introduction to medicinal products part 2 Flashcards

(35 cards)

1
Q

examples of powdered dosage forms?

A

effervescent powders (contain the drug, acid carbonate)
dusting powders (applied topically)
powders for syrup (for those difficulty swallowing)

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2
Q

why does segregation or de-mixing happen

A

size and density differences

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3
Q

how to prevent segregation?

A

granulation

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4
Q

what gives a good granulation

A

granules with correct ratios and narrow particle size distribution

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5
Q

why is preventing segregation important?

A

ensure patient receives same dose of API every time

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6
Q

pros of using powders/granules?

A

more stable than liquid preparations therefore increased shelf life
more convenient for drugs with high dosage
faster dissolution rate compared to tablets

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7
Q

cons of powders/granules

A

less convenient for patient to carry
not convenient for low dosage drugs
not suitable for drugs that are inactive in the stomach
can cause stability problems

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8
Q

why are tablets sometimes used over powders

A

convenient to handle
more stable

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9
Q

how is a tablet formed

A

hopper fills die with powder
upper punch lowered compressing the powder into a tablet
tablet ejected

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10
Q

What do powders, tablets, and capsules have in common?

A

they need dissolution to happen to be effective i.e need to be in a solution to be absorbed- molecularly dispersed form

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11
Q

what is the rate of dissolution?

A

the rate at which drug particles becomes drug molecules diffused into solvent

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12
Q

one way of the dissolution of a saturated solubility of solid increased?

A

addition of excipients

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13
Q

what is the role of a disintegrant?

A

makes sure the tablet breaks into fragments when in contact with liquid by facilitating water uptake or rupturing tablet by swelling

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14
Q

examples of disintegrant?

A

cellulose, starch

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15
Q

what is the role of dissolution enhancer?

A

required if drug has low aqueous solubility (dissolution is the rate limiting step) so temporarily increases solubility

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16
Q

examples of dissolution enhancer?

A

magnesium oxide

17
Q

what is the rate of dissolution effected by?

A

excipients present

18
Q

what are the kinds of release?

A

immediate release- drug released rapidly after being taken
modified release- prolonged, pulsatile, delayed

19
Q

difference between prolonged, immediate and delayed release

A

refer to introduction of medicinal products part 2 slide 16

20
Q

what is pulsatile release?

A

tablets released in two or more pulses

21
Q

what coating is used for tablets with delayed release?

A

enteric coating

22
Q

what is enteric coating

A

polymers that are insoluble in acid but dissolve in neutral/ slightly alkaline conditions in the gut

23
Q

characteristics of hard capsules?

A

have a cap and a body (shell)
colour aided for identification

24
Q

what is the shell of a capsule for

A

to hide hide mask the taste of the filling

25
what can hard capsules be filled with?
non aqueous liquids or dry solids
26
relationship between shell and the contents?
they shouldn't interfere with each other
27
what must a good hard capsule be able to do?
the shell should dissolve rapidly in gastrointestinal fluids contents in shell should disperse rapidly
28
how is dissolution rate increased in a capsule?
by adding excipients
29
why is dissolution rate faster with excipients
if the contents of the capsule have a more porous mass there's an increase in surface area so dissolution rate is faster
30
what do soft capsules contain?
liquid or semi-solid
31
difference between hard capsule and soft?
shell in one piece for soft
32
where is the drug contained in a soft capsule?
in solution or suspension in the matix
33
Hydrophobic matrix example
triglyceride vegetable oils
34
hydrophilic matrix example
polyethylene glycol
35
what is the shell of soft capsule made of?
gelatine, plasticizer, water