Claims for Patent: 6,413,549

Summary for Patent: 6,413,549

Title:	Fast-Dispersing solid oral dosage form containing coarse particles
Abstract:	This invention is directed to an oral solid, rapidly disintegrating, freeze-dried dosage form containing coarse particles of a pharmaceutically active material which are uncoated or coated with a polymer or lipid material. Preferably, the oral dosage form comprises coarse particles having a size in the range of 50 micron to 400 micron. The oral solid rapidly disintegrating dosage form according to the present invention preferably disintegrates in the oral cavity in less than 10 seconds.
Inventor(s):	Green; Richard (Wiltshire, GB), Kearney; Patrick (Swindon, GB)
Assignee:	R. P. Scherer Corporation (Basking Ridge, NJ)
Application Number:	09/335,177
Patent Claims:	1. A freeze-dried oral solid rapidly disintegrating dosage form comprising coarse particles consisting of a pharmaceutically active material, said coarse particles having a size within the range of 50 .mu.m to 400 .mu.m, which are coated with a polymer or lipid material in a matrix comprising a carrier material and a structure forming agent, wherein said carrier material is selected from the group consisting of water soluble and water-dispersible carrier materials, wherein said dosage form disintegrates in water in less than 10 seconds. 2. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 1, wherein said carrier material is gelatin and said structure-forming agent is a polyhydric alcohol. 3. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 2, wherein said polyhydric alcohol is selected from mannitol and sorbitol. 4. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 1, wherein said coarse particles are coated with a coating which delays release of the pharmaceutically active substance beyond the point of disintegration of said form on the tongue. 5. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 4, wherein said coating is selected from the group consisting of a polymeric materials and a lipid material. 6. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 5, wherein said polymeric material is selected from the group consisting of cellulose, a cellulose derivative, an acrylic derivative, polyglycolic-polylactic acid, polyvinyl alcohol, gelatin, collagen and polyethylene glycol. 7. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 6, wherein said cellulose derivative is selected from the group consisting of ethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, hydroxypropylcellulose, methylcellulose, cellulose acetate, cellulose acetate phthalate and hydroxypropylmethylcellulosephthalate, and said acrylic derivative is a polymethacrylate. 8. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 5, wherein said coating is selected from the group consisting of a wax, lanolin, stearic acid, a stearic acid derivative, a phospholipid and a glycolipid. 9. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 8, wherein stearic acid derivative is selected from the group consisting of a glycerol ester, a fixed oil and a fat. 10. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 1, wherein said structure-forming agent is present in the amount of 1 to 5% by weight. 11. A freeze-dried oral solid rapidly disintegrating dosage form according to claim 1, wherein said coarse particles have a size in the range of 100 .mu.m to 400 .mu.m. 12. A freeze-dried oral solid rapidly disintegrating dosage form comprising coarse particles consisting of a pharmaceutically active material which are coated with a polymer or lipid material in a matrix comprising a carrier material and a structure forming agent, wherein said carrier material is selected from the group consisting of water soluble and water-dispersible carrier materials, wherein said coarse particles have a size of at least 100 .mu.m.