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Testing the efficiency of aerosol containment during cell sorting.
Curr Protoc Cytom. 2001 May; Chapter 3:Unit 3.3.CP

Abstract

Production of droplets and microdroplets (aerosols) is part of the normal operation of a cell sorter. These aerosols may contain toxic, carcinogenic, or teratogenic fluorophores or known or unknown pathogens from viable biological specimens. Most newer models of commercially available instruments incorporate features designed to reduce the production of aerosols and prevent their release into the room. This unit presents two protocols for assessment of aerosol containment on jet-in-air flow sorters. In both procedures, lytic T4 bacteriophage is run through the instrument at high concentrations to tag aerosol droplets. The instrument is tested in normal operating mode and in simulated failure mode. Aerosols are detected by plaque formation on susceptible E. coli lawns. With the continuing increase in the sorting of viable human cells, it is vital for cytometrists to be aware of the potential dangers.

Authors+Show Affiliations

UCLA School of Medicine, Los Angeles, California, USA.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18770706

Citation

Schmid, I, et al. "Testing the Efficiency of Aerosol Containment During Cell Sorting." Current Protocols in Cytometry, vol. Chapter 3, 2001, pp. Unit 3.3.
Schmid I, Hultin LE, Ferbas J. Testing the efficiency of aerosol containment during cell sorting. Curr Protoc Cytom. 2001;Chapter 3:Unit 3.3.
Schmid, I., Hultin, L. E., & Ferbas, J. (2001). Testing the efficiency of aerosol containment during cell sorting. Current Protocols in Cytometry, Chapter 3, Unit 3. https://doi.org/10.1002/0471142956.cy0303s01
Schmid I, Hultin LE, Ferbas J. Testing the Efficiency of Aerosol Containment During Cell Sorting. Curr Protoc Cytom. 2001;Chapter 3:Unit 3.3. PubMed PMID: 18770706.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Testing the efficiency of aerosol containment during cell sorting. AU - Schmid,I, AU - Hultin,L E, AU - Ferbas,J, PY - 2008/9/5/pubmed PY - 2008/9/25/medline PY - 2008/9/5/entrez SP - Unit 3.3 EP - Unit 3.3 JF - Current protocols in cytometry JO - Curr Protoc Cytom VL - Chapter 3 N2 - Production of droplets and microdroplets (aerosols) is part of the normal operation of a cell sorter. These aerosols may contain toxic, carcinogenic, or teratogenic fluorophores or known or unknown pathogens from viable biological specimens. Most newer models of commercially available instruments incorporate features designed to reduce the production of aerosols and prevent their release into the room. This unit presents two protocols for assessment of aerosol containment on jet-in-air flow sorters. In both procedures, lytic T4 bacteriophage is run through the instrument at high concentrations to tag aerosol droplets. The instrument is tested in normal operating mode and in simulated failure mode. Aerosols are detected by plaque formation on susceptible E. coli lawns. With the continuing increase in the sorting of viable human cells, it is vital for cytometrists to be aware of the potential dangers. SN - 1934-9300 UR - https://www.unboundmedicine.com/medline/citation/18770706/Testing_the_efficiency_of_aerosol_containment_during_cell_sorting_ L2 - https://doi.org/10.1002/0471142956.cy0303s01 DB - PRIME DP - Unbound Medicine ER -