E2 L4 - Emulsion Flashcards

1
Q

A system of two immiscible liquids in which one is dispensed as droplets (e.g. water phase + oil phase)

A

Emulsion

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2
Q

Dispersed phase

A

“water in oil” (water is dispersed, oil is continuous)

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3
Q

Continuous phase (=external phase)

A

Determines organoleptic properties (taste, smell, feel) of the emulsion

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4
Q

Oral: Oil in water

A

to mask the tase of an oil
to enhance absorption of an oil

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5
Q

External: Oil in water

A

water washable vanishing cream

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6
Q

External water in oil

A

for cleansing skin – cold cream

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7
Q

IV Lipid emulsion

A

Oil in water

Oil has to be very small so it does not block the blood vessel

Oil can provide more calories than solutions

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8
Q

Emulsifying agents

A

Added to stabilize the emulsion

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9
Q

Three types of emulsifiers

A

Surfactants
Polymers
Fine divided particles

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10
Q

Three strategies of emulsifiers

A

Use surface activation (surfactants)
Use polymer (provide steric interest so they do not merge)
one purpose: Improve stability

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11
Q

Surfactant

A

Empty vials
Hydrophilic and hydrophobic (amphipathic)
Align (hydrophilic - water; hydrophobic - oil)
Separate
Surface activation

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12
Q

Hydrophilic colloid - polymer

A

Align with surface of the barrier
create barrier

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13
Q

Fine particles

A

Smaller than polymer
Particles CANNOT MERGE because there is barrier created on the surface

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14
Q

Which emulsifier is more different than the other two?

A

Surfactant
Surfactant - reduces interfacial tension
other two - do not reduce interfacial tension, just stop the things from merging

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15
Q

Surface active agents - surfactants

A

Molecules that contain both a hydrophilic and hydrophobic region
Orient at the liquid-liquid or liquid-air interface and lower interfacial tension

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16
Q

Log C

A

Concentration of surfactant

17
Q

Surfactants reduce surface tension to a certain extent why?

A

Over a certain concentration, it stops reducing tension
Forms micelles
Too much - they start to form their own assemblies, so they are not reducing surface tension anymore (since they are forming small vesicles themselves
When this happen: CMC - critical micelle count

18
Q

Know different types of surfactant chains, if they are anionic or cationic, and if they are a zwitterion or not

A

-

19
Q

Hydrophile-lipophile balance

A

A measure of the relative contributions of the hydrophilic and lipophilic regions of a surfactant

Calculated according to an empirical formula

Ranges 0-20 for non-ionic surfactants

Low HLBs indicate greater lipid solubility

In practice, a mix of emulsifying agents is used to get a desired HLB

20
Q

HLB equation

A

HLB = aX + (1-a)Y

X: HLB of surfactant 1

Y: HLB of surfactant 2

A: Fraction of surfactant 1 in the surfactant mix

Bigger than 10 - hydrophilic
Smaller than 10 - hydrophobic

HLB = X * a + y(1-a)

21
Q

Rule of Bancroft (1913)

A

A relative solubility of the surfactant determines they type of emulsion (i.e. the phase in which a surfactant is more soluble becomes the continuous phase)
E.g. a surfactant with a high HLB (>10, soluble in water) forms an o/w emulsion

22
Q

Micelles

A

As the concentration of a surfactant increases above a critical concentration, (the CMC) the surfactant molecules self-associate into small aggregates called MICELLES
The micelles formed in water have the hydrophobic groups of the surfactant oriented TOWARD the core of the micelle. The center of the micelle represents a lipid-like region that is capable of dissolving water-insoluble drugs

23
Q

Hydrophobic colloids

A

Hydrophilic polymers
Used for O/W emulsions – hydrophilic

Form a multimolecular film at the interface and increase the viscosity of water

Do NOT lower the interfacial tension

Ex: Acacia, tragacanth, gelatin

Natural polymers

24
Q

Finely divided solid particles

A

Particles less than a micron can adsorb at the interface and form a film of fine particles
Ex:
Bentonite, magnesium, aluminum silicate, aluminum hydroxide: Hydrophilic O/W emulsion
Charcoal: Hydrophobic, for W/O emulsion

25
Q

Predicting type of emulsion

A

The phase in which the emulsifier is most soluble will be the external (=continuous) phase

Surface active agents

HLB < 10: W/O

HLB > 10: O/W

Hydrophilic colloids: Only O/W

Finely divided solids

Hydrophilic if contact angle < 90degrees O/W

Hydrophobic if contact angle >90 W/O

**Obtuse – hydrophobic

Acute – hydrophilic**

26
Q

Phase volume ratio

A

Phase volume ratio:

Volume of oil phase/Total volume of the emulsion

0-26%: O/W only

26-74%: either

74-100% W/O only

27
Q

T/F: emulsifier is a surfactant

A

FALSE - Correct to say surfactant is an emulsifier, NOT that emulsifier is surfactant (it is a subtype of emulsifier, but not the only one)

28
Q

Instability of emulsion - creaming

A

V = d2(pi-pe)980/18n (Stokes Law)

V = velocity of sedimentation

D: diameter of droplets

Pi: density of internal phase

Pe: density of external phase

980 cm/sec2: gravity constant

Reversible as long as the interfacial film is effective in maintaining the integrity of individual droplets

Droplets stay as droplets – shake before use

Natural process

29
Q

Instability of Emulsion - Coalescence

A

Droplet size increases because the interfacial film is unable to maintain the integrity of individual droplets

Irreversible and WILL ULTIMATELY lead to a layer of oil and a layer of water (broken emulsion)

Cannot fic by shaking bottle

Must be reformulated

Molecules bump together and fuse – irreversible

30
Q

Instability of Emulsion - Phase inversion

A

Big problem in IN

Hard water

Due to phase volume ratio exceeding 74%

Rule of thumb: keep the phase volume ratio <50%

O/W emulsion stabilized w/sodium stearate can be inverted to W/O type using “hard” water (containing calcium)

Conversion of Na stearate to Ca stearate