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首页> 外文期刊>Field Analytical Chemistry and Technology >Field Detection and Identification of a Bioaerosol Suite by Pyrolysis-Gas Chromatography-Ion Mobility Spectrometry
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Field Detection and Identification of a Bioaerosol Suite by Pyrolysis-Gas Chromatography-Ion Mobility Spectrometry

机译:热解-气相色谱-离子迁移谱法现场检测和鉴定生物气溶胶套件

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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 Er-winia 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 1 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).
机译:改进了热解气相色谱-离子迁移谱(Py-GC-IMS)独立生物检测器,以向IMS检测器模块提供更多热解化合物信息。发现与连续工作相比,连续流过热解管的空气载气,空气流率和热解率可提高IMS检测器检测到的热解化合物的相对质量和数量。这些改进使得在室外测试场景中获得的生物气溶胶与标准GC-IMS生物气溶胶数据集之间的相关性更加可信。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,用于革兰氏阴性欧文氏草(EH)和卵清蛋白蛋白质的气溶胶。枯草芽孢杆菌变种的革兰氏阳性孢子差异最小。 globigii(BG)来自早期的工作。先前的室外气溶胶挑战涉及一种生物的检测,即EH或BG。在加拿大西部的大草原上散布了生物气溶胶,并测试了Py-GC-IMS检测生物气溶胶的能力。当前的户外试验系列包括三种不同的生物气雾剂挑战。进行了四十二项试验,在30项试验中,对GC-IMS数据域生物标志物峰的简单面积计算与正确的生物气溶胶攻击相关(71%)。在另外7个试验中,确定气雾剂的状态为生物学起源。另外两项试验没有明显,明确的GC-IMS生物学反应,因为它们是空白喷水。可重复的检测极限浓度为每升空气中小于0.5的含细菌分析物的颗粒。为了实现这种低浓度,使用了一个气溶胶浓缩器在2.2分钟内浓缩了2000 1空气。先前的室外气雾剂试验表明,Py-GC-IMS设备在确定生物气雾剂的存在方面是可靠的检测器。当前的一系列户外试验提供了一个平台,显示了当操作者不知道传播时间时,Py-GC-IMS可以提供​​比气溶胶的生物或非生物分析更具体的信息。显示Py-GC-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(卵清蛋白)的气溶胶。

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