首页> 外文期刊>Chromatographia >Development of an Analytical Method for Strong Mutagens/Carcinogens, 3,9-Dinitrofluoranthene and Dinitropyrene Isomers, in the Environment and Their Particle-Size Distribution in Airborne Particles
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Development of an Analytical Method for Strong Mutagens/Carcinogens, 3,9-Dinitrofluoranthene and Dinitropyrene Isomers, in the Environment and Their Particle-Size Distribution in Airborne Particles

机译:环境中强突变体/致癌物,3,9-二硝基荧蒽和二硝基py异构体的分析方法及其在空中颗粒中的粒径分布

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3,9-Dinitrofluoranthene (DNF) and 1,3-, 1,6-, and 1,8-dinitropyrene (DNP) isomers are classified as "possible human carcinogens (Group 2B)" by the International Agency for Research on Cancer (IARC). In the present study, we developed an analytical method for DNF and DNP isomers, which is composed of efficient purification of nitroarenes from impurities and separation of nitroarenes from each other using high-performance liquid chromatography (HPLC) and two-dimensional HPLC analysis. These nitroarenes are reduced to corresponding aminoarenes online and sensitively quantified by their fluorescence. We adopted this analytical method for surface soil and airborne particle samples. In the chromatograms of HPLC analysis, DNF and DNP isomers were sufficiently separated from each other and no interfering peaks were observed around DNF and DNP isomers. DNF and 1,3-, 1,6-, and 1,8-DNP isomers were detected in the ranges of 47-579, 27-165, 30-238, and 34-228 pg g(-1) of soil, respectively, from all analyzed samples (n = 6). The contribution ratios of DNF to the mutagenicity toward Salmonella typhimurium TA98 without a metabolic system (S9) were high in the range of 11.6-36.6 %. When classified airborne particles, namely, < 1.1, 1.1-2.0, 2.0-3.3, 3.3-7.0, and > 7.0 mu m in size, were analyzed, amounts of DNF were 64, 14, 13, 6, and 5 fg m(-3), respectively, and DNF tended to be detected in smaller airborne particles. This is the first report on an analytical method for DNF in the environment and the particle-size distribution of DNF in airborne particles.
机译:国际癌症研究机构将3,9-二硝基荧蒽(DNF)和1,3-,1,6-和1,8-二硝基py(DNP)异构体归类为“可能的人类致癌物(第2B组)”( IARC)。在本研究中,我们开发了一种DNF和DNP异构体的分析方法,该方法包括使用杂质进行高效液相色谱(HPLC)和二维HPLC分析,从杂质中高效纯化硝基芳烃,并将硝基芳烃彼此分离。这些硝基芳烃在线还原为相应的氨基芳烃,并通过其荧光灵敏地定量。我们对表层土壤和空气中的颗粒样品采用了这种分析方法。在HPLC分析的色谱图中,DNF和DNP异构体彼此充分分离,并且在DNF和DNP异构体周围未观察到干扰峰。在47-579、27-165、30-238和34-228 pg g(-1)的土壤中检测到DNF和1,3-,1,6-和1,8-DNP异构体,分别来自所有分析样本(n = 6)。在没有代谢系统(S9)的情况下,DNF对鼠伤寒沙门氏菌TA98致突变性的贡献率很高,在11.6-36.6%的范围内。分析分类的空气传播颗粒,即<1.1、1.1-2.0、2.0-3.3、3.3-7.0和> 7.0微米时,DNF的量为64、14、13、6和5 fg m( -3)和DNF倾向于在较小的空气传播颗粒中检测到。这是有关环境中DNF的分析方法以及空气中颗粒中DNF粒度分布的第一份报告。

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