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Characterization of reaerosolization from impingers in an effort to improve airborne virus sampling

机译:表征撞击源的再气溶胶化,以改善机载病毒采样

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To assess the impact of reaerosolization from liquid impingement methods on airborne virus sampling. An AGI-30 impinger containing particles [MS2 bacteriophage or 30-nm polystyrene latex (PSL)] of known concentration was operated with sterile air. Reaerosolized particles as a function of sampling flow rate and particle concentration in the impinger collection liquid were characterized using a scanning mobility particle sizer. Reaerosolization from the impinger was also compared to that from a BioSampler. Results show that reaerosolization increases as flow rate increases. While the increased particle concentration in the impinger collection liquid leads to an increase in the reaerosolization of PSL particles, it does not necessarily lead to an increase in the reaerosolization of virus particles. Reaerosolization of virus particles begins to decrease as the particle concentration in the impinger collection liquid rises above 10e PFU mlp#. This phenomenon results from aggregation of viral particles at high concentrations. Compared with micron-sized particles, nanosized virus particles are easier to aerosolize because of reduced inertia. Reaerosolization from the BioSampler is demonstrated to be significantly less than that from the impinger. Reaerosolization from impingement sampling methods is a mode of loss in airborne virus sampling, although it is not as significant a limitation as the primary particle size of the aerosol. Utilizing a BioSampler coupled with short sampling periods to prevent high accumulative concentrations can minimize the impact of reaerosolization. This study confirms reaerosolization of virus particles to be a mode of loss in impingement sampling and identifies methods to minimize the loss.
机译:评估液体撞击方法的再气雾化对机载病毒采样的影响。用无菌空气操作含有已知浓度的颗粒[MS2噬菌体或30 nm聚苯乙烯胶乳(PSL)]的AGI-30冲击器。使用扫描迁移率粒度仪对再雾化的颗粒作为采样速率和冲击收集器液体中颗粒浓度的函数进行了表征。还比较了撞击器的再雾化与BioSampler的再雾化。结果表明,随着流速的增加,再气溶胶化也增加。冲击器收集液中增加的颗粒浓度会导致PSL颗粒的再气溶胶化增加,但并不一定会导致病毒颗粒的再气溶胶化程度增加。随着冲击器收集液中的颗粒浓度升高到10e PFU mlp#以上,病毒颗粒的再雾化作用开始降低。这种现象是由于高浓度病毒颗粒的聚集引起的。与微米级颗粒相比,纳米级病毒颗粒由于惯性降低而更易于雾化。已证明,BioSampler的再雾化效果明显小于冲击器的再雾化效果。撞击采样方法中的再雾化是空气传播病毒采样中的一种损失方式,尽管它不像气雾剂的原始粒径那样重要。利用BioSampler加上较短的采样周期来防止高浓度累积,可以最大程度地减少再气溶胶化的影响。这项研究证实了病毒颗粒的再雾化是冲击采样中的一种损失方式,并确定了使损失最小化的方法。

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