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Table 2 Pharmacokinetic parameters of total radiolabeled components in selected tissues/matrices, calculated from the radioactivity concentrations determined by QWBA after a 2 mg/kg oral dose of [14C]diclofenac sodium in treated rats (n = 3 animals/time point) and in control rats (n = 1 animal/time point).

From: Preferential uptake of the non steroid anti-inflammatory drug diclofenac into inflamed tissues after a single oral dose in rats

Treated rats

(Carrageenan injected)

tmax (h)

Cmax (nmol/g)

AUC(0-tlast) (h*(nmol/g))

tlast (h)

t1/2 (h)

Control footpads

1

0.16

0.92

8

1.80

Inflamed footpads

4

1.30

16.00

24

5.30

Inflamed nape neck

8

1.30

20.00

24

7.10

Blood

4

2.20

27.00

24

5.10

Kidney (cortex)

4

9.80

105.00

24

5.20

Liver

4

5.40

62.00

24

5.70

Control rats

(Saline injected)

tmax (h)

Cmax (nmol/g)

AUC(0-tlast) (h*(nmol/g))

tlast (h)

t1/2 (h)

Control footpads

1

0.20

1.1

8

2.60

Injected footpads

1

0.12

0.30

4

1.60

Injected nape neck

1

0.18

0.77

8

2.90

Blood

4

1.90

22.00

24

4.90

Kidney (cortex)

4

8.20

88.00

24

5.30

Liver

4

4.00

45.00

24

5.50