Contamination Flashcards
What are the Different Types of Contamination?
- Product Related
- Foreign Material
Describe Product Related Contamination
- 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
Describe Foreign Material Contamination
- 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
Describe Fibre as a Foreign Material Contaminant
- Usually identified using polarised light microscopy
- Variety fibres found within same sample = more serious contamination issue
Describe Glass Particles as a Foreign Material Contaminant
- 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
Describe Silicone as a Foreign Material Contaminant
- 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
Describe the Control of Dust Contamination
- 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
How can Product Related Contamination be Prevented?
- 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
Describe Drug Counterfeiting
- 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
Describe Cross Contamination
- Contamination of a starting material, or of a product with another starting material or product
What does the risk of accidental cross-contamination arise from?
- 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
Define Disinfectants
- Process of removing micro-organisms from surface of objects
Define Antiseptics
- Destruction or inhibition of micro-organisms on living tissues to limit/prevent harmful effects of infection
Define Preservatives
- Limit proliferation of micro-organisms that may be introduced into non-sterile products such as oral and topical
Why do we add preservatives?
- Prevent microbial spoilage of product, minimise risk of infection
Should preservatives be added?
- Yes: Multidose medication bottles
- Avoid: Younger paediatric patients
Which Preservative to use?
- Wide spectrum of antimicrobial activity
- Chemically and physically stable over the shelf-life of product
- Not compromise the quality or performance of product, pack or delivery system
- Low toxicity
What factors are the basis for selecting a preservative?
- Effectiveness
- Effect of pH on preservative
- Safety and comfort of patient
Describe Effectiveness in terms of the Basis for selecting a preservative
What are the factors that limit effectiveness?
- Require broad spectrum antimicrobial
- Factors that limit effectiveness
- Inactivation due to interaction with container
- Adsorption onto suspended solids
- Entrapment of preservative within mielles or surfactants
Describe the Effect of pH on Preservatives
- Many preservatives are weak organic acids
- Partition coefficient
- [HA]org: concentration of preservative in organic phase at equilibrium
- [HA]aq: concentration of preservative in aqueous phase at equilibrium
Describe Safety and Comfort of Patient in terms of Preservatives
- Toxicity
- Hypersensitivitiy/irritation to skin
- Odour
- Taste
What are the Types of Preservatives?
- Acids and Esters
- Esters of p-hydroxybenzoic acid (parabens)
- Alcohols (aliphatic)
- Alcohols (Arakyl and highly substituted aliphatic)
- Bronopol
What are the Main Disadvantages of Acids and Esters as Preservatives?
- Low pKa, most active at pH below 4
What are the Advantages and Disadvantages of Esters of p-hydroxybenzoic acid (parabens) as Preservatives?
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Advantages:
- Prepared to overcome pH dependence
- Active against broad spectrum of microorganisms
- More effective against Gram +ve
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Diadvantages:
- Inactivation by non-ionic surfactants
- Reduced activity against bacteria; especially pseudomonads
- Limited solubility in water
- As chain length increases, hydrophobicity increases and antimicrobial activity increases