CA2798702A1 - Alcoholresistant metoprolol-containing extended-release oral dosage forms - Google Patents

Alcoholresistant metoprolol-containing extended-release oral dosage forms Download PDF

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Publication number
CA2798702A1
CA2798702A1 CA2798702A CA2798702A CA2798702A1 CA 2798702 A1 CA2798702 A1 CA 2798702A1 CA 2798702 A CA2798702 A CA 2798702A CA 2798702 A CA2798702 A CA 2798702A CA 2798702 A1 CA2798702 A1 CA 2798702A1
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CA
Canada
Prior art keywords
percent
weight
granule
amount
dosage form
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA2798702A
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French (fr)
Inventor
Ehab Hamed
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Cima Labs Inc
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Cima Labs Inc
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Filing date
Publication date
Application filed by Cima Labs Inc filed Critical Cima Labs Inc
Publication of CA2798702A1 publication Critical patent/CA2798702A1/en
Abandoned legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives

Abstract

This disclosure relates to an extended release oral dosage form comprising a matrix containing a viscosity modifier (but no lipid) and coated granules containing metoprolol or a pharmaceutically acceptable salt or solvate thereof. The dosage form has alcohol resistance and may also have crush resistance.

Claims (39)

  1. WHAT IS CLAIMED IS:
    An extended release oral dosage form comprising:
    a matrix, wherein the matrix comprises a viscosity modifier in an amount from about 1 to about 60 percent by weight of the dosage form; and coated granules comprising metoprolol or a pharmaceutically acceptable salt or solvate thereof;
    wherein the matrix does not contain a lipid.
  2. 2. An extended release oral dosage form comprising:
    a matrix, wherein the matrix comprises a viscosity modifier in an amount from about 1 to about 60 percent by weight of the dosage form; and coated granules comprising metoprolol or a pharmaceutically acceptable salt or solvate thereof;
    wherein the matrix does not contain a lipid;
    in which the percent of metoprolol released after 2 hours in a solution of 0.1N
    hydrochloric acid and 40% alcohol is no more than 10 percentage points greater than the percent of said metoprolol released in a solution of 0.1N hydrochloric acid in the absence of alcohol.
  3. 3. An extended release oral dosage form comprising:
    a matrix, wherein the matrix comprises a viscosity modifier in an amount from about 1 to about 60 percent by weight of the dosage form; and coated granules comprising metoprolol or a pharmaceutically acceptable salt or solvate thereof;
    wherein the matrix does not contain a lipid;
    in which the release of metoprolol from the dosage form 6 hours after testing is less than about 80 percent when tested in 500m1 of 0.1N hydrochloric acid solution using USP dissolution apparatus.
  4. 4. The dosage form of claim 1 or 2 or 3, wherein the viscosity modifier is selected from the group consisting of. sodium alginate, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, methylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, crosslinked polyacrylic acid, gelatin, pectins, gums, polyethylene oxides, Konjac flour, carrageenan, xanthan gum, or mixtures thereof.
  5. 5. The dosage form of claim 1 or 2 or 3, wherein the viscosity modifier is a gelling polymer.
  6. 6. The dosage form of claim 5, wherein the gelling polymer is selected from the group consisting of. natural and synthetic starches, natural and synthetic celluloses, acrylates, and polyalkylene oxides.
  7. 7. The dosage form of claim 6, wherein the gelling polymer is selected from the group consisting of. hydroxypropylmethylcellulose, hydroxypropylcellulose, methylcellulose, hydroxyethylcellulose, and carboxymethylcellulose.
  8. 8. The dosage form of claim 7, wherein the gelling polymer is hydroxypropylmethylcellulose.
  9. 9. The dosage form of claim 1 or 2 or 3, wherein the viscosity modifier is present in an amount from about 25 to about 45 percent by weight of the dosage form.
  10. 10. The dosage form of claim 1 or 2 or 3, wherein the coated granules comprise:
    a granule comprising metoprolol or a pharmaceutically acceptable salt or solvate thereof in an amount from about 10 to about 90 percent by weight of the granule, a first strong film former in an amount from about 1 to about 90 percent by weight of the granule, a second viscosity modifier in an amount from about 1 to about 90 percent by weight of the granule, and a fat/wax in an amount from about 0 to about 40 percent by weight of the granule; and a coating on the granule, wherein the coating is present in an amount from about 5 to about 70 percent by weight of the coated granule, and wherein the coating comprises a second strong film former in an amount from about 1 to about 50 percent by weight of the coated granule, and an anti-adherent in an amount from about 0 to about 30 percent by weight of the coated granule.
  11. 11. The dosage form of claim 10, wherein the coating is present in an amount from about 30 to about 70 percent by weight of the coated granule.
  12. 12. The dosage form of claim 11, wherein the coating is present in an amount from about 35 to about 55 percent by weight of the coated granule.
  13. 13. The dosage form of claim 10, wherein the first strong film former and the second strong film former are the same.
  14. 14. The dosage form of claim 10, wherein the first and second strong film formers are independently selected from the group consisting of. natural and synthetic starches, natural and synthetic celluloses, acrylics, vinylics, resins, methacrylate or shellac.
  15. 15. The dosage form of claim 14, wherein the first and second strong film formers are independently selected from the group consisting of. ethylcellulose; Ammonio Methacrylate Copolymer, Type B; Ammonio Methacrylate Copolymer, Type A; Amino Methacrylate Copolymer; Ethyl Acrylate and Methyl Methacrylate Copolymer Dispersion; Methacrylic Acid Copolymer, Type A; Methacrylic Acid Copolymer, Type B; and shellac.
  16. 16. The dosage form of claim 15, wherein the first and second strong film formers are ethylcellulose.
  17. 17. The dosage form of claim 10, wherein the first strong film former is present in an amount from about 5 to about 40 percent by weight of the granule.
  18. 18. The dosage form of claim 10, wherein the first strong film former is present in an amount from about 10 to about 30 percent by weight of the granule.
  19. 19. The dosage form of claim 10, wherein the second viscosity modifier is selected from the group consisting of. sodium alginate, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, methylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, crosslinked polyacrylic acid, gelatin, pectins, gums, polyethylene oxides, Konjac flour, carrageenan, xanthan gum, or mixtures thereof.
  20. 20. The dosage form of claim 19, wherein the second viscosity modifier is selected from the group consisting of: hydroxypropylmethylcellulose, hydroxypropylcellulose, methylcellulose, hydroxyethylcellulose, and carboxymethylcellulose.
  21. 21. The dosage form of claim 20, wherein the second viscosity modifier is hydroxypropylmethylcellulose.
  22. 22. The dosage form of claim 10, wherein the second viscosity modifier is present in an amount from about 1 to about 60 percent by weight of the granule.
  23. 23. The dosage form of claim 10, wherein the second viscosity modifier is present in an amount from about 5 to about 30 percent by weight of the granule.
  24. 24. The dosage form of claim 10, wherein the fat/wax is selected from the group consisting of. glycerol fatty esters and waxes.
  25. 25. The dosage form of claim 24, wherein the fat/wax is selected from the group consisting of. glycerol behenate, carnauba wax and bees wax.
  26. 26. The dosage form of claim 25, wherein the fat/wax is glycerol behenate.
  27. 27. The dosage form of claim 1 or 2 or 3, wherein the coated granules comprise:
    a granule consisting essentially of metoprolol or a pharmaceutically acceptable salt or solvate thereof in an amount from about 10 to about 90 percent by weight of the granule, a first strong film former in an amount from about 1 to about 90 percent by weight of the granule, and a second viscosity modifier in an amount from about 1 to about 90 percent by weight of the granule;
    and a coating on the granule, wherein the coating is present in an amount from about 5 to about 70 percent by weight of the coated granule, and wherein the coating comprises a second strong film former in an amount from about 1 to about 50 percent by weight of the coated granule, and an anti-adherent in an amount from about 0 to about 30 percent by weight of the coated granule.
  28. 28. The dosage form of claim 27, wherein the anti-adherent is present in an amount from about 10 to about 25 percent by weight of the coated granule.
  29. 29. The dosage form of claim 27, wherein the anti-adherent is magnesium stearate present in an amount from about 10 to about 25 percent by weight of the coated granule.
  30. 30. The dosage form of claim 27, wherein metoprolol or a pharmaceutically acceptable salt or solvate thereof is present in an amount from about 50 to about 90 percent by weight of the granule.
  31. 31. The dosage form of claim 27, wherein metoprolol or a pharmaceutically acceptable salt or solvate thereof is present in an amount from about 60 to about 90 percent by weight of the granule.
  32. 32. An alcohol-resistant extended release oral dosage form comprising: a matrix, wherein the matrix comprises a first viscosity modifier in an amount from about 5 to about 45 percent by weight of the dosage form; and coated granules, wherein the coated granules comprise: a granule comprising metoprolol or a pharmaceutically acceptable salt or solvate thereof in an amount from about 10 to about 90 percent by weight of the granule, a first strong film former in an amount from about 1 to about 90 percent by weight of the granule, a second viscosity modifier in an amount from about 1 to about 90 percent by weight of the granule, and a fat/wax in an amount from about 0 to about 40 percent by weight of the granule; and a coating on the granule, wherein the coating is present in an amount from about 5 to about 70 percent by weight of the coated granule, and wherein the coating comprises a second strong film former in an amount from about 1 to about 50 percent by weight of the coated granule, and an anti-adherent in an amount from about 10 to about 25 percent by weight of the coated granule; and wherein the matrix does not comprise a lipid.
  33. 33. An alcohol-resistant extended release oral dosage form comprising a matrix, wherein the matrix comprises a first viscosity modifier in an amount from about 25 to about 45 percent by weight of the dosage form; and coated granules, wherein the coated granules comprise: a granule consisting essentially of metoprolol or a pharmaceutically acceptable salt or solvate thereof in an amount from about 50 to about 90 percent by weight of the granule, a first strong film former in an amount from about 5 to about 40 percent by weight of the granule, a second viscosity modifier in an amount from about 5 to about 30 percent by weight of the granule, and a coating on the granule, wherein the coating is present in an amount from about 30 to about 70 percent by weight of the coated granule, and wherein the coating comprises a second strong film former in an amount from about 10 to about 50 percent by weight of the coated granule, and an anti-adherent in an amount from about 10 to about 25 percent by weight of the coated granule; and wherein the matrix does not comprise a lipid.
  34. 34. An alcohol-resistant extended release oral dosage form comprising a matrix, wherein the matrix comprises hydroxypropylmethylcellulose in an amount from about 25 to about 45 percent by weight of the dosage form; and coated granules, wherein the coated granules comprise: a granule consisting essentially of metoprolol or a pharmaceutically acceptable salt or solvate thereof in an amount from about 60 to about 90 percent by weight of the granule, ethylcellulose in an amount from about 10 to about 30 percent by weight of the granule, hydroxypropylmethylcellulose in an amount from about 5 to about 20 percent by weight of the granule; and a coating on the granule, wherein the coating is present in an amount from about 30 to about 55 percent by weight of the coated granule, and wherein the coating comprises ethylcellulose in an amount from about 10 to about 50 percent by weight of the coated granule, and magnesium stearate in an amount from about 10 to about 25 percent by weight of the coated granule; and wherein the matrix does not comprise a lipid.
  35. 35. An alcohol-resistant extended release oral dosage form comprising a matrix, wherein the matrix comprises hydroxypropylmethylcellulose in an amount of about 30 percent by weight of the dosage form; and coated granules, wherein the coated granules comprise: a granule consisting essentially of metoprolol succinate in an amount of about 70 to about 80 percent by weight of the granule, ethylcellulose in an amount from about 10 to about 20 percent by weight of the granule, and hydroxypropylmethylcellulose in an amount from about 5 to about 20 percent by weight of the granule; and a coating on the granule, wherein the coating is present in an amount from about 30 to about 55 percent by weight of the coated granule, and wherein the coating consists essentially of ethylcellulose in an amount from about 10 to about 50 percent by weight of the coated granule, and magnesium stearate in an amount from about 10 to about 25 percent by weight of the coated granule; and wherein the matrix does not comprise a lipid.
  36. 36. A method of producing a tablet dosage form according to any of claims 1 to above comprising:
    (1) granulating metoprolol or a pharmaceutically acceptable salt or solvate thereof, a first strong film former, a second viscosity modifier and optionally a fat/wax in a granulator in the presence of alcohol (e.g. ethanol) followed by milling and drying;
    (2) coating the granules formed in step (1) above in a fluid bed using a second strong film former and an anti-adherent in an alcohol (e.g. ethanol) solvent;
    (3) mixing the coated granules formed in step (2) above with a first viscosity modifier and any excipients such as fillers, lubricants, coloring or flavoring agents to form a blend; and (4) compressing the blended mixture formed in step (3) using a conventional tablet press to form tablets.
  37. 37. A sustained-release oral dosage form for twice-a-day administration comprising:
    a matrix, wherein the matrix comprises a viscosity modifier in an amount from about 20 to about 60 percent by weight of the dosage form and wherein the C
    max changes less than about 50% when food is ingested with the dosage form compared to when food is not ingested with the dosage form; and coated granules comprising metoprolol or a salt form thereof.
  38. 38. The sustained-release oral dosage form of claim 37, wherein the coated granules comprise a coating comprising a fatty acid ester and wherein the dosage form is crush resistant.
  39. 39. The sustained-release oral dosage form of claim 37, wherein the matrix comprises less than 1% fat/wax on a weight basis.
CA2798702A 2010-05-11 2011-05-09 Alcoholresistant metoprolol-containing extended-release oral dosage forms Abandoned CA2798702A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US33353110P 2010-05-11 2010-05-11
US61/333,531 2010-05-11
PCT/US2011/035770 WO2011143120A1 (en) 2010-05-11 2011-05-09 Alcoholres i stant metoprolol - containing extended - release oral dosage forms

Publications (1)

Publication Number Publication Date
CA2798702A1 true CA2798702A1 (en) 2011-11-17

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CA2798702A Abandoned CA2798702A1 (en) 2010-05-11 2011-05-09 Alcoholresistant metoprolol-containing extended-release oral dosage forms

Country Status (6)

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US (1) US8927025B2 (en)
EP (1) EP2568977A1 (en)
JP (1) JP2013526523A (en)
CA (1) CA2798702A1 (en)
MX (1) MX2012012991A (en)
WO (1) WO2011143120A1 (en)

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