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Techniques for dispersion of microorganisms into air

Reponen, T., Willeke, K., Ulevicius, V., Grinshpun, S. A. and Donnelly, J.
1997
Aerosol Science and Technology, 27(3), 405-421


Reponen, T., Willeke, K., Ulevicius, V., Grinshpun, S. A. and Donnelly, J., (1997), "Techniques for dispersion of microorganisms into air", Aerosol Science and Technology, 27(3), 405-421.
Abstract:
Many commercially available devices initially developed for dispersion of biologically inert particles have been adopted for aerosolization of microorganisms in laboratory settings. However, these dispersion devices are not always adequate for microbial particles, as they do not simulate natural release into air. Wet dispersion methods are appropriate for viruses and most bacteria, whereas dry methods are more suitable for most fungal and actinomycete spores. Characteristics of the resulting aerosol are dependent on the dispersing shear forces and the sensitivity and agglomeration of the tested microorganisms. Consequently, each microbial group may need a specific dispersion techniques. The following devices have been developed and tested in this study: the bubbling aerosol disperser, the agar-tube disperser, and the swirling-flow disperser. Testing included the evaluation of both physical and microbiological characteristics of aerosolized microorganisms. Each of the dispersers has shown several advantages over commercially available ones. When used for the dispersion of bacteria form the liquid suspension, the bubbling aerosol disperser was found to produce considerably fewer amounts of microbial fragments and much lower levels of microbial metabolic injury than the commercially available Collision nebulizer. Fungal spores dispersed from their colonies by the agar-tube disperser were found to have a more stable aerosol concentration and a lower fraction of agglomerates than achievable by conventional powder dispersion. The swirling-flow dispersion technique was used for aerosolization of actinomycetes because the agar-tube disperser could not provide a stable concentration of these spores due to their smaller size. The tests have shown that new methods minimize the changes of properties of the microorganisms during their aerosolization in the laboratory.

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Author Information and Other Publications Notes
Reponen, T.
Dr.Tiina Reponen, Research Associate Professor Department of Environmental Health University of Cincinnati
     
Willeke, K.
  1. Aerosol characteristics of airborne actinomycetes and fungi
  2. Bioaerosol collection by a new electrostatic precipitator
  3. Characteristics of airborne actinomycete spores
  4. Collection of airborne microorganisms by a new electrostatic precipitator
  5. Collection of bioaerosol particles by impaction: effect of fungal spore agglomeration and bounce
  6. Collection of fungal spores on air filters and spore reentrainment from filters into air
  7. Development and evaluation of aerosol generators for biological materials
  8. Effect of impact stress on microbial recovery on an agar surface
  9. Effect of relative humidity on the aerodynamic diameter and respiratory deposition of fungal spores
  10. Evaluation of a new personal sampler for enumerating airborne spores
  11. Fungal fragments as indoor air biocontaminants
  12. Improved aerosol collection by combined impaction and centrifugal motion
  13. Inlet sampling efficiency of bioaerosol samplers
  14. Long-term sampling of airbome bacteria and fungi into a non-evaporating liquid
  15. Performance characteristics of the button personal inhalable aerosol sampler
  16. Performance of Air-O-Cell, Burkard, and Button samplers for total enumeration of airborne spores
  17. Performance of bioaerosol samplers: collection characteristics and sampler design considerations
  18. Release of lead-containing particles from a wall enclosure
  19. Release of Streptomyces albus propagules from contaminated surfaces
  20. Source strength of fungal spore aerosolization from moldy building material  
Ulevicius, V.
  1. Development and evaluation of aerosol generators for biological materials
  2. Effect of impact stress on microbial recovery on an agar surface
  3. Effect of relative humidity on the aerodynamic diameter and respiratory deposition of fungal spores  
Grinshpun, S. A.
  1. Aerodynamic versus physical size of spores: measurement and implication for respiratory deposition
  2. Aerosol characteristics of airborne actinomycetes and fungi
  3. Bioaerosol collection by a new electrostatic precipitator
  4. Characteristics of airborne actinomycete spores
  5. Collection of airborne microorganisms by a new electrostatic precipitator
  6. Collection of airborne spores by circular single-stage impactors with small jet-to-plate distance
  7. Collection of bioaerosol particles by impaction: effect of fungal spore agglomeration and bounce
  8. Collection of fungal spores on air filters and spore reentrainment from filters into air
  9. Development and evaluation of aerosol generators for biological materials
  10. Effect of impact stress on microbial recovery on an agar surface
  11. Effect of relative humidity on the aerodynamic diameter and respiratory deposition of fungal spores
  12. Evaluation of a new personal sampler for enumerating airborne spores
  13. Field Testing of New Aerosol Sampling Method With a Porous Curved Surface as Inlet
  14. Fungal fragments as indoor air biocontaminants
  15. Fungal spore source strength tester: laboratory evaluation of a new concept
  16. Improved aerosol collection by combined impaction and centrifugal motion
  17. Inlet sampling efficiency of bioaerosol samplers
  18. Long-term sampling of airbome bacteria and fungi into a non-evaporating liquid
  19. Performance characteristics of the button personal inhalable aerosol sampler
  20. Performance of Air-O-Cell, Burkard, and Button samplers for total enumeration of airborne spores
  21. Release of lead-containing particles from a wall enclosure
  22. Release of Streptomyces albus propagules from contaminated surfaces  
Donnelly, J.
  1. Effect of impact stress on microbial recovery on an agar surface  



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