IE810036L - Sustained release compositions - Google Patents
Sustained release compositionsInfo
- Publication number
- IE810036L IE810036L IE810036A IE3681A IE810036L IE 810036 L IE810036 L IE 810036L IE 810036 A IE810036 A IE 810036A IE 3681 A IE3681 A IE 3681A IE 810036 L IE810036 L IE 810036L
- Authority
- IE
- Ireland
- Prior art keywords
- amount
- milligrams
- release controlling
- agent
- controlling agent
- Prior art date
Links
- 238000013268 sustained release Methods 0.000 title abstract 2
- 239000012730 sustained-release form Substances 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 abstract 7
- 239000003814 drug Substances 0.000 abstract 3
- 230000003628 erosive effect Effects 0.000 abstract 3
- 230000001737 promoting effect Effects 0.000 abstract 3
- 229940124597 therapeutic agent Drugs 0.000 abstract 3
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 abstract 1
- 229920000623 Cellulose acetate phthalate Polymers 0.000 abstract 1
- 229920002261 Corn starch Polymers 0.000 abstract 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 abstract 1
- 229940081734 cellulose acetate phthalate Drugs 0.000 abstract 1
- 239000008120 corn starch Substances 0.000 abstract 1
- 229960002390 flurbiprofen Drugs 0.000 abstract 1
- SYTBZMRGLBWNTM-UHFFFAOYSA-N flurbiprofen Chemical compound FC1=CC(C(C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-UHFFFAOYSA-N 0.000 abstract 1
- 229960001680 ibuprofen Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 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
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
A sustained release pharmaceutical composition in table-t form comprises an effective amount of an orallyactive therapeutic agent, 0.8 to 1. 6% by weight of a release controlling agent and 1.0 to 7.5% by weight of an erosion promoting agent, the relative amounts of the components being such that a criticality factor calculated according to equation I lies in the range 20 to 450. Equation 1 is <IMG> I wherein CF is the criticality factor, CA is the. amount of therapeutic agent per tablet in milligrams divided by the amount of release controlling agent per tablet in milligrams and CS is the amount of erosion promoting agent per tablet in milligrams divided by the amount of release controlling agent per-tablet in milligrams, Suitable therapeutic agents include acetylsalicylic acid, ibuprofen and flurbiprofen. A preferred release controlling agent is cellulose acetate phthalate and a preferred erosion promoting agent is corn starch.
[CA1140466A]
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11143080A | 1980-01-11 | 1980-01-11 | |
| US06/194,453 US4308251A (en) | 1980-01-11 | 1980-10-17 | Controlled release formulations of orally-active medicaments |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE810036L true IE810036L (en) | 1981-07-11 |
| IE50806B1 IE50806B1 (en) | 1986-07-23 |
Family
ID=26808896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE36/81A IE50806B1 (en) | 1980-01-11 | 1981-01-09 | Pharmaceutical compositions |
Country Status (22)
| Country | Link |
|---|---|
| JP (1) | JPS56103110A (en) |
| AT (1) | AT374681B (en) |
| AU (1) | AU542824B2 (en) |
| BE (1) | BE886998A (en) |
| CA (1) | CA1140466A (en) |
| CH (1) | CH646604A5 (en) |
| DE (1) | DE3100191A1 (en) |
| DK (1) | DK6181A (en) |
| ES (2) | ES8205353A1 (en) |
| FI (1) | FI76927C (en) |
| FR (1) | FR2473308B1 (en) |
| GB (1) | GB2067072B (en) |
| GR (1) | GR73843B (en) |
| IE (1) | IE50806B1 (en) |
| IN (1) | IN151913B (en) |
| IT (1) | IT1221041B (en) |
| LU (1) | LU83052A1 (en) |
| NL (1) | NL8100037A (en) |
| NO (1) | NO156153C (en) |
| NZ (1) | NZ195933A (en) |
| SE (1) | SE447450B (en) |
| ZA (1) | ZA81136B (en) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2496082A (en) * | 1947-05-24 | 1950-01-31 | Ashenfelter William | Scaffold structure |
| IT1144911B (en) * | 1981-03-19 | 1986-10-29 | Pharmatec Spa | CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION CONTAINING IBUPROFEN |
| JPS59227817A (en) * | 1983-06-07 | 1984-12-21 | Toyo Jozo Co Ltd | Long-acting bredinin preparation for oral administration |
| JPH0662404B2 (en) * | 1983-06-14 | 1994-08-17 | シンテックス・ファーマシユーテイカルズ・インターナシヨナル・リミテツド | Controlled-release naproxen and naproxen sodium tablets |
| ZA836030B (en) * | 1983-08-16 | 1985-02-27 | Verex Lab | Constant order release solid dosage indomethacin formulation and method of treating arthritis and other inflammatory conditions |
| ZA836031B (en) * | 1983-08-16 | 1985-02-27 | Verex Lab | Constant release rate solid dosage theophylline formulation |
| US4774091A (en) * | 1983-10-14 | 1988-09-27 | Sumitomo Pharmaceuticals Company, Ltd. | Long-term sustained-release preparation |
| US4855134A (en) * | 1983-10-14 | 1989-08-08 | Sumitomo Pharmaceuticals Company, Limited | Sustained-release preparation |
| DE3486029T2 (en) * | 1983-10-14 | 1993-05-13 | Sumitomo Pharma | IFN PREPARATION WITH DELAYED DELIVERY FOR PARENTAL ADMINISTRATION. |
| US5385738A (en) * | 1983-10-14 | 1995-01-31 | Sumitomo Pharmaceuticals Company, Ltd. | Sustained-release injection |
| CA1277601C (en) * | 1985-12-27 | 1990-12-11 | Shigeji Sato | Method for producing sustained release formulation |
| GB8601204D0 (en) * | 1986-01-18 | 1986-02-19 | Boots Co Plc | Therapeutic agents |
| US4968508A (en) * | 1987-02-27 | 1990-11-06 | Eli Lilly And Company | Sustained release matrix |
| IL85538A (en) * | 1987-02-27 | 1991-09-16 | Lilly Co Eli | Sustained release matrix tablet formulations containing hydrophilic and enteric polymers |
| AU6403196A (en) * | 1995-06-30 | 1997-02-05 | Baylor University | Polyester/carboxylic acid composite materials |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2953497A (en) * | 1953-06-03 | 1960-09-20 | Howard A Press | Therapeutic tablets |
| BE604564A (en) * | 1960-06-06 | |||
| US3577514A (en) * | 1968-06-10 | 1971-05-04 | Pfizer | Sustained release pharmaceutical tablets |
| US3773920A (en) * | 1971-07-14 | 1973-11-20 | Nikken Chemicals Co Ltd | Sustained release medicinal composition |
| US3906086A (en) * | 1971-07-19 | 1975-09-16 | Richard G Powers | Timed-release aspirin |
| GB1500300A (en) * | 1975-01-06 | 1978-02-08 | Ciba Geigy Ag | Pharmaceutical preparation for the treatment of circulatory disorders |
| JPS5411226A (en) * | 1977-06-24 | 1979-01-27 | Shin Etsu Chem Co Ltd | Disintegratable granule |
-
1980
- 1980-12-23 IN IN1418/CAL/80A patent/IN151913B/en unknown
- 1980-12-23 NZ NZ195933A patent/NZ195933A/en unknown
-
1981
- 1981-01-05 AU AU65976/81A patent/AU542824B2/en not_active Ceased
- 1981-01-06 FR FR8100087A patent/FR2473308B1/en not_active Expired
- 1981-01-07 NL NL8100037A patent/NL8100037A/en not_active Application Discontinuation
- 1981-01-07 DE DE19813100191 patent/DE3100191A1/en active Granted
- 1981-01-08 CH CH9281A patent/CH646604A5/en not_active IP Right Cessation
- 1981-01-08 DK DK6181A patent/DK6181A/en not_active Application Discontinuation
- 1981-01-08 BE BE0/203426A patent/BE886998A/en unknown
- 1981-01-08 GB GB8100522A patent/GB2067072B/en not_active Expired
- 1981-01-08 ES ES498369A patent/ES8205353A1/en not_active Expired
- 1981-01-08 JP JP157881A patent/JPS56103110A/en active Pending
- 1981-01-09 LU LU83052A patent/LU83052A1/en unknown
- 1981-01-09 NO NO810062A patent/NO156153C/en unknown
- 1981-01-09 ZA ZA00810136A patent/ZA81136B/en unknown
- 1981-01-09 CA CA000368219A patent/CA1140466A/en not_active Expired
- 1981-01-09 FI FI810056A patent/FI76927C/en not_active IP Right Cessation
- 1981-01-09 GR GR63828A patent/GR73843B/el unknown
- 1981-01-09 SE SE8100104A patent/SE447450B/en not_active IP Right Cessation
- 1981-01-09 IT IT47537/81A patent/IT1221041B/en active
- 1981-01-09 IE IE36/81A patent/IE50806B1/en unknown
- 1981-01-09 AT AT0005481A patent/AT374681B/en not_active IP Right Cessation
-
1982
- 1982-01-29 ES ES509179A patent/ES509179A0/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| NO156153C (en) | 1987-08-05 |
| IT8147537A0 (en) | 1981-01-09 |
| GB2067072B (en) | 1983-08-10 |
| IN151913B (en) | 1983-09-03 |
| GR73843B (en) | 1984-05-07 |
| FI810056L (en) | 1981-07-12 |
| SE447450B (en) | 1986-11-17 |
| ATA5481A (en) | 1983-10-15 |
| JPS56103110A (en) | 1981-08-18 |
| BE886998A (en) | 1981-07-08 |
| ES8301629A1 (en) | 1982-12-16 |
| ES498369A0 (en) | 1982-06-01 |
| AU542824B2 (en) | 1985-03-14 |
| CH646604A5 (en) | 1984-12-14 |
| NL8100037A (en) | 1981-08-03 |
| NZ195933A (en) | 1982-11-23 |
| FR2473308B1 (en) | 1985-07-19 |
| IT1221041B (en) | 1990-06-21 |
| FI76927B (en) | 1988-09-30 |
| ES8205353A1 (en) | 1982-06-01 |
| AU6597681A (en) | 1981-07-16 |
| AT374681B (en) | 1984-05-25 |
| ZA81136B (en) | 1982-01-27 |
| ES509179A0 (en) | 1982-12-16 |
| LU83052A1 (en) | 1982-09-10 |
| DE3100191A1 (en) | 1981-12-10 |
| DE3100191C2 (en) | 1988-09-01 |
| IE50806B1 (en) | 1986-07-23 |
| GB2067072A (en) | 1981-07-22 |
| NO810062L (en) | 1981-07-13 |
| CA1140466A (en) | 1983-02-01 |
| NO156153B (en) | 1987-04-27 |
| SE8100104L (en) | 1981-07-12 |
| DK6181A (en) | 1981-07-12 |
| FR2473308A1 (en) | 1981-07-17 |
| FI76927C (en) | 1989-01-10 |
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