Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
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 Amountin 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...
|