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Table 2 Pharmacokinetics of intravenous artelinate and artesunate in plasma from P. coatneyi infected rhesus monkeys

From: Comparative pharmacokinetics and pharmacodynamics of intravenous artelinate versus artesunate in uncomplicated Plasmodium coatneyi-infected rhesus monkey model

Pharmacokinetics

Rx

Parent compound (P)

Metabolite (M)

M/P

% AUC0–20

Parameter

Unit

Median

25th IQT

75th IQT

pa

Median

25th IQT

75th IQT

pa

AUC0–∞

C bmax

mM

IV AL

60.2

55.9

65.3

<0.0001

10.9

9.10

13.4

<0.0001

0.18

 

IV AS

28.2

24.3

38.0

7.23

6.52

7.41

 

0.26

 

t c1/2

min

IV AL

28.2

25.8

35.4

<0.0001

42.2

33.2

47.6

0.02

1.50

 

IV AS

3.47

3.09

5.15

31.1

25.0

34.5

8.97

 

AUC d0–∞

mM min

IV AL

3706

2845

4218

<0.0001

1260

944

1519

<0.0001

0.33

 

IV AS

288

260

399

453

415

494

1.58

 

AUC e0–20

mM min

IV AL

925

849

1028

<0.0001

117

100

153

0.7

 

24.6

IV AS

288

253

394

116

107

122

 

97.0

Clf

L kg−1 min−1

IV AL

5.60

4.85

7.88

<0.0001

      

IV AS

72.3

52.4

79.9

      

V gz

L kg−1

IV AL

0.259

0.241

0.294

0.07

      

IV AS

0.397

0.311

0.507

      
  1. aMann Whitney Test
  2. b C max maximum concentration of drug reached in plasma
  3. c t 1/2 elimination half-life
  4. d AUC 0–∞ area under the concentration–time curve from zero to infinity
  5. e AUC 0–20 area under the concentration–time curve from zero to 20 min
  6. f Cl apparent total body clearance
  7. g V z volume of distribution