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Table 6 Pharmacokinetic parameters of COS 2 and COS 3 after intragastric administration and intravenous administration (data derived from non-compartmental model, mean ± SD, n = 6)

From: Pharmacokinetics, bioavailability and tissue distribution of chitobiose and chitotriose in rats

Parameters

Unit

i.g. COS 2

i.g. COS 3

i.v. COS 2

i.v. COS 3

100 mg/kg

500 mg/kg

100 mg/kg

500 mg/kg

100 mg/kg

100 mg/kg

AUC0-t

mg/L·h

4.09 ± 0.68

16.38 ± 2.19

4.81 ± 0.65

20.01 ± 4.29

820.24 ± 67.60

1340.53 ± 130.92

AUC0-∞

mg/L·h

4.30 ± 1.08

16.61 ± 2.32

5.40 ± 0.76

21.44 ± 5.51

821.81 ± 68.03

1340.55 ± 130.93

MRT0-t

h

4.12 ± 1.21

3.71 ± 0.82

4.14 ± 1.60

4.02 ± 1.47

0.44 ± 0.06

0.38 ± 0.11

MRT0-∞

h

6.49 ± 3.95

4.20 ± 0.94

6.57 ± 2.45

5.63 ± 3.00

0.46 ± 0.07

0.39 ± 0.11

t1/2z

h

5.52 ± 6.50

3.95 ± 1.84

5.09 ± 1.83

5.90 ± 3.52

0.84 ± 0.33

0.58 ± 0.12

Tmax

h

0.75 ± 0.00

0.79 ± 0.10

0.71 ± 0.10

0.92 ± 0.13

0.08 ± 0.00

0.08 ± 0.00

CLZ/F

L/h/kg

24.43 ± 5.81

30.63 ± 4.58

18.82 ± 2.64

24.84 ± 7.41

0.12 ± 0.01

0.08 ± 0.01

VZ/F

L/kg

162.32 ± 136.07

167.10 ± 64.50

134.33 ± 38.50

189.30 ± 78.96

0.15 ± 0.06

0.06 ± 0.02

Cmax

mg/L

1.53 ± 0.34

5.61 ± 1.46

2.33 ± 0.60

7.88 ± 1.87

2137.85 ± 335.25

3312.24 ± 160.94

F0-∞

%

0.52

0.40

0.40

0.32

N/A

N/A

  1. i.g., intragastric administration; i.v., intravenous administration