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Table 2 The main pharmacokinetic parameters after oral administration of 25, 50, and 100 mg/kg for MOIG, and 1650 mg/kg for MO or intravenous administration of 25 mg/kg MOIG in female rats (n = 3, mean ± SD)

From: Pharmacokinetics and tissue distribution of monotropein and deacetyl asperulosidic acid after oral administration of extracts from Morinda officinalis root in rats

Parameters

Component

po-MOIG-25

po-MOIG-50

po-MOIG-100

po-MO-1650

iv-MOIG-25

AUC0-t (μg·h/L)

MON

1988 ± 870

3083 ± 1184

2963 ± 397

1504 ± 244

19,098 ± 4740

DA

3133 ± 1580

6572 ± 884

5727 ± 992

4254 ± 3301

8910 ± 2343

AUC0-∞ (μg·h/L)

MON

2040 ± 815

3178 ± 1290

2981 ± 400

1507 ± 243

19,129 ± 4743

DA

3221 ± 1536

6661 ± 935

5785 ± 1024

4308 ± 3367

8945 ± 2349

AUMC0-∞ (μg·h/L)

MON

10,005 ± 3510

16,892 ± 14,358

8895 ± 1596

5589 ± 407

17,847 ± 2842

DA

20,444 ± 6912

41,101 ± 9585

29,163 ± 7495

25,789 ± 23,049

9214 ± 715

MRT (h)

MON

5.28 ± 2.38

4.78 ± 2.64

2.99 ± 0.43

3.75 ± 0.34

0.98 ± 0.31

DA

6.77 ± 1.35

6.12 ± 0.60

4.99 ± 0.44

5.66 ± 0.71

1.08 ± 0.31

t1/2 (h)

MON

3.61 ± 1.03

4.01 ± 2.35

2.08 ± 0.50

2.51 ± 0.34

1.76 ± 1.32

DA

4.43 ± 1.12

3.66 ± 0.35

3.64 ± 0.43

3.38 ± 0.44

2.20 ± 1.86

Tmax (h)

MON

0.94 ± 0.00

1.33 ± 0.29

0.92 ± 0.14

0.92 ± 0.14

0.03 ± 0.00

DA

2.17 ± 0.76

1.83 ± 0.58

2.33 ± 0.58

2.08 ± 1.18

0.03 ± 0.00

Vd (L/g)

MON

0.08 ± 0.05

0.09 ± 0.04

0.10 ± 0.04

4.07 ± 1.16

0.003 ± 0.002

DA

0.07 ± 0.06

0.04 ± 0.01

0.09 ± 0.01

2.50 ± 1.25

0.009 ± 0.006

CL (L/g·h)

MON

0.014 ± 0.005

0.018 ± 0.009

0.034 ± 0.05

1.114 ± 0.183

0.001 ± 0.000

DA

0.010 ± 0.006

0.008 ± 0.001

0.018 ± 0.003

0.532 ± 0.287

0.003 ± 0.001

Cmax (μg/L)

MON

475 ± 160

761 ± 184

899 ± 197

405 ± 102

25,719 ± 12,174

DA

445 ± 218

863 ± 112

966 ± 171

584 ± 419

12,340 ± 5992

F (%)

MON

10.66 ± 4.26

8.31 ± 3.37

3.90 ± 0.52

3.94 ± 0.64

DA

36.01 ± 17.17

37.23 ± 5.23

16.17 ± 2.86

24.08 ± 18.82