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10 Cards in this Set

  • Front
  • Back
Steady-state Levels vs. PK-parameters

Both c(inf)max and c(inf)min are
--directly proportional to the dose D0
--indirectly proportional to the volume of distribution VD
steady state levels: elimination rate constant and dosing interval

Steady-state levels increase rapidly if:
the value of the product ke * T is decreased below about 0.7
steady state levels vs half life

for one compartment situations:
t 1/2 = ln2/ke
steady state levels vs half life

substitution instead of ke
(eq)
ke * T= 0.693 * T/ t 1/2 < 0.7

0.7 = the conditin for the drug accumulation
steady state levels vs half life

significant accumulation if the dosing interval is shorter than the half-life
T < t 1/2


multiples of 24 (3*8, 4*6...)
dosages that are shorter than half life
Time Course of Drug Amount in the Body I

Time course of the plasma concentration for each dosing interval is :
c(t) = cmax * e^-ke * t
For each interval, the minimum plasma concentration is achieved for t = T

(eq)
c(min)/c(max) = e ^- ke * T = f
time course of drug amount in the body I

The drug amount at the beginning of the dosing interval will decline to the fraction f at the end of the dosing interval
f= n(min)/n(max) = e^-ke * T
(0 < or equal f < or equal 1)
time course of drug amount in the body II
see slide 6, 7, 8
minimum and maximun drug amounts VIII
see the rest of the slides...