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.
Z rozdziału 7:
Now Playing
Pharmacokinetic Models
386 Wyświetleń
Pharmacokinetic Models
86 Wyświetleń
Pharmacokinetic Models
75 Wyświetleń
Pharmacokinetic Models
153 Wyświetleń
Pharmacokinetic Models
189 Wyświetleń
Pharmacokinetic Models
58 Wyświetleń
Pharmacokinetic Models
144 Wyświetleń
Pharmacokinetic Models
59 Wyświetleń
Pharmacokinetic Models
190 Wyświetleń
Pharmacokinetic Models
372 Wyświetleń
Pharmacokinetic Models
132 Wyświetleń
Pharmacokinetic Models
88 Wyświetleń
Pharmacokinetic Models
91 Wyświetleń
Pharmacokinetic Models
192 Wyświetleń
Pharmacokinetic Models
138 Wyświetleń
See More
Copyright © 2025 MyJoVE Corporation. Wszelkie prawa zastrzeżone