WO2012039789A1 - Fabrication de formes pharmaceutiques à densité variable utilisant l'énergie de radiofréquence - Google Patents

Fabrication de formes pharmaceutiques à densité variable utilisant l'énergie de radiofréquence Download PDF

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Publication number
WO2012039789A1
WO2012039789A1 PCT/US2011/029158 US2011029158W WO2012039789A1 WO 2012039789 A1 WO2012039789 A1 WO 2012039789A1 US 2011029158 W US2011029158 W US 2011029158W WO 2012039789 A1 WO2012039789 A1 WO 2012039789A1
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WO
WIPO (PCT)
Prior art keywords
tablet
forming
dosage form
electrode
energy
Prior art date
Application number
PCT/US2011/029158
Other languages
English (en)
Inventor
Christopher E. Szymczak
Frank J. Bunick
Harry S. Sowden
Joseph R. Luber
Leo B. Kriksunov
Original Assignee
Mcneil-Ppc, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US12/887,544 external-priority patent/US8871263B2/en
Priority to AU2011306064A priority Critical patent/AU2011306064B2/en
Priority to RU2013118328/02A priority patent/RU2013118328A/ru
Priority to BR112013006522A priority patent/BR112013006522A2/pt
Priority to EP11710980.1A priority patent/EP2618995A1/fr
Priority to KR1020137009864A priority patent/KR20130136464A/ko
Application filed by Mcneil-Ppc, Inc. filed Critical Mcneil-Ppc, Inc.
Priority to MX2013003287A priority patent/MX343047B/es
Priority to CN201180045941.1A priority patent/CN103140346B/zh
Priority to CA2810623A priority patent/CA2810623A1/fr
Priority claimed from US13/052,219 external-priority patent/US8858210B2/en
Publication of WO2012039789A1 publication Critical patent/WO2012039789A1/fr
Priority to HK13111498.9A priority patent/HK1184111A1/zh

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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
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
    • 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
    • A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
    • A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
    • 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
    • A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B30—PRESSES
    • B30B—PRESSES IN GENERAL
    • B30B11/00—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses
    • B30B11/02—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space
    • B30B11/027—Particular press methods or systems
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B30—PRESSES
    • B30B—PRESSES IN GENERAL
    • B30B11/00—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses
    • B30B11/02—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space
    • B30B11/08—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space co-operating with moulds carried by a turntable
    • B30B11/085—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space co-operating with moulds carried by a turntable for multi-layer articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B30—PRESSES
    • B30B—PRESSES IN GENERAL
    • B30B11/00—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses
    • B30B11/02—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space
    • B30B11/08—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space co-operating with moulds carried by a turntable
    • B30B11/10—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses using a ram exerting pressure on the material in a moulding space co-operating with moulds carried by a turntable intermittently rotated
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B30—PRESSES
    • B30B—PRESSES IN GENERAL
    • B30B15/00—Details of, or accessories for, presses; Auxiliary measures in connection with pressing
    • B30B15/34—Heating or cooling presses or parts thereof

Definitions

  • Pharmaceuticals intended for oral administration are typically provided in tablet form. Tablets are swallowed whole, chewed in the mouth, or disintegrated in the oral cavity. Soft tablets that either are chewed or dissolve in the mouth are often employed in the administration of pharmaceuticals where it is impractical to provide a tablet for swallowing whole. With chewable tablets, the act of chewing helps to break up the tablet particles as the tablet disintegrates and may increase the rate of absorption by the digestive tract. Soft tablets are also advantageous where it is desirable to make a pharmaceutically active agent available topically in the mouth or throat for both local effects and/or systemic absorption. Soft tablets are also utilized to improve drug administration in pediatric and geriatric patients. Soft tablets designed to disintegrate in the mouth prior to swallowing are particularly useful for improving compliance of pediatric patients.
  • soft tablets are made by compaction of a blend of powdered ingredients and typically include a pharmaceutically active agent, flavoring, and/or binders.
  • the powder blend is typically fed into the cavity of a die of a tablet press and a tablet is formed by applying pressure. Hardness of the resulting tablet is a direct function of the compaction pressure employed and the compatibility of the ingredients in the formulation.
  • a softer tablet, having an easier bite-through, may be prepared by employing reduced compaction pressures.
  • the resulting tablet is softer, but also more fragile, brittle, and easily chipped and disadvantageously can involve complex and costly processing steps. Examples of soft tablets designed to disintegrate in the mouth without chewing are disclosed in U.S. Patent Nos. 5,464,632, 5,223,264, 5,178,878, 6,589,554, and 6,224,905.
  • the present invention relates to the discovery of a machine and a process for making dosage forms, such as chewable or orally
  • the present invention relates to the discovery of the manufacture of such a dosage form having varying levels of hardness and thickness, thereby able to deliver a unique consumer experience Summary of the Invention
  • the present invention features a machine for the production of a solid dosage form (e.g., a tablet) including: (a) a die platen having one or more forming cavities each having an inner wall, a first opening at the surface of one side of the die platen, and a second opening at the surface on the opposite side of the die platen; (b) one or more first forming tools each adapted to move into one of the forming cavities through the first opening of the forming cavity; (c) one or more second forming tools each adapted to move adjacent to one of the second openings or into one of the forming cavities through the second opening of the forming cavity; (d) at least one first RF electrode operably associated with the one or more first forming tools, the one or more second forming tools, or the inner wall of the one or more forming cavities; and (e) at least one second RF electrode operably associated with the one or more first forming tools, the one or more second forming tools, or the inner wall of the one or more forming cavities; wherein the machine
  • solid dosage forms include tablets (e.g., swallowable, chewable, and orally disintegrating tablets), gums, and lozenges.
  • the present invention also features a method of making a dosage form using such a machine by: (a) adding a powder blend to a forming cavity; (b) moving a first forming tool into the forming cavity through the first opening of the forming cavity such that the powder blend is formed into the shape of the dosage form within the forming cavity between the first forming tool and a second forming tool; (c) conducting RF energy between the first electrode and the second electrode such that the energy heats the powder blend within the forming cavity to form the dosage form; and (d) removing the dosage form from the forming cavity.
  • the present invention features a machine for the production of a solid dosage form, the machine including: (a) a die platen having one or more forming cavities each having an inner wall, a first opening at the surface of one side of the die platen, and a second opening at the surface on the opposite side of the die platen; (b) one or more first forming tools having a dosage form contacting first surface, each of the one or more first forming tools adapted to move into one of the cavities through the first opening of the forming cavity; (c) one or more second forming tools having a dosage form contacting second surface, each of the one or more second forming tools adapted to move into one of the cavities through the second opening of the forming cavity; (d) at least one first RF electrode operably associated with the one or more first forming tools, the one or more second forming tools, or the inner wall of the one or more forming cavities; and (e) at least one second RF electrode operably associated with the one or more first forming tools, the one or more second forming tools
  • the present invention features a method of making a solid dosage form using such a machine, the method including the steps of: (a) adding a powder blend to a forming cavity; (b) moving a first forming tool into the forming cavity through the first opening of the forming cavity such that the powder blend is formed into the shape of the dosage form within the forming cavity between the dosage form contacting first surface and the dosage form contacting second surface; (c) conducting RF energy between the first electrode and the second electrode such that the energy heats the powder blend within the forming cavity to form the dosage form; and (d) removing the dosage form from the forming cavity.
  • the present invention features a tablet including at least one pharmaceutically active ingredient, wherein the shape of said tablet includes at least one major face wherein: (i) the peak penetration resistance at the perimeter of said major face of the tablet is at least about 10% greater than the peak penetration resistance at the center of said major face; and (ii) the tablet disintegrates in the mouth when placed on the tongue in less than about 30 seconds.
  • the present invention features a tablet including at least one pharmaceutically active ingredient, wherein the shape of said tablet includes at least one major face wherein: (i) the peak penetration resistance at the center of said major face is less than 250 grams and (ii) the tablet disintegrates in the mouth when placed on the tongue in less than about 30 seconds.
  • FIGS. 1 A-F are cross-section, side views of an embodiment of the invention showing the manufacture of tablet 4a from powder blend 4 within die platen 2.
  • FIGS. 2A-H are cross-section, side views of an embodiment of the invention showing the manufacture of a bilayer tabletl2 from powder blends 10 and 1 1 within die platen 2.
  • FIGS. 3A-G are cross-section, side views of an embodiment of the invention showing the manufacture of tablet 40 containing preformed inserts 30 and 31 from powder blend 20 within die platen 2.
  • FIGS. 4A and 4B are a perspective view of a rotary indexing machine 195.
  • FIGS. 5 A and 5B are top views of the rotary indexing machine 195 in the dwell position.
  • FIGS. 6A and 6B are section views of the lower forming tool assemblyl 10 in the start position of the manufacturing cycle.
  • FIG. 7 is a section view through the RF station rotary indexing machine 195 prior to compacting powder blend 101.
  • FIG. 8 is a section view through the RF station rotary indexing machine 195 prior showing the manufacture of tablets 101a.
  • FIG. 9 is a section view through tablet ejection station 160 before tablets 101a have been ejected.
  • FIG. 10 is a section view through tablet ejection station 160 after tablets 101 a have been ejected into blister 190.
  • FIGS. 1 1 A-F are cross sections of alternate embodiments of forming tools and the die platen.
  • FIGS. 12A-D are cross sections of alternate embodiments of forming tools and the die platen.
  • FIG. 13A is a cross section of forming tools having a wave-shaped surface.
  • FIG. 13B is a perspective view of forming tools having a wave-shaped surface.
  • FIG. 14 is a cross section of forming tools having protrusions at the surface.
  • FIG. 15 A is a cross section of forming tools having a contacting surface that are movable.
  • FIG. 15B is a perspective of forming tools having a contacting surface that are movable and the resulting tablet having a major face with various average peak penetration resistances.
  • FIG. 16 is a cross section of forming tools that contain a spring.
  • the present invention features a method of making a dosage form using such a machine by: (a) adding a powder blend to a forming cavity; (b) moving a first forming tool into the forming cavity through the first opening of the forming cavity such that the powder blend is formed into the shape of the dosage form within the forming cavity between the first forming tool and a second forming tool; (c) conducting RF energy between the first electrode and the second electrode such that the energy heats the powder blend within the forming cavity to form the dosage form; and (d) removing the dosage form from the forming cavity. While the specific embodiments herein focus on tablets, other dosage forms such as lozenges and chewing gums can also be made by such machine and process.
  • the tablet is manufactured by compacting a powder blend containing a pharmaceutically active agent (as discussed herein), a meltable binder (as discussed herein), and optionally a pharmaceutically-acceptable carrier.
  • the carrier contains one or more suitable excipients for the formulation of tablets.
  • suitable excipients include, but are not limited to, fillers, adsorbents, disintegrants, lubricants, glidants, sweeteners, superdisintegrants, flavor and aroma agents, antioxidants, preservatives, texture enhancers, and mixtures thereof.
  • suitable excipients include, but are not limited to, fillers, adsorbents, disintegrants, lubricants, glidants, sweeteners, superdisintegrants, flavor and aroma agents, antioxidants, preservatives, texture enhancers, and mixtures thereof.
  • One or more of the above ingredients may be present on the same particle of the powder blend.
  • Suitable fillers include, but are not limited to, carbohydrates (as discussed herein) and water insoluble plastically deforming materials (e.g., microcrystalline cellulose or other cellulosic derivatives), and mixtures thereof.
  • Suitable adsorbents include, but are not limited to, water-insoluble adsorbents such as dicalcium phosphate, tricalcium phosphate, silicified microcrystalline cellulose (e.g., such as distributed under the PROSOLV brand (Pen West Pharmaceuticals, Patterson, NY)), magnesium aluminometasilicate (e.g., such as distributed under the NEUSILIN brand (Fuji Chemical Industries (USA) Inc., Robbinsville, NJ)), clays, silicas, bentonite, zeolites, magnesium silicates, hydrotalcite, veegum, and mixtures thereof.
  • water-insoluble adsorbents such as dicalcium phosphate, tricalcium phosphate, silicified microcrystalline cellulose (e.g., such as distributed under the PROSOLV brand (Pen West Pharmaceuticals, Patterson, NY)), magnesium aluminometasilicate (e.g., such as distributed under the NEUSILIN brand (Fu
  • Suitable disintegrants include, but are not limited to, sodium starch glycolate, cross-linked polyvinylpyrrolidone, cross-linked carboxymethylcellulose, starches, microcrystalline cellulose, and mixtures thereof.
  • Suitable lubricants include, but are not limited to, long chain fatty acids and their salts, such as magnesium stearate and stearic acid, talc, glycerides waxes, and mixtures thereof.
  • Suitable glidants include, but are not limited to, colloidal silicon dioxide.
  • sweeteners include, but are not limited to, synthetic or natural sugars; artificial sweeteners such as saccharin, sodium saccharin, aspartame, acesulfame, thaumatin, glycyrrhizin, sucralose, dihydrochalcone, alitame, miraculin, monellin, and stevside; sugar alcohols such as sorbitol, mannitol, glycerol, lactitol, maltitol, and xylitol; sugars extracted from sugar cane and sugar beet (sucrose), dextrose (also called glucose), fructose (also called laevulose), and lactose (also called milk sugar); isomalt, salts thereof, and mixtures thereof.
  • artificial sweeteners such as saccharin, sodium saccharin, aspartame, acesulfame, thaumatin, glycyrrhizin, sucralose, dihydr
  • superdisintegrants include, but are not limited to, croscarmellose sodium, sodium starch glycolate and cross-linked povidone (crospovidone).
  • the tablet contains up to about 5% by weight of such superdisintegrant.
  • flavors and aromatics include, but are not limited to, essential oils including distillations, solvent extractions, or cold expressions of chopped flowers, leaves, peel or pulped whole fruit containing mixtures of alcohols, esters, aldehydes and lactones; essences including either diluted solutions of essential oils, or mixtures of synthetic chemicals blended to match the natural flavor of the fruit (e.g., strawberry, raspberry and black currant); artificial and natural flavors of brews and liquors, e.g., cognac, whisky, rum, gin, sherry, port, and wine; tobacco, coffee, tea, cocoa, and mint; fruit juices including expelled juice from washed, scrubbed fruits such as lemon, orange, and lime; spear mint, pepper mint, wintergreen, cinnamon, cacoe/cocoa, vanilla, liquorice, menthol, eucalyptus, aniseeds nuts (e.g., peanuts, coconuts, hazelnuts, chestnuts, walnuts, colanuts), almonds, raisins; and
  • antioxidants include, but are not limited to, tocopherols, ascorbic acid, sodium pyrosulfite, butylhydroxytoluene, butylated hydroxyanisole, edetic acid, and edetate salts, and mixtures thereof.
  • preservatives include, but are not limited to, citric acid, tartaric acid, lactic acid, malic acid, acetic acid, benzoic acid, and sorbic acid, and mixtures thereof.
  • texture enhancers include, but are not limited to, pectin, polyethylene oxide, and carrageenan, and mixtures thereof. In one embodiment, texture enhancers are used at levels of from about 0.1% to about 10% percent by weight.
  • the powder blend has an average particle size of less than 500 microns, such as from about 50 microns to about 500 microns, such as from about 50 microns and 300 microns. Particles in this size range are particularly useful for direct compacting processes.
  • the tablet may be a made from a powder blend that is substantially free of hydrated polymers.
  • substantially free is less than 5%, such as less than 1%, such as less than 0.1%, such as completely free (e.g., 0%).
  • Such a composition is advantageous for maintaining an immediate release dissolution profile, minimizing processing and material costs, and providing for optimal physical and chemical stability of the tablet.
  • powder blend/ tablet is substantially free of directly compressible water insoluble fillers.
  • Water insoluble fillers include but are not limited to microcrystalline cellulose, directly compressible microcrystalline cellulose, celluloses, water insoluble celluloses, starch, cornstarch and modified starches. As described in this embodiment, substantially free is less than 2 percent, e.g. less than 1 percent or none.
  • the powder blend/tablet of the present invention includes at least one meltable binder.
  • the meltable binder has a melting point of from about 40 °C to about 140 °C, such as from about 55 °C to about 100 °C.
  • the softening or melting of the meltable binder(s) results in the sintering of the tablet shape through the binding of the softened or melted binder with the pharmaceutically active agent and/or other ingredients within the compacted powder blend.
  • the meltable binder is a RF-meltable binder.
  • an RF-meltable binder is a solid binder that can be softened or melted upon exposure to RF energy.
  • the RF-meltable binder typically is polar and has the capability to re- harden or resolidify upon cooling.
  • the meltable binder is not a RF-meltable binder.
  • the powder blend contains an excipient that heats upon exposure to RF energy (e.g., a polar excipient), such that the resulting heat from is able to soften or melt the meltable binder.
  • excipients include, but are not limited to, polar liquids such as water and glycerin; powdered metals and metal salts such as powdered iron, sodium chloride, aluminum hydroxide, and magnesium hydroxide; stearic acid; maltodextrin and sodium stearate.
  • meltable binders include amorphous carbohydrate polymers.
  • amorphous carbohydrate polymer is a molecule having a plurality of carbohydrate monomers wherein such molecule has a crystallinity of less than 20%, such as less than 10%, such as less than 5%.
  • amorphous carbohydrate polymers include, but are not limited to hydrogenated starch hydrosolate, polydextrose, and oligosaccharides.
  • oligosaccharides include, but are not limited to, fructo-oligosaccharide, galacto-oligosaccharide malto-oligosaccharide, inulin, and isolmalto-oligosaccharide
  • meltable binders examples include: fats such as cocoa butter, hydrogenated vegetable oil such as palm kernel oil, cottonseed oil, sunflower oil, and soybean oil; mono, di, and triglycerides; phospholipids; cetyl alcohol; waxes such as Carnauba wax, spermaceti wax, beeswax, candelilla wax, shellac wax, microcrystalline wax, and paraffin wax; water soluble polymers such as polyethylene glycol,
  • polycaprolactone polycaprolactone, GlycoWax-932, lauroyl macrogol-32 glycerides, and stearoyl macrogol-32 glycerides; polyethylene oxides; and sucrose esters.
  • the meltable binder is a RF-meltable binder
  • the RF- meltable binder is a polyethylene glycol (PEG), such as PEG-4000.
  • PEG polyethylene glycol
  • a particularly preferred RF-meltable binder is PEG having at least 95% by weight of the PEG particles less than 100 microns (as measured by conventional means such as light or laser scattering or sieve analysis) and a molecular weight between 3000 and 8000 Daltons.
  • the meltable binder(s) may be present at level of about 0.01 percent to about 70 percent of the powder blend/tablet, such as from about 1 percent to about 50 percent, such as from about 10 percent to about 30 percent of the powder blend/tablet.
  • the average particle size of the binder is less than 250 microns, such as less than 100 microns.
  • the powder blend contains at least one carbohydrate.
  • the carbohydrate can contribute to the dissolvability and mouth feel of the tablet, aid in distributing the meltable binder across a broader surface area, and diluting and cushioning the pharmaceutically active agent.
  • carbohydrates include, but are not limited to, water-soluble compressible carbohydrates such as sugars (e.g., dextrose, sucrose, maltose, isomalt, and lactose), starches (e.g., corn starch), sugar-alcohols (e.g., mannitol, sorbitol, maltitol, erythritol, lactitol, and xylitol), and starch hydrolysates (e.g., dextrins, and maltodextrins).
  • sugars e.g., dextrose, sucrose, maltose, isomalt, and lactose
  • starches e.g., corn starch
  • the carbohydrate(s) may be present at level of about 5 percent to about 95 percent of the powder blend/tablet, such as from about 20 percent to about 90 percent or from about 40 percent to about 80 percent of the powder blend/tablet.
  • the particle size of the of carbohydrate can influence the level of meltable binder used, wherein a higher particle size of carbohydrate provides a lower surface area and subsequently requires a lower level of meltable binder. In one embodiment, wherein the carbohydrate(s) is greater than 50% by weight of the powder blend and the mean particle size of the carbohydrate(s) is greater than 100 microns, then the meltable binder is from about 10 to about 30 percent by weight of the powder blend/tablet.
  • the powder blend/tablet of the present invention includes at least one
  • a pharmaceutically active agent is an agent (e.g., a compound) that is permitted or approved by the U.S. Food and Drug Administration, European Medicines Agency, or any successor entity thereof, for the oral treatment of a condition or disease.
  • Suitable pharmaceutically active agents include, but are not limited to, analgesics, anti-inflammatory agents, antipyretics, antihistamines, antibiotics (e.g., antibacterial, antiviral, and antifungal agents), antidepressants, antidiabetic agents, antispasmodics, appetite suppressants, bronchodilators,
  • cardiovascular treating agents e.g., statins
  • central nervous system treating agents e.g., cough suppressants, decongestants, diuretics, expectorants, gastrointestinal treating agents, anesthetics, mucolytics, muscle relaxants, osteoporosis treating agents, stimulants, nicotine, and sedatives.
  • suitable gastrointestinal treating agents include, but are not limited to: antacids such as aluminum-containing pharmaceutically active agents (e.g., aluminum carbonate, aluminum hydroxide, dihydroxyaluminum sodium carbonate, and aluminum phosphate), bicarbonate-containing pharmaceutically active agents, bismuth- containing pharmaceutically active agents (e.g., bismuth aluminate, bismuth carbonate, bismuth subcarbonate, bismuth subgallate, and bismuth subnitrate), calcium-containing pharmaceutically active agents (e.g., calcium carbonate), glycine, magnesium-containing pharmaceutically active agents (e.g., magaldrate, magnesium aluminosilicates, magnesium carbonate, magnesium glycinate, magnesium hydroxide, magnesium oxide, and magnesium trisilicate), phosphate-containing pharmaceutically active agents (e.g., aluminum phosphate and calcium phosphate), potassium-containing pharmaceutically active agents (e.g., potassium bicarbonate), sodium-containing pharmaceutically active agents (e.g.,
  • gastrointestinal cytoprotectives such as sucraflate and misoprostol
  • gastrointestinal prokinetics such as prucalopride; antibiotics for H. pylori, such as clarithromycin, amoxicillin, tetracycline, and metronidazole; antidiarrheals, such as bismuth subsalicylate, kaolin, diphenoxylate, and loperamide; glycopyrrolate; analgesics, such as mesalamine; antiemetics such as ondansetron, cyclizine, diphenyhydroamine, dimenhydrinate, meclizine, promethazine, and hydroxyzine; probiotic bacteria including but not limited to lactobacilli; lactase; racecadotril; and antiflatulents such as
  • polydimethylsiloxanes e.g., dimethicone and simethicone, including those disclosed in United States Patent Nos. 4,906,478, 5,275,822, and 6,103,260
  • isomers thereof e.g., isomers thereof
  • pharmaceutically acceptable salts and prodrugs e.g., esters
  • antihistamines and decongestants include, but are not limited to, bromopheniramine, chlorcyclizine, dexbrompheniramine, bromhexane, phenindamine, pheniramine, pyrilamine, thonzylamine, pripolidine, ephedrine, phenylephrine, pseudoephedrine, phenylpropanolamine, chlorpheniramine, dextromethorphan, diphenhydramine, doxylamine, astemizole, terfenadine, fexofenadine, naphazoline, oxymetazoline, montelukast, propylhexadrine, triprolidine, clemastine, acrivastine, promethazine, oxomemazine, mequitazine, buclizine, bromhexine, ketotifen, terfenadine, ebastine, oxatamide,
  • cough suppressants and expectorants include, but are not limited to, diphenhydramine, dextromethorphan, noscapine, clophedianol, menthol, benzonatate, ethylmorphone, codeine, acetylcysteine, carbocisteine, ambroxol, belladona alkaloids, sobrenol, guaiacol, and guaifenesin; isomers thereof; and pharmaceutically acceptable salts and prodrugs thereof.
  • muscle relaxants include, but are not limited to, cyclobenzaprine and chlorzoxazone metaxalone, orphenadrine, and methocarbamol; isomers thereof; and pharmaceutically acceptable salts and prodrugs thereof.
  • appetite suppressants include, but are not limited to,
  • anesthetics include, but are not limited to dyclonine, benzocaine, and pectin and pharmaceutically acceptable salts and prodrugs thereof.
  • statins include but are not limited to atorvastin, rosuvastatin, fluvastatin, lovastatin, simvustatin, atorvastatin, pravastatin and pharmaceutically acceptable salts and prodrugs thereof.
  • the pharmaceutically active agent included within the tablet is selected from phenylephrine, dextromethorphan, pseudoephedrine, acetaminophen, cetirizine, aspirin, nicotine, ranitidine, ibuprofen, ketoprofen, loperamide, famotidine, calcium carbonate, simethicone, chlorpheniramine, methocarbomal, chlophedianol, ascorbic acid, pectin, dyclonine, benzocaine and menthol, and pharmaceutically acceptable salts and prodrugs thereof.
  • the pharmaceutically active agents of the present invention may also be present in the form of pharmaceutically acceptable salts, such as acidic/anionic or basic/cationic salts.
  • Pharmaceutically acceptable acidic/anionic salts include, and are not limited to acetate, benzenesulfonate, benzoate, bicarbonate, bitartrate, bromide, calcium edetate, camsylate, carbonate, chloride, citrate,
  • dihydrochloride edetate, edisylate, estolate, esylate, fumarate, glyceptate, gluconate, glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, pamoate, pantothenate, phosphate/diphospate, polygalacturonate, salicylate, stearate, subacetate, succinate, sulfate, tannate, tartrate, teoclate, tosylate and triethiodide.
  • Pharmaceutically acceptable basic/cationic salts include, and are not limited to
  • ethylenediamine lithium, magnesium, meglumine, potassium, procaine, sodium and zinc.
  • the pharmaceutically active agents of the present invention may also be present in the form of prodrugs of the pharmaceutically active agents.
  • prodrugs will be functional derivatives of the pharmaceutically active agent, which are readily convertible in vivo into the required pharmaceutically active agent.
  • Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in "Design of Prodrugs", ed. H. Bundgaard, Elsevier, 1985.
  • the invention provides the esters, amides, and other protected or derivatized forms of the described compounds.
  • the pharmaceutically active agents according to this invention may accordingly exist as enantiomers. Where the pharmaceutically active agents possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention. Furthermore, some of the crystalline forms for the pharmaceutically active agents may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the pharmaceutically active agents may form solvates with water (e.g., hydrates) or common organic solvents, and such solvates are also intended to be encompassed within the scope of this invention.
  • the pharmaceutically active agent or agents are present in the tablet in a therapeutically effective amount, which is an amount that produces the desired therapeutic response upon oral administration and can be readily determined by one skilled in the art. In determining such amounts, the particular pharmaceutically active agent being administered, the bioavailability characteristics of the pharmaceutically active agent, the dose regime, the age and weight of the patient, and other factors must be considered, as known in the art.
  • the pharmaceutically active agent may be present in various forms.
  • the pharmaceutically active agent may be dispersed at the molecular level, e.g. melted, within the tablet, or may be in the form of particles, which in turn may be coated or uncoated.
  • the particles typically have an average particle size of from about 1 to about 2000 microns.
  • such particles are crystals having an average particle size of from about 1 to about 300 microns.
  • the particles are granules or pellets having an average particle size of from about 50 to about 2000 microns, such as from about 50 to about 1000 microns, such as from about 100 to about 800 microns.
  • the pharmaceutically active agent may be present in pure crystal form or in a granulated form prior to the addition of the taste masking coating.
  • Granulation techniques may be used to improve the flow characteristics or particle size of the pharmaceutically active agents to make it more suitable for compaction or subsequent coating.
  • Suitable binders for making the granulation include but are not limited to starch, polyvinylpyrrolidone, polymethacrylates, hydroxypropylmethylcellulose, and hydroxypropylcellulose.
  • the particles including pharmaceutically active agent(s) may be made by cogranulating the pharmaceutically active agent(s) with suitable substrate particles via any of the granulation methods known in the art. Examples of such granulation method include, but are not limited to, high sheer wet granulation and fluid bed granulation such as rotary fluid bed granulation.
  • the pharmaceutically active agent has an objectionable taste
  • pharmaceutically active agent may be coated with a taste masking coating, as known in the art.
  • suitable taste masking coatings are described in U.S. Patent No. 4,851,226, U.S. Patent No. 5,075,1 14, and U.S. Patent No. 5,489,436.
  • Commercially available taste masked pharmaceutically active agents may also be employed.
  • acetaminophen particles which are encapsulated with ethylcellulose or other polymers by a coacervation process, may be used in the present invention.
  • Coacervation- encapsulated acetaminophen may be purchased commercially from Eurand America, Inc. (Vandalia, Ohio) or from Circa Inc. (Dayton, Ohio).
  • swellable, erodible hydrophilic materials for use as a release modifying excipient for use in the modified release coating include water swellable cellulose derivatives, polyalkylene glycols, thermoplastic polyalkylene oxides, acrylic polymers, hydrocolloids, clays, and gelling starches.
  • water swellable cellulose derivatives include sodium carboxymethylcellulose, cross-linked
  • EUDRAGIT S and poly(methacrylic acid, methyl methacrylate) 1 : 1 (available from Rohm Pharma GmbH under the tradename EUDRAGIT L).
  • USP 24 specifies that in pH 5.8 phosphate buffer, using USP apparatus 2 (paddles) at 50 rpm, at least 80% of the acetaminophen contained in the tablet is released there from within 30 minutes after dosing, and for ibuprofen tablets, USP 24 specifies that in pH 7.2 phosphate buffer, using USP apparatus 2 (paddles) at 50 rpm, at least 80% of the ibuprofen contained in the tablet is released there from within 60 minutes after dosing. See USP 24, 2000 Version, 19 - 20 and 856 (1999).
  • the dissolution characteristics of the pharmaceutically active agent are modified: e.g. controlled, sustained, extended, retarded, prolonged, delayed and the like.
  • the particle size of the pharmaceutically active agent causes more void spaces to be present in the tablet, wherein a higher particle size of the pharmaceutically active agent subsequently requires a lower level of meltable binder.
  • the pharmaceutically active agent or coated pharmaceutically active agent(s) is greater than 50% of the blend by weight of the powder blend/tablet and the mean particle size of the carbohydrate is greater than 100 microns
  • the meltable binder is from about 10 to about 30 percent by weight of the powder blend/tablet.
  • meltable binder is from about 10 to about 20 percent by weight of the powder blend/tablet.
  • the meltable binder is heated from about 30°C to about 60 °C.
  • the pharmaceutically active agent is the meltable binder.
  • the pharmaceutically active agent is in the form of a particle that is coated with the meltable binder.
  • the susceptibility to RF energy of the pharmaceutically active agent can have an impact on the type of energy and/or temperature used during the heating step as well as the type of the meltable binder used.
  • the processing of the tablet is free of a wet or hot melt granulation step.
  • the materials are directly blended prior to the addition of heat.
  • the materials are directly blended and compressed prior to the addition of heat.
  • the powder blend is fed into the tablet die of an apparatus that applies pressure to form the tablet shape (e.g., by light compaction such as tamping).
  • Any suitable compacting apparatus may be used, including, but not limited to, a conventional unitary or rotary tablet press.
  • the tablet shape may be formed by compaction using a rotary tablet press (e.g., such as those commercially available from Fette America Inc., Rockaway, NJ. or Manesty Machines LTD,
  • the tablet shape is heated after it is removed from the tablet press. In another embodiment, the tablet shape is heated within the tablet press.
  • the tablet's construction may be highly porous, use a minimal amount of binder, and/or have a low density. Such tablets, therefore, are somewhat fragile and soft.
  • a minimum of tamping/compaction force is desired to achieve the orally disintegrating property (low density).
  • the heat source and the heat sink are two distinct machines or steps requiring material to be transferred from one apparatus to the other.
  • the energy must be added to the tablet to achieve the binding effect and then must be removed from the product to solidify and strengthen it for its final handling packaging and use.
  • One of the unique and unanticipated attributes of one embodiment of the manufacturing process of the present invention is that heat source and heat sink are part of the same apparatus.
  • the metallic forming tool e.g., a die punch
  • the metallic forming tool which was at room temperature removed so much heat from the treated tablet shape (due to its high thermal conductivity) that the surface of the resulting tablet was unacceptable due to the fact that uniform melting within the powder blend had not taken place.
  • the compaction step (e.g., tamping) which occurs prior to the addition of the RF energy utilizes a compaction force which is less than the force required to compress a chewable or swallowable tablet.
  • the compaction force is less than about 1000 pounds per square inch (e.g., less than about 500 pounds per square inch, such as less than 200 pounds per square inch, such as less than 50 pounds per square inch).
  • the energy is applied while the powder blend is under such force.
  • the compaction step occurs in an indexed manner, where one set of tablets are compacted simultaneously, before rotating to another indexing station.
  • the compaction step occurs at a single indexing station and the application of RF energy occurs at a separate indexing station.
  • a third indexing station is present wherein the ejection of the tablet or multiple tablets occurs, wherein the lower forming tool is raised up through and up to the surface of the die.
  • the compaction step is performed through the addition of air pressure or hydraulic cylinder to the top of the upper forming tools.
  • multiple tablets are ejected simultaneously and separated from the surface of the indexing station and removed via a take-off bar.
  • the tablet shape may be prepared by the compaction methods and apparatus described in United States Patent Application Publication No. 20040156902.
  • the tablet shape may be made using a rotary compression module including a fill zone, insertion zone, compression zone, ejection zone, and purge zone in a single apparatus having a double row die construction.
  • the dies of the compression module may then be filled using the assistance of a vacuum, with filters located in or near each die.
  • the purge zone of the compression module includes an optional powder blend recovery system to recover excess powder blend from the filters and return the powder blend to the dies.
  • the RF energy source is projected through the die table of a rotary press into the appropriate electrode within the forming tool or the forming cavity.
  • the die table is constructed of non-conductive material.
  • a portion of the tablet shape may be prepared by a wet- granulation method, in which the excipients and a solution or dispersion of a wet binder (e.g., an aqueous cooked starch paste or solution of polyvinyl pyrrolidone) are mixed and granulated.
  • a wet binder e.g., an aqueous cooked starch paste or solution of polyvinyl pyrrolidone
  • Suitable apparatus for wet granulation include low shear mixers (e.g., planetary mixers), high shear mixers, and fluid beds (including rotary fluid beds).
  • the resulting granulated material may then be dried, and optionally dry-blended with further ingredients (e.g., excipients such as, for example, the meltable binder described in the invention herein, lubricants, colorants, and the like).
  • the final dry blend is then suitable for compaction by the methods described herein. Methods for direct compaction and wet
  • the tablet shape is prepared by the compaction methods and apparatus described in issued U.S. Patent No. 6,767,200. Specifically, the tablet shape is made using a rotary compression module including a fill zone, compression zone, and ejection zone in a single apparatus having a double row die construction as shown in FIG. 6 therein.
  • the dies of the compression module are preferably filled using the assistance of a vacuum, with filters located in or near each die.
  • FIGS. 3A - 3G show another embodiment of the invention where preformed inserts 30 and 31 are inserted into tablet shape 20a as shown in FIGS. 3A - 3D.
  • Forming tools 1 and 3, die platen 2, tablet shape 20, and preformed inserts 30 and 31 are then moved to the compaction and RF heating station as shown in FIG 3E.
  • RF heating is accomplished as described above in FIG. 1C to produce a multi-component tablet 40 shown in FIGS. 2F and 2G.
  • FIGS. 4A and 4B show two views of a rotary indexing machine 195 which is designed to create large quantities of tablets.
  • the configuration of the apparatus shown is designed to manufacture fragile tablets with minimized risk of damaging them as they are moved through the various manufacturing steps.
  • This embodiment of the invention is comprised of an indexing table 170 having four sets of die platens 175 each having sixteen cavities, powder feeder 100, RF generator 150, a machine frame 140, moving RF electrode assemblies 120 and 130, lower forming tool assembly 1 10, upper forming tool assembly 210, tablet ejection station 160, indexer drive system 180, blister package web 190, and blister lid material roll 191.
  • Figure 5A is a top view of the apparatus in the dwell position.
  • Figure 5B is a top view of the apparatus as the indexing table 170 rotates between stations in direction "A".
  • Figure 6A depicts a section view through the lower forming tool assembly 110 in a start position of the manufacturing cycle.
  • the lower forming tools 1 1 which are made of an electrically conductive metallic material such as brass or stainless steel, are retained in retainer plate 1 12 (e.g., made of aluminum or steel).
  • Heated block 1 17 is attached to the retainer plate 1 12 and contains fluid passages 117b. Heated (or optionally cooling) fluid is circulated through the heated block 1 17 by connections to flexible hoses 1 19a and 1 19b which form a supply and return circuit.
  • Figure 6B depicts a section through the powder feeder station 100 of the apparatus.
  • powdered powder blend 101 is gravity fed into die platen 171.
  • Movable cam segment 118 is adjusted up or down in direction "B" to vary the volume of the forming cavity 171a by changing the amount that the lower forming tools 1 1 1 penetrate into the die platen 171.
  • This adjustable volume feature enables the precise dose of powdered powder blend to be selected for a desired tablet weight.
  • the rim of feeder 102 scrapes against the die platen 171 to create a level powder surface relative to the surface of the die platen 171.
  • a lower movable RF electrode 121 is shown, movable in direction "D". It is represented in its down position.
  • the linear movement is generated by linear actuators which are typically devises such as air cylinders or servo motors.
  • Two air cylinders are depicted in Figure 7.
  • Air cylinder bodies 141 and 142 apply pressure to guide rods 144 and 143.
  • Moving platens 132 and 122 are connected to the guide rods and provide an electrically isolated mounting for electrode plates 131 and 121.
  • RF generator 150 connects to the electrode plates 131 and 121 through wires 185 and 184.
  • a movable upper RF electrode assembly 130, movable in direction "C" is shown in its up position.
  • Upper forming tools 133, retainer plate 134, and heated block 135 are all attached to the movable RF electrode plate 131 and, consequently, move up and down with it.
  • Powder blend 101 is within die platen 171.
  • Figure 8 is a section through the same RF station but shows the RF electrodes 131 and 121 pressing against the respective forming tool assemblies 133 and 1 1 1 to both compact and apply RF energy to powder blend 101 creating tablet 101 a. After application of the RF energy is stopped, the moveable RF electrode plates retract, and the indexing plate 170, die platen 171, and lower forming tool assembly 1 10 are indexed to the next station.
  • Figure 10 is a section through the same assembly after the ejector pins 161 have pushed finished tablets 101a through the die platen 171. This direct placement of tablet into blister helps prevent breakage that could occur while using typical means such as feeders or by dumping tablets into transport drums.
  • the presence of a hydrophobic lubricant can disadvantageously compromise the disintegration or dissolution properties of a tablet.
  • the tablet is substantially free of a hydrophobic lubricant.
  • Hydrophobic lubricants include magnesium stearate, calcium stearate and aluminum stearate.
  • the RF energy is delivered while the tablet shape is being formed. In one embodiment, the RF energy is delivered once the tablet shape is formed. In one embodiment, the RF energy is delivered after the tablet shape has been removed from the die.
  • the RF energy is applied for a sufficient time to soften and melt substantially all (e.g., at least 90%, such as at least 95%, such as all) of the binder within the tablet shape. In one embodiment, the RF energy is applied for a sufficient time to soften and melt only a portion (e.g., less than 75%, such as less than 50%, such as less than 25%) of the binder within the tablet shape, for example only on a portion of the tablet shape, such as the outside of the tablet shape.
  • the forming tools can be constructed to achieve localized heating effects and can also be configured to shape the electric field that is developed across the tools.
  • Figure 1 1A shows one such configuration.
  • An RF generator 200 is connected to RF electrode plates 201 and 202.
  • Forming tools 205 and 204 are constructed of an electrically conductive material and they have an attachment 207 and 208 which are made of electrical and RF energy insulative material such as ceramic, Teflon®, polyethylene, or high density polyethylene.
  • Die platen 203 is also constructed of electrical and RF energy insulative material. This configuration creates greater distance between the conductive forming tools to weaken the electric field which is beneficial for producing thin tablets without the risk of an electric arc forming which would damage the product and tooling.
  • Figures 12B and 12C depict two embodiments where the die platen comprises a respective center portion 245 and 254 that are electrically conductive and respective outer portions 244/246 and 252/253 is are made of electrical and RF energy insulative material.
  • Figure 12B further includes insulating component 220 around the surface of lower forming tool 219.
  • Figure 12D is a further embodiment where the forming tools 263 and 262 are made of electrical and RF energy insulative material.
  • the die platen portions 264 and 265 are made of electrical and RF energy insulative material, but there are two respective electrically conductive portions 267 and 266 which are attached to the RF generator circuit 200. In this configuration, the electric field is applied in the horizontal direction across the tablet shape 206.
  • FIG. 13A and 13B depict such a configuration.
  • a wave-shaped forming tools 270 and 273 are shown to create a tablet 272 within die platen 271 with a unique appearance.
  • the profiles of the forming tool surfaces are equidistant as shown by dimension "X".
  • the tablet shape there is a single powder blend forming the tablet shape which is then heated with the RF energy.
  • the tablet is formed of at least two different powder blends, at least one powder blend being RF-curable and at least one formulation being not RF-curable. When cured with RF energy, such tablet shape develops two or more dissimilarly cured zones. In one embodiment, the outside area of the tablet shape is cured, while the middle of the tablet shape is not cured. By adjusting the focus of the RF heating and shape of the RF electrodes, the heat delivered to the tablet shape can be focused to create customized softer or harder areas on the finished tablet.
  • the RF energy is combined with a second source of heat including but not limited to infrared, induction, or convection heating.
  • a second source of heat including but not limited to infrared, induction, or convection heating.
  • the addition of the second source of heat is particularly useful with a secondary non-RF -meltable binder present in the powder blend.
  • the present invention features a tablet, wherein the shape of said tablet includes at least one major face (i.e., the largest side of the tablet) wherein the peak penetration resistance (described below) at the perimeter (i.e., at the edge) of said major face of the tablet is at least about 10% greater than the peak penetration resistance at the center of said major face.
  • a tablet is depicted in FIG. 15B, wherein tablet 300 has an upper major face 301, a lower major face 302, and a side 303.
  • upper major face 301 has two regions have different hardness (e.g., a measured by the average peak penetration resistance); namely perimeter region 304 (i.e., at the perimeter of the upper major face) and center region 305 (i.e., at the center of the upper major face).
  • perimeter region 304 i.e., at the perimeter of the upper major face
  • center region 305 i.e., at the center of the upper major face.
  • center region 305 is raised (e.g., thicker) as compared to perimeter region 304
  • such tablets having varying surface hardness may be manufactured but utilizing modified forming tools.
  • the machine includes: (a) a die platen having one or more forming cavities each having an inner wall, a first opening at the surface of one side of the die platen, and a second opening at the surface on the opposite side of the die platen; (b) one or more first forming tools having a dosage form contacting first surface, each of the one or more first forming tools adapted to move into one of the cavities through the first opening of the forming cavity; (c) one or more second forming tools having a dosage form contacting second surface, each of the one or more second forming tools adapted to move into one of the cavities through the second opening of the forming cavity; (d) at least one first RF electrode operably associated with the one or more first forming tools, the one or more second forming tools, or the inner wall of the one or more forming cavities; and (e) at least one second RF electrode operably associated with the one or more first forming tools
  • the present invention features a method of making a solid dosage form using such a machine, the method including the steps of: (a) adding a powder blend to a forming cavity; (b) moving a first forming tool into the forming cavity through the first opening of the forming cavity such that the powder blend is formed into the shape of the dosage form within the forming cavity between the dosage form contacting first surface and the dosage form contacting second surface; (c) conducting RF energy between the first electrode and the second electrode such that the energy heats the powder blend within the forming cavity to form the dosage form; and (d) removing the dosage form from the forming cavity.
  • upper forming tool 370 has an upper flexible dosage form contacting surface 391 and upper recess 381
  • lower forming tool 373 has a lower flexible dosage form contacting surface 390 and lower recess 380.
  • RF generator 200 are attached to RF electrode plates 20 land 202, and upper forming tool 370 and lower forming tool 273 are constructed if electrically conductive material.
  • Contacting surfaces 390 and 391 are made of flexible RF insulative material, such as Teflon®.
  • Die platen 271 is also constructed of electrical and RF insulative material.
  • powder blend 272 As powder blend 272 is heated with the RF energy from the RF electrode plates 201 and 202, the powder blend 272 expands and causes contacting surfaces 390 and 391 to respectively move (e.g., flex) into recesses 381 and 380. As a result, as depicted in
  • the major face 301 of tablet 300 has a raised center region 305, which also is less hard than perimeter region 304.
  • powder blend 272 expands against the movable pistons 402 and 405 overcoming the spring preload force and pushing the pistons back into the forming tool sleeves 401 and 406.
  • springs 403 and 407 depicted in this embodiment enable an automatic expansion feature, a similar effect can be accomplished by other non spring actuated means such as a by actuating the movable pistons by a cam, an air cylinder, or a servomotor or other similar mechanical means.
  • the thickness at the perimeter of the major face(s) of the tablet is greater than the thickness at the center of the tablet.
  • Such tablets with a raised parameter on the surface of the major face(s) can be made with forming tools depicted in Figures 1 IE and 1 IF.
  • an upper forming tool assembly and a lower forming tool assembly are respectively comprised of an outer forming tool sleeves 501 and 506, Teflon® plugs 502 and 505, and metal pins 503 and 507.
  • metal pins 503 and 507 assist in focusing energy to the center of the powder blend 272 within die platen 271.
  • metal pins 503 and 507 are removed, resulting in less RF energy being transferred to the tablet.
  • the thickness of the tablet at the center region of the major face is different than the thickness at the perimeter of the major face (e.g., thicker or thinner). In one embodiment, there are two major faces of the tablet wherein only one center region is expanded or contracted with respect to the perimeter of the same face. In one embodiment, wherein the center region is expanded, the ratio of the thickness at the center to the thickness of at the perimeter is at least about 1.1 : 1 for example at least about 1.3: 1. In one embodiment, wherein the perimeter is thicker, the ratio of the thickness at the perimeter to the center is at least about 1.1 : 1 , for example at least about 1.3: 1.
  • the radius of curvature at the center of the tablet face is substantially different than the radius of curvature of the tablet face at the perimeter region.
  • the radius of curvature at the center of the tablet face may be at least 10% or at least 50% less than the radius of curvature of the tablet face in the perimeter region.
  • an insert is incorporated into the tablet shape before the RF energy is delivered.
  • examples include solid compressed forms or beads filled with a liquid composition. Such incorporation of an insert is depicted in Figs. 3A-3G.
  • the pharmaceutically active agent is in the form of a gel bead, which is liquid filled or semi-solid filled.
  • the gel bead(s) are added as a portion of the powder blend.
  • the tablet of this invention has the added advantage of not using a strong compaction step, allowing for the use of liquid or semisolid filled particles or beads which are deformable since they will not rupture following the reduced pressure compaction step.
  • These bead walls may contain gelling substances such as: gelatin; gellan gum; xanthan gum; agar; locust bean gum; carrageenan; polymers or polysaccharides such as but not limited to sodium alginate, calcium alginate, hypromellose, hydroxypropyl cellulose and pullulan; polyethylene oxide; and starches.
  • the bead walls may further contain a plasticizer such as glycerin, polyethylene glycol, propylene glycol, triacetin, triethyl citrate and tributyl citrate.
  • the pharmaceutically active agent may be dissolved, suspended or dispersed in a filler material such as but not limited to high fructose corn syrup, sugars, glycerin, polyethylene glycol, propylene glycol, or oils such as but not limited to vegetable oil, olive oil, or mineral oil.
  • a filler material such as but not limited to high fructose corn syrup, sugars, glycerin, polyethylene glycol, propylene glycol, or oils such as but not limited to vegetable oil, olive oil, or mineral oil.
  • the insert is substantially free of RF-absorbing ingredients, in which case application of the RF energy results in no significant heating of the insert itself.
  • the insert contains ingredients and are heated upon exposure to RF energy and, thus, such inserts can be used to soften or melt the meltable binder.
  • the tablet includes at least two layers, e.g., with different types and/or concentrations of binders and/or other ingredients or different concentrations of pharmaceutically active agents. Such an embodiment is shown in FIGS. 2A-2D.
  • the tablet includes two layers, one layer having orally disintegrating properties and another layer being chewable or swallowable.
  • one layer has a meltable binder and another layer does not have a meltable binder.
  • one layer is compacted at higher compaction force versus the other layer.
  • both layers contain same amount of the meltable binder, but have different amount of pharmaceutically active agents and/or other excipients.
  • all properties of the two layers are identical but the colors of the two layers are different.
  • the powder blend further contains one or more effervescent couples.
  • effervescent couple contains one member from the group consisting of sodium bicarbonate, potassium bicarbonate, calcium carbonate, magnesium carbonate, and sodium carbonate, and one member selected from the group consisting of citric acid, malic acid, fumaric acid, tartaric acid, phosphoric acid, and alginic acid.
  • the combined amount of the effervescent couple(s) in the powder blend/tablet is from about 2 to about 20 percent by weight, such as from about 2 to about 10 percent by weight of the total weight of the powder blend/tablet.
  • the tablet is designed to disintegrate in the mouth when placed on the tongue in less than about 60 seconds, e.g. less than about 45 seconds, e.g. less than about 30 seconds, e.g. less than about 15 seconds.
  • the tablet meets the criteria for Orally Disintegrating Tablets (ODTs) as defined by the draft Food and Drug Administration guidance, as published in April, 2007.
  • ODTs Orally Disintegrating Tablets
  • the tablet meets a two-fold definition for orally disintegrating tablets including the following criteria: 1) that the solid tablet is one which contains medicinal substances and which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue and 2) be considered a solid oral preparation that disintegrates rapidly in the oral cavity, with an in vitro disintegration time of
  • the tablet is contained next to another edible form.
  • this edible form is a hard candy or compressed ring that holds the powder blend during compaction and/or the RF heating step.
  • the outer hard candy form may be made using uniplast rolling or roping and subsequent cutting and stamping, as well as depositing into molds.
  • the hard candy portion contains one or more sugars selected from the group consisting of isomalt, sucrose, dextrose, corn syrup, lactitol, and lycasin. In one embodiment, the hard candy portion contains at least 50% (such as at least 75%, such as at least 90%) by weight of such sugar(s).
  • the outer edible form contains a pharmaceutically active agent and the inner tablet contains a second portion of the same pharmaceutically active agent that is in the outer edible form.
  • the outer edible form contains a pharmaceutically active agent and the inner tablet contains a different pharmaceutically active agent than that in the outer edible form.
  • the outer edible form disintegrates at a rate of at least 10 times, such as at least 20 times, the rate of the inner tablet.
  • the first and second portions can be the same or different.
  • the tablet having an outer edible form and an inner tablet is coated with an immediate release sugar coating or film coating.
  • the step following the fusing (heating) and subsequent cooling of the tablet would involve further sugar or film coating in a coating pan.
  • the tablet is prepared such that the tablet is relatively soft (e.g., capable of disintegrating in the mouth or being chewed).
  • the hardness of the tablet is preferably less than about 3 kiloponds per square centimeter (kp/cm 2 ) (e.g., less than about 2 kp/cm 2 , such as less than about 1 kp/cm 2 ).
  • Hardness is a term used in the art to describe the diametral breaking strength as measured by conventional pharmaceutical hardness testing equipment, such as a
  • Schleuniger Hardness Tester In order to compare values across different size tablets, the breaking strength must be normalized for the area of the break. This normalized value, expressed in kp/cm 2 , is sometimes referred in the art as tablet tensile strength.
  • tablet hardness testing is found in Leiberman et al., Pharmaceutical Dosage Forms— Tablets, Volume 2, 2.sup.nd ed., Marcel Dekker Inc., 1990, pp. 213-217, 327- 329.
  • a more preferred test for hardness of the tablet of the present invention relies upon a Texture Analyzer TA-XT2i to measure the peak penetration resistance of the tablet.
  • the texture analyzer is fitted with a flat faced cylindrical probe having a length longer than the thickness of the tablet (e.g., 26 mm) and a diameter of fromlmm to 2 mm.
  • the tablet rests upon a platform fitted with a cylindrical die having a cavity.
  • the diameter of the cavity is equal or greater than the diameter of the probe and less than the diameter of the tablet face (e.g., the die cavity may have a diameter of about 6 mm and a depth of about 25 mm).
  • the texture analyzer is employed to measure and report the force in grams as the probe moves at 0.05 millimeters per second through the tablet, until the probe passes through at least 80% of the thickness of the tablet.
  • the maximum force required to penetrate the tablet is referred to herein as the peak resistance to penetration ("peak penetration resistance").
  • the peak penetration resistance at the center of a major face is less than 2500 grams, such as less than about 1500 grams, such as less than about 500 grams. In one embodiment, the peak penetration resistance at the center of a major face is from about 2 grams to about 2000 grams, such as from about 30 grams to about 1000 grams, such as from about 100 grams to about 500 grams.
  • the peak penetration resistance of the tablet varies between different regions in the tablet.
  • the peak penetration resistance measured at the perimeter is higher than the peak penetration resistance at the center of a major face.
  • the peak penetration resistance of the tablet at the perimeter may be at least about 10% greater than the peak penetration resistance at the center of a major face, such as at least about 30%, such as at least about 100%, such as at least about 200% greater.
  • the ratio of the peak penetration resistance of the tablet at the perimeter to the peak penetration resistance at the center of a major face is at least about 1.1 : 1, such as at least about 1.3: 1, such as at least about 2: 1, such as at least about 3: 1.
  • the peak penetration resistance at the center of a major face is from about 10 grams to about 500 grams and the peak penetration resistance at the perimeter of the tablet is from about 50 grams to about 1000 grams, such as the peak penetration resistance at the center of a major face is from about 50 grams to about 350 grams and the peak penetration resistance at the perimeter of the tablet is from about 100 grams to about 750 grams
  • the density of the tablet is less than about 2 g/cc (e.g., less than about 0.9 g/cc, such as less than about 0.8 g/cc, such as less than about 0.7 g/cc). In one embodiment, the difference in the density of the powdered material following the compaction step is less than about 40 percent (e.g., less than about 25 percent, such as less than about 15 percent).
  • the density of the tablet is different between the center of the major face of the tablet and the perimeter of the major face. In one embodiment, the density of 25 percent of the surface area of the major face of the tablet when measured from the outer perimeter is at least 10 percent greater than the density of 25 percent of the surface area of the tablet when measured from the center portion. In one embodiment the density of 25 percent of the surface area of the tablet when measured from the outer perimeter is from about 0.6 g/cc to about 1.2 g/cc and the density of 25 percent of the surface area of the center of the tablet is from about 0.1 g/cc to about 0.59 g/cc. Tablets Coatings
  • the tablet includes an additional outer coating (e.g., a translucent coating such as a clear coating) to help limit the friability of the tablet.
  • an additional outer coating e.g., a translucent coating such as a clear coating
  • Suitable materials for translucent coatings include, but are not limited to, hypromellose, hydroxypropylcellulose, starch, polyvinyl alcohol, polyethylene glycol, polyvinylalcohol and polyethylene glycol mixtures and copolymers, and mixtures thereof. Tablets of the present invention may include a coating from about 0.05 to about 10 percent, or about 0.1 to about 3 percent by weight of the total tablet.
  • the surface of the dosage form is further exposed to infrared energy wherein the majority (at least 50 percent, such as least 90 percent, such as at least 99 percent) of the wavelength of such infrared energy is from about 0.5 to about 5 micrometers such as from about 0.8 to about 3.5 micrometers (e.g., by use of a wavelength filter).
  • the infrared energy source is a quartz lamp with a parabolic reflector (e.g., to intensify the energy) and a filter to remove unwanted frequencies. Examples of such infrared energy sources include the SPOT IR 4150 (commercially available from Research, Inc., Eden Prairie, MN). Use of Tablet
  • the tablets may be used as swallowable, chewable, or orally disintegrating tablets to administer the pharmaceutically active agent.
  • the present invention features a method of treating an ailment, the method including orally administering the above-described tablet wherein the tablet includes an amount of the pharmaceutically active agent effective to treat the ailment.
  • ailments include, but are not limited to, pain (such as headaches, migraines, sore throat, cramps, back aches and muscle aches), fever, inflammation, upper respiratory disorders (such as cough and congestion), infections (such as bacterial and viral infections), depression, diabetes, obesity, cardiovascular disorders (such as high cholesterol, triglycerides, and blood pressure), gastrointestinal disorders (such as nausea, diarrhea, irritable bowel syndrome and gas), sleep disorders, osteoporosis, and nicotine dependence.
  • the method is for the treatment of an upper respiratory disorder, wherein the pharmaceutically active agent is selected from the group of phenylephrine, cetirizine, loratadine, fexofenadine, diphenhydramine, dextromethorphan, chlorpheniramine, chlophedianol, and pseudoephedrine.
  • the pharmaceutically active agent is selected from the group of phenylephrine, cetirizine, loratadine, fexofenadine, diphenhydramine, dextromethorphan, chlorpheniramine, chlophedianol, and pseudoephedrine.
  • the "unit dose” is typically accompanied by dosing directions, which instruct the patient to take an amount of the pharmaceutically active agent that may be a multiple of the unit dose depending on, e.g., the age or weight of the patient.
  • the unit dose volume will contain an amount of pharmaceutically active agent that is therapeutically effective for the smallest patient.
  • suitable unit dose volumes may include one tablet.
  • Example 1 Manufacture of Powder Blend Containing Loratadine
  • the loratadine powder blend for an orally disintegrating tablet containing the ingredients of Table 1 , is manufactured as follows: Table 1 : Loratadine Powder Blend Formulation
  • sucralose, colorant, and flavor were placed together into a 500cc sealable plastic bottle.
  • the mixture was then blended end-over-end manually for approximately 2 minutes.
  • the resulting mixture, the dextrose monohydrate, loratadine, and the polyethylene oxide were then added to another 500cc sealable plastic bottle and mixed end-over-end manually for approximately 5 minutes.
  • the resulting mixture was then added to a planetary bowl mixer, and the simethicone DClOO was added and mixed for approximately 3 minutes.
  • the polyethylene glycol 4000 and the maltodextrin were added to the mixture and mixed for approximately 3 minutes.
  • Example 2 Manufacture of Orally Disintegrating Tablet Containing Loratadine
  • a portion of the powder blend from Example 1 was placed into a 1/2 inch diameter forming cavity of an electrically insulative Teflon die platen.
  • the powder blend was then tamped between an upper and lower flat- faced metal forming tools into a shape conformal to the surface of the forming tools.
  • the tamping pressure was typically between 10 and approximately 50 psi of pressure.
  • the forming tools, die platen and tablet shape were then placed between the upper RF electrode and lower RF electrode powered by an RF heating unit using a COSMOS Model C10X16G4 (Cosmos Electronic Machine Corporation, Farmingdale, NY) RF generator having an output of 4 KW of power, frequency of 27 MHz, and the vacuum capacitor is set at 140.
  • COSMOS Model C10X16G4 Cosmos Electronic Machine Corporation, Farmingdale, NY
  • the diphenhydramine powder blend for an orally disintegrating tablet containing the ingredients of Table 2, was manufactured as follows.
  • the sucralose, yellow colorant, flavors, polyethylene glycol and maltodextrin from the formula in Table 2 were passed through a 20 mesh screen.
  • the sieved materials were placed into a 500cc plastic bottle and blended end over end with the remaining materials in Table 2.
  • the powder blend was placed into the forming cavity, tamped, and activated with RF energy as described in Example 2 for approximately 2 to 5 seconds to form the orally disintegrating tablet and subsequently removed from the die platen.
  • Example 5 Manufacture of Orally Disintegrating Tablet Placebo Containing
  • the placebo powder blend for a comparative chewable placebo tablet containing the ingredients of Table 5, was manufactured as follows.
  • the sucralose, yellow color, and flavors were passed through a 20 mesh screen prior to blending.
  • the sieved materials were blended with the remaining materials in the formula in Table 5 and added to a 500cc plastic bottle and blended end over end for approximately 3 minutes and discharged.
  • the tablets were compressed using two different compression forces as follows: Tablets (a) were compressed on a single station manual Carver press (commercially available from Carver Press Corporation in Wabash, Indiana) at 0.7 Metric tons (6.86 KiloNewtons) and Tablets (b) were compressed at 0.25 Metric tons (2.45 KiloNewtons). Tablets (b) were extremely friable and fragile given the low amount of pressure applied to the formulation.
  • the placebo powder blend for a chewable tablet containing the ingredients of Table 6, was manufactured as follows.
  • the sucralose, yellow color, flavors, and citric acid were passed through a 20 mesh screen prior to blending.
  • the sieved materials were blended with the remaining materials in the formula in Table 6 and added to a 500cc plastic bottle and blended end over end for approximately 3 minutes and discharged.
  • the tablets were compressed using two different compression forces as follows: Tablets (a) were lightly compressed on a single station manual Carver press at 0.7 Metric tons (6.86 KiloNewtons) and Tablets (b) were compressed at 0.25 Metric tons (2.45 KiloNewtons). Tablets (b) were extremely friable and fragile given the low amount of pressure applied to the formulation.
  • Example 7b (2) 451 1 1.21 5.00 493.5 0.910
  • the ODT tablets of the present invention (Examples 3, 4, and 5) have densities ranging from 0.541-0.635 mg/mm 3
  • the comparative chewable tablets of Examples 6 and 7 had densities ranging from 0.890 - 1.240 mg/mm 3 .
  • the ODT tablets of the present invention thus, had densities approximately half of that of the comparative examples.
  • Example 3 The tablets of the present invention (Example 3) disintegrated immediately following the addition of the water as indicated by the probe distance, which increased from 0 mm to greater than 1 mm between 10 and 20 seconds.
  • the tablets from Example 6a which were representative of chewable tablets, disintegrated in 84.30 seconds from the addition of water as measured by the change in slope in the texture analyzer, where tablets of Example 3 were completely disintegrated in 6.99 seconds from the addition of water.
  • the loratadine powder blend for an orally disintegrating tablet, containing the ;redients of Table 9, is manufactured as follows: Table 9: Loratadine Powder Blend Formulation
  • sucralose, colorant, and flavor are placed together into a 500cc sealable plastic bottle.
  • the mixture is then blended end-over-end manually for approximately 2 minutes.
  • the resulting mixture, the dextrose monohydrate, and the loratadine, are then added to another 500cc sealable plastic bottle and mixed end-over-end manually for approximately 5 minutes.
  • the polyethylene glycol 4000 and the maltodextrin is added to the mixture and mixed for approximately 3 minutes.
  • Example 1 1 Manufacture of Orally Disintegrating Tablet
  • a portion of the powder blend from Example 10 is placed into an electrically insulative Teflon®, or ceramic die block, approximately 0.50" in diameter and 0.175" thick.
  • the powder blend is then tamped between an upper and lower forming tools into a shape conforming to the surface of the forming tools.
  • the forming tools are metal and have a recessed center, which covers approximately 80% of the surface area. Covering the entire upper surface of the tool is a thin, flat, flexible Teflon disc (approximately 0.020 - 0.100" thick) as depicted in Figure 15 A.
  • the tamping pressure is typically between 10 and approximately 100 psi of pressure.
  • Example 12 Orally Disintegrating Tablet Placebo Produced Utilizing Rf Energy comprising Dextrose Monohydrate and Forming Tools with Hollowed Centers
  • the powder blend is placed into an upper and lower set of 1 ⁇ 2 inch flat faced forming tools with hollowed centers, and conductive rings. Covering the entire upper surface of the tool is a thin, flat, flexible Teflon disc (approximately 0.020 - 0.100" thick) as depicted in Figure 15.
  • the powder blend is activated with Rf energy for
  • Example 12 The powder blend from Example 12 are placed into an upper and lower set of 1 ⁇ 2 inch flat faced forming tools as depicted in Figures 1 IE or 1 IF with Teflon® plugs in the center of the forming tool (with or without an additional metal pin) and activated with Rf energy for approximately 2 seconds as described in Example 2 to form an orally disintegrating tablet and subsequently removed from the die.
  • This method produced tablets with a perimeter that was slightly raised as compared to the center at the two major faces.
  • Comparative data from marketed fast dissolving tablet products is shown in Table 12. The following comparative products were tested: Migranin 400mg Ibuprofen Dragees (Reckitt Benckisser Healthcare, GmbH, Manheim, Germany); Nurofen Meltlets Ibuprofen 200mg Self Dissolving Tablets (Crookes Healthcare, Nottingham, UK);
  • Claritin Reditabs lOmg Loratadine (Schering-Plough, Memphis, TN); Imodium Instant Melt Tablets, 2mg Loperamide HC1 (McNeil Products LTD, Maidenhead, Berkshire, UK); Alavert Loratadine Orally Disintegrating Tablet, lOmg (Wyeth Consumer
  • the samples of Examples 12 and 13 had a range of the ratio of PRP of from 1.3 : 1 to 18.6: 1, while the comparative orally disintegrating products had a range of the ratio of PRP of from 0.35 to 1.07: 1

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Abstract

La présente invention a trait à un comprimé qui inclut au moins une matière pharmaceutiquement active, la forme dudit comprimé incluant au moins une face majeure où : (i) la résistance à la pénétration maximale sur le périmètre de ladite face majeure du comprimé est au moins d'environ 10 % supérieure à la résistance à la pénétration maximale au centre de ladite face majeure ; et (ii) le comprimé se désintègre dans la bouche lorsqu'il est placé sur la langue en moins d'environ 30 secondes. La présente invention a également trait à une machine et à un procédé de fabrication dudit comprimé.
PCT/US2011/029158 2010-09-22 2011-03-21 Fabrication de formes pharmaceutiques à densité variable utilisant l'énergie de radiofréquence WO2012039789A1 (fr)

Priority Applications (9)

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CA2810623A CA2810623A1 (fr) 2010-09-22 2011-03-21 Fabrication de formes pharmaceutiques a densite variable utilisant l'energie de radiofrequence
RU2013118328/02A RU2013118328A (ru) 2010-09-22 2011-03-21 Производство дозированных форм с различной плотностью с использованием радиочастотного излучения
BR112013006522A BR112013006522A2 (pt) 2010-09-22 2011-03-21 afbricação de formas de dosagem com densidade variável mediante o uso de energia de radiofrequência
EP11710980.1A EP2618995A1 (fr) 2010-09-22 2011-03-21 Fabrication de formes pharmaceutiques à densité variable utilisant l'énergie de radiofréquence
KR1020137009864A KR20130136464A (ko) 2010-09-22 2011-03-21 고주파 에너지를 이용한 가변 밀도 투여 형태의 제조
AU2011306064A AU2011306064B2 (en) 2010-09-22 2011-03-21 Manufacture of variable density dosage forms utilizing radiofrequency energy
MX2013003287A MX343047B (es) 2010-09-22 2011-03-21 Fabricacion de formas de dosificacion de densidad variable con el uso de energia de radiofrecuencia.
CN201180045941.1A CN103140346B (zh) 2010-09-22 2011-03-21 利用射频能量制造可变密度剂型
HK13111498.9A HK1184111A1 (zh) 2010-09-22 2013-10-11 利用射頻能量製造可變密度劑型

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US12/887,544 US8871263B2 (en) 2009-09-24 2010-09-22 Manufacture of tablet in a die utilizing radiofrequency energy and meltable binder
US12/887,569 US8807979B2 (en) 2009-09-24 2010-09-22 Machine for the manufacture of dosage forms utilizing radiofrequency energy
US12/887,569 2010-09-22
US12/887,552 2010-09-22
US12/887,544 2010-09-22
US12/887,552 US9610224B2 (en) 2009-09-24 2010-09-22 Manufacture of tablet in a die utilizing powder blend containing water-containing material
US13/052,219 2011-03-21
US13/052,219 US8858210B2 (en) 2009-09-24 2011-03-21 Manufacture of variable density dosage forms utilizing radiofrequency energy

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US8343533B2 (en) 2009-09-24 2013-01-01 Mcneil-Ppc, Inc. Manufacture of lozenge product with radiofrequency
US20110318411A1 (en) 2010-06-24 2011-12-29 Luber Joseph R Multi-layered orally disintegrating tablet and the manufacture thereof
US9233491B2 (en) 2012-05-01 2016-01-12 Johnson & Johnson Consumer Inc. Machine for production of solid dosage forms
US9511028B2 (en) * 2012-05-01 2016-12-06 Johnson & Johnson Consumer Inc. Orally disintegrating tablet
US9445971B2 (en) * 2012-05-01 2016-09-20 Johnson & Johnson Consumer Inc. Method of manufacturing solid dosage form
US20130295174A1 (en) * 2012-05-01 2013-11-07 Mcneil-Ppc, Inc. Tablet comprising a first and second region
DE102013002267A1 (de) * 2013-02-12 2014-08-14 Michael Hager Tablettenpresse
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US9839212B2 (en) * 2015-04-16 2017-12-12 Bio-Lab, Inc. Multicomponent and multilayer compacted tablets
WO2017078557A1 (fr) * 2015-11-05 2017-05-11 Анатолий Викторович ЗАЗУЛЯ Fabrication d'un comprimé possédant un mécanisme d'augmentation de l'efficacité thérapeutique d'un médicament au moyen d'une dose à l'échelle nanométrique d'un homologue
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