Pharmacology Summary Flashcards

Incomplete

1
Q

Pharmacodynamics meaning

A

What a drug does to the body

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

Pharmacokinetics meaning

A

What the body does to a drug

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

What are receptors?

A

Class of cellular macromolecules

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

What is an agonist?

A

Drug that binds to a receptor

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

What is affinity?

A

Strength of association between ligand and receptor

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

What is efficacy?

A

Ability of an agonist to evoke a cellular response

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

Do agonists have affinity and efficacy?

A

Agonists have affinity and efficacy

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

What is an antagonist?

A

Drug that blocks the actions of an agonist

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

Do antagonist possess affinity and efficacy?

A

Possess affinity but lacks efficacy

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

What is competitive antagonism?

A

Binding of agonist and antagonist occur at the same site

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

Does competitive antagonism affect maximal response?

A

No

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

How is competitive antagonism overcame?

A

Increasing concentration of agonist

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

What is non-competitive antagonism?

A

Agonist binds at one site and antagonist binds at a separate site

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

During non-competitive antagonism what does antagonist binding cause?

A

Activation cannot occur when is bound

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

Does non-competitive antagonism effect maximal response?

A

It decreases maximal response

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

Does a concentration increase of agonist effect maximal response?

A

No

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is absorption?

A

Process by which a drug enters the body from its site of administration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is distribution?

A

Process by which drug leaves circulation and enters the tissues perfused with blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is metabolism?

A

Process by which tissue enzymes catalyse chemical conversion of a drug to a more polar form that is more readily excreted from the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is excretion?

A

Process that removes the drug from the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What factors control drug absorption?

A

Solubility
Chemical stability
Lipid to water partition coefficient
Degree of inonisation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

How does solubility affect drug absorption?

A

Drug must be able to dissolve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

How does chemical stability affect drug absorption?

A

Some drug may be dissolved by acid

24
Q

How does lipid to water partition coefficient affect drug absorption?

A

Rate of diffusion of drug increases with lipid solubility

25
What affects the degree of ionisation?
pKa of the drug and local pH
26
What is the Henderson-Hasselbalch equation?
pH = pKa + log([A⁻]/[HA])
27
What is pKa?
pH in which 50% of drug is ionised and 50% is unionised
28
If Ka is large?
Strong acid
29
What is oral availability?
Fraction of drug that reaches systemic circulation after oral ingestion
30
What is systemic availability?
Fraction of drug that reaches systemic circulation after absorption
31
What are the routes of administration?
Enteral Parenteral
32
How are enteral drugs absorbed?
Via the gut
33
How are Parenteral drugs absorbed?
Not via the gut
34
Examples of enteral methods of administration
Oral Sublingual Rectal
35
Examples of parenteral methods of administration
Intravenous Intramuscular and subcutaneous Inhalation Topical
36
What is a feature of drugs within systemic circulation?
Can be distributed to one or more body fluid compartment
37
Are drugs evenly distributed within the body?
No
38
What is volume distribution?
Apparent volume in which a drug is dissolved
39
What is the volume distribution equation for IV?
Vd = dose/plasma concentration
40
What is MEC?
Minimum effective concentration
41
What is MTC?
Maximum tolerated concentration
42
Formula for therapeutic ratio
Therapeutic Ratio = MTC/MEC
43
What does a high therapeutic ratio indicate?
That drug is safe
44
What is the rate of elimination directly proportional to?
Drug concentration
45
How is plasma concentration effected by elimination?
Falls exponentially
46
Half life equation
T1/2 = 0.693 * Vd / CL
47
What is clearance?
The volume of plasma cleared of drug in unit of time
48
Equation for rate of clearance
Rate of elimination = clearance * plasma concentration
49
After how many half lives is steady state reached?
5
50
When does steady state exist?
Rate of drug administration = rate of drug elimination
51
Equation to determine Cpss (Steady state concentration)
Cpss = maintainance does rate / clearance
52
During oral dosing how does the plasma concentration behave?
Fluctuates about an average steady state value
53
What is Vd?
Volume of distribution
54
What is volume of distribution?
Volume into which a drug appears to be distributed with a concentration equal to that of plasma
55
What is loading dose?
Use of an initial higher dose of drug before stepping down to lower maintenance dose
56
Why is loading dose used?
Decreases time to stead state in drugs with a long half life
57
What is half life?
Time for the concentration of drug plasma to halve