Contamination Flashcards
1
Q
What are the Different Types of Contamination?
A
- Product Related
- Foreign Material
2
Q
Describe Product Related Contamination
A
- Impurities arise during storage
- Chemical instability of the pharmaceutical substance
- Chemical decomposition catalysed by light, traces of acid or alkali, traces of metallic impurities, air oxidation, carbon, dioxide and water vapours
- Chemical instability of the pharmaceutical substance
3
Q
Describe Foreign Material Contamination
A
- Foreign products are introduced into a drug
- Foreign ingredients or products
- Impurities in the ingredients
- Endotoxins
- Particulate matter
- Micro-organisms
- Products or substances other than product manufactured
4
Q
Describe Fibre as a Foreign Material Contaminant
A
- Usually identified using polarised light microscopy
- Variety fibres found within same sample = more serious contamination issue
5
Q
Describe Glass Particles as a Foreign Material Contaminant
A
- Can be generated by fracture of the vial neck or opening, from external sources such as other vials, glassware and lighting and from delamination of the inner vial surface
- Sink rapidly to the bottom of the vial when the liquid is agitated
6
Q
Describe Silicone as a Foreign Material Contaminant
A
- Used as a lubricant for rubber stoppers and plungers
- ‘Sloughs off’ - ends up in product
- Can interact with protein based drugs or active ingredients producing particles
- Silicone oil = oil droplets = hazy appearance
7
Q
Describe the Control of Dust Contamination
A
- Dust is a carrier of microbes and contaminants
- Ambient bacteria are removed by filtration
- Internal bacterial distribution can be controlled by directional air flow and air flushing or dilution
8
Q
How can Product Related Contamination be Prevented?
A
- Should be protected from light
- Darkened glass, metal containers
- Materials susceptible to oxidation by air or attack by moisture
- Sealed containers
- Air from containers can be displaced by an inert gas e.g. N
- Can be prevented by adding suitable antioxidants which are capable of undergoing oxidation as the expense of the substances
9
Q
Describe Drug Counterfeiting
A
- A pharmaceutical product which is deliberately and fraudulently mislabelled with respect to identity and/or source
- Branded and Generic Products:
- Products with correct or incorrect ingredients
- Products without active ingredients
- Products with incorrect quantity of active ingredient
- Fake packaging
10
Q
Describe Cross Contamination
A
- Contamination of a starting material, or of a product with another starting material or product
11
Q
What does the risk of accidental cross-contamination arise from?
A
- The uncontrolled release of dust, gases, vapours, sprays or organisms from materials and products in process
- From residues on equipment and from operators’ clothing
- Things that are more sensitive e.g. injection, parenteral, opthalmics
12
Q
Define Disinfectants
A
- Process of removing micro-organisms from surface of objects
13
Q
Define Antiseptics
A
- Destruction or inhibition of micro-organisms on living tissues to limit/prevent harmful effects of infection
14
Q
Define Preservatives
A
- Limit proliferation of micro-organisms that may be introduced into non-sterile products such as oral and topical
15
Q
Why do we add preservatives?
A
- Prevent microbial spoilage of product, minimise risk of infection