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Table 10 Forced degradation study results for lamivudine

From: A new validated stability-indicating RP-HPLC method for simultaneous quantification of dolutegravir and lamivudine in bulk and pharmaceutical dosage form

S.No

Sample name

% assay

% degradation

Purity angle

Purity threshold

Purity flag

1

Controlled sample

100.1

--

0.310

1.375

No

2

Acid degradation

95.1

5.0

0.325

0.463

No

3

Alkaline degradation

96.9

3.2

0.575

1.081

No

4

Peroxide degradation

94.8

5.3

1.612

2.175

No

5

Thermal degradation

98.3

1.8

0.268

0.294

No

6

UV degradation

99.7

0.4

0.318

0.335

No

7

Water degradation

98.4

1.7

0.264

0.298

No