Pharmacokinetics Flashcards

1
Q

volume w/in body necessary to account for the initial concentration of drug in plasma following a given dose
(no actual anatomical correlate)

A

Volume of Distribution

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2
Q

drugs with ____ Vd undergo limited distribution.

In the case of IV doses, they will?

A

low

remain in the bloodstream

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3
Q

When the rate of drug moving into the tissues greatly exceeds the rate leaving tissues, Volume of Distribution will be

A

large

drug accumulates outside of bloodstream

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4
Q

Is there an upper limit for Volume of Distribution

A

no

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5
Q

What conditions can affect the animals normal Vd?

A

edema, liver disease (reduction in plasma proteins)

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6
Q

In zero order kinetics, the drug will be eliminated at a ______

A

constant rate (unrelated to concentration)

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7
Q

When is the amount of drug eliminated proportional to its concentration?

A

1+ Orders

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8
Q

What time of kinetics is safer with regards to elimination and total body burden?

A

1+ order

BUT any can convert to zero order when SATURATED

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9
Q

When is half life constant for a drug?

A

when it obeys 1st order kinetics

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10
Q

Two phases of drug transport after dosing?

Which is used for calculations?

A

Redistribution(alpha) & elimination (beta)

Elimination!

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11
Q

Using half lives is helpful for predicting levels ______________ but not ______________

A

in blood

not in tissues

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12
Q

time to achieve ___________ in plasma depends solely ON THE HALF LIFE

A

Steady-State Concentrations

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13
Q

What does Steady-state plasma concentration mean?

A

concentration is fluctuating in a consistent way (peaks and troughs stay the same for 6 half-lives)

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14
Q

Requires approximately ____ half-lives of sustained drug administration to achieve steady-state

A

5

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15
Q

Giving dosage more frequently will _______ both the peaks and troughs and vice versa for less frequent dosage.

A

elevate

ratio Cpmin/Cpmax is increased however

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16
Q

How will increasing the dose affect the peaks and troughs(Cpmax and Cpmin)?

A

elevate both

17
Q

How does giving a dose more frequently affect the accumulation in a tissue?

A

increase accumulation

18
Q

How is accumulation affected by dosing interval?

A

less frequent dosing -> less accumulation

vice versa

19
Q

R (accumulation factor) is a function of ?

A

ratio of dose interval / drug half life

20
Q

What is a function of the dose interval relative to half-life?

A

R(accumulation factor) but also peak-to-trough concentration (Cpmax55:Cpmin55)

21
Q

When dosing interval equals the half-life Cpmin is ________ Cpmax

A

1/2

22
Q

When the dosing interval equals 2 half, Cpmax is ________ Cpmin

A

4x

23
Q

How will steady state be affected by slow absorption?

A

reduces both peak and trough levels