Enoxaparin Sodium | ||||
Source | Intestinal mucosa of pigs | |||
Quality standard |
USP |
EP |
||
characters |
Appearance |
/ |
white or almost white;?hygroscopic powder | |
solubility |
/ |
freely soluble in water | ||
identification | The spectra exhibit maxima at 231±2nm | The 13C NMR spectrum obtained is similar to that obtained with the appropriate specific Enoxaparin sodium CRS | ||
The spectra are similar | 15 -25 % bearing the 1,6-anhydro structure at the reducing end of their chain | |||
Anti- Xa activity/?anti-?IIa?: 3.3-5.3 | Anti- Xa activity/?anti-?IIa?: 3.3-5.3 | |||
Mw :?3800?-5000Da, M≤2000?:?12.0%-20.0%,???????????????????????????????M≥8000:NMT 18.0%, M2000-8000:68.0%-82.0% | Mw :?3800?-5000Da, M≤2000?:?12.0%-20.0%,???????????????????????????????M≥8000:NMT 18.0%, M2000-8000:68.0%-82.0% | |||
Meets the requirements for Sodium Content | It complies with the test for sodium | |||
Appearance of solution | / | clear;NMT: intensity?6 | ||
Specific Absorbance | 14.0-20.0 (on the dried basis) | 14.0-20.0 (on the dried basis),determined at 231nm | ||
pH | 6.2-7.7 | 6.2-7.7 | ||
Benzyl alcohol | ≤?0.1% | ≤?0.1% | ||
Molar ratio of Sulfate carboxylate | ≥?1.8 | ≥?1.8 | ||
Nitrogen | 1.8?%-2.5 %?(on the dried basis) | 1.5 %-2.5 %?(on the dried basis) | ||
Sodium | 11.3%?-13.5%?(on the dried basis) | 11.3%?-13.5%?(on the dried basis) | ||
Loss on drying | ≤?10.0% | ≤?10.0% | ||
Bacterial endotoxins | <0.01EU/U | <0.01EU/IU | ||
Assay | Anti- Xa activity | 90-125 IU/mg (on the dried basis) | 90-125 IU/mg (on the dried basis) | |
Anti- IIa activity | 20-35 IU/mg (on the dried basis) | 20-35 IU/mg (on the dried basis) |