Crystalline forms of naltrexone methobromide
View Patent ↗The present invention relates to novel crystalline forms of naltrexone methobromide including hydrated and solvated forms. The invention also describes methods of preparing the various crystalline forms. The present invention also relates to pharmaceutical compositions containing crystalline forms of naltrexone methobromide, as well as methods of treating or preventing opioid induced side effects by administering the pharmaceutical compositions.
1. A crystalline form of naltrexone methobromide Form II characterized by an x-ray diffraction pattern having at least four characteristic peaks expressed in degrees 2θ (±0.2°) selected from 8.0, 8.3, 10.7, 14.1, 14.5, 16.0, 17.3, 17.5, 20.0, 21.6, 22.1, 24.2, 24.6, 25.6, and 26.2.
2. The crystalline form of naltrexone methobromide of claim 1 characterized by an x-ray diffraction pattern having at least eight characteristic peaks expressed in degrees 2θ (±0.2°) selected from 8.0, 8.3, 10.7, 14.1, 14.5, 16.0, 17.3, 17.5, 20.0, 21.6, 22.1, 24.2, 24.6, 25.6, and 26.2.
3. The crystalline form of naltrexone methobromide of claim 1 characterized by an x-ray diffraction pattern having at least ten characteristic peaks expressed in degrees 2 θ (±0.2°) selected from 8.0, 8.3, 10.7, 14.1, 14.5, 16.0, 17.3, 17.5, 20.0, 21.6, 22.1, 24.2, 24.6, 25.6, and 26.2.
4. The crystalline form of naltrexone methobromide of claim 1 characterized by a powder x-ray diffraction pattern as shown in FIG. 2 .
5. The crystalline form of naltrexone methobromide of claim 1 comprising bound methanol.
6. The crystalline form of naltrexone methobromide of claim 1 comprising from about 4.9% to 7.5% bound methanol.
7. The crystalline form of naltrexone methobromide of claim 1 characterized by a differential scanning calorimetry thermogram taken at a heating rate of 5° C./min, in a closed pan that exhibits a large endothermic transition at approximately 25° C. to 150° C.
8. The crystalline form of naltrexone methobromide of claim 1 characterized by no loss of mass prior to sublimation above 150° C.
9. A crystalline form of naltrexone methobromide Form III characterized by an x-ray diffraction pattern having at least eight characteristic peaks expressed in degrees 2θ (±0.2°) selected from 7.7, 12.9, 13.6, 15.4, 16.2, 17.6, 18.7, 19.7, 21.2, 21.9, 23.3, 24.5, 26.3, 28.6, and 35.9.
10. The crystalline form of naltrexone methobromide of claim 9 characterized by an x-ray diffraction pattern having at least eight characteristic peaks expressed in degrees 2θ (±0.2°) selected from 7.7, 12.9, 13.6, 15.4, 16.2, 17.6, 18.7, 19.7, 21.2, 21.9, 23.3, 24.5, 26.3, 28.6, and 35.9.
11. The crystalline form of naltrexone methobromide of claim 9 characterized by an x-ray diffraction pattern having at least ten characteristic peaks expressed in degrees 2 θ (±)0.2°) selected from 7.7, 12.9, 13.6, 15.4, 16.2, 17.6, 18.7, 19.7, 21.2, 21.9, 23.3, 24.5, 26.3, 28.6, and 35.9.
12. The crystalline form of naltrexone methobromide of claim 9 characterized by a powder x-ray diffraction pattern as shown in FIG. 3 .
13. The crystalline form of naltrexone methobromide of claim 9 comprising bound water.
14. The crystalline form of naltrexone methobromide of claim 9 comprising from about 3.5% to about 6.0% water by mass.
15. The crystalline form of naltrexone methobromide of claim 9 characterized by a differential scanning calorimetry thermogram taken at a heating rate of 5° C./min. in a closed pan that exhibits a large endothermic transition below 75° C.
16. The crystalline form of naltrexone methobromide of claim 9 characterized by no loss of mass prior to sublimation above 75° C.
17. A pharmaceutical composition comprising a therapeutically-effective amount of the crystalline form of naltrexone methobromide Form II of claim 1 .
18. A pharmaceutical composition comprising a therapeutically-effective amount of the crystalline form of naltrexone methobromide Form III of claim 9 .