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. 2016 Aug 9;31:e2016016. doi: 10.5620/eht.e2016016

Table 1.

Effects of co-administration of BST extract with MDZ on the pharmacokinetic parameters of MDZ and 1ʹ-OH-MDZ (n=3)

Parameters BST extract (g/kg) Oral administration of MDZ
Intraperitoneal administration of MDZ
AUC (mg-min/mL) Cmax (mg/mL) Half-life (min) Tmax (min) AUC (mg-min/mL) Cmax (mg/mL) Half-life (min) Tmax (min)
MDZ 0.0 45.7±2.9 0.7±0.1 167.3±116.8 5.0±0.0 234.5±9.5 4.5±0.1 23.1±1.5 11.7±1.7
0.5 33.9±6.5 0.7±0.1 59.3±15.3 8.3±3.3 220.1±26.2 4.5±0.5 25.0±3.1 10.0±0.0
1.0 16.9±4.1** 0.3±0.1 79.1±1.2 26.7±16.9 197.9±7.8 3.9±0.2 23.1±0.8 9.0±1.3
1'-OH MDZ 0.0 3540.8±312.7 43.1±8.5 55.3±0.0 50.0±10.0 18.9±0.8 0.2±0.01 159.8±11.2 20.0±5.0
0.5 3189.7±907.0 42.9±12.6 71.8±12.3 16.7±7.3 18.2±0.3 0.1±0.01 166.0±6.1 13.8±1.3
1.0 1901.0±194.2* 21.4±2.5 101.1±1.7 31.7±15.9 18.2±0.4 0.1±0.0 169.0±11.3 21.0±3.8

Data are presents as mean±standard errors.

BST, Banha-sasim-tang; MDZ, midazolam; 1ʹ-OH-MDZ, 1ʹ-hydroxymidazolam; AUC, area under the plasma concentration-time curve; Cmax, maximum plasma concentration; Tmax, maximum plasma concentration

*

p<0.05

**

p<0.01 compared to the vehicle-treated group.