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. 2020 Mar 15;12(3):268. doi: 10.3390/pharmaceutics12030268

Table 1.

Pharmacokinetic parameters of DWP16001, dapagliflozin, and ipragliflozin after a single oral administrations of DWP16001, dapagliflozin, and ipragliflozin at a dose of 1 mg/kg in ICR mice, respectively.

Parameters DWP16001 Dapagliflozin Ipragliflozin
Plasma Cmax (ng/mL) 371.4 ± 108.6 274.8 ± 143.6 409.6 ± 59.1
Tmax (h) 0.7 ± 0.3 0.5 ± 0.0 0.6 ± 0.2
AUC72h (μg∙h/mL) 1.69 ± 0.34 0.48 ± 0.18 * 1.96 ± 0.41
AUC (μg∙h/mL) 1.73 ± 0.34 0.55 ± 143.8 * 1.97 ± 0.41
t1/2 (h) 3.8 ± 1.4 2.1 ± 0.2 * 3.1 ± 0.5
Kidney AUC72h (μg∙h/g tissue) 139.2 ± 5.19 26.30 ± 3.34 * 73.65 ± 7.05 *
AUC ratio 85.0 ± 16.1 64.6 ± 31.8 38.4 ± 5.3 *
t1/2 (h) 125.5 ± 80.4 24.9 ± 5.4 * 24.3 ± 5.7 *

Area under curve (AUC) ratio: Ratios of Kidney AUC to plasma AUC; Data expressed as mean ± SD from five mice; *: p < 0.05, compared with DWP16001 group.