Aerosol Hazards

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    Aerosol Hazards

    in the Laboratory

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    Aerosol Hazards

    Objectives

    Identify major aerosol-producing activities

    List the major factors affecting the ability ofairborne microbes to cause infection

    Describe the limitations of workplace

    monitoring for aerosols

    Describe the effects of the physical

    environment on aerosol transport and removal

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    Episodes of Single-Source,

    Multiple Laboratory Infections

    Disease Probable Source

    ofInfection

    Maximum Distance

    From Source

    Number

    Persons

    Infected

    Brucellosis Centrif ugation Basement to 3rd floor 94

    Coccidioidomycosis Culture transfer solid media 2 Building floors 13

    Coxsackie Virus

    infection

    Spilled tube of infected

    mouse tissue on floor

    5 feet (estimated) 2

    Murine Typhus Intranasal inoculation of mice 6 feet (estimated) 6

    Tularemia 20 petri plates dropped 70 feet 5

    Venezuelan

    encephalitis

    9 lyophilized ampoules

    dropped

    4th floor stairs to 3rdor

    5th24

    Reitman and Wedum, 1956

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    What is an Aerosol?

    Particles suspended in a gas

    0.5 Q- Q in diameter

    In this instance the gas is air

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    Approximate

    Size Ranges ofVarious

    Bioaerosols

    Particles Diameters ()

    Smoke 0.001 0.1

    Viruses 0.015 0.45

    Bacteria 0.3 5

    Cat Ag-bearing

    particles

    5)

    Fungal spores 2.0 50

    Algae cells/clusters 1 100+

    Protozoa 2 100+

    Dermatophagoides

    fecal pellets ~20

    Fern spores 20 60

    Pollen 1

    0 - 100

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    Unscrewing Bottle Cap

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    Withdrawing Needle from Septum Cap

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    Vortex Mixing

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    Blowing Out the Last Drop

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    Blender Lid Open After Stop

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    Aerosols Produced from Laboratory Operations1010 bacteria/ml culture 10 min

    Blender, opened at once 106

    Sonicator, with bubbling 106

    Pipetting, vigorous 10

    6

    Dropping culture 3 x 105

    Splash on centrifuge rotor 105

    Drop spill on zonal rotor 2 x 104

    Blender, opened at 1 minute 2 x 104

    Pipetting, carefully 104

    Dimmick et al., 1973

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    Aerosol and Surface Recovery from Pipetting

    Operations of 109/ml B. subtilis

    (average time 3 minutes; 1 ml pipette; ea. 2 ml bulb)Chatigny et al, 1979

    RUN Airborne CFUSettled CFU

    Hands Area

    1 2,040 35,800 3,700

    2 657 22,000 860

    3 2,050 14,800 1,700

    4 388 9,300 550

    5 5,110 6,900 2,100

    6 649 228,000 2,900

    Average 1,820 52,800 1,970

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    Aerosols from Animal Cage Cleaning

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    Factors Affecting Survival of

    Aerosolized Organisms

    Environmental temperature, relative

    humidity

    Suspending Medium pH, specific gravity,

    constituents, e.g., protein

    Surface porous vs. non-porous

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    Factors Affecting Character of

    Aerosols

    Energy Input

    Low Large particles

    High Small particles

    Infectious Units/Particle

    organisms/unit, volume of original

    suspension Persistence particle size

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    Estimated Small Particle Aerosol Dose

    from Pipetting 1010/ml - min

    At 3 feet - 1,200 At 10 feet - 50

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    Estimated Small Particle Aerosol Dose

    from Blender 1010/ml 5 min

    At 3 feet - 2,000

    At 10 feet - 200

    Dimmick 1973 et. al.

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    Aerosol Dispersion in a Poorly

    Ventilated Room

    Dimmick 1973 et. al.

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    Summary

    Aerosols are generated from most

    laboratory tasks

    Aerosols can spread through a building

    and effect many people

    Contamination is often heaviest in work

    areas and on worker hands