Co-solvent compositions and methods for improved delivery of dantrolene therapeutic agents
The present invention provides for methods of using tert-butyl alcohol (TBA) co-solvent systems in the formulation and production of a pharmaceutical agent with low solubility. The present invention also provides for pharmaceutical compositions made using the novel co-solvent system. In one embodiment, the invention provides for a method of making dantrolene sodium (DS) formulation for intravenous use (DS-IV). This instantaneous reconstitution of the DS-IV product constitutes a significant improvement in the pharmacotherapy of patients undergoing malignant hyperthermia during surgery.
1. A stable and lyophilized formulation of an active pharmaceutical compound made by the process comprising a) dissolving the active pharmaceutical compound in an alkaline solution of water and organic co-solvent solution comprising between about 1% to about 99% (v/v) organic co-solvent to form a pre-lyophilization solution; and b) lyophilizing the pre-lyophilization solution to form a powder; where the co-solvent is selected from the group consisting of one or more of tertiary butanol, n-propanol, n-butanol, isopropanol, ethanol, and methanol; where the active pharmaceutical compound has the formula:
wherein
A has the formula
in which R is from one to two substitutes selected from the group consisting of nitro, cyano, amino, chloro, bromo, acetyl, carboxy, methyl, trifluoromethyl, and hydrogen;
X is a member of the group consisting of carbonyl and methylene; and
Y is a member of the group consisting of hydroxyethyl, butyl, hydrogen, and r-pyridylethyl;
wherein step b) comprises:
i) freezing the pre-lyophilization solution to a temperature below about −40° C. to form a frozen solution;
ii) holding the frozen solution at or below −40° C. for at least 2 hours;
iii) ramping the frozen solution to a primary drying temperature between about −40° C. and about 20° C. to form a dried cake;
iv) holding for about 30 to about 70 hours;
v) ramping the dried cake to a secondary drying temperature between about 25° C. and about 40° C.; and
vii) holding for about 5 to about 40 hours to form the stable and lyophilized formulation.
2. The stable and lyophilized formulation of claim 1 , wherein the active pharmaceutical compound is selected from the group consisting of:
1-[5-(p-nitrophenyl)furfurylideneamino]hydantoin,
1-[5-(p-aminophenyl)furfurylideneamino]hydantoin,
1-[5-(m-chlorophenyl)furfurylideneamino]hydantoin,
1-[5-(p-chlorophenyl)furfurylideneamino]hydantoin,
1-[5-(2,4-dichlorophenyl)furfurylideneamino]hydantoin,
1-[5-(2-methyl-4-nitrophenyl)furfurylideneamino]hydantoin,
1-[5-(p-nitrophenyl)furfurylideneaminio]-2-imidazolidinone, and
1-[5-(p-cyanophenyl)furfurylideneamino]hydantoin.
3. The stable and lyophilized formulation of claim 1 , wherein the active pharmaceutical compound is dantrolene sodium.
4. The stable and lyophilized formulation of claim 3 wherein the residual concentration of organic co-solvent is less than about 0.5%.
5. The stable and lyophilized formulation of claim 3 wherein the concentration of dantrolene sodium degradants in the final lyophilized product is less than about 8%.
6. The stable and lyophilized formulation of claim 3 , wherein the formulation is packaged in a vial or other pharmaceutically acceptable container.
7. An injectable formulation of dantrolene sodium formed by reconstituting the lyophilized dantrolene sodium powder of claim 3 with a diluent suitable for intravenous administration.
8. The injectable formulation of claim 7 , wherein the injectable formulation comprises about 10 mg to about 30 mg of lyophilized dantrolene sodium powder.
9. The injectable formulation of claim 7 , wherein the injectable formulation comprises about 15 mg to about 25 mg of lyophilized dantrolene sodium powder.
10. The stable and lyophilized formulation of claim 3 , wherein the organic co-solvent is tertiary butanol.
11. The stable and lyophilized formulation of claim 3 , made by a process further comprising the step of adding an excipient and a pH adjusting agent before lyophilization.
12. The stable and lyophilized formulation of claim 11 , wherein the excipient comprises mannitol and the pH adjusting agent comprises sodium hydroxide.
13. The stable and lyophilized formulation of claim 12 , wherein the pre-lyophilization solution comprises dantrolene sodium at a concentration of about 0.1 to about 5 mg/mL, mannitol at a concentration of about 2 to about 100 mg/mL, tertiary butanol at a concentration of about 1 to about 99% (v/v) and an amount of sodium hydroxide adequate to adjust the pH to a range of from about 9.5 to about 10.5.
14. The stable and lyophilized formulation of claim 12 , wherein the pre-lyophilization solution comprises tertiary butanol at a concentration of about 1% to 30%.
15. The stable and lyophilized formulation of claim 3 , wherein the formulation is about 96% by weight or greater dantrolene sodium.
16. The stable and lyophilized formulation of claim 3 , wherein the formulation can be reconstituted in about 20 seconds or less.
17. The stable and lyophilized formulation of claim 1 , wherein step b) results in a freeze-drying cycle of about 54 hours or less.
18. The stable and lyophilized formulation of claim 3 , wherein the vial or other pharmaceutically acceptable container contains about 10 to about 500 mg of dantrolene sodium per vial or container.
19. The injectable formulation of claim 7 , wherein the injectable formulation is useful for the treatment of malignant hyperthermia.