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This technique is particularly important with drugs which:-
1) have good water solubility;
2) are not tightly bound to plasma protein;
3) are smaller (< 500) molecular weight; and
4) have a small apparent volume of distribution.
Conversely drugs which are tightly bound or extensively stored or distributed into tissues are only poorly removed by this route, or process.
A simulation of drug concentration with and without dialysis is shown in Figure 27.3.1.
Figure 27.3.1 Drug Concentration during and after Dialysis
These data were simulation using a one compartment model using Boomer (Macintosh, UNIX, and DOS .BAT files). Maybe you could try changing this to a two-compartment model and seeing what happens.
Copyright 2001-3 David W. A. Bourne (david@boomer.org)