad by application of amines for CO2 capture and storage (CO2 capture Mongstad (CCM) project). As part of the CO2 capture process, nitrosamines and nitramines may be emitted. Toxicological testing of nitrosamines and nitramines indicate a genotoxic potential of these substances. Here we present a risk characterization and assessment for five nitrosamines (N-Nitrosodi-methylamine (NDMA) N-Nitrosodi-ethylamine (NDEA), N-Nitroso-morpholine (NNM), N-Nitroso-piperidine (NPIP), and Dinitroso-piperazine (DNP)) and two nitramines (N-Methyl-nitramine (NTMA), Dimethyl-nitramine (NDTMA)), which are potentially emitted from the CO2 capture plant (CCP). Human health risk assessment of genotoxic non-threshold substances is a heavily debated topic, and no consensus methodology exists internationally. Extrapolation modeling from high-dose animal exposures to low-dose human exposures can be crucial for the final risk calculation. In the work presented here, different extrapolation models are discussed, and suggestions on applications are given. Then, preferred methods for calculating derived minimal effect level (DMEL) are presented with the selected nitrosamines and nitramines.
大气中二氧化碳(CO₂)的排放和累积对环境和气候变化构成了挑战。蒙斯塔德通过应用胺类进行二氧化碳捕集与封存(蒙斯塔德二氧化碳捕集(CCM)项目)来应对这一挑战。作为二氧化碳捕集过程的一部分,亚硝胺和硝胺可能会排放出来。对亚硝胺和硝胺的毒理学测试表明这些物质具有遗传毒性潜力。在此,我们针对五种亚硝胺(N-亚硝基二甲胺(NDMA)、N-亚硝基二乙胺(NDEA)、N-亚硝基吗啉(NNM)、N-亚硝基哌啶(NPIP)和二亚硝基哌嗪(DNP))以及两种硝胺(N-甲基硝胺(NTMA)、二甲基硝胺(NDTMA))进行了风险特征描述和评估,这些物质可能从二氧化碳捕集工厂(CCP)排放出来。对具有遗传毒性的无阈值物质进行人类健康风险评估是一个备受争议的话题,国际上不存在共识性的方法。从高剂量动物暴露外推至低剂量人类暴露的建模对于最终的风险计算可能至关重要。在本文所呈现的工作中,讨论了不同的外推模型,并给出了应用建议。然后,针对选定的亚硝胺和硝胺,介绍了计算导出最小效应水平(DMEL)的首选方法。