Laboratory Comparison of Hand-Cleansing Agents

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Questions and Answers

What does a rating of '+++' indicate regarding microbial contamination levels?

  • Little contamination
  • No contamination
  • Moderate contamination
  • A lot of contamination (correct)

When evaluating the effectiveness of a hand-cleansing agent, which aspect should be examined for diversity?

  • The temperature of the water used
  • Physical characteristics like color and texture (correct)
  • The timing of the hand-washing process
  • The absolute number of microbes only

What might affect the observed effectiveness of various hand-cleansing agents besides the agent itself?

  • The type of table used during the experiment
  • Variations in technique among students (correct)
  • The cleanliness of the lab section
  • The size of the student's hands

Which of the following interpretations indicates that the cleansing agent was very effective?

<p>Excellent (D)</p> Signup and view all the answers

What aspect of microbial persistence should students consider after washing their hands?

<p>The characteristics of different microbes (B)</p> Signup and view all the answers

What is the purpose of allowing agar plates to cool in an upright position?

<p>To ensure they solidify properly for agar deeps (D)</p> Signup and view all the answers

At what temperature and duration are media typically sterilized in an autoclave?

<p>121 °C for 15 minutes (B)</p> Signup and view all the answers

What happens to brain-heart infusion agar (BHIA) when removed from the autoclave?

<p>It remains liquid until it cools down (B)</p> Signup and view all the answers

How should agar plates be prepared to avoid airborne contamination?

<p>By using sterile Petri dishes and a lid as shield (B)</p> Signup and view all the answers

What is the correct procedure to check for growth in tubes and plates?

<p>Store them at room temperature for 24 hours before examination (A)</p> Signup and view all the answers

What should you avoid doing when transferring organisms with a loop?

<p>Dig into the agar or scoop up a glob of growth (D)</p> Signup and view all the answers

Why is the technique called 'fishtail streak'?

<p>It resembles the movement of a fish's tail in water (A)</p> Signup and view all the answers

What adjustment should be made when transferring a BSL-2 organism?

<p>Make appropriate procedural adjustments (A)</p> Signup and view all the answers

What is the correct order of steps after picking up a sterile agar slant?

<p>Remove the cap, flame the tube's lip, touch the loop to the growth (D)</p> Signup and view all the answers

When handling culture tubes, what should you do after touching the loop to the growth on the agar?

<p>Gently withdraw the loop and make a fishtail motion (A)</p> Signup and view all the answers

What is the primary goal when using a loop for transferring cultures?

<p>To pick up and inoculate the smallest amount visible (D)</p> Signup and view all the answers

What is the recommended procedure for flaming the culture tube?

<p>Flame the culture tube's lip after removing the cap (B)</p> Signup and view all the answers

Which action should be taken immediately after making the fishtail streak?

<p>Flame the loop again to sterilize it (D)</p> Signup and view all the answers

What is crucial to remember when withdrawing the culture tube from the wire?

<p>Keep the loop steady to avoid cutting the agar (D)</p> Signup and view all the answers

What should be done with the culture tube after touching the loop to the growth?

<p>Flame it and replace the cap before putting it down (C)</p> Signup and view all the answers

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Study Notes

Hand-Cleansing Agents

  • Relative growth contamination scale: +++ (a lot), ++ (moderate), + (little), 0 (none).
  • Emphasize consistency in evaluation despite subjective interpretations of contamination levels.
  • Observe diversity in microbial growth by noting colors, shapes, textures, and the number of different organisms.

Questions on Effectiveness

  • Identify which hand-washing agent effectively removed microbes from fingertips.
  • Determine the least effective agent for microbial removal.
  • Consider variables influencing differences between individuals’ finger cleanliness.
  • Recognize any persistent microbes post-washing and explore possible factors causing retention.

Media Preparation and Handling

  • Weigh ingredients accurately before suspending them in distilled or deionized water.
  • Heating may be necessary to ensure complete dissolution of media ingredients.
  • Media sterilization: autoclave at 121 °C for 15 minutes.

Types of Media

  • Tubed media types: broth, agar slant, agar deep tube.
  • Agar slants are allowed to solidify at an angle; agar deeps solidify upright.
  • Agar plates are prepared by pouring sterilized medium into sterile Petri dishes.

Microbial Culture Handling

  • Proper handling of culture tubes includes flaming and maintaining sterility during transfers.
  • Utilize a loop to inoculate agar surfaces carefully without damaging the media.
  • Maintain a sterile environment to avoid contamination during transfers.

Labeling Protocols

  • Always label sterile media with name, date, medium type, and inoculum source.
  • Consistent adherence to labeling ensures accurate tracking of cultures and experiments.

Miscellaneous Techniques

  • Employ "fishtail" streaking technique for loop inoculation on agar, resembling the motion of a fish tail.
  • Keep hands steady and flaming techniques consistent for ensuring proper sterilization between transfers.

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