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Table 3 The main pharmacokinetic parameters of rifaximin in mammary glands following an intramammary administration with a single dose of 50, 100, 200, and 400 μg/gland in mice, analyzed by non-compartment and two-compartment models

From: A PK/PD model for the evaluation of clinical rifaximin dosage for the treatment of dairy cow mastitis induced by Escherichia coli

Parameters

Administered Dose (µg/gland) (n = 6)

50

100

200

400

 

non-compartment

 T1/2

6.18

7.45

6.84

7.19

6.92 ± 0.48

 MRT

6.76

7.42

6.80

7.11

7.02 ± 0.27

 AUC24

170.23

414.31

653.22

1287.03

 

 Cmax

25.01

49.73

83.17

162.17

 

two-compartment models

 MRT

9.10

11.34

9.08

10.46

10.00 ± 0.96

 AUC24

175.41

469.08

677.08

1400.29

 

 Cmax

27.08

53.07

87.31

165.99

 

 V1

1.85

1.88

2.29

2.41

2.11 ± 0.28

 CL1

0.29

0.21

0.30

0.29

2.07 ± 0.04

 V2

0.75

0.53

0.39

0.58

0.56 ± 0.15

 CL2

1.13

1.21

1.14

0.40

0.97 ± 0.38

  1. T1/2 is the half-life of rifaximin in the mammary gland, MRT is the average dwell time, AUC24 represents the area under the curve when the drug is administered for 0–24 h, Cmax is the maximum drug concentration after drug infusion