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Table 2 Assay results for the determination of the studied drugs in their synthetic mixture and co-formulated tablets.

From: Development and validation of a repharsed phase- HPLC method for simultaneous determination of rosiglitazone and glimepiride in combined dosage forms and human plasma

Sample

Concentration taken (μg/mL)

Concentration found (μg/mL)

% Found

Reference method [14]

1- Synthetic mixture(a)

ROS

GLM

ROS

GLM

ROS

GLM

ROS

GLM

 

0.25

0.125

0.249

0.127

99.60

101.60

99.10

100.27

 

0.5

0.25

0.501

0.251

100.20

100.40

100.64

98.18

 

1.0

0.5

1.013

0.506

101.30

101.20

98.00

99.73

 

5.0

2.5

4.966

0.473

99.32

98.92

  
 

10.0

5.0

10.005

5.014

100.05

100.28

  
 

15.0

7.5

15.131

7.473

100.87

99.64

  
 

25.0

12.5

25.047

12.473

100.19

99.78

  

X'

    

100.22

100.26

99.25

99.06

SD

    

0.68

0.92

1.33

1.08

%RSD

    

0.68

0.92

  

±%Error

    

0.26

0.35

  

t- test

    

1.58

1.80

  

F- test

    

3.83

1.37

  

2-AvandarylTM tablets(b) (4 mg ROS + 2 mg GLM/tablet)

0.25

0.125

0.253

0.123

101.20

98.40

98.10

101.56

 

1.0

0.5

0.994

0.511

99.4

102.20

99.27

98.50

 

5.0

2.5

5.038

2.543

100.76

101.72

100.71

100.40

 

10.0

5.0

10.215

4.946

102.15

98.92

  

X'

    

100.88

100.31

99.36

100.15

SD

    

1.14

1.93

1.31

1.54

%RSD

    

1.14

1.93

  

±%Error

    

0.57

0.97

  

t- test

    

1.65

0.12

  

F- test

    

1.32

1.32

  
  1. N.B.:
  2. (a) The values of tabulated t and F are (2.31) and (5.14) respectively at p = 0.05
  3. (b) The values of tabulated t and F are (2.57) and (9.550 respectively at p = 0.05