Field detection and identification of a bioaerosol suite by pyrolysis-gas chromatography-ion mobility spectrometry*

A. Snyder, A. Tripathi, W. Maswadeh, J. Ho, M. Spence
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引用次数: 34

Abstract

Improvements were made to a pyrolysis-gas chromatography-ion mobility spectrometry (Py-GC-IMS) stand-alone biodetector to provide more pyrolyzate compound information to the IMS detector module. Air carrier gas flowing continuously through the pyrolysis tube, the rate of air flow, and pyrolysis rate were found to improve the relative quality and quantity of pyrolyzate compounds detected by the IMS detector compared to earlier work. These improvements allowed a greater degree of confidence in the correlation of biological aerosols obtained in outdoor testing scenarios to a standard GC-IMS biological aerosol dataset. The airflow improvement allowed more biomarker compounds to be observed in the GC-IMS data domain for aerosols of gram-negative Erwinia herbicola (EH) and ovalbumin protein as compared to previous studies. Minimal differences were observed for gram-positive spores of Bacillus subtilis var. globigii (BG) from that of earlier work. Prior outdoor aerosol challenges dealt with the detection of one organism, either EH or BG. Biological aerosols were disseminated in a Western Canadian prairie and the Py-GC-IMS was tested for its ability to detect the biological aerosols. The current series of outdoor trials consisted of three different biological aerosol challenges. Forty-two trials were conducted and a simple area calculation of the GC-IMS data domain biomarker peaks correlated with the correct bioaerosol challenge in 30 trials (71%). In another 7 trials, the status of an aerosol was determined to be biological in origin. Two additional trials had no discernible, unambiguous GC-IMS biological response, because they were blank water sprays. Reproducible limits of detection were at a concentration of less than 0.5 bacterial analyte-containing particle per liter of air. In order to realize this low concentration, an aerosol concentrator was used to concentrate 2000 l of air in 2.2 min. Previous outdoor aerosol trials have shown the Py-GC-IMS device to be a credible detector with respect to determining the presence of a biological aerosol. The current series of outdoor trials has provided a platform to show that the Py-GC-IMS can provide information more specific than a biological or non-biological analysis to an aerosol when the time of dissemination is unknown to the operator. The Py-GC-IMS is shown to be able to discriminate between aerosols of a gram-positive spore (BG), a gram-negative bacterium (EH), and a protein (ovalbumin). © 2001 John Wiley & Sons, Inc. Field Analyt Chem Technol 5: 190–204, 2001
热分解-气相色谱-离子迁移谱法对生物气溶胶的现场检测和鉴定*
对热解-气相色谱-离子迁移谱(Py-GC-IMS)独立生物检测器进行了改进,为IMS检测器模块提供更多的热解化合物信息。与之前的工作相比,载气在热解管中连续流动、气流速率和热解速率可以提高IMS检测器检测到的热解产物的相对质量和数量。这些改进使得在室外测试情景中获得的生物气溶胶与标准GC-IMS生物气溶胶数据集的相关性具有更大的可信度。与以前的研究相比,气流的改善使得在GC-IMS数据域中可以观察到更多的生物标志物化合物,用于革兰氏阴性Erwinia除草剂(EH)和卵清蛋白的气溶胶。观察到革兰氏阳性芽孢枯草芽孢杆菌变种globigii (BG)与早期工作的差异很小。以前的室外气溶胶挑战处理一种生物的检测,EH或BG。生物气溶胶散布在加拿大西部的草原上,并测试了Py-GC-IMS检测生物气溶胶的能力。目前的一系列户外试验包括三种不同的生物气溶胶挑战。进行了42次试验,对30次试验(71%)中GC-IMS数据域生物标志物峰与正确的生物气溶胶挑战相关的简单面积计算。在另外7项试验中,气溶胶的状态被确定为生物来源。另外两项试验没有明显的、明确的GC-IMS生物反应,因为它们是空白水喷雾。检测的重现限为每升空气中含有细菌分析物的颗粒浓度小于0.5。为了实现这种低浓度,使用气溶胶浓缩器在2.2分钟内浓缩2000升空气。以前的室外气溶胶试验表明,Py-GC-IMS设备是确定生物气溶胶存在的可靠探测器。目前的一系列室外试验提供了一个平台,表明当操作者不知道气溶胶的传播时间时,Py-GC-IMS可以提供比生物或非生物分析更具体的信息。经证明,pygc - ims能够区分革兰氏阳性孢子(BG)、革兰氏阴性细菌(EH)和蛋白质(卵白蛋白)的气溶胶。©2001 John Wiley & Sons, Inc化学工程学报(英文版),2001,31 (5):391 - 394
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