Sterility techniques Flashcards

1
Q

Heat sterilisation can only be done with ________ products. If they are moisture resistant, then __________. If they are moisture sensitive, then __________.

A

thermostable
moist heat sterilisation
dry heat sterilisation

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2
Q

Moist heat sterilisation is carried out in an instrument called an _______

A

autoclave

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3
Q

Steam can either be ________ within the steriliser (e.g. portable bench sterilises; in which steam is constantly in contact with ______ - known as ‘___’ steam.)
OR
Steam can be supplied under _____ from a separate boiler (as ‘___’ ______ steam with NO water droplets

A

generated
water
wet
dry saturated

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4
Q

Which is visible?

Saturated steam or wet steam

A

wet steam

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5
Q

Which is invisible?

Saturated steam or wet steam

A

saturdate

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6
Q

Saturated steam is in ________ equilibrium with the water which has produced it

A

thermal

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7
Q

Saturated steam turns to wet steam once it is released to the _______, where part of it condenses by transferring its ____ to the surrounding air (and clouds of white _____ and tiny droplets of _____ are formed)

A

atmosphere
heat
vapour
water

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8
Q

Compare killing potential of wet steam and dry saturated steam at the same temperature.

A

same

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9
Q

Although killing potential of ‘wet’ steam is the same as that of
‘dry’ saturated steam at the same temperature, wet steam is more likely to soak a _____ ____, creating physical difficulties for further steam penetration

A

porous load

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10
Q

Superheated steam: is an ________ sterilising agent
(created by heating wet or saturated steam beyond the ______ steam point; less efficient, becoming equivalent to ___ heat)

A

inefficient
saturated
dry

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11
Q

What are the adverse effects of air?

A
  • Air is driven off from water and may be trapped in porous loads (e.g gauze, surgical dressings)
  • Air is a poor conductor of heat and inhibits heat flow
  • Steam containing air will be at a lower temp than pure steam (and so sterilisation temp will not be achieved)
  • Removal of air is important to ensure efficient autoclaving
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12
Q

Autoclaves are ________ steel vessels designed to withstand the steam pressures employed in sterilisation. There are two types:

A

stainless
portable sterilisers (labs)
large scale sterilisers (hospitals)

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13
Q

What are the three stages for autoclaves?

A
  1. Air removal (via downward displacement with steam/ evacuation) and steam admission
  2. Heating/ sterilising (holding stage)
  3. Drying/ cooling
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14
Q

What are the two main types of LARGE autoclaves?

A
  • downward displacement autoclaves - a.k.a bottled fluid sterilisers (min temp 121 for 15 mins)
  • high pre-vacuum autoclave - for porous loads (min temp 134 for 3 mins)
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15
Q

Whenever possible, aqueous injections are ______ sterilised by autoclaving. The exception is if they are _________ drugs.

A

terminally

thermolabile

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16
Q

SAL for heat processes?

A

10^-6

17
Q

SAL for filtration?

A

10^-3

18
Q

Does filtration involve terminal sterilisation?

A

NO! It must be followed by aseptic transference of sterilised solution to final containers which are then sealed, and recontamination at this stage remains a possibilty

19
Q

Desirable qualities of filter?

A
  • mechanically strong and flexible (even when wet)
  • biologically inert and easily cleaned
  • non pyrogenic
  • does not clog
  • removes all particles of given size
  • minimal fibre shedding/ chemical release
  • can be sterilised by steam
  • flow rates are acceptable
20
Q

Advantages of filtration methods

A
  • particle removal (both viable and non viable cells)
  • can process large volumes
  • pyrogens are not generated (as organisms are removed)
  • filter material can be varied according to the product
21
Q

Disadvantages of filtration methods

A
  • post filtration aseptic processing is necessary
  • pyrogens are not removed
  • possibility of sorption of active ingredients
  • viruses and mycoplasmas not removed
22
Q

In order to release filtered products, what info must be recorded/ stated?

A
  • type of filter used
  • pressure differential and filter time records
  • bio-burden data (pre filtration)
  • adherence to documented procedures
  • filter integrity testing
  • sterility test results
  • details of sterilisation components
  • environment monitoring
  • operator testing