PULSATILE RELEASE COMPOSITION OF THERAPEUTIC AGENT

• US 20110311628A1
• Filed: 03/08/2010
• Published: 12/22/2011
• Est. Priority Date: 03/09/2009
• Status: Abandoned Application

• Current Assignee: Council of Scientific & Industrial Research
• Original Assignee: Council of Scientific & Industrial Research
• Inventors: Kulkarni, Mohan Gopalkrishna, Muthusamy, Ramesh
• Application Number:
  US13/254,008
• Publication Number:
  US 20110311628A1
• Time in Patent Office: Days
• US Class Current: 424/482
• CPC Class Codes: A61K 47/34 Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers A61K47/10 takes precedence
• CPC Class Codes: A61K 8/91 Graft copolymers A61K8/89 takes precedence
• CPC Class Codes: A61K 9/2853 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers, poly(lactide-co-glycolide)
• CPC Class Codes: A61K 9/5084 Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs tablets containing such a mixture A61K9/2077
• CPC Class Codes: A61P 11/06 Antiasthmatics
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: A61P 31/00 Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system

Abstract

A pulsatile release composition which releases the content rapidly after a predetermined lag time comprising a drug containing a core, coated with a pH sensitive graft copolymer. The coating suppresses the drug release at acidic pH prevalent in the stomach and releases it either immediately or after a lag time in the intestinal region. Combinations of multiple numbers of coated and uncoated units provide a sequential pulsatile release of same or different therapeutic agents.

Claims

1. A pulsatile release composition for oral administration comprising therapeutically active agent and pharmaceutically acceptable ingredients as a core unit and the said core unit is coated with pH sensitive graft copolymer having the formula 1

2. The pulsatile release composition as claimed in claim 1, wherein the backbone is poly (ester-ether) or polyester.

3. The pulsatile release composition as claimed in claim 1, wherein the diol is selected from the group consisting of aliphatic diol, cycloaliphatic diol and aromatic diol.

4. The pulsatile release composition as claimed in claim 3, wherein the aliphatic diol is selected from the group consisting of diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, tripropylene glycol, polyethylene glycol (M_n˜

200), polyethylene glycol (M_n˜

400), polyethylene glycol (M_n˜

1000), polyethylene glycol (M_n˜

2000), 1,2-ethane diol, 1,3-propane diol, 1,2-propane diol, 2-methyl-1,3-propane diol, 1,4-butane diol, 1,3-butane diol, 1,2-butane diol, 1,5-pentane diol, 1,6-hexane diol, 1,7-heptane diol, 1,8-octane diol, 1,9-nonane diol and 1,12-dodecane diol.

5. The pulsatile release composition as claimed in claim 3, wherein the cycloaliphatic diol is 1,4-cyclohexanedimethanol.

6. The pulsatile release composition as claimed in claim 3, wherein the aromatic diol is bis(2-hydroxyethyl)terephthalate.

7. The pulsatile release composition as claimed in claim 1, wherein the dicarboxylic acid is selected from the group consisting of succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid and dodecanedioic acid.

8. The pulsatile release composition as claimed in claim 1, wherein the acid anhydride is selected from succinic anhydride and phthalic anhydride.

9. The pulsatile release composition as claimed in claim 1, wherein the monomer containing pendent unsaturation is an epoxy monomer selected from glycidyl methacrylate and glycidyl acrylate or a diol monomer selected from trimethylolpropane monomethacrylate and trimethylolpropane monoacrylate.

12. The pulsatile release composition as claimed in claim 1, wherein the acidic monomer (D) is a carboxylic acid selected from acrylic acid and methacrylic acid.

13. The pulsatile release composition as claimed in claim 1, wherein the plasticizer is preferably di-n-butyl phthalate

14. The pulsatile release composition as claimed in claim 1, wherein the therapeutically active agent comprises anti-inflammatory drugs further comprising ibuprofen, ketoprofen, indomethacin, diclofenac and naproxen, cardiovascular drugs comprising verapamil, nifedepine, captopril, propranolol, atenolol and diltiazem, antibiotic drugs comprising ampicillin and cephalexin, analgesic drugs comprising acetylsalicylic acid, acetaminophen, oxycodone and morphine, and anti-asthmatic drugs comprising aminophylline, theophylline and salbutamol.

20. The pulsatile release composition as claimed in claim 1, wherein core unit contains same or different therapeutically active agent.

22. The pulsatile release composition as claimed in claim 1, wherein pharmaceutically acceptable ingredients are selected from, but not limited to the group consisting of, filler selected from microcrystalline cellulose and lactose monohydrate, binder selected from hydroxypropyl methyl cellulose and polyvinyl pyrrolidone, lubricant selected from magnesium stearate and talc and glidant, preservatives, colorants and flavorants.

23. The pulsatile release composition as claimed in claim 22, wherein glidant is preferably aerosil.

24. The pulsatile release composition as claimed in claim 1, wherein the pH sensitive graft copolymer coat is 7-25% of the total weight of each coated unit.

25. The pulsatile release composition as claimed in claim 1, wherein the plasticizer is 5-30% of the weight of the pH sensitive graft copolymer of claim 1 on the weight of said coat.

26. The pulsatile release composition as claimed in claim 1, wherein the therapeutically active agent comprises 20-70% of the total weight of each unit and the pharmaceutically acceptable ingredients comprises 20-60% of the total weight of each unit.

28. The pulsatile release composition as claimed in claim 1, wherein the pharmaceutically acceptable ingredients comprise filler 9-54%, a binder 5-15%, a lubricant 0.5-2% and a glidant 0.2-1% of the total weight of each unit and the units are tablets.

30. The pulsatile release composition as claimed in claim 1, wherein process for the preparation of the said composition comprises the steps of:

I. dry granulating and mixing the therapeutically active agent and pharmaceutically acceptable ingredients to obtain granular mixture;

II. compressing the granular mixture as obtained in step (I) into tablets;

III. dissolving pH sensitive graft copolymer and plasticizer in solvent mixture to obtain 10% solution;

IV. coating the tablets as obtained in step (II) with 10% solution of the pH sensitive graft copolymer and plasticizer as obtained in step (III) to obtain coated tablets;

V. drying the coated tablets as obtained in step (IV) to obtain pulsatile release composition for oral administration.

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