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Table 6 Robustness results at different conditions

From: Development and validation by statistical treatment of stability indicating RP-HPLC method for quantification of Orlistat in Orlistat-loaded solid dispersion

Condition

Recovery % (±SD)

2.5 μg/ml

5 μg/ml

7.5 μg/ml

HPLC 2

97 ± 2.45

98 ± 2.76

101 ± 1.67

Mobile phase with composition 84:15:1 (methanol, acetonitrile and 2% phosphoric acid)

99 ± 3.51

101 ± 2.12

102 ± 2.73

Flow rate 1.2 ml/min

98 ± 4.78

99 ± 3.85

104 ± 3.76