pharmacokinetics MT1 Flashcards

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

A

independant

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
Q

zero or first order kinetics?
there are limited number of enzymes/receptors for the amount of drug

A

zero order kinetics

25
Q

zero or first order kinetics?
the rate of transfer does not depend on how much drug is available

A

zero order kinetics

26
Q

zero or first order kinetics?
rate of transfer does depend on how much of the drug is available

A

first order kinetics

27
Q

we can predict the rate of decline of drugs following first order kinetics using __________

A

half life

28
Q

________ 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

A

terminal half-life

29
Q

what is the equation for half life for first order kinetics

A

t(1/2) = 0.693 Vd/Cl

30
Q

is half life directly or inversely proportional to Clearance

A

inversely

31
Q

is half life directly or inversely proportional to volume distribution

A

directly