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航空燃料燃烧产生的初级颗粒物的毒理学评价。

Toxicological evaluation of primary particulate matter emitted from combustion of aviation fuel.

机构信息

Department of Pharmacological and Biomolecular Sciences (DiSFeB) "Rodolfo Paoletti", Università degli Studi di Milano, 20133, Milan, Italy.

National Institute for Public Health and the Environment (RIVM), 3720 BA, Bilthoven, the Netherlands.

出版信息

Chemosphere. 2024 Sep;363:142958. doi: 10.1016/j.chemosphere.2024.142958. Epub 2024 Jul 26.

DOI:10.1016/j.chemosphere.2024.142958
PMID:39069102
Abstract

Recently, Sustainable Aviation Fuel (SAF) blends and novel combustion technologies have been introduced to reduce aircraft engine emissions. However, there is limited knowledge about the impact of combustion technology and fuel composition on toxicity of primary Particulate Matter (PM) emissions, comparable to regulated non-volatile PM (nvPM). In this study, primary PM was collected on filters using a standardised approach, from both a Rich-Quench-Lean (RQL) combustion rig and a bespoke liquid fuelled Combustion Aerosol Standard (CAST) Generator burning 12 aviation fuels including conventional Jet-A, SAFs, and blends thereof. The fuels varied in aromatics (0-25.2%), sulphur (0-3000 ppm) and hydrogen (13.43-15.31%) contents. Toxicity of the collected primary PM was studied in vitro utilising Air-Liquid Interface (ALI) exposure of lung epithelial cells (Calu-3) in monoculture and co-culture with macrophages (differentiated THP-1 cells). Cells were exposed to PM extracted from filters and nebulised from suspensions using a cloud-based ALI exposure system. Toxicity readout parameters were analysed 24 h after exposure. Results showed presence of genotoxicity and changes in gene expression at dose levels which did not induce cytotoxicity. DNA damage was detected through Comet assay in cells exposed to CAST generated samples. Real-Time PCR performed to investigate the expression profile of genes involved in oxidative stress and DNA repair pathways showed different behaviours after exposure to the various PM samples. No differences were found in pro-inflammatory interleukin-8 secretion. This study indicates that primary PM toxicity is driven by wider factors than fuel composition, highlighting that further work is needed to substantiate the full toxicity of aircraft exhaust PM inclusive of secondary PM emanating from numerous engine technologies across the power range burning conventional Jet-A and SAF.

摘要

最近,可持续航空燃料 (SAF) 混合物和新型燃烧技术已被引入,以减少飞机发动机排放。然而,对于燃烧技术和燃料成分对原始颗粒物 (PM) 排放毒性的影响,我们的了解有限,这与规定的非挥发性 PM (nvPM) 相当。在这项研究中,使用标准化方法从 Rich-Quench-Lean (RQL) 燃烧装置和燃烧 12 种航空燃料的定制液体燃料燃烧气溶胶标准 (CAST) 发生器收集了原始 PM ,这些燃料包括常规 Jet-A、SAF 及其混合物。燃料中的芳烃(0-25.2%)、硫(0-3000ppm)和氢(13.43-15.31%)含量各不相同。在体外利用单层肺上皮细胞 (Calu-3) 和与巨噬细胞 (分化的 THP-1 细胞) 共培养的空气-液界面 (ALI) 暴露研究收集的原始 PM 的毒性。细胞用从过滤器中提取的 PM 进行暴露,并用基于云的 ALI 暴露系统从悬浮液中喷雾 PM。暴露 24 小时后分析毒性读出参数。结果表明,在未引起细胞毒性的剂量水平下,存在遗传毒性和基因表达变化。彗星试验检测到暴露于 CAST 生成样品的细胞中的 DNA 损伤。进行实时 PCR 以研究参与氧化应激和 DNA 修复途径的基因的表达谱,结果表明暴露于各种 PM 样品后表现出不同的行为。未发现促炎细胞因子白细胞介素-8 分泌的差异。本研究表明,原始 PM 的毒性受燃料成分以外的更广泛因素驱动,这表明需要进一步研究以证实包括源自燃烧传统 Jet-A 和 SAF 的众多发动机技术的二次 PM 在内的飞机排气 PM 的全部毒性。

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