ADME lab Flashcards

1
Q

organ clearance of a drug is influenced by:

A
  • organ blood flow
  • plasma protein binding
  • organs intrinsic ability to eliminate the drugs
    (so larger drug dose does not change the clearance values)
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2
Q

if a drug has high renal clearance - what does it imply about the filtration through the kidney

A

will probably be both filtered and actively transported from the blood to the urine

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3
Q

what is the difference between pharmacokinetic half life and the normal half life of a drug

A

pharmacokinetic half life - the half life of the drug in the plasma
half life - the half life of the drug in the body

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4
Q

if drug A is eliminated from the body slower than drug B, what would you expect the half life of drug A to be compared to drug B

A

longer

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5
Q

how do we measure drug clearance

A

(fractional single pass elimination) x (blood flow rate of the organ)

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6
Q

what is the bioavailability of a drug

A

the proportion of the drug that reaches the systemic circulation in an active form

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7
Q

does oral or IV administration lead to longer lasting drug concentrations and why

A

oral - because the release is delayed

IV will have higher and faster conc, but oral will have longer effect

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8
Q

what are three ways in which a drug may have bioavailability of less than 100%

A
  • first pass metabolism in the liver
  • incomplete drug absorption
  • bacterial metabolism in the intestine (if via oral absorption)
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9
Q

what is the volume of distribution

A

the volume into which the total amount of drug in the body would need to be dissolved to achieve the conc that is observed in the blood

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