Magnesium-containing oxytocin formulations and methods of use
Disclosed are methods and compositions for the treatment of autism spectrum disorder, related disorders and symptoms of such disorders, comprising co-administration of an oxytocin peptide and magnesium ions. Co-administration of an oxytocin peptide and magnesium ions results in a synergistic or enhanced effect on reducing social and communication deficits in a patient suffering from an autism spectrum disorder.
1. A method for treating a disorder selected from an autism spectrum disorder, a social anxiety disorder, or a social communication disorder, comprising administering to a subject in need thereof an oxytocin peptide and a magnesium salt formulated in an aqueous solution for intranasal administration, wherein the aqueous solution comprises about 8 μg to about 1000 μg of the oxytocin peptide, wherein the magnesium salt is capable of providing between 0.11% to 1.65% (w/v) of magnesium ions, and wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio selected from the group consisting of: about 1:1000, about 1:1100, about 1:1200, about 1:1400, and about 1:1600.
2. The method of claim 1 , wherein the magnesium salt is one or both of magnesium chloride and magnesium citrate.
3. The method of claim 1 , wherein the aqueous solution comprises about 8 μg to about 80 μg of the oxytocin peptide.
4. The method of claim 1 , wherein the disorder is an autism spectrum disorder.
5. The method of claim 1 , wherein the subject in need thereof manifests one or more symptoms associated with an autism spectrum disorder.
6. The method of claim 1 , wherein the disorder is social and communication deficits.
7. The method of claim 1 , wherein the disorder is an anxiety.
8. The method of claim 1 , wherein the oxytocin peptide is human oxytocin SEQ ID NO: 1.
9. A method for treating a disorder selected from an autism spectrum disorder, a social anxiety disorder, or a social communication disorder, comprising administering to a subject in need thereof an oxytocin peptide and a magnesium salt formulated in an aqueous solution for intranasal administration, wherein the aqueous solution comprises about 8 μg to about 1000 μg of the oxytocin peptide, wherein the magnesium salt is capable of providing 0.11% to 1.65% (w/v) of magnesium ions, wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio selected from the group consisting of the ratios: about 1:1000, about 1:1100, about 1:1200, about 1:1400, and about 1:1600, and wherein the volume of the aqueous solution administered is between about 5 μL and about 1000 μL.
10. The method of claim 9 , wherein the aqueous solution comprises about 8 μg to about 80 μg of the oxytocin peptide.
11. The method of claim 9 , wherein the aqueous solution is administered in a volume between about 50 μL and about 200 μL.
12. The method of claim 11 , wherein the aqueous solution is administered using a metered nasal device in 1 to 4 units of about 50 μL per unit.
13. The method of claim 11 , wherein the aqueous solution is administered using a metered nasal device in 1 to 2 units of about 100 μL per unit.
14. The method of claim 9 , wherein the disorder is an autism spectrum disorder.
15. The method of claim 9 , wherein the subject in need thereof manifests one or more symptoms associated with an autism spectrum disorder.
16. The method of claim 9 , wherein the disorder is social and communication deficits.
17. The method of claim 9 , wherein the disorder is an anxiety.
18. The method of claim 9 , wherein the oxytocin peptide is human oxytocin SEQ ID NO:1.
19. The method of claim 9 , wherein the aqueous solution is contained in a device for intranasal administration.
20. The method of claim 19 , wherein the device for intranasal administration is a nasal pump apparatus.
21. The method of claim 20 , wherein the nasal pump apparatus comprises a reservoir bottle attached to a pump actuator.
22. The method of claim 21 , wherein the pump actuator is metered to deliver a volume of about 50 μL.
23. The method of claim 20 , wherein the nasal pump apparatus comprises a reservoir bottle attached to an aerosolizer.
24. The method of any one of claims 20 to 23 , wherein the nasal pump apparatus comprises one or more of the following:
(i) a filter for preventing back flow,
(ii) a metal-Tree fluid path, and
(iii) a plastic material stable to gamma-radiation.
25. The method of claim 9 , wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio of about 1:1000.
26. The method of claim 9 , wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio of about 1:1100.
27. The method of claim 9 , wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio of about 1:1200.
28. The method of claim 9 , wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio of about 1:1400.
29. The method of claim 9 , wherein the aqueous solution has an oxytocin peptide to magnesium ions molar ratio of about 1:1600.