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Table 1 Optimized chromatographic conditions for the analysis of vildagliptin by RP-HPLC

From: Bioequivalence study of different brands of vildagliptin in healthy human subjects

Drug

Time (min)

Mobile buffer (%A)

Phase ACN (%B)

Flow rate (ml/min)

Detection wavelength (nm)

Injection volume (μl)

Retention time (min)

Vildagliptin

0

95

5

    

5

80

20

    

10

50

50

    

15

20

80

1

210

20

11

17

5

95

    

19

95

5

    

20

95

5

    
  1. Linear regression was performed to determine the drug concentration in the range of 10–1000 ng/ml (r2 = 0.9992). The lower limit of quantitation was 10.0 ng/ml with the accuracy (%) and precision (CV %) of 97.37 and 1.48, respectively