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Table 1 Optimized chromatographic conditions

From: Development and validation of RP HPLC method for the estimation of Sofosbuvir and related impurity in bulk and pharmaceutical dosage form

Parameters

Results

Elution

Isocratic

Mobile phase

0.1 % trifluroacetic acid in 1000 ml water:acetonitrile (50:50)

Column

Agilent Eclipse XDB C18, 4.6 × 250 mm, 5μ

Flow rate

1.0 ml/min

Detection

260.0 nm

Injection volume

20 μl

Temperature

Ambient

Retention time

3.674 min for sofosbuvir and 5.704 min for phosphoryl impurity

Run time

25 min