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. 2015 Jan 28;5(4):207–227. doi: 10.1016/j.jtcme.2014.11.041

Table 20.

Estimated pharmacokinetic data on geniposide in rat blood following geniposide administration (10, 30, and 100 mg kg−1, intravenously).

Parameters Geniposide 10 mg/kg−1
Geniposide 30 mg/kg−1
Geniposide 100 mg/kg−1
With out acupuncture With acupuncture Without acupuncture With acupuncture Without acupuncture With acupuncture
A. Blood
AUC (min μgml−1) 417 ± 17 486 ± 59 1102 ± 32 1235 ± 128 4759 ± 601 4233 ± 411
MRT (min) 15 ± 1 15 ± 1 18 ± 1 17 ± 2 17 ± 2 17 ± 2
Cl (ml min−1 kg−1) 24 ± 1 22 ± 2 27 ± 1 26 ± 3 23 ± 3 25 ± 2
B. Liver
AUC (min μgml−1) 550 ± 107 637 ± 76
MRT (min) 16 ± 2 19 ± 3
C. Bile
AUC (min μgml−1) 1039 ± 136 1001 ± 90
MRT (min) 37 ± 2 39 ± 1
AUC liver/AUC blood 1.34 ± 0.27 1.41 ± 0.24
AUC bile/AUC blood 2.50 ± 0.33 2.10 ± 0.10

Data are expressed as mean ± standard error of the mean from six individual micro-dialysis experiments at each dose treatment.

AUC = area under the concentration-time curve; Cl = clearance; MRT = mean residence time.