Kakimoto Kensaku, Nagayoshi Haruna, Konishi Yoshimasa, Kajimura Keiji, Ohura Takeshi, Hayakawa Kazuichi, Toriba Akira
Osaka Prefectural Institute of Public Health, 1-3-69, Nakamichi, Higashinari-ku, Osaka 537-0025, Japan; Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192, Japan.
Osaka Prefectural Institute of Public Health, 1-3-69, Nakamichi, Higashinari-ku, Osaka 537-0025, Japan.
Chemosphere. 2014 Sep;111:40-6. doi: 10.1016/j.chemosphere.2014.03.072. Epub 2014 Apr 19.
This study estimates atmospheric concentrations of chlorinated polycyclic aromatic hydrocarbons (ClPAHs) and polycyclic aromatic hydrocarbons (PAHs) in East Asia using a Gas Chromatograph with High Resolution Mass Spectrometer (GC-HRMS). ClPAHs are ubiquitously generated from PAHs through substitution, and some ClPAHs show higher aryl hydrocarbon receptor (AhR)-mediated activities than their parent PAHs. Atmospheric particles were collected using a high-volume air sampler equipped with a quartz-fiber filter. We determined the ClPAH concentrations of atmospheric particles collected in Japan (Sapporo, Sagamihara, Kanazawa, and Kitakyushu), Korea (Busan), and China (Beijing). The concentrations of ClPAHs were highest in the winter Beijing sample, where the total mean concentration was approximately 15-70 times higher than in the winter samples from Japan and Korea. The concentrations of Σ19ClPAHs and Σ9PAHs were significantly correlated in the Kanazawa and the Busan samples. This indicates that within those cities ClPAHs and PAHs share the same origin, implying direct chlorination of parent PAHs. Toxic equivalent concentrations (TEQs) of the total ClPAHs and PAHs were lowest in Kanazawa in the summer, reaching 1.18 and 2610fg-TEQm(-3) respectively, and highest in Beijing in the winter, reaching 627 and 4240000fg-TEQm(-3) respectively.
本研究使用配备高分辨率质谱仪的气相色谱仪(GC-HRMS)估算东亚地区大气中氯代多环芳烃(ClPAHs)和多环芳烃(PAHs)的浓度。ClPAHs是由PAHs通过取代反应普遍生成的,一些ClPAHs表现出比其母体PAHs更高的芳烃受体(AhR)介导活性。使用配备石英纤维滤膜的大容量空气采样器收集大气颗粒物。我们测定了在日本(札幌、相模原、金泽和北九州)、韩国(釜山)和中国(北京)采集的大气颗粒物中的ClPAH浓度。北京冬季样本中的ClPAH浓度最高,其总平均浓度比日本和韩国冬季样本中的浓度高出约15至70倍。在金泽和釜山样本中,Σ19ClPAHs和Σ9PAHs的浓度显著相关。这表明在这些城市中,ClPAHs和PAHs具有相同的来源,意味着母体PAHs发生了直接氯化反应。总ClPAHs和PAHs的毒性当量浓度(TEQs)在夏季的金泽最低,分别达到1.18和2610fg-TEQm(-3),而在冬季的北京最高,分别达到627和4240000fg-TEQm(-3)。