Orally disintegrating tablets and methods of manufacture
View Patent ↗A tablet that rapidly disintegrates in the oral cavity comprising a compressed blend of rapidly dispersing microgranules prepared by granulating a sugar alcohol or a saccharide or a mixture thereof having an average particle size less than about 30 microns and a disintegrant, and a taste-masked microcapsule containing at least one drug, the microcapsule being prepared by granulating a pharmaceutically acceptable formulation comprising at least one drug in a therapeutically effective amount and at least one polymeric binder that improves resilience of the microgranules, wet milling the granulated mass, and microencapsulating the milled granules to provide microcapsules.
1. A tablet that rapidly disintegrates in the oral cavity comprising a compressed blend of:
rapidly dispersing microgranules comprising a sugar alcohol or a saccharide or a mixture thereof having an average particle size not more than about 30 microns, and a disintegrant, and
taste-masked microcapsules containing at least one drug, prepared by granulating a pharmaceutically acceptable formulation comprising the at least one drug in a therapeutically effective amount and at least one polymeric binder imparting resilient characteristics to the resulting microcapsules, wet milling the granulated mass, and coating the milled granules with one or more polymers to provide taste-masked microcapsules,
wherein not less than 60% of the at least one drug from said tablet dissolves in about 60 minutes when dissolution tested using USP Apparatus 2 (paddle at 50 RPM, 900 mL of 0.1N HCl at 37° C.).
2. The tablet of claim 1 prepared by a process comprising the steps of:
(a) granulating the pharmaceutically acceptable formulation comprising at least one drug in a therapeutically effective amount and at least one polymeric binder imparting resilient characteristics to the resulting microcapsules, and optionally one or more diluents and one or more disintegrants, and
(b) wet milling the granulated mass using a size reduction mill to produce microgranules which resist breakage during coating for taste-masking and whose average particle size is not more than about 300 μm,
(c) microencapsulating the microgranules to provide microcapsules with an average particle size of not more than about 400 μm,
(d) separately granulating a sugar alcohol or a saccharide or a mixture thereof having an average particle size less than about 30 μm and a disintegrant to provide rapidly dispersing microgranules,
(e) blending the taste-masked microcapsules from step (c) and rapidly dispersing microgranules from step (d) optionally with additional pharmaceutical ingredients,
(f) compressing the blend from step (e) to form a tablet.
3. The tablet of claim 1 which is produced by:
(a) granulating a powder mixture into rapidly dispersing microgranules with a fixed particle diameter, the powder mixture comprising a sugar alcohol, a saccharide or a combination thereof, each of which having an average particle diameter of not more than 30 μm;
(b) granulating, wet milling and drying a pharmaceutically acceptable formulation comprising at least one drug with an average particle size of not more than about 50 μm, at least one polymeric binder imparting resilient characteristics to the resulting microcapsules, and optionally a diluent(s) and a disintegrant, said microgranule exhibiting not more than 15% fines (passing through 140 mesh screen) when tested in accordance with the procedure for friability test;
(c) encapsulating the microgranules of the at least one drug of step (b) by coacervation in a cyclohexane solution comprising ethylcellulose,
(d) mixing the rapidly dispersing microgranules from step (a) and the microcapsules from step (c) and optionally other pharmaceutically acceptable ingredients and compressing the mixture into a predetermined shape.
4. The tablet as set forth in claim 1 comprising rapidly dispersing microgranules comprising a sugar alcohol, a saccharide or a combination thereof, each of which has an average particle size of not more than about 30 μm, in the amount of about 30% to about 70% by weight of the tablet; a taste-masked microcapsule having an average particle diameter of not more than about 400 μm in the amount of about 0.01% to about 30% by weight of the tablet; a disintegrant in the amount of about 1.0% to about 10% by weight of the tablet; and optionally other pharmaceutically acceptable ingredients; said tablet being compressed into a predetermined shape.
5. The tablet of claim 4 wherein said sugar alcohol or saccharide is selected from the group consisting of D-mannitol, sorbitol, xylitol, maltitol, lactose and combinations thereof; and wherein the disintegrant is selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose, low substituted hydroxypropyl cellulose, and combinations thereof, each of which have an average particle diameter of not more than about 30 μm.
6. The tablet of claim 4 wherein said at least one drug is selected from the group consisting of H 2 antagonists, proton pump inhibitors, H 5 agonists, and selective histamine H 1 receptor antagonists, each of which having an average particle size of not more than about 50 μm.
7. The tablet of claim 6 wherein the disintegrant is selected from the group consisting of cross-linked polyvinylpyrrolidone (crospovidone), cross-linked carmellose of sodium, low substituted hydroxypropylcellulose, and mixtures thereof.
8. The tablet as set forth in claim 7 wherein the polymeric binder imparting resilient characteristics to the resulting microcapsules used for the granulation of the at least one drug is selected from the group consisting of hydroxypropylcellulose (HPC) of viscosity of 100 cps or higher, hydroxypropyl methylcellulose (HPMC), modified starches.
9. The tablet as set forth in claim 8 wherein the sugar alcohol is D-mannitol.
10. The tablet as set forth in claim 9 wherein the saccharide is lactose.
11. The tablet as set forth in claim 6 wherein the at least one drug is selected from the group consisting of ranitidine, cimetidine, famotidine, omeprazole, lansoprazole, sumatriptan, rezatriptan, zolmitriptan and cetirizine.
12. The tablet as set forth in claim 11 wherein the at least one drug is sumatriptan.
13. The tablet as set forth in claim 12 wherein the disintegrant is crospovidone.
14. The tablet as set forth in claim 13 wherein said polymeric binder is selected from the group consisting of hydroxypropylcellulose (HPC) of viscosity of 100 cps or higher, hydroxypropyl methylcellulose (HPMC) of viscosity of 100 cps or higher, modified starches, and combinations thereof.
15. The tablet as set forth in claim 1 wherein the disintegration time in the buccal cavity of the tablet is not more than 120 seconds.
16. A method for manufacturing a tablet that disintegrates in the oral cavity comprising the steps of:
(a) granulating a pharmaceutically acceptable formulation comprising at least one drug in a therapeutically effective amount and at least one polymeric binder imparting resilient characteristics to the resulting microcapsules, and optionally one or more diluents and one or more disintegranst, and
(b) wet milling the granulated mass using a size reduction mill to produce granules which resist breakage during coacervation for taste-masking and whose average particle size is not more than 300 μm,
(c) microencapsulating said microgranules with one or more polymers to provide taste-masked microcapsules with an average particle size of not more than 400 μm,
(d) separately granulating a sugar alcohol or a saccharide or a mixture thereof having an average particle size less than 30 μm and at least one disintegrant to provide rapidly dispersing microgranules,
(e) blending the taste-masked microcapsules from step (c) and rapidly dispersing microgranules from step (d) optionally with additional pharmaceutical ingredients,
(f) compressing the blend from step (e) to form a tablet, wherein not less than 60% of the drug from said tablet dissolves in about 60 minutes when dissolution tested using USP Apparatus 2 (paddle at 50 RPM, 900 mL of 0.1N HCl at 37° C.).
17. The method of claim 16 wherein an intrabuccally rapidly disintegrating tablet is produced which comprises a sugar alcohol, a saccharide or a combination thereof, each of which have an average particle size of not more than about 30 μm, in the amount of about 30% to about 70% by weight of the tablet, an active ingredient having an average particle diameter of not more than about 50 μm in the amount of about 0.01% to about 30% by weight of the tablet, a disintegrant in the amount of about 1.0% to about 10% by weight of the tablet, and optionally other pharmaceutically acceptable ingredients.
18. The method of claim 17 wherein the step of compressing includes compressing the mixture into a predetermined shape using a tablet press and pre-lubricating the dies and punches prior to tablet compression.
19. The method of claim 18 wherein the blend is internally lubricated prior to its compression on a tablet press.
20. The method of claim 17 wherein the sugar alcohol, the saccharide or the combination thereof, is selected from the group consisting of D-mannitol, sorbitol, xylitol, maltitol, and lactose and the disintegrant is selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose, and low substituted hydroxypropyl cellulose, each of which have an average particle diameter of not more than about 30 μm.
21. The method of claim 20 wherein the at least one drug is selected from the group consisting of H 2 antagonists, proton pump inhibitors, 5-HT 1 receptor agonists, each of which have an average particle size of not more than 50 μm, and is granulated with one or more diluents and at least one polymeric binder imparting resilient characteristics to the resulting microcapsules.
22. The method of claim 21 wherein the disintegrant is selected from the group consisting of cross-linked polyvinylpyrrolidone (crospovidone), cross-linked carmellose of sodium, low substituted hydroxypropyl cellulose, and mixtures thereof.
23. The method of claim 22 wherein said polymeric binder imparting resilient characteristics to the resulting microcapsules used for the granulation of the active is selected from the group consisting of hydroxypropylcellulose (HPC) of viscosity of 100 cps or higher, hydroxypropyl methylcellulose (HPMC) of viscosity of 100 cps or higher, modified starch, and mixtures thereof.
24. The method of claim 23 wherein the tablet disintegrates within 60 seconds in the buccal cavity, the sugar is D-mannitol having an average particle size of not more than about 30 μm, the disintegrant is crospovidone, the active ingredient is ranitidine or sumatriptan having an average particle size of not more than about 50 μm, and the polymeric binder is HPMC with a viscosity of 100 cps or higher, modified starch, or mixtures thereof.