Measurement of antimicrobial activity 3 (Part 2) Flashcards

1
Q

Define sterile.

A

The COMPLETE absence of life. Absence of prions is desired but difficult to demonstrate.

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2
Q

Name some products that need to be sterile.

A
  • injections
  • ophthalmic preparation
  • dialysis solutions
  • implants
  • certain surgical dressings
  • surgical instruments e.g. syringes, rubber gloves, needles, catheters
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3
Q

What is terminal sterilisation?

A

When you make the product under non sterile conditions using non sterile ingredients and then sterilise it at the end of the process

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4
Q

What is aseptic manufacturing?

A

When you make the product under sterile conditions using sterile ingredients

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5
Q

Sterilisation process concentration on the destruction or physical removal of all microorganisms in a product. The processes are designed to remove the most problematic microorganisms (e.g. the smallest bacteria in filtration processes or the most heat- resistant bacterial spores in heat sterilisation). WHY?

A

This principle is that the elimination of the most problematic species will have led to the elimination of all less resistant microorganisms

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6
Q

The choice of sterilisation method is determined largely by the ability of the product to ______ the physical stresses applied during the process such as:

A

withstand

  • elevated temperature (autoclaving, dry heat)
  • irradiation
  • reactive gas (ethylene oxide)
  • filtration (using MO proof filter)
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7
Q

What is the simplest sterilisation method? And what are the conditions? e.g. temp + duration

A

moist heat sterilisation

121 degrees for 15 minutes

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8
Q

The choice of sterilization method depends on the _________ of the product

A

thermostability (e.g. moist heat sterilisation can only be applied to drugs that are heat-stable in aqueous solution and are not subject to hydrolysis)

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9
Q

If standard moist heat cannot be used, what is a suitable alternative?

A

Filtration in combination with aseptic processing

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10
Q

Is aseptic processing the same as sterilisation?

A

NO! Aseptic processing by itself is not a method of sterilisation, rather of preventing contamination

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11
Q

What are suitable reference organisms for testing sterilisation efficiency? Give examples

A

The most durable bacterial spores

  • Geobacillus stearothermophilus - formerly known as Bacillus stearothermophilus - for moist heat
  • certain strains of Bacillus subtilis for dry heat and gaseous sterilisation and
  • Bacillus pumilus for ionising radiation)
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12
Q

READ

A
  • Sterilisation processes are usually based on the ability to deal with a ‘worst case’ scenario
  • It is usually assumed that organisms within the
    products are no more resistant than the reference spores or isolates (however, resistance may be altered or lost entirely by laboratory subculture; resistance characteristics of the reference strains must be regularly checked)
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13
Q

D value is the

A

resistance of an organism to a sterilising agent. It is also used to indicate the rate of kill (but it does not quantify the amount of microbial killing)

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14
Q

What quantifies the amount of microbial killing?

A

inactivation factor

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15
Q

In terms of survival 10^-2 spores/ml means how many survivors in how man ml?

A

1 survivor in ever 100 ml of liquid

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16
Q

Z value represents

A

the increase in temperature necessary to reduce the D-value of an organism by 90%

17
Q

The elimination of viable microorganisms from a product is a _________-dependent process

A

time (influenced by duration of biocidal action and initial bioburden)

18
Q

For pharmaceutical products, the most frequent standard is that the probability of a non-sterile unit is 1 in 1 million units processed (i.e. 10^ -6). SO for an initial burden of 10^2 spores, an IF = ____ will be needed to achieve the sterility assurance of 10^-6

A

10^-8

  • The sterilisation will need to produce sufficient lethality to get an 8 log reduction in viable organisms
  • Will require exposure of the product to eight times the D-value of the organism (i.e. IF = No/N = 10t/D; so 10t/D = 108; so t = 8 x D)
19
Q

Bioburden is

A

the concentration of microorganisms in a

material

20
Q

Contamination on surfaces, including equipment, may be measured using

A

swabs or contact plates

21
Q

Microbial load in the atmosphere may be determined

by use of ‘_____ _____’ or by use of air samplers

A

settle plates

22
Q

What are some difficulties of sterility testing?

A
  • need trained operators
  • need media that can grow a wide range of microbial contaminants
  • hard to demonstrate a negative
  • difficult eliminating antimicrobial activity