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Table 5 Determination of ebastine in its dosage forms by the proposed HPLC method

From: Validated stability indicating liquid chromatographic determination of ebastine in pharmaceuticals after pre column derivatization: Application to tablets and content uniformity testing

Proposed method

Comparison method [4]

Preparation

Amount taken (μg/ml)

Amount found (μg/ml)

% Recovery

% Recovery

Bastab ® tablets

0.3

0.2974

99.14

99.23

 

0.7

0.6981

99.72

99.61

 

1.0

1.0094

100.94

100.61

 

3.0

3.0036

100.12

 
 

5.0

4.9835

99.67

 
 

6.0

5.9844

99.74

 

Xˉ ± SD

  

99.88 ± 0.61

99.82 ± 0.71

Student's t test

  

0.39(2.02)*

 

Variance ratio F test

  

1.35(3.78)*

 

Evastine ® syrup

0.3

0.30216

100.72

100.12

 

0.7

0.69615

99.45

99.61

 

1.0

1.0011

100.11

99.51

 

3.0

3.0144

100.48

 
 

5.0

5.031

100.62

 
 

6.0

5.9994

99.99

 

Xˉ ± SD

  

100.23 ± 0.48

99.75 ± 0.33

Student's t test

  

0.23(2.02)*

 

Variance ratio F test

  

2.12(3.78)*

 
  1. *Figures between parentheses are the tabulated t and F values at p = 0.05 [20].*