Suspensions (exam 2) Flashcards

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
Q

compounding mechanism to decrease particle size

A

trituration

26
Q

suspensions for neonates should not include

A

preservatives
alcohol
color
flavors

27
Q

which type of powder requires a wetting agent? and why?

A

hydrophobic powders

not wet by water

28
Q

how does wetting agents work?

A

disperse air in the particles
disperse particles
allow penetration of dispersion medium into powder

29
Q

examples of wetting agents (2-5%)

A

alcohol
glycerin
propylene glycol
surfactants

30
Q

suspending agents are added to

A

thicken the dispersion medium

31
Q

examples of suspending agents (1%)

A

carboxymethylcellulose
methylcellulose
microcrystalline cellulose
polyvinyl pyrrolidone

32
Q

examples of flocculating agents

A

clays
electrolytes
nonionic surfactants
ionic surfactants

33
Q

why is a portion of the vehicle used to wash mixing equipment?

A

to ensure correct drug concentration in the suspension

34
Q

suspensions are physically

A

unstable systems

35
Q

beyond use date when stability is not known

36
Q

packaging and storage of suspensions

A

wide mouth containers
adequate airspace above liquid
tight, light resistant container
protect from freezing and excessive heat
stored in fridge

37
Q

types of suspensions

A

ready to use form of suspensions
dry powders for oral suspension
extemporaneously compounded suspensions

38
Q

usual adult dose of an oral suspension is

A

5 ml (1 tsp)

39
Q

pediatric dosing of suspension is

A

dose calibrated number of drops