Home

intercompartmental

Intercompartmental refers to processes or transfers that occur between compartments within a system. In physiology and pharmacokinetics, compartments are conceptual spaces representing groups of tissues or fluids with relatively uniform characteristics. Intercompartmental transfer describes the movement of substances, such as drugs or metabolites, from one compartment to another. This transfer is typically described by rate constants (for example k12, k21) that quantify the speed of exchange between compartments. In a two-compartment model, for instance, the central compartment often corresponds to blood plasma, while peripheral compartments represent tissues; the observed concentration-time profile after administration is shaped by intercompartmental distribution in addition to elimination from the system.

Mechanisms and factors influencing intercompartmental transfer include membrane permeability, tissue perfusion, binding to proteins or intracellular

In pharmacokinetics, intercompartmental transfer explains why a drug does not vanish from the bloodstream immediately after

components,
tissue
composition,
and
barriers
such
as
the
blood-brain
barrier.
Lipophilicity,
molecular
size,
and
protein
binding
affect
both
the
rate
and
extent
of
exchange.
Intercompartmental
modeling
uses
differential
equations
to
describe
the
flow
of
material
between
compartments;
solutions
yield
distribution
and
elimination
phases
and
help
predict
tissue
concentrations.
administration
but
instead
shows
rapid
distribution
to
highly
perfused
organs
followed
by
slower
equilibration
with
other
tissues
such
as
fat
or
muscle.
This
concept
aids
in
dose
optimization,
interpretation
of
concentration
data,
and
understanding
tissue
pharmacokinetics.
The
term
also
applies
more
broadly
to
exchange
between
compartments
in
biological,
physiological,
or
engineered
systems.