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Size distributions of particle-generated hydroxyl radical (·OH) in surrogate lung fluid (SLF) solution and their potential sources

机译:替代肺液(SLF)溶液中颗粒生成的羟基自由基(·OH)及其潜在来源的尺寸分布

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Although it is known that increases in ambient particulate matter (PM) levels are associated with elevated occurrence of adverse health outcomes, the understanding of the mechanisms of PM-related health effects is limited by our knowledge of how particle size and composition are altered subsequent to inhalation through respiratory-deposited processing. Here we present a particle-generated hydroxyl radical (center dot OH) study of the size-resolved particles as particles are inhaled in the human respiratory tract (RT), and we show that accumulation-mode particles are significant factors (71-75%) in center dot OH generation of lung-deposited particles using Multiple-Path Particle Dosimetry (MPPD) model. The ability of PM to catalyze center dot OH generation is mainly related to transition metals, particularly towards the upper regions of the RT (75%), and to quinones deeper in the lung (42-46%). Identification of this generation ability induced by chemical composition has shown that four potential sources (biomass burning, incomplete combustion, mobile & industry, and mineral dust) are responsible for center dot OH generation. With center dot OH-forming ability after PM inhalation implicated as the first step towards revealing the subsequent toxic processes, this work draws a connection between the detailed center dot OH chemistry occurring on size-resolved particles and a possible toxicological mechanism based on chemical composition and sources. (C) 2020 Elsevier Ltd. All rights reserved.
机译:虽然已知环境颗粒物质(PM)水平的增加与不利健康结果的发生升高相关,但是对PM相关健康效应的机制的理解受到我们对粒子尺寸和组成在后续改变的改变通过呼吸沉积加工吸入。在这里,我们提出了粒子产生的羟基 - 自由基(中心点OH)研究的尺寸分离的颗粒作为颗粒在人类呼吸道(RT)中吸入,并且我们表明积累 - 模式颗粒是重要因素(71-75% )使用多径粒子剂量(MPPD)模型,在中心点OH生成肺沉积的颗粒。 PM至催化中心点OH生成的能力主要与过渡金属相关,特别是朝向RT(75%)的上部区域,并在肺中更深的醌(42-46%)。通过化学组成诱导的这种产生能力的鉴定表明,四种潜在来源(生物质燃烧,不完全燃烧,移动和工业和矿物粉尘)负责中心点OH生成。随着中央点OH形成能力后,PM吸入作为揭示随后有毒过程的第一步,该作品在尺寸分辨颗粒上发生的详细中心点OH化学和基于化学成分的可能的毒理学机制之间的联系来源。 (c)2020 elestvier有限公司保留所有权利。

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