Drug distribution Flashcards

1
Q

What happens once a drug has been absorbed

A

must be available for biological action and distribution to the tissues

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

Define drug distribution

A

Transfer of a Drug between the Blood and the Extra Vascular Fluids and Tissues of the body activating the drug

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

What kind of drug is biologically active

A

an unbound drug

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

What is Tmax and Cmax

A

The time to maximum plasma concentration (Tmax)

maxiumum plasma concentration (Cmax)

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

The area under the drug concentration-time curve represents

A

the amount of drug which reaches the systemic circulation and is available for action

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

The bioavailability of a drug is dependant on

A

extent of absorption and first pass metabolism

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

Drugs binding to proteins in the plasma can be affected by

A
Renal failure
Hypoalbuminaemia (Low plasma proteins)
Pregnancy
Other drugs
Saturability of binding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

The less bound a drug is to plasma protein increases its ability to

A

cross the cell membrane and be activated

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

When is plasma protein binding matter

A

when binding is above 90%
because if unbound level changes above 90% there is a massive proportional increase in the amount of free drug
also important when tissue distribution is small

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

Volume Of Distribution

A

overall distribution of drug within the body observed in blood concentrations

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

The greater volume distribution increases the time of what

A

clearance

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

Define clearance

A

the theoretical volume of fluid from which a drug is completely removed over a period of time - basic measure of elimination

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

What is clearance dependant on

A

concentration
Urine flow rate
metabolism
biliary excretion for hepatic clearance.

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

What organs help clearance

A

Liver
Kidney
maybe gut

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

If liver and kidneys not working what is the result

A

accumulated drug resulting in toxicity

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

Define the half life

A

the time taken for the drug concentration in the blood to decline to half of the current value

17
Q

What is half life dependant on

A

volume of distribution and rate of clearance

18
Q

If half life of drug prolonged and medicine is continued this increases the volume distribution leading to

A

toxicity

19
Q

What do we need to know to work out how often a drug can be administrated

A

half life

20
Q

Define Drug elimination

A

the removal of active drug and matabolites from the body

21
Q

What are the two parts of drug elimination

A

Drug metabolism

drug elimination

22
Q

What are the primary organs for drug excretion

A

the kidneys

23
Q

Where are drugs usually metabolised

A

Liver

24
Q

where will all unbound drugs be filtered at

A

glomerulus in kidneys as long as they aren’t to big

25
Q

Factors that affect the glomerular filtration rate will reduce

A

the clearance of the drug

26
Q

what is entero-hepatic circulation

A

Many drugs are then reabsorbed from the bile into the circulation

27
Q

when does entero-hepatic circulation stop

A

when drug is metabolised in the liver or excreted by the kidneys

28
Q

where are drugs usually conjugated - i.e. the chemical substances is terminated

A

the liver

29
Q

Damage to the liver may reduce the rates of conjugation resulting in

A

reabsorption or an accumulation resulting in toxicity

30
Q

What are the factors that effect drug distribution

A

Plasma protein binding
Blood flow - tissue mass ratio
Membrane characteristics - blood brain barrier
Transport mechanisms
Diseases and other drugs (esp renal failure, liver disease, obesity)
Elimination

31
Q

where are some drugs selectively accumulated and what can this lead to

A

kidneys
eye
bone
selective toxicity

32
Q

What is the transfer of drugs to the brain modified by and why

A

blood brain barrier - as is much less permeable to water-soluble drugs than is the membrane between plasma and other tissues

33
Q

what does the duration and intensity of the pharmacological effect depend mostly on

A

renal function