Compressible resilient granules and formulations prepared therefrom

• US 20080069889A1
• Filed: 09/05/2007
• Published: 03/20/2008
• Est. Priority Date: 03/07/2006
• Status: Abandoned Application

• Current Assignee: Capricorn Pharma Incorporated
• Original Assignee: Capricorn Pharma Incorporated
• Inventors: Cherukuri, S.
• Application Number:
  US11/899,601
• Publication Number:
  US 20080069889A1
• Time in Patent Office: Days
• US Class Current: 424/493
• CPC Class Codes: A61K 31/07 Retinol compounds, e.g. vitamin A retinoic acids A61K31/203
• CPC Class Codes: A61K 31/12 Ketones
• CPC Class Codes: A61K 31/355 Tocopherols, e.g. vitamin E
• CPC Class Codes: A61K 31/375 Ascorbic acid, i.e. vitamin C; Salts thereof
• CPC Class Codes: A61K 31/4415 Pyridoxine, i.e. Vitamin B6 pyridoxal phosphate A61K31/675
• CPC Class Codes: A61K 31/455 Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
• CPC Class Codes: A61K 31/51 Thiamines, e.g. vitamin B1
• CPC Class Codes: A61K 31/525 Isoalloxazines, e.g. riboflavins, vitamin B2
• CPC Class Codes: A61K 31/59 Compounds containing 9, 10- seco- cyclopenta[a]hydrophenanthrene ring systems
• CPC Class Codes: A61K 31/714 Cobalamins, e.g. cyanocobalamin, i.e. vitamin B12
• CPC Class Codes: A61K 47/26 Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
• CPC Class Codes: A61K 47/36 Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
• CPC Class Codes: A61K 9/1652 Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin homeopathic globules A61K9/1623
• CPC Class Codes: A61K 9/205 Polysaccharides, e.g. alginate, gums; Cyclodextrin
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

The present invention provides resilient self-adhering granules which comprise a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa·s to about 250,000 mPa·s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m². The present invention also provides oral dosage compositions comprising the resilient self-adhering granules and methods for making and using the resilient self-adhering granules.

Claims

1. A resilient self-adhering granule which comprises a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa·

s to about 250,000 mPa·

s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m².

2. The granule according to claim 1, wherein the polysaccharide is selected from the group consisting of simple sugars, complex sugars, fibers, starches, pectins, dextrins, dextrans, natural gums, synthetic gums, mucilages, derivatives thereof, components thereof, and mixtures thereof.

3. The granule according to claim 2, wherein the polysaccharide is a dextrin.

4. The granule according to claim 1, wherein the binder is selected from the group consisting of syrups, emulsifiers, fats, waxes, gums, plasticizers, and mixtures thereof.

5. The granule according to claim 4, wherein the binder is selected from the group consisting of maltitol syrups, acetylated mono-, di-, or triglycerides, polyethyleneglycol esters, bee'"'"'s wax, carnuba wax, spermaceti, mineral oils, paraffins, microcrystalline waxes, polyethylene wax, gum Arabica, gum tragacanth, gum acacia, fiber gums, and mixtures thereof.

6. The granule according to claim 5, wherein the binder is maltitol syrup.

7. The granule according to claim 1, wherein the binder has a viscosity of about 10,000 mPa·

s.

8. The granule according to claim 1, further comprising a sugar alcohol selected from the group consisting of arabitol, erythritol, hydrogenated starch hydrolysates, isomalt, lactitol, maltitol, mannitol, sorbitol, xylitol, galactitol, inositol, ribitol, dithioerythritol, dithiothreitol, glycerol, derivatives thereof, and mixtures thereof.

9. The granule according to claim 8, wherein the sugar alcohol is maltitol.

10. The granule according to claim 1, further comprising an active agent selected from the group consisting of analgesics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antibiotics, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, immunosuppressants, antithyroid agents, antiviral agents, anxiolytic sedatives including hypnotics and neuroleptics, astringents, beta-adrenoceptor blocking agents, blood products and substitutes, cardiac inotropic agents, contrast media, corticosteroids, cough suppressants including expectorants and mucolytics, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics including antiparkinsonian agents, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, sex hormones including steroids, anti-allergic agents, stimulants and anoretics, sympathomimetics, thyroid agents, vasodilators, xanthines, antitussives, decongestants, alkaloids, laxatives, antacids, ion exchange resins, anti-cholesterolemics, antipyretics, analgesics including acetaminophen, aspirin, non-steroidal anti-inflammatory drugs and opioids, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psycho-tropics, antimanics, stimulants, gastrointestinal agents, sedatives, anti-diarrheal preparations, anti-anginal drugs, vasodilators, vasoconstrictors, migraine treatments, tranquilizers, anti-psychotics, antitumor drugs, antithrombotic drugs, hypnotics, anti-emetics, anti-nausants, anti-convulsants, neuromuscular drugs, hyper- and hypoglycemic spasmodics, uterine relaxants, antiobesity drugs, anabolic drugs, erythropoetic drugs, antiasthmatics, mucolytics, anti-uricemic drugs, and mixtures thereof.

11. The granule according to claim 10, wherein the active agent is selected from the group consisting of analgesics, antibiotics, lipid regulating agent, antihistamines, antineoplastic agents, and antiviral agents.

12. The granule, according to claim 10, wherein the active agent is homogenous throughout the granule or is coated on the surface of the granule.

13. The granule according to claim 10, wherein the active agent is in immediate release form or in controlled release form.

14. The granule of claim 1, further comprising a nutritional supplement selected from the group consisting of calcium-containing materials, stannol esters, hydroxycitric acid, vitamins, minerals, herbals, spices, and mixtures thereof.

15. The granule according to claim 13, wherein the nutritional supplement is a calcium containing material, a zinc containing material, or vitamin C.

16. The granule according to claim 1, wherein the granule withstands pressures of up to 50 kilonewtons/m² without losing its resiliency.

17. An oral dosage composition comprising resilient self-adhering granules which comprise a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa·

s to about 250,000 mPa·

s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m² and the granules have agglomerated to form the oral dosage composition.

18. The composition according to claim 17, wherein the polysaccharide is selected from the group consisting of simple sugars, complex sugars, fibers, starches, pectins, dextrins, dextrans, natural gums, synthetic gums, mucilages, derivatives thereof, components thereof, and mixtures thereof.

19. The composition according to claim 17, wherein the binder is selected from the group consisting of syrups, emulsifiers, fats, waxes, gums, plasticizers, and mixtures thereof.

20. The composition according to claim 17, wherein the binder has a viscosity of about 10,000 mPa·

s.

21. The composition according to claim 17, further comprising a sugar alcohol selected from the group consisting of arabitol, erythritol, hydrogenated starch hydrolysates, isomalt, lactitol, maltitol, mannitol, sorbitol, xylitol, galactitol, inositol, ribitol, dithioerythritol, dithiothreitol, glycerol, derivatives thereof, and mixtures thereof.

22. The composition according to claim 17, further comprising an active agent selected from the group consisting of analgesics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antibiotics, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, immunosuppressants, antithyroid agents, antiviral agents, anxiolytic sedatives including hypnotics and neuroleptics, astringents, beta-adrenoceptor blocking agents, blood products and substitutes, cardiac inotropic agents, contrast media, corticosteroids, cough suppressants including expectorants and mucolytics, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics including antiparkinsonian agents, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, sex hormones including steroids, anti-allergic agents, stimulants and anoretics, sympathomimetics, thyroid agents, vasodilators, xanthines, antitussives, decongestants, alkaloids, laxatives, antacids, ion exchange resins, anti-cholesterolemics, antipyretics, analgesics including acetaminophen, aspirin, non-steroidal anti-inflammatory drugs and opioids, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psycho-tropics, antimanics, stimulants, gastrointestinal agents, sedatives, anti-diarrheal preparations, anti-anginal drugs, vasodilators, vasoconstrictors, migraine treatments, tranquilizers, anti-psychotics, antitumor drugs, antithrombotic drugs, hypnotics, anti-emetics, anti-nausants, anti-convulsants, neuromuscular drugs, hyper- and hypoglycemic spasmodics, uterine relaxants, antiobesity drugs, anabolic drugs, erythropoetic drugs, antiasthmatics, mucolytics, anti-uricemic drugs, and mixtures thereof.

23. The composition according to claim 17, wherein the oral dosage composition is in the form of a tablet that has been scored at least once.

24. The composition according to claim 23, wherein the tablet is broken into two portions and the breaking results in substantially no material loss.

25. The composition according to claim 24, wherein the two broken portions may be reformed with substantially no material loss.

26. The composition according to claim 17, further comprising non-resilient granules.

27. The composition according to claim 26, wherein the resilient granules comprise an active agent and the non-resilient granules comprise an inactive agent,

28. The composition according to claim 26, wherein the resilient granules comprise an inactive agent and the non-resilient granules comprise an active agent,

29. The composition according to claim 26, wherein the resilient granules comprise an active agent in immediate release form and the non-resilient granules comprise the same active agent in delayed release form.

30. The composition according to claim 26, wherein the resilient granules comprise an active agent in delayed release form and the non-resilient granules comprise the same active agent in immediate release form.

31. The composition according to claim 26, wherein the resilient granules comprise a first active agent and the non-resilient granules comprise a second active agent, and further wherein the first and second active agents can both be in immediate release form, can both be in delayed release form, or one active agent can be in immediate release form and the other active agent can be in delayed release form.

32. The composition according to claim 17, wherein a first portion of the resilient granules comprises an active agent and a second portion of the resilient granules comprises an inactive agent.

33. The composition according to claim 17, wherein a first portion of the resilient granules comprises an active agent in immediate release form and a second portion of the resilient granules comprises the same active agent in delayed release form.

34. The composition according to claim 17, wherein a first portion of the resilient granules comprises a first active agent and a second portion of the resilient granules comprises a second active agent, and further wherein the first and second active agents can both be in immediate release form, can both be in delayed release form, or one active agent can be in immediate release form and the other active agent can be in delayed release form.

35. A method for making a resilient self-adhering granule which comprises a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa·

s to about 250,000 mPa·

s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m², which comprises the steps of;

(a) mixing and heating the polysaccharide and binder in a mixer to form a reaction mixture; and

(b) extruding the reaction mixture from step (a), cooling the reaction mixture to room temperature, milling the reaction mixture to a particular granule size, and cooling the reaction mixture in a freezer.

36. The method according to claim 35, wherein the polysaccharide is selected from the group consisting of simple sugars, complex sugars, fibers, starches, pectins, dextrins, dextrans, natural gums, synthetic gums, mucilages, derivatives thereof, components thereof, and mixtures thereof.

37. The method according to claim 35, wherein the binder is selected from the group consisting of syrups, emulsifiers, fats, waxes, gums, plasticizers, and mixtures thereof.

38. The method according to claim 35, wherein the binder has a viscosity of about 10,000 mPa·

s.

39. The method according to claim 35, further comprising a sugar alcohol selected from the group consisting of arabitol, erythritol, hydrogenated starch hydrolysates, isomalt, lactitol, maltitol, mannitol, sorbitol, xylitol, galactitol, inositol, ribitol, dithioerythritol, dithiothreitol, glycerol, derivatives thereof, and mixtures thereof.

40. The method according to claim 35, further comprising an active agent selected from the group consisting of analgesics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antibiotics, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, immunosuppressants, antithyroid agents, antiviral agents, anxiolytic sedatives including hypnotics and neuroleptics, astringents, beta-adrenoceptor blocking agents, blood products and substitutes, cardiac inotropic agents, contrast media, corticosteroids, cough suppressants including expectorants and mucolytics, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics including antiparkinsonian agents, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, sex hormones including steroids, anti-allergic agents, stimulants and anoretics, sympathomimetics, thyroid agents, vasodilators, xanthines, antitussives, decongestants, alkaloids, laxatives, antacids, ion exchange resins, anti-cholesterolemics, antipyretics, analgesics including acetaminophen, aspirin, non-steroidal anti-inflammatory drugs and opioids, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psycho-tropics, antimanics, stimulants, gastrointestinal agents, sedatives, anti-diarrheal preparations, anti-anginal drugs, vasodilators, vasoconstrictors, migraine treatments, tranquilizers, anti-psychotics, antitumor drugs, antithrombotic drugs, hypnotics, anti-emetics, anti-nausants, anti-convulsants, neuromuscular drugs, hyper- and hypoglycemic spasmodics, uterine relaxants, antiobesity drugs, anabolic drugs, erythropoetic drugs, antiasthmatics, mucolytics, anti-uricemic drugs, and mixtures thereof.

41. A method for administering an oral dosage composition to a subject comprising:

a) providing resilient self-adhering granules which comprises a polysaccharide present in an amount from about 10 wt % to about 90 wt % and a binder having a viscosity from about 5,000 mPa·

s to about 250,000 mPa·

s present in an amount from about 90 wt % to about 10 wt %, wherein the granule is capable of reversible agglomeration at or below 6,500 kilonewtons/m²; and

b) administering the oral dosage composition to a subject'"'"'s oral cavity, wherein the majority of the resilient self-adhering granules is released in the gastrointestinal tract.

42. The method according to claim 41, wherein the polysaccharide is selected from the group consisting of simple sugars, complex sugars, fibers, starches, pectins, dextrins, dextrans, natural gums, synthetic gums, mucilages, derivatives thereof, components thereof, and mixtures thereof.

43. The method according to claim 41, wherein the binder is selected from the group consisting of syrups, emulsifiers, fats, waxes, gums, plasticizers, and mixtures thereof.

44. The method according to claim 41, wherein the binder has a viscosity of about 10,000 mPa·

s.

45. The method according to claim 41, further comprising a sugar alcohol selected from the group consisting of arabitol, erythritol, hydrogenated starch hydrolysates, isomalt, lactitol, maltitol, mannitol, sorbitol, xylitol, galactitol, inositol, ribitol, dithioerythritol, dithiothreitol, glycerol, derivatives thereof, and mixtures thereof.

46. The method according to claim 41, further comprising an active agent selected from the group consisting of analgesics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antibiotics, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, immunosuppressants, antithyroid agents, antiviral agents, anxiolytic sedatives including hypnotics and neuroleptics, astringents, beta-adrenoceptor blocking agents, blood products and substitutes, cardiac inotropic agents, contrast media, corticosteroids, cough suppressants including expectorants and mucolytics, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics including antiparkinsonian agents, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, sex hormones including steroids, anti-allergic agents, stimulants and anoretics, sympathomimetics, thyroid agents, vasodilators, xanthines, antitussives, decongestants, alkaloids, laxatives, antacids, ion exchange resins, anti-cholesterolemics, antipyretics, analgesics including acetaminophen, aspirin, non-steroidal anti-inflammatory drugs and opioids, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psycho-tropics, antimanics, stimulants, gastrointestinal agents, sedatives, anti-diarrheal preparations, anti-anginal drugs, vasodilators, vasoconstrictors, migraine treatments, tranquilizers, anti-psychotics, antitumor drugs, antithrombotic drugs, hypnotics, anti-emetics, anti-nausants, anti-convulsants, neuromuscular drugs, hyper- and hypoglycemic spasmodics, uterine relaxants, antiobesity drugs, anabolic drugs, erythropoetic drugs, antiasthmatics, mucolytics, anti-uricemic drugs, and mixtures thereof.

47. The method according to claim 41, further comprising non-resilient granules.

48. The method according to claim 47, wherein the resilient granules comprise an active agent and the non-resilient granules comprise an inactive agent,

49. The method according to claim 47, wherein the resilient granules comprise an inactive agent and the non-resilient granules comprise an active agent,

50. The method according to claim 47, wherein the resilient granules comprise an active agent in immediate release form and the non-resilient granules comprise the same active agent in delayed release form.

51. The method according to claim 47, wherein the resilient granules comprise an active agent in delayed release form and the non-resilient granules comprise the same active agent in immediate release form.

52. The method according to claim 47, wherein the resilient granules comprise a first active agent and the non-resilient granules comprise a second active agent, and further wherein the first and second active agents can both be in immediate release form, can both be in delayed release form, or one active agent can be in immediate release form and the other active agent can be in delayed release form.

53. The method according to claim 41, wherein a first portion of the resilient granules comprises an active agent and a second portion of the resilient granules comprises an inactive agent.

54. The method according to claim 41, wherein a first portion of the resilient granules comprises an active agent in immediate release form and a second portion of the resilient granules comprises the same active agent in delayed release form.

55. The method according to claim 41, wherein a first portion of the resilient granules comprises a first active agent and a second portion of the resilient granules comprises a second active agent, and further wherein the first and second active agents can both be in immediate release form, can both be in delayed release form, or one active agent can be in immediate release form and the other active agent can be in delayed release form.