Lecture 12 Flashcards

emulsions (2/15)

1
Q

emulsion

A

a system of two immiscible liquids in which one is dispersed as droplets
example - water phase + oil phase

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2
Q

two phases of emulsions

A

dispersed phase
continuous phase (external) – determines organoleptic properties

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3
Q

applications of emulsions

A

oral, external, intravenous lipid (O/W)

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4
Q

O/W oral

A

used to mask the taste of an oil (mineral oil emulsion as a laxative)
used to enhance absorption of an oil (vitamin a/d, cod liver oil)

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5
Q

o/w external

A

water-washable
vanishing cream

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6
Q

w/o external

A

for cleansing skin
cold cream

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7
Q

intravenous lipid emulsion

A

o/w only
for parenteral nutrition
100mL of 20% lipid emulsion provides 200kcal, while 100mL of 5% dextrose only provides 20kcal
smallest capillaries are 5 mcm (critical that the droplet size is less 1 mcm to avoid embolisms)

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8
Q

emulsifying agents

A

emulsifiers
added to stabilize the emulsion

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9
Q

types of emulsifying agents

A

surface active agents (surfactants, monomolecular film)
hydrophilic colloids (polymers, multimolecular film)
finely divided solid particles (solid particle film)

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10
Q

surfactants

A

molecules that contain both a hydrophilic region and a hydrophobic region
orient at the liquid-liquid or liquid-air interface and lower interfacial or surface tension
act as clamp to bind oil and water together

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11
Q

types of surfactants

A

anionic - alkyl sulfate, alkylbenzene sulfonate
cationic - alkyltrimethylammonium bromide, alkylpyridinium chloride
zwitterionic - alkyl betaine, alkyldimethylamine oxide
nonionic - alcohol ethoxylate, poly-poly-poly block copolymer

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12
Q

hydrophile-lipophile balance (HLB)

A

a measure of the relative contributions of the hydrophilic and lipophilic regions of a surfactant
calculated according to an empirical formula
ranges from 0 to 20 for non-ionic surfactants

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13
Q

low HLBs

A

indicate greater lipid solubility

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14
Q

HLB of a mixture equation

A

aX + (1-a)Y
X – HLB of surfactant 1
Y – HLB of surfactant 2
a – fraction of surfactant 1 in the surfactant mixture

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15
Q

rule of bancroft (1913)

A

a relative solubility of the surfactant determines the type of emulsion (= the phase in which the surfactant is more soluble becomes the continuous phase)

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16
Q

surfactant with high HLB

A

soluble in water
forms an o/w emulsion

17
Q

micelles

A

small aggregates that form as surfactant molecules self-associate, occurs as the concentration of a surfactant increases above a critical concentration (CMC)
have hydrophobic groups of the surfactants oriented toward the center/core

18
Q

core of the micelle

A

represents a lipid-like region that is capable of dissolving water-insoluble drugs

19
Q

hydrophilic colloids

A

hydrophilic polymers
used in O/W emulsion
form a multimolecular film at the interface and increase the viscosity of water
does not lower the interfacial tension
examples - acacia, tragacanth, gelatiun

20
Q

finely divided solid particles

A

particles less than a micron can adsorb at the interface and form a film of fine particle

21
Q

hydrophilic finely divided solid particles

A

bentonite
magnesium aluminum silicate
aluminum hydroxide
used for O/W emulsion

22
Q

hydrophobic finely divided solid particles

A

charcoal
used for W/O emulsions

23
Q

predicting type of emulsion

A

based on surface active agents, hydrophilic colloids, or finely divided solid

24
Q

surfactant predicts emulsion type

A

HLB less than 10, W/O
HLB greater than 10, O/W

25
Q

hydrophilic colloids predicts emulsion type

A

only O/W

26
Q

finely divided solids predict emulsion type

A

hydrophilic if contact angle is less than 90, O/W
hydrophobic if contact angle is greater than 90, W/O

27
Q

phase volume ratio

A

volume of oil phase / total volume of the emulsion
0-26 –> O/W only
26-74 –> either O/W or W/O
74-100 –> W/O only

28
Q

creaming

A

reversible as long as the interfacial film is effective in maintaining integrity of individual droplets
Stokes Law

29
Q

Stokes Law

A

velocity of sedimentation

(squared diameter of droplets)(density of internal phase - density of external phase)980
/
18(viscosity of external phase)

30
Q

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 be fixed by shaking
must be reformulated

31
Q

phase inversion

A

due to phase volume ratio exceeding 74% (should keep the ratio below 50%)
O/W emulsion stabilized with sodium stearate can be inverted to W/O type using hard water – containing calcium (high HLB to low HLB)

32
Q

instability of emulsion factors

A

creaming
coalescence
phase inversion