Suspension Dosage Forms Flashcards

1
Q

What are pharmaceutical applications of suspensions?

A
  • All new products (unless problematic)
  • Paediatrics
  • Geriatrics
  • Administration of water-insoluble drugs
  • Enteral fed patients
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2
Q

What should be considered in lansoprazole suspensions? (enteral feeding tubes)

A

*should be diluted as too viscous to administer via fine bore tube

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3
Q

What should be considered for augmentin suspension? (enteral feeding tube)

A

*should be diluted to half strength to avoid ‘caking’

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4
Q

What should be considered with diazepam suspension? (enteral feeding tubes)?

A

*not recommended due to adoption onto plastic tubing

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5
Q

What should be considered with sucralfate suspension? (enteral feeding tubes)

A

Not recommended due to ‘bezoar’
formation (aggregates of undigested
material) in patients with impaired
gastric emptying, due to binding of
sucralfate to protein in the food

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6
Q

Describe the way suspensions disperse

A
  • Course dispersion in which insoluble particles, generally > 1 μm, are
    dispersed within a liquid medium which is usually aqueous
  • Settle out
  • Shake to stay suspended
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7
Q

What is an ideal suspension?

A
  • Homogeneous during dosing
  • Easy to re-suspend
  • Proper viscosity
  • Particles should be small and uniform in size
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8
Q

How can you work out if a suspension is flocculated or not?

A

work out ratio = Vs/Vt ~ h/h0

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9
Q

What is the system like in suspensions?

A
  • In deflocculated systems the
    particles are not associated
  • During flocculation, particles come
    together attracted by weak forces to
    form flocs
    *pressure leads to close packing at the bottom = cake
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10
Q

How is caking prevented?

A

*using flocculating agents in the formulation

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11
Q

What are some flocculating agents?

A

*electrolytes (reduces electrical forces of repulsion)
*surfactants (hydrated layers around particles and formation of liquid bridges)
*polymers (structured vehicles and inter particulate interactions)

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12
Q

How does zeta potential affect caking?

A

higher zeta = caking
lower zeta = non caking

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13
Q

Entail what happens what Va > Vr (small)

A
  • Weakly attracted clusters form
  • Flocculation = ‘form into an aggregated lumpy or fluffy mass’
  • Re-disperse upon shaking
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14
Q

Entail what happens when Va > Vr (large)

A
  • Close packed arrangement at the bottom of the container
  • Particles in the lowest layers are ‘pressed’ together by the weight of
    the particles above → Produces a course compact mass
  • The repulsive barrier can be overcome and ‘caking’ can ensue
  • A ‘caked’ suspension cannot be re-dispersed
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15
Q

What is entailed in a flocculated system?

A
  • Particles are aggregated
  • Fast sedimentation
  • “Fluffy” sediment
  • Large sedimentation volume
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16
Q

What is entailed in a deflocculated system?

A
  • Particles remain as discrete units
  • Slower sedimentation
  • Compact sediment
  • Small sedimentation volume
17
Q

What is the best DVLO for suspensions?

A

*secondary minimum

18
Q

What is needed to achieve controlled flocculation?

A

*particle size
*use of electrolytes to control electrostatic repulsion
*addition of flocculating agents