Moe Birget, Yuan Chungang, Li Jinhua, Du Haiying, Gabos Stephan, Le X Chris, Li Xing-Fang
Division of Analytical & Environmental Toxicology, Department of Laboratory Medicine & Pathology, Faculty of Medicine & Dentistry, University of Alberta , Edmonton, Alberta, Canada T6G 2G3.
Alberta Centre for Toxicology, Department of Physiology & Pharmacology, Faculty of Medicine, University of Calgary , Calgary, Alberta, Canada T2N 4N1.
Chem Res Toxicol. 2016 Jun 20;29(6):972-80. doi: 10.1021/acs.chemrestox.6b00004. Epub 2016 May 19.
The development of a unique bioassay for cytotoxicity analysis of coal fly ash (CFA) particulate matter (PM) and its potential application for air quality monitoring is described. Using human cell lines, A549 and SK-MES-1, as live probes on microelectrode-embedded 96-well sensors, impedance changes over time are measured as cells are treated with varying concentrations (1 μg/mL-20 mg/mL) of CFA samples. A dose-dependent impedance change is determined for each CFA sample, from which an IC50 histogram is obtained. The assay was successfully applied to examine CFA samples collected from three coal-fired power plants (CFPs) in China. The samples were separated into three size fractions: PM2.5 (<2.5 μm), PM10-2.5 (2.5 μm < x < 10 μm), and PM10 (>10 μm). Dynamic cell-response profiles and temporal IC50 histograms of all samples show that CFA cytotoxicity depends on concentration, exposure time (0-60 h), and cell-type (SK-MES-1 > A549). The IC50 values differentiate the cytotoxicity of CFA samples based on size fraction (PM2.5 ≈ PM10-2.5 ≫ PM10) and the sampling location (CFP2 > CFP1 ≈ CFP3). Differential cytotoxicity measurements of particulates in human cell lines using cell-electronic sensing provide a useful tool for toxicity-based air quality monitoring and risk assessment.
本文描述了一种用于分析粉煤灰(CFA)颗粒物(PM)细胞毒性的独特生物测定方法的开发及其在空气质量监测中的潜在应用。使用人细胞系A549和SK-MES-1作为嵌入微电极的96孔传感器上的活体探针,在细胞用不同浓度(1μg/mL - 20mg/mL)的CFA样品处理时,测量随时间的阻抗变化。为每个CFA样品确定剂量依赖性阻抗变化,从中获得IC50直方图。该测定方法成功应用于检测从中国三个燃煤电厂(CFP)收集的CFA样品。样品被分为三个粒径部分:PM2.5(<2.5μm)、PM10 - 2.5(2.5μm < x < 10μm)和PM10(>10μm)。所有样品的动态细胞反应曲线和时间IC50直方图表明,CFA细胞毒性取决于浓度、暴露时间(0 - 60小时)和细胞类型(SK-MES-1 > A549)。IC50值根据粒径部分(PM2.5 ≈ PM10 - 2.5 ≫ PM10)和采样地点(CFP2 > CFP1 ≈ CFP3)区分CFA样品的细胞毒性。使用细胞电子传感在人细胞系中对颗粒物进行差异细胞毒性测量,为基于毒性的空气质量监测和风险评估提供了一种有用的工具。