8. Pharmacokinetic calculations, principles of pharmacotherapy (bioavailability, loading dose, maintenance dose) Flashcards

1
Q

One-compartment vs two-compartment model

A

In one compartment model only elimination is considered. In 2 compartment disribution + elimination

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2
Q

Apparent volume distribution (Vd)

A

Ratio of the total amount of drug in the body to the plasma concentration of the drugs. Vd = D/C

Lower Vd -› drug distributed mainly in blood
Higher Vd -› better distibution of the drug in the body

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3
Q

Difference in blood concentration of the drug in IM and SC administration

A

SC -› drug stays in the plasma for longer period of time

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4
Q

Bioavalability (F) -?

A

is the ration between two AUC (area under curve)

reflects the actual body exposure to drug after administration. (comparing it to IV data)

F = AUC(x - way of adm) x D(iv) / AUC(iv) x D(x)

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5
Q

Clearance (Cl) - ?

A

volume of plasma that is cleared of drug per time unit (ml/min or l/hour)

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6
Q

Loading dose

A

Dose given with one adminisration (or repeated few times quickly) with which the desired drug consentration can be reached immediately

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7
Q

Maintenace dose

A

The dose needed to maintain the concentration within the theraupetic window when given repeatedly at a constant interval

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8
Q

When is steady state reached?

A

Between 4 and 5 administration. Time to steady state is independent of dosage

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