Crystalline and amorphous forms of naltrexone hydrochloride
View Patent ↗The present invention relates to novel crystalline forms of naltrexone hydrochloride including hydrated and solvated forms and a novel amorphous form. The invention also describes methods of preparing the various crystalline forms. The present invention also relates to pharmaceutical compositions containing crystalline and amorphous forms of naltrexone hydrochloride, as well as methods of treating addictive behavior by administering the pharmaceutical compositions.
1. A crystalline form of naltrexone hydrochloride hydrate selected from the group consisting of:
(a) Form II having an x-ray diffraction pattern having characteristic peaks expressed in degrees 2θ (±0.2°) at 8.0, 10.8, 11.7, 12.9, 15.9, 17.1, 18.5, 20.8, 23.5, and 26.4;
(b) Form VIII having an x-ray diffraction pattern having characteristic peaks expressed in degrees 2θ (±0.2°) at 11.4, 11.8, 13.1, 13.5, 15.9, 19.6, 22.6, 23.1, 24.5, and 25.8; and
(c) Form XI having an x-ray diffraction pattern having characteristic peaks expressed in degrees 2θ (±0.2°) at 8.3, 11.5, 11.9, 16.5, 17.2, 21.9, 23.8, and 27.3.
2. The crystalline form of naltrexone hydrochloride of claim 1 (a), having a powder x-ray diffraction pattern substantially as shown in FIG. 2 ; wherein the crystalline form comprises bound water.
3. The crystalline form of naltrexone hydrochloride of claim 1 (b), having a powder x-ray diffraction pattern substantially as shown in FIG. 8 ; wherein the crystalline form comprises bound water.
4. The crystalline form of naltrexone hydrochloride of claim 1 (c), having a powder x-ray diffraction pattern substantially as shown in FIG. 12 ; wherein the crystalline form comprises bound water.
5. A pharmaceutical composition comprising a therapeutically-effective amount of one or more of the naltrexone hydrochloride forms chosen from claim 1 and one or more pharmaceutically acceptable carriers, excipients or diluents thereof.
6. A method of treating alcohol dependence in a patient suffering therefrom, comprising the step of administering to said patient a therapeutically-effective amount of one or more of the naltrexone hydrochloride forms chosen from claim 1 .
7. A method of making a crystalline form of naltrexone hydrochloride comprising: (i) adding an amount of naltrexone hydrochloride to a solvent system selected from the group consisting of methanol, isopropanol, ethanol, water, n-butanol, acetone, glacial acetic acid, ethyl acetate, methylene chloride, chloroform, acetonitrile, THF, hexane, toluene, DMSO, ethyl ether, and mixtures thereof, to create a nearly saturated solution; and (ii) evaporating the solvent system from the solution for an amount of time sufficient to induce crystallization of at least one crystalline form of naltrexone hydrochloride, wherein the crystalline form of naltrexone hydrochloride is selected from the forms set forth in claim 1 .
8. A method of making a crystalline form of naltrexone hydrochloride comprising: (i) dissolving naltrexone hydrochloride in a first solvent system in a first container, wherein the first solvent system is selected from the group consisting of methanol and ethanol; (ii) adding a second solvent system to a second container, wherein the second solvent system is selected from the group consisting of ethyl acetate, hexane, chloroform, and ethyl ether, and wherein the second container is configured to receive the first container; and (iii) placing the first container in the second container for an amount of time sufficient to induce crystallization of at least one crystalline form of naltrexone hydrochloride, wherein the crystalline form of naltrexone hydrochloride is selected from the forms set forth in claim 1 .
9. A method of converting a first crystalline form of naltrexone hydrochloride to a second crystalline form of naltrexone hydrochloride comprising: (i) adding an amount of the first crystalline form of naltrexone hydrochloride to a solvent system selected from the group consisting of methanol, isopropanol, ethanol, water, n-butanol, acetone, glacial acetic acid, ethyl acetate, methylene chloride, chloroform, acetonitrile, THE, hexane, toluene, DMSO, ethyl ether, and mixtures thereof to form a saturated solution; (ii) adding an additional amount of the first crystalline form of naltrexone hydrochloride to form a slurry; (iii) stirring the slurry for an amount of time sufficient to convert the first crystalline form of naltrexone hydrochloride to the second crystalline form of naltrexone hydrochloride; and (iv) filtering the solvent system from the slurry, wherein the second crystalline form of naltrexone hydrochloride is selected from the forms set forth in claim 1 .
10. A method of making a crystalline form of naltrexone hydrochloride comprising: (I) forming a mixture comprising naltrexone hydrochloride and a solvent system selected from the group consisting of methanol, isopropanol, ethanol, water, n-butanol, acetone, glacial acetic acid, ethyl acetate, methylene chloride, chloroform, acetonitrile, THE, hexane, toluene, DMSO, ethyl ether, and mixtures thereof; (ii) heating the mixture; (iii) adding an amount of hydrochloric acid to the heated mixture; and (iv) cooling the resulting solution to induce crystallization of at least one crystalline form of naltrexone hydrochloride, wherein the crystalline form of naltrexone hydrochloride is selected from the forms set forth in claim 1 .