Transnasal anticonvulsive pharmaceutical composition comprising poorly soluble anticonvulsant
There is provided a transnasal anticonvulsive pharmaceutical composition including a poorly soluble anticonvulsant. The anticonvulsive pharmaceutical composition comprising a poorly soluble anticonvulsant as an active component, which is transnasally spray-administered, comprises diethylene glycol monoethyl ether and fatty acid ester, wherein the fatty acid ester is selected from the group consisting of caprylocaproyl polyoxylglyceride, isopropyl palmitate, oleoyl polyoxylglyceride, sorbitan monolaurate 20, methyl laurate, ethyl laurate, and polysorbate 20. Also, the anticonvulsive pharmaceutical composition comprising a poorly soluble anticonvulsant as an active component, which is transnasally spray-administered, comprises diethylene glycol monoethyl ether, fatty acid ester, methylpyrrolidone, water and alcohol. Therefore, the transnasal anticonvulsive pharmaceutical composition may be useful to highly enhance the bioavailability of the poorly soluble anticonvulsant. Also, the transnasal anticonvulsive pharmaceutical composition may be useful to allow the poorly soluble anticonvulsant to show the improved viscosity and/or enhanced solubility in order to effectively deliver the poorly soluble anticonvulsant at a therapeutic dose.
1. An anticonvulsive pharmaceutical composition for transnasal administration, consisting essentially of:
about 1% to about 20% by weight of a poorly soluble anticonvulsant,
about 40% to about 60% by weight of diethylene glycol monoethyl ether,
about 5% to about 30% by weight of methylpyrrolidone,
about 1% to about 5% by weight of water,
about 5% to about 10% by weight of alcohol, and
fatty acid ester which is methyl laurate at about 5% to about 15% by weight of the pharmaceutical composition and/or propylene glycol monocaprylate at about 5% to about 25% by weight of the pharmaceutical composition.
2. The anticonvulsive pharmaceutical composition of claim 1 , wherein the poorly soluble anticonvulsant is diazepam or lorazepam.
3. The anticonvulsive pharmaceutical composition of claim 1 , wherein the poorly soluble anticonvulsant is diazepam.
4. The anticonvulsive pharmaceutical composition of claim 1 , wherein the alcohol is ethanol.
5. The anticonvulsive pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has a kinematic viscosity of 10 mm 2 /sec or less for transnasal spray-administration.
6. The anticonvulsive pharmaceutical composition of claim 1 , wherein the fatty acid ester is methyl laurate at about 5% to about 15% by weight of the pharmaceutical composition and propylene glycol monocaprylate at about 5% to about 25% by weight of the pharmaceutical composition.
7. A method for treating a convulsion in a subject, comprising:
transnasally administering to the subject in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 1 .
8. The method of claim 7 , wherein the transnasally administering comprises transnasally spraying the pharmaceutical composition.
9. The anticonvulsive pharmaceutical composition of claim 1 , wherein the poorly soluble anticonvulsant is diazepam at about 5% to about 15% by weight.
10. An anticonvulsive pharmaceutical composition for transnasal administration, consisting essentially of:
about 1% to about 20% by weight of diazepam,
about 40% to about 60% by weight of diethylene glycol monoethyl ether,
about 5% to about 30% by weight of methylpyrrolidone,
about 1% to about 5% by weight of water,
about 5% to about 10% by weight of ethanol,
about 5% to about 15% by weight of methyl laurate, and
about 5% to about 25% by weight of propylene glycol monocaprylate.
11. A method for treating a convulsion in a subject, comprising:
transnasally administering to the subject in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 10 .
12. The method of claim 11 , wherein the transnasally administering comprises transnasally spraying the pharmaceutical composition.
13. An anticonvulsive pharmaceutical composition for transnasal administration, consisting essentially of:
about 5% to about 15% by weight of diazepam,
about 40% to about 60% by weight of diethylene glycol monoethyl ether,
about 5% to about 30% by weight of methylpyrrolidone,
about 1% to about 5% by weight of water,
about 5% to about 10% by weight of ethanol,
about 5% to about 15% by weight of methyl laurate, and
about 5% to about 25% by weight of propylene glycol monocaprylate.
14. A method for treating a convulsion in a subject, comprising:
transnasally administering to the subject in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 13 .
15. The method of claim 14 , wherein the transnasally administering comprises transnasally spraying the pharmaceutical composition.