EP0461202A1 - Composition contenant une enzyme pour le nettoyage de verres de contact et methode pour un tel nettoyage - Google Patents
Composition contenant une enzyme pour le nettoyage de verres de contact et methode pour un tel nettoyageInfo
- Publication number
- EP0461202A1 EP0461202A1 EP19900906421 EP90906421A EP0461202A1 EP 0461202 A1 EP0461202 A1 EP 0461202A1 EP 19900906421 EP19900906421 EP 19900906421 EP 90906421 A EP90906421 A EP 90906421A EP 0461202 A1 EP0461202 A1 EP 0461202A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polymer
- terpolymer
- membrane
- composition according
- hydrogen peroxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 55
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 20
- 239000012528 membrane Substances 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000001301 oxygen Substances 0.000 claims abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- 229920003176 water-insoluble polymer Polymers 0.000 claims abstract description 3
- 230000003197 catalytic effect Effects 0.000 claims abstract 5
- 239000012736 aqueous medium Substances 0.000 claims abstract 4
- 238000000034 method Methods 0.000 claims description 23
- 238000000576 coating method Methods 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 20
- 229920001897 terpolymer Polymers 0.000 claims description 12
- 102000016938 Catalase Human genes 0.000 claims description 11
- 108010053835 Catalase Proteins 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 9
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 7
- 239000004014 plasticizer Substances 0.000 claims description 7
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 230000000249 desinfective effect Effects 0.000 claims description 2
- 230000000063 preceeding effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 4
- 230000035699 permeability Effects 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 11
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 238000004659 sterilization and disinfection Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229940117958 vinyl acetate Drugs 0.000 description 6
- 239000012530 fluid Substances 0.000 description 5
- 230000002147 killing effect Effects 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 230000000937 inactivator Effects 0.000 description 3
- 229940073584 methylene chloride Drugs 0.000 description 3
- 229960004793 sucrose Drugs 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229920001688 coating polymer Polymers 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 235000013681 dietary sucrose Nutrition 0.000 description 2
- 229960004716 idoxuridine Drugs 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000010296 bead milling Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 210000004087 cornea Anatomy 0.000 description 1
- 239000003405 delayed action preparation Substances 0.000 description 1
- 238000009837 dry grinding Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L12/00—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor
- A61L12/08—Methods or apparatus for disinfecting or sterilising contact lenses; Accessories therefor using chemical substances
- A61L12/12—Non-macromolecular oxygen-containing compounds, e.g. hydrogen peroxide or ozone
- A61L12/124—Hydrogen peroxide; Peroxy compounds
- A61L12/126—Hydrogen peroxide; Peroxy compounds neutralised with catalase or peroxidase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/04—Enzymes or microbial cells immobilised on or in an organic carrier entrapped within the carrier, e.g. gel or hollow fibres
Definitions
- Disinfection of contact lenses is mainly carried out by treat ⁇ ing the lenses once a day (or up to once a week) with an aqueous hydrogen peroxide (3 %) solution.
- the killing effect depends on the concentration of the hydrogen peroxide solu- tion and the time during which the lenses are in contact with the solution. Minimum 1,5 % during minimum 20 minutes is regarded to give a sufficiently killing effect.
- the removal of the hydrogen peroxide can be carried out in different ways.
- The-most common way is the use of platinum as a catalyst for the decomposition of hydrogen peroxide and the use of the enzyme catalase for the same purpose.
- the method based on platinum is carried out in such a way that a plate of platinum is mounted on the bottom of the di ⁇ sinfection vessel.
- a plate of platinum is mounted on the bottom of the di ⁇ sinfection vessel.
- the solution of hydrogen peroxide is added the decomposition process starts immediately.
- Each plate of platinum is intended for three months daily use.
- a new plate gives a rapid decomposition process, which can je- opardize the killing effect, whereas a plate, which has been used for some time, gives a remarkably reduced decomposition effect with big risk for remaining high concentrations of hydrogen peroxide after the recommended treating time, 6 h. Accordingly the risk of damages on the eye is big.
- the advantage of the method with the decomposition with pla ⁇ tinum is that it is regarded as easy to use by the user be ⁇ cause disinfection and decomposition is started at the same time and the user needs not do anything with the lenses un- til after 6 h when the process is ready.
- catalase for the decomposi ⁇ tion of hydrogen peroxide is carried out in such a way that catalase is added either as a solution or in the form of a tablet approximately, 20-30 minutes after the lenses have been placed in 3 % hydrogen .peroxide.
- the decomposition then starts immediately and goes very rapidly and completely.
- the disadvantage of the method is that the users consider the method more complicated to use than the method with platinum due to the fact that it requires two operations by the user at two different occasions.
- An ideal tablet preparation of a hydrogen peroxide inactiva- tor shall thus be able to give a slow decomposition at the beginning and a rapid decomposition after the disinfection is completed.
- This invention is intended to fulfil the following requirements:
- a disinfection-process for contact lenses, which when initiated by the user does not require any further acti ⁇ on until the process is complete and the lenses are rea ⁇ dy for use.
- a predetermined concentration of hydrogen peroxide shall be maintained during a specific period of time in order to secure a complete disinfection.
- the decomposition rate shall be increased in order to secure that no hydrogen peroxide remains after the desired period of time (during the night).
- the invention comprises that tablet cores containing a cata ⁇ lytic substance such as catalase, is coated with a membrane, which consists of a water insoluble polymer which contains water soluble particles of a defined size and amount. The particles will be dissolved by the hydrogen peroxide solu ⁇ tion and a macroporous membrane is formed. Hydrogen peroxide penetrates through this membrane and a reaction starts bet- ween the hydrogen peroxide and catalase, whereby hydrogen pe ⁇ roxide decomposes for oxygen and water.
- a cata ⁇ lytic substance such as catalase
- the decomposition of the hydrogen peroxide is initially slow, but concurrently with the formation of more oxygen the membrane is expanded by the gas pressure and the penetration capacity of the mem ⁇ brane is increased, whereby catalase is released to the sur ⁇ rounding hydrogen peroxide solution and the reaction rate and the decomposition will increase.
- the polymer forming Jhe membrane should have good funifor ⁇ ming and adhesive properties and should be easily soluble in organic solvents, such as acetone and methylene chloride.
- Suitable polymers are derivatives of cellulose, acrylpoly- mers and vinylpolymers.
- the coating polymer is a polymer, which contains 80-95 per cent by weight of vinyl chloride, 1-19 per cent by weight vinylacetate and 0-10 per cent vinylalcohol.
- the coating should also preferably include a plastisizer.
- the amount of the p astisizer may vary between 30 and 150 per cent by weight of the polymer coating.
- suitable plastisizers are acetyltributylcitrate, polyethylene glycol , blown castor oil and glyceryltriacetate.
- the coating can al ⁇ so include sodium bicarbonate as a stabilizing agent.
- the poreforming substance which is used according to tfie in ⁇ vention should be very water soluble, insoluble in the sol ⁇ vent, which is used for the coating, and toxicologically acceptable in the amounts used.
- perfered are sugars, such as sucrose and lactose and salts, such as sodium chloride.
- the particle size of the poreforming substance may vary bet ⁇ ween 0,1 and 100, preferably between 0,5 and 50 urn.
- the ra- tio between the amount of porecreating substance and coating polymer depends on the desired property. Usually this ratio should exceed 5 and preferably be between 10 and 30.
- the co ⁇ ating comprises a terpolymer of
- the amount of plasticizer exceeds 30 per cent by weight of the terpolymer.
- the amount of plasticizer varies between 50 and 150 per cent by weight of the terpolymer.
- the ratio porecreating agent to terpolymer should preferably exceed 5. Most preferably this ratio should vary between 10 and 30.
- the coating thickness depends also on the desired property. It can vary between 5 and 300 ⁇ , preferably between 10 and 200 ⁇ m.
- the coating procedure according to the invention can prefer ⁇ ably be carried out in the folowing manner:
- a terpolymer containing (w/w%) 80-95 '/. VC (vinyl- chloride), 1-19 % VAC (vinylacetate), and 1-10 % V0H (vlnylalcohol) is dissolved in a solvent, e.g. acetone, methylenechloride, methylethylketone, or mixtures aceto ⁇ ne and ethanol , acetone and methylenechloride, or the like.
- a solvent e.g. acetone, methylenechloride, methylethylketone, or mixtures aceto ⁇ ne and ethanol , acetone and methylenechloride, or the like.
- a suspension of the pore-creating substance is produced as fol ows:
- the pore-creating particles are ground either by dry milling in a ball mill or by wet-milling in a glass bead milling device to a defined particle size, preferably between 0,5 urn and 50 ⁇ m.
- the particles are dispersed in solvents or mixtures of solvents, such as those previ ⁇ ously mentioned, and mixed with the terpolymer solution.
- the ratio between pore-creating substance and terpolymer in the coating fluid is as previously described for the ratio in the coating.
- the coating fluid may, as previ ⁇ ously stated, include a plasticizer and sodium bicarbonate.
- the coating fluid in the form of a suspension, is then applied on cores by conventional coating procedure.
- coating procedures are pan coating, manual or spray-coating, W ⁇ rster coating, and other fluid-bed coating procedures.
- Coloring matter can also be incorporated in the coating fluid, and insoluble co ⁇ loring materials are preferred.
- Example 1 The following examples further illustrate the invention but should not be construed as limiting the invention.
- Example 1 The following examples further illustrate the invention but should not be construed as limiting the invention.
- Tablets including catalase (commercially available from Allergan) in a sufficient amount for decomposition of 10 ml hydrogen peroxide (3 %) were coated according to the proce ⁇ dure described above with a membrane consisting of 1 mg ter ⁇ polymer of vinylchloride, vinylacetate and vinylalcohol as a water insoluble membrane, 0,2 mg acetyltributylcitrate, 0,1 mg blown castor oil, 5,6 mg saccharose and 0,2 mg sodium bicarbonate. Acetone' as used as a solvent for the coating.
- the catalase containing tablets from Allergan were coated by a coating fluid having the following composition:
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Microbiology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Eyeglasses (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Oxygen, Ozone, And Oxides In General (AREA)
- Catalysts (AREA)
Abstract
L'invention concerne une composition comprenant un noyau doté d'une matière catalytique pour la décomposition du peroxyde d'hydrogène en oxygène et eau. Ladite composition est caractérisée par le fait que le noyau est entouré d'une membrane, qui peut s'étendre en milieu aqueux et qui comprend un polymère insoluble dans l'eau et une matière porogène soluble dans l'eau, distribuée de manière aléatoire dans le polymère, permettant l'augmentation de la perméabilité de la membrane vis à vis de la matière catalytique au fur et à mesure que la membrane s'étend dans le milieu aqueux.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8901279 | 1989-04-10 | ||
| SE8901279A SE8901279D0 (sv) | 1989-04-10 | 1989-04-10 | Komposition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0461202A1 true EP0461202A1 (fr) | 1991-12-18 |
Family
ID=20375626
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19900906421 Withdrawn EP0461202A1 (fr) | 1989-04-10 | 1990-04-05 | Composition contenant une enzyme pour le nettoyage de verres de contact et methode pour un tel nettoyage |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0461202A1 (fr) |
| JP (1) | JPH04506159A (fr) |
| AU (1) | AU5528490A (fr) |
| SE (1) | SE8901279D0 (fr) |
| WO (1) | WO1990011786A1 (fr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2026714A1 (fr) * | 1989-11-03 | 1991-05-04 | Peter Gyulai | Composes detruisant le peroxyde d'hydrogene et methode d'utilisation |
| JPH05504496A (ja) * | 1990-02-27 | 1993-07-15 | アラーガン、インコーポレイテッド | 過酸化水素分解組成物およびその使用方法 |
| DK0517758T3 (da) * | 1990-02-27 | 1999-08-09 | Allergan Inc | Hydrogenperoxid-destruerende sammensætninger og fremgangsmåder til fremstilling og anvendelse af samme |
| US5145644A (en) | 1990-12-20 | 1992-09-08 | Allergan, Inc. | Hydrogen peroxide destroying compositions and methods of making and using same |
| ES2041561B1 (es) * | 1991-05-07 | 1994-06-01 | Dirygesa Sl | Procedimiento para desinfectar y limpiar lentes de contacto. |
| JPH08507700A (ja) * | 1992-12-28 | 1996-08-20 | ボシュ アンド ロム インコーポレイテッド | 水性媒体内に活性物質を制御放出する組成物 |
| JP3381172B2 (ja) | 1993-01-26 | 2003-02-24 | アラーガン、インコーポレイテッド | コンタクトレンズ消毒用組成物および方法 |
| US5362647A (en) * | 1993-02-12 | 1994-11-08 | Allergan, Inc. | Compositions and methods for destroying hydrogen peroxide |
| JP2002508530A (ja) | 1997-12-12 | 2002-03-19 | シュノプティク アクティーゼルスカブ | 物質の定時解放のための容器 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8332489D0 (en) * | 1983-12-06 | 1984-01-11 | Contactasol Ltd | Contact lenses |
| DE3666914D1 (en) * | 1985-07-10 | 1989-12-21 | Ciba Geigy Ag | Cleaning set for contact lenses |
| DE3524659C2 (de) * | 1985-07-10 | 1999-02-18 | Novartis Ag | Kontaktlinsenpflegesatz |
| EP0265253A3 (fr) * | 1986-10-24 | 1990-01-10 | Kingston Technologies, Inc. | Enzyme dispersé stabilisé |
| DE3721574A1 (de) * | 1987-06-30 | 1989-01-12 | Kettelhack Riker Pharma Gmbh | Arzneimittel in form von pellets mit enzymatisch kontrollierter arzneistoff-freisetzung |
-
1989
- 1989-04-10 SE SE8901279A patent/SE8901279D0/xx unknown
-
1990
- 1990-04-05 JP JP2506386A patent/JPH04506159A/ja active Pending
- 1990-04-05 AU AU55284/90A patent/AU5528490A/en not_active Abandoned
- 1990-04-05 WO PCT/SE1990/000227 patent/WO1990011786A1/fr not_active Ceased
- 1990-04-05 EP EP19900906421 patent/EP0461202A1/fr not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9011786A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5528490A (en) | 1990-11-05 |
| SE8901279D0 (sv) | 1989-04-10 |
| WO1990011786A1 (fr) | 1990-10-18 |
| JPH04506159A (ja) | 1992-10-29 |
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