The two-compartment model for intravenous (IV) bolus administration illustrates drug distribution in the body, subdividing it into central and peripheral compartments. This model operates on the concept of two-compartment kinetics. The drug's plasma concentration shows a bi-exponential decline following IV bolus administration, signaling the presence of two disposition processes: distribution and elimination.
The disparity between drug input and the sum of drug transfer rates between compartments and elimination determines the rate of change in drug concentration. The transfer constants k12 and k21 depict the rate at which the drug moves between these compartments.
The method of residuals is employed to estimate these transfer constants and other pharmacokinetic parameters. In this method, the slope of the residual line provides the elimination rate constant (k). From k, we can calculate the elimination half-life (t1/2). Other essential pharmacokinetic parameters like the volume of distribution (Vd) and clearance (Cl) can also be determined using suitable equations. All these parameters help in understanding the behavior of the drug within the body.
From Chapter 7:
Now Playing
Pharmacokinetic Models
321 Views
Pharmacokinetic Models
76 Views
Pharmacokinetic Models
68 Views
Pharmacokinetic Models
139 Views
Pharmacokinetic Models
156 Views
Pharmacokinetic Models
53 Views
Pharmacokinetic Models
138 Views
Pharmacokinetic Models
47 Views
Pharmacokinetic Models
181 Views
Pharmacokinetic Models
295 Views
Pharmacokinetic Models
112 Views
Pharmacokinetic Models
73 Views
Pharmacokinetic Models
84 Views
Pharmacokinetic Models
185 Views
Pharmacokinetic Models
127 Views
See More
Copyright © 2025 MyJoVE Corporation. All rights reserved