Research Article
Development and Validation of Stability Indicating Spectroscopic Method for Content Analysis of Ceftriaxone Sodium in Pharmaceuticals
Table 5
Results for stability of drug under forced degradation study.
| | Parameters studied | Conc. taken (g/mL) | Conc. found (g/mL) | % degradation | % recovery |
| | Acid hydrolysis | 20 | 7.80 | 11.0 | 89.0% | | Alkaline hydrolysis | 20 | 20.07 | ā0.35 | 100.35% | | Oxidative degradation | 20 | 18.41 | 7.95 | 92.05% | | UV degradation | 20 | 21.69 | ā8.45 | 108.45% | | Thermal degradation | 20 | 19.31 | 3.45 | 96.55% |
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