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. 2020 Aug 28;42(2):311–322. doi: 10.1038/s41401-020-0481-8

Table 2.

Pharmacokinetic parameters of forsythin, M1 (aglycone), M2 (M1 sulfate), and M7 (M1 glucuronide) following administration of 100 mg forsythin capsules in 8 healthy subjects.

Parameters Forsythin M1 M2 M7
Cmax (ng/mL) 31.8 ± 6.5 3.81 ± 1.24 1450 ± 792 72.2 ± 55.1
Tmax (h) 1.25 (0.75–3.00) 11.0 (4.00–14.0) 5.00 (1.00–12.0) 6.00 (1.00–12.0)
Cmax1 (ng/mL) 29.7 ± 8.23 1.88 ± 0.97 893 ± 462 35.7 ± 29.6
Tmax1 (h) 1.25 (0.72–2.00) 0.75 (0.50–3.00) 0.875 (0.25–2) 1.25 (0.72–2.50)
Cmax2 (ng/mL) 22.0 ± 13.6 3.30 ± 1.79 1203 ± 946 59.8 ± 58.3
Tmax2 (h) 2.50 (3.00–6.00) 6.00 (2.50–12.0) 6.00 (3.00–12.0) 6.00 (2.50–12.0)
AUC0–t (h·ng/mL) 111 ± 34 31.3 ± 11.8 9700 ± 1890 417 ± 132
AUC0–∞ (h·ng/mL) 114 ± 34 45.3 ± 7.39 9860 ± 1960 477 ± 127
t1/2 (h) 1.75 ± 0.26 4.57 ± 2.88 4.36 ± 1.61 3.32 ± 1.47
Vz/F (L) 2370 ± 731
CL/F (L/h) 942 ± 265

Cmax maximum observed plasma concentration, Tmax time of the maximum concentration, AUC0–t area under the concentration–time curve from time zero to the last measurable concentration, AUC0–∞ area under the concentration–time curve from 0 h to the infinite time, tmax time to the Cmax, t1/2 apparent elimination half-life, Vz/F apparent volume of distribution, CL/F apparent clearance.