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  • 标题:A method for assessing carcinogenic risk of air fine particle-associated polycyclic aromatic hydrocarbons by considering bioaccessibility in lung fluids
  • 本地全文:下载
  • 作者:Xinlei Liu ; Yuejiao Wang ; Zelin Shen
  • 期刊名称:MethodsX
  • 印刷版ISSN:2215-0161
  • 电子版ISSN:2215-0161
  • 出版年度:2019
  • 卷号:6
  • 页码:558-566
  • DOI:10.1016/j.mex.2019.03.009
  • 语种:English
  • 出版社:Elsevier
  • 摘要:Graphical abstractDisplay OmittedAbstractThis study was conducted to evaluate the inhalation carcinogenic risk of PAHs in biochar fine particles using total concentration-based assessment approach and bioaccessibility-based assessment approach. Only limit PAHs in particles can be released in simulated lung fluids, leading to a low bioaccessibility (only ranging from 0.34% to 1.48% for biochar fine particles and from 3.21% to 44.2% for PM2.5), which would significantly affect health risk assessment. Therefore, bioaccessibility should always be favored over more traditional evaluations based on total concentration, while evaluating inhalation health risks of biochar-bound PAHs. To prove the broad applicability of bioaccessibility-based assessment approaches, we also compared health risk of actual atmospheric particles (PM2.5collected from Nanjing, China) using total concentration-based approaches and bioaccessibility-based approaches.•Proposed bioaccessibility-based approaches for assessing biochar risk are more accurate than traditional total concentration-based approaches;•Proposed bioaccessibility-based approaches can be applied to health risk assessment of actual air particles;•A more practical method was proposed to evaluate the bioaccessibility of PAHs in biochar fine particles or other specific component of atmospheric particle matters: using wet sieving method to prepare fine particles, using volatile organic solvent-drying method to load14C-PAHs on fine particles, and using desorption experiments to determine bioaccessibility of PAHs.
  • 关键词:Biochar fine particles;PM2.5;Polycyclic aromatic hydrocarbons;Simulated lung fluids;Bioaccessibility;Carcinogenic risk assessment
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