Cyanocobalamin low viscosity aqueous formulations for intranasal delivery
View Patent ↗A stable pharmaceutical mercury-free aqueous solution of cyanocobalamin comprised of cyanocobalamin and water wherein said solution of cyanocobalamin is suitable for intranasal administration, has a viscosity less than about 1000 cPs, and wherein said solution of cyanocobalamin has a bioavailability of cyanocobalamin when administered intranasally of at least about 7% relative to an intramuscular injection of cyanocobalamin with the proviso that the solution is essentially free of mercury and mercury-containing compounds. The present invention is also directed towards a method for elevating the vitamin B12 levels in the cerebral spinal fluid (CSF) comprising administering intranasally a sufficient amount of a mercury-free cyanocobalamin solution so as to increase the average ratio of vitamin B12 in the CSF to that in the blood serum (B12 CSF/B12 Serum×100) to at least about 1.1 comprising intranasally administering an aqueous solution of a cyanocobalamin, wherein said solution of cyanocobalamin has a bioavailability of at least 7% relative to an intramuscular injection of a cyanocobalamin.
1. A method of administering cyanocobalamin, comprising infusing the nose of a subject in need thereof with an aqueous solution comprising a pharmaceutically effective amount of cyanocobalamin at a concentration of about 0.5% of total weight of solution, wherein the solution has a viscosity of less than 1000 cPs, and wherein the solution has a bioavailability of about 7% or more relative to the bioavailability of an intramuscular injection containing cyanocobalamin at a concentration of 0.1% of the total weight based on a same volume as the solution.
2. The method of claim 1 wherein the solution has a bioavailability of about 9% or more relative to the bioavailability of the intramuscular injection of cyanocobalamin.
3. The method of claim 1 wherein the solution has a bioavailability of about 10% or more relative to the bioavailability of the intramuscular injection of cyanocobalamin.
4. The method of claim 1 wherein the solution has a bioavailability of about 11% or more relative to the bioavailability of the intramuscular injection of cyanocobalamin.
5. The method of claim 1 wherein the solution has a bioavailability of about 12% or more relative to the bioavailability of the intramuscular injection of cyanocobalamin.
6. The method of claim 1 , wherein the solution comprises cyanocobalamin, water, and one or more components selected from the group consisting of: a buffer, a preservative, and a humectant.
7. The method of claim 6 , wherein the buffer is selected from the group consisting of: citric acid, sodium citrate, monopotassium phosphate, disodium phosphate, potassium biphthalate, sodium hydroxide, sodium acetate, acetic acid, and combinations thereof.
8. The method of claim 6 , wherein the preservative is selected from the group consisting of: benzyl alcohol, parabens thimerosal, chlorobutanol, benzethonium chloride, and benzalkonium chloride.
9. The method of claim 6 , wherein the humectant is selected from the group consisting of: sorbitol, propylene glycol, and glycerin.
10. A method of administering cyanocobalamin, comprising infusing the nose of a subject in need thereof with an aqueous solution comprising: a pharmaceutically effective amount of cyanocobalamin at a concentration of about 0.5% of total weight of solution, citric acid, sodium citrate, benzaikonium chloride, and glycerin, wherein the solution has a viscosity of less than 1000 cPs, and wherein the solution has a bioavailability of about 7% or more relative to the bioavailability of an intramuscular injection containing cyanocobalamin at a concentration of 0.1% of the total weight based on a same volume as the solution.
11. The method of claim 1 wherein the solution has a bioavailability of about 8% or more relative to the bioavailability of the intramuscular injection of cyanocobalamin.