F1 ADME & clinical pharmacology 1 Flashcards

1
Q

What is pharmacokinetics?

A

the time course of a drug from absorption to elimination

determines the drug regimen for a drug - dose, how often

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2
Q

What does ADME stand for?

A

Absorption, distribution, metabolism, excretion

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3
Q

What are the 3 mechanisms of drug absorption?

A

active transport- for drug structurally related to endogenous chemicals
bulk flow of water - small water soluble drug
passive diffusion- movement of most drugs

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4
Q

Are weak acids and bases ionised and absorbed in the stomach?

A

weak acids - unionised therefore absorbed

weak bases - ionised and not absorbed

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5
Q

Does presence of food increase time of drug in stomach?

A

yes

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6
Q

Which type of acid drugs have slowed absorption?

A

acid stable drugs

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7
Q

Why are acid labile drugs more readily broken down?

A

stay longer in stomach

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8
Q

Why are PPIs given gesture-resistant capsules?

A

are acid labile

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9
Q

Where is the major site or absorption?

A

small intestines

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10
Q

Do the small intestines have good blood flow?

A

yes

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11
Q

Why are most weak acids & bases absorbed in small intestines?

A

high levels of uncharged drug

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12
Q

What is first pass metabolism?

A

drug absorbed from small intestines go to liver via hepatic portal vein, some drug metabolised before reaching the systemic circulation

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13
Q

How do you calculate bioavailability F?

A

F= AUC oral/AUC iv

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14
Q

How do you calculate single dose?

A

=amount given/ F

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15
Q

What is clearance?

A

the volume of plasma cleared of a drug in unit time) measure of amount of drug removed by body

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16
Q

What are the units for clearance?

A

(mL/min) use L/h

17
Q

What is volume of distribution (Vd)?

A

the apparent vol in which a drug is dissolved in a body

18
Q

How do you calculate Vd?

A

= amount in body/conc

= does/ conc at t=0

19
Q

What does first order kinetic tell us about elimination and concentration of drug?

A

rate if elimination is proportional to concentration of drug

20
Q

What is the equation of first order kinetics and what does each part represent?

A
Ct= Coe^-kt 
Ct= conc at t=t 
Co= conc at t=0 
k= rate constant 
t= time
21
Q

What does rate constant mean?

A

k is the fraction of drug eliminated per unit time

k= clearance/ Vd

22
Q

What is half life?

A

time for conc to decrease by 50%

23
Q

How do you calculate half life?

A

t (0.5) = ln2/K or 0.693/K