gels creams and ointments Flashcards

1
Q

What is a gel

A

Non-fluid colloidal network or polymer network that is expanded
throughout its whole volume by a fluid.

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2
Q

what is swelling constrained by

A

constrained by intermolecular interactions or cross-links within
the molecular network, which confers structural rigidity.

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3
Q

what is swelling due to

A

solvent infiltration into the molecular network, thus

unfolding and expanding the molecular network

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4
Q

gels are what kinds of semi-solids

A

viscoelastic

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5
Q

name the type 1 gel

A

chemical gel

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6
Q

name the type 2 gel

A

physical gel

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7
Q

describe the type 1 chemical gel + give an example

A

Irreversible polymer network.
– Covalently cross-linked.
– Often uses a covalent cross-linker.
– Example: polyacrylamide gel.

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8
Q

describe the type 2 physical gel + give an example

A

Reversible polymer network.
– Weak intermolecular bonds (e.g. H-bonds).
– Sol-gel transition in response to specific stimulus (e.g. heat, pH).
– Example: agarose gel

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9
Q

what fluid phase does a hydrogel have

A

water

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10
Q

what fluid phase does an alcogel have

A

alcohol

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11
Q

what fluid phase does organogel have

A

organic solvent

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12
Q

which fluid phase does oleogel have

A

oil

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13
Q

which fluid phase does xerogel have

A

none

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14
Q

which fluid phase does aerogel

A

air

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15
Q

which fluid phase does cryogel have

A

produced throughfreezing

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16
Q

indications of pharmaceuitcal gels

A
Analgesic (e.g. ibuprofen).
– Anti-inflammatory (e.g. diclofenac).
– Anti-bacterial (e.g. clindamycin).
– Anti-fungal (e.g. miconazole).
– Local anaesthetics (e.g. lidocaine)
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17
Q

advvantages of gel:

A

Topical and parenteral drug delivery.
• Controlled release.
• Dose form retention.
• Environmentally sensitive gels:
– Conditional drug release triggered by changes in environmental
conditions, e.g. pH, temperature.
• In-situ gelling systems:
– Controlled release: administer in liquid form, drug release in semi-solid
form.
– In-situ gelling can be triggered by physiological environment, e.g. body
heat.

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18
Q

what are the basic components of pharmaceuticel gel

A

Drug.
– Solvent: dissolves drug and excipients, usually aqueous.
– Gelling agent: forms molecular network, provides structural rigidity,
entraps drug.

19
Q

what other components are in pharmaceutical gels

A

Cosolvent—enhance drug solubility.
– pH regulator (buffer)—enhance solubility of ionisable drugs, avoid skin
irritation.
– Preservative—inhibit microbial growth in aqueous gels.
– Penetration enhancer—enhance drug absorption into skin.

20
Q

describe a solid

A

– Liquid state.
– Colloidal dispersion (two or more components) of freely diffusing gelling
agent.
– Not a solution (single component).

21
Q

describe a gel

A

Solid-like state.
– Molecules of gelling agent interact covalently or non-covalently, polymer
network develops.
– Constrained by intermolecular bonds, physical entanglement or cross-links.
– Gelling agent not freely diffusing.

22
Q

what is the gel point

A

point of incipient polymer network formation.

23
Q

what does gel point depend on

A

chemical composition of the gel formulation,

24
Q

what are cellulosics

A

Cellulose and derivatives.

25
Q

what are carbomers

A

Cross-linked polyacrylic acid polymers.

26
Q

how can gel viscosity and swelling be enhanced

A

by neutralisation
with a base (e.g. triethanolamine) or by adding hydroxyl donors (e.g.
polyols, sugar alcohols) to promote hydrogen bonding.

27
Q

what is a cream

A

semi-solid emulsion

Dispersed system stabilised using a suitable emulsifier.

28
Q

name the two types of cream

A

hydrophillic

lipophlic

29
Q

what are the characteristics of hydrophillic cream

A

Non-greasy.
– Miscible with skin secretions.
– Water-washable.
– Non-occlusive.

30
Q

characteristics of lipophilic cream

A

– Somewhat greasy (less so than ointments).
– Less miscible with skin secretions than O/W.
– Less water-washable than O/W.
– Somewhat occlusive (less so than ointments).

31
Q

what does a cream need

A

Drug.
– Continuous phase.
– Dispersed phase.
– Emulsifier—stabilise emulsion.

32
Q

To ensure sufficient dose and even dispersion of ingredients:

A

Good solubility in either phase.

– Or, incorporate solids homogenously by trituration.

33
Q

To ensure stable emulsion:

A

Choice of suitable emulsifiers, commonly amphiphilic surfactants.
– Hydrophile-lipophile balance (HLB) and Bancroft’s rule.

34
Q

recall bancrofts rule in terms of emulsifier

A

High HLB emulsifier, O/W emulsion.

– Low HLB emulsifier, W/O emulsion.

35
Q

recall HLB in terms of emulsifier

A

Hydrophilic emulsifier: High HLB (>10).

– Lipophilic emulsifier: Low HLB (<10)

36
Q

what is an emulsion

A

continuous phase is a gel.

O/W or W/O.

37
Q

what is an emulgel

A

Emulsion + gel.

38
Q

advantages of emulgel:

A

– Incorporation of poorly water soluble drugs in a water-based
formulation.
– Non-greasy.
– Good patient acceptability.
– Dual release control mechanisms.
– Viscous continuous phase enhances emulsion stability.
– Thixotropy enhances spreadability

39
Q

what is an ointment

A

semi-solid dosage form, usually anhydrous with a hydrophobic oily
base, intended for external application to the skin or mucous membran

40
Q

Types of ointment

A

Hydrophobic (oleaginous) ointment.
– Water emulsifying ointment.
– Hydrophilic (greaseless) ointment.

41
Q

describe a hydrocarbon base

A

Occlusive—emollient effect.
– Not water-washable.
– Greasy.
– Petrolatum (paraffin).

42
Q

describe a absorption bases

A

– Form w/o emulsions with skin secretions.
– W/O emulsifier.
– Emollient effect.
– Lanolin and derivatives.

43
Q

describe a water-removable base for water emulsifying ointment

A

Form O/W emulsions with skin secretions.
– O/W emulsifier.
– Water-washable.
– Cetostearyl alcohol, cetomacrogol.

44
Q

describe water-soluble base

A

Water-washable.
– Non-greasy.
– Macrogols (polyethylene glycols = PEG).