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. 2016 Feb 1;37(4):530–544. doi: 10.1038/aps.2015.103

Table 3. Plasma pharmacokinetics of paeoniflorin (5) in rats receiving a 30-min intravenous infusion of XueBiJing injection.

PK parameter 5 mL/kg (Paeoniflorin, 5.7 mg/kg) 10 mL/kg (Paeoniflorin, 11.4 mg/kg) 20 mL/kg (Paeoniflorin, 22.8 mg/kg)
C30 min (μmol/L) 24.6±5.0 48.6±3.6 95.3±16.8
AUC0-∞ (μmol/L·h) 13.8±3.2 28.4±3.7 56.0±9.8
t1/2 (h) 0.37±0.15 0.43±0.09 0.47±0.21
MRT (h) 0.55±0.05 0.56±0.03 0.58±0.04
CLtot, p (L·h−1·kg−1) 0.90±0.22 0.85±0.11 0.87±0.16
VSS (L/kg) 0.26±0.02 0.26±0.02 0.31±0.06

C30 min, concentration at 30 min after dosing; AUC0-∞, area under the plasma concentration-time curve from zero to infinity; t1/2, elimination half-life; MRT, mean residence time; CLtot,p, total plasma clearance; VSS, apparent volume of distribution at steady state.