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Field Detection And Identification of a Bioaerosol Suite By Pyrolysis-Gas Chromatography-Ion Mobility Spectrometry

机译:热解 - 气相色谱离子迁移光谱法的生物溶胶套件的场检测及鉴定

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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 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 particles per liter of air (ACPLA). In order to realize this low concentration, an aerosol concentrator was used to concentrate 2000 liters of air in 2.2 minutes. 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:对热解 - 气相色谱 - 离子迁移率(Py-GC-IMS)独立生物法进行改进,以向IMS检测器模块提供更热解的化合物信息。通过热解管连续流动的空气载体气体,空气流速和热解率流动,以改善IMS检测器与早期工作相比检测到的热解酸盐化合物的相对质量和量。这些改进允许更大程度的信心对在室外测试场景中获得的生物气溶胶的相关性,以标准GC-IMS生物气溶胶数据集。与先前的研究相比,气流改善允许在GC-IMS数据结构域中观察更多的生物标志物化合物,以用于革兰氏阴性Erwinia Herbicola(EH)和卵磷蛋白蛋白的气溶胶。对于枯草芽孢杆菌VAR的革兰氏阳性孢子,观察到最小差异。来自早期工作的Globigii(BG)。在户外气溶胶挑战挑战,检测一个有机体,eh或bg。在西加拿大草原中散发生物气溶胶,测试了Py-GC-IMS以检测生物气溶胶的能力。目前系列的户外试验包括三种不同的生物气溶胶挑战。进行了四十两项试验,并且GC-IMS数据域生物标志物峰的简单区域计算与30试验中的正确的生物溶胶攻击相关(71%)。在另外7种试验中,确定气溶胶的状态是生物学原产地。另外两项额外试验没有可辨别,明确的GC-IMS生物反应,因为它们是空白喷水。可再现的检测限浓度为每升空气(ACPLA)的含有小于0.5个含细菌分析物颗粒的浓度。为了实现这种低浓度,气溶胶浓缩器用于将2000升空气浓缩2.2分钟。以前的户外气溶胶试验表明Py-GC-IMS装置是一种可靠的检测器,相对于确定生物气溶胶的存在。目前的一系列户外试验提供了一个平台,以表明Py-GC-IMS可以在传播时间未知的情况下,将Py-GC-IMS提供比生物学或非生物学分析更具特异性的信息。 Py-GC-IMS被证明能够区分革兰氏阳性孢子(BG)的气溶胶,革兰氏阴性细菌(EH)和蛋白质(卵磷酸酯)。

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