MXPA04005955A - SISTEMA DE CARBOHIDRATOS CO-PROCESADOS COMO UNA MATRIZ DE DISOLUCION RáPIDA PARA FORMAS DE DOSIFICACION SOLIDAS. - Google Patents
SISTEMA DE CARBOHIDRATOS CO-PROCESADOS COMO UNA MATRIZ DE DISOLUCION RáPIDA PARA FORMAS DE DOSIFICACION SOLIDAS.Info
- Publication number
- MXPA04005955A MXPA04005955A MXPA04005955A MXPA04005955A MXPA04005955A MX PA04005955 A MXPA04005955 A MX PA04005955A MX PA04005955 A MXPA04005955 A MX PA04005955A MX PA04005955 A MXPA04005955 A MX PA04005955A MX PA04005955 A MXPA04005955 A MX PA04005955A
- Authority
- MX
- Mexico
- Prior art keywords
- mannitol
- composition according
- sorbitol
- composition
- present
- Prior art date
Links
- 150000001720 carbohydrates Chemical class 0.000 title abstract description 49
- 239000007909 solid dosage form Substances 0.000 title abstract description 21
- 239000011159 matrix material Substances 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 261
- 210000000214 mouth Anatomy 0.000 claims abstract description 30
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 113
- 229930195725 Mannitol Natural products 0.000 claims description 113
- 239000000594 mannitol Substances 0.000 claims description 113
- 235000010355 mannitol Nutrition 0.000 claims description 113
- 239000000600 sorbitol Substances 0.000 claims description 89
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 88
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 73
- 239000002245 particle Substances 0.000 claims description 68
- 238000000034 method Methods 0.000 claims description 55
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 47
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- 239000004480 active ingredient Substances 0.000 claims description 30
- 238000001035 drying Methods 0.000 claims description 30
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- 239000000126 substance Substances 0.000 claims description 18
- 229910002027 silica gel Inorganic materials 0.000 claims description 16
- 239000000741 silica gel Substances 0.000 claims description 16
- 229920002785 Croscarmellose sodium Polymers 0.000 claims description 14
- 239000008119 colloidal silica Substances 0.000 claims description 14
- 239000007884 disintegrant Substances 0.000 claims description 14
- 238000001694 spray drying Methods 0.000 claims description 12
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 11
- 229960000913 crospovidone Drugs 0.000 claims description 11
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 claims description 11
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 claims description 11
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 229940079832 sodium starch glycolate Drugs 0.000 claims description 8
- 239000008109 sodium starch glycolate Substances 0.000 claims description 8
- 229920003109 sodium starch glycolate Polymers 0.000 claims description 8
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 claims description 7
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 11
- 238000004090 dissolution Methods 0.000 description 11
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- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 7
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000004376 Sucralose Substances 0.000 description 5
- 238000005056 compaction Methods 0.000 description 5
- MVPICKVDHDWCJQ-UHFFFAOYSA-N ethyl 3-pyrrolidin-1-ylpropanoate Chemical compound CCOC(=O)CCN1CCCC1 MVPICKVDHDWCJQ-UHFFFAOYSA-N 0.000 description 5
- 238000005469 granulation Methods 0.000 description 5
- 229940034008 mannitol / sorbitol Drugs 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- BALXUFOVQVENIU-KXNXZCPBSA-N pseudoephedrine hydrochloride Chemical compound [H+].[Cl-].CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 BALXUFOVQVENIU-KXNXZCPBSA-N 0.000 description 5
- 229940045902 sodium stearyl fumarate Drugs 0.000 description 5
- 235000019408 sucralose Nutrition 0.000 description 5
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- MKXZASYAUGDDCJ-SZMVWBNQSA-N LSM-2525 Chemical compound C1CCC[C@H]2[C@@]3([H])N(C)CC[C@]21C1=CC(OC)=CC=C1C3 MKXZASYAUGDDCJ-SZMVWBNQSA-N 0.000 description 4
- 235000009754 Vitis X bourquina Nutrition 0.000 description 4
- 235000012333 Vitis X labruscana Nutrition 0.000 description 4
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- 229960004543 anhydrous citric acid Drugs 0.000 description 4
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- 239000003814 drug Substances 0.000 description 4
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- 239000007788 liquid Substances 0.000 description 4
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 238000004064 recycling Methods 0.000 description 4
- BNRNXUUZRGQAQC-UHFFFAOYSA-N sildenafil Chemical compound CCCC1=NN(C)C(C(N2)=O)=C1N=C2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(C)CC1 BNRNXUUZRGQAQC-UHFFFAOYSA-N 0.000 description 4
- 238000010561 standard procedure Methods 0.000 description 4
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 3
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 3
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- 238000007907 direct compression Methods 0.000 description 3
- 239000011363 dried mixture Substances 0.000 description 3
- 235000003599 food sweetener Nutrition 0.000 description 3
- 239000000845 maltitol Substances 0.000 description 3
- 235000010449 maltitol Nutrition 0.000 description 3
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 3
- 229940035436 maltitol Drugs 0.000 description 3
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 3
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- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 3
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- 229960000620 ranitidine Drugs 0.000 description 1
- JQXXHWHPUNPDRT-WLSIYKJHSA-N rifampicin Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C([O-])=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N1CC[NH+](C)CC1 JQXXHWHPUNPDRT-WLSIYKJHSA-N 0.000 description 1
- 229960001225 rifampicin Drugs 0.000 description 1
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- WTGQALLALWYDJH-MOUKNHLCSA-N scopolamine hydrobromide (anhydrous) Chemical compound Br.C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 WTGQALLALWYDJH-MOUKNHLCSA-N 0.000 description 1
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- 239000002002 slurry Substances 0.000 description 1
- LXMSZDCAJNLERA-ZHYRCANASA-N spironolactone Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)SC(=O)C)C[C@@]21CCC(=O)O1 LXMSZDCAJNLERA-ZHYRCANASA-N 0.000 description 1
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- 239000011550 stock solution Substances 0.000 description 1
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- MBGGBVCUIVRRBF-UHFFFAOYSA-N sulfinpyrazone Chemical compound O=C1N(C=2C=CC=CC=2)N(C=2C=CC=CC=2)C(=O)C1CCS(=O)C1=CC=CC=C1 MBGGBVCUIVRRBF-UHFFFAOYSA-N 0.000 description 1
- 229960003329 sulfinpyrazone Drugs 0.000 description 1
- 229960000894 sulindac Drugs 0.000 description 1
- MLKXDPUZXIRXEP-MFOYZWKCSA-N sulindac Chemical compound CC1=C(CC(O)=O)C2=CC(F)=CC=C2\C1=C/C1=CC=C(S(C)=O)C=C1 MLKXDPUZXIRXEP-MFOYZWKCSA-N 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- KQKPFRSPSRPDEB-UHFFFAOYSA-N sumatriptan Chemical compound CNS(=O)(=O)CC1=CC=C2NC=C(CCN(C)C)C2=C1 KQKPFRSPSRPDEB-UHFFFAOYSA-N 0.000 description 1
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- 239000006188 syrup Substances 0.000 description 1
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- IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 description 1
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- KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
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- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
-
- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/485—Morphinan derivatives, e.g. morphine, codeine
-
- 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
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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- 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
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
- A61K9/2081—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets with microcapsules or coated microparticles according to A61K9/50
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Emergency Medicine (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Pain & Pain Management (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Biophysics (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34136601P | 2001-12-17 | 2001-12-17 | |
| US10/274,227 US7118765B2 (en) | 2001-12-17 | 2002-10-18 | Co-processed carbohydrate system as a quick-dissolve matrix for solid dosage forms |
| PCT/US2002/040506 WO2003051338A1 (en) | 2001-12-17 | 2002-12-17 | Co-processed carbohydrate system as a quick-dissolve matrix for solid dosage forms |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04005955A true MXPA04005955A (es) | 2005-03-31 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04005955A MXPA04005955A (es) | 2001-12-17 | 2002-12-17 | SISTEMA DE CARBOHIDRATOS CO-PROCESADOS COMO UNA MATRIZ DE DISOLUCION RáPIDA PARA FORMAS DE DOSIFICACION SOLIDAS. |
Country Status (9)
| Country | Link |
|---|---|
| US (4) | US7118765B2 (https=) |
| EP (1) | EP1465604B1 (https=) |
| JP (1) | JP4472988B2 (https=) |
| AU (1) | AU2002351396B2 (https=) |
| CA (1) | CA2470601C (https=) |
| ES (1) | ES2429529T3 (https=) |
| MX (1) | MXPA04005955A (https=) |
| WO (1) | WO2003051338A1 (https=) |
| ZA (1) | ZA200404998B (https=) |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7815937B2 (en) * | 1998-10-27 | 2010-10-19 | Biovail Laboratories International Srl | Quick dissolve compositions and tablets based thereon |
| CA2348452A1 (en) * | 1998-10-27 | 2000-05-04 | Biovail Technologies Ltd. | Microparticles containing peg and/or peg glyceryl esters |
| US7118765B2 (en) * | 2001-12-17 | 2006-10-10 | Spi Pharma, Inc. | Co-processed carbohydrate system as a quick-dissolve matrix for solid dosage forms |
| FR2834889B1 (fr) * | 2002-01-18 | 2004-04-02 | Roquette Freres | Forme pharmaceutique solide orodispersible |
| FR2834894B1 (fr) * | 2002-01-21 | 2004-02-27 | Servier Lab | Composition pharmaceutique orodispersible de piribedil |
| DE10232113A1 (de) | 2002-07-16 | 2004-01-29 | Bayer Ag | Vardenafil Hydrochlorid Trihydrat enthaltende Arzneimittel |
| US7282217B1 (en) * | 2003-08-29 | 2007-10-16 | Kv Pharmaceutical Company | Rapidly disintegrable tablets |
| JP3841804B2 (ja) | 2003-10-15 | 2006-11-08 | 富士化学工業株式会社 | 口腔内速崩壊性錠剤用の組成物 |
| US8349361B2 (en) | 2003-10-15 | 2013-01-08 | Fuji Chemical Industry Co., Ltd. | Composition for rapid disintegrating tablet in oral cavity |
| JP5179757B2 (ja) * | 2004-02-17 | 2013-04-10 | トランセプト ファーマシューティカルズ， インコーポレイティド | 口腔粘膜を介して催眠剤をデリバリーするための組成物及びその使用方法 |
| US20050214365A1 (en) * | 2004-03-24 | 2005-09-29 | Gulf Pharmaceutical Industries | [Instant dissolving tablet composition for loratidine and desloratidine] |
| DE602005013232D1 (de) * | 2004-07-01 | 2009-04-23 | Lek Pharmaceuticals | Schnell zerfallende im mund dispergierbare zusammensetzung mit nicht-filamentösen mitverarbeiteten polyol-teilchen und verkieselter mikrokristalliner cellulose |
| ATE521343T1 (de) * | 2004-11-24 | 2011-09-15 | Teva Pharma | Im mund zerfallende zusammensetzungen von rasagilin |
| DE102005009241A1 (de) * | 2005-03-01 | 2006-09-07 | Bayer Healthcare Ag | Arzneiformen mit kontrollierter Bioverfügbarkeit |
| DE102005009240A1 (de) | 2005-03-01 | 2006-09-07 | Bayer Healthcare Ag | Arzneiformen mit verbesserten pharmakokinetischen Eigenschaften |
| US20060264458A1 (en) * | 2005-05-03 | 2006-11-23 | Jie Du | Quinine dosage forms and methods of use thereof |
| CN1686089B (zh) * | 2005-05-08 | 2010-08-18 | 北京健健康康生物技术有限公司 | 一种可直接压片的木糖醇颗粒及其制备方法 |
| EP1883408A4 (en) * | 2005-05-25 | 2009-11-11 | Transcept Pharmaceuticals Inc | SOLID COMPOSITIONS AND METHODS FOR TREATMENT OF INSOMNIA IN THE NIGHT |
| US20070287740A1 (en) * | 2005-05-25 | 2007-12-13 | Transcept Pharmaceuticals, Inc. | Compositions and methods of treating middle-of-the night insomnia |
| US20070225322A1 (en) * | 2005-05-25 | 2007-09-27 | Transoral Pharmaceuticals, Inc. | Compositions and methods for treating middle-of-the night insomnia |
| IL169678A (en) | 2005-07-14 | 2010-11-30 | Innova Sa | Sweetener compositions |
| US20090186896A1 (en) * | 2005-09-29 | 2009-07-23 | Bayer Healthcare Ag | PDE Inhibitors and Combinations Thereof for the Treatment of Urological Disorders |
| US20070092553A1 (en) * | 2005-10-21 | 2007-04-26 | Pfab Lp | Compositions and methods of making rapidly dissolving lonically masked formulations |
| US8497258B2 (en) | 2005-11-12 | 2013-07-30 | The Regents Of The University Of California | Viscous budesonide for the treatment of inflammatory diseases of the gastrointestinal tract |
| US8425935B2 (en) | 2005-12-21 | 2013-04-23 | Basf Se | Pharmaceutical formulation for producing rapidly disintegrating tablets |
| FR2898492B1 (fr) * | 2006-03-15 | 2008-06-06 | Pierre Fabre Medicament Sa | Comprimes orodispersibles de domperidone |
| US20090208576A1 (en) | 2006-03-31 | 2009-08-20 | Gandhi Anilkumar S | Orally Disintegrating Tablets |
| US9084434B2 (en) * | 2006-09-27 | 2015-07-21 | Little Calumet Holdings Llc | Probiotic oral dosage forms |
| WO2008089773A1 (fr) * | 2007-01-22 | 2008-07-31 | Crd Saidal | Formulation d'une matrice a desintegration rapide |
| WO2008089772A1 (fr) * | 2007-01-22 | 2008-07-31 | Crd Saidal | Formulation d'un comprime orodispersible a base d'acide acetylsalicylique enrobe |
| CN102083410B (zh) | 2007-06-06 | 2013-04-17 | 巴斯夫欧洲公司 | 用于制备迅速崩解的片剂的药物制剂 |
| KR20160083132A (ko) | 2007-06-06 | 2016-07-11 | 바스프 에스이 | 급속 붕해 정제의 제조를 위한 제약 제제 |
| US8685457B2 (en) * | 2007-06-06 | 2014-04-01 | Basf Se | Pharmaceutical formulation for the production of rapidly disintegrating tablets |
| EP2042160A1 (de) * | 2007-09-14 | 2009-04-01 | Basf Se | Mittel für die Behandlung von Mund und Rachen in Form von Tabletten |
| DE102008012295A1 (de) | 2008-03-03 | 2009-09-17 | Südzucker AG Mannheim/Ochsenfurt | Gemisch zur Herstellung von schnell zerfallenden Tabletten |
| WO2009124357A1 (en) * | 2008-04-10 | 2009-10-15 | Malvin Leonard Eutick | Fast dissolving oral formulations for critical drugs |
| TR201808694T4 (tr) * | 2008-06-20 | 2018-07-23 | Merck Patent Gmbh | Doğrudan sıkıştırılabilen ve hızlı parçalanan tablet matrisi. |
| FR2933299B1 (fr) | 2008-07-04 | 2012-02-03 | Roquette Freres | Mannitol orodispersible |
| EP2385769A4 (en) * | 2008-12-15 | 2014-08-20 | Valeant Pharmaceuticals Luxembourg S R L | QUICKLY SOLUBLE VITAMIN FORMULATION AND METHOD FOR THEIR USE |
| US20110027374A1 (en) * | 2008-12-16 | 2011-02-03 | Maria Oksana Bachynsky | Capecitabine rapidly disintegrating tablets |
| US20100189791A1 (en) | 2009-01-23 | 2010-07-29 | Teva Pharmaceutical Industries, Ltd. | Delayed release rasagiline malate formulation |
| EP2218444A3 (en) | 2009-01-23 | 2010-08-25 | Teva Pharmaceutical Industries, Ltd. | Delayed release rasagiline formulation |
| MX2011009053A (es) * | 2009-03-09 | 2012-04-02 | Spi Pharma Inc | Excipientes de compresion directa con alta capacidad de compactacion y durables y sistemas de excipiente. |
| JP2012521393A (ja) * | 2009-03-26 | 2012-09-13 | ロイヤル カレッジ オブ サージェオンズ イン アイルランド | 口腔内分散性錠剤 |
| PL2238974T3 (pl) * | 2009-04-09 | 2013-09-30 | E Pharma Trento S P A | Granulat do stosowania w preparatach tabletek ulegających rozpadowi w ustach |
| US20100285164A1 (en) | 2009-05-11 | 2010-11-11 | Jrs Pharma | Orally Disintegrating Excipient |
| US8497290B2 (en) * | 2009-05-27 | 2013-07-30 | Takeda Pharmaceuticals U.S.A., Inc. | Thiocolchicine derivatives, method of making and methods of use thereof |
| US20110097401A1 (en) | 2009-06-12 | 2011-04-28 | Meritage Pharma, Inc. | Methods for treating gastrointestinal disorders |
| EP2451447B1 (de) * | 2009-07-10 | 2017-10-11 | Merck Patent GmbH | Wasserarmes tablettierhilfsmittel und verfahren zu seiner herstellung |
| JP6038651B2 (ja) * | 2009-07-10 | 2016-12-07 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | 錠剤を製造するための組成物の調製方法 |
| DK3254676T3 (en) * | 2009-10-30 | 2019-03-11 | Ix Biopharma Ltd | QUICK-SOLVING SOLID DOSAGE FORM |
| US12186426B2 (en) | 2009-10-30 | 2025-01-07 | Ix Biopharma Ltd. | Solid dosage form |
| US20110150986A1 (en) * | 2009-12-18 | 2011-06-23 | Kristin Arnold | Quinine formulations, method of making, and metho of use thereof |
| US20110178180A1 (en) * | 2010-01-18 | 2011-07-21 | Kurt Nielsen | Deuterium-enriched colchicine, thiocolchicine, and derivatives thereof; methods of preparation; and use thereof |
| EP2526086A2 (en) * | 2010-01-22 | 2012-11-28 | Mutual Pharmaceutical Company, Inc. | Thiocolchicine and colchicine analogs, methods of making and methods of use thereof |
| EP2384742A1 (en) | 2010-05-03 | 2011-11-09 | The Jordanian Pharmaceutical Manufacturing Co. | Pharmaceutical excipient, method for its preparation and use thereof |
| AU2011305572B2 (en) | 2010-09-20 | 2016-08-04 | Diane Goll | Microencapsulation process and product |
| AU2012241189A1 (en) * | 2010-10-26 | 2014-04-24 | Ix Biopharma Pte Ltd | Fast Dissolving Solid Dosage Form |
| US8715729B2 (en) | 2010-12-22 | 2014-05-06 | Basf Se | Rapidly disintegrating, solid coated dosage form |
| CN107252419A (zh) | 2010-12-22 | 2017-10-17 | 巴斯夫欧洲公司 | 快速崩解的固体包衣剂型 |
| JP2014507454A (ja) | 2011-03-09 | 2014-03-27 | ビーエーエスエフ ソシエタス・ヨーロピア | 速崩錠を製造するための医薬製剤 |
| US9265757B2 (en) | 2011-08-25 | 2016-02-23 | Aptapharma Inc. | Methods of administering antihistamines |
| CN104159583B (zh) * | 2012-02-22 | 2018-04-13 | 富山化学工业株式会社 | 含有1‑(3‑(2‑(1‑苯并噻吩‑5‑基)乙氧基)丙基)氮杂环丁烷‑3‑醇或其盐的固体药物组合物 |
| IN2014DN09416A (https=) | 2012-04-25 | 2015-07-17 | Spi Pharma Inc | |
| WO2013171164A1 (en) | 2012-05-14 | 2013-11-21 | EJP Pharmaceutical ApS | Compositions and formulations for the treatment of halitosis |
| FI126168B (en) | 2012-09-18 | 2016-07-29 | Novaldmedical Ltd Oy | A method for coating pharmaceutical substrates |
| SG11201502425WA (en) * | 2012-10-11 | 2015-05-28 | Ix Biopharma Ltd | Solid dosage form |
| US9579330B2 (en) | 2012-11-22 | 2017-02-28 | Bayer Pharma Aktiengesellschaft | Use and application regimen of a pharmaceutical composition containing levonorgestrel and a COX inhibitor for on-demand contraception |
| US10207004B2 (en) | 2014-04-04 | 2019-02-19 | Douxmatok Ltd | Method for producing sweetener compositions and sweetener compositions |
| US20160242439A1 (en) | 2014-04-04 | 2016-08-25 | Douxmatok Ltd | Method for producing sweetener compositions and sweetener compositions |
| US10231476B2 (en) | 2014-04-04 | 2019-03-19 | Douxmatok Ltd | Sweetener compositions and foods, beverages, and consumable products made thereof |
| WO2016061486A1 (en) | 2014-10-16 | 2016-04-21 | Cargill, Incorporated | Process for preparing a directly compressible erythritol & uses thereof |
| FR3038836B1 (fr) * | 2015-07-17 | 2017-07-14 | Roquette Freres | Granules de mannitol pour compression directe |
| EP3135272A1 (en) | 2015-08-31 | 2017-03-01 | Basf S.A. | Compositions for mouth wash in the form of tablets |
| EP3419659A1 (en) | 2016-02-23 | 2019-01-02 | The Regents of the University of Colorado, A Body Corporate | Compositions and methods for making and using thermostable immunogenic formulations with increased compatibility of use as vaccines against one or more pathogens |
| US10076494B2 (en) | 2016-06-16 | 2018-09-18 | Dexcel Pharma Technologies Ltd. | Stable orally disintegrating pharmaceutical compositions |
| US10064820B2 (en) | 2016-09-30 | 2018-09-04 | Aptapharma Inc. | Antihistamine compositions, combinations, and use thereof |
| EP3740197A4 (en) | 2018-01-16 | 2021-11-10 | Applied Materials, Inc. | METAL OXIDE ENCAPSULATED COMPOSITIONS OF THE ACTIVE SUBSTANCE AND PROCESS FOR THEIR MANUFACTURING |
| WO2020018845A1 (en) * | 2018-07-18 | 2020-01-23 | Anewsha Holding Group Llc | Rapidly dissolving pharmaceutical compositions and method of manufacturing |
| KR20220051385A (ko) | 2019-08-27 | 2022-04-26 | 어플라이드 머티어리얼스, 인코포레이티드 | 약제 용해도 조절을 위한 증기상 코팅들 |
| EP4021423A4 (en) | 2019-08-27 | 2023-11-08 | Applied Materials, Inc. | Vapor phase coating technology for pharmaceutical abuse deterrent formulations |
| US11464827B2 (en) | 2020-03-10 | 2022-10-11 | Anewsha Holding Group Llc | Antiviral pharmaceutical compositions and method of manufacturing |
| EP4149450A4 (en) * | 2020-05-15 | 2024-06-19 | SPI Pharma, INC. | Compositions and methods for hardening |
| TWI870622B (zh) | 2020-10-02 | 2025-01-21 | 美商應用材料股份有限公司 | 製備氧化矽塗佈藥品的低溫處理 |
| EP4408402A4 (en) | 2021-09-30 | 2025-08-06 | Applied Materials Inc | LOW TEMPERATURE SILICON OXIDE COATING FOR PHARMACEUTICAL APPLICATIONS |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3145146A (en) | 1961-10-31 | 1964-08-18 | Warner Lambert Pharmaceutical | Modified mannitol for pharmaceutical tablets |
| DE3245170A1 (de) | 1982-12-07 | 1984-06-07 | Merck Patent Gmbh, 6100 Darmstadt | Verbesserter sorbit, verfahren zur herstellung und verwendung |
| JPH0830005B2 (ja) | 1985-09-25 | 1996-03-27 | ゲルゲリイ、ゲルハルト | 崩壊性錠剤とその製造方法 |
| US4990537A (en) | 1988-07-11 | 1991-02-05 | Banyu Pharmaceutical Co., Ltd. | Anti influenza agent |
| ES2058546T3 (es) | 1988-09-30 | 1994-11-01 | Rhone Poulenc Rorer Ltd | Formulaciones farmaceuticas granulares. |
| US5583215A (en) | 1990-06-25 | 1996-12-10 | Towa Chemical Industry Co., Ltd. | Crystalline mixture solid containing maltitol and a process for preparing it |
| IE67345B1 (en) | 1991-03-12 | 1996-03-20 | Akzo Nv | Low dose dry pharmaceutical preparations |
| US5464632C1 (en) | 1991-07-22 | 2001-02-20 | Prographarm Lab | Rapidly disintegratable multiparticular tablet |
| DE69331839T2 (de) | 1992-01-29 | 2002-12-12 | Takeda Chemical Industries, Ltd. | Schnellösliche Tablette und ihre Herstellung |
| FR2710637B1 (fr) | 1993-09-28 | 1995-12-08 | Roquette Freres | Mannitol pulvérulent de friabilité modérée et son procédé de préparation. |
| US5576014A (en) | 1994-01-31 | 1996-11-19 | Yamanouchi Pharmaceutical Co., Ltd | Intrabuccally dissolving compressed moldings and production process thereof |
| US5635210A (en) * | 1994-02-03 | 1997-06-03 | The Board Of Regents Of The University Of Oklahoma | Method of making a rapidly dissolving tablet |
| DE4439858A1 (de) | 1994-11-08 | 1996-05-09 | Merck Patent Gmbh | Durch Co-Sprühtrocknung erhältliche Polyol-Zusammensetzung |
| DE19615418A1 (de) * | 1996-04-22 | 1997-10-23 | Merck Patent Gmbh | Polyol-Zusammensetzung |
| DE19617487A1 (de) | 1996-05-02 | 1997-11-06 | Merck Patent Gmbh | Geschmacksverbesserung von Arzneimittelwirkstoffen |
| US5957471A (en) * | 1996-10-28 | 1999-09-28 | Weeks; Bruce V. | Snow vehicle |
| EP0839526A3 (en) | 1996-10-31 | 1999-01-07 | Takeda Chemical Industries, Ltd. | Solid pharmaceutical preparation with fast buccal disintegration or dissolution |
| CA2271839A1 (en) | 1996-11-15 | 1998-05-28 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Process for the production of shaped or unshaped polyol materials |
| US6024981A (en) | 1997-04-16 | 2000-02-15 | Cima Labs Inc. | Rapidly dissolving robust dosage form |
| AU730650B2 (en) | 1997-05-01 | 2001-03-08 | Nissan Chemical Industries Ltd. | Benzimidazole derivative |
| FR2766089B1 (fr) | 1997-07-21 | 2000-06-02 | Prographarm Lab | Comprime multiparticulaire perfectionne a delitement rapide |
| ATE346589T1 (de) | 1997-10-15 | 2006-12-15 | Merck Patent Gmbh | Herstellung eines direkt verpressbaren tablettierhilfsstoffes |
| FI107732B (fi) * | 1998-03-18 | 2001-09-28 | Xyrofin Oy | Laktitolin kiteyttäminen, kiteinen laktitolituote ja sen käyttö |
| DE19820957A1 (de) | 1998-05-11 | 1999-11-25 | Merck Patent Gmbh | Verfahren zur Herstellung von Mannit |
| GT199900061A (es) | 1998-05-15 | 2000-10-14 | Pfizer | Formulaciones farmaceuticas. |
| US20020071864A1 (en) | 1999-03-25 | 2002-06-13 | Yuhan Corporation | Rapidly disintegrable tablet for oral administration |
| WO2000057857A1 (en) | 1999-03-25 | 2000-10-05 | Yuhan Corporation | Rapidly disintegrable tablet for oral administration |
| DE19927537A1 (de) | 1999-06-16 | 2000-12-21 | Merck Patent Gmbh | Sprühtrocknungsanlage und Verfahren zu ihrer Verwendung |
| US6740339B1 (en) | 1999-06-18 | 2004-05-25 | Takeda Chemical Industries, Ltd. | Quickly disintegrating solid preparations |
| US6284270B1 (en) | 1999-08-04 | 2001-09-04 | Drugtech Corporation | Means for creating a mass having structural integrity |
| US6248359B1 (en) * | 2000-01-05 | 2001-06-19 | Laboratorios Phoenix U.S.A., Inc. | Multi-tablet oxybutynin system for treating incontinence |
| WO2002015880A2 (en) | 2000-08-25 | 2002-02-28 | Merck Patent Gmbh | Powdered mannitol and mannitol-containing compositions |
| US6733781B2 (en) * | 2000-12-06 | 2004-05-11 | Wyeth | Fast dissolving tablet |
| US6814978B2 (en) * | 2000-12-29 | 2004-11-09 | Mcneil-Ppc, Inc. | Process for preparing a soft tablet |
| WO2002070013A1 (en) | 2001-03-06 | 2002-09-12 | Kyowa Hakko Kogyo Co., Ltd. | Utilization of spray-dried powder containing sugar alcohol |
| JPWO2002069934A1 (ja) | 2001-03-06 | 2004-07-02 | 協和醗酵工業株式会社 | 口腔内速崩壊性製剤 |
| US6723348B2 (en) * | 2001-11-16 | 2004-04-20 | Ethypharm | Orodispersible tablets containing fexofenadine |
| DE10161402A1 (de) | 2001-12-13 | 2003-06-18 | Merck Patent Gmbh | Verfahren zur Herstellung von direkt tablettierbarem beta-Mannit |
| US7118765B2 (en) | 2001-12-17 | 2006-10-10 | Spi Pharma, Inc. | Co-processed carbohydrate system as a quick-dissolve matrix for solid dosage forms |
-
2002
- 2002-10-18 US US10/274,227 patent/US7118765B2/en not_active Expired - Lifetime
- 2002-12-17 CA CA 2470601 patent/CA2470601C/en not_active Expired - Lifetime
- 2002-12-17 EP EP20020787055 patent/EP1465604B1/en not_active Revoked
- 2002-12-17 MX MXPA04005955A patent/MXPA04005955A/es active IP Right Grant
- 2002-12-17 WO PCT/US2002/040506 patent/WO2003051338A1/en not_active Ceased
- 2002-12-17 JP JP2003552271A patent/JP4472988B2/ja not_active Expired - Lifetime
- 2002-12-17 ES ES02787055T patent/ES2429529T3/es not_active Expired - Lifetime
- 2002-12-17 AU AU2002351396A patent/AU2002351396B2/en not_active Expired
-
2004
- 2004-06-24 ZA ZA2004/04998A patent/ZA200404998B/en unknown
-
2006
- 2006-06-06 US US11/448,523 patent/US8545889B2/en not_active Expired - Fee Related
-
2013
- 2013-09-27 US US14/038,924 patent/US9138413B2/en not_active Expired - Fee Related
-
2015
- 2015-08-31 US US14/840,232 patent/US10702605B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2470601C (en) | 2012-10-02 |
| ZA200404998B (en) | 2005-07-27 |
| US7118765B2 (en) | 2006-10-10 |
| EP1465604A1 (en) | 2004-10-13 |
| US20060251716A1 (en) | 2006-11-09 |
| WO2003051338A1 (en) | 2003-06-26 |
| US8545889B2 (en) | 2013-10-01 |
| EP1465604A4 (en) | 2006-11-08 |
| AU2002351396B2 (en) | 2008-09-25 |
| US10702605B2 (en) | 2020-07-07 |
| EP1465604B1 (en) | 2013-07-17 |
| US20160051680A1 (en) | 2016-02-25 |
| CA2470601A1 (en) | 2003-06-26 |
| AU2002351396A1 (en) | 2003-06-30 |
| US20030118642A1 (en) | 2003-06-26 |
| JP2005520796A (ja) | 2005-07-14 |
| JP4472988B2 (ja) | 2010-06-02 |
| HK1067544A1 (en) | 2005-04-15 |
| US20140023707A1 (en) | 2014-01-23 |
| ES2429529T3 (es) | 2013-11-15 |
| US9138413B2 (en) | 2015-09-22 |
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