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Table 4 Stability results of tofacitinib in forced degradation study

From: Design of experiment-driven stability-indicating RP-HPLC method for the determination of tofacitinib in nanoparticles and skin matrix

Study performed

Stress condition

% of Tofacitinib degraded

Degradation peaks with retention time (min)

Acid hydrolysis

0.5 M Hydrochloric acid

14.78 ± 0.04%

3.67, 3.8 and 4.6

Base hydrolysis

0.5 M sodium hydroxide

75 ± 0.06%

5.4

Oxidative

2% hydrogen peroxide

20.25 ± 0.04%

3.7 and 4.6

Thermal

Water

1.5 ± 0.02%

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