Emulsion
The invention relates to an orally administrable chewable composition in unit dosage form comprising an oil-in-water emulsion in which the aqueous phase is gelled and in which the oil phase comprises a physiologically tolerable unsaturated fatty acid ester.
1. An orally administrable chewable composition in unit dosage form comprising a chewable, set oil-in-water emulsion in which the aqueous phase is gelled and constitutes about 50% to 60% wt. of the unit dosage form, wherein said aqueous phase comprises gelatin in an amount of about 10% to 25% wt. of the aqueous phase and wherein the oil phase comprises a physiologically tolerable omega-3 or omega-6 fatty acid ester and constitutes about 40% of the dose unit, and wherein the unit dosage form has an overall dose unit weight of 0.25 to 3 g, and wherein the composition, upon chewing, remains free of bad odor and taste.
2. The composition as claimed in claim 1 , wherein the omega-3 or omega-6 fatty acid ester is a physiologically tolerable triglyceride.
3. The composition as claimed in claim 1 , wherein the omega-3 or omega-6 fatty acid ester is a fish oil.
4. The composition as claimed in claim 1 , wherein said aqueous phase further comprises polysaccharides.
5. The composition as claimed in claim 1 , wherein said aqueous phase further comprises carageenan.
6. The composition as claimed in claim 1 , further comprising at least 1% wt. xylitol.
7. The composition as claimed in claim 1 , further comprising a citrus flavor.
8. The composition as claimed in claim 1 , wherein said aqueous phase further comprises a water soluble vitamin.
9. The composition as claimed in claim 1 in animal, doll, vehicle, rod, strip or tube shape.
10. A package comprising an air-tight compartment containing one dose unit of a composition as claimed in claim 1 .
11. The package as claimed in claim 10 in the form of a blister pack.
12. A method of treatment of a human by oral administration of an effective amount of an active agent in oil form or dissolved in an oil comprising administering said active agent in a chewable composition according to claim 1 .
13. The method as claimed in claim 12 , wherein said active agent is an analgesic.
14. The method as claimed in claim 12 , wherein said active agent is a triglyceride.