Research Article
Safety Assessment of Ubiquinol Acetate: Subchronic Toxicity and Genotoxicity Studies
Table 3
Dose confirmation & homogeneity analysis.
| Day of Dose Formulation used for administration | % Recovery of analysed concentration | (Dose Confirmation) | Low dose | Mid dose | High dose | (37.5 mg/mL) | (75.0 mg/mL) | (150.0 mg/mL) |
| Day 0 | 104.15 | 104.28 | 101.31 | Day 49 | 96.74 | 97.58 | 98.10 | Day 90 | 94.94 | 95.62 | 95.68 |
| Day of Dose Formulation used for administration | % Recovery of analysed concentration | (Homogeneity) | Low dose | Mid dose | High dose | (37.5 mg/mL) | (75.0 mg/mL) | (150.0 mg/mL) | Top | Middle | Bottom | Top | Middle | Bottom | Top | Middle | Bottom |
| Day 0 | 102.32 | 103.30 | 103.39 | 103.40 | 104.42 | 104.84 | 106.28 | 107.59 | 105.63 | Day 49 | 98.07 | 97.82 | 96.33 | 98.42 | 98.88 | 98.61 | 98.68 | 99.70 | 98.87 | Day 90 | 96.06 | 96.11 | 93.87 | 96.19 | 96.86 | 97.11 | 97.57 | 96.78 | 96.56 |
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Note: acceptable limits of % recovery: from 85 to 115 %.
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