Crystals and process of making 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid
The present invention relates to a novel crystals of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid and methods of making the zwitterion of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.
1. A pharmaceutical composition comprising a Form α crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid, wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 10.2±0.3, 11.3±0.3, 11.8±0.3, 14.0±0.3, 14.3±0.3, 14.7±0.3, 16.1±0.3, and 18.3±0.3 degrees 2-theta.
2. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 10.2±0.25, 11.3±0.25, 11.8±0.25, 14.0±0.25, 14.3±0.25, 14.7±0.25, 16.1±0.25, and 18.3±0.25 degrees 2-theta.
3. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 10.2±0.2, 11.3±0.2, 11.8±0.2, 14.0±0.2, 14.3±0.2, 14.7±0.2, 16.1±0.2, and 18.3±0.2 degrees 2-theta.
4. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 14.0±0.2, 14.3±0.2, 14.7±0.2 degrees 2-theta.
5. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2±0.2, 11.3±0.2, 14.0±0.2, 14.3±0.2, and 14.7±0.2 degrees 2-theta.
6. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2±0.2, 11.3±0.2, 11.8±0.2, 14.0±0.2, 14.3±0.2, 14.7±0.2, 16.1±0.2, and 18.3±0.2 degrees 2-theta.
7. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 1.
8. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .
9. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 2 .
10. The pharmaceutical composition of claim 1 , wherein the Form α crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 3 .
11. The pharmaceutical composition of claim 1 , in a dosage form suitable for oral administration.
12. The pharmaceutical composition of claim 11 , wherein the dosage form is a solid.
13. The pharmaceutical composition of claim 11 , wherein the dosage form is selected from the group consisting of a tablet, a caplet, a hard gelatin capsule, a starch capsule, a hydroxypropyl methylcellulose (HPMC) capsule, and a soft elastic gelatin capsule.
14. The pharmaceutical composition of claim 11 , wherein the dosage form as administered is a liquid.
15. The pharmaceutical composition of claim 11 , wherein the dosage form as administered is selected from the group consisting of a suspension, a solution, a syrup, and an emulsion.
16. The pharmaceutical composition of claim 11 , wherein the dosage form is a tablet.
17. A method of treating an opioid receptor disorder in a mammal comprising administering to the mammal an effective amount of the pharmaceutical composition of claim 1 .
18. The method of claim 17 , wherein the opioid receptor disorder is selected from the group consisting of irritable bowel syndrome, pain and a combination of both.
19. The method of claim 17 , wherein the opioid receptor disorder is irritable bowel syndrome.
20. The method of claim 17 , wherein the opioid receptor disorder is pain.
21. A pharmaceutical composition comprising a Form β crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid, wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 11.0±0.3, 12.4±0.3, 14.9±0.3, 15.2±0.3, 22.1±0.3, 25.6±0.3, 27.4±0.3, and 30.4±0.3 degrees 2-theta.
22. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 11.0±0.25, 12.4±0.25, 14.9±0.25, 15.2±0.25, 22.1±0.25, 25.6±0.25, 27.4±0.25, and 30.4±0.25 degrees 2-theta.
23. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having any three or more powder X-ray diffraction peaks selected from the group consisting of powder X-ray diffraction peaks at about 11.0±0.2, 12.4±0.2, 14.9±0.2, 15.2±0.2, 22.1±0.2, 25.6±0.2, 27.4±0.2, and 30.4±0.2 degrees 2-theta.
24. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0±0.2, 12.4±0.2, and 15.2±0.2 degrees 2-theta.
25. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0±0.2, 12.4±0.2, 14.9±0.2, 15.2±0.2, and 22.1±0.2, degrees 2-theta.
26. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0±0.2, 12.4±0.2, 14.9±0.2, 15.2±0.2, 22.1±0.2, 25.6±0.2, 27.4±0.2, and 30.4±0.2 degrees 2-theta.
27. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 2.
28. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .
29. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 4 .
30. The pharmaceutical composition of claim 21 , wherein the Form β crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 5 .
31. The pharmaceutical composition of claim 21 , in a dosage form suitable for oral administration.
32. The pharmaceutical composition of claim 31 , wherein the dosage form is a solid.
33. The pharmaceutical composition of claim 31 , wherein the dosage form is selected from the group consisting of a tablet, a caplet, a hard gelatin capsule, a starch capsule, a hydroxypropyl methylcellulose (HPMC) capsule, and a soft elastic gelatin capsule.
34. The pharmaceutical composition of claim 31 , wherein the dosage form as administered is a liquid.
35. The pharmaceutical composition of claim 31 , wherein the dosage form as administered is selected from the group consisting of a suspension, a solution, a syrup, and an emulsion.
36. The pharmaceutical composition of claim 31 , wherein the dosage form is a tablet.
37. A method of treating an opioid receptor disorder in a mammal comprising administering to the mammal an effective amount of the pharmaceutical composition of claim 21 .
38. The method of claim 37 , wherein the opioid receptor disorder is selected from the group consisting of irritable bowel syndrome, pain and a combination of both.
39. The method of claim 37 , wherein the opioid receptor disorder is irritable bowel syndrome.
40. The method of claim 37 , wherein the opioid receptor disorder is pain.