8. Pharmacokinetic calculations, principles of pharmacotherapy (bioavailability, loading dose, maintenance dose) Flashcards
One-compartment vs two-compartment model
In one compartment model only elimination is considered. In 2 compartment disribution + elimination
Apparent volume distribution (Vd)
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
Difference in blood concentration of the drug in IM and SC administration
SC -› drug stays in the plasma for longer period of time
Bioavalability (F) -?
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)
Clearance (Cl) - ?
volume of plasma that is cleared of drug per time unit (ml/min or l/hour)
Loading dose
Dose given with one adminisration (or repeated few times quickly) with which the desired drug consentration can be reached immediately
Maintenace dose
The dose needed to maintain the concentration within the theraupetic window when given repeatedly at a constant interval
When is steady state reached?
Between 4 and 5 administration. Time to steady state is independent of dosage