Description Usage Arguments Details Value Note Author(s) References Examples
These functions calculate steady-state properties from the parameters of a one-compartment pharmacokinetic model, assuming all doses occur in the post- distribution phase (tau >> tmax).
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cl |
apparent clearance (L/h) |
v |
apparent volume (L) |
ka |
absorption constant (h^-1) |
tau |
steady-state trough-to-trough interval (h) |
dose |
dose (arbitrary units) |
time |
arbitrary time point, <= tau |
... |
other arguments, ignored |
acr
calculates accumulation ratio (unitless, called by css
).
ke
calculates the elimination constant (h^-1, called by css
).
css
calculates steady-state compartment concentration (dose units per L)
at a given time. cavg
calculates average concentration over dosing interval.
cmin
and cmax
calculate minimum and maximum steady-state concentrations; they
call css
, passing either tau
itself or tmax
for the time argument.
tmax
calculates the time of the maximum concentration.
auc
calculates area under the curve.
Note that for the post-distributive assumption to hold, tau
must be very large
relative to the time needed for drug disposition. To the extent that it does not
hold, these functions give biased results.
numeric
Multiple properties can be calculated within the same function or loop, since
all arguments can be passed even if not needed. For example, the same five
arguments can be passed, even un-named, to cmax
and tmax
(tmax
will ignore dose).
But be sure to pass by name the same arguments to cmax
and cavg
: the latter will
ignore unused arguments but has the common arguments in a different order.
Tim Bergsma
Gibaldi M, Perrier D. Multiple dosing. Pharmacokinetics. New York: Marcel Dekker, Inc., 1982: p. 113- 144.
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