Calculate C(t) for a 3-compartment linear model
calc_sd_3cmt(t, dose, dur = NULL, tinf = NULL, ...) calc_sd_3cmt_linear_bolus(t, dose, ...) calc_sd_3cmt_linear_oral_1_lag(t, dose, ...) calc_sd_3cmt_linear_infusion(t, dose, tinf, ...) calc_sd_3cmt_linear_oral_0(t, dose, dur, ...) calc_sd_3cmt_linear_oral_0_lag(t, dose, dur, ...) calc_sd_3cmt_linear_oral_1(t, dose, ...)
t
: Time after dose (h)dose
: Dosedur
: Duration of zero-order absorption (h)tinf
: Duration of infusion (h)...
: Passed to calc_derived_3cpt()
Concentration of drug at requested time (t
) after a single dose, given provided set of parameters and variables.
calc_sd_3cmt_linear_bolus()
: Calculate C(t) for a 3-compartment linear model after a single IV bolus dosecalc_sd_3cmt_linear_oral_1_lag()
: Calculate C(t) for a 3-compartment linear model after a single oral dosecalc_sd_3cmt_linear_infusion()
: Calculate C(t) for a 3-compartment linear model after a single IV infusioncalc_sd_3cmt_linear_oral_0()
: Calculate C(t) for a 3-compartment linear model after a single dose, with zero-order absorptioncalc_sd_3cmt_linear_oral_0_lag()
: Calculate C(t) for a 3-compartment linear model after a single dose, with zero-order absorption and a lag timecalc_sd_3cmt_linear_oral_1()
: Calculate C(t) for a 3-compartment linear model after a single oral doseCt <- calc_sd_3cmt_linear_bolus(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, dose = 100) Ct <- calc_sd_3cmt_linear_oral_1_lag(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, ka = 1, dose = 100, tlag = 1.5) Ct <- calc_sd_3cmt_linear_infusion(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, dose = 100, tinf=1) Ct <- calc_sd_3cmt_linear_oral_0(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, dur = 1, dose = 100) Ct <- calc_sd_3cmt_linear_oral_0_lag(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, dur = 1, dose = 100, tlag=1.5) Ct <- calc_sd_3cmt_linear_oral_1(t = 11.75, CL = 3.5, V1 = 20, V2 = 500, V3 = 200, Q2 = 0.5, Q3 = 0.05, ka = 1, dose = 100)
Bertrand J & Mentre F (2008). Mathematical Expressions of the Pharmacokinetic and Pharmacodynamic Models implemented in the Monolix software. http://lixoft.com/wp-content/uploads/2016/03/PKPDlibrary.pdf
Rowland M, Tozer TN. Clinical Pharmacokinetics and Pharmacodynamics: Concepts and Applications (4th). Lippincott Williams & Wilkins, Philadelphia, 2010.
Justin Wilkins, justin.wilkins@occams.com
Bill Denney, wdenney@humanpredictions.com