Table 3.
PK/PD model parameters for atorvastatin
| ADAPT parameter | Value | Corresponding parameter in Narwal et al. [14] |
|---|---|---|
| PK component | ||
| K 21 (h−1) | 3.5 | K a |
| V 1 (L) | 3250 | V 1 |
| V 3 (L)a | 2170 | V 2 |
| K 13 (h−1) | 0.578 | Q/V 1 |
| K 31 (h−1) | 0.866 | Q/V 3 |
| K 14 (h−1) | 0.155 | CLpm/V 1 |
| K 41 (h−1) | 0.175 | CLmp/V m |
| V 4 (L) | 137 | V m |
| K 40 (h−1) | 0.847 | CLm/V m |
| PD component | ||
| k in (mg/dL·h) | 1.14 | –b |
| E max | 0.489 | –b |
| EC50 (ng/mL) | 22.3 | c |
| k out (mg/dL·h)/(mg/dL) | 0.0114 | –b |
The following model parameters were set to zero: K 10, V 5, K 45, K 54, and τ
For the ADAPT parameters, single-digit subscripts correspond to the compartment numbers in the models. Two-digit subscripts indicate flux between numbered compartments
CL clearance, EC 50 concentration producing half-maximal inhibition, E max maximum inhibitory effect, K CL/V, m metabolite, p parent compound, PD pharmacodynamic, PK pharmacokinetic, Q intercompartmental clearance, V volume
aCalculated as a secondary parameter in ADAPT
bFrom Kim et al. [13]
cFrom Dansette et al. [17]