WO2006061990A1 - コンタクトレンズ用液剤組成物 - Google Patents
コンタクトレンズ用液剤組成物 Download PDFInfo
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- WO2006061990A1 WO2006061990A1 PCT/JP2005/021438 JP2005021438W WO2006061990A1 WO 2006061990 A1 WO2006061990 A1 WO 2006061990A1 JP 2005021438 W JP2005021438 W JP 2005021438W WO 2006061990 A1 WO2006061990 A1 WO 2006061990A1
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- Prior art keywords
- contact lens
- composition
- contact lenses
- liquid composition
- solution
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Classifications
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- 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
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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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/717—Celluloses
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/008—Polymeric surface-active agents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0078—Compositions for cleaning contact lenses, spectacles or lenses
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
Definitions
- the present invention relates to a liquid composition for contact lenses, and is particularly suitable as an ophthalmic solution with improved safety for the eyes while ensuring the function of removing contact stains and preventing the adhesion of stains thereto.
- the present invention relates to a liquid composition for contact lenses that can be used.
- contact lenses have been used by being classified into non-hydrous contact lenses and hydrous contact lenses, or roughly divided into node contact lenses and soft contact lenses.
- dirt such as protein and eye grease derived from tear fluid can easily adhere to and accumulate on the surface of the contact lens during its use. Dirt such as protein or fat existing on the fingertips may adhere to the contact lens surface, and such dirt may cause the contact lens to become less transparent or have a foreign object feeling due to the adhered dirt. This may cause a feeling of wearing such as the occurrence of eyelids, a decrease in visual acuity, and may cause eye disorders such as corneal inflammation and conjunctival hyperemia.
- Permissible Document 5 reveals that an ophthalmic composition with good wettability of a contact lens can be provided by combining a predetermined nonionic surfactant and a viscous agent.
- an anionic surfactant having a specific structure called AKYPO RLM-100 etc. terminal CH of polyoxyethylene long chain alkyl ether
- An aqueous cleaning composition for contact lenses having an OH group in an acid form) as an active ingredient has also been clarified.
- Patent Document 1 Japanese Patent Laid-Open No. 7-76700
- Patent Document 2 Japanese Patent Laid-Open No. 4-370197
- Patent Document 3 Japanese Patent Laid-Open No. 9-87682
- Patent Document 4 Japanese Patent Laid-Open No. 10-108899
- Patent Document 5 Pamphlet of International Publication No. 97Z28827
- Patent Document 6 US Patent No. 4808239 Specification
- the present invention has been made against the background of vigorous circumstances.
- the problem is to maintain the function of removing dirt such as lipid stains attached to the outer contour lens and the function of effectively suppressing the adhesion of dirt such as proteins to the surface of the contact lens. It is possible to cause damage to the cornea due to the destruction of the layer, etc., to provide a liquid composition for contact lenses that is highly safe for the living body, and to effectively wet the surface of the contact lenses.
- Another object of the present invention is to provide an ophthalmic solution composition that can be suitably used as an ophthalmic solution for contact lenses. Means for solving the problem
- the present inventors have been used as a component of ophthalmic liquid preparations, and have been used as a specific non-ion that is relatively safe.
- the surfactant is contained at a specific low concentration, specifically near the critical micelle concentration, and polyethylene glycol is contained in a large proportion relative to the strong nonionic surfactant.
- Ophthalmic solution composition that does not affect the tear film while retaining the ability to dissolve lipid stains on contact lenses and the ability to suppress adhesion of protein stains to contact lenses. It was found that can be obtained.
- the present invention has been completed on the basis of strong knowledge, and the first aspect is that a polyoxyethylene sorbitan alkylate, a polyoxyethylene-cured castor is contained in an aqueous medium. At least one nonionic surfactant selected from the group consisting of oil, polyoxyethylene stearate and polyoxyethylene polyoxypropylene block copolymer within the range of 0.0001-0.04 w / w%. And a polyethylene glycol is contained in a proportion of 20 parts by weight or more with respect to 1 part by weight of the nonionic surfactant.
- the polyethylene glycol has an average molecular weight of 1000 to 100,000.
- the polyoxyethylene sorbitan alkylate includes a polyoxyethylene sorbitan model. Nolate is preferably used.
- hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinylinol pyrrolidone, polybulal alcohol, chondroitin sulfate and hyaluronate A configuration in which at least one thickening agent selected from the group consisting of is further contained in the liquid composition for contact lenses is advantageously employed.
- the osmotic pressure of the liquid composition is in an osmotic pressure ratio with respect to physiological saline, from 0.85 to L 5 It is adjusted so that it is within the range of 5.
- isotonic agents as the sixth aspect, isotonic agents, pH buffering agents, chelating agents, preservatives, bactericides, cooling agents, anti-inflammatory agents, vasoconstrictors
- a composition that further contains at least one additive selected from the group consisting of vitamins and amino acids is also employed.
- the seventh aspect force containing K + within the range of 2 mEq ZL to 30 mEqZL of the liquid composition composition force for contact lenses as described above is advantageously employed.
- the liquid composition for contact lenses as described above can be advantageously used as an ophthalmic solution for contact lenses.
- the specific nonionic property that is relatively safe as a compounding component of the ophthalmic detergent Since it is contained at a very low concentration of 0.04 wZw% or less, its ability to solubilize lipids even in the presence of such nonionic surfactants Therefore, it is thought that there is not enough force to destroy the tear film and dissolve all the oil film, and as a result, damage to the cornea due to tear film destruction, etc.
- the contact lens liquid composition according to the present invention is imparted with a surface activity performance due to the presence of a nonionic surfactant, even though the concentration is low. According to it, contact lenses Effectively moisten the surface There are also effects that can be achieved.
- the present invention even if the content of the nonionic surfactant is such a low concentration, a practically sufficient effect of removing lipid stains can be exhibited.
- the presence of a large proportion of polyethylene glycol can effectively improve the lipid solubilization rate of the contact lens solution composition according to the present invention, and can advantageously enhance the removal action of dirt such as lipid dirt. It also has features. That is, in order to remove lipids, it is necessary to liquidize lipid stains adhering to the lens surface in the cleaning process. Polyethylene glycol can penetrate into the lipids, thereby causing contamination. Can be liquefied and lifted up, and it is considered that the solubilizing action of the nonionic surfactant can be effectively extracted, so that an effective dirt removing effect can be exhibited. is there.
- the polyethylene glycol used in the present invention also has a function of inducing precipitation due to interaction with a protein.
- a protein By suppressing or preventing direct deposition on the surface, it is possible to advantageously exert the effect of suppressing the adhesion of dirt, such as protein contamination on the contact lens.
- the liquid composition for contact lenses according to the present invention as described above effectively removes dirt such as lipid stains adhering to the contact lens, and also has an effect of suppressing the adhesion of dirt such as proteins. It can be used advantageously, and can effectively wet the surface of contact lenses with a hydrophobic surface, but does not cause problems such as damage to the cornea due to tear film destruction. For this reason, as an ophthalmic solution for a contact lens as in the eighth aspect of the present invention described above, it is used for instillation on an eye on which a contact lens is worn. 'Effects can be exerted advantageously.
- polyethylene glycol having an average molecular weight within a predetermined range is used, and according to the third embodiment of the present invention, polyoxyethylene sorbitan alkylate is used as a polyoxyethylene sorbitan alkylate.
- polyoxyethylene sorbitan monooleate is used as a polyoxyethylene sorbitan alkylate.
- a predetermined thickener is further added according to the fourth aspect of the present invention, or a predetermined thickener according to the sixth aspect is included.
- the additive is further contained, it is imparted to the liquid composition for contact lenses with a further characteristic power according to each component, and its practicality can be further enhanced.
- the concentration of potassium ions (K +) in the liquid composition composition for contact lenses as in the seventh aspect described above is adjusted so as to be within a predetermined range. It becomes close to the composition, and the biocompatibility of the liquid composition can be further improved.
- ophthalmic solutions have osmotic pressure adjusted to the same level as tears in order to increase biocompatibility, but sodium chloride sodium (NaCl) is mainly used as a tonicity adjusting agent.
- NaCl sodium chloride sodium
- salt NaCl is an indispensable component for the living body, the physiological function is maintained by the presence of an appropriate amount of other electrolytes such as K + and Ca2 + at the same time. It is.
- moderate potassium (K +) is also present in the tears, and the same amount of rhodium as in tears may be present in the vaginal eye drops that maintain the physiological function of the eye tissue. Desirable.
- FIG. 1 is a graph showing the relationship between the shaking time of each test solution and physiological saline obtained in Example 1 and the results of absorbance measurement.
- FIG. 2 is a graph showing the lipid solubilization rate for each test solution and physiological saline obtained in Example 1.
- FIG. 3 is a graph showing the relationship between each test solution and the amount of protein attached to the contact lens obtained in Example 3.
- such a liquid composition composition for contact lenses mainly comprises an aqueous medium, and contains a predetermined nonionic surfactant at a low concentration as one of essential components therein.
- a nonionic surfactant used there Polyoxyethylene sorbitan alkylate, polyoxyethylene hydrogenated castor oil, polyethylene stearate, and polyoxyethylene polyoxypropylene block copolymer that have been used as a component of ophthalmic solutions and are considered relatively safe At least one of them can be selected and used.
- the lipid solubilizing ability can be advantageously enhanced, and polyoxyl is a component that has been used as a component of ophthalmic solutions in Japan and has a mild surface activity.
- Various commercially available products such as ethylene sorbitan alkylate, especially polyoxyethylene sorbitan monooleate, for example, polysorbate 80 (trade name: Nikko Chemicals Co., Ltd.), are preferably used.
- nonionic surfactant should achieve the object of the present invention at a low concentration of 0.001 to 0.04 wZw%, preferably 0.001 to 0.03 wZw%. Thus, it is contained in the contact lens solution composition. It should be noted that if the content of the nonionic surfactant to be produced is less than the above lower limit, the detergency is extremely reduced because it is much lower than the critical micelle concentration (CMC). If the amount exceeds the upper limit, problems such as destruction of the tear film and damage to the corneal epithelium are likely to occur.
- CMC critical micelle concentration
- Polyethylene glycol which is another essential component of the liquid composition for contact lenses according to the present invention, is generally a polyether having hydroxyl groups at both ends obtained by ring-opening polymerization of ethylene oxide. In the present invention, it is used as a component that improves the lipid solubility rate of the nonionic surfactant described above and suppresses the adhesion of dirt such as protein dirt, and Fully fulfilling such a function Force to be contained so as to be a ratio of 20 parts by weight or more with respect to 1 part by weight of the non-ionic surfactant, which is contained in the liquid composition for contact lenses In general, the amount is 0.01 to 5. OwZw%, preferably 0.1 to 1. OwZw%.
- polyethylene glycol content is too low, there are problems that it is difficult to effectively act on solubilization of lipids, and that the effect of preventing the adhesion of protein stains such as protein stains is insufficient, and the content increases. This is because problems such as swelling and deformation of the contact lens are likely to be caused if too much.
- powerful polyethylene glycol has an average molecular weight because it can sufficiently achieve the object of the present invention, suppress adsorption uptake into the contact lens, and at the same time ensure sufficient solubility in water.
- a force in the range of 1000 to 100,000 is preferably used.
- the polyethylene glycol power having an average molecular weight in the range of 3000 to 20000 is advantageously used in the present invention.
- the liquid composition for contact lenses according to the present invention has a feeling of use that is more excellent for contact lenses by adjusting the viscosity of such a liquid composition and improving its moisture retention and wettability.
- At least one kind of thickening agent that gives the strength is further contained.
- examples of such a thickener include hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinyl pyrrolidone, polyvinyl alcohol, chondroitin sulfate, hyaluronate and the like. Among them, it is a component that has been used as a component of ophthalmic solutions in Japan, and it is expected to be effective in removing lipid adhering to contact lenses.
- the content of the thickener is generally about 0.05 to 0.8 wZw%, preferably about 0.1 to 0.8 wZw%.
- the content of this thickener is small, there is a problem that a sufficient thickening effect cannot be obtained, and when it exceeds the upper limit, the viscosity becomes too high and the usability is poor. When this happens, the same problem occurs.
- the liquid composition for contact lenses according to the present invention has a large osmotic pressure. It is usually used for contact lenses because it may cause irritation to the eyes, affect the shape of the contact lens, or cause eye damage if it becomes too small or too small. It is generally desirable that the osmotic pressure of a liquid composition is close to that of tears by adding an isotonic agent (osmotic pressure adjusting agent) or the like.
- the pressure ratio (assuming the osmotic pressure of the physiological saline is 1) is adjusted to a range of about 0.85 to about L 55, preferably about 0.9 to 1.5.
- the osmotic pressure adjusting agent used for adjusting the osmotic pressure is generally at least one selected from the group consisting of sodium chloride, potassium chloride, saccharides, sugar alcohols, polyhydric alcohols or ethers thereof, or ester forces thereof.
- the above compound power will be used.
- the pH value of such a liquid composition is usually adjusted to about 5.3 to 8.5, particularly around 7.0 by adding a suitable pH adjusting agent or buffering agent. It is desirable.
- a suitable pH adjusting agent or buffering agent used for the adjustment of such a pH
- the pH adjusting agent used for the adjustment of such a pH whereas such as sodium hydroxide or hydrochloric acid is used, the P H of the liquid composition, to effectively and eye range mentioned above
- a pH buffering agent for keeping the temperature within a safe range various kinds of conventionally known pH buffers are appropriately selected and used.
- carboxylic acids such as phosphoric acid, boric acid and citrate, acids such as oxycarboxylic acid and salts thereof (for example, sodium salt), and Good-Buffer tris (hydroxymethyl) aminomethane ( TRIS), bis (2-hydroxyethyl) iminotris (hydroxymethyl) methane (Bis-Tris), sodium hydrogen carbonate, etc.
- TRIS Good-Buffer tris (hydroxymethyl) aminomethane
- Bis-Tris bis (2-hydroxyethyl) iminotris (hydroxymethyl) methane
- sodium hydrogen carbonate etc.
- contact lenses particularly soft contact lenses, generally have the potential to deposit or adsorb calcium or the like as dirt from tears.
- a chelating agent is also advantageously added to the liquid composition for contact lenses that prevents adsorption.
- Such chelating agents include, for example, ethylenediamine tetraacetic acid (EDTA) and its salts, such as ethylenediamine tetraacetic acid ⁇ 2 sodium (EDTA.2Na), ethylenediamine amine acetic acid ⁇ 3 sodium (EDTA.3). Na) and the like.
- the liquid composition for contact lenses according to the present invention is advantageous in disinfecting or sterilizing effects for eyes and contact lenses, and further, preserving and preserving effects of the liquid composition for contact lenses. Therefore, a preservative having a preservative effect or a bactericidal effect or a bactericidal agent is appropriately added to the liquid composition.
- preservatives and fungicides in general, those having antiseptic or bactericidal efficacy, excellent compatibility with eyes and contact lenses, and those that are unlikely to cause damage such as allergies are desired. Appropriate ones are selected from various publicly known ones and used alone or in combination.
- sorbic acid for example, sorbic acid, potassium sorbate, benzoic acid or a salt thereof, paraethyl benzoate, butyl paraoxybenzoate, propyl parabenzoate, methyl parabenzoate, chlorobutanol, Perborates such as perborate or sodium perborate, diacid chloride and the like may be mentioned.
- the fungicide include biguanide fungicides such as polyhexamethylene biguanide (PHMB) and quaternary ammonium salt fungicides such as polyquaterum.
- the ophthalmic composition according to the present invention can be used as a single dose type that can be used once, or disclosed in JP-A-2002-80055, It is also possible to use it as a multi-dose type using a protruding container with such a filter.
- menthol borneol, camphor, gera-ol, eucalyptus oil, bergamot oil, etc.
- a refreshing agent such as Wikiyo oil, heart force oil, rose oil or cool mint.
- the liquid composition for contact lenses according to the present invention includes glycyrrhizic acid and its salt, ⁇ -, in order to suppress intraocular inflammation caused by wearing stress lenses or the like.
- Anti-inflammatory agents such as aminocaproic acid, allantoin, and sodium azulene sulfonate and nafazoline nitrate and tetrahydrozoline hydrochloride, which are effective in relieving eye fatigue while acting on the scleral blood vessels in the eyeball to relieve eye redness.
- Vasoconstrictor such as vitamin A (including retinol palmitate, j8—power rotin, etc.), vitamin B
- the liquid composition for contact lenses according to the present invention which contains various ingredients such as beer, has a concentration of potassium ions (K +) contained in the liquid composition for improving the biocompatibility thereof.
- K + potassium ions
- the concentration of potassium ions (K +) contained in the liquid composition for improving the biocompatibility thereof.
- it is adjusted to be within a range of about 2 mEqZL to 30 mEqZL, preferably about 4 mEqZL to 28 mEqZL. If this potassium ion concentration is too low or too high, the Ocular Surface may be adversely affected.
- This potassium ion is introduced as a KC1 added as an isotonic agent or various additive ingredients of K salt type, and the total amount thereof is within the above-mentioned range. Is adjusted.
- the liquid composition for contact lenses according to the present invention is prepared by adding and incorporating the above-described components in an appropriate amount in an appropriate aqueous medium, as in the prior art.
- the aqueous medium used at that time is highly water-safe if it is a solution mainly composed of water. Needless to say, any of them can be used as long as they are sufficiently ophthalmically acceptable.
- no special method is required, and the components are dissolved in an arbitrary order in an aqueous medium as in the case of preparing a normal aqueous solution. Thus, it can be easily obtained.
- the liquid composition for contact lenses according to the present invention obtained as described above is excellent in safety for the eyes, does not destroy the tear film, or damage the corneal epithelium. Since it does not adversely affect the shape or physical properties of the contact lens, it is advantageously used as an ophthalmic solution, so that the above-described effect of the present invention can be effectively exhibited. .
- the appropriate amount of the ophthalmic solution in the state of wearing a contact lens is the same as that of conventionally known eye drops or eye drops. However, it will be instilled.
- the contact lens solution composition according to the present invention when used as a contact lens solution that is not an eye drop, the contact lens is washed or rinsed with a powerful ophthalmic composition, for example. After that, the contact lens is worn with the liquid composition attached to the surface of the contact lens, or the contact lens is immersed in a powerful liquid composition for a certain period of time and stored. Remove the lens and wear it as it is. When used in this manner, the effects of the liquid composition composition for contact lenses according to the present invention are advantageously exhibited.
- contact lens cleaning solution In addition to the above contact lens solution, contact lens cleaning solution, contact lens rinsing solution, contact lens preserving solution and the like for the purpose of single use, cleaning, rinsing, sterilization and storage, etc.
- Any known liquid agent conventionally used for contact lens care such as a multi-purpose solution, intended for two or more uses can be mentioned, and its use is limited in any way It is not a thing.
- the contact lens solution composition according to the present invention is used as an ophthalmic solution for contact lenses or a contact lens solution
- the types of contact lenses are not limited. For example, soft contact lenses and hard contact lens forces classified into non-water content, low water content, high water content, etc. There is no question.
- test solutions 17 having a pH of 6.5 were added to purified water by adding and dissolving prescribed compounding ingredients in various proportions shown in Table 1 below. Prepared.
- the osmotic pressure of the seven kinds of test solutions obtained was about 1.1 in terms of the osmotic pressure ratio with respect to physiological saline.
- HPMC2910 used in the preparation of a powerful test solution is hydroxypropylmethylcellulose (Metrouse TC-1E manufactured by Shin-Etsu Chemical Co., Ltd.) as a thickener, and PEG # 6000 Is polyethylene glycol having an average molecular weight of 6000 (manufactured by Fluka Bio Chemika), and polysorbate 80 is polyoxyethylene sorbitan monooleate (TO—manufactured by Nikko Chemicals Co., Ltd.), a nonionic surfactant. 1 0M).
- the amount of borax used was determined in such a ratio that the pH of each test solution was 6.5.
- a colored lipid obtained by mixing triglyceride as a lipid and Sudan I as a pigment at a weight ratio of 99: 1 is put in a predetermined test bottle. Coughed After that, add 20 ml of the test solution or physiological saline solution obtained above to a vigorous test bottle, accommodate it, and then cover the opening of the test bottle with an appropriate lid. About each. Next, each of the test bottles containing the colored lipid and the liquid preparation prepared in this way is shaken at a constant speed for 1 to 24 hours at a temperature of 25 ° C., and is further allowed to stand for a predetermined time.
- each supernatant liquid in each test bottle was collected, and each of the supernatant liquids was measured at a wavelength of 485.5 nm by a spectrophotometer (manufactured by Shimadzu Corporation, self-recording spectrophotometer UV-2200). The absorbance at was measured.
- Table 2 below shows the measurement results of the absorbance of the supernatant in each test bottle when the shaking time for the above test bottles is 1, 3, 6, 9, and 24 hours. This is shown in Figure 1 as well.
- Test Solution 1 and Test Solution 2 and Test Solution 3 and Test Solution 4 show almost the same value in the amount of lipid solubility.
- Test Solution 1 and Test Solution 3 use polyethylene glycol and a nonionic surfactant (polysorbate 80) in combination.
- Test Solution 2 and Test Solution 4 are nonionic surfactant (polysorbate 80) and the power of the two substances is ⁇ (polyethylene glycol must be added). ) Is understood.
- polyethylene glycol reduces the amount of lipid soluble matter due to the surface active ability of nonionic surfactants when used in combination with nonionic surfactants. It is understood that only the lipid solubility rate is increased. In addition, increasing the solubility rate without affecting the amount of lipid solubility does not affect the lipid soil components such as eye oil more quickly when instilled. Therefore, the removal treatment can be advantageously performed, and therefore, it is possible to obtain a more effective cleaning liquid in the cleaning action when used in combination with polyethylene glycol than when the nonionic surfactant is used alone. It can be done.
- Example 1 Based on the results of Example 1 above, in order to conduct a comparative study of Test Solution 1 and Test Solution 3 that use two components of polyethylene glycol and a nonionic surfactant (Polysorbate 80) together, A Ni-BUT (Non-invasive Tear Break-up Time) measurement test was conducted to investigate the effect on the surface.
- Ni-BUT Non-invasive Tear Break-up Time
- the content of the polysorbate 80, a nonionic surfactant is approximately 10 times the critical micelle concentration, and the test solution 1 that is set to a concentration near the critical micelle concentration is higher. It is understood that it is very safe and favorable to the power.
- the lysozyme concentration in the artificial tears after immersion for 5 minutes was measured with a high performance liquid chromatography.
- the amount of lysozyme adhering to the contact lens was calculated from the difference between the lysozyme concentration in the artificial tear before immersion of the contact lens and the lysozyme concentration in the artificial tear after immersion of the contact lens.
- test solution 6 containing 0.01% of a nonionic surfactant (polysorbate 80) and 0.10% of polyethylene glycol, and nonionic
- test solution 7 containing 0.01% of the surfactant (polysorbate 80) and 0.20% of polyethylene glycol, where polysorbate 80
- a remarkable difference is observed between the ratio of 1:10 and 1:20, and it can be found that the former test solution 6 has less protein adhesion than the latter test solution 7.
- the amount ratio of nonionic surfactant (polysorbate 80) to polyethylene glycol is 1:20.
- a range of ⁇ 1: 50 is considered preferable.
- polysorbate 80 which is a nonionic surfactant used for preparing the test solution in Example 1
- other nonionic surfactants such as polyoxyethylene hydrogenated castor oil, polyoxyethylene stearate or Polyoxyethylene Polyoxypropylene block copolymer (manufactured by BASF) was used in the same manner as in Example 1, and even in the test solution prepared, polyethylene glycol having an average molecular weight of 4000 ( Even when using Nakarai Testa Co., Ltd., it is possible to effectively remove lipid stains attached to the surface of the contact lens being worn, and effectively attach proteins.
- an ophthalmic liquid composition that is suppressed and safe for a living body can be obtained.
- the blending ratio of polysorbate 80 as a nonionic surfactant which is a blending component of Test Solution 1 in Example 1, is 0.001 wZw%, and the blending amount of polyethylene glycol (PEG # 6000) is 0.05 wZw.
- PEG # 6000 polyethylene glycol
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Abstract
Description
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05809155A EP1845405A4 (en) | 2004-12-06 | 2005-11-22 | LIQUID COMPOSITION FOR CONTACT LENSES |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004353394A JP4642449B2 (ja) | 2004-12-06 | 2004-12-06 | コンタクトレンズ用液剤組成物 |
JP2004-353394 | 2004-12-06 |
Publications (1)
Publication Number | Publication Date |
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WO2006061990A1 true WO2006061990A1 (ja) | 2006-06-15 |
Family
ID=36577821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/021438 WO2006061990A1 (ja) | 2004-12-06 | 2005-11-22 | コンタクトレンズ用液剤組成物 |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1845405A4 (ja) |
JP (1) | JP4642449B2 (ja) |
WO (1) | WO2006061990A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008206915A (ja) * | 2007-02-28 | 2008-09-11 | Toray Ind Inc | 化合物の滅菌方法およびこれを用いた医療材料の製造方法 |
JP4751482B2 (ja) * | 2008-07-22 | 2011-08-17 | 株式会社メニコン | コンタクトレンズ用液剤 |
JP2012198538A (ja) * | 2012-03-12 | 2012-10-18 | Menicon Co Ltd | コンタクトレンズ用組成物 |
US8647658B2 (en) | 2007-08-31 | 2014-02-11 | Novartis Ag | Contact lens products |
US8689971B2 (en) | 2007-08-31 | 2014-04-08 | Novartis Ag | Contact lens packaging solutions |
US9829723B2 (en) | 2015-12-03 | 2017-11-28 | Novartis Ag | Contact lens packaging solutions |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5369346B2 (ja) * | 2008-12-25 | 2013-12-18 | 株式会社メニコンネクト | コンタクトレンズ用の装着・保存・点眼用の組成物 |
JPWO2022030421A1 (ja) * | 2020-08-03 | 2022-02-10 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08122717A (ja) * | 1994-08-29 | 1996-05-17 | Seiko Epson Corp | 電解イオン水消毒装置及び消毒中和方法 |
JP2001181208A (ja) * | 1999-12-27 | 2001-07-03 | Fuso Pharmaceutical Industries Ltd | 涙液分泌促進組成物 |
JP2001302518A (ja) * | 2000-02-15 | 2001-10-31 | Rohto Pharmaceut Co Ltd | 官能改善方法および官能改善剤 |
JP2003057610A (ja) * | 2001-08-09 | 2003-02-26 | Ophtecs Corp | コンタクトレンズ用液剤組成物 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5870208A (ja) * | 1981-10-22 | 1983-04-26 | Toyo Contact Lens Co Ltd | コンタクトレンズ用洗浄剤 |
US4734222A (en) * | 1986-04-03 | 1988-03-29 | Ciba-Geigy Corporation | Composition and method for cleaning soft and hard contact lenses |
JP3610986B2 (ja) * | 1994-12-28 | 2005-01-19 | 株式会社トーメー | コンタクトレンズ用洗浄消毒液およびそれを用いたコンタクトレンズの洗浄消毒方法 |
JPH09206362A (ja) * | 1996-02-05 | 1997-08-12 | Tomey Technol Corp | コンタクトレンズ用消毒洗浄組成物及びそれを用いたコンタクトレンズの消毒洗浄方法 |
FR2762849B1 (fr) * | 1997-05-05 | 1999-06-18 | Essilor Int | Solution aqueuse d'entretien des lentilles de contact |
JP2000109892A (ja) * | 1998-10-02 | 2000-04-18 | Rohto Pharmaceut Co Ltd | 多糖含有コンタクトレンズ用液剤 |
JP2000347142A (ja) * | 1999-06-02 | 2000-12-15 | Tomey Corp | コンタクトレンズ用洗浄・保存液剤 |
JP3793483B2 (ja) * | 2002-06-05 | 2006-07-05 | 日本瓦斯工事株式会社 | 三種混合装置 |
JP4361294B2 (ja) * | 2003-02-25 | 2009-11-11 | ロート製薬株式会社 | ケトチフェン含有組成物 |
-
2004
- 2004-12-06 JP JP2004353394A patent/JP4642449B2/ja not_active Expired - Lifetime
-
2005
- 2005-11-22 WO PCT/JP2005/021438 patent/WO2006061990A1/ja active Application Filing
- 2005-11-22 EP EP05809155A patent/EP1845405A4/en not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08122717A (ja) * | 1994-08-29 | 1996-05-17 | Seiko Epson Corp | 電解イオン水消毒装置及び消毒中和方法 |
JP2001181208A (ja) * | 1999-12-27 | 2001-07-03 | Fuso Pharmaceutical Industries Ltd | 涙液分泌促進組成物 |
JP2001302518A (ja) * | 2000-02-15 | 2001-10-31 | Rohto Pharmaceut Co Ltd | 官能改善方法および官能改善剤 |
JP2003057610A (ja) * | 2001-08-09 | 2003-02-26 | Ophtecs Corp | コンタクトレンズ用液剤組成物 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1845405A4 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008206915A (ja) * | 2007-02-28 | 2008-09-11 | Toray Ind Inc | 化合物の滅菌方法およびこれを用いた医療材料の製造方法 |
US8647658B2 (en) | 2007-08-31 | 2014-02-11 | Novartis Ag | Contact lens products |
US8689971B2 (en) | 2007-08-31 | 2014-04-08 | Novartis Ag | Contact lens packaging solutions |
US9162784B2 (en) | 2007-08-31 | 2015-10-20 | Novartis Ag | Contact lens packaging solutions |
US9348061B2 (en) | 2007-08-31 | 2016-05-24 | Novartis Ag | Contact lens products |
JP4751482B2 (ja) * | 2008-07-22 | 2011-08-17 | 株式会社メニコン | コンタクトレンズ用液剤 |
JP2012198538A (ja) * | 2012-03-12 | 2012-10-18 | Menicon Co Ltd | コンタクトレンズ用組成物 |
US9829723B2 (en) | 2015-12-03 | 2017-11-28 | Novartis Ag | Contact lens packaging solutions |
Also Published As
Publication number | Publication date |
---|---|
EP1845405A1 (en) | 2007-10-17 |
EP1845405A4 (en) | 2008-05-14 |
JP2006162899A (ja) | 2006-06-22 |
JP4642449B2 (ja) | 2011-03-02 |
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