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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