Methods of preventing the serotonin syndrome and compositions for use thereof
The present invention is directed at methods for preventing or minimizing the intensity of the serotonin syndrome in humans and lower animals which comprises administering proserotonergic agents and serotonin surge protectors. The present invention is also directed to pharmaceutical compositions comprising proserotonergic agents and serotonin surge protectors useful for carrying out the method of the present invention.
1. A method of reducing the intensity of the serotonin syndrome in a human to whom levorphanol is being administered, the method comprising orally administering to the human a pharmaceutical composition comprising a blend of
a) an effective amount of levorphanol and
b) a serotonin surge protector (SSP) selected from the group consisting of:
i) hydrogenated vegetable oils;
ii) coconut oil products;
iii) polyoxyethylene stearates;
iv) polyoxyethylene distearates;
v) glycerol monostearate; and
vi) waxes that are poorly soluble in water and that have a melting point in the range from 40 to 100 degrees Celsius;
the SSP being present in an amount sufficient to extend release of the levorphanol, relative to the same composition lacking the SSP,
wherein the blend has a melting point greater than 20 degrees Celsius.
2. The method of claim 1 , wherein the blend comprises at least two of i)-vi).
3. The method of claim 1 , wherein the blend comprises at least three of i)-vi).
4. The method of claim 1 , wherein the blend further comprises
c) a thixotrope in an amount sufficient to increase the viscosity of the blend when it is combined with a solvent.
5. The method of claim 4 , wherein the thixotrope is selected from the group comprising silicon dioxide or a mixture of silicon dioxide and aluminum oxide.
6. The method of claim 4 , wherein the blend further comprises
d) a release rate modifier in an amount effective to modify the rate of release of levorphanol from the composition following administration of the composition to the human.
7. The method of claim 1 , wherein the blend further comprises a release rate modifier in an amount effective to modify the rate of release of levorphanol from the composition following administration of the composition to the human.
8. The method of claim 7 , wherein an aqueous solution of the release rate modifier exhibits a greater viscosity at 40 degrees Celsius than at approximately 20 degrees Celsius.
9. The method of claim 8 , wherein the release rate modifier is soluble in water at approximately 20 degrees Celsius, but is substantially insoluble in water at 40 degrees Celsius.
10. The method of claim 7 , wherein the release rate modifier is a hydroxypropyl methyl cellulose.
11. The method of claim 1 , wherein the blend comprises a hydrogenated vegetable oil selected from the group consisting of hydrogenated cottonseed oil, hydrogenated palm oil, hydrogenated palm kernel oil, hydrogenated soybean oil, and combinations of these.
12. The method of claim 1 , wherein the blend comprises a coconut oil product selected from the group consisting of coconut oil, fractionated coconut oil, cetyl alcohol, lauric acid and medium chain triglycerides, and combinations of these.
13. The method of claim 12 , wherein the coconut oil product is fractionated coconut oil.
14. The method of claim 1 , wherein the blend comprises at least one of
i) a polyoxyethylene stearate selected from the group consisting of polyoxyl 2, 4, 6, 8, 12, 20, 30, 40, 50, 100 and 150 stearates and combinations of these and
ii) a polyoxyethylene distearate selected from the group consisting of polyoxyl 4, 8, 12, 32 and 150 distearates and combinations of these.
15. The method of claim 1 , wherein the blend comprises a wax selected from the group consisting of glyceryl behenate, glyceryl palmitostearate, glyceryl monostearate, stearoyl macrogolglycerides, lauroyl macrogolglycerides, carnauba waxes, petroleum waxes, cetyl ester waxes, hydrogenated castor oils, lanolin alcohols, cetostearyl alcohols, beeswaxes, and combinations of these.
16. A method of reducing the incidence of the serotonin syndrome in a human to whom levorphanol is being administered, the method comprising orally administering to the human a pharmaceutical composition comprising a blend of
a) an effective amount of levorphanol and
b) a serotonin surge protector (SSP) selected from the group consisting of:
i) hydrogenated vegetable oils;
ii) coconut oil products;
iii) polyoxyethylene stearates;
iv) polyoxyethylene distearates;
v) glycerol monostearate; and
vi) waxes that are poorly soluble in water and that have a melting point in the range from 40 to 100 degrees Celsius;
the SSP being present in an amount sufficient to extend release of levorphanol, relative to the same composition lacking the SSP,
wherein the blend has a melting point greater than 20 degrees Ceisius,
whereby incidence of the serotonin syndrome in the human is decreased, relative to incidence of the serotonin syndrome in the same human being administered levorphanol alone.
17. The method of claim 16 , wherein the blend comprises a pharmaceutically acceptable salt of levorphanol.
18. The method of claim 16 , wherein the blend comprises levorphanol tartrate.
19. The method of claim 1 , wherein the blend comprises a pharmaceutically acceptable salt of levorphanol.
20. The method of claim 1 , wherein the blend comprises levorphanol tartrate.