pharmacokinetics MT1 Flashcards

(32 cards)

1
Q

this is the branch of pharmacology concerned with the movement of drugs within the body/what the body does to the drug

A

pharmacokinetics

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1
Q

what are the factors that determine blood concentration of a drug?

A
  • size of administered dose
  • extent of absorption
  • rate of absorption
  • extent od drug distribution
  • extent of elimination
  • rate of elimination
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2
Q

this is how much of a drug gets absorbed

A

extent of absorption

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3
Q

what determines the extent of absorption of a drug

A

formulation

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4
Q

this is how quickly a drug gets absorbed

A

rate of absorption

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5
Q

what determines the rate of absorption

A

route

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6
Q

this is how well a drug spreads and goes into organs

A

extent of drug distribution

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7
Q

what determines the extent of drug distribution

A

depends partly on volume/site of distrbution

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8
Q

this is how much and how well a drug can leave the body

A

extent of elimination

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9
Q

this is how quickly the drug can leave the body

A

rate of elimination

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10
Q

the manner in which a drug is taken is called a __________. this depends on the therapeutic objectives (e.g. cure, prevention, etc.)

A

dosage regimen

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11
Q

Managing a proper dosing regimen to treatment of patients with various diseases requires the maintenance of enough drug systematic exposure which in an effective range to have a certain duration and intensity of effect, but doesn’t give adverse effects. It is necessary to keep the dosage regimen within the _______________

A

therapeutic window

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12
Q

this is a model used in determining drug movement in the body; its the simplest way to view the entry, disposition, and exit of the drug from the body where the body acts like a single, uniform compartment

A

single compartment open model

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13
Q

the rate of change in concentration over time (dC/dt) in the body (reservoir) in a one compartment open model is dependant on these two factors

A
  • how much drug there is in the body (reservoir)
  • how well the drug is eliminated
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14
Q

how much drug there is in the body/reservoir depends on what two factors

A
  • the size of the reservoir for the drug
  • the dose given
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15
Q

how well the drug is eliminated depends on what two factors

A
  • rate of elimination
  • capacity of the elimination organs to remove the drug
16
Q

What are the two types of elimination processes?

A

Zero Order elimination/kinetics and First order elimination/kinetics

17
Q

this elimination process is the mass of the drug that is eliminated/transferred is constant with respect to time

A

zero order kinetics

18
Q

this elimination process is the mass of the drug that is eliminated/transferred is never constant with reprint to time

A

first order kinetics

19
Q

for a zero order process, drug transfer is at a constant rate, ______________ of the plasma concentration

20
Q

for frist order process, the rate of drug transfer is not constant and is _________ of the plasma concentration

A

dependant - the more drug the faster its eliminated

21
Q

for first order kinetics, the rate of change of concentration with respect to time depends on what two factors

A
  • how much drug there is initially
  • the elimination capacity
22
Q

zero or first order kinetics?
the number of enzymes/receptors is higher than the amount of drug

A

first order kinetics

23
Q

zero or first order kinetics?
accumulation of drug in the body leads to toxicity

A

zero order kinetics

24
zero or first order kinetics? there are limited number of enzymes/receptors for the amount of drug
zero order kinetics
25
zero or first order kinetics? the rate of transfer does not depend on how much drug is available
zero order kinetics
26
zero or first order kinetics? rate of transfer does depend on how much of the drug is available
first order kinetics
27
we can predict the rate of decline of drugs following first order kinetics using __________
half life
28
________ is constant for a particular drug following first order kinetics - this helps to predict the length of time it takes for a drug to leave the body - it also helps to determine how long its takes to reach a steady state drug levels in the body after multiple dosing
terminal half-life
29
what is the equation for half life for first order kinetics
t(1/2) = 0.693 Vd/Cl
30
is half life directly or inversely proportional to Clearance
inversely
31
is half life directly or inversely proportional to volume distribution
directly