Dosage Forms II Exam 1 Flashcards

1
Q

What are the types of liquid dosage forms?

A

Solution, Emulsion, Suspension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the advantages of solutions?

A

homogeneous, no problems of content uniformity
easy to manufacture
good bioavailability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are two things to know when designing a buffer?

A

important for stability, controls pH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Why is a weak acid with a pKa close to the desired pH selected?

A

because the reaction they undergo will not significantly change the concentration of the solution and allows only a small change in pH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How do you design a buffer with a specific pH and buffering capacity?

A

by adding a weak acid with a pKa similar to the desired pH of the solution and provides maximum stability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What can be done to minimize irritation if pH of solution cannot match the pH of body fluid?

A

minimize buffering capacity, minimize volume, and administer slowly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are antimicrobial preservatives mechanism of action?

A

they absorb to the bacterial membrane and disrupt it; membrane is lipophilic and has a negative surface charge

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the function of each excipient in a solution dosage form?

A

alcohols- Ethanol, Benzyl Alcohol, Chlorobutanol
acids- Benzoic acid, Sorbic acid
parabens- Propyl paraben, butyl paraben, methyl paraben, and ethyl paraben
quaternary ammonium compounds- Benzalkonium Chloride(Zephirin), Cetyltrimethylammonium chlroide(Cepryn)
antioxidants- Free-radical scavengers(Propyl, octyl, dodecyl esters of gallic acid, BHA, BHT, Tocopherols, Vitamin E, Reducing agents(Sodium bisulfite, Ascorbic acid, Thiols)
chelating agents (Citric acid, EDTA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the type of emulsions?

A

Oil in water; Water in oil (dispersed & continuous phase)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the clinical applications of Emulsions?

A

Oral, External, Intravenous lipid emulsion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the molecular basis of interfacial tension and how do surfactants alter the interfacial tension?

A

less molecules are at the interface then in the bulk phase; these molecules at the interface contact other molecules and experience different forces of attraction
-surfactants have both a hydrophilic and hydrophobic region and lower the overall interface tension (form micelles)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the role of interfacial tension in production of an emulsion and stability of the emulsion?

A

lower the interfacial tension the more stable the emulsion is

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How do micelles form in solutions of surfactants and their utility?

A

form at the liquid-liquid or liquid-air interface to lower the interfacial tension which causes micelles as surfactant concentration is increased

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the mechanism by which surfactants, hydrophilic colloids, and finely divided solids act as emulsifying agents?

A

surfactants form micelles, hydrophilic colloids form a multi molecular film and increase the viscosity of water, finely divided solid particles forms a film of fine particles and absorb at the interface

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the basis of physical instability of emulsions?

A

Creaming (how quickly it will float to surface or sediment; reversible), Coalescence (droplet size increases; irreversible) Phase inversion (O/W emulsion stabilized by W/O using hard water)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the typical components of an emulsion and how to manufacture an emulsion?

A

Benzyl Alcohol-Preservative
Cetyl Alcohol- Emulsifier, Thickening agent
Glycerin- Humectant
Liquid Petrolatum- Oil Phase
Magnesium aluminum silicate- Emulsifier
Water- Aqueous phase

17
Q

Why would you select a suspension dosage form rather than a solution?

A

There is more chemical stability than solutions, can taste better, and can be more soluble

18
Q

When is a suspension preferred to a tablet dosage form?

A

easier to swallow, dose is more flexible, dissolution rate is faster

19
Q

What are the desirable properties of an ideal suspension?

A

-not settle rapidly
-particles settled should be redispersed easily
-easy to administer
-particle size remains constant during storage

20
Q

What factors affect the velocity of sedimentation of a suspension dosage form?

A

the diameter, density of the liquid and solid, viscosity of the liquid, gravity

21
Q

What are the common methods of particle size reduction?

A

-Micropulverization
-Fluid energy grinding
-Spray drying

22
Q

What processes occur during aging of a suspension to bring G toward zero?

A

aggregation and crystal growth

23
Q

What interparticle forces are important in suspension dosage forms?

A

Van der Waals attractive force, Hydration repulsive force, Electrostatic repulsive force, Steric repulsive force

24
Q

Differentiate dispersion vs. flocculation

A

dispersion has repulsive forces as dominant force; repel eachother and do not aggregate; usually hard to redisperse
flocculation- repulsive and attractive forces are in balance; easy to redisperse

25
Q

What is the basis between Newtonian and non-Newtonian flows?

A

-Newtonian flow is when the fluids stresses are proportional to the velocity vector; reciprocal of slope is viscosity
-Non-Newtonian flow is either plastic, pseudoplastic or dilatant; requires a threshold of shear stress for flow

26
Q

How is shear-thinning rheology used to prepare suspensions?

A

Shear-thinning rheology is the strength of the attractive force of the secondary minimum; present in plastic and Pseudoplastic

27
Q

compare different suspension approaches

A

-Dispersed suspension (Stokes law approach)cloudy suspension and forms non-suspendable sediment
-Controlled Flocculation; fast rate of sedimetation nut easily redispersed by shaking
-Structured vehicle; no sedimentation, thick if unidisturbed and thin if disturbed

28
Q

What are the usual components of suspension dosage forms?

A

Magnesium aluminum silicate- Structured vehicle system
Carboxymethylcellulose sodium- Structured vehicle system
Polysorbate 80- Wetting agent (sufactant)
Disodium EDTA-Chelating agent
Potassium sorbate- Buffering agent, Preservative
Water- Vehicle

29
Q

What is a polymer?

A

a large molecule comprised of many small repeating units “monomer”

30
Q

compare synthetic polymers vs. Natural polymers

A

Natural polymers are Nucleic acids (DNA,RNA), Proteins (Gelatin) and Polysaccharides (cellulose, chitosan, alginic acid)
Synthetic polymers include Polyethylene, Teflon, Kevlar, Mylon, silicon ribber, rayon

31
Q

How do you name a polymer?

A

Poly + repeating unit (in singular form)

32
Q

What is condensation polymerization?

A

2 monomers react to become one with HCL as a by product; ex. Nylon

33
Q

What is addition polymerization?

A

aka Free-radical polymerization; chain polymerization
intitiated by a radical and then terminated by an inert molecule