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Table 2 Summary of plasma pharmacokinetic parameters of JOTROLTM (resveratrol) (PK population)

From: Safety and pharmacokinetics of a highly bioavailable resveratrol preparation (JOTROL TM)

 

Treatment A

Treatment B

Analyte

Parameter (unit)

N

Mean

SD

CV%

N

Mean

SD

CV%

Resveratrol

AUC0-t (h*ng/mL)

21

149

108

72

16

480

256

53

Plasma

AUC0-inf (h*ng/mL)

1

215

-

-

5

574

325

57

Residual Area (%)

1

5.48

-

-

5

5.55

4.08

74

Cmax (ng/mL)

21

127

116

91

16

455

409

90

T1/2 el (h)

1

1.26

-

-

5

2.74

1.71

63

Kel (/h)

1

0.552

-

-

5

0.332

0.162

49

 

Treatment A

Treatment B

Analyte

Parameter (unit)

N

Median

Min

Max

N

Median

Min

Max

Resveratrol

Tmax (h)

21

0.999

0.25

2.01

16

1

0.496

2.001

 

Treatment A

Treatment B

Analyte

Parameter (unit)

N

Mean

SD

CV%

N

Mean

SD

CV%

Urine

Ae0-t (ng)

21

22700

17100

75

16

54300

27100

50

Rmax (ng/h)

21

12100

10000

82

16

39300

53700

137

TRmax (h)

21

1.5

2.49

166

16

0.678

0.384

57

CLR (L/h)

21

0.25

0.28

112

16

0.14

0.09

63

 

Treatment C

Treatment D

Analyte

Parameter (unit)

N

Mean

SD

CV%

N

Mean

SD

CV%

Resveratrol

AUC0-t (h*ng/mL)

18

886

456

52

14

306

201

66

Plasma

AUC0-inf (h*ng/mL)

3

611

172

28

2

613

373

61

Residual Area (%)

3

3.76

1.45

39

2

3.7

4.12

111

Cmax (ng/mL)

18

805

590

73

14

205

207

101

T1/2 el (h)

3

1.6

0.4

25

2

1.71

1.22

72

Kel (/h)

3

0.455

0.13

29

2

0.547

0.392

72

 

Treatment C

Treatment D

Analyte

Parameter (unit)

N

Median

Min

Max

N

Median

Min

Max

Resveratrol

Tmax (h)

18

1.025

0.251

2

14

1.497

0.499

2.002

 

Treatment C

 

Analyte

Parameter (unit)

N

Mean

SD

CV%

Urine

Ae0-t (ng)

18

143000

127000

88

Rmax (ng/h)

18

63400

57700

91

TRmax (h)

18

0.974

0.796

82

CLR (L/h)

18

0.19

0.18

95

  1. No urinary data collected in treatment D
  2. N number of observations, SD standard deviation, CV coefficient of variation, Min minimum, Max maximum