Hero graphic - researchers in a lab

Preventing Aerosol Production

Examples of Aerosol-Producing Activities in the Lab

  • Carelessly removing gloves
  • Pouring liquids
  • Removing (“popping off”) stoppers
  • Opening lyophilized cultures, snap top tubes, bottles
  • Blowing out pipettes
  • Shaking or vortexing open tubes, stirring
  • Dropping/breakage of culture containers
  • Flaming inoculating needles, loops, or slides
  • Inserting a hot loop into a culture
  • Pulling needles out of septum, filling a syringe
  • Centrifugation steps such as filling centrifuge tubes, removing plugs or caps from tubes after centrifugation, removing supernatant, resuspending sedimented pellets, breakage of tubes during centrifugation, and centrifugation itself
  • Sonicating, homogenizing, blending, grinding, cell disruption with French press
  • Cell sorters
  • Vacuum and aspirating equipment
  • Intranasal inoculation of animals
  • Cage cleaning, changing animal bedding
  • Harvesting infected material from animals, eggs, and other virology procedures
  • Necropsies of infected animals

Safe Work Practices to Minimize the Creation of and Exposure to Aerosols

Laboratory workers should learn and follow (as appropriate) these practices. Using a combination of 
the appropriate safety equipment and safe procedures is the primary method to minimize the creation 
of and exposure to aerosols.
 
Lab Safety Equipment to Protect Personnel from Aerosols
  • A certified biological safety cabinet (class I or II) is the primary barrier to protect worker from aerosols if working with RG2 or higher agents.
  • Centrifuges with safety centrifuge cups.
  • Vacuum line trap and filter systems are used to protect the vacuum system from aerosols.
Safe Work Practices for Centrifugation
  • Routinely inspect centrifuge to ensure that leakage is not occurring.
  • Do not overfill centrifuge tubes. Wipe the outside of the tubes with disinfectant after they are filled and sealed.
  • Centrifugation may be performed in a centrifuge that is contained within a biological safety cabinet or other physical containment device.
  • If a whole centrifuge containment device is not available, internal aerosol containment devices (e.g., sealed canisters, safety cups or buckets with covers, heat sealed tubes or sealed rotors, etc) should be used.
  • Aerosol containment devices should be removed from the centrifuge and opened in a biological safety cabinet. If a biological safety cabinet is unavailable, a minimum of 10 minutes settling time should be allowed before opening.
Safe Work Practices for Blending, Sonicating, Grinding, and Lyophilizing
  • Operate blender, sonicator, and grinder in a biological safety cabinet, or place a towel moistened with disinfectant over the top of blender, grinder, or sonicator.
  • Use safety blenders designed to prevent leakage.
  • If leak-proof blender is not available, regularly inspect the bottom of the blender for leakage.
  • Avoid glass blenders.
  • Allow aerosols to settle for at least 5 minutes before opening blender.
  • Filter lyophilizer vacuum pump exhaust through HEPA filters or vent into a biological safety cabinet.
  • Autoclave or disinfect all equipment promptly after use.
 
Safe Work Practices for Pipetting
  • Drain a pipette with tip against the inner wall of the receiving vessel. Never forcibly expel any hazardous material from a pipette.
  • Carefully eject the disposable pipette tips to minimize aerosol formation. A wetted towel in the bottom of the dispensing container (which is often a glass beaker) will keep the pipette tip from bouncing around   in the container, thereby minimizing aerosol production.
  • Place reusable pipettes horizontally in a pan filled with enough liquid disinfectant to completely cover them.
  • Mouth pipetting is prohibited; mechanical pipetting devices are used.

Other Safety Precautions

  • Minimize air bubbles when filling a syringe. Place a pad moistened with disinfectant over the tip of the needle when expelling air.
  • Use a shielded electric incinerator or hot bead sterilizer to sterilize inoculating loops. Disposable plastic loops and culture needles are good alternatives to open flames.
  • If a spill occurs that may generate aerosols, leave the area, close the door, wait 30-60 minutes to allow dissipation of aerosols. See the GW biosafety manual for spill cleanup.
  • Wear gloves when handling infectious materials, or infected animals.
PDF version for your lab's biosafety manual.