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Measuring containment of viable infectious cell sorting in high-velocity cell sorters.
Cytometry A. 2003 Apr; 52(2):122-30.C

Abstract

BACKGROUND

With the advent of high-speed sorters, aerosols are a considerable safety concern when sorting viable infectious materials. We describe a four-part safety procedure for validating the containment.

METHODS

This procedure includes aerosol containment, physical barriers, environmental controls, and personal protection. The Aerosol Management System (AMS) produces a negative pressure within the sort chamber, where aerosols are forced through a HEPA filter. Physical barriers include the manufacturer's standard plastic shield and panels. The flow cytometer was contained within a BSL-3 laboratory for maximum environmental control, and the operator was protected by a respiratory system. Containment was measured by using highly fluorescent Glo-Germ particles under the same conditions as the cell sort.

RESULTS

Escaping aerosols were vacuumed for 10 min onto a glass slide and examined. With the AMS active and the cytometer producing the maximum aerosols possible, Glo-Germ particles remained within the sort chamber. Measurements taken directly outside the door averaged fewer than one particle per slide, and those taken at 2 ft away and on top of the sorter were completely negative.

CONCLUSIONS

With this monitoring system in place, aerosols can be efficiently measured, thus reducing the risk to the operator while sorting viable infectious cells.

Authors+Show Affiliations

Vaccine Research Center, NAID, National Institute of Health, Bethesda, Maryland 20892-3015, USA. sperfetto@nih.govNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Validation Study

Language

eng

PubMed ID

12655656

Citation

Perfetto, Stephen P., et al. "Measuring Containment of Viable Infectious Cell Sorting in High-velocity Cell Sorters." Cytometry. Part a : the Journal of the International Society for Analytical Cytology, vol. 52, no. 2, 2003, pp. 122-30.
Perfetto SP, Ambrozak DR, Koup RA, et al. Measuring containment of viable infectious cell sorting in high-velocity cell sorters. Cytometry A. 2003;52(2):122-30.
Perfetto, S. P., Ambrozak, D. R., Koup, R. A., & Roederer, M. (2003). Measuring containment of viable infectious cell sorting in high-velocity cell sorters. Cytometry. Part a : the Journal of the International Society for Analytical Cytology, 52(2), 122-30.
Perfetto SP, et al. Measuring Containment of Viable Infectious Cell Sorting in High-velocity Cell Sorters. Cytometry A. 2003;52(2):122-30. PubMed PMID: 12655656.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Measuring containment of viable infectious cell sorting in high-velocity cell sorters. AU - Perfetto,Stephen P, AU - Ambrozak,David R, AU - Koup,Richard A, AU - Roederer,Mario, PY - 2003/3/26/pubmed PY - 2004/1/30/medline PY - 2003/3/26/entrez SP - 122 EP - 30 JF - Cytometry. Part A : the journal of the International Society for Analytical Cytology JO - Cytometry A VL - 52 IS - 2 N2 - BACKGROUND: With the advent of high-speed sorters, aerosols are a considerable safety concern when sorting viable infectious materials. We describe a four-part safety procedure for validating the containment. METHODS: This procedure includes aerosol containment, physical barriers, environmental controls, and personal protection. The Aerosol Management System (AMS) produces a negative pressure within the sort chamber, where aerosols are forced through a HEPA filter. Physical barriers include the manufacturer's standard plastic shield and panels. The flow cytometer was contained within a BSL-3 laboratory for maximum environmental control, and the operator was protected by a respiratory system. Containment was measured by using highly fluorescent Glo-Germ particles under the same conditions as the cell sort. RESULTS: Escaping aerosols were vacuumed for 10 min onto a glass slide and examined. With the AMS active and the cytometer producing the maximum aerosols possible, Glo-Germ particles remained within the sort chamber. Measurements taken directly outside the door averaged fewer than one particle per slide, and those taken at 2 ft away and on top of the sorter were completely negative. CONCLUSIONS: With this monitoring system in place, aerosols can be efficiently measured, thus reducing the risk to the operator while sorting viable infectious cells. SN - 1552-4922 UR - https://www.unboundmedicine.com/medline/citation/12655656/Measuring_containment_of_viable_infectious_cell_sorting_in_high_velocity_cell_sorters_ DB - PRIME DP - Unbound Medicine ER -