Drug Absorption Flashcards

1
Q

What is pharmacokinetics?

A

What the body does to the drug (metabolism etc)

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2
Q

What does ADME stand for?

A

Absorption
Distribution
Metabolism
Excretion

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3
Q

What is absorption?

A

Process by which unchanged drugs enter the circulation

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4
Q

What is distribution?

A

Dispersion or a drug among fluids and tissues of the body

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5
Q

What is metabolism?

A

Transformation of a drug into daughter compounds

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6
Q

What is excretion?

A

Removal of drugs/ metabolites from the body

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7
Q

Why is ADME important (5)?

A
Safe and intelligent use of medicines by all doctors 
Designing dose regimens
Monitoring treatment compliance
Medicine licensing requirement
Substance abuse monitoring
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8
Q

What does the choice of delivery rate depend on (4)?

A

Speed of onset
Convenience
Bioavailability
Side effects/ specificity of action

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9
Q

What is bioavailability?

A

Proportion of administered drug reaching the system circulation

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10
Q

What is the bioavailability for IV drugs?

A

100%

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11
Q

What are the routes of administration?

A

Oral

IV

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12
Q

What are the three options of delivery for IV drugs?

A

Subcutaneous
Intramuscular
Intravenous

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13
Q

Where is subcutaneous IV?

A

Under the epithelium

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14
Q

Where is intramuscular IV?

A

In the muscle

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15
Q

Where is Intravenous IV?

A

Into the blood vessel

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16
Q

What is the BAR availability of drugs?

A

Amount of drugs to reach the bloodstream

17
Q

What is transcellular?

A

Through cells

18
Q

What is paracellular?

A

Between cells

19
Q

How can drug absorption occur?

A

Active transport through cells
Facilitated diffusion through cells
Passive diffusion

20
Q

What is ficks law?

A

Rate of diffusion = surface area x concentration difference x permeability

21
Q

What is drug permeability governed by?

A

Molecular size, lipid solubility and presence of charged or ionisable groups

22
Q

What does the extent of drug ionisation depend on?

A

pH of environment and the acid/ base dissociation constant of the drug

23
Q

What must drugs be to diffuse across cell membranes?

A

Uncharged

24
Q

What drugs are absorbed most effectively?

A

Nonionisable, lipophilic drugs

25
Q

What do the Henderson-hasselbalch equations do?

A

Predict the extent of ionisation

26
Q

In the Henderson-hasselbalch equations, when does pH=pKa?

A

When drug is 50% ionised

27
Q

What will happen to acidic drugs when the pH decreases?

A

More unionised

28
Q

What will happen to alkali drugs when the pH increases?

A

More unionised

29
Q

Is aspirin acidic or basic?

A

Weak acid

30
Q

What form is aspirin in in the stomach?

A

Unionised

31
Q

How can aspirin not move back from bloodstream to stomach?

A

Once it is absorbed into the bloodstream, it ionises so it can’t be reabsorbed

32
Q

What is ion trapping?

A

Acidic drugs are absorbed efficiently into stomach whereas basic drugs aren’t and give versa

33
Q

Where do oral basic drugs get absorbed into the bloodstream?

A

In the intestine, where the surface area compensates for low absorbance efficiency

34
Q

What are the lipinski rules?

A

A set of rules that help to determine specific properties of a developing drug

35
Q

Give the lipinski rules

A

Molecular weight <500Da
No more than 5 h-bond donors
No more than 10 h-bond acceptors
LogP<5 (partition coefficient)