WO2015114656A2 - Mucoadhesive tablet of pregabalin - Google Patents
Mucoadhesive tablet of pregabalin Download PDFInfo
- Publication number
- WO2015114656A2 WO2015114656A2 PCT/IN2015/000033 IN2015000033W WO2015114656A2 WO 2015114656 A2 WO2015114656 A2 WO 2015114656A2 IN 2015000033 W IN2015000033 W IN 2015000033W WO 2015114656 A2 WO2015114656 A2 WO 2015114656A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- mucoadhesive
- mucoadhesive tablet
- pregabalin
- tablet according
- tablet
- Prior art date
Links
- 230000003232 mucoadhesive effect Effects 0.000 title claims abstract description 59
- AYXYPKUFHZROOJ-ZETCQYMHSA-N pregabalin Chemical compound CC(C)C[C@H](CN)CC(O)=O AYXYPKUFHZROOJ-ZETCQYMHSA-N 0.000 title claims abstract description 38
- 229960001233 pregabalin Drugs 0.000 title claims abstract description 36
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 230000008961 swelling Effects 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 12
- 229940079593 drug Drugs 0.000 claims abstract description 11
- 239000003814 drug Substances 0.000 claims abstract description 11
- 230000002496 gastric effect Effects 0.000 claims abstract description 11
- 239000003349 gelling agent Substances 0.000 claims abstract description 11
- 230000014759 maintenance of location Effects 0.000 claims abstract description 10
- 210000002784 stomach Anatomy 0.000 claims abstract description 10
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 9
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 8
- 229920002125 Sokalan® Polymers 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 6
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 6
- 229920003109 sodium starch glycolate Polymers 0.000 claims description 6
- 239000008109 sodium starch glycolate Substances 0.000 claims description 6
- 229940079832 sodium starch glycolate Drugs 0.000 claims description 6
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 5
- 229960000913 crospovidone Drugs 0.000 claims description 5
- 238000007907 direct compression Methods 0.000 claims description 5
- 239000002552 dosage form Substances 0.000 claims description 5
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 claims description 5
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 claims description 5
- 235000010413 sodium alginate Nutrition 0.000 claims description 5
- 239000000661 sodium alginate Substances 0.000 claims description 5
- 229940005550 sodium alginate Drugs 0.000 claims description 5
- 241000416162 Astragalus gummifer Species 0.000 claims description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 4
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims description 4
- 229920001615 Tragacanth Polymers 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 229940071826 hydroxyethyl cellulose Drugs 0.000 claims description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 4
- 239000012729 immediate-release (IR) formulation Substances 0.000 claims description 4
- 229940016286 microcrystalline cellulose Drugs 0.000 claims description 4
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 4
- 239000008108 microcrystalline cellulose Substances 0.000 claims description 4
- 235000010487 tragacanth Nutrition 0.000 claims description 4
- 239000000196 tragacanth Substances 0.000 claims description 4
- 229940116362 tragacanth Drugs 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- KUQWZSZYIQGTHT-UHFFFAOYSA-N hexa-1,5-diene-3,4-diol Chemical compound C=CC(O)C(O)C=C KUQWZSZYIQGTHT-UHFFFAOYSA-N 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 229920002785 Croscarmellose sodium Polymers 0.000 claims description 2
- 229920003134 Eudragit® polymer Polymers 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- 229920002594 Polyethylene Glycol 8000 Polymers 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- 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 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 229960001681 croscarmellose sodium Drugs 0.000 claims description 2
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 claims description 2
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920000193 polymethacrylate Polymers 0.000 claims description 2
- 229940032147 starch Drugs 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000000230 xanthan gum Substances 0.000 claims description 2
- 235000010493 xanthan gum Nutrition 0.000 claims description 2
- 229920001285 xanthan gum Polymers 0.000 claims description 2
- 229940082509 xanthan gum Drugs 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 abstract description 6
- 239000003826 tablet Substances 0.000 description 31
- 210000001035 gastrointestinal tract Anatomy 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000007916 tablet composition Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229940009697 lyrica Drugs 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 0 CC(C)C[C@](CCN)CC(*)=O Chemical compound CC(C)C[C@](CCN)CC(*)=O 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229940124277 aminobutyric acid Drugs 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000036765 blood level Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000004751 neurological system process Effects 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 210000001187 pylorus Anatomy 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0065—Forms with gastric retention, e.g. floating on gastric juice, adhering to gastric mucosa, expanding to prevent passage through the pylorus
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
Definitions
- the present invention relates to a mucoadhesive tablet comprising pregabalin with pharmaceutically acceptable excipients, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach. Further it relates to a process for the preparation of the mucoadhesive tablet
- Pregabalin is an analogue of the physiologically important endogenous neurotransmitter [gamma] -amino butyric acid (GABA), which is involved in the regulation of neural processes.
- GABA physiologically important endogenous neurotransmitter
- Pregabalin is disclosed in U.S. Patent Nos. 6,197,819 and 5,563,175, which describe its use in the treatment of seizure disorders.
- U.S. Patent No. 6,117,906 discloses the use of pregabalin in treating anxiety, while U.S. Patent No. 6,001 ,876 discloses its use in treating pain.
- pregabalin is available as conventional immediate-release capsules marketed by CP Pharms/Pfizer under the brand name Lyrica ® .
- Lyrica ® Capsules requires two or three times a day dosing.
- a once-daily tablet is desirable.
- pregabalin cannot be absorbed in the entire gastrointestinal tract (GIT).
- GIT gastrointestinal tract
- Pregabalin is only absorbed in the upper sections of the gut. It is therefore desirable to have a dosage form which has a longer retention time in the upper GIT and which, during that time, releases the active agent continuously over a longer period of time.
- the U.S. Publication Application No. 2007/0269511 discloses a pregabalin formulation containing matrix forming agent and a swelling agent, wherein the matrix forming agent is polyvinyl acetate and polyvinylpyrrolidone, and the swelling agent is cross-linked polyvinylpyrrolidone.
- the U.S. Publication Application No. 2010/0255067 describes pharmaceutical compositions comprising pregabalin, a hydrophobic release controlling agent, and other pharmaceutically acceptable excipients.
- the U.S. Publication Application No. 2013/149253 describes oral dosage form for the modified release of pregabalin, comprising pregabalin in a matrix comprising a swelling agent, a matrix former and a buoyancy agent or alternatively a sedimentation agent. Therefore, a mucoadhesive tablet that retains in the upper parts of the gastrointestinal tract would be an ideal dosage form for pregabalin.
- the objective of the present invention is to develop a mucoadhesive tablet of pregabalin.
- the primary object of the invention is to provide a mucoadhesive tablet comprising pregabalin with pharmaceutically acceptable excipients, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- Another object of the invention is to provide a mucoadhesive tablet comprising pregabalin with at least mucoadhesive excipient, at least one swelling agent and at least one gelling agent, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- Another object of the invention is to provide a process for the preparation of a mucoadhesive tablet of pregabalin.
- the invention relates to a mucoadhesive tablet comprising pregabalin with pharmaceutically acceptable excipients, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- the invention in another embodiment, relates to a mucoadhesive tablet comprising pregabalin with at least mucoadhesive excipient, at least one swelling agent and at least One gelling agent, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- the invention relates to a mucoadhesive tablet comprising pregabalin with polyethylene oxide (PEO) as mucoadhesive excipient, cross-linked homopolymers of l-vinyl-pyrrolidin-2-one (Crospovidone) as swelling agent, and sodium alginate as gelling agent.
- PEO polyethylene oxide
- Cross-linked homopolymers of l-vinyl-pyrrolidin-2-one (Crospovidone) as swelling agent
- sodium alginate sodium alginate
- the invention relates to a mucoadhesive tablet comprising pregabalin with tragacanth as mucoadhesive excipient, sodium starch glycolate as swelling agent, and polymers of acrylic acid cross-linked with polyalkenyl ethers or divinyl glycol such as carbomers (carbopols) as gelling agent.
- the invention relates to a process for the preparation of a mucoadhesive tablet of pregabalin, preferably direct compression method.
- the present invention relates to a mucoadhesive tablet comprising pregabalin with pharmaceutically acceptable excipients, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- the "mucoadhesive tablet” remains in the patient's stomach following oral administration, which is substantially longer than the average residence time of a corresponding immediate release dosage form.
- the present invention may employ any pharmaceutically acceptable form of pregabalin, including its free form (zwitter ion), and its pharmaceutically acceptable complexes, acid addition salts, base addition salts solvates, hydrates, and polymorphs.
- the present invention relates to a mucoadhesive tablet comprising pregabalin with at least mucoadhesive excipient, at least one swelling agent and at least one gelling agent, wherein the mucoadhesive tablet maintains gastric retention for the time period during which the drug is released into the stomach.
- the "mucoadhesive excipient" of the present invention includes polyethylene glycol (PEG 8000), Tragacanth, polymethacrylate derivatives (Eudragit), polyethylene oxide (PEO) or combinations or copolymers thereof.
- the mucoadhesive excipient is generally used in an amount ranging from about 5% to about 20% by weight of the tablet composition .
- the "swelling agent" of the present invention includes croscarmellose sodium, sodium starch glycolate (SSG), microcrystalline cellulose (MCC), starch, cross- linked homopolymers of 1 -vinyl-pyrrolidin-2-one (Crospovidone) or combinations or copolymers thereof.
- the swelling agent absorbs water from the gastric fluid and thereby the tablet expands in size larger than the pylorus.
- the swelling agent is generally used in an amount ranging from about 5% to about 30% by weight of the tablet composition.
- the "gelling agent" of the present invention includes polyvinyl pyrrol idone (PVP), polymers of acrylic acid cross-linked with polyalkenyl ethers or divinyl glycol such as carbomers (carbopols), alginates, preferably sodium alginate, hydroxyalkyl cellulose, especially hydroxyethyl cellulose (HEC), xanthan gum or combinations or copolymers thereof.
- PVP polyvinyl pyrrol idone
- carbomers carbomers
- alginates preferably sodium alginate
- hydroxyalkyl cellulose especially hydroxyethyl cellulose (HEC)
- HEC hydroxyethyl cellulose
- xanthan gum xanthan gum or combinations or copolymers thereof.
- the gelling agent includes excipient that forms a gel when in contact with gastric fluid and thereby modulates the drug release characteristics of the tablet.
- the gelling agent is generally used in an amount ranging from about 0.5% to about 40% by weight
- the mucoadhesive tablet may also comprise further pharmaceutically acceptable excipients such as diluents, binders, rate-controlling agents, lubricants, wetting agent, glidants and coating excipients.
- excipients such as diluents, binders, rate-controlling agents, lubricants, wetting agent, glidants and coating excipients.
- the mucoadhesive tablet of pregabalin is designed for once-daily administration and achieves bioequivalence with immediate release dosage form of pregabalin that is taken two- or three-times daily.
- the invention in another embodiment, relates to a process for the preparation of a mucoadhesive tablet of pregabalin. It can be prepared by routine tableting method including direct compression, granulation and pelletization methods. Preferably, the process for the preparation is direct compression method.
- Example 1 Mucoadhesive Tablet by Direct Compression approach
- the mucoadhesive tablet of the present invention is prepared by Direct Compr method in the procedural steps as described below. Manufacturing Process:
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN215/MUM/2014 | 2014-01-22 | ||
IN215MU2014 IN2014MU00215A (enrdf_load_stackoverflow) | 2014-01-22 | 2015-01-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2015114656A2 true WO2015114656A2 (en) | 2015-08-06 |
WO2015114656A3 WO2015114656A3 (en) | 2015-12-17 |
Family
ID=53757863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2015/000033 WO2015114656A2 (en) | 2014-01-22 | 2015-01-20 | Mucoadhesive tablet of pregabalin |
Country Status (2)
Country | Link |
---|---|
IN (1) | IN2014MU00215A (enrdf_load_stackoverflow) |
WO (1) | WO2015114656A2 (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108159011A (zh) * | 2018-03-16 | 2018-06-15 | 中国药科大学 | 一种双相控释的普瑞巴林胃滞留缓释片及其制备方法 |
JP2018118966A (ja) * | 2017-01-23 | 2018-08-02 | 日新製薬株式会社 | 3位が置換されたγ−アミノ酪酸誘導体を含有する圧縮固形医薬組成物。 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2012322323B2 (en) * | 2011-10-11 | 2016-04-21 | Sun Pharmaceutical Industries Limited | A gastroretentive dosage system and process of preparation thereof |
-
2015
- 2015-01-20 IN IN215MU2014 patent/IN2014MU00215A/en unknown
- 2015-01-20 WO PCT/IN2015/000033 patent/WO2015114656A2/en active Application Filing
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018118966A (ja) * | 2017-01-23 | 2018-08-02 | 日新製薬株式会社 | 3位が置換されたγ−アミノ酪酸誘導体を含有する圧縮固形医薬組成物。 |
CN108159011A (zh) * | 2018-03-16 | 2018-06-15 | 中国药科大学 | 一种双相控释的普瑞巴林胃滞留缓释片及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
WO2015114656A3 (en) | 2015-12-17 |
IN2014MU00215A (enrdf_load_stackoverflow) | 2015-08-28 |
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