L13 - Suspensions - Introduction Flashcards

1
Q

what im a solution in pharmacy terms

A
  • solution is a liquid system
  • formed from various combination of phases
  • at the end the solution is a one-phase system where at equilibrium all the ingredients are disperased eenly at the molecular level
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2
Q

in a solution: what are the other components added to make up a formulation

3 examples

A
  • preservatves
  • buffers
  • flavours
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3
Q

What is a characteristic of the appearance of a solution

A
  • opticaly clear
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4
Q

what is a suspension

A
  • a dispersion of solid materials, generally the drug, in a liquid phase
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5
Q

what are the differences in pharmacy between a solution and a suspension

A
  • solid material (usually the drug) does not dissolve in the liquid phase in a suspension#
    • drug remains as solid particles
    • these particles are distributed throughout the liqud phase
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6
Q

what is the dispersed phased and the liquid phase

A
  • a suspension describes a dispersion of solid materials (the dispersed phase) in liquid (the continuous phase)
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7
Q

in general term, in a suspension, what influences the physical and chemical behaviour

A

particle size

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8
Q

what are the typical size of particles in a pharmaceutical suspension?

what are the different types of suspension

A
  • particle size in typical pharmaceutical suspension are between 0.1µm and 10µm
  • colloidal suspension
    • upto 1µm
  • coarse suspension
    • >1µm
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9
Q

what is the appearance of suspension

how does it change

A
  • suspension are not opotically clear and appear cloudy unless the size of the particles is within the colloidal range
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10
Q

what is the rational of pharmaceutical suspension

A
  • durgs with low solubility in the contineous phase
  • patient acceptability
    • a liquid form, rather than a solid dosage form
  • drugs that have an unpleasant taste in soluble form can be made into insoluble form
    • more palatable
    • e.g. chloramphenicol (soluble) → chloramphenicol palmitate (insolbule)
  • oral suspension
    • drug already finely divided form → optimal dissolution in GI tract → increased absorbtiion
  • stability
    • freshly prepared just before use
  • modify drug release
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