Carvedilol phosphate
The invention encompasses novel amorphous and crystalline forms of carvedilol phosphate, carvedilol hydrogen phosphate, and carvedilol dihydrogen phosphate as well as methods of making the novel amorphous and crystalline forms. Also disclosed are pharmaceutical compositions comprising the novel amorphous and crystalline forms and uses thereof.
1. A crystalline form of carvedilol dihydrogen phosphate characterized by data selected from the group consisting of:
(a) X-ray powder diffraction reflections at about: 7.6, 9.8, 10.9, 21.2 and 25.0 degrees two theta±0.2 degrees two theta;
(b) any five peaks selected from the following list of PXRD peaks at about: 7.6, 8.5, 9.8, 10.9, 12.0, 13.3, 15.2 and 16.9±0.2 degrees two theta;
(c) X-ray powder diffraction reflections at about: 7.6, 10.9, 13.3, 15.2 and 18.8 degrees two theta±0.2 degrees two theta;
d) X-ray powder diffraction reflections at about: 7.6, 8.5, 9.8, 15.2 and 16.9±0.2 degrees two theta;
(e) X-ray powder diffraction reflections at about: 7.6, 9.8, 10.9, 14.7, 15.2 and 22.8±0.2 degrees two theta;
(f) X-ray powder diffraction reflections at about: 7.6, 8.5, 9.8, 13.3 and 15.2±0.2 degrees two theta; and
(g) an X-ray powder diffraction pattern substantially as depicted in FIG. 26 or FIG. 27 .
2. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by X-ray powder diffraction reflections at about: 7.6, 9.8, 10.9, 21.2 and 25.0 degrees two theta±0.2 degrees two theta.
3. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by any five peaks selected from the following list of PXRD peaks at about: 7.6, 8.5, 9.8, 10.9, 12.0, 13.3, 15.2 and 16.9±0.2 degrees two theta.
4. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by X-ray powder diffraction reflections at about: 7.6, 10.9, 13.3, 15.2 and 18.8 degrees two theta±0.2 degrees two theta.
5. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by X-ray powder diffraction reflections at about: 7.6, 8.5, 9.8, 15.2 and 16.9±0.2 degrees two theta.
6. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by X-ray powder diffraction reflections at about: 7.6, 9.8, 10.9, 14.7, 15.2 and 22.8±0.2 degrees two theta.
7. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by X-ray powder diffraction reflections at about: 7.6, 8.5, 9.8, 13.3 and 15.2±0.2 degrees two theta.
8. The crystalline form carvedilol dihydrogen phosphate of claim 1 , further characterized by a solid-state 13 C-NMR spectrum having chemical shift resonances at about 155.3, 145.3 and 127.7±0.2 ppm.
9. The crystalline form carvedilol dihydrogen phosphate of claim 1 , further characterized by a solid-state 13 C NMR spectrum having chemical shift differences between the lowest ppm resonance in the chemical shift area of 100 to 180 ppm and another in the chemical shift area of 100 to 180 ppm of about 52.6, 42.6 and 25±0.1 ppm.
10. The crystalline form carvedilol dihydrogen phosphate of claim 1 characterized by an X-ray powder diffraction pattern substantially as depicted in FIG. 26 or FIG. 27 .
11. The crystalline form carvedilol dihydrogen phosphate of claim 1 , further characterized by a solid-state 13 C NMR spectrum substantially as depicted in FIG. 28 or 28 a.
12. The crystalline form carvedilol dihydrogen phosphate of claim 1 containing less than about 20% by weight of other crystalline forms of carvedilol and carvedilol phosphate salts.
13. The crystalline form carvedilol dihydrogen phosphate of claim 1 containing less than about 20% by weight of crystalline carvedilol dihydrogen phosphate Form I; wherein carvedilol dihydrogen phosphate Form I is characterized by X-ray powder diffraction reflections at about: 7.0, 8.0, 11.4 and 16.0 degrees two theta±0.2 degrees two theta.
14. The crystalline form carvedilol dihydrogen phosphate of claim 12 containing less than about 10% by weight of other crystalline forms of carvedilol and carvedilol phosphate salts.
15. The crystalline form carvedilol dihydrogen phosphate of claim 14 containing less than about 5% by weight of other crystalline forms of carvedilol and carvedilol phosphate salts.
16. The crystalline form carvedilol dihydrogen phosphate of claim 15 containing less than about 1% by weight of other crystalline forms of carvedilol and carvedilol phosphate salts.
17. The crystalline form carvedilol dihydrogen phosphate of claim 13 containing less than about 10% by weight of crystalline carvedilol dihydrogen phosphate Form I.
18. The crystalline form carvedilol dihydrogen phosphate of claim 17 containing less than about 5% by weight of crystalline carvedilol dihydrogen phosphate Form I.
19. The crystalline form carvedilol dihydrogen phosphate of claim 18 containing less than about 1% by weight of crystalline carvedilol dihydrogen phosphate Form I.