Pharmacology Flashcards

1
Q

What are the three major routes of drug administration?

A

Topical, Transdermal and Subcutaneous

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

What does the stratum corneum consist of?

A

Cornerocytes (hardened, dead keratinocytes), surrounded by intercellular lipids forming 10-30 sheets of tissue that are constantly shed (desquamated) and renewed

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

What is the differences between these routes and which is the principle route?

A

Principle route is intercellular

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

Why can steriods be stored in the Stratum Coneneum?

A

The “mortar” is highly lipophillic, allowing highly lipophillic drugs such as steriods to be stored

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

Describe the “brick and mortar” model

A

Brick: corneocytes suspended in aggegated keratin filaments embedded in a matrix of filagrin. Adjacent corneocytes are held together by corneodesmosomes

Mortar: Multiple bilayers of intercellular lipids (ceramides, cholesterol and free fatty acids). Highly hydrophobic and can act as a reservior for lipid soluble drugs (eg steriods).

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

What is the most effective way for drugs to enter across the stratum corneum both locally and systemically?

A

Via intercellular route, and normally only allows the diffusion of small, hydrophobic drugs.

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

What two factors dictate the choice of vehicle?

A

1) Physicochemical properties of the drug
2) The clincal condition

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

What is Fick’s law of diffusion?

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

What other factors does Kp, the permeability coefficient, take into account within Fick’s Law of Diffusion?

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

What is the concentration of the drug and the partition coefficient of the drug highly dependant on?

A

The vehicle

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

What are the important factors when considering the rate and extent of absorption of a topically applied drug?

A
  • Solubility of the drug in vehicle (Cv)
  • Maximising the movement (or partitioning) or the drug from vehicle to the stratum corneum (Km)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Comment on each of these stages of drug absorption

A

1) Lipophilic drug is good for absorption. If in a lipophillic base, likes to dissolve, therefore vehicle retains drug
2) Can expect good partitioning
3) Hydrophillic cannot diffuse rapidly through strateum corneum

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

What is the driving force for percutaneous absorption?

A

The concentration of soluble drug in the vehicle

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

How can percutaneous absorption be enhanced?

A

By increasing the concentration of soluble drug in the vehicle. To do this, an inclusion of excipients such as propylene glycol can enhance solubility.

17
Q

Why are topically applied drugs generally poorly absorbed?

A

Because only a small fraction partitions into the stratum corneum

18
Q

What are the physical and chemical conditions which can improve partitioning?

A
  • Hydration of the skin by occlusion (prevention of water loss) by using ointments, creams or even cling film!
  • Increase the solubilty of hydrophobic drugs by inclusion of excipients such as propylene glycol
19
Q

Why should non specific prescribing be avoided, in particular reference to hydrocortisone?

A

Hydrocortisone comes in many forms and the salt can can vastly influence potency

20
Q

What must be considered when prescribing?

A

Where is the drug being applied, skin thickness, hydration of the skin, intergrity of the epidermis, drug concentration, vehicle, the drug salt

21
Q

What can glucocorticosteriod features vary with?

A

-Body site, state of skin, occlusion, vehicle, concentration of drug and form of drug

22
Q

Explain the mechanism of glucocorticosteriods in relation to this diagram

A
23
Q

Why is the skin an attractive route or drug administration for a systemic effect?

A
24
Q

When is Transdermal drug delivery suitable and what are the advantages and disadvantages?

A
25
Q
A