Dispersi Kasar Part 1

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    , ..,

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    :

    , () ,

    ( )

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    ( )

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    What is a dispersion at molecular level?

    What makes them physically stable?

    Interfacial Phenomena

    Coarse dispersion 10 to 50 m Fine dispersion 0.5 to 10 m

    Colloidal 1 nm to 0.5 m

    What happens at interface is critical!!

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    Suitable For Drugs with low solubility

    Pharmaceutical suspensions are uniform dispersions ofsolid drug particles in a vehicle in which the drug hasminimum solubility. Colloidal suspension 1 nm to 0.5 m Coarse suspension 1 to 100 m

    May be for oral, ophthalmic, parenteral, or topical use

    Oral suspensions may be aqueous preparations withflavored, sweetened vehicles or powder products fororal suspension

    Marketed preparations: ready-to-use dry powders which must be reconstituted before administration

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    10

    10

    10

    10

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    flocculation or caking

    determined by forces of attraction (van der Waals)versus forces of repulsion (electrostatic)

    deflocculated repulsion> attraction

    affected by [electrolytes]

    flocculated

    attraction > repulsion

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    Electric Double Layer

    ----

    ++++

    +

    -+

    -

    ++

    -

    +- ++ -

    +

    tightly

    bound

    diffuse

    electroneutral

    --++ + - -- +

    gegenion

    Nernst potential

    zeta potential

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    Electrical Double LayerElectrical Double Layer

    ----

    -

    ---+

    +

    +

    +

    Surface

    ()

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    , , , . .

    , .

    12/19/2013 2013 12

    .

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    Resuspend easily upon shaking Settle slowly after shaking

    H m n mix f r Ph i ll n

    chemically stable during its shelf life

    Sterile (parenteral, ocular)

    Gets into syringe (parenteral, ocular)

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    Controlled Flocculation

    electrolytes most widely used

    reduce zeta potential

    decrease force of repulsion

    change pH

    bridge formation

    polymers adsorb to particle surface

    bridging

    viscosity, thixotropy

    protective colloid action

    most effective

    alcohol reduction in zeta potential

    surfactants form adsorbed monolayers on

    particle surface efficacy is dependent on charge,

    concentration

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    State Rate of settling Sedimentationvolume

    Nature

    Flocculated Fast High Porous, easy toredisperse

    Deflocculated Slow Low Compact, difficultto redisperse

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    The suspension shall form

    loose networks of flocksthat settle rapidly, do notform cakes and are easy toresus end.

    flock

    Settling and aggregationmay result in formation ofcakes (suspension) that isdifficult to resuspend or

    phase separation (emulsion) cake

    Cake & Flock must be Controlled

    by Zeta Potensial, Viscosity andParticle Size

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    12/19/2013 2013 20

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    : 181818182222

    (((( )

    : ( )

    (: )

    ( )

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    F = Vu /V0 ; ideally, F should be equal to 1.0

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    : 181818182222

    (((( )

    ,

    , ,

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    (

    !

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    )

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    Determine the absolute viscosity of syrup using a ball of radius of 0.2 cm.The density of the ball is 2.33g/cc and the density of the syrup is 1.33 g/cc

    at 250 C. The rate of falling is 4.35 cm/sec.

    Determine the velocity of settling of sulfur in water. The average particleradius is 5.5 m. The density of sulfur and water at 250 C. is 1.96 and. ., . . . .

    If the height of the bottle is 10 cm how long will it take to completelysettle?

    Particle size determination:

    From the previous example, calculate the average particle size of sulfur.

    What is the necessary viscosity to reduce the sedimentation rate from0.0071 cm/sec to 0.00071 cm/sec?