Drug Absorption Flashcards

1
Q

correct pharmacological effect - effect of drug on the body

A

Pharmacodynamic

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

drug to site of action
what your body does to the drug?
how removed?
ADME

A

Pharmacokinetic

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

drug into patient

A

Pharmaceutical

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

The time to peak concentration

A

(Tmax)

The more rapid the rate of absorption, the earlier the drug concentration peak.

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

The peak concentration

A

(Cmax)

Increasing dose does not reduce the time at which peak concentration is reached but does increase the peak concentration

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

Total exposure to drug; amount of drug reaching systemic circulation

A

AUC

The area under the drug concentration-time curve represents the amount of drug which reaches the systemic circulation.

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

measure of the range at which a drug is safe and active

A

therapeutic index

Index lower - oral - plasma conc low - compared to other route of administration

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

drug is active over a range of concentrations

A

therapeutic range

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

A drug given _________ has 100% bioavailability.

A

intravenously

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

Factors affecting bioavailability (oral) - list 5

A
Formulation
Ability of drug to pass physiological barriers/transport across memb- Particle size, Lipid solubility, pH and ionisation (unionised - cross lipid but do not dissolve in H20 / ionised cannot cross memb
GI effects
First pass metabolism
Slow release preparations
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Does ionised drug cross the membrane?

A

No.

Most drugs are weak acids or bases; the degree of ionisation depends on the pH of the environment.

Most drugs do not completely ionise in water.

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

The ability of a drug to diffuse across a lipid barrier

A

a lipid-water partition coefficient.

This is the ratio of the amount of drug which dissolves in the lipid and water phase when they are in contact.

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

To pass across a lipid layer a drug must be in solution and ________ soluble.

A

lipid

A drug that is not lipid soluble may not be absorbed at all, for example gentamicin.

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

To undergo active transport drugs must resemble ______

A

naturally occurring compounds.

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

____________occurs through inter-cellular pores and is the major mechanism through which drugs cross the capillary walls.

A

Filtration

normal method for water soluble molecules with a molecular weight of 100 or less.

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

Metabolism of drug (gut –> liver) prior to reaching systemic circulation

A

First Pass metabolism

17
Q

Which drug administration avoids first pass metabolism?

A

IM, Sublingual, subcutaneuous, rectal,buccal, transdermal

18
Q

Which drug administration undergoes first pass metabolism?

A

oral

19
Q

Relation between local pH and degree of Ionisation
Henderson-Hasselbach
ion trapping

A

Diffusion-Ionisation

20
Q

conc of ionised = unionised same

A

pH = pKa

21
Q

Sublingual (SL)

A

under tongue

bypass first met

22
Q

buccal

A

cheek - inside mouth

23
Q

Despite route of administration, same dosage of drug = same AUC = same half life - T or F?

A

True