KOFIS Flashcards

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1
Q

What is suspension

A

Preparation where you can see particulates , at least one active ingredient, each drop has equal amounts.

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2
Q

Oral liquid

A

-Ready made
-Reconstituted- like antibiotics-come as powders you add water, and it turns into
the medicine
-Suspension- shake well before use
-Dosing accuracy- use syringe -most accurate way- make sure you have the right
dose
What are some su

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3
Q

Why is particle size important

A

Slow rate of sedimentation (small- harder for drug to sink at the bottom) (large- heavier so sink at the bottom quicker)
Storage

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4
Q

Advantages of suspensions

A

Draggability, swallobitility, absorption and modification of drug release

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5
Q

Disadvantages of suspensions

A

Patient compliance- have to shake before use
Dosing accuracy -less accurate than solutions
Storage conditions effect of disperse system
Transportation- can be bulky heavy or leak

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6
Q

Suspension formulation

A

Controlled flocculations -have lose drug particles that can be easily distributed before dispensing
-system is controllably flocculated to ensure the formulation is redispersed before
use

• Structured vehicle/solution
-increase viscosity to reduce sedimentation

-use polymers to reduce rate of sedimentation for suspended drug particles
-polymer added to increase viscosity

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7
Q

2 types of controlled flocculations

A

Indiffusible suspension:
contains light insoluble powders
when shaken disperse evenly throughout the vehicle
long enough to allow for an accurate dose to be poured out
some examples can include: light magnesium carbonate BP, magnesium trisilicate BP

Diffusible suspension:
Contains heavy insoluble powders
When shaken don’t disperse evenly throughout the vehicle
long enough to allow an accurate dose to be poured, therefore vehicle is thickened (requires a suspending agent) to slow down the rate of sedimentation, viscosity and particle size
some examples can include: aspirin BP, Calamine BP, gaviscon

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8
Q

Suspending Agents (have to know 2 of each)

A

natural polysaccharides: acacia gum bp, starch bp,
semi-synthetic polysaccharides: methyl cellulose bp, sodium carboxy methyl cellulose BP
Clays: aluminium magnesium silicate bp, bentonite bp
synthetic: carbomer Bp, polyvinyl alcohol bp
others: gelatin bp

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9
Q

Polymers

A

Polymers are defines as long chain molecules that can be made or occur naturally
generally rope like molecules that are made by joining many monomers (single) together
types of polymers: linear, branched, crosslinked
can be either chemical or physical

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10
Q

Conditions for bridging flocculation

A

good absorbers, good solvent, very low polymer density, and long polymers, polymers can be formed between particles and they can also form flocs

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11
Q

Examples of flavourings (need to know 1 of each)

A

flavoured syrups: blackcurrant syrup bp
aromatic waters: concentrated peppermint water bp
spirits: lemon spirit bp
extracts: liquid liquorice extract bp

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12
Q

topical formulations

A

composed of drug in a suitable semi-solid base
drug is suspended or dissolved in a semi-solid base
base could be either hydrophobic or hydrophilic
base plays role in drug release behaviour
if hydrophobic or hydrophilic base is chosen, drug release is different depending on each

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13
Q

Drugs are

A

dissolved or-completely mixed into ointment
dispersed in the-drug molecules suspended in base
ointment base-are greasy and is immiscible

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14
Q

ointment bases are

A

Anhydrous-contains no H2O
Greasy
Immiscible with skin secretions-so can be hard to apply because when you sweat, the sweat will form atop and adsorb to the surface
mixture of waxes (solid at rt), fats (semisolid at rt), oils (liquid at rt)

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15
Q

preparation of ointments

A

fusion
melt base in water bath
high mp to low mp
as base coold, add ingredients with decreasing mp
stir continuously (homogenous mix)
leave to set

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16
Q

creams

A

Viscous semi-solid emulsions for external use (topical applications)
Drugs can be dissolved or dispersed
w/o (oily creams):
natural emulsifiers (Bees wax or wool fat)
Creamy white of translucent, stiff - needs to be appealing to the eye so patient uses it
emollient (moisturisers)
w/o (Aqueous Creams):
Synthetic emulsifiers (macrogol or cetomacrogol)
good for absorption and presentation of drugs
thin, white and smooth
can wash off with water easily

17
Q

preparation of creams and pastes

A

oily phase
melt fatty bases
cool to 60 degrees and disperse oil miscible ingredients

18
Q

what are pharmaceutical pastes?

A

Semisolid preparations for External Use
Very fine powders (high proportion ~50%)
Non-greasy base such as liquid paraffin or glycerol
Stiff and don’t spread well

19
Q

application of pastes

A

Localised delivery (lesion or plaque)
Dressings (absorbent for wound exudates, antiseptic, protective, soothing)
Nappy Products (absorbent ammonia in urine)

20
Q

definition of gels

A

Formed by the aggregation of colloidal particles or polymers

21
Q

what are colloids?

A

They are particles with a size less than 1μm
Dispersed phase = particles or droplets
Continuous phase = solution media

22
Q

classification of colloids

A

Colloidal dispersions: Particle droplets in dispersion medium, Thermodynamically unstable after phase separation
True solutions of macromolecular materials: Natural polymeric materials such as proteins and cellulose, Stable thermodynamically and can be redispersed after phase separation
Associate colloids: Surfactants (micelles), Thermodynamically stable

23
Q

gel formulation

A

Particles link together to form an interlaced network
creates rigid structure
the continuous phase is held together withing the meshes
between the fibres the gel is dispersed

24
Q

advantages of gels

A

stability
aesthetic
rapid release
rapid absorption
suitable for topical application
easy to wash off

25
Q

what are emulsions?

A

they are prepared when oil and water are mixed together

26
Q

what are surfactants?

A

surface active agents
have to be balanced

27
Q

classification of surfactants

A

cationic (quaternary ammonia), irritant to skin
cationic (carboxylates, sulphonates, phosphates),
amphoterics (betaines), main characteristics depend on ph
nonionic (hydrophilic groups that have no charge), main span and tween
polymeric surfactants (pluronics), Excellent dispersing & stabilising power for hydrophobic particles in water, Highly concentrated suspensions can be made, Polymeric surfactants modified for use as surfactants

28
Q

advantages of surfactants

A

cost
low toxicity
biodegradable

29
Q

disadvantages of surfactants

A

Precipitation in Ca2+ and Mg3+ ions
To avoid precipitation
Carboxylates modified with hydrophilic groups

30
Q

what are the uses of surfactants

A

Wetting and spreading
Emulsification
Stabilising
Solubilising

31
Q

pros of emulsions

A

Druggability
* Solubility issues and lipophilic drugs
* Creams are semi solid emulsions
Palatability
* e.g., cod liver oil emulsion
Swallowability
* Flavoured aqueous phase
Absorption
* Improved absorption and bioavailability
Stability
* Separation of incompatible ingredients

32
Q

cons of emulsions

A

Patients Compliance
* Shake well before use
Dose Accuracy
* Dispersed phase
Storage conditions
* Stability of dispersed phase
Microbial contamination
* Emulsifier, water
Transportation
Bulky, Heavy, Breakage, Leakage

33
Q

tests for emulsions

A

Dilution test
Dye test
Electric conductivity test

34
Q

about suppositories and pessaries

A

Generally for local (treatment of infections) rather than systemic effects
For introduction into body cavities (melt and release drug)
Good for drug inactivated by GI tract, liver

35
Q

pros of suppositories

A

Local effect-deliver drug directly to Rectum, Vagina, Urethra
Bowel evacuation (suppository used to
trigger defecation) for surgical interventions
Unconscious patients
Patients in seizures
Vomiting (regurgitation)
Systemic effect (first pass-metabolism)
Not exposed to harsh GI conditions
Drugs irritating to stomach can be given

36
Q

cons of suppositories

A

Unacceptable (cultures)
Difficult to self-administer
patient mobility (disability)
arthritis
Variable/erratic absorption
Mucosal irritation (indomethacin-rashes)
Installation may trigger defecation
High cost of manufacture
Disease state can affect absorption
Not well researched (lack of comparable data)