Toxicity Decreases with the Decay of Environmentally Persistent Free Radicals in Particulate Matter from Incomplete Solid Fuel Burning

IF 8.9 2区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Environmental Science & Technology Letters Environ. Pub Date : 2024-05-03 DOI:10.1021/acs.estlett.4c00333
Anyuan Cheng, Xiu Chen, Di Wu and Qing Li*, 
{"title":"Toxicity Decreases with the Decay of Environmentally Persistent Free Radicals in Particulate Matter from Incomplete Solid Fuel Burning","authors":"Anyuan Cheng,&nbsp;Xiu Chen,&nbsp;Di Wu and Qing Li*,&nbsp;","doi":"10.1021/acs.estlett.4c00333","DOIUrl":null,"url":null,"abstract":"<p >Environmentally persistent free radicals (EPFRs) have been linked to the generation of reactive oxygen species (ROS) and adverse health effects. However, there remains a knowledge gap regarding the dynamic changes in reactivity and toxicity during the decay process of EPFRs emitted from incomplete solid fuel burning, which are identified as a primary source of EPFRs. Here, we report the decay behavior of EPFRs in particulate matter (PM) emitted from typical solid fuel burning and the associated ROS generation and cytotoxic effects. The EPFRs in freshly produced PM first undergo rapid exponential decay with lifetimes ranging from 15 to 97 h and are categorized as fast-decay EPFRs. The relative content of fast-decay EPFRs was 40.5 ± 15.3%, while the remaining portion, defined as slow-decay EPFRs, displayed an extremely slow rate of decay. ROS generation and cytotoxicity decreased by 38.8 ± 11.4% and 62.5 ± 12.6%, respectively, following the depletion of fast-decay EPFRs, which were further demonstrated to be responsible for the variations in PM reactivity and toxicity. These new findings underscore the importance of considering the decay process of EPFRs in assessments of PM toxicity.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":null,"pages":null},"PeriodicalIF":8.9000,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science & Technology Letters Environ.","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.estlett.4c00333","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Environmentally persistent free radicals (EPFRs) have been linked to the generation of reactive oxygen species (ROS) and adverse health effects. However, there remains a knowledge gap regarding the dynamic changes in reactivity and toxicity during the decay process of EPFRs emitted from incomplete solid fuel burning, which are identified as a primary source of EPFRs. Here, we report the decay behavior of EPFRs in particulate matter (PM) emitted from typical solid fuel burning and the associated ROS generation and cytotoxic effects. The EPFRs in freshly produced PM first undergo rapid exponential decay with lifetimes ranging from 15 to 97 h and are categorized as fast-decay EPFRs. The relative content of fast-decay EPFRs was 40.5 ± 15.3%, while the remaining portion, defined as slow-decay EPFRs, displayed an extremely slow rate of decay. ROS generation and cytotoxicity decreased by 38.8 ± 11.4% and 62.5 ± 12.6%, respectively, following the depletion of fast-decay EPFRs, which were further demonstrated to be responsible for the variations in PM reactivity and toxicity. These new findings underscore the importance of considering the decay process of EPFRs in assessments of PM toxicity.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
不完全固体燃料燃烧产生的微粒物质中环境持久性自由基的衰变导致毒性降低
环境持久性自由基(EPFRs)与活性氧(ROS)的产生和对健康的不良影响有关。然而,关于不完全固体燃料燃烧排放的环境持久性自由基(EPFRs)在衰变过程中反应性和毒性的动态变化仍然是一个知识空白,而不完全固体燃料燃烧已被确定为环境持久性自由基的主要来源。在这里,我们报告了典型固体燃料燃烧排放的颗粒物(PM)中 EPFRs 的衰变行为以及相关的 ROS 生成和细胞毒性效应。新产生的可吸入颗粒物中的 EPFRs 首先会发生快速指数衰变,寿命从 15 到 97 小时不等,被归类为快速衰变 EPFRs。快衰变 EPFR 的相对含量为 40.5 ± 15.3%,其余部分衰变速度极慢,被定义为慢衰变 EPFR。快衰变 EPFR 消耗殆尽后,ROS 生成和细胞毒性分别降低了 38.8 ± 11.4% 和 62.5 ± 12.6%,这进一步证明了它们是造成 PM 反应性和毒性变化的原因。这些新发现强调了在评估可吸入颗粒物毒性时考虑EPFR衰变过程的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Environmental Science & Technology Letters Environ.
Environmental Science & Technology Letters Environ. ENGINEERING, ENVIRONMENTALENVIRONMENTAL SC-ENVIRONMENTAL SCIENCES
CiteScore
17.90
自引率
3.70%
发文量
163
期刊介绍: Environmental Science & Technology Letters serves as an international forum for brief communications on experimental or theoretical results of exceptional timeliness in all aspects of environmental science, both pure and applied. Published as soon as accepted, these communications are summarized in monthly issues. Additionally, the journal features short reviews on emerging topics in environmental science and technology.
期刊最新文献
Issue Editorial Masthead Issue Publication Information Environmental Science & Technology Letters Presents the 2023 Excellence in Review Awards: We’re in This Together Global Impact of Particulate Nitrate Photolysis on Fine Sulfate Aerosol Mechanistic Insights into Di-2-ethylhexyl Phthalate (DEHP)-Induced Metabolic Disruption: Integrating Gut Hormone Secretion and Metabolomics in Colonic Organoids
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1