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Table 12 Robustness studies (different column) for standard and test solutions of phosphoryl impurity

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

Injection no.

Peak area (AU)

Retention time (min)

Standard

Test

Standard

Test

1

33533

35324

6.095

6.102

2

33964

33955

6.096

6.105

3

34743

33980

6.103

6.106

Mean

34080

34420

6.098

6.105

Std. dev

613.28

783.28

0.004

0.002

% RSD

1.800

2.276

0.069

0.032

% Assay

99.77