Research Article
Development and Validation of a Discriminating In Vitro Dissolution Method for Oral Formulations Containing Satranidazole
Table 8
Change in wavelength.
| Time (minutes) | At 318 | At 320 | At 322 |
| Average % release ± SD | 0 | 0 | 0 | | 5 | 8.95 ± 0.5456 | 85.12 ± 0.7678 | 83.98 ± 0.6789 | 10 | 34.01 ± 0.4345 | 98.23 ± 0.6678 | 97.31 ± 0.8012 | 15 | 44.25 ± 0.5987 | 99.81 ± 0.8978 | 98.12 ± 0.5612 | 30 | 66.87 ± 0.6745 | 101.29 ± 0.7809 |
99.24 ± 0.6769 | 45 | 77.12 ± 0.7568 | 76.84 ± 0.5982 | 77.46 ± 0.8145 | 60 | 85.93 ± 0.4768 | 87.09 ± 0.3780 | 85.76 ± 0.4568 |
| Average at 60 min | 86.26 ± 0.6744 | % RSD at 60 min | 0.839 |
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