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onsider a 3 - compartment model of pharmacokinetics ( drug delivery ) where the patient is receiving a drug by IV infusion. The drug is

onsider a 3-compartment model of pharmacokinetics (drug delivery) where the patient is receiving a drug
by IV infusion. The drug is input into the Central compartment and then is transported to and from two
peripheral compartments - one of highly perfused tissues and one of scarcely perfused tissues and organs.
Assume constant volume in each compartment. The concentration in each compartment is written as
C1(t),C2(t),C3(t) and assume C1(0)=C2(0)=C3(0)=0.
a. For the diagram above, write three model equations (using an unsteady state mass balance approach)
for the concentration of the drug in all three compartments. The input rate can be given as m0mgmin
and the infusion will last for 20 minutes.
b. Use 'ode15s' to solve your model from part a) over a time interval of 20 minutes. Use the model
parameters from the table below. The infusion is input at a rate of 0.004mgmin per kilogram of
body mass. Assume the patient is 70kg.
c. After 20 minutes, the infusion is stopped. Modify your equations in part a to indicate this. Use 'ode 15s'
to solve for the concentration of the drug in each compartment during this time after the infusion has
stopped over a period of 5 hours (use appropriate "initial" conditions here). What are the drug
concentrations in each compartment at the end of this time?
d. Concatenate your two plots from b and c to show a full time course of the drug concentrations from
the start of the infusion and the five following hours. All plots should be clearly labeled.
e. What is the maximum concentration of the drug in the blood? At what time (minutes after the infusion
is started) does this occur?
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