US20050053654A1 - Orodispersible tablets containing fexofenadine - Google Patents
Orodispersible tablets containing fexofenadine Download PDFInfo
- Publication number
- US20050053654A1 US20050053654A1 US10/495,007 US49500704A US2005053654A1 US 20050053654 A1 US20050053654 A1 US 20050053654A1 US 49500704 A US49500704 A US 49500704A US 2005053654 A1 US2005053654 A1 US 2005053654A1
- Authority
- US
- United States
- Prior art keywords
- granules
- fexofenadine
- pharmaceutically acceptable
- acceptable salts
- weight
- 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
Links
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- 229960003592 fexofenadine Drugs 0.000 title claims abstract description 106
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- RRJFVPUCXDGFJB-UHFFFAOYSA-N Fexofenadine hydrochloride Chemical compound Cl.C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RRJFVPUCXDGFJB-UHFFFAOYSA-N 0.000 claims description 3
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- 230000001419 dependent effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000012738 dissolution medium Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- MVPICKVDHDWCJQ-UHFFFAOYSA-N ethyl 3-pyrrolidin-1-ylpropanoate Chemical compound CCOC(=O)CCN1CCCC1 MVPICKVDHDWCJQ-UHFFFAOYSA-N 0.000 description 1
- 235000020937 fasting conditions Nutrition 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 239000000938 histamine H1 antagonist Substances 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 229940087875 leukine Drugs 0.000 description 1
- 229960003511 macrogol Drugs 0.000 description 1
- 229940057948 magnesium stearate Drugs 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- ITVGXXMINPYUHD-CUVHLRMHSA-N neohesperidin dihydrochalcone Chemical compound C1=C(O)C(OC)=CC=C1CCC(=O)C(C(=C1)O)=C(O)C=C1O[C@H]1[C@H](O[C@H]2[C@@H]([C@H](O)[C@@H](O)[C@H](C)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 ITVGXXMINPYUHD-CUVHLRMHSA-N 0.000 description 1
- 229940089953 neohesperidin dihydrochalcone Drugs 0.000 description 1
- 235000010434 neohesperidine DC Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 229940100691 oral capsule Drugs 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 239000007935 oral tablet Substances 0.000 description 1
- 229940096978 oral tablet Drugs 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 210000003254 palate Anatomy 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229940069328 povidone Drugs 0.000 description 1
- 206010039083 rhinitis Diseases 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 108010038379 sargramostim Proteins 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 206010041232 sneezing Diseases 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 229940045902 sodium stearyl fumarate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
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
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K9/14—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
- 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
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5026—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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1611—Inorganic compounds
Definitions
- the present invention concerns orodispersible tablets comprising coated granules of fexofenadine.
- the invention also concerns said coated granules of fexofenadine, a process for the preparation thereof and the use of said orodispersible tablets.
- orodispersible tablets means tablets which are able to disintegrate in the buccal cavity in less than 60 seconds, preferably in less than 40 seconds, upon contact with saliva by formation of an easy-to-swallow suspension.
- the disintegration time corresponds to the time between the moment when the tablet is placed in the buccal cavity in contact with saliva and the moment when the suspension (resulting from the disintegration without chewing of the tablet) is swallowed
- Fexofenadine is a well known synthetic antiallergenic with the chemical name ( ⁇ )-4-[1-hydroxy-4-[4(hydroxydiphenylmethyl)-1-piperidinyl]-butyl] ⁇ , ⁇ -dimethyl benzeneacetic acid.
- Fexofenadine a metabolite of terfenadine, is an antihistamine with selective peripheral H1-receptor antagonist activity.
- Fexofenadine is known from e.g. U.S. Pat. No. 4,254,129. It is acknowledged in the art and is commercially available, in particular as an oral tablet or capsule, under the trade name Allegra®.
- the tablets commercially available under the trade name Allegra® contain 30, 60, or 180 mg fexofenadine hydrochloride (depending on the dosage) and, as excipients, croscarmellose sodium, magnesium stearate, microcrystalline cellulose and pregelatinized starch. Said tablets are coated with a film coating based on hydroxypropyl methylcellulose, mixture of iron oxides, polyethylene glycol, povidone, silicone dioxide, and titanium dioxide.
- Fexofenadine is highly active via oral administration. While numerous pharmaceutical compositions for oral administration have been proposed, there still exists a need for commercially acceptable fexofenadine formulations for oral administration with good patient convenience and acceptance, especially for children or the elderly.
- fexofenadine Another difficulty in the formulation of fexofenadine in oral pharmaceutical compositions is the low solubility of fexofenadine, especially in gastric conditions (solubility of 0.2 mg of fexofenadine HCl per ml of pH 1.2 aqueous buffer solution).
- coated granules containing fexofenadine, which have taste-masking properties while permitting rapid release of the active substance from the granules and allowing rapid absorption in the body after oral administration.
- a tablet containing fexofenadine as active ingredient in the form of coated granules and a mixture of excipients containing at least one disintegrating agent, a soluble diluent agent and a lubricant, and optionally a swelling agent, an antistatic agent, a permeabilising agent, sweeteners, flavoring agents and colors.
- the present invention relates to orodispersible tablets which are able to disintegrate in the buccal cavity upon contact with saliva by formation of an easy-to-swallow suspension, in less than 60 seconds, preferably in less than 40 seconds, such tablets containing fexofenadine as active ingredient in the form of coated granules, and a mixture of excipients comprising at least one disintegrating agent, a soluble diluent agent, a lubricant and optionally a swelling agent, an antistatic agent, a permeabilising agent, sweeteners, flavoring agents and colors.
- the tablets according to the invention disintegrate in the buccal cavity and present a release of the active ingredient which is equivalent to the conventional formulation, they nevertheless have a pleasant taste.
- the orodispersible tablets of the invention are found to show high stability and physical integrity, e.g. during storage, handling, packaging and the like, while maintaining very good disintegration performance.
- Fexofenadine may be used in the form of its racemate or a single enantiomer, in free base form or in acid addition salt form of the racemate or one of its single enantiomers.
- An acid addition salt form may be prepared from the free base form in a conventional manner and vice-versa.
- suitable acid addition salt forms include hydrochloride, lactate and ascorbate, preferably hydrochloride. Fexofenadine in the form of a hydrochloride salt is preferred.
- fexofenadine particles present a particle size such that 100% of the particles have an average size of less than 20 ⁇ m.
- fexofenadine in anyone of said forms is present as coated granules.
- the tablet according to the invention has a hardness of not less than 15 N, when measured with the test method of the European Pharmacopeia (2.9.8).
- the tablet according to the invention contains coated granules of fexofenadine, or one of its pharmaceutically acceptable salts, and a mixture of excipients, the ratio of the mixture of excipients to the coated granules is 0.4 to 9, preferably 1.5 to 5 and even more preferably 2 to 3 parts by weight, the mixture of excipients comprising:
- the disintegrating agent is selected from the group consisting of croscarmellose, available as e.g. Ac-di-sol®, crospovidone available as e.g. Kollidon CL®, and mixtures thereof.
- the soluble diluent agent used in the tablets presents binding properties.
- the soluble diluent agent with binding properties consists of a polyol having less than 13 carbon atoms and being either in the form of a directly compressible product with an average particle size of 100 to 500 ⁇ m, or in the form of a powder with an average particle size of less than 100 ⁇ m, this polyol preferably being selected from the group comprising mannitol, xylitol, sorbitol and maltitol, it being Understood that sorbitol cannot be used alone and that, in the case where there is only one soluble diluent agent with binding properties, it is used in the form of the directly compressible product, whereas in the case where there are at least two soluble diluent agents with binding properties, one is present in the directly compressible form and the other is present in powder form, it then being possible for the polyols to be the same, the ratio of directly compressible poly
- the proportion of disintegrating agent is from 3 to 15% by weight, preferably 5 to 15% by weight, in the case of a mixture, each disintegrating agent being comprised between 1 and 10% by weight, preferably 5 to 10% by weight, and the proportion of soluble diluent agent being 30 to 90% by weight, preferably 40 to 60% by weight, based in each case on the weight of the tablet.
- the lubricant is selected from the group consisting of magnesium stearate, stearic acid, sodium stearyl fumarate, micronised polyoxyethyleneglycol (micronised Macrogol 6000), leukine, sodium benzoate and mixtures thereof.
- the amount of lubricant is from 0 to 3%, preferably from 1 to 2% by weight, based on the weight of the tablet.
- the lubricant can be dispersed within the mixture of excipients, or according to an advantageous embodiment, sprayed over the outer surface of the tablet.
- the lubricant is in powder form and is, at least in part, disposed on the surface of the tablets.
- the permeabilising agent allows the creation of a hydrophilic network which facilitates the penetration of saliva and hence assists the disintegration of the tablet.
- the permeabilising agent is selected from the group comprising especially silica with a high affinity for aqueous solvents, such as colloidal silica (Aerosil®), precipitated silica (Sylo ⁇ d® FP 244), maltodextrins, ⁇ -cyclodextrins and mixtures thereof.
- colloidal silica Alignin®
- precipitated silica Sylo ⁇ d® FP 244
- maltodextrins ⁇ -cyclodextrins and mixtures thereof.
- the amount of permeabilising agent is between 0 and 5%, preferably from 0.5 to 2% by weight, based on the weight of the tablet.
- a swelling agent can be incorporated in the mixture of excipients.
- Said swelling agent is selected from the group consisting of starch, modified starch or microcristalline cellulose.
- An antistatic agent can be incorporated as a flow aid, said antistatic agent being selected from the group consisting of micronised or non micronised talc, fumed silica (Aerosil® R972), colloidal silica (Aerosil®200), precipitated silica (Sylo ⁇ d® FP 244), and mixtures thereof.
- the sweetener which can be included in the mixture of excipients, can be selected from the group consisting of especially aspartam, potassium acesulfame, sodium saccharinate, neohesperidin dihydrochalcone, sucralose, monoammonium glycyrrhizinate, and mixtures thereof.
- flavorings and colors are those conventionally used in pharmacy for the preparation of tablets.
- the present invention also relates to the coated granules of fexofenadine or one of its pharmaceutically acceptable salts.
- the taste-masking of fexofenadine is achieved by coating granulated microcrystals of fexofenadine with one or more polymers.
- the granules of fexofenadine, or one of its pharmaceutically acceptable salts are characterized in that the granules are coated and that they contain:
- the granulation excipients can also include disintegrating agents and/or surfactants.
- the binder is selected from the group consisting of cellulosic polymers, such as ethylcellulose, hydroxypropylcellulose and hydroxypropylmethyl cellulose, acrylic polymers, such as insoluble acrylate ammoniomethacrylate copolymer, polyacrylate or polymethacrylic copolymer, povidones, copovidones, polyvinylalcohols, alginic acid, sodium alginate, starch, pregelatinized starch, sucrose and its derivatives, guar gum, polyethylene glycol, preferably an acrylic polymer, most preferably Eudragit® E100, and mixtures thereof.
- cellulosic polymers such as ethylcellulose, hydroxypropylcellulose and hydroxypropylmethyl cellulose
- acrylic polymers such as insoluble acrylate ammoniomethacrylate copolymer, polyacrylate or polymethacrylic copolymer, povidones, copovidones, polyvinylalcohols, alginic
- a diluent agent is used.
- the diluent agent is selected from the group consisting of microcrystalline cellulose, sucrose, dicalcium phosphate, starches, lactose and polyols of less than 13 carbon atoms, such as mannitol, xylitol, sorbitol, maltitol, pharmaceutically acceptable amino acids, such as glycin, and their mixtures.
- the antistatic agent which can be used as flow aid, is selected from the group consisting of micronised or non micronised talc, fumed silica (Aerosil® R972), colloidal silica (Aerosil200), precipitated silica (Sylo ⁇ d® FP244) and mixtures thereof.
- Conventional pharmaceutically acceptable sweetening agents and/or colouring agents can be incorporated into the granules of fexofenadine.
- the granule of fexofenadine or one of its pharmaceutically acceptable salts is in the form of a core of granulated microcrystals of fexofenadine, coated with at least one layer comprising fexofenadine.
- Said coated core is characterized in that the core and the layer comprise each from 70% to 95%, preferably 80% to 95% by weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof, the balance to 100% being formed with at least one binder, and that said coated core is advantageously a sphere.
- the core and the layer comprise each from 70% to 95%, preferably 80% to 95% by weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof, the balance to 100% being formed with at least one binder, and that said coated core is advantageously a sphere.
- the granules comprise:
- the granules are coated with a coating composition containing at least one coating polymer selected from the group consisting of cellulosic polymers, acrylic polymers and their mixtures.
- ethylcellulose, hydroxypropylcellulose (HPC) and hydroxypropylmethylcellulose (HPMC) are advantageously used.
- insoluble acrylate ammoniomethacrylate copolymer (Eudragit® RL100 or RS100 or Eudragit® RL30D or RS30D), polyacrylate (Eudragit®NE30D), or methacrylic copolymers (Eudragit® L100-55 or Eudragit® L30D, Eudragit® E100, Eudragit® EPO . . . ) are advantageously used, alone, in combination or in admixture with pH-dependent polymers. Eudragit® E100 or a mixture of Eudragit® EPO and Eudragit®NE30D are preferred.
- the binder and the coating polymer are the same polymer.
- the prepared coating liquid is either water-based or prepared with organic solvents. According to an advantageous embodiment, this coating liquid is suitable to be sprayed with conventional spray layering equipment, as for example a fluidized bed equipped with a top insert or bottom (Bruster) insert.
- permeabilising agents plasticizers, soluble agents, disintegrating agents and surfactants are added as coating additives.
- the plasticizer is selected in the group consisting of triacetine, triethylacetate, triethylcitrate (Eudraflex®), ethylphthalate, or mixtures thereof.
- the plasticizer is used in proportions of at most about 30%, preferably 10% by weight of the coating polymers.
- the soluble agents are selected in particular among the polyols having less than 13 carbon atoms.
- the disintegrating agent or a surfactant which could be added during the granulation and the coating steps allow improved dissolution.
- the surfactant may be an anionic, nonionic, cationic or amphoteric surfactant.
- the disintegrating agent is selected from the group consisting of croscarmellose, available as e.g. Ac-di-sol®, crospovidone available as e.g. Kollidon CL®, and mixtures thereof.
- the particle size range of coated granules comprising fexofenadine, or one of its pharmaceutically acceptable salts is adapted for obtaining an effective taste masking with an acceptable coating factor and a good mouthfeel.
- the coated granules according to the invention have a particle size distribution between 150 ⁇ m and 500 ⁇ m, preferably between 150 ⁇ m and 425 ⁇ m, such that at least 50%, preferably at least 70% of the granules have a particle size ranging between 150 and 425 ⁇ m and less than 15% of the granules have a particle size less than 150 ⁇ m.
- the particle sizes are measured according to conventional methods, preferably by sieving.
- a granulation step is needed in order to obtain such particle size distribution.
- coated granules according to the invention comprise:
- the invention also relates to a process for the preparation of coated granules of fexofenadine, which comprises the successive steps consisting in:
- the invention also concerns a process for preparing orodispersible tablets comprising coated granules of fexofenadine, or one of its pharmaceutically acceptable salts.
- the process comprises the successive steps consisting in:
- the lubricant can be mixed with the excipients for the tablet, but can advantageously be sprayed on the surface of the punches before tabletting.
- the mixing, granulating and coating steps can be performed in different or in the same equipment, each step being performed in the presence of a mixture of excipients which are identical or different.
- each step is performed on a fluidized air-bed, such as for example, but not limited to Glatt GPCG-1, GPCG-3, GPCG-5 or GPCG 120.
- a fluidized air-bed such as for example, but not limited to Glatt GPCG-1, GPCG-3, GPCG-5 or GPCG 120.
- bottom, top and tangential spray methods can be used as well as layering method, bottom spray method of coating being preferred.
- various punches may be used, with diameters comprised between 8 and 17 mm, depending upon the dosage of the tablet.
- Various shapes may be used, such as for example, flat shape, advantageously with bevelled edges or polo punches.
- the orodispersible tablets of the present invention show rapid disintegration in the buccal cavity upon contact with saliva without chewing, in less than 60 seconds, preferably in less than 40 seconds, have a pleasant taste and palatability and thus have particularly good patient convenience and patient acceptance due to their increased ease of administration and ingestion.
- the tablets of the invention show surprisingly high physical stability and are easy to handle and package.
- the tablet of the invention presents the following composition:
- isopropanol is used as solvent and removed during the coating and granulation processes.
- the tablet of the invention has the following composition:
- Fexofenadine Coated Granules Fexofenadine HCl 40-80% Eudragit ® E100 20-60% Precipitated silica 0-5% the percentages being calculated by weight of coated granules,
- Excipients for the Formulation of the Tablet Fexofenadine coated granules 10-45% Mannitol powder and/or granular 50-90% Crospovidone 2-15% Precipitated silica 0-5% Magnesium stearate 0-5% Sucralose 0-5% Flavors 0-2% the percentages being calculated by weight of the tablet.
- isopropanol is used as solvent and removed during the coating and granulation processes.
- the tablets are particularly effective in treating seasonal allergic rhinitis, in adults and children 6 years of age and older.
- the present invention also concerns-the use of a coated granules of fexofenadine with a mixture of excipients, as described above, for the manufacture of a medicament for the treatment of symptoms associated with seasonal allergic rhinitis.
- the present invention relates also to methods for the treatment of symptoms associated with seasonal allergic rhinitis, in which the tablets of fexofenadine according to the invention are orally administered.
- Symptoms treated effectively include sneezing, rhinorrhea, itchy nose/palate/throat, itchy/watery, rhinitis.
- the utility of the tablets of the present invention may be observed in standard bioavailability tests or standard animal models, for example ascertaining dosages of the present tablets giving blood levels of fexofenadine hydrochloride equivalent to blood levels having a therapeutical effect on administration of known fexofenadine oral dosage forms, e.g. a tablet.
- an indicated daily dosage is in the range from about 10 mg to about 500 mg per day, preferably from 30 mg to 180 mg, conveniently administered, for example, in divided doses up to four times a day or once daily.
- Preferred dosages, expressed as fexofenadine HCl, for children 6 to 11 years of age are about 30 mg two times a day, and for adults and children 12 years of age and older from about 60 mg two times a day, or 180 mg once a day.
- Particle size of Fexofenadine HCl used for the manufacture of granules of examples 1 to 4 is measured with conventional laser equipment.
- Particle size distribution has following characteristics: D 10% 2.1 ⁇ m D 50% 5.3 ⁇ m D 90% 11.1 ⁇ m
- Examples 1 to 4 relate to the preparation of coated granules of fexofenadine.
- the thus obtained granules were coated in a fluidized bed equipped with a top insert, by spraying thereon a dispersion of 465 g of a mixture of Eudragit EPO/Eudragit NE30D (50/50) in water at 16% (weight/weight).
- the amount of coating was of 12.5% by weight with respect to the weight of the granules of fexofenadine HCl.
- the dissolution rates of the thus obtained coated granules were measured with the following method: Apparatus USP Apparatus II (Paddle method) Speed 50 rpm Volume 900 mL of HCl 0.001 N pH 3.0* Temperature 37.0° C. ⁇ 0.5° C. Sampling (5 mL) 2.5, 7.5, 15, 30 and 60 minutes HPLC Detection UV at 220 nm HPLC column Zorbax SB-Phenyl, 5 ⁇ m, 4.6 ⁇ 250 mm. Injection volume 20 ⁇ L Mobile Phase Acetonitrile: 0.03 M Acetic acid containing Triethylamine pH 5.25 (36:64). Dissolution medium HCl 0.001 N adjusted to pH 3.0 ⁇ 0.05 (if necessary) with o-Phosphoric acid.
- the amount of coating was of 40% by weight with respect to the weight of the granules of fexofenadine HCl.
- the particle size distribution (Sieve method) is given in the following table. TABLE 2 Sieve operture After Granulating step After Coating step >0.500 mm 14.5% 5.7% 0.425 mm-0.500 mm 13.0% 24.1% 0.355 mm-0.425 mm 20.0% 9.5% 0.250 mm-0.355 mm 30.5% 28.9% 0.150 mm-0.250 mm 21.5% 31.5% ⁇ 0.150 mm 0.5% 0.3%
- the amount of coating was of 38% by weight with respect to the weight of the granules of fexofenadine HCl.
- the obtained granules were coated in a fluidized bed equipped with a Wurster insert, by spraying thereon a solution of Eudragit E100 in isopropanol at 10% (weight/weight) containing 1% of Sylo ⁇ d FP 244.
- the amount of coating was of 30% by weight with respect to the weight of the granules of fexofenadine HCl.
- Examples 5-8 relate to the preparation of tablets.
- Three types of tablets T 1 , T2, T3 were prepared using coated granules of fexofenadine presenting different coating ratios.
- the coated granules of fexofenadine were obtained as in example 3 above but using the three different coating ratios of 30, 35 and 40. Then, an amount of each type of said coated granules corresponding to 180 mg of fexofenadine HCl was thoroughly blended for 15 minutes with the following tablet excipients.
- the percentages are expressed as percentage of the total weight of a tablet.
- the homogeneous obtained blend was introduced in a tabletting machine equipped with 14 mm-diameter polo shape punches.
- T4 three types of tablets (T4, T5, T6) presenting coated granules of fexofenadine with coating ratios of 30, 35, 40 were prepared but using an amount of fexofenadine HCl equivalent to 30 mg per tablet.
- the homogeneous obtained blend was introduced in a tabletting machine equipped with polo shape punches as described in the table.
- Results are displayed in the table 8 TABLE 8 Tablets T4 T5 T6 Coated granule ratio 30 35 40 (% by weight) Punch diameter 8 mm 7 mm 6 mm Weight 153 mg 131 mg 115 mg Hardness 44 N 39 N 45 N Disintegration time 15-20 sec. 15-20 sec 20-25 sec. in mouth Mouthfeel Complies Complies Complies Complies Complies Complies Taste Complies Complies Tablets T4, T5 and T6 present an acceptable taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- Tablets T7 according to the formula of T2 of example 5 are manufactured, using a ratio of Mannitol powder/Mannitol granular ratio of 1/1, containing an amount of fexofenadine HCl equivalent to 180 mg per tablet.
- the homogeneous obtained blend was introduced in a tabletting machine equipped with 14 mm-diameter polo shape punches.
- T8 T9, T10 Three types of tablets (T8, T9, T10 ) according to the formula T2 of example 5 were manufactured but using three different ratios of crospovidone of 5, 7.5 and 10% by weight.
- the homogeneous obtained blend was introduced in a tabletting machine equipped with 14mm-diameter polo shape.
- Tablets T8, T9 and T10 were thus obtained.
- the disintegrating time in mouth, the hardness, the mouthfeell and taste were evaluated, the results are displayed in table 10.
- Taste Complies Complies
- Tablets T8, T9 and T10 present an acceptable taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- T11 and T12 are given below: Fexofenadine HCl coated granules T11 T12 Fexofenadine HCl 48.4% 58.2% Eudragit E100 47.4% 37.7% Silica 4.2% 4.1%
Abstract
The present invention concerns orodispersible tablets, which are able to disintegrate in the buccal cavity upon contact with saliva by formation of an easy-to-swallow suspension, in less than 60 seconds, preferably in less than 40 seconds, containing fexofenadine in the form of coated granules, and a mixture of excipients comprising at least one disintegrating agent, a soluble diluent agent, a lubricant and optionally a swelling agent, a permeabilising agent, sweeteners, flavoring agents and colors; the process for obtaining such orodispersible tablets and the coated granules incorporated therein and the use of said orodispersible tablets in the treatment of seasonal allergic rhinitis.
Description
- The present invention concerns orodispersible tablets comprising coated granules of fexofenadine. The invention also concerns said coated granules of fexofenadine, a process for the preparation thereof and the use of said orodispersible tablets.
- In the context of the present invention, the term “orodispersible tablets” means tablets which are able to disintegrate in the buccal cavity in less than 60 seconds, preferably in less than 40 seconds, upon contact with saliva by formation of an easy-to-swallow suspension.
- The disintegration time corresponds to the time between the moment when the tablet is placed in the buccal cavity in contact with saliva and the moment when the suspension (resulting from the disintegration without chewing of the tablet) is swallowed
- Fexofenadine is a well known synthetic antiallergenic with the chemical name (±)-4-[1-hydroxy-4-[4(hydroxydiphenylmethyl)-1-piperidinyl]-butyl]α,α-dimethyl benzeneacetic acid.
- Fexofenadine, a metabolite of terfenadine, is an antihistamine with selective peripheral H1-receptor antagonist activity.
- Fexofenadine is known from e.g. U.S. Pat. No. 4,254,129. It is acknowledged in the art and is commercially available, in particular as an oral tablet or capsule, under the trade name Allegra®.
- The tablets, commercially available under the trade name Allegra® contain 30, 60, or 180 mg fexofenadine hydrochloride (depending on the dosage) and, as excipients, croscarmellose sodium, magnesium stearate, microcrystalline cellulose and pregelatinized starch. Said tablets are coated with a film coating based on hydroxypropyl methylcellulose, mixture of iron oxides, polyethylene glycol, povidone, silicone dioxide, and titanium dioxide.
- Fexofenadine is highly active via oral administration. While numerous pharmaceutical compositions for oral administration have been proposed, there still exists a need for commercially acceptable fexofenadine formulations for oral administration with good patient convenience and acceptance, especially for children or the elderly.
- One particular difficulty in the formulation of fexofenadine in oral pharmaceutical compositions is its unpleasant, strong bitter taste and aftertaste.
- Another difficulty in the formulation of fexofenadine in oral pharmaceutical compositions is the low solubility of fexofenadine, especially in gastric conditions (solubility of 0.2 mg of fexofenadine HCl per ml of pH 1.2 aqueous buffer solution).
- It is therefore highly desirable to develop coated granules, containing fexofenadine, which have taste-masking properties while permitting rapid release of the active substance from the granules and allowing rapid absorption in the body after oral administration.
- Furthermore, some patients, especially children and the elderly, experience difficulties swallowing the tablets, even with liquids.
- It is estimated that 50% of the population have problems swallowing the tablets. This leads to poor, or even noncompliance, with the treatment and thus has a negative impact on the efficiency of the treatment (H. Seager, 1998, J. Pharm. Pharmacol. 50, 375-382).
- Oral disintegrable multiparticulate tablets have already been described in U.S. Pat. No. 5,464,632, U.S. Pat. No. 6,106,861, WO 00/27357 and WO00/51568, the contents of which are hereby incorporated by reference. The active ingredient is in the form of coated microcrystals or coated microgranules.
- Up to now, no oral formulations of fexofenadine exist which are specifically suitable for patients having difficulties when swallowing or for patients taking the drugs with no liquids.
- It is thus highly desirable to remedy this situation and to develop an orodispersible tablet, containing fexofenadine, which has taste-masking properties and presents a pleasant palatability such that the administration of the tablet is not unpleasant for the patient and which allows the obtaining of pharmacokinetic parameters at least bioequivalent to those which are obtained with conventional oral formulations of fexofenadine, for example tablets such as those available under the trademark Allegra®.
- The Applicant has now surprisingly found that these characteristics can be obtained by formulating a tablet containing fexofenadine as active ingredient in the form of coated granules, and a mixture of excipients containing at least one disintegrating agent, a soluble diluent agent and a lubricant, and optionally a swelling agent, an antistatic agent, a permeabilising agent, sweeteners, flavoring agents and colors.
- The present invention relates to orodispersible tablets which are able to disintegrate in the buccal cavity upon contact with saliva by formation of an easy-to-swallow suspension, in less than 60 seconds, preferably in less than 40 seconds, such tablets containing fexofenadine as active ingredient in the form of coated granules, and a mixture of excipients comprising at least one disintegrating agent, a soluble diluent agent, a lubricant and optionally a swelling agent, an antistatic agent, a permeabilising agent, sweeteners, flavoring agents and colors.
- Surprisingly, although the tablets according to the invention disintegrate in the buccal cavity and present a release of the active ingredient which is equivalent to the conventional formulation, they nevertheless have a pleasant taste.
- Furthermore, the orodispersible tablets of the invention are found to show high stability and physical integrity, e.g. during storage, handling, packaging and the like, while maintaining very good disintegration performance.
- Fexofenadine may be used in the form of its racemate or a single enantiomer, in free base form or in acid addition salt form of the racemate or one of its single enantiomers. An acid addition salt form may be prepared from the free base form in a conventional manner and vice-versa. Examples of suitable acid addition salt forms include hydrochloride, lactate and ascorbate, preferably hydrochloride. Fexofenadine in the form of a hydrochloride salt is preferred.
- In a preferred embodiment, fexofenadine particles present a particle size such that 100% of the particles have an average size of less than 20 μm.
- In the tablets according to the invention, fexofenadine in anyone of said forms is present as coated granules.
- In the present patent application, the term “fexofenadine” is employed for designating anyone of its specific forms.
- According to an advantageous embodiment, the tablet according to the invention, has a hardness of not less than 15 N, when measured with the test method of the European Pharmacopeia (2.9.8).
- According to an advantageous embodiment, the tablet according to the invention contains coated granules of fexofenadine, or one of its pharmaceutically acceptable salts, and a mixture of excipients, the ratio of the mixture of excipients to the coated granules is 0.4 to 9, preferably 1.5 to 5 and even more preferably 2 to 3 parts by weight, the mixture of excipients comprising:
-
- at least one disintegrating agent,
- a soluble diluent agent,
- a lubricant,
- and optionally a permeabilising agent, a swelling agent, an antistatic agent, sweeteners, flavoring agents and colors.
- The disintegrating agent is selected from the group consisting of croscarmellose, available as e.g. Ac-di-sol®, crospovidone available as e.g. Kollidon CL®, and mixtures thereof.
- According to an advantageous embodiment of the invention, the soluble diluent agent used in the tablets presents binding properties. The soluble diluent agent with binding properties consists of a polyol having less than 13 carbon atoms and being either in the form of a directly compressible product with an average particle size of 100 to 500 μm, or in the form of a powder with an average particle size of less than 100 μm, this polyol preferably being selected from the group comprising mannitol, xylitol, sorbitol and maltitol, it being Understood that sorbitol cannot be used alone and that, in the case where there is only one soluble diluent agent with binding properties, it is used in the form of the directly compressible product, whereas in the case where there are at least two soluble diluent agents with binding properties, one is present in the directly compressible form and the other is present in powder form, it then being possible for the polyols to be the same, the ratio of directly compressible polyol to powder polyol being 99/1 to 20/80, preferably 80/20 to 20/80.
- The proportion of disintegrating agent is from 3 to 15% by weight, preferably 5 to 15% by weight, in the case of a mixture, each disintegrating agent being comprised between 1 and 10% by weight, preferably 5 to 10% by weight, and the proportion of soluble diluent agent being 30 to 90% by weight, preferably 40 to 60% by weight, based in each case on the weight of the tablet.
- The lubricant is selected from the group consisting of magnesium stearate, stearic acid, sodium stearyl fumarate, micronised polyoxyethyleneglycol (micronised Macrogol 6000), leukine, sodium benzoate and mixtures thereof.
- The amount of lubricant is from 0 to 3%, preferably from 1 to 2% by weight, based on the weight of the tablet.
- The lubricant can be dispersed within the mixture of excipients, or according to an advantageous embodiment, sprayed over the outer surface of the tablet. Thus, according to an advantageous embodiment of the tablets of the invention, the lubricant is in powder form and is, at least in part, disposed on the surface of the tablets.
- The permeabilising agent allows the creation of a hydrophilic network which facilitates the penetration of saliva and hence assists the disintegration of the tablet.
- The permeabilising agent is selected from the group comprising especially silica with a high affinity for aqueous solvents, such as colloidal silica (Aerosil®), precipitated silica (Syloïd® FP 244), maltodextrins, β-cyclodextrins and mixtures thereof.
- The amount of permeabilising agent is between 0 and 5%, preferably from 0.5 to 2% by weight, based on the weight of the tablet.
- A swelling agent can be incorporated in the mixture of excipients. Said swelling agent is selected from the group consisting of starch, modified starch or microcristalline cellulose.
- An antistatic agent can be incorporated as a flow aid, said antistatic agent being selected from the group consisting of micronised or non micronised talc, fumed silica (Aerosil® R972), colloidal silica (Aerosil®200), precipitated silica (Syloïd® FP 244), and mixtures thereof.
- The sweetener which can be included in the mixture of excipients, can be selected from the group consisting of especially aspartam, potassium acesulfame, sodium saccharinate, neohesperidin dihydrochalcone, sucralose, monoammonium glycyrrhizinate, and mixtures thereof.
- The flavorings and colors are those conventionally used in pharmacy for the preparation of tablets.
- The present invention also relates to the coated granules of fexofenadine or one of its pharmaceutically acceptable salts.
- The taste-masking of fexofenadine is achieved by coating granulated microcrystals of fexofenadine with one or more polymers.
- According to an advantageous embodiment of the invention, the granules of fexofenadine, or one of its pharmaceutically acceptable salts, are characterized in that the granules are coated and that they contain:
-
- microcrystals of fexofenadine, or one of its pharmaceutically acceptable salts,
- at least one binder,
- optionally a diluent agent, an antistatic agent, a sweetening agent and/or a coloring agent.
- Furthermore, the granulation excipients can also include disintegrating agents and/or surfactants.
- The binder is selected from the group consisting of cellulosic polymers, such as ethylcellulose, hydroxypropylcellulose and hydroxypropylmethyl cellulose, acrylic polymers, such as insoluble acrylate ammoniomethacrylate copolymer, polyacrylate or polymethacrylic copolymer, povidones, copovidones, polyvinylalcohols, alginic acid, sodium alginate, starch, pregelatinized starch, sucrose and its derivatives, guar gum, polyethylene glycol, preferably an acrylic polymer, most preferably Eudragit® E100, and mixtures thereof.
- Optionally, in order to enhance the granulation of the fexofenadine or one of its pharmaceutically acceptable salts, a diluent agent is used.
- The diluent agent is selected from the group consisting of microcrystalline cellulose, sucrose, dicalcium phosphate, starches, lactose and polyols of less than 13 carbon atoms, such as mannitol, xylitol, sorbitol, maltitol, pharmaceutically acceptable amino acids, such as glycin, and their mixtures.
- The antistatic agent, which can be used as flow aid, is selected from the group consisting of micronised or non micronised talc, fumed silica (Aerosil® R972), colloidal silica (Aerosil200), precipitated silica (Syloïd® FP244) and mixtures thereof.
- Conventional pharmaceutically acceptable sweetening agents and/or colouring agents can be incorporated into the granules of fexofenadine.
- In a particular embodiment, the granule of fexofenadine or one of its pharmaceutically acceptable salts, is in the form of a core of granulated microcrystals of fexofenadine, coated with at least one layer comprising fexofenadine.
- Said coated core is characterized in that the core and the layer comprise each from 70% to 95%, preferably 80% to 95% by weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof, the balance to 100% being formed with at least one binder, and that said coated core is advantageously a sphere. Such a specific structure has previously been described by the Applicant in the French patent application FR 00 14803.
- According to another embodiment of the invention, the granules comprise:
-
- from 10% to 95%, preferably from 50% to 70% of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
- at most 20%, preferably at most 10% by weight of the binder, relative to the weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
- at most 5%, preferably 2% by weight of the antistatic agent, relative to the weight of said granules
- optionally a diluent agent for the balance to 100%.
- In order to ensure efficient taste masking, and a dissolution profile of the active substance such that more than 70% of the active substance is released in 30 minutes, preferably more than 90% is released in 30 minutes, the granules are coated with a coating composition containing at least one coating polymer selected from the group consisting of cellulosic polymers, acrylic polymers and their mixtures.
- Among the cellulosic polymers, ethylcellulose, hydroxypropylcellulose (HPC) and hydroxypropylmethylcellulose (HPMC), are advantageously used.
- Among the acrylic polymers, insoluble acrylate ammoniomethacrylate copolymer (Eudragit® RL100 or RS100 or Eudragit® RL30D or RS30D), polyacrylate (Eudragit®NE30D), or methacrylic copolymers (Eudragit® L100-55 or Eudragit® L30D, Eudragit® E100, Eudragit® EPO . . . ) are advantageously used, alone, in combination or in admixture with pH-dependent polymers. Eudragit® E100 or a mixture of Eudragit® EPO and Eudragit®NE30D are preferred.
- In a preferred embodiment, the binder and the coating polymer are the same polymer.
- The prepared coating liquid is either water-based or prepared with organic solvents. According to an advantageous embodiment, this coating liquid is suitable to be sprayed with conventional spray layering equipment, as for example a fluidized bed equipped with a top insert or bottom (würster) insert.
- Optionally permeabilising agents, plasticizers, soluble agents, disintegrating agents and surfactants are added as coating additives.
- The plasticizer is selected in the group consisting of triacetine, triethylacetate, triethylcitrate (Eudraflex®), ethylphthalate, or mixtures thereof. The plasticizer is used in proportions of at most about 30%, preferably 10% by weight of the coating polymers.
- The soluble agents are selected in particular among the polyols having less than 13 carbon atoms.
- The disintegrating agent or a surfactant which could be added during the granulation and the coating steps allow improved dissolution.
- The surfactant may be an anionic, nonionic, cationic or amphoteric surfactant.
- The disintegrating agent is selected from the group consisting of croscarmellose, available as e.g. Ac-di-sol®, crospovidone available as e.g. Kollidon CL®, and mixtures thereof.
- The particle size range of coated granules comprising fexofenadine, or one of its pharmaceutically acceptable salts is adapted for obtaining an effective taste masking with an acceptable coating factor and a good mouthfeel.
- Advantageously the coated granules according to the invention have a particle size distribution between 150 μm and 500 μm, preferably between 150 μm and 425 μm, such that at least 50%, preferably at least 70% of the granules have a particle size ranging between 150 and 425 μm and less than 15% of the granules have a particle size less than 150 μm. The particle sizes are measured according to conventional methods, preferably by sieving.
- A granulation step is needed in order to obtain such particle size distribution.
- In a particular embodiment, the coated granules according to the invention comprise:
-
- from 10% to 95%, preferably 40 to 75% of granules of fexofenadine, or one of its pharmaceutically acceptable salts, preferably fexofenadine HCl,
- from 5 to 90%, preferably 10 to 70% and even more preferably from 25 to 55% of a coating polymer, preferably Eudragit® E100, the percentages being expressed by weight relative to the weight of the granules of fexofenadine, or one of its pharmaceutically acceptable salts,
- from 0 to 10% of a permeabilising agent, preferably colloidal silica, the percentages being expressed by weight relative to the weight of the coating polymer.
- Determination of workable proportions in any particular instance will generally be within the capability of the person skilled in the art. All indicated proportions and relative weight ranges described above are accordingly to be understood as being indicative of preferred or individually inventive teachings only and not as limiting the invention in its broadest aspect.
- Details concerning any of the excipients of the invention may be found in Fiedler, H. P. “Lexikon der Hilfsstoffe für Pharmazie, Kosmetik und angrenzende Gebiete”, Editio Cantor Verlag Aulendorf, Aulendorf, 4th revised and expanded edition (1996); “Handbook of Pharmaceutical Excipients”, 2nd Edition, Editors A. Wade and P. J. Weller (1994), Joint publication of American Pharmaceutical Association, Washington, USA and The Pharmaceutical Press, London, England; or may be obtained from the relevant manufacturers, the contents of which are hereby incorporated by reference.
- The invention also relates to a process for the preparation of coated granules of fexofenadine, which comprises the successive steps consisting in:
-
- dry mixing the microcrystals of fexofenadine or one of its pharmaceutically acceptable salts optionally with an antistatic agent and/or a diluent agent;
- granulating the mixture obtained in the above step by spraying of a solution or suspension of at least one binder,
- optionally applying a layer over the thus obtained granules by spraying thereon a suspension, or a solution comprising fexofenadine, or one of its pharmaceutically acceptable salts with at least one binder,
- coating the thus obtained granules with a suspension of a coating composition,
- drying the thus obtained coated granules.
- The invention also concerns a process for preparing orodispersible tablets comprising coated granules of fexofenadine, or one of its pharmaceutically acceptable salts.
- The process comprises the successive steps consisting in:
-
- dry mixing the microcrystals of fexofenadine, or one of its pharmaceutically acceptable salts, optionally with an antistatic agent, a diluent agent, a permeabilising agent, a sweetening agent and/or a coloring agent;
- granulating the thus obtained mixture by spraying thereon a solution or a suspension of at least one binder,
- optionally applying a layer over the thus obtained granules by spraying thereon a suspension, or a solution comprising fexofenadine, or one of its pharmaceutically acceptable salts with at least one binder.
- coating the thus obtained granules by spraying thereon a suspension, a dispersion or a solution of the coating composition,
- drying the thus obtained coated granules,
- dry mixing coated granules and a mixture of excipients consisting of at least one disintegrating agent, a soluble diluent agent, and optionally a lubricant, a permeabilising agent, a swelling agent, sweeteners, an antistatic agent, flavorings and colors,
- compressing the mixture of coated granules and excipients into a tablet.
- The lubricant can be mixed with the excipients for the tablet, but can advantageously be sprayed on the surface of the punches before tabletting.
- In this process the mixing, granulating and coating steps can be performed in different or in the same equipment, each step being performed in the presence of a mixture of excipients which are identical or different.
- For granulating, high shear mixer, planetary mixer or fluidized bed with insert used for bottom spray, granulation, tangential spray granulation, top spray granulation can be used, bottom spray granulation being preferred.
- In an advantageous embodiment, each step is performed on a fluidized air-bed, such as for example, but not limited to Glatt GPCG-1, GPCG-3, GPCG-5 or GPCG 120.
- For coating, bottom, top and tangential spray methods can be used as well as layering method, bottom spray method of coating being preferred.
- For compressing the mixture of coated granules and excipients into a tablet, various punches may be used, with diameters comprised between 8 and 17 mm, depending upon the dosage of the tablet.
- Various shapes may be used, such as for example, flat shape, advantageously with bevelled edges or polo punches.
- The orodispersible tablets of the present invention show rapid disintegration in the buccal cavity upon contact with saliva without chewing, in less than 60 seconds, preferably in less than 40 seconds, have a pleasant taste and palatability and thus have particularly good patient convenience and patient acceptance due to their increased ease of administration and ingestion.
- In addition the tablets of the invention show surprisingly high physical stability and are easy to handle and package.
- According to a preferred embodiment, the tablet of the invention presents the following composition:
-
- granules of Fexofenadine HCl coated with Eudragit® E100,
- and a mixture of excipients consisting of Eudragit® E100, mannitol powder, mannitol granular, Crospovidone, precipitated silica, sweeteners and flavors.
- For the preparation of said tablets, isopropanol is used as solvent and removed during the coating and granulation processes.
- According to an advantageous embodiment, the tablet of the invention has the following composition:
- Fexofenadine Coated Granules
Fexofenadine HCl 40-80% Eudragit ® E100 20-60% Precipitated silica 0-5%
the percentages being calculated by weight of coated granules, - Excipients for the Formulation of the Tablet
Fexofenadine coated granules 10-45% Mannitol powder and/or granular 50-90% Crospovidone 2-15% Precipitated silica 0-5% Magnesium stearate 0-5% Sucralose 0-5% Flavors 0-2%
the percentages being calculated by weight of the tablet. - For the preparation of said tablets, isopropanol is used as solvent and removed during the coating and granulation processes.
- The tablets are particularly effective in treating seasonal allergic rhinitis, in adults and children 6 years of age and older.
- The present invention also concerns-the use of a coated granules of fexofenadine with a mixture of excipients, as described above, for the manufacture of a medicament for the treatment of symptoms associated with seasonal allergic rhinitis.
- The present invention relates also to methods for the treatment of symptoms associated with seasonal allergic rhinitis, in which the tablets of fexofenadine according to the invention are orally administered.
- Symptoms treated effectively include sneezing, rhinorrhea, itchy nose/palate/throat, itchy/watery, rhinitis.
- The utility of the tablets of the present invention may be observed in standard bioavailability tests or standard animal models, for example ascertaining dosages of the present tablets giving blood levels of fexofenadine hydrochloride equivalent to blood levels having a therapeutical effect on administration of known fexofenadine oral dosage forms, e.g. a tablet.
- The appropriate dosage will, of course, vary depending upon, for example, the host and the nature and severity of the condition being treated. However, in general satisfactory results in animals are indicated to be obtained by daily treatments. In humans an indicated daily dosage is in the range from about 10 mg to about 500 mg per day, preferably from 30 mg to 180 mg, conveniently administered, for example, in divided doses up to four times a day or once daily. Preferred dosages, expressed as fexofenadine HCl, for children 6 to 11 years of age are about 30 mg two times a day, and for adults and children 12 years of age and older from about 60 mg two times a day, or 180 mg once a day.
- The invention is illustrated more in detail in the following examples.
- Particle size of Fexofenadine HCl used for the manufacture of granules of examples 1 to 4 is measured with conventional laser equipment.
- Particle size distribution has following characteristics:
D10% 2.1 μm D50% 5.3 μm D90% 11.1 μm - In the examples below, the following excipients are used:
-
- Methacrylic polymer sold under tradename Eudragit®EPO or Eudragit® E100.
- Polyacrylate sold under the tradename Eudragit® NE30D.
- Mannitol powder
- Mannitol granular 300
- Sucralose
- Aspartam
- Peppermint, wildberry as flavoring agents
- Precipitated silica sold under the name Syloïd FP244
- Polyvinylpyrrolidone sold under the name PVP K90
- Examples 1 to 4 relate to the preparation of coated granules of fexofenadine.
- Granulating Step
- 500 g of fexofenadine HCl mixed with 15 g of Syloïd FP 244 were granulated in a fluidized bed with 465 g of a mixture of Eudragit EPO/Eudragit NE30D (50/50) in water at 16% (weight/weight).
- Coating Step:
- The thus obtained granules were coated in a fluidized bed equipped with a top insert, by spraying thereon a dispersion of 465 g of a mixture of Eudragit EPO/Eudragit NE30D (50/50) in water at 16% (weight/weight).
- The amount of coating was of 12.5% by weight with respect to the weight of the granules of fexofenadine HCl.
- The dissolution rates of the thus obtained coated granules were measured with the following method:
Apparatus USP Apparatus II (Paddle method) Speed 50 rpm Volume 900 mL of HCl 0.001 N pH 3.0* Temperature 37.0° C. ± 0.5° C. Sampling (5 mL) 2.5, 7.5, 15, 30 and 60 minutes HPLC Detection UV at 220 nm HPLC column Zorbax SB-Phenyl, 5 μm, 4.6 × 250 mm. Injection volume 20 μL Mobile Phase Acetonitrile: 0.03 M Acetic acid containing Triethylamine pH 5.25 (36:64). Dissolution medium HCl 0.001 N adjusted to pH 3.0 ± 0.05 (if necessary) with o-Phosphoric acid. - The results are given in the following table 1:
TABLE 1 Dissolved fexofenadine in % (w/w) 5 minutes 55% 10 minutes 70% 15 minutes 75% 30 minutes 85% - More than 80% of fexofenadine is dissolved after 30 minutes, taste-masking is efficient.
- Granulating Step
- 500 g of fexofenadine HCl mixed with 15 g of Syloïd FP244 were granulated in a fluidized bed with 30 g of an aqueous solution of PVP K90 at 8% (weight/weight).
- Coating Step:
- The thus obtained granules were coated in a fluidized bed equipped with a top insert, by spraying thereon a mixture of Eudragit EPO/Eudragit NE30D (60/40) in water at 16% (weight/weight)
- The amount of coating was of 40% by weight with respect to the weight of the granules of fexofenadine HCl.
- The particle size distribution (Sieve method) is given in the following table.
TABLE 2 Sieve operture After Granulating step After Coating step >0.500 mm 14.5% 5.7% 0.425 mm-0.500 mm 13.0% 24.1% 0.355 mm-0.425 mm 20.0% 9.5% 0.250 mm-0.355 mm 30.5% 28.9% 0.150 mm-0.250 mm 21.5% 31.5% <0.150 mm 0.5% 0.3% - The dissolution rates of said granules were measured as indicated in example 1 above.
- The results are given in the following table 3:
TABLE 3 Dissolved fexofenadine in % (w/w) 5 minutes 65% 10 minutes 85% 15 minutes 100% 30 minutes 100% - More than 80% of fexofenadine is dissolved after 30 minutes, taste-masking is efficient.
- Granulating Step
- 1000 g of fexofenadine HCl mixed with 30 g of Syloïd FP 244 were granulated in a fluidized bed equipped with a Wurster insert with 1 500 g of an solution of Eudragit E100 in isopropanol at 12% (weight/weight).
- Coating Step:
- The thus obtained granules were coated in a fluidized bed equipped with a top insert, by spraying thereon a polymeric dispersion of 3 900 g of Eudragit E100 in isopropanol at 12% (weight/weight) containing 1% of Syloïd FP 244.
- The amount of coating was of 38% by weight with respect to the weight of the granules of fexofenadine HCl.
- The particle size distribution (Sieve method) is given in the following table.
TABLE 4 Sieve operture Coated granules >0.600 mm 0% 0.500 mm-0.600 mm 1.0% 0.425 mm-0.500 mm 9.2% 0.355 mm-0.425 mm 18.6% 0.250 mm-0.355 mm 36.2% 0.150 mm-0.250 mm 30.2% 0.090 mm-0.150 mm 3.4% <0.090 mm 1.4% - The dissolution rates of said granules were measured as indicated in example 1 above.
- The results are given in the following table 5:
TABLE 5 Dissolved fexofenadine in % (w/w) 5 minutes 55% 10 minutes 85% 15 minutes 95% 30 minutes 100% - More than 80% of fexofenadine is dissolved after 30 minutes, taste-masking is efficient.
- Granulating Step
- 1000 g of fexofenadine HCl mixed with 30 g of Syloïd FP 244 were granulated in a planetary mixer with 400 g of an solution of Eudragit E100 in isopropanol at 12% (weight/weight).
- Coating Step:
- The obtained granules were coated in a fluidized bed equipped with a Wurster insert, by spraying thereon a solution of Eudragit E100 in isopropanol at 10% (weight/weight) containing 1% of Syloïd FP 244.
- The amount of coating was of 30% by weight with respect to the weight of the granules of fexofenadine HCl.
- The dissolution rates of said granules were measured as indicated in example 1 above.
- The results are given in the following table 6:
TABLE 6 Dissolved fexofenadine in % (w/w) 5 minutes 40% 10 minutes 80% 15 minutes 95% 30 minutes 100%
100% of fexofenadine is dissolved after 30 minutes, taste-masking is efficient.
- Examples 5-8 relate to the preparation of tablets.
- Three types of tablets T1, T2, T3 were prepared using coated granules of fexofenadine presenting different coating ratios. The coated granules of fexofenadine were obtained as in example 3 above but using the three different coating ratios of 30, 35 and 40. Then, an amount of each type of said coated granules corresponding to 180 mg of fexofenadine HCl was thoroughly blended for 15 minutes with the following tablet excipients.
Crospovidone 10% Silica 0.5% Magnesium stearate 0.5% Aspartame 2% Flavor 1% Mannitol powder(60 μm)/granular (330 μm) (2/1) qs 100% - The percentages are expressed as percentage of the total weight of a tablet.
- The homogeneous obtained blend was introduced in a tabletting machine equipped with 14 mm-diameter polo shape punches.
- These tablets T1, T2 and T3 were obtained.
- For each tablet thus obtained, the weight, hardness, disintegrating time in mouth, mouthfeel and taste were measured.
- The results are displayed in the table 7
TABLE 7 Tablets T1 T2 T3 Coated granule ratio 30 35 40 (% by weight) Weight 920 mg 780 mg 690 mg Hardness 44 N 39 N 45 N Disintegration time 15-20 sec. 15-20 sec 20-25 sec. in mouth Mouthfeel Complies Complies Complies Taste Complies Complies Complies
T1, T2, T3 present an acceptable dissolution rate with good taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- As in example 5, three types of tablets (T4, T5, T6) presenting coated granules of fexofenadine with coating ratios of 30, 35, 40 were prepared but using an amount of fexofenadine HCl equivalent to 30 mg per tablet.
- The homogeneous obtained blend was introduced in a tabletting machine equipped with polo shape punches as described in the table.
- Results are displayed in the table 8
TABLE 8 Tablets T4 T5 T6 Coated granule ratio 30 35 40 (% by weight) Punch diameter 8 mm 7 mm 6 mm Weight 153 mg 131 mg 115 mg Hardness 44 N 39 N 45 N Disintegration time 15-20 sec. 15-20 sec 20-25 sec. in mouth Mouthfeel Complies Complies Complies Taste Complies Complies Complies
Tablets T4, T5 and T6 present an acceptable taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- Tablets T7 according to the formula of T2 of example 5 are manufactured, using a ratio of Mannitol powder/Mannitol granular ratio of 1/1, containing an amount of fexofenadine HCl equivalent to 180 mg per tablet.
- The homogeneous obtained blend was introduced in a tabletting machine equipped with 14 mm-diameter polo shape punches.
- The disintegration time in the mouth, the mouthfeel and taste were evaluated.
- The results are displayed in the table 9.
TABLE 9 Tablets T7 Disintegration time in mouth 25 sec. Mouthfeel Complies Taste Complies
Tablets T7 with a mannitol powder/granular ratio of 1/1 (w/w) present a good taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- Three types of tablets (T8, T9, T10 ) according to the formula T2 of example 5 were manufactured but using three different ratios of crospovidone of 5, 7.5 and 10% by weight.
- The homogeneous obtained blend was introduced in a tabletting machine equipped with 14mm-diameter polo shape.
- Tablets T8, T9 and T10 were thus obtained. The disintegrating time in mouth, the hardness, the mouthfeell and taste were evaluated, the results are displayed in table 10.
TABLE 10 Tablets T8 T9 T10 Crospovidone ratio 5 7.5 10 (% by weight) Hardness 44 N 45 N 45 N Disintegration time 20-25 sec. 20-25 sec 20-25 sec. in mouth Mouthfeel Complies Complies Complies Taste Complies Complies Complies
Tablets T8, T9 and T10 present an acceptable taste and pleasant mouthfeel and disintegrate in buccal cavity in less than 30 seconds.
- A bioequivalence study was conducted with two tablets (T11 and T12) according to the invention versus Allegra® 180 mg (Reference).
- 15 subjects received T11 versus Reference and 13 subjects received T12, each versus Reference
- The respective compositions of T11 and T12 are given below:
Fexofenadine HCl coated granules T11 T12 Fexofenadine HCl 48.4% 58.2% Eudragit E100 47.4% 37.7% Silica 4.2% 4.1% - Tablets
Coated granules corresponding to 30% 180 mg of Fexofenadine HCl Crospovidone 5% Silica 0.5% Magnesium stearate 1% Sucralose 2% Flavor 0.2% Mannitol powder(60 μm)/granular (330 μm) (1/1) qs 100% - Said tablets were prepared according to the process of example 5 above. The tablets (Prototype and Reference) were administered to fasting patients. Pharmacokinetic parameters obtained for each prototype A and B and Reference are listed in tables 11 and 12:
TABLE 11 Test 1 (n = 15)-mean values AUC (CV) Cmax (CV) Tmax (CV) Reference 3132.2 453.8 2.0 T11 3804.4 571.2 2.9 (% as exp. versus reference) (121) (126) (144)
T11 under fasting conditions has slightly higher bioavailability relative to the reference.
-
TABLE 12 Test 2 (n = 13)-mean values AUC Cmax Tmax Reference 3017.0 457.3 2.2 T12 3047.1 409.8 2.6 (% as exp. versus reference) (101) (90) (115)
T12 under fasting is bioequivalent relative to the reference tablet.
Claims (23)
1-13. (canceled)
14. Granules of fexofenadine, or one of its pharmaceutically acceptable salts, wherein the granules are coated and contain:
microcrystals of fexofenadine, or one of its pharmaceutically acceptable salts,
at least one binder selected from the group consisting of cellulosic polymers, such as ethylcellulose, hydroxypropylcellulose and hydroxypropylmethylcellulose, acrylic polymers such as insoluble acrylate ammoniomethacrylate copolymer, polyacrylate or polymethacrylic copolymer, povidones, copovidones, polyvinylalcohols, alginic acid, sodium alginate, starch, pregelatinized starch, sucrose and its derivatives, guar gum, polyethylene glycol and mixtures thereof.
15. Granules according to claim 14 which further contain a diluent agent selected from the group consisting of microcrystalline cellulose, sucrose, dicalcium phosphate starches, lactose, polyols of less than 13 carbon atoms such as mannitol, xylitol, sorbitol, maltitol, pharmaceutically acceptable amino acids such as glycin, and their mixtures, an antistatic agent selected from the group consisting of micronised or non micronised talc, fumed silica, precipitated and colloidal silica, a sweetening agent or a coloring agent.
16. Granules according to claim 14 , which further comprise a disintegrating agent selected from the group consisting of croscarmellose, crospovidone and mixtures thereof or a surfactant which can be an anionic, nonionic, cationic or amphoteric surfactant.
17. Granules according to claim 15 , comprising:
from 10% to 95% of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
at most 20% by weight of the binder, relative to the weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
at most 5% of the antistatic agent, relative to the weight of said granules.
18. Granules according to claim 17 , comprising:
from 50% to 70% of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
at most 10% by weight of the binder, relative to the weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof,
at most 2% by weight of the antistatic agent, relative to the weight of said granules.
19. Granules according to claim 17 , further comprising a diluent agent for the balance to 100%.
20. Granules according to claim 18 , further comprising a diluent agent for the balance to 100%.
21. Granules according to claim 14 , wherein they are coated with a coating composition containing at least one coating polymer selected rom the group consisting of cellulosic polymers such as ethylcellulose, hydroxypropylcellulose and hydroxypropylmethylcellulose, acrylic polymers such as insoluble acrylate amoniomethacrylate copolymer, polyacrylate or methacrylic copolymers, and mixtures thereof.
22. Granules according to claim 21 , wherein the coating composition further contains permeabilizing agents, plasticizers, soluble agents, disintegrating agents or surfactants.
23. Granules according to claim 14 comprising:
from 10% to 95% of granules of fexofenadine, or one of its pharmaceutically acceptable salts.
from 5 to 90% of a coating polymer, the percentages being expressed by weight relative to the weight of the granules of the fexofenadine, or one of its pharmaceutically acceptable salts.
from 0 to 10% of a permeabilising agent, the percentages being expressed by weight relative to the weight of the coating polymer.
24. Granules according to claim 23 comprising:
from 40 to 75% of granules of fexofenadine, or one of its pharmaceutically acceptable salts,
from 10 to 70% of a coating polymer, the percentages being expressed by weight relative to the weight of the granules of the fexofenadine, or one of its pharmaceutically acceptable salts.
from 0 to 10% of colloidal silica as permeabilising agent, the percentages being expressed by weight relative to the weight of the coating polymer.
25. Granules according to claim 24 , comprising from 25 to 55% of a coating polymer.
26. Granules according to claim 23 , comprising fexofenadine hydrochloride.
27. Coated granules of fexofenadine, or one of its pharmaceutically acceptable salts, according to claim 14 , which are coated with a coating layer containing fexofenadine wherein the granules and the coating layer comprise each from 70% to 95% by weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof, the balance to 100% being formed with at least one binder.
28. Coated granules of fexofenadine, or one of its pharmaceutically acceptable salts, according to claim 27 , which are coated with a coating layer containing fexofenadine wherein the granules and the coating layer comprise each from 80% to 95% by weight of fexofenadine, or one of the pharmaceutically acceptable salts thereof, the balance to 100% being formed with at least one binder.
29. Process for the preparation of granules according to claim 14 wherein it comprises the successive steps consisting in:
dry mixing the microcrystals of the fexofenadine or one of its pharmaceutically acceptable salts;
granulating the mixture obtained in the above step by spraying of a solution or suspension of at least one binder,
coating the thus obtained granules with a suspension of a coating composition,
drying the thus obtained coated granules.
30. Process for the preparation of granules according to claim 15 , wherein it comprises the successive steps consisting in:
dry mixing the microcrystals of the fexofenadine or one of its pharmaceutically acceptable salts with an antistatic agent or a diluent agent;
granulating the mixture obtained in the above step by spraying of a solution or suspension of at least one binder,
coating the thus obtained granules with a suspension of a coating composition,
drying the thus obtained coated granules.
31. Process for the preparation of granules according to claim 27 wherein it comprises the successive steps consisting in:
dry mixing the microcrystals of the fexofenadine or one of its pharmaceutically acceptable salts;
granulating the mixture obtained in the above step by spraying of a solution or suspension of at least one binder,
applying a layer over the thus obtained granules by spraying thereon a suspension, or a solution comprising fexofenadine, or one of its pharmaceutically acceptable salts with at lease one binder,
coating the thus obtained granules with a suspension of a coating composition,
drying the thus obtained coated granules.
32. Process according to claim 31 wherein it comprises the successive steps consisting in:
dry mixing the microcrystals of the fexofenadine or one of its pharmaceutically acceptable salts with an antistatic agent or a diluent agent;
granulating the mixture obtained in the above step by spraying of a solution or suspension of a least one binder,
applying a layer over the thus obtained granules by spraying thereon a suspension, or a solution comprising fexofenadine, or one of its pharmaceutically acceptable salts with at least one binder,
coating the thus obtained granules with suspension of a coating composition,
drying the thus obtained coated granules.
33. Process for the preparation of tablets according to claim 31 , comprising the successive steps consisting in:
preparing coated granules of fexofenadine, or one of its pharmaceutically acceptable salts,
dry mixing coated granules and a mixture of excipients consisting of at least one disintegrating agent and a soluble diluent agent,
compressing the mixture of coated granules and excipients into a tablet.
34. Process for the preparation of tablets according to claim 31 , wherein the mixture of excipients further comprises a lubricant, a permeabilising agent, a swelling agent, sweeteners, an antistatic agent, flavorings and colors.
35-36. (canceled).
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Cited By (4)
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Publication number | Priority date | Publication date | Assignee | Title |
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AU2003209673B2 (en) * | 2002-03-08 | 2007-10-18 | M/S. Ind-Swift Limited | Tasteless directly compressible fast-dissolving complexes and pharmaceutical formulations thereof |
US20050147670A1 (en) * | 2002-05-29 | 2005-07-07 | Impax Laboratories Inc. | Oral disintegrating dosage forms |
US20030228370A1 (en) * | 2002-06-11 | 2003-12-11 | Michel Serpelloni | Orodispersible solid pharmaceutical form |
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US20070048373A1 (en) * | 2005-08-30 | 2007-03-01 | Cima Labs Inc. | Dried milled granulate and methods |
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Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4239901A (en) * | 1976-10-14 | 1980-12-16 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Pyrazol-1-ylphenylacetic acids |
US4254129A (en) * | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
US4341759A (en) * | 1975-11-17 | 1982-07-27 | Aktiebolaget Hassle | Granule having controlled release properties |
US5075114A (en) * | 1990-05-23 | 1991-12-24 | Mcneil-Ppc, Inc. | Taste masking and sustained release coatings for pharmaceuticals |
US5213811A (en) * | 1991-09-13 | 1993-05-25 | Sterling Drug Inc. | Oral sustained-release drug compositions |
US5460828A (en) * | 1993-01-28 | 1995-10-24 | Recordati S.A., Chemical And Pharmaceutical Company | Process for the preparation of microgranules suitable for suspension in fluids |
US5464632A (en) * | 1991-07-22 | 1995-11-07 | Laboratoires Prographarm | Rapidly disintegratable multiparticular tablet |
US5578316A (en) * | 1992-06-04 | 1996-11-26 | Smithkline Beecham Corporation | Palatable pharmaceutical compositions |
US6106861A (en) * | 1997-07-21 | 2000-08-22 | Laboratoires Prographarm | Multiparticulate tablet disintegrating in less than 40 seconds in the mouth |
US6113942A (en) * | 1995-02-28 | 2000-09-05 | Aventis Pharmaceuticals Inc. | Pharmaceutical composition for piperidinoalkanol compounds |
US6117452A (en) * | 1998-08-12 | 2000-09-12 | Fuisz Technologies Ltd. | Fatty ester combinations |
US6120803A (en) * | 1997-08-11 | 2000-09-19 | Alza Corporation | Prolonged release active agent dosage form adapted for gastric retention |
US6267811B1 (en) * | 1998-12-21 | 2001-07-31 | Stora Enso North America Corp. | Talc slurry dispersion |
US20040101568A1 (en) * | 2000-11-16 | 2004-05-27 | Etienne Bruna | Microgranules based on active principle and method for making same |
US7067149B1 (en) * | 1998-11-06 | 2006-06-27 | Ethypharm | Fast disintegrating tablet |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100193121B1 (en) * | 1990-05-23 | 1999-06-15 | 조셉 에프. 셔츠, 안드레아 엘. 콜비 | Taste masking and sustained release coatings |
EP1380308B1 (en) * | 1996-07-12 | 2008-07-09 | Daiichi Pharmaceutical Co., Ltd. | Quickly disintegrable compression-molded materials and process for producing the same |
FR2790387B1 (en) | 1999-03-01 | 2001-05-18 | Prographarm Laboratoires | ORODISPERSIBLE TABLET HAVING LOW FRIABILITY AND PROCESS FOR THE PREPARATION THEREOF |
KR20010006835A (en) * | 1999-03-25 | 2001-01-26 | 김선진 | Rapidly disintegrable tablet for oral administration |
JP3435664B2 (en) * | 1999-12-08 | 2003-08-11 | ヤンセンファーマ株式会社 | Oral fast disintegrating tablet and method for producing the same |
EP1269995A1 (en) * | 2000-03-27 | 2003-01-02 | Kyowa Hakko Kogyo Co., Ltd. | Easy-to-take granule |
US20020119196A1 (en) * | 2000-12-21 | 2002-08-29 | Narendra Parikh | Texture masked particles containing an active ingredient |
US6723348B2 (en) * | 2001-11-16 | 2004-04-20 | Ethypharm | Orodispersible tablets containing fexofenadine |
-
2001
- 2001-11-16 US US09/995,975 patent/US6723348B2/en not_active Expired - Lifetime
-
2002
- 2002-11-14 WO PCT/EP2002/014917 patent/WO2003041683A2/en active Application Filing
- 2002-11-14 PL PL02368610A patent/PL368610A1/en not_active Application Discontinuation
- 2002-11-14 ES ES02803040T patent/ES2269817T3/en not_active Expired - Lifetime
- 2002-11-14 CN CN201010176984A patent/CN101849917A/en active Pending
- 2002-11-14 CN CNA02822602XA patent/CN1592622A/en active Pending
- 2002-11-14 CA CA2466580A patent/CA2466580C/en not_active Expired - Lifetime
- 2002-11-14 KR KR1020097019922A patent/KR20090117899A/en not_active Application Discontinuation
- 2002-11-14 KR KR1020047007536A patent/KR101020809B1/en active IP Right Grant
- 2002-11-14 DE DE60213861T patent/DE60213861T2/en not_active Expired - Lifetime
- 2002-11-14 US US10/495,007 patent/US20050053654A1/en not_active Abandoned
- 2002-11-14 HU HU0402293A patent/HU229570B1/en unknown
- 2002-11-14 AU AU2002356786A patent/AU2002356786A1/en not_active Abandoned
- 2002-11-14 EP EP02803040A patent/EP1458387B1/en not_active Expired - Lifetime
- 2002-11-14 AT AT02803040T patent/ATE335483T1/en not_active IP Right Cessation
- 2002-11-14 JP JP2003543570A patent/JP2005513008A/en active Pending
-
2005
- 2005-03-19 HK HK05102404A patent/HK1069340A1/en not_active IP Right Cessation
-
2010
- 2010-06-01 JP JP2010125743A patent/JP5525920B2/en not_active Expired - Lifetime
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4341759A (en) * | 1975-11-17 | 1982-07-27 | Aktiebolaget Hassle | Granule having controlled release properties |
US4239901A (en) * | 1976-10-14 | 1980-12-16 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Pyrazol-1-ylphenylacetic acids |
US4254129A (en) * | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
US5075114A (en) * | 1990-05-23 | 1991-12-24 | Mcneil-Ppc, Inc. | Taste masking and sustained release coatings for pharmaceuticals |
US5464632A (en) * | 1991-07-22 | 1995-11-07 | Laboratoires Prographarm | Rapidly disintegratable multiparticular tablet |
US5464632C1 (en) * | 1991-07-22 | 2001-02-20 | Prographarm Lab | Rapidly disintegratable multiparticular tablet |
US5213811A (en) * | 1991-09-13 | 1993-05-25 | Sterling Drug Inc. | Oral sustained-release drug compositions |
US5578316A (en) * | 1992-06-04 | 1996-11-26 | Smithkline Beecham Corporation | Palatable pharmaceutical compositions |
US5460828A (en) * | 1993-01-28 | 1995-10-24 | Recordati S.A., Chemical And Pharmaceutical Company | Process for the preparation of microgranules suitable for suspension in fluids |
US6113942A (en) * | 1995-02-28 | 2000-09-05 | Aventis Pharmaceuticals Inc. | Pharmaceutical composition for piperidinoalkanol compounds |
US6106861A (en) * | 1997-07-21 | 2000-08-22 | Laboratoires Prographarm | Multiparticulate tablet disintegrating in less than 40 seconds in the mouth |
US6120803A (en) * | 1997-08-11 | 2000-09-19 | Alza Corporation | Prolonged release active agent dosage form adapted for gastric retention |
US6117452A (en) * | 1998-08-12 | 2000-09-12 | Fuisz Technologies Ltd. | Fatty ester combinations |
US7067149B1 (en) * | 1998-11-06 | 2006-06-27 | Ethypharm | Fast disintegrating tablet |
US6267811B1 (en) * | 1998-12-21 | 2001-07-31 | Stora Enso North America Corp. | Talc slurry dispersion |
US20040101568A1 (en) * | 2000-11-16 | 2004-05-27 | Etienne Bruna | Microgranules based on active principle and method for making same |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090136568A1 (en) * | 2004-10-29 | 2009-05-28 | Mayne Pharma International Pty Ltd | Tabletting process |
US20100330180A1 (en) * | 2004-10-29 | 2010-12-30 | Stefan Lukas | Tabletting process |
US8715724B2 (en) | 2004-10-29 | 2014-05-06 | Mayne Pharma International Pty Ltd | Tabletting process |
US20090317558A1 (en) * | 2008-06-23 | 2009-12-24 | Cornell University | Multiplexed Electrospray Deposition Apparatus |
US20100029691A1 (en) * | 2008-08-04 | 2010-02-04 | Advanced Drug Delivery Systems Pharmaceuticals, LLC | Fast onset orodispersable tablets |
WO2010017111A1 (en) * | 2008-08-04 | 2010-02-11 | Adds Pharmaceuticals Llc | Fast onset orodispersable tablets |
US8343978B2 (en) | 2008-08-04 | 2013-01-01 | Adds Pharmaceuticals Llc | Fast onset orodispersable tablets |
US10869877B2 (en) | 2014-10-08 | 2020-12-22 | Mayne Pharma International Pty. Ltd. | Controlled release doxycycline |
Also Published As
Publication number | Publication date |
---|---|
PL368610A1 (en) | 2005-04-04 |
HUP0402293A2 (en) | 2005-02-28 |
EP1458387B1 (en) | 2006-08-09 |
JP2005513008A (en) | 2005-05-12 |
WO2003041683A3 (en) | 2003-08-28 |
ATE335483T1 (en) | 2006-09-15 |
KR101020809B1 (en) | 2011-03-09 |
CN1592622A (en) | 2005-03-09 |
CN101849917A (en) | 2010-10-06 |
US6723348B2 (en) | 2004-04-20 |
CA2466580C (en) | 2011-06-07 |
KR20090117899A (en) | 2009-11-13 |
DE60213861D1 (en) | 2006-09-21 |
HU229570B1 (en) | 2014-02-28 |
EP1458387A2 (en) | 2004-09-22 |
HK1069340A1 (en) | 2005-05-20 |
ES2269817T3 (en) | 2007-04-01 |
WO2003041683A2 (en) | 2003-05-22 |
KR20050044512A (en) | 2005-05-12 |
AU2002356786A1 (en) | 2003-05-26 |
US20030099700A1 (en) | 2003-05-29 |
DE60213861T2 (en) | 2007-03-08 |
JP5525920B2 (en) | 2014-06-18 |
JP2010184938A (en) | 2010-08-26 |
HUP0402293A3 (en) | 2011-05-30 |
CA2466580A1 (en) | 2003-05-22 |
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