Suspensions (exam 2) Flashcards

(39 cards)

1
Q

dispersed system

A

liquid preperation containing undissolved or immiscible drug in a vehicle

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2
Q

phases in a suspension

A

dispersed phase
dispersing phase/medium (vehicle)

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3
Q

label for suspensions

A

shake well

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4
Q

coarse dispersions

A

contain large particles
ex: suspensions, emulsions

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5
Q

fine dispersions

A

contain small particles
ex: magmas, gels

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6
Q

suspensions are liquid preparations containing _________________ in a liquid phase in which particles are ___________________

A

solid drug particles dispersed

not soluble

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7
Q

pharmaceutical suspensions has to possess

A

therapeutic efficacy
chemical stability
permanency of preparation
esthetic appeal

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8
Q

routes of administration for suspensions

A

oral
topical
ophthalmic
parenteral

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9
Q

reasons to formulate a suspension

A

when a drug is insoluble
when a drug is unstable in solution
when the taste is bad, needs to be overcome

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10
Q

suspensions contain

A

large solid drug particles

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11
Q

sedimentation

A

particles tend to settle, redisperse upon shaking

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12
Q

__________________ is very important to the accurate administration of doses

A

uniform redistribution

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13
Q

caking of suspension

A

rigid cohesion of particles that resists breakdown upon shaking

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14
Q

what can prevent caking?

how?

A

flocculation

enhances particle dispersability

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15
Q

what type of particles produce more stable suspensions?

A

barrel shaped particles

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16
Q

flocs resist complete settling, but flocculated particles ________________ than fine particles

A

settle faster

17
Q

stokes equation says sedimentation rate can be decreased by

A

reduce the particles size (dispersed phase)
increase the viscosity of the suspension (dispersion medium)

18
Q

zeta potential

A

voltage difference between ions in tightly bund layer and electroneutral region

19
Q

the magnitude of the zeta potential gives an indication of

A

the stability of the dispersion system

20
Q

suspension with zeta potential between -30mV and +30mV

21
Q

suspension with zeta potential more than +30mV or less than -30mV

22
Q

micropulverization

A

for oral and topical solutions
mill and beaters produce fine drug power

23
Q

grinding

A

for parenteral and ophthalmic solutions
rotating hammers/pins produce very fine particles

24
Q

spray drying

A

cone shaped apparatus rapidly dries and produces very very small particles

25
compounding mechanism to decrease particle size
trituration
26
suspensions for neonates should not include
preservatives alcohol color flavors
27
which type of powder requires a wetting agent? and why?
hydrophobic powders not wet by water
28
how does wetting agents work?
disperse air in the particles disperse particles allow penetration of dispersion medium into powder
29
examples of wetting agents (2-5%)
alcohol glycerin propylene glycol surfactants
30
suspending agents are added to
thicken the dispersion medium
31
examples of suspending agents (1%)
carboxymethylcellulose methylcellulose microcrystalline cellulose polyvinyl pyrrolidone
32
examples of flocculating agents
clays electrolytes nonionic surfactants ionic surfactants
33
why is a portion of the vehicle used to wash mixing equipment?
to ensure correct drug concentration in the suspension
34
suspensions are physically
unstable systems
35
beyond use date when stability is not known
14 days
36
packaging and storage of suspensions
wide mouth containers adequate airspace above liquid tight, light resistant container protect from freezing and excessive heat stored in fridge
37
types of suspensions
ready to use form of suspensions dry powders for oral suspension extemporaneously compounded suspensions
38
usual adult dose of an oral suspension is
5 ml (1 tsp)
39
pediatric dosing of suspension is
dose calibrated number of drops