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Future Journal of Pharmaceutical Sciences

Table 2 System suitability parameters

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

Parameters

Sofosbuvir

Phosphoryl impurity

Retention time

3.674 min

5.704 min

Theoretical plates

6144.731

9453.104

Tailing factor

1.366

1.269

Resolution

0.000

9.617

Peak area

5971771

33349

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