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Table 4 The pharmacokinetic parameters of flibanserin in rat plasma after oral administration

From: A rapid and sensitive UPLC-MS/MS method for the determination of flibanserin in rat plasma: application to a pharmacokinetic study

Parameters

Unit

Mean

po 10 mg/kg

SD

RSD/%

AUC(0–t)

μg/L h

351,658.00

77,499.85

22.0

AUC(0–∞)

μg/L h

356,517.60

77,670.82

21.8

MRT(0–t)

h

2.70

0.29

10.7

MRT(0–∞)

h

2.88

0.29

10.2

t1/2z

h

2.03

0.66

32.7

Tmax

h

0.79

0.19

23.7

Vz/F

L/kg

0.09

0.04

42.5

CLz/F

L/h/kg

0.03

0.01

27.6

Cmax

μg/L

108,224.40

25,506.58

23.6