non-compartmental analysis Flashcards

1
Q

What PK properties can we quantitate?

A

Absorption
Distribution
Metabolism
Elimination

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2
Q

The rate of absorption describes how ________ a drug is absorbed. It is characterized by ________ and _______ in pharmacokinetics.

A

quick; first-order absorption rate constant (ka); the time it takes to reach the maximum plasma concentration (tmax)

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3
Q

The extent of absorption describes how _______ a drug is absorbed. It is characterized by _____ and _____ in pharmacokinetics.

A

much; bioavailability (F); AUC

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4
Q

For intravenous administration, the bioavailability value should be _______. For non-intravenous administration, the bioavailability value should be _______.

A

F=1; 0<F<1

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5
Q

T/F - Dose in the system can be interpreted as the amount of drug in the body except for the unabsorbed drug in the GI.

A

True

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6
Q

In pharmacokinetics, drug distribution is primarily characterized by _______, which represents _______ (distribution of drug in tissue/distribution of drug in plasma/relative distribution of drug between tissue and plasma).

A

volume of distribution; relative distribution of drug between tissue and plasma

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7
Q

Elimination consists of _______ and _______.

A

metabolism; excretion

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8
Q

Total clearance is a proportionality constant relating _______ to _______.

A

the rate of elimination; plasma drug concentration

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9
Q

T/F A drug is considered being eliminated only after it leaves the body

A

False - A drug is considered to be eliminated after it is metabolized and transformed to a different chemical species.

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10
Q

Disposition = ________ + ________

A

distribution + elimination

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11
Q

disposition = ________ + ________ + ________

A

distribution + metabolism + excretion

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12
Q

List 3 examples that when dose is changed, the PK variable will change proportionally under linear PK

A

concentration (C), AUC, elimination rate (dA/dt)

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13
Q

List 5 examples that when dose is changed, the PK variable will stay unchanged under linear PK

A

V, CL, ka, t1/2, k

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14
Q

List the 3 primary PK parameters

A

V - volume of distribution
CL - clearance
ka - absorption rate

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15
Q

List 3 secondary PK parameters

A

t1/2, Cmax, tmax, AUC, F

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16
Q

T/F If a drug has a large volume of distribution, its total clearance is likely to be low.

A

F - a drug having a large volume of distribution does not mean that the drug will have a low total clearance. The information is sufficient for us to make the interpretation.

17
Q

T/F - If a drug has a low total clearance, there will be more drug in the tissue and thus the volume of distribution should be large.

A

F - If a drug has a low total clearance, there will be more drug in both of the tissue and plasma and thus the volume of distribution should be unchanged.

18
Q

T/F - If the ka of a drug increases, its V and CL will increase

A

F - If the ka of a drug increases, its V and CL will be likely to stay the same

19
Q

If a drug has a V value of 15 L, it will be likely to distribute in _________

A

blood/plasma, interstitial/extracellular fluid

20
Q

If a drug has a V value of 25 L, it will be likely to reach ________

A

intracellular space

21
Q

Regarding mass balance, dose = ________ + ________ + _________ + __________

A

amount at the absorption site; amount in body; amount metabolized; amount excreted

22
Q

Regarding mass balance, rate of change of drug in body = _________ - _________

A

input rate; output rate

23
Q

Regarding mass balance, rate of change of drug in body = _______ - (_______ + _______) = _________- __________ - _________

A

rate of absorption - (rate of excretion + rate of metabolism) = rate of absorption - rate of metabolism - rate of excretion

24
Q

When ready state is reached, input rate ______ output rate

A

equals