Crystalline form of dextral oxiracetam, preparation method therefor and use thereof
View Patent ↗The present invention provides a crystalline form of dextral oxiracetam. The crystalline form has a diffraction peak when a diffraction angle, 2θ, is 17.12±0.2°, 18.88±0.2°, 19.24±0.2°, 21.18±0.2°, 24.88±0.2°. The crystalline form having oxiracetam can promote synthesis of phosphorylcholine and phosphoethanolamine, boosts cerebral metabolism, has a stimulating function on a specific central nervous pathway through a blood-brain barrier, improves the intelligence and memory, has an obvious effect on a memory dysfunction, and has special biologic activity in the field of sedation and the antiepileptic field. The method for preparing the crystalline form is simple and is suitable for industrial production.
1. A crystalline form III of dextral oxiracetam having diffraction peaks at diffraction angles 2θ of 17.12±0.2°, 18.88±0.2°, 19.24±0.2°, 21.18±0.2°, and 24.88±0.2°.
2. The crystalline form III of dextral oxiracetam according to claim 1 , characterized in that the crystalline form III of dextral oxiracetam has a relative peak intensity of 100% at the diffraction angle 2θ of 18.88±0.2°; a relative peak intensity of more than 80% and less than 100% at diffraction angles 2θ of 21.18±0.2° and 24.88±0.2°; and a relative peak intensity of not less than 60% at the diffraction angles 2θ of 17.12±0.2° and 19.24±0.2°.
3. The crystalline form III of dextral oxiracetam according to claim 1 , characterized in that the crystalline form III of dextral oxiracetam has diffraction peaks at diffraction angles 2θ of 17.12±0.2°, 18.88±0.2°, 19.24±0.2°, 20.66±0.2°, 20.84±0.2°, 21.18±0.2°, 21.82±0.2°, 22.94±0.2°, 24.88±0.2°, and 31.52±0.2°.
4. The crystalline form III of dextral oxiracetam according to claim 1 , characterized in that the crystalline form III of dextral oxiracetam has diffraction peaks at diffraction angles 2θ of 14.44±0.2°, 17.12±0.2°, 18.88±0.2°, 19.24±0.2°, 19.78±0.2°, 20.66±0.2°, 20.84±0.2°, 21.18±0.2°, 21.82±0.2°, 22.94±0.2°, 23.24±0.2°, 24.88±0.2°, 30.46±0.2°, 31.40±0.2°, and 31.52±0.2°.
5. The crystalline form III of dextral oxiracetam according to claim 1 , characterized in that the crystalline form has a powder diffraction pattern as shown in FIG. 1 .
6. A method of preparing the crystalline form III of dextral oxiracetam according to claim 1 , applying the following steps: dissolving dextral oxiracetam in n-propanol to form a supersaturated solution, and then cooling the solution in a low temperature environment of from −12° C. to −21° C. to form crystals, separating the crystals by filtration, and drying to obtain the crystal form III of dextral oxiracetam.
7. The method of preparing the crystalline form III of dextral oxiracetam according to claim 6 , characterized in that the method applies the following steps: adding dextral oxiracetam into the n-propanol in a concentration of from 10 mg/mL to 55 mg/mL, stirring continuously, dissolving by heating at from 35° C. to 90° C., and filtering to form the supersaturated solution; then sealing the supersaturated solution and cooling it in a low temperature environment of from −12° C. to −21° C. to form crystals, separating the crystals by filtration, and drying to obtain the crystal form III of dextral oxiracetam.
8. The method of preparing the crystalline form III of dextral oxiracetam according to claim 6 , characterized in that the low temperature environment is from −17° C. to −19° C.
9. A method for treating or preventing epilepsy in a patient in need thereof comprising: administering the crystalline form III of dextral oxiracetam according to claim 1 .
10. The method of claim 9 , wherein the crystalline form III of dextral oxiracetam is administered in the form of a pharmaceutical composition comprising the crystalline form III of dextral oxiracetam and pharmaceutically acceptable excipients.
11. The method according to claim 10 , characterized in that the composition is tablets, powders, granules, injections, capsules, dripping pills, sustained release formulations, or lyophilized powders for injection.