Drug compositions containing controlled release hypromellose matrices

• US 20070048377A1
• Filed: 08/25/2006
• Published: 03/01/2007
• Est. Priority Date: 08/26/2005
• Status: Abandoned Application

• Current Assignee: BPSI Holdings, LLC
• Original Assignee: BPSI Holdings, LLC
• Inventors: Fegely, Kurt, Young, Cara, Rajabi-Siahboomi, Ali, Rege, Pankaj
• Application Number:
  US11/510,359
• Publication Number:
  US 20070048377A1
• Time in Patent Office: Days
• US Class Current: 424/468
• CPC Class Codes: A61K 31/275 Nitriles; Isonitriles
• CPC Class Codes: A61K 9/1635 obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
• CPC Class Codes: A61K 9/1652 Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin homeopathic globules A61K9/1623
• CPC Class Codes: A61K 9/2027 obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
• CPC Class Codes: A61K 9/2031 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
• CPC Class Codes: A61K 9/2054 Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
• CPC Class Codes: A61K 9/2077 Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets

Abstract

This invention is directed to a controlled release formulation for an oral dosage form that is formulated into a swellable, hydrophilic matrix. The controlled release formulation contains a mixture of hypromellose and polyvinyl acetate phthalate and allows pharmaceutically active ingredients combined therewith to be released in a controlled release manner.

Claims

1. A controlled release formulation for use in oral dosage forms, comprising a mixture containing hypromellose and polyvinyl acetate phthalate, said polyvinyl acetate phthalate being present in amount which is effective to provide controlled release of a pharmaceutically active ingredient in vitro when said mixture is compressed into a swellable, hydrophilic matrix.

2. The controlled release formulation of claim 1, further comprising an anionic polymer.

3. The controlled release formulation of claim 2, wherein said anionic polymer is selected from the group consisting of sodium carboxymethylcellulose, sodium alginate, xanthan gum, Carbopol (cross-linked acrylic acid polymers), cellulose acetate phthalate, hydroxypropyl-methylcellulose phthalate, methacrylic acid copolymer, hydroxyppropylmethyl acetate succinate, and mixtures thereof.

4. The controlled release formulation of claim 1, further comprising a pharmaceutically active ingredient or a nutritional supplement.

5. The controlled release formulation of claim 1, further comprising an auxiliary hydrophilic cellulosic polymer.

6. The controlled release formulation of claim 5, wherein said auxiliary hydrophilic cellulosic polymer is selected from the group consisting of hydroxypropylcellulose, hydroxyethylcellulose, polyvinyl acetate and mixtures thereof.

7. The controlled release formulation of claim 1, wherein the amount of hypromellose is from about 8 to about 60% by wt.

8. The controlled release formulation of claim 7, wherein the amount of hypromellose is from about 15 to about 45% by wt.

9. The controlled release formulation of claim 8, wherein the amount of hypromellose is from about 25 to about 35% by wt.

10. The controlled release formulation of claim 1, wherein the amount of said polyvinyl acetate phthalate is from about 4 to about 60% by wt. of the mixture.

11. The controlled release formulation of claim 10, wherein the amount of said polyvinyl acetate phthalate is from about 8 to about 45% by wt. of the mixture.

12. The controlled release formulation of claim 11, wherein the amount of said polyvinyl acetate phthalate is from about 15 to about 35% by wt. of the mixture.

13. The controlled release formulation of claim 1, wherein the polyvinyl acetate phthalate is co-processed with titanium dioxide.

14. The controlled release formulation of claim 5, where the amount of auxiliary hydrophilic cellulosic polymer ranges from >

0 up to about 100 percent by weight of anionic polymer.

15. The controlled release formulation of claim 1, further comprising a member of the group consisting of lubricants, flow aids, diluents, binding agents, disintegrants, binders, solubility enhancers, pH modulating agents and mixtures thereof.

16. The controlled release formulation of claim 4, wherein the pharmaceutically active ingredient or a nutritional supplement is from about 0.001 to about 60% by weight of the mixture.

17. The controlled release formulation of claim 16, wherein the pharmaceutically active ingredient or a nutritional supplement is from about 5.0 to about 40% by weight of the mixture.

18. The controlled release formulation of claim 17, wherein the pharmaceutically active ingredient or a nutritional supplement is from about 10 to about 30% by weight of the mixture.

19. The controlled release formulation of claim 1, wherein the hypromellose and polyvinyl acetate phthalate are wet granulated with a pharmaceutically active ingredient.

20. The controlled release formulation of claim 15, wherein the lubricant is selected from the group consisting of stearic acid, calcium, magnesium stearate, poloxamer, polyethylene glycol, hydrogenated vegetable oil, and mixtures thereof.

21. The controlled release formulation of claim 15, wherein the flow aid is selected from the group consisting of colloidal silicon dioxide, talc, magnesium stearate, polyethylene glycol, magnesium stearate and mixtures thereof.

22. The controlled release formulation of claim 15, wherein the diluent is selected from the group consisting of microcrystalline cellulose, lactose, dicalcium phosphate, pregelatinized starch, native starch, mannitol, sucrose, talc and mixtures thereof.

23. The controlled release formulation of claim 15, wherein the disintegration aid is selected from the group consisting of crospovidone, croscarmellose sodium, sodium starch glycolate, hydroxypropylcellulose (low-substituted), starch, calcium carbonate, carboxymethylcellulose calcium, and mixtures thereof.

24. The controlled release formulation of claim 15, wherein the solubility enhancer is selected from the group consisting of lecithin, poloxamer, polyoxyethylene-fatty acid esters, sorbitan esters, and mixtures thereof.

25. The controlled release formulation of claim 15, wherein the pH modulating agent is selected from the group consisting of citric acid, fumaric acid, tartaric acid, sodium citrate, sodium tartrate, sodium bicarbonate and mixtures thereof.

26. The controlled release formulation of claim 15, wherein the member of said group is present in an amount of from about 0.001 to about 50% by weight of the mixture.

27. The controlled release formulation of claim 4, wherein said hypromellose and said polyvinyl acetate phthalate are dry blended prior to being mixed with said pharmaceutical active ingredients or said nutritional supplementary.

28. The controlled release formulation of claim 4, wherein said dry blend of said hypromellose and said polyvinyl acetate phthalate are dispersed in an aqueous solution prior to being combined with said pharmaceutical active ingredients or said nutritional supplementary.

29. An oral solid dosage form comprising the controlled release formulation of claim 1.

30. A method of preparing an oral solid dosage form, comprising providing the controlled release formulation of claim 4 and compressing the formulation into an oral solid dosage form.