Table 4.
Observed and modelled drug exposure pharmacokinetic parameters for 75 mg immediate release tablets of dipyridamole.
PK Parameter | Ricevuti et al. ± SD | PBPK Using Experimental Biphasic InForm PRC Value ± SD (% PE) | PBPK Using Experimental D-P PRC Value ± SD (% PE) | PBPK Using Default Simulator Precipitation Values ± SD (% PE) | PBPK with no Precipitation ± SD (% PE) |
---|---|---|---|---|---|
AUC (mg/L h) | 4.13 ± 0.52 | 4.12 ± 1.49 (0.24%) | 3.58 ± 1.32 (13.32%) | 2.81 ± 1.13 (31.96%) | 5.28 ± 1.98 (27.85%) |
Cmax (mg/L) | 0.93 ± 0.13 | 0.83 ± 0.21 (10.75%) | 0.71 ± 0.18 (23.66%) | 0.49 ± 0.15 (47.31%) | 1.14 ± 0.29 (22.58%) |