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Table 1 Forced degradation study results

From: Development and validation of stability-indicating UPLC method for the determination of gliclazide and its impurities in pharmaceutical dosage forms

Stress conditions

% Degradation

Purity angle

Purity threshold

Purity flag

Unstressed condition

0

0.068

0.317

No

Treated with 1 N (5 mL) HCL solution for 45 min on benchtop

5.5

0.088

0.416

No

Treated with 1 N (5mL) NaOH solution for 2 h at 95 °C

5.8

0.056

0.357

No

Treated with 3% (5 mL) H2O2 solution for 1 h at benchtop

13.9

0.058

0.308

No

Treated with H2O (5 mL) for 2 h 90 °C

18.4

0.297

0.314

No

Kept in oven at 105 °C for and 72 h

0.9

0.089

0.408

No

Kept in humidity chamber for 120 h at 75%

Relative humidity and 40 °C

0.1

0.102

0.421

No