Methylprednisolone sodium succinate is a glucocorticoid receptor agonist with immunosuppressive and anti-inflammatory activity that can be converted to active prednisolone in vivo, thereby activating GR-mediated gene expression. In addition, Methylprednisolone sodium succinate can be used to construct a rat model of hormonal femoral head necrosis.
| Molecular Weight | 496.5 |
| Formula | C26H33NaO8 |
| CAS Number | 2375-03-3 |
| Form | Solid |
| Solubility (25°C) | Water 50 mg/mL (ultrasonic) DMSO 25 mg/mL |
| Storage | 4°C, dry, sealed |
| Species | Mouse | Rat | Rabbit | Guinea pig | Hamster | Dog |
| Weight (kg) | 0.02 | 0.15 | 1.8 | 0.4 | 0.08 | 10 |
| Body Surface Area (m2) | 0.007 | 0.025 | 0.15 | 0.05 | 0.02 | 0.5 |
| Km factor | 3 | 6 | 12 | 8 | 5 | 20 |
| Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
| Animal A Km |
For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.
[2] Foteini Stefania Koumpa, et al. BMJ Case Rep. Sudden irreversible hearing loss post COVID-19
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