WO1994001092A1 - Composition for controlled release of an active substance and method for the preparation of such a composition - Google Patents
Composition for controlled release of an active substance and method for the preparation of such a composition Download PDFInfo
- Publication number
- WO1994001092A1 WO1994001092A1 PCT/NL1993/000140 NL9300140W WO9401092A1 WO 1994001092 A1 WO1994001092 A1 WO 1994001092A1 NL 9300140 W NL9300140 W NL 9300140W WO 9401092 A1 WO9401092 A1 WO 9401092A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- active substance
- composition
- release
- amylose
- composition according
- Prior art date
Links
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
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
Definitions
- composition for controlled release of an active substance and method for the preparation of such a composition
- the invention relates to a composition for delayed release of an active substance in a target environment, the active substance being incorporated in a polysaccharide matrix.
- compositions for delayed release of an active substance for example for delayed release of a medicament for oral administration in the gastrointestinal tract of a mammal, have advantages, inter alia because the administration of the active substance can take place in a small number of doses and because a more constant concentration is obtained in the target environment.
- compositions for delayed release are known in diverse forms.
- One form of delayed release can comprise the presence of a matrix containing the active substance therein, which matrix slowly dissolves in the water- containing environment and thus releases the active substance in a delayed manner;
- a composition of this type is, for example, disclosed in European Patent Application EP-A-24l,179-
- a composition of this type in which the matrix is formed by a natural polysaccharide such as xanthan is disclosed in International Patent Application WO-A-87,05212.
- the active substance is packaged in an insoluble capsule which is provided with a water-soluble stopper, as disclosed, inter alia, in British Patent Application 2,241,485.
- compositions for delayed release are compositions from which the active substance is released by erosion, as is disclosed, for example, in European Patent Application EP-A-38l,l ⁇ 2.
- the use of heat-modified starch as the matrix for the controlled release of medicaments for oral administration is described by J. Herman and J.P. Remon, Int. J. Pharmaceutics , 56, 51-63 and 65-70 (1989).
- Amylose a straight-chain starch fraction
- British Patent 1,072,795 describes the use of "retrograded” amylose, i.e. associated amylose
- EP-A-343.993 discribes the use of "glassy” amylose, i.e. one of the types of amorphous amylose, as a release-delaying material for active substances.
- compositions for the delayed release of an active substance frequently have the disadvantage that release of the active substance does not proceed in accordance with an ideal zero order rate, that is to say with a constant amount per unit time, but at a first order rate, that is to say with an amount which decreases per unit time, or poorer; in addition, the materials used as matrix are often expensive.
- the aim of the invention is to provide a composition, and a method for the preparation thereof, which releases an active substance as far as possible in accordance with a zero order curve and which, in addition, is harmless to health and/or the environment and which, moreover, is economical in use.
- composition according to the invention which to this end is characterised in that the matrix material in which the active substance is incorporated comprises an essentially crystalline, straight-chain glucan.
- the glucan is preferably an ⁇ -glucan and in particular an ⁇ -l,4-glucan and preferably has essentially a helix structure.
- An ⁇ -l,4-glucan is understood to be an essentially straight-chain polysaccharide which is composed of anhydroglucose units which are linked to one another by ⁇ -bridges via the 1-position and 4-position.
- Other straight-chain glucans can also be used if these are able to assume a helical structure, such as, for example, ⁇ -l,3-glucans.
- Suitable ⁇ -l,4-glucans are in general starch fractions and starch derivatives.
- the ⁇ -l,4-glucan can, for example, be an amylose.
- Amylose is a straight chain of ⁇ -l,4-anhydroglucose units which has a degree of polymerisation (DP) of the order of 100 - 1,000.
- DP degree of polymerisation
- amylose V an amylose which has an amorphous structure and is precipitated from an aqueous solution by magnesium sulphate.
- Use is made of a product having a crystalline structure which may be derived from amylose V.
- This so-called helical amylose or crystalline amylose can be obtained from amylose by dissolving in water and complexing with a complex-forming agent such as 1-butanol, after which the complex-forming agent can be removed by careful spray-drying or by treatment with a suitable solvent, such as ethanol, methanol or acetone.
- a suitable solvent such as ethanol, methanol or acetone.
- the crystalline and/or helical amylose to be used in the com- positions according to the invention can also be obtained directly from starch, in a similar process using a complexing agent, further including washing the complex to remove amylopectin.
- Suitable complexing agents for preparing crystalline, helical amylose by precipitating amylose from an aqueous solution include 1,1,2,2-tetrachloroethane, cyclohexane, 1,1,1- and 1,1,2-trichloroethane, benzene, chloroform, fluorobenzene, o-xylene, 2,3- dimethylbutane, C 3 -C 8 alcohols and phenols, such as butanol, amyl alcohol, cyclohexanol, hexanol and 2-octanol, isopropyl ketone, quinoline, chloral hydrate, butyric acid etc. See e.g. J. Muetgeert, Advances in Carbohydrate Chemistry, Vol. 16 Ed. Melville, Wolfrom, Acad. Press (1961).
- Derivatives which are obtained by debranching branched glucans, in particular amylopectins, are also suitable.
- the ⁇ -1,6 bonds of amylopectin are broken, preferably enzymatically (see Kobayashi, S. et al.. Cereal Chem. 63, 71-74 (1968) and Netherlands patents 160,615 and 165. 00) with the formation of amylodextrin, a straight-chain dextrin.
- This has an average chain length (DP) of the order of 15 - 75. with a maximum between 15 and 25 and a maximum between 5 and 75-
- Amylodextrin like the helical amylose, occurs in helix form with approximately 6 to 7 anhydroglucose units per winding.
- the crystalline ⁇ -l,4-glucans suitable for use in the present compositions can be distinguished from unsuitable types of glucans by their infrared spctrum.
- the crystalline amylose and amylodextrin, just like cyclodextrin, have sharp absorptions at about 1150, lO ⁇ O and 1020 cm "1 , whereas amorphous amylose only exhibits broad or undistinguished absorptions at these frequencies.
- tablets and other administra ⁇ tion forms which comprise such crystalline straight-chain glucans as matrix-forming material are subject to little or no disintegration and little or no attack by ⁇ -amylase, an enzyme which usually splits starch, for example in the digestive tract, or by acid.
- ⁇ -amylase an enzyme which usually splits starch, for example in the digestive tract, or by acid.
- the tablets are found to be resistant to breaking and often more resistant to breaking than microcrystalline cellulose (for example Avicel ).
- the matrix material contains at least 5 % by weight of water. If the material contains less than 5% of water a usable release pattern is obtained but the strength is then no better than that, or even worse than that, of microcrystalline cellulose. Preferably, the material contains no more than 25 % by weight, and more preferably no more than 20 % by weight of water. In particular, the matrix material contains 7-l6 % by weight of water.
- the matrix material can contain other fillers and auxiliaries.
- the presence of non-crystalline amylose up to a content of, for example, 25 % by weight does not interfere.
- Many types of starch contain about 25 % of amylose and if these starches is used to prepare amylodextrin by debraching the amylopectin, this residual amylose there ⁇ fore does not have to be removed if the starch is used as starting material for the matrix-forming material.
- Suitable auxiliaries are the auxiliaries known per se for compositions of active substances, such as lubricants, for example magnesium stearate, auxiliary solvents, pH regulators, preservatives, disintegrating agents, colorants, flavourings and the like.
- auxiliaries which modify the release pattern of the active substance from the matrix such as auxiliaries which in themselves are inactive, for example lactose, or active auxiliaries such as ⁇ -amylase, which can help the matrix material to disintegrate from inside to out, can also advantageously be present.
- the active substance can be present in the matrix material in virtually any desired concentration.
- the amount of active substance can make up, for example, 0.1 - 80 % by weight of the composition, partly depending on the desired dosage. More particularly, the amount is between 0.5 and 50 % by weight. Within this range, a release rate is obtained which is independent of the remaining amount of active substance, that is to say which has a zero order curve. This is also an unexpected aspect of the compositions according to the invention.
- the rate of release of the composition according to the invention can be adjusted by varying one or more of the following parameters: active substance concentration in the matrix material, dosage unit form, in particular the surface area/capacity ratio, force under which the composition is pressed, presence of disintegration-promoting agents, for example lactose or ⁇ -amylase, or disintegration-retarding agents, such as a coating or an inert filler.
- active substance concentration in the matrix material dosage unit form, in particular the surface area/capacity ratio, force under which the composition is pressed
- disintegration-promoting agents for example lactose or ⁇ -amylase
- disintegration-retarding agents such as a coating or an inert filler.
- the active substance can be of diverse natures.
- it can be medicaments for oral, rectal, vaginal or transdermal administration, diagnostic agents, feedstuffs or conditioning agents, flavourings, manure or nutrients to be added to water or soil, preservatives, vaccine substances, hormones, genetic material, control agents, attractants, growth promoters and the like.
- the active substances can be either organic or inorganic. Mixtures of active substance can also be administered by means of the composition according to the invention. Release can take place in an aqueous medium, such as the gastrointestinal tract of animals, or in plants or in the soil, but also into the air.
- composition according to the invention is suitable, in particular, for the controlled release of substances of low molecular weight, such as those having a molecular weight of less than 1,000 daltons (D) .
- D daltons
- the hydrophilicity of the active compound is also of importance for the rate of release.
- hydrophilic substances having a molecular weight of up to about 1,500 Da still be effectively released, whilst for hydrophobic substances the practical upper limit will be at about 500 Da.
- composition can also be provided with a coating which provides further protection or further control of the release or, for example, has a colouring or taste function.
- the composition can also be in the form of a capsule in which the matrix material containing active substance is present, for example in granular form or powder form.
- composition according to the invention can be in any desired form, such as tablets, powders, granules, plasters and implants.
- Tablets can be pressed directly after mixing the active substance with the straight-chain glucan as matrix material and any other auxiliaries. Preferably, however, the mixture is granulated before or after physical mixing of the active substance and matrix material and is then tableted.
- Example II Example II
- Example IV The release of the active substance was determined from 3 tablets in an aqueous medium, buffer pH 6.8, over a period of 8 hours and is shown in Fig. 3 as a percentage of the original amount which has gone into solution.
- Example IV The release of the active substance was determined from 3 tablets in an aqueous medium, buffer pH 6.8, over a period of 8 hours and is shown in Fig. 3 as a
- Example VII Amylodextrin matrix tablets containing 30 % of potassium dichromate were prepared.
- Example X The release of atrazine from amylodextrin matrix tablets containing 30 % by weight of active substance was determined.
- Example XI 100 g of amylodextrin were stirred with 2 g of carvone in a round- bottomed flask. Tablets 13 mm in cross section weighing 300 mg were pressed in a press mould (Specac Ltd, Kent, GB) from the mixture thus obtained. Pressing time 5 min; pressing force varying from 5 to 50 kN.
- amylose is chosen as raw material the washing steps needed to remove the amylopectin may be omitted. For the remainder, the procedure is similar as described above. It may be noted that many other complexing agents may be used instead of 2-methyl-l-butanol. However, the critical concentration of each complexing agent should be taken into account: with starch the critical concentration is used, and with amylose the critical or a higher concentration may be used. The critical concentration of a number of complexing agents is summarised below (form J. Muetgeert, Advances in Carbohydrate Chemistry, Vol. 16, Acad. Press (1961), p.
- complexing agent critical concentration in g per 100 ml of water
- 1-butanol 4.2
- isopropyl ketone 0.6
- amyl alcohol 1.8
- cyclohexanol 0.5
- 1-hexanol 0.3
- phenol 2.5
- Tablets of helical amylose (crystalline amylose, prepared according to example XII) , containing 2 % or 10 % by weight respectively of theophylline-monohydraat were prepared. After mixing granulated crystalline amylose and the appropriate amount theophylline, tablets were struck under a force of 10 kN. The tablets weighed 300 mg, comprising 6 or 30 mg of theophylline and had a diameter of 9 mm. Release of the active substance from the tablet was determined in an aqueous medium, buffer pH 6, over a period of 13 hours and is shown in Fig. 13. This figure shows a zero order release, both for the 2 % tablet (solid line) and for the 10 % tablet (broken line) .
- Example XIV Tablets of helical amylose (crystalline amylose, prepared according to Example XII) , containing or 10 % by weight of theophylline- monohydraat were prepared. After mixing dry granulated ("slugged") crystalline amylose and the appropriate amount theophylline, tablets were struck under a force of 10 kN. The tablets weighed 300 mg, comprising 30 mg of theophylline and had a diameter of 9 mm. Release of the active substance from the tablet was determined in an aqueous medium, buffer pH 6, over a period of 13 hours and is shown in Fig. 14. This figure shows a zero order release.
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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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/356,256 US5585114A (en) | 1992-07-03 | 1993-07-02 | Composition for controlled release of an active substance and method for the preparation of such a composition |
AU45893/93A AU678166B2 (en) | 1992-07-03 | 1993-07-02 | Composition for controlled release of an active substance and method for the preparation of such a composition |
DE69305346T DE69305346T2 (en) | 1992-07-03 | 1993-07-02 | COMPOSITION FOR THE CONTROLLED DELIVERY OF AN ACTIVE SUBSTANCE AND METHOD FOR THE PRODUCTION THEREOF |
JP6503185A JPH07508533A (en) | 1992-07-03 | 1993-07-02 | Compositions for controlled release of active substances and methods for preparing such compositions |
EP93916292A EP0648116B1 (en) | 1992-07-03 | 1993-07-02 | Composition for controlled release of an active substance and method for the preparation of such a composition |
GR960403674T GR3022195T3 (en) | 1992-07-03 | 1996-12-30 | Composition for controlled release of an active substance and method for the preparation of such a composition. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL9201195A NL9201195A (en) | 1992-07-03 | 1992-07-03 | PREPARATION FOR THE REGULATED DELIVERY OF AN ACTIVE SUBSTANCE AND METHOD FOR PREPARING SUCH A PREPARATION. |
NL9201195 | 1992-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994001092A1 true WO1994001092A1 (en) | 1994-01-20 |
Family
ID=19861014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1993/000140 WO1994001092A1 (en) | 1992-07-03 | 1993-07-02 | Composition for controlled release of an active substance and method for the preparation of such a composition |
Country Status (12)
Country | Link |
---|---|
US (1) | US5585114A (en) |
EP (1) | EP0648116B1 (en) |
JP (1) | JPH07508533A (en) |
AT (1) | ATE143801T1 (en) |
AU (1) | AU678166B2 (en) |
CA (1) | CA2139494A1 (en) |
DE (1) | DE69305346T2 (en) |
DK (1) | DK0648116T3 (en) |
ES (1) | ES2095658T3 (en) |
GR (1) | GR3022195T3 (en) |
NL (1) | NL9201195A (en) |
WO (1) | WO1994001092A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996009815A1 (en) * | 1994-09-27 | 1996-04-04 | Coöperatieve Verkoop- En Productievereniging Van Aardappelmeel En Derivaten Avebe B.A. | Starch products as tabletting excipient, method for preparing same, and method for making tablets |
WO1997034932A2 (en) * | 1996-03-20 | 1997-09-25 | British Technology Group Limited | Compositions containing starch excipients |
WO1999009066A1 (en) * | 1997-08-14 | 1999-02-25 | 9068-3293 Quebec Inc. | Preparation of pregelatinized high amylose starch and debranched starch useful as an excipient for controlled release of active agents |
WO1999030691A2 (en) * | 1997-12-18 | 1999-06-24 | Ato B.V. | Composition for the controlled release of active compounds |
WO2011117884A1 (en) * | 2010-03-22 | 2011-09-29 | Cadila Healthcare Limited | Stable pharmaceutical compositions comprising fesoterodine |
US8759604B2 (en) | 2005-12-09 | 2014-06-24 | Sca Hygiene Products Ab | Absorbent product |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2743496B1 (en) * | 1996-01-15 | 1998-04-10 | Univ Rennes | MACROPOROUS COMPOSITE SUPPORT FOR DRUG SUBSTANCE (S) FOR USE AS BONE RECONSTRUCTION MATERIAL AND PROCESS FOR PREPARING THE SAME |
US5879707A (en) * | 1996-10-30 | 1999-03-09 | Universite De Montreal | Substituted amylose as a matrix for sustained drug release |
NZ527832A (en) | 2001-03-13 | 2006-03-31 | Penwest Pharmaceuticals Co | Chronotherapeutic dosage forms |
JP3742335B2 (en) * | 2001-12-20 | 2006-02-01 | 富士通株式会社 | I / O buffer circuit |
US7081261B2 (en) * | 2002-05-14 | 2006-07-25 | National Starch And Chemical Investment Holding Corporation | Resistant starch prepared by isoamylase debranching of low amylose starch |
US6929817B2 (en) * | 2002-05-14 | 2005-08-16 | National Starch & Chemical Investment Holding Corporation | Slowly digestible starch product |
US6890571B2 (en) * | 2002-05-14 | 2005-05-10 | National Starch And Chemical Investment Holding Corporation | Slowly digestible starch product |
US20040185097A1 (en) * | 2003-01-31 | 2004-09-23 | Glenmark Pharmaceuticals Ltd. | Controlled release modifying complex and pharmaceutical compositions thereof |
EP1645568A4 (en) | 2003-07-11 | 2007-06-27 | Asahi Kasei Chemicals Corp | Functional starch powder |
JP4716871B2 (en) * | 2003-08-26 | 2011-07-06 | 江崎グリコ株式会社 | Additives for tablets |
BRPI0414311A (en) | 2003-09-19 | 2008-03-04 | Penwest Pharmaceutical Co | controlled release dosage forms |
KR20110073618A (en) * | 2008-10-23 | 2011-06-29 | 헨켈 코포레이션 | Vaginal pellets comprising debranched starch |
Citations (7)
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---|---|---|---|---|
GB1072795A (en) * | 1963-08-28 | 1967-06-21 | Eastman Kodak Co | Solid composition containing fat-soluble vitamins and processes for making it |
US3490742A (en) * | 1966-01-14 | 1970-01-20 | Staley Mfg Co A E | Compressed tablets |
US3493652A (en) * | 1962-09-14 | 1970-02-03 | Charles W Hartman | Controlled release medicament |
WO1985003414A1 (en) * | 1984-01-31 | 1985-08-15 | Scm Corporation | Encapsulation matrix composition and encapsulate containing same |
WO1987005212A1 (en) * | 1986-03-07 | 1987-09-11 | Eurand Italia S.P.A. | Formulation for preparing sustained release drugs for oral administration |
WO1989000045A1 (en) * | 1987-06-30 | 1989-01-12 | Riker Laboratories, Incorporated | Pellets with enzymatically controlled drug release |
EP0343993A1 (en) * | 1988-05-26 | 1989-11-29 | Btg International Limited | Delayed release formulations |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0747539B2 (en) * | 1986-10-22 | 1995-05-24 | 東京田辺製薬株式会社 | Bile acid solid formulation |
CA2041774C (en) * | 1990-11-27 | 1994-04-19 | Mircea A. Mateescu | Use of cross-linked amylose as a matrix for the slow release of biologically active compounds |
-
1992
- 1992-07-03 NL NL9201195A patent/NL9201195A/en not_active Application Discontinuation
-
1993
- 1993-07-02 DE DE69305346T patent/DE69305346T2/en not_active Expired - Fee Related
- 1993-07-02 DK DK93916292.1T patent/DK0648116T3/en active
- 1993-07-02 JP JP6503185A patent/JPH07508533A/en active Pending
- 1993-07-02 ES ES93916292T patent/ES2095658T3/en not_active Expired - Lifetime
- 1993-07-02 EP EP93916292A patent/EP0648116B1/en not_active Expired - Lifetime
- 1993-07-02 US US08/356,256 patent/US5585114A/en not_active Expired - Fee Related
- 1993-07-02 AU AU45893/93A patent/AU678166B2/en not_active Ceased
- 1993-07-02 CA CA002139494A patent/CA2139494A1/en not_active Abandoned
- 1993-07-02 AT AT93916292T patent/ATE143801T1/en not_active IP Right Cessation
- 1993-07-02 WO PCT/NL1993/000140 patent/WO1994001092A1/en active IP Right Grant
-
1996
- 1996-12-30 GR GR960403674T patent/GR3022195T3/en unknown
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
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US3493652A (en) * | 1962-09-14 | 1970-02-03 | Charles W Hartman | Controlled release medicament |
GB1072795A (en) * | 1963-08-28 | 1967-06-21 | Eastman Kodak Co | Solid composition containing fat-soluble vitamins and processes for making it |
US3490742A (en) * | 1966-01-14 | 1970-01-20 | Staley Mfg Co A E | Compressed tablets |
WO1985003414A1 (en) * | 1984-01-31 | 1985-08-15 | Scm Corporation | Encapsulation matrix composition and encapsulate containing same |
WO1987005212A1 (en) * | 1986-03-07 | 1987-09-11 | Eurand Italia S.P.A. | Formulation for preparing sustained release drugs for oral administration |
WO1989000045A1 (en) * | 1987-06-30 | 1989-01-12 | Riker Laboratories, Incorporated | Pellets with enzymatically controlled drug release |
EP0343993A1 (en) * | 1988-05-26 | 1989-11-29 | Btg International Limited | Delayed release formulations |
Non-Patent Citations (1)
Title |
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PATENT ABSTRACTS OF JAPAN vol. 12, no. 349 22 October 1986 * |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996009815A1 (en) * | 1994-09-27 | 1996-04-04 | Coöperatieve Verkoop- En Productievereniging Van Aardappelmeel En Derivaten Avebe B.A. | Starch products as tabletting excipient, method for preparing same, and method for making tablets |
NL9401572A (en) * | 1994-09-27 | 1996-05-01 | Avebe Coop Verkoop Prod | Starch products such as tableting excipient, method of preparation thereof, and method of making tablets. |
US6010717A (en) * | 1994-09-27 | 2000-01-04 | Arends-Scholte; Anna Willemina | Starch products as tabletting excipient, method for preparing same, and method for making tablets |
WO1997034932A2 (en) * | 1996-03-20 | 1997-09-25 | British Technology Group Limited | Compositions containing starch excipients |
WO1997034932A3 (en) * | 1996-03-20 | 2001-04-26 | British Tech Group | Compositions containing starch excipients |
WO1999009066A1 (en) * | 1997-08-14 | 1999-02-25 | 9068-3293 Quebec Inc. | Preparation of pregelatinized high amylose starch and debranched starch useful as an excipient for controlled release of active agents |
WO1999030691A2 (en) * | 1997-12-18 | 1999-06-24 | Ato B.V. | Composition for the controlled release of active compounds |
WO1999030691A3 (en) * | 1997-12-18 | 2002-10-10 | Ato Bv | Composition for the controlled release of active compounds |
US8759604B2 (en) | 2005-12-09 | 2014-06-24 | Sca Hygiene Products Ab | Absorbent product |
WO2011117884A1 (en) * | 2010-03-22 | 2011-09-29 | Cadila Healthcare Limited | Stable pharmaceutical compositions comprising fesoterodine |
Also Published As
Publication number | Publication date |
---|---|
DK0648116T3 (en) | 1997-03-24 |
DE69305346D1 (en) | 1996-11-14 |
EP0648116A1 (en) | 1995-04-19 |
JPH07508533A (en) | 1995-09-21 |
US5585114A (en) | 1996-12-17 |
ES2095658T3 (en) | 1997-02-16 |
CA2139494A1 (en) | 1994-01-20 |
GR3022195T3 (en) | 1997-03-31 |
AU678166B2 (en) | 1997-05-22 |
NL9201195A (en) | 1994-02-01 |
ATE143801T1 (en) | 1996-10-15 |
DE69305346T2 (en) | 1997-04-30 |
AU4589393A (en) | 1994-01-31 |
EP0648116B1 (en) | 1996-10-09 |
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