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评估ELITE流式细胞仪上的气溶胶控制情况。

Assessment of aerosol containment on the ELITE flow cytometer.

作者信息

Ferbas J, Chadwick K R, Logar A, Patterson A E, Gilpin R W, Margolick J B

机构信息

Department of Infectious Diseases and Microbiology, Graduate School of Public Health, University of Pittsburgh, Pennsylvania, USA.

出版信息

Cytometry. 1995 Mar 15;22(1):45-7. doi: 10.1002/cyto.990220109.

Abstract

Biohazardous aerosols generated during cell sorting have been of increased concern recently because of interest in sorting specimens containing human immunodeficiency virus type 1 (HIV-1). Current flow cytometers have features designed to contain such aerosols within the sorting chamber, but the efficacy of these features has not been established. Therefore, we tested aerosol containment by two ELITE flow cytometers (Coulter Cytometry, Inc., Hialeah, FL) during sorting of specimens containing high titers of bacteriophage. Agar plates confluent with susceptible Escherichia coli were used to detect infectious units released from the sorting chamber. Under recommended operating conditions very few infectious units were released from the sorting chambers. Release increased when the center stream was not optimally collected in a vacuum-exhausted tube or the chamber door was not completely closed. Failure of the negative pressure and high efficiency particle air (HEPA) filtration features had less of an effect. The data indicate that these standard safety features provide a rational expectation of safety for the flow cytometry operator.

摘要

由于对含有1型人类免疫缺陷病毒(HIV-1)的标本进行分选的兴趣,细胞分选过程中产生的生物危害气溶胶最近受到了越来越多的关注。当前的流式细胞仪具有旨在将此类气溶胶限制在分选腔内的特性,但这些特性的有效性尚未得到证实。因此,我们在对含有高滴度噬菌体的标本进行分选期间,通过两台ELITE流式细胞仪(库尔特细胞计数公司,佛罗里达州希亚莱)测试了气溶胶的限制情况。使用长满易感大肠杆菌的琼脂平板来检测从分选腔释放的感染单位。在推荐的操作条件下,分选腔释放的感染单位极少。当中心流未在真空排气管中得到最佳收集或腔门未完全关闭时,释放量会增加。负压和高效空气过滤器(HEPA)过滤特性失效的影响较小。数据表明,这些标准安全特性为流式细胞术操作人员提供了合理的安全预期。

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