Crystalline salts of psilocin
Crystalline salts of psilocin are disclosed. The beneficial and therapeutic uses of the crystalline psilocin salts and of compositions containing the crystalline psilocin salts are also disclosed. The disclosure sets out methods of making and characterizing the crystalline psilocin salts.
1. A crystalline form of a salt or cocrystal of nicotinic acid and psilocin (4-hydroxy-N,N-dimethyltryptamine) having about a 1:1 stoichiometry, and exhibiting an X-ray powder diffraction pattern having at least three peaks at the following 2θ diffraction angles: 10.2, 11.4, 12.4, 14.0, 15.1, 15.6, 17.2, 17.5, 18.4, 19.2, 20.0, 22.4, 23.5, 24.1, 25.0, and 25.2 °2θ±0.2 °2θ.
2. The crystalline form of claim 1 , wherein the crystalline form exhibits an X-ray powder diffraction pattern having at least four peaks at the following 2θ diffraction angles: 10.2, 11.4, 12.4, 14.0, 15.1, 15.6, 17.2, 17.5, 18.4, 19.2, 20.0, 22.4, 23.5, 24.1, 25.0, and 25.2 °2θ±0.2 °2θ.
3. The crystalline form of claim 1 , wherein the crystalline form exhibits an X-ray powder diffraction pattern having at least five peaks at the following 2θ diffraction angles: 10.2, 11.4, 12.4, 14.0, 15.1, 15.6, 17.2, 17.5, 18.4, 19.2, 20.0, 22.4, 23.5, 24.1, 25.0, and 25.2 °2θ±0.2 °2θ.
4. The crystalline form of claim 1 , wherein the crystalline form has an X-ray powder diffraction pattern as shown in FIG. 6 .
5. The crystalline form of claim 1 , wherein the crystalline form comprises a crystal having unit cell parameters substantially equal to the following:
Crystal system
Triclinic
Space group
P1 (1) or P 1 (2)
Unit cell parameters
a = 9.343 Å
α = 76.04°
b = 9.595 Å
β = 71.26°
c = 11.079 Å
γ = 74.13°
Unit cell volume (Å 3 )
891.7.
6. The crystalline form of claim 1 , wherein the crystalline form further exhibits one or more of the following characteristics:
an endothermic event having peak maximum at about 189° C., measured by differential scanning calorimetry;
a thermogravimetric analysis thermogram as shown in FIG. 9 ; or
a solution 1 H NMR spectrum in d 6 -DMSO comprising one or more chemical shift peaks at about 2.9 ppm, 3.3 ppm, 3.5 ppm, 6.4 ppm, 6.8 ppm, 6.9 ppm, 7.0 ppm, 7.4 ppm, 8.3 ppm, 8.5 ppm, or 9.1 ppm.
7. The crystalline form of claim 6 , wherein the crystalline form has a differential scanning calorimetry thermogram as shown in FIG. 8 .
8. The crystalline form of claim 6 , wherein the crystalline form has a solution 1 H NMR spectrum in d 6 -DMSO comprising at least the characteristic chemical shift peaks at about 6.4 ppm and about 9.1 ppm.
9. The crystalline form of claim 6 , wherein the crystalline form has a solution 1 H NMR spectrum as shown in FIG. 10 .
10. A pharmaceutical composition comprising the crystalline form of claim 1 , and at least one pharmaceutically acceptable carrier.
11. The pharmaceutical composition of claim 10 , wherein the pharmaceutical composition is an oral formulation.
12. The pharmaceutical composition of claim 10 , wherein the pharmaceutical composition is in an oral solid dosage form.
13. A method for preparing the crystalline form of claim 1 , comprising:
reacting psilocin with nicotinic acid, to precipitate the salt or cocrystal of psilocin and nicotinic acid in a crystalline form.
14. The method of claim 13 , further comprising:
dissolving or suspending or grinding the psilocin and/or the acid in an organic solvent selected from the group consisting of an alcohol, ether, ketone, alkane, and a mixture thereof.
15. The method of claim 14 , wherein the organic solvent is diethyl ether, isopropyl alcohol, acetone, ethanol, methyl ethyl ketone, methyl tertiary-butyl ether, hexane, or a mixture thereof.
16. The method of claim 15 , wherein the organic solvent is isopropyl alcohol.
17. A method of treating a disease or disorder in a subject in need thereof, comprising:
administering to the subject in need thereof a therapeutically effective amount of the crystalline form of claim 1 ,
wherein the disease or disorder is a psychiatric of psychotic disorder, a neurocognitive disease or disorder, autism spectrum disorder (ASD), chronic pain, inflammatory disease or disorder, stroke, epilepsy disorder, amyotrophic lateral sclerosis (ALS), or combinations therefore.
18. The method of claim 17 , wherein the disease or disorder is a psychiatric or psychotic disorder selected from the group consisting of attention-deficit hyperactivity disorder (ADHD), anxiety disorder, sleep-wake disorder, impulse-control disorder, conduct disorder, depressive disorder, major depressive disorder (MDD), post-traumatic stress disorder (PTSD), obsessive-compulsive disorder, bipolar disorder, schizophrenia, and combinations thereof.
19. The method of claim 17 , wherein the disease or disorder is a neurocognitive disease or disorder selected from the group consisting of Alzheimer's disease, Lewy body dementia, traumatic brain injury, HIV infection, Parkinson's disease, Huntington's disease, and combinations thereof.