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Table 4 Robustness parameters

From: RP-HPLC method development and validation for the quantification of Efonidipine hydrochloride in HME processed solid dispersions

Parameter

Method condition

Mean peak Area ± SD

%RSD

Rt ± SD

%RSD

Original

Variation

Flow rate (ml/min)

1.2

1.4

19,425.2 ± 91.61

0.472

3.45 ± 0.036

1.04

1.2

1.0

Mobile phase (ACN to pH 2.5 phosphate buffer)

85:15

87:13

19,352.7 ± 79.95

0.41

3.43 ± 0.04

1.16

85:15

83:17

  1. Concentration: 10 μg/ml