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L19 - drug sol & DR 5

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

classification of surfactants

Back (Answer)

(charge carried by polar part) - cationic - anionic - non ionic - zwitterionic

#2
Front (Question)

non-ionic surfactants

Back (Answer)

• OH and ether groups • less polar than ionised group • need more units to produce effective polar moiety

#3
Front (Question)

polyoxyethylene chains as non ionic surfactants

Back (Answer)

• chains of these with 20 or more ether groups linked to non polar moiety • several chains linked to cyclic sugar linked to alkyl groups • POE (number) = number of monomeric polyoxyethylene groups in molecules

#4
Front (Question)

application os anionic surfactants

Back (Answer)

• cheap • toxicity (external) • O/W emulsifiers

#5
Front (Question)

applications for cationic surfactants

Back (Answer)

• disinfectants due to preservative properties • O/W emulsifiers • toxicity

#6
Front (Question)

application of non ionic surfactants

Back (Answer)

• O/W and W/O emulsifiers • low toxicity and low irritancy • oral and parenteral use

#7
Front (Question)

ionic parenteral surfactant appication

Back (Answer)

hemolysis of RBC and destruction of T lymphocyte cell

#8
Front (Question)

applications of non ionic parenteral surfactants

Back (Answer)

• phospholipids • polysorbates • cremophor • toxicity of non ionic residue contamination of ethylene oxide

#9
Front (Question)

micellisation

Back (Answer)

• alt method to adsorption • causes strong water water interactions that would be prevented if surfactant molecules were in sol as single molecules between water molecules • hydrophobic effect

#10
Front (Question)

hydrophobic portion of surface active drugs

Back (Answer)

• aromatic or heterocyclic ring system • tranqulizers • antidepressants • antihistamines • antibiotics

#11
Front (Question)

solubilisation

Back (Answer)

process where water insoluble/ early soluble substances brought into aq sol by incorporation into micelles

#12
Front (Question)

core of micelle

Back (Answer)

hydrocarbons

#13
Front (Question)

palisade layer of micelle

Back (Answer)

• hydrocarbon • polar parts • some water

#14
Front (Question)

surface or mantle of micelle

Back (Answer)

polar head groups + water

#15
Front (Question)

site of solubilisation

Back (Answer)

• depends on chemical nature of solubilisate • the more polar the solute, the more likely to be solubilised close to the surface • the polar region of a non-ionic micelle is significantly larger than that of ionic micelle

#16
Front (Question)

how to quantify micellar solubilisation?

Back (Answer)

solubilisation capacity (k)

#17
Front (Question)

what is solubilisation capacity, k?

Back (Answer)

• aka solubilisation ratio and efficiency • measures the ability of a surfactant to solubilise a solute

#18
Front (Question)

what is the molar solubilisation capacity?

Back (Answer)

moles of solute that can be solubilised by 1 mole of micellar surfactant

#19
Front (Question)

how to calculate solubilisation capacity?

Back (Answer)

• K = Stotal - Swater / Csurfactant - c.m.c OR • K = Sm/Cmic Sm = molar solubility of the solute in the micelle Cmic = molar conc of micellar surfactants

#20
Front (Question)

what happens if you increase HC chain of non-polar region?

Back (Answer)

• larger non polar region will solubilise more solute • decrease c.m.c

#21
Front (Question)

what happens if you introduce a polar group or double bond to chain of low polarity solutes?

Back (Answer)

it is equivalent to decreasing length of HC chain

#22
Front (Question)

what happens if your surfactant is branched?

Back (Answer)

smaller micelles

#23
Front (Question)

semi polar solutes

Back (Answer)

surface and palisade region largely unaffected by non polar region

#24
Front (Question)

are long chains good surfactant?

Back (Answer)

no, bad solubility - due to decrease in cmc - which decreases surfactant sol - so reduces amount of surfactant that can be used - increasing chain length in 2 C decreases solubility 10 fold