WO1995000617A1 - Composition for cleaning and wetting contact lenses - Google Patents

Composition for cleaning and wetting contact lenses Download PDF

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Publication number
WO1995000617A1
WO1995000617A1 PCT/US1994/006788 US9406788W WO9500617A1 WO 1995000617 A1 WO1995000617 A1 WO 1995000617A1 US 9406788 W US9406788 W US 9406788W WO 9500617 A1 WO9500617 A1 WO 9500617A1
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WO
WIPO (PCT)
Prior art keywords
composition
contact lens
cleaning
surface active
wetting
Prior art date
Application number
PCT/US1994/006788
Other languages
French (fr)
Inventor
Chimpiramma Potini
Stanley J. Wrobel
Hong J. Zhang
Edward J. Ellis
Original Assignee
Polymer Technology Corporation
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Polymer Technology Corporation filed Critical Polymer Technology Corporation
Priority to DE69422813T priority Critical patent/DE69422813T2/en
Priority to AU72082/94A priority patent/AU684805B2/en
Priority to BR9407263A priority patent/BR9407263A/en
Priority to KR1019950705684A priority patent/KR100341671B1/en
Priority to EP94921307A priority patent/EP0703967B1/en
Publication of WO1995000617A1 publication Critical patent/WO1995000617A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3738Alkoxylated silicones
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0078Compositions for cleaning contact lenses, spectacles or lenses
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/90Betaines

Definitions

  • This invention relates to compositions for the care of contact lenses and methods employing such compositions.
  • a care regimen for contact lenses involves various functions, such as regularly cleaning the lens with a contact lens solution containing a surface active agent. Rinsing of the contact lens is generally required following cleaning to remove loosened debris. Additionally, the regimen may include treatment to disinfect the lens, treatment to render the lens surface more wettable prior to insertion in the eye, or treatment to condition (e.g, lubricate or cushion) the lens surface so that the lens is more comfortable in the eye. As a further example, a contact lens wearer may need to rewet the lens during wear by administering directly in the eye a solution commonly referred to as rewetting drops.
  • Multipurpose contact lens solutions may be designed for the individual segments of the care regimen.
  • multipurpose contact lens solutions have gained popularity, i.e., solutions which can be used for several segments of the care regimen.
  • Multipurpose contact lens solutions which effectively clean the contact lens, and can also be used to treat the lens immediately prior to insertion of the lens in the eye, represent the more difficult multipurpose solutions to develop.
  • Conventional surface active agents used as primary cleaning agents in the cleaning segment of the regimen, as well as various other components such as antimicrobial agents included as a preservative or disinfectant, tend to be irritating to the eye. Additionally, the surface active agents must not inhibit the wetting or conditioning function of the solution.
  • a principal component of the compositions of this invention is a silicone polymer containing an alkyleneoxide side chain.
  • compositions for cleaning soft and silicone contact lenses which contain a polyoxyalkylene modified silicone resin and at least one fatty acid amide or nitrogen analog thereof.
  • a broad class of modified silicone resins are mentioned, the described silicone resins are preferably block copolymers having the formula:
  • T is alkyl of from 1 to 3 carbon atoms, usually methyl
  • T' is alkyl of from 1 to 6 carbon atoms, usually 3 to 4 carbon atoms
  • n is an integer of from 2 to 30, and x and y are numbers within various ranges.
  • the silicone resin in the Chen patent was reported as not particularly effective as a primary cleaning agent for contact lens deposits. Additionally, neither the Chen patent nor the Sibley patents suggests that the compositions can wet or condition a contact lens, or that the compositions are sufficiently nonirritating for in-eye use.
  • this invention provides an aqueous composition for cleaning and wetting contact lenses which comprises a silicone polymer containing an alkyleneoxide side chain, and a surface active agent having cleaning activity for contact lens deposits.
  • compositions provide effective cleaning activity, and are effective at wetting surfaces of the lens.
  • the compositions achieve the desired cleaning for a wide variety of contact lens deposits but are relatively nonirritating to the eye.
  • the composition is sufficiently nonirritating that contact lenses treated with the compositions can be inserted directly in the eye, i.e., without the need to rinse the composition from the lens, or the composition can be administered directly in the eye for use as a rewetting solution.
  • the invention provides a wetting solution for contact lenses, comprising the described silicone polymer containing an alkyleneoxide side chain.
  • the composition of the invention is an aqueous composition which comprises a silicone polymer containing an alkyleneoxide side chain, and a surface active agent having cleaning activity for contact lens deposits.
  • Preferred silicone polymers are represented by the formula:
  • each R is independently selected from the group consisting of C ⁇ Cn alkyl and phenyl; each R' is independently an alkyleneoxide containing radical; x is 0 or an integer of at least 1, preferably 1 to 200; and y is an integer of at least 1, preferably 1 to 200.
  • R' is an alkyleneoxide containing radical of the formula:
  • R 2 is an alkylene radical having 1 to 6 carbon atoms
  • EO is the ethyleneoxide radical -(C 2 H4O)-;
  • PO is the propyleneoxide radical , preferably -(CH 2 CH(CH 3 )0)-; and each of m and n is independently 0 or an integer of at least 1, preferably m is at least 1.
  • Preferred silicone polymers include dimethylpolysiloxanes having at least one pendant side chain provided by the R' radical, i.e., dimethylpolysiloxanes wherein at least one methyl group attached to silicon is replaced with the alkyleneoxy pendant side chain, including several materials available under the CTFA (Cosmetic, Toiletry and Fragrance Association, Inc.) name dimethicone copolyol.
  • CTFA Cosmetic, Toiletry and Fragrance Association, Inc.
  • alkoxylated silicone polymers available under the tradename Dow Corning ® 193 from Dow Corning, Midland, Michigan, USA.
  • the silicone polymer may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.002 to about 1 weight percent, with about 0.002 to about 0.1 weight percent being especially preferred.
  • the composition further includes at least one surface active agent having cleaning activity for contact lens deposits. This ensures that the composition has good cleaning activity.
  • surface active agent having cleaning activity for contact lens deposits.
  • preferred silicone polymers such as Dow Corning 193 are surfactants, they are not particularly effective cleaning agents for removing deposits from contact lenses.
  • compositions of the present invention provide excellent cleaning and wetting of contact lenses.
  • a surface active agent having good cleaning ability, as well as various optional components tending to be irritating to the eye
  • the compositions exhibit minimal or no eye irritation in that the subject silicone polymer alleviates the irritation potential of the composition.
  • the silicone polymers contribute to the ability of the compositions to wet lenses treated with the compositions. When lenses are treated with the compositions, the hydrophobic silicone portion of these silicone polymers tend to loosely associate with the lens surface, whereby the pendant alkyleneoxy side chain extends from the lens surface to enhance wettability of the lens surface.
  • a wide variety of surface active agents are known in the art as a primary cleaning agent, including anionic, cationic, nonionic and amphoteric surface active agents.
  • anionic surface active agents include sulfated and sulfonated surface active agents, and physiologically acceptable salts thereof, which provide good cleaning activity for lipids, proteins, and other contact lens deposits.
  • Examples include sodium lauryl sulfate, sodium laureth sulfate (sodium salt of sulfated ethoxylated lauryl alcohol) , ammonium laureth sulfate (ammonium salt of sulfated ethoxylated lauryl alcohol) , sodium trideceth sulfate (sodium salt of sulfated ethoxylated tridecyl alcohol) , sodium dodecylbenzene sulfonate, disodium lauryl or laureth sulfosuccinate (disodium salt of a lauryl or ethoxylated lauryl alcohol half ester of sulfosuccinic acid) , disodium oleamido sulfo
  • Nonionic surface active agents having good cleaning activity include certain polyoxyethylene, polyoxypropylene block copolymer (poloxamer) surface active agents, including various surface active agents available under the tradename Pluronic from BASF Corp., e.g., Pluronic P104 or L64.
  • the poloxamers' which may be employed as a primary cleaning agent in the compositions of this invention have an HLB value less than 18, generally about 12 to about 18.
  • Other representative nonionic surface active agents include: ethoxylated alkyl phenols, such as various surface active agents available under the tradenames Triton (Union Carbide, Tarrytown, New York, USA) and Igepal (Rhone-Poulenc, Cranbury, New Jersey, USA) ; polysorbates such as polysorbate 20, including the polysorbate surface active agents available under the tradename Tween (ICI Americas, Inc., Wilmington, Delaware, USA.); and alkyl glucosides and polyglucosides such as products available under the tradename Plantaren (Henkel Corp. , Hoboken, New Jersey, USA) .
  • compositions may include a cationic surface active agent.
  • cationic surface active agents include triquaternary phosphate esters, such as various cationic surface active agents available from Mona Industries, Inc., Patterson, New Jersey, USA under the tradename Monaquat.
  • compositions may include an amphoteric surface active agent.
  • Amphoteric surface active agents include fatty acid amide betaines, such as the cocoamidoalkyl betaines available under the tradename Tego-Betain (Goldschmidt Chemical Corp. , Hopewell, Virginia, USA).
  • Other amphoterics include imidazoline derivatives such as cocoamphopropionates available under the tradename Miranol (Rhone-Poulenc) , and N-alkylamino acids such as lauramino propionic acid available under the tradename Mirataine (Rhone- Poulenc) .
  • Silicone polymers having a pendant side chain containing an ionizable group include silicone polymers having a pendant side chain containing an ionizable group.
  • Dimethylpolysiloxanes containing a pendant side chain having a sulfonate or sulfosuccinate radical are available under the tradenames Silube WS-100 and Silube SS-154-100 (Siltech, Inc., Norcross, Georgia, USA).
  • Dimethylpolysiloxanes containing a pendant side chain having a phosphobetaine radical are available under the tradename Silicone Phosphobetaine (Siltech, Inc.), dimethylpolysiloxanes containing a pendant side chain having an amphoteric radical are available under the tradename Siltech Amphoteric (Siltech, Inc.), and dimethylpolysiloxanes substituted with propyleneglycol betaine are available under the tradename Abil B 9950 from Goldschmidt Chemical Corp., Hopewell, Virginia, USA.
  • Such silicone polymers are especially compatible in the compositions of this invention, and exhibit less irritation than many conventional cleaning agents such as the above-described anionic surface active agents.
  • the surface active agents having cleaning activity for contact lens deposits may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.005 to about 2 weight percent, with about 0.01 to about 0.1 weight percent being especially preferred.
  • the composition includes a polyethyleneoxy (PEO) containing material (in addition to any silicone polymer which contains PEO in the pendant side chain) , especially a PEO-containing material having a hydrophile-lipophile balance (HLB) of at least about 18.
  • PEO polyethyleneoxy
  • HLB hydrophile-lipophile balance
  • Preferred PEO-containing materials include homopoly ers of polyethylene glycol or polyethyleneoxide having the high HLB value, and certain poloxamers such as materials commercially available from BASF under the tradenames Pluronic F108 and Pluronic F127.
  • Other preferred PEO-containing materials include ethoxylated glucose derivatives, such as the ethoxylated products available under the tradename Glucam (Amerchol Corp.
  • the PEO-containing materials may be employed at about 0.001 to about 10 weight percent, preferably at about 0.001 to about 5 weight percent.
  • the cleaning compositions include as necessary buffering agents for buffering or adjusting pH of the composition, and/or tonicity adjusting agents for adjusting the tonicity of the composition.
  • Representative buffering agents include: alkali metal salts such as potassium or sodium carbonates, acetates, borates, phosphates, citrates and hydroxides; and weak acids such as acetic, boric and phosphoric acids.
  • Representative tonicity adjusting agents include: sodium and potassium chloride, and those materials listed as buffering agents.
  • the tonicity agents may be employed in an amount effective to adjust the osmotic value of the final composition to a desired value.
  • the buffering agents and/or tonicity adjusting agents may be included up to about 10 weight percent.
  • the silicone polymer contributes to the wetting ability of the composition.
  • the composition may include as necessary a supplemental wetting agent.
  • Representative wetting agents include: the aforementioned PEO-containing materials; cellulosic materials such as cationic cellulosic polymers, hydroxypropyl ethylcellulose, hydroxyethyl cellulose and methylcellulose; polyvinyl alcohol; and polyvinyl pyrrolidone.
  • Such additives when present, may be used in a wide range of concentrations, generally about 0.1 to about 10 weight percent.
  • an antimicrobial agent is included in the composition in an antimicrobially effective amount, i.e., an amount which is effective to at least inhibit growth of microorganisms in the composition.
  • the composition can be used to disinfect a contact lens treated therewith.
  • antimicrobial agents are known in the art as useful in contact lens solutions, including: chlorhexidine (1,l'-hexamethylene-bis[5-(p- chlorophenyl) biguanide]) or water soluble salts thereof, such as chlorhexidine gluconate; polyhexamethylene biguanide (a polymer of hexamethylene biguanide, also referred to as polyaminopropyl biguanide) or water-soluble salts thereof, such as the polyhexamethylene biguanide hydrochloride available under the trade name Cosmocil CQ (ICI Americas Inc.); benzalkonium chloride; and polymeric quaternary ammonium salts.
  • the antimicrobial agent may be included at 0.00001 to about 5 weight percent, depending on the specific agent.
  • compositions may further include a sequestering agent (or chelating agent) which can be present up to about 2.0 weight percent.
  • sequestering agents include ethylenediaminetetraacetic acid (EDTA) and its salts, with the disodium salt (disodium edetate) being especially preferred.
  • Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon or a fluorosilicon polymer.
  • Soft contact lenses include hydrophilic hydrogel lenses.
  • a contact lens is cleaned by exposing the lens to the cleaning composition, preferably by immersing the lens in the composition, followed by agitation, such as by rubbing the composition on the lens surface.
  • the lens is then rinsed to remove the composition along with contaminants.
  • the composition may also be used to rinse the lenses, or alternately, a separate solution can be used.
  • the composition When the composition is used to rinse the lenses, the composition will usually adequately wet the lens surface. Due to the low irritation potential of the composition, the lens can then be inserted directly in the eye. Alternately, the cleaned lens can be subsequently treated with the composition, such as soaking the lens in the composition for sufficient time to ensure adequate wetting the lens surface.
  • the composition including an antimicrobial agent
  • the treated lens can then be inserted directly in the eye.
  • a second embodiment of the invention provides a composition for wetting a contact lens comprising as an essential component the silicone polymer containing an alkyleneoxide side chain, wherein the composition is sufficiently nonirritating that contact lenses treated with the composition can be inserted directly in the eye.
  • the wetting composition can be applied directly in the eye as a rewetting solution.
  • the wetting composition may include any of the components described for the cleaning and wetting composition, preferably an antimicrobial agent as a preservative or disinfectant, a buffering agent and/or a tonicity adjusting agent, and if desired, a supplemental wetting agent.
  • compositions listed in the following tables can be prepared by the following general procedure.
  • compositions can be prepared by adding the individual components to water.
  • a representative method follows.
  • the salts and wetting agents such as sodium chloride, potassium chloride, disodium edetate, cellulosic components, and/or polyvinyl alcohol (PVA) , are added to premeasured, heated water with mixing.
  • This first composition is allowed to cool, filtered, and sterilized.
  • the sodium phosphate, potassium phosphate, PEO-containing material, the silicone polymer, the surface active agents and/or glycerin are added to premeasured water with mixing and then sterilized and filtered.
  • the antimicrobial agents are added to the remaining amount of premeasured water, and the three compositions are combined with mixing.
  • PVA 0.11 0.15 cationic cellulosic 0.010 polymer (Polymer JR-30M, Amerchol) hydroxypropy1 0.50 0.55 methylcellulose sodium phosphate 0.56 0.56 potassium phosphate 0.11 0.11 polyethylene glycol 0.10 0.10 (Polyox WSR-301, 1%, Union Carbide) glycerin 0.020 0.050 alkoxylated silicone —— 0.005 polymer (193, Dow Corning)
  • compositions of Examples 1 and Comparative Example 1 were evaluated for cleaning and wetting efficacy. It is noted that the composition of Comparative Example 1 did not include the silicone polymer having a pendant alkyleneoxy group.
  • oven-dried fluorosilicone rigid, gas permeable (RGP) contact lenses were either: rubbed with the composition, inserted onto a subject's eye, and evaluated for non-wetted areas; or agitated with the composition without rubbing, inserted onto a subject's eye, and evaluated for non-wetted areas.
  • Table 1A shows the average percent of lens area remaining non- wetted with each method of wetting (rubbing or agitation) ; the "Combined" column combines the trials for the two methods.
  • the anterior surfaces of fluorosilicone RGP contact lenses were contaminated with Vaseline ® Intensive Care lotion.
  • the contaminated lenses were either: rubbed with the composition, inserted onto a subject's eye, and evaluated for contaminated areas; or agitated with the composition without rubbing, inserted onto a subject's eye, and evaluated for contaminated areas.
  • Table IB shows the average percent of lens area showing lipid contamination after each method of cleaning (rubbing or agitation) ; the third column combines the trials for the two methods.
  • compositions were also evaluated in toxicity testing. Five drops of the compositions were instilled onto the superior li bus of non-wearers of contact lenses. For subjects who are wearers of RGP lenses, lenses were rubbed with a large amount of the composition and then inserted directly on the eye. The composition of Example 1 scored better than Comparative Example 1, inducing no complaints of stinging, itching or burning. TABLE 2
  • compositions in Table 2 were tested according to the following procedure on twenty wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for at least five minutes', and then the soaked lenses were inserted directly (i.e., without rinsing) onto the subject's eye. The amount of irritation occurring within the first 20-30 seconds after insertion was rated by the subjects using the following scale:
  • each composition was then instilled directly into both eyes of each subject (one drop every 5 minutes) . Again, the amount of irritation occurring within the first 20-30 minutes after instillation of each drop was rated using the above scale.
  • Deionized Water 100 100 100 100 (qs to) pH 7.3 7.3 7.3 7.3 7.3
  • Osmolality 344 345 342 341 (mOsm/kg water)
  • the compositions in Table 3, and a saline solution as a control were tested according to the following procedure on twenty-one wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for about 8 to 10 minutes. Then, the lenses were removed from the case, additional solution was added to the back surface of the lens.es, and the lenses were inserted onto the subject's eyes. After waiting periods of approximately 10 minutes, the procedure was repeated for the remaining solutions, with various compositions presented to the subjects in random order. The subjects rated irritation based on the above scale of 0 to 8. The average irritation ratings are listed in Table 3A. The comparison of Example 11 and saline is considered statistically significant.
  • compositions were tested for insertional blur, i.e., the time required after insertion for the subject's vision to return to baseline acuity.
  • the average time for vision to clear (after insertion) is listed in Table 3A. TABLE 3A
  • Osmolality 363 351 341 (mOsm/kg water)

Abstract

Compositions for the care of contact lenses include a silicone polymer containing an alkyleneoxide side chain.

Description

COMPOSITION FOR CLEANING AND WETTING CONTACT LENSES
BACKGROUND OF THE INVENTION This invention relates to compositions for the care of contact lenses and methods employing such compositions.
A care regimen for contact lenses involves various functions, such as regularly cleaning the lens with a contact lens solution containing a surface active agent. Rinsing of the contact lens is generally required following cleaning to remove loosened debris. Additionally, the regimen may include treatment to disinfect the lens, treatment to render the lens surface more wettable prior to insertion in the eye, or treatment to condition (e.g, lubricate or cushion) the lens surface so that the lens is more comfortable in the eye. As a further example, a contact lens wearer may need to rewet the lens during wear by administering directly in the eye a solution commonly referred to as rewetting drops.
Separate solutions may be designed for the individual segments of the care regimen. For convenience purposes, multipurpose contact lens solutions have gained popularity, i.e., solutions which can be used for several segments of the care regimen. Multipurpose contact lens solutions which effectively clean the contact lens, and can also be used to treat the lens immediately prior to insertion of the lens in the eye, represent the more difficult multipurpose solutions to develop. Conventional surface active agents used as primary cleaning agents in the cleaning segment of the regimen, as well as various other components such as antimicrobial agents included as a preservative or disinfectant, tend to be irritating to the eye. Additionally, the surface active agents must not inhibit the wetting or conditioning function of the solution.
A principal component of the compositions of this invention is a silicone polymer containing an alkyleneoxide side chain.
U.S. Patent No. 4,613,380 (Chen) reports tests evaluating the effectiveness of various agents for removing lipid deposits from silicone elastomer contact lenses. A silicone polymer containing an alkyleneoxy side chain (Dow Corning® 190) , designated in the patent as "Surfactant 1", was employed as a comparative example in tests for effectiveness at removing lipid deposits from the contact lenses.
U.S. Patent Nos. 4,048,122 and 4,126,587 (Sibley et al.) describe compositions for cleaning soft and silicone contact lenses which contain a polyoxyalkylene modified silicone resin and at least one fatty acid amide or nitrogen analog thereof. Although a broad class of modified silicone resins are mentioned, the described silicone resins are preferably block copolymers having the formula:
TSi(0(SiMe20)x(CnH2nO)yT'3 wherein T is alkyl of from 1 to 3 carbon atoms, usually methyl, T' is alkyl of from 1 to 6 carbon atoms, usually 3 to 4 carbon atoms, n is an integer of from 2 to 30, and x and y are numbers within various ranges.
It will be appreciated that the silicone resin in the Chen patent was reported as not particularly effective as a primary cleaning agent for contact lens deposits. Additionally, neither the Chen patent nor the Sibley patents suggests that the compositions can wet or condition a contact lens, or that the compositions are sufficiently nonirritating for in-eye use.
SUMMARY OF THE INVENTION
In a first embodiment, this invention provides an aqueous composition for cleaning and wetting contact lenses which comprises a silicone polymer containing an alkyleneoxide side chain, and a surface active agent having cleaning activity for contact lens deposits.
The compositions provide effective cleaning activity, and are effective at wetting surfaces of the lens. The compositions achieve the desired cleaning for a wide variety of contact lens deposits but are relatively nonirritating to the eye. According to preferred embodiments, the composition is sufficiently nonirritating that contact lenses treated with the compositions can be inserted directly in the eye, i.e., without the need to rinse the composition from the lens, or the composition can be administered directly in the eye for use as a rewetting solution.
In a second embodiment, the invention provides a wetting solution for contact lenses, comprising the described silicone polymer containing an alkyleneoxide side chain.
DETAILED DESCRIPTION OF THE INVENTION In a first embodiment, the composition of the invention is an aqueous composition which comprises a silicone polymer containing an alkyleneoxide side chain, and a surface active agent having cleaning activity for contact lens deposits.
Preferred silicone polymers are represented by the formula:
R R R R
R-S Ii-O-(-SIi-O-)χ-(-SIi-O-)y-SIi-R R R R' R
wherein: each R is independently selected from the group consisting of C^Cn alkyl and phenyl; each R' is independently an alkyleneoxide containing radical; x is 0 or an integer of at least 1, preferably 1 to 200; and y is an integer of at least 1, preferably 1 to 200.
Preferably, R' is an alkyleneoxide containing radical of the formula:
-R2-0-(EO)m-(PO)n-H wherein R2 is an alkylene radical having 1 to 6 carbon atoms;
EO is the ethyleneoxide radical -(C2H4O)-;
PO is the propyleneoxide radical , preferably -(CH2CH(CH3)0)-; and each of m and n is independently 0 or an integer of at least 1, preferably m is at least 1.
Preferred silicone polymers include dimethylpolysiloxanes having at least one pendant side chain provided by the R' radical, i.e., dimethylpolysiloxanes wherein at least one methyl group attached to silicon is replaced with the alkyleneoxy pendant side chain, including several materials available under the CTFA (Cosmetic, Toiletry and Fragrance Association, Inc.) name dimethicone copolyol. Especially preferred are the alkoxylated silicone polymers available under the tradename Dow Corning® 193 from Dow Corning, Midland, Michigan, USA.
The silicone polymer may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.002 to about 1 weight percent, with about 0.002 to about 0.1 weight percent being especially preferred.
The composition further includes at least one surface active agent having cleaning activity for contact lens deposits. This ensures that the composition has good cleaning activity. Although preferred silicone polymers such as Dow Corning 193 are surfactants, they are not particularly effective cleaning agents for removing deposits from contact lenses.
Applicants have found that the compositions of the present invention provide excellent cleaning and wetting of contact lenses. Despite the inclusion of a surface active agent having good cleaning ability, as well as various optional components tending to be irritating to the eye, the compositions exhibit minimal or no eye irritation in that the subject silicone polymer alleviates the irritation potential of the composition. Additionally, the silicone polymers contribute to the ability of the compositions to wet lenses treated with the compositions. When lenses are treated with the compositions, the hydrophobic silicone portion of these silicone polymers tend to loosely associate with the lens surface, whereby the pendant alkyleneoxy side chain extends from the lens surface to enhance wettability of the lens surface.
A wide variety of surface active agents are known in the art as a primary cleaning agent, including anionic, cationic, nonionic and amphoteric surface active agents.
Representative anionic surface active agents include sulfated and sulfonated surface active agents, and physiologically acceptable salts thereof, which provide good cleaning activity for lipids, proteins, and other contact lens deposits. Examples include sodium lauryl sulfate, sodium laureth sulfate (sodium salt of sulfated ethoxylated lauryl alcohol) , ammonium laureth sulfate (ammonium salt of sulfated ethoxylated lauryl alcohol) , sodium trideceth sulfate (sodium salt of sulfated ethoxylated tridecyl alcohol) , sodium dodecylbenzene sulfonate, disodium lauryl or laureth sulfosuccinate (disodium salt of a lauryl or ethoxylated lauryl alcohol half ester of sulfosuccinic acid) , disodium oleamido sulfosuccinates, and dioctyl sodium sulfosuccinate (sodium salt of the diester of a 2-ethylhexyl alcohol and sulfosuccinic acid) .
Nonionic surface active agents having good cleaning activity include certain polyoxyethylene, polyoxypropylene block copolymer (poloxamer) surface active agents, including various surface active agents available under the tradename Pluronic from BASF Corp., e.g., Pluronic P104 or L64. (In contrast with the high-HLB PEO-containing materials, the poloxamers' which may be employed as a primary cleaning agent in the compositions of this invention have an HLB value less than 18, generally about 12 to about 18.) Other representative nonionic surface active agents include: ethoxylated alkyl phenols, such as various surface active agents available under the tradenames Triton (Union Carbide, Tarrytown, New York, USA) and Igepal (Rhone-Poulenc, Cranbury, New Jersey, USA) ; polysorbates such as polysorbate 20, including the polysorbate surface active agents available under the tradename Tween (ICI Americas, Inc., Wilmington, Delaware, USA.); and alkyl glucosides and polyglucosides such as products available under the tradename Plantaren (Henkel Corp. , Hoboken, New Jersey, USA) .
The compositions may include a cationic surface active agent. Representative cationic surface active agents include triquaternary phosphate esters, such as various cationic surface active agents available from Mona Industries, Inc., Patterson, New Jersey, USA under the tradename Monaquat.
Additionally, the compositions may include an amphoteric surface active agent. Amphoteric surface active agents include fatty acid amide betaines, such as the cocoamidoalkyl betaines available under the tradename Tego-Betain (Goldschmidt Chemical Corp. , Hopewell, Virginia, USA). Other amphoterics include imidazoline derivatives such as cocoamphopropionates available under the tradename Miranol (Rhone-Poulenc) , and N-alkylamino acids such as lauramino propionic acid available under the tradename Mirataine (Rhone- Poulenc) .
Surface active agents having cleaning activity for contact lens deposits include silicone polymers having a pendant side chain containing an ionizable group. Dimethylpolysiloxanes containing a pendant side chain having a sulfonate or sulfosuccinate radical are available under the tradenames Silube WS-100 and Silube SS-154-100 (Siltech, Inc., Norcross, Georgia, USA). Dimethylpolysiloxanes containing a pendant side chain having a phosphobetaine radical are available under the tradename Silicone Phosphobetaine (Siltech, Inc.), dimethylpolysiloxanes containing a pendant side chain having an amphoteric radical are available under the tradename Siltech Amphoteric (Siltech, Inc.), and dimethylpolysiloxanes substituted with propyleneglycol betaine are available under the tradename Abil B 9950 from Goldschmidt Chemical Corp., Hopewell, Virginia, USA. Such silicone polymers are especially compatible in the compositions of this invention, and exhibit less irritation than many conventional cleaning agents such as the above-described anionic surface active agents.
The surface active agents having cleaning activity for contact lens deposits may be employed at about 0.001 to about 5 weight percent of the composition, preferably at about 0.005 to about 2 weight percent, with about 0.01 to about 0.1 weight percent being especially preferred.
According to preferred embodiments, the composition includes a polyethyleneoxy (PEO) containing material (in addition to any silicone polymer which contains PEO in the pendant side chain) , especially a PEO-containing material having a hydrophile-lipophile balance (HLB) of at least about 18. These high-HLB PEO-containing materials are useful for further reducing the irritation potential of the surface active agent or other components in the compositions, and in some cases the PEO-containing materials may contribute to the wetting ability of the composition.
Preferred PEO-containing materials include homopoly ers of polyethylene glycol or polyethyleneoxide having the high HLB value, and certain poloxamers such as materials commercially available from BASF under the tradenames Pluronic F108 and Pluronic F127. Other preferred PEO-containing materials include ethoxylated glucose derivatives, such as the ethoxylated products available under the tradename Glucam (Amerchol Corp. , Edison, New Jersey, USA) , and high HLB ethoxylated nonionic ethers of sorbitol or glycerol, such as products available under the tradename Ethosperse, including sorbeth-20 supplied as Ethosperse SL-20 and glycereth-26 supplied as Ethosperse G-26 (Lonza Inc., Fair Lawn, New Jersey, USA) .
When present, the PEO-containing materials may be employed at about 0.001 to about 10 weight percent, preferably at about 0.001 to about 5 weight percent.
The cleaning compositions include as necessary buffering agents for buffering or adjusting pH of the composition, and/or tonicity adjusting agents for adjusting the tonicity of the composition. Representative buffering agents include: alkali metal salts such as potassium or sodium carbonates, acetates, borates, phosphates, citrates and hydroxides; and weak acids such as acetic, boric and phosphoric acids. Representative tonicity adjusting agents include: sodium and potassium chloride, and those materials listed as buffering agents. The tonicity agents may be employed in an amount effective to adjust the osmotic value of the final composition to a desired value. Generally, the buffering agents and/or tonicity adjusting agents may be included up to about 10 weight percent. As mentioned, the silicone polymer contributes to the wetting ability of the composition. The composition may include as necessary a supplemental wetting agent. Representative wetting agents include: the aforementioned PEO-containing materials; cellulosic materials such as cationic cellulosic polymers, hydroxypropyl ethylcellulose, hydroxyethyl cellulose and methylcellulose; polyvinyl alcohol; and polyvinyl pyrrolidone. Such additives, when present, may be used in a wide range of concentrations, generally about 0.1 to about 10 weight percent.
According to preferred embodiments, an antimicrobial agent is included in the composition in an antimicrobially effective amount, i.e., an amount which is effective to at least inhibit growth of microorganisms in the composition. Preferably, the composition can be used to disinfect a contact lens treated therewith. Various antimicrobial agents are known in the art as useful in contact lens solutions, including: chlorhexidine (1,l'-hexamethylene-bis[5-(p- chlorophenyl) biguanide]) or water soluble salts thereof, such as chlorhexidine gluconate; polyhexamethylene biguanide (a polymer of hexamethylene biguanide, also referred to as polyaminopropyl biguanide) or water-soluble salts thereof, such as the polyhexamethylene biguanide hydrochloride available under the trade name Cosmocil CQ (ICI Americas Inc.); benzalkonium chloride; and polymeric quaternary ammonium salts. When present, the antimicrobial agent may be included at 0.00001 to about 5 weight percent, depending on the specific agent.
The compositions may further include a sequestering agent (or chelating agent) which can be present up to about 2.0 weight percent. Examples of preferred sequestering agents include ethylenediaminetetraacetic acid (EDTA) and its salts, with the disodium salt (disodium edetate) being especially preferred.
The compositions are useful for hard and soft contact lenses. Hard lenses include polymethylmethacrylate lenses and rigid gas permeable (RGP) lenses formed of a silicon or a fluorosilicon polymer. Soft contact lenses include hydrophilic hydrogel lenses.
A contact lens is cleaned by exposing the lens to the cleaning composition, preferably by immersing the lens in the composition, followed by agitation, such as by rubbing the composition on the lens surface. The lens is then rinsed to remove the composition along with contaminants. The composition may also be used to rinse the lenses, or alternately, a separate solution can be used.
When the composition is used to rinse the lenses, the composition will usually adequately wet the lens surface. Due to the low irritation potential of the composition, the lens can then be inserted directly in the eye. Alternately, the cleaned lens can be subsequently treated with the composition, such as soaking the lens in the composition for sufficient time to ensure adequate wetting the lens surface. When treating lenses with the composition including an antimicrobial agent, it is preferred to soak the lenses for sufficient time to disinfect the lenses, in which case the composition is used for cleaning, disinfecting and wetting the lens. The treated lens can then be inserted directly in the eye.
A second embodiment of the invention provides a composition for wetting a contact lens comprising as an essential component the silicone polymer containing an alkyleneoxide side chain, wherein the composition is sufficiently nonirritating that contact lenses treated with the composition can be inserted directly in the eye. Alternately, the wetting composition can be applied directly in the eye as a rewetting solution. The wetting composition may include any of the components described for the cleaning and wetting composition, preferably an antimicrobial agent as a preservative or disinfectant, a buffering agent and/or a tonicity adjusting agent, and if desired, a supplemental wetting agent. The following examples further illustrate preferred embodiments of the invention.
The compositions listed in the following tables can be prepared by the following general procedure.
The compositions can be prepared by adding the individual components to water. A representative method follows. The salts and wetting agents, such as sodium chloride, potassium chloride, disodium edetate, cellulosic components, and/or polyvinyl alcohol (PVA) , are added to premeasured, heated water with mixing. This first composition is allowed to cool, filtered, and sterilized. The sodium phosphate, potassium phosphate, PEO-containing material, the silicone polymer, the surface active agents and/or glycerin are added to premeasured water with mixing and then sterilized and filtered. The antimicrobial agents are added to the remaining amount of premeasured water, and the three compositions are combined with mixing.
TABLE 1
Component COMP 1 EX 1 sodium chloride 0.78 0.78 potassium chloride 0.056 0.056 disodium edetate 0.056 0.056
PVA 0.11 0.15 cationic cellulosic 0.010 — polymer (Polymer JR-30M, Amerchol) hydroxypropy1 0.50 0.55 methylcellulose sodium phosphate 0.56 0.56 potassium phosphate 0.11 0.11 polyethylene glycol 0.10 0.10 (Polyox WSR-301, 1%, Union Carbide) glycerin 0.020 0.050 alkoxylated silicone —— 0.005 polymer (193, Dow Corning)
Polysorbate 20 0.008 0.010
(Tween-20, ICI Americas) polyhexamethylene 0.003 0.003 biguanide (Cosmocil CQ, 20%, ICI Americas)
Deionized Water 100 100
(q.s. to) pH 7.3 7.3
Osmolality 354 370
(mOsm/kg water)
The compositions of Examples 1 and Comparative Example 1 were evaluated for cleaning and wetting efficacy. It is noted that the composition of Comparative Example 1 did not include the silicone polymer having a pendant alkyleneoxy group.
To evaluate wetting potential of the compositions, oven-dried fluorosilicone rigid, gas permeable (RGP) contact lenses were either: rubbed with the composition, inserted onto a subject's eye, and evaluated for non-wetted areas; or agitated with the composition without rubbing, inserted onto a subject's eye, and evaluated for non-wetted areas. Table 1A shows the average percent of lens area remaining non- wetted with each method of wetting (rubbing or agitation) ; the "Combined" column combines the trials for the two methods.
TABLE 1A Percent of Lens Surface Remaining Non-wetted
Composition Rubbed Agitated Combined
EX 1 0% 6% 3%
COMP 1 32% 18% 25%
To evaluate cleaning efficacy, the anterior surfaces of fluorosilicone RGP contact lenses were contaminated with Vaseline® Intensive Care lotion. The contaminated lenses were either: rubbed with the composition, inserted onto a subject's eye, and evaluated for contaminated areas; or agitated with the composition without rubbing, inserted onto a subject's eye, and evaluated for contaminated areas. Table IB shows the average percent of lens area showing lipid contamination after each method of cleaning (rubbing or agitation) ; the third column combines the trials for the two methods.
TABLE IB Percent of Lens Surface Showing Lipid Contamination
Composition Rubbed Agitated Combined
EX 1 4% 1% 3%
COMP 1 8% 4% 6%
The compositions were also evaluated in toxicity testing. Five drops of the compositions were instilled onto the superior li bus of non-wearers of contact lenses. For subjects who are wearers of RGP lenses, lenses were rubbed with a large amount of the composition and then inserted directly on the eye. The composition of Example 1 scored better than Comparative Example 1, inducing no complaints of stinging, itching or burning. TABLE 2
Component EX 2 EX 3 EX 4 EX 5 EX 6 EX 7 sodium 0.70 0.70 0.70 0.70 0.70 0.70 chloride potassium 0.040 0.040 0.040 0.040 0.040 0.040 chloride disodium 0.050 0.050 0.050 0.050 0.050 0.050 edetate hydroxypropyl 0.55 0.55 0.60 0.60 0.60 0.60 methylcellulose sodium 0.55 0.55 0.55 0.55 0.55 0.55 phosphate potassium 0.11 0.11 0.11 0.11 0.11 0.11 phosphate
Polyox WSR-301 0.10 0.10 0.10 0.10 0.10 0.10 (1%)
PVA 1.50 glycerin 0.050 0.050 0.050 0.050 0.050 0.050 alkoxylated 0.015 0.015 0.015 0.015 0.015 0.015 silicone polymer (193, Dow Corning)
Tween-20 0.025 0.025 amphoteric — — 0.030 dimethylpolysiloxane (Siltech-Ampho, Siltech) sulfosuccinate — — — 0.030 dimethylpolysiloxanes (Silube SS-154-00, Siltech) silicone betaine — — — — 0.030 (Abil B 9950, Goldschmidt) phosphobetaine — — — — — 0.030 dimethylpolysiloxane (Siltech Phosphobetaine)
PHMB 0.003 0.003 0.003 0.003 0.003 0.003
Deionized 100 100 100 100 100 100 Water (q.s. to) pH 7.3 7.3 7.3 7.3
Osmolality 346 349 347 338
(mOsm/kg water) The compositions in Table 2 were tested according to the following procedure on twenty wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for at least five minutes', and then the soaked lenses were inserted directly (i.e., without rinsing) onto the subject's eye. The amount of irritation occurring within the first 20-30 seconds after insertion was rated by the subjects using the following scale:
0 = no irritation
1
2 = very mild irritation
3
4 = mild irritation
5
6 = moderate irritation
7
8 = severe irritation
Additionally, five drops of each composition were then instilled directly into both eyes of each subject (one drop every 5 minutes) . Again, the amount of irritation occurring within the first 20-30 minutes after instillation of each drop was rated using the above scale.
The entire procedure was repeated on separate days until each subject had tested each composition. The average rating at insertion and following instillation of each drop is listed in Table 2A. TABLE 2 Average Irritation Rating
Drop Number Overall
Comp Insertion 1 2 3 4 5 Average
EX 2 1.0 0.8 1.1 1.5 1.6 1.7 1.28
EX 3 0.8 0.8 0.9 1.1 1.4 1.3 1.03
EX 4 0.9 1.5 1.2 1.4 1.3 1.5 1.26
EX 5 0.8 0.6 0.8 1.2 1.3 1.4 1.02
EX 6 0.9 0.8 0.9 0.9 0.8 0.8 0.82
EX 7 0.8 0.8 0.7 0.9 1.0 1.0 0.83
TABLE 3
Component EX 8 EX 9 EX 10 EX 11 sodium chloride 0.70 0.70 0.70 0.70 potassium chloride 0.040 0.040 0.040 0.040 disodium edetate 0.050 0.050 0.050 0.050 hydroxypropyl 0.55 0.55 0.55 0.55 methylcellulose sodium phosphate 0.55 0.55 0.55 0.55 potassium phosphate 0.11 0.11 0.11 0.11
Methyl gluceth-20 0.10 0.10 0.10 0.10 (Glucam E-20, Amerchol)
PVA 0.15 alkoxylated 0.015 0.015 0.015 0.015 silicone polymer (193, Dow Corning)
Tween-20 0 . 025 0 . 020 0.025 0.020
Tego-Betaine L7 0. 010 0.010 (30%)
PHMB (20%) 0.0025 0.0025 0.0025 0.0025
Chlorhexidine 0.0165 0.0165 0.0165 0.0165 gluconate (20%)
Deionized Water 100 100 100 100 (qs to) pH 7.3 7.3 7.3 7.3
Viscosity 28.7 28.7 24.6 25.7 (cp at 25°C)
Osmolality 344 345 342 341 (mOsm/kg water) The compositions in Table 3, and a saline solution as a control, were tested according to the following procedure on twenty-one wearers of RGP contact lenses. First, each subject's lenses were soaked in a composition for about 8 to 10 minutes. Then, the lenses were removed from the case, additional solution was added to the back surface of the lens.es, and the lenses were inserted onto the subject's eyes. After waiting periods of approximately 10 minutes, the procedure was repeated for the remaining solutions, with various compositions presented to the subjects in random order. The subjects rated irritation based on the above scale of 0 to 8. The average irritation ratings are listed in Table 3A. The comparison of Example 11 and saline is considered statistically significant.
Additionally, the compositions were tested for insertional blur, i.e., the time required after insertion for the subject's vision to return to baseline acuity. The average time for vision to clear (after insertion) , and the range of time for vision to clear for all subjects, is listed in Table 3A. TABLE 3A
Average Average Range of Irritation Time to Clear Time to Clear
Saline 1.38 3 seconds 1-9 seconds
EX 9 1.10 14 seconds 4-33 seconds
EX 10 0.71 18 seconds 5-42 seconds
EX 8 0.57 19 seconds 3-60 seconds
EX-11 0.38 14 seconds 11-60 seconds
Additional examples of preferred multipurpose compositions suitable for cleaning and wetting contact lenses are given in Table 4.
TABLE 4
Component EX 12 EX 13 EX 14 sodium chloride 0.70 0.78 0.70 potassium chloride 0.040 0.17 0.040 disodium edetate 0.050 0.050 0.050 hydroxypropyl 0.55 0.60 0.60 methylcellulose sodium phosphate 0.55 0.28 0.55 potassium phosphate 0.11 0.55 0.11
Glucam E-20 0.10 0.10 0.10 alkoxylated 0.015 0.015 0.015 silicone polymer (193, Dow Corning)
Tween-20 0.025 0.020 0.020
Tego-Betaine L7 0.010 0.010 0.010 (30%)
PHMB (20%) 0.0025 0.0025 0.0025
CHG (20%) 0.0165 0.0165 0.0165
Deionized Water 100 100 100 (q.s. to)
PH 7.4 7.3 7.3
Viscosity 30.6 34.6 33.4 (cp at 25°C)
Osmolality 363 351 341 (mOsm/kg water)
Although certain preferred embodiments have been described, it is understood that the invention is not limited thereto and modifications and variations would be evident to a person of ordinary skill in the art.
We claim:

Claims

1. An aqueous composition for cleaning and wetting a contact lens comprising:
(a) a silicone polymer containing an alkyleneoxide side chain; and
(b) a surface active agent having cleaning activity for contact lens deposits.
2. The composition of claim 1, wherein the silicone polymer is a dimethylpolysiloxane having at least one pendant alkyleneoxide side chain.
3. The composition of claim 1, wherein the silicone polymer is represented by the formula:
i-R
Figure imgf000028_0001
wherein: each R is independently selected from the group consisting of
Figure imgf000028_0002
alkyl and phenyl; each R' is independently an alkyleneoxide containing radical; x is 0 or an integer of at least 1; and y is an integer of at least 1.
4. The composition of claim 3, wherein R' is -R2-0-(EO)m-(PO)n-H wherein R2 is an alkylene radical having 1 to 6 carbon atoms; EO is an ethyleneoxide radical; PO is a propyleneoxide radical; and each of m and n is independently 0 or an integer of least 1.
5. The composition of claim 1, comprising a nonionic surface active agent having cleaning action for contact lens deposits.
6. The composition of claim 5, wherein the nonionic surface active agent includes a polysorbate surface active agent.
7. The composition of claim 1, comprising a cocoamidoalkyl betaine surface active agent.
8. The composition of claim 1, further comprising an antimicrobial agent.
9. The composition of claim 1, further comprising a polyethyleneoxide-containing material.
10. The composition of claim 9, wherein the polyethyleneoxide-containing material is a selected from the group consisting of ethoxylated ethoxylated glucose derivatives, ethoxylated ethers of sorbitol, and mixtures thereof.
11. The composition of claim 1, further comprising a buffering agent or tonicity adjusting agent.
12. The composition of claim 1, further comprising a wetting agent selected from the group consisting of a cellulosic material, polyvinyl alcohol, polyvinyl pyrrolidone, and mixtures thereof.
13. The composition of claim 1, wherein said composition is sufficiently nonirritating for application to the eye.
14. A composition for wetting a contact lens comprising a silicone polymer containing an alkyleneoxide side chain, wherein said composition is sufficiently nonirritating for application to the eye.
"15. A method for cleaning and wetting a contact lens comprising exposing said contact lens to an aqueous composition which comprises a silicone polymer containing an alkyleneoxide side chain, and a surface active agent having cleaning activity for contact lens deposits.
16. The method of claim 15, comprising:
(a) rubbing said composition against the contact lens and rinsing the contact lens to remove contaminants; and
(b) subsequently treating the contact lens with said composition to wet the surface of the contact lens for insertion in the eye.
17. The method of claim 16, further comprising inserting the treated lens directly in the eye.
18. A method for cleaning, disinfecting and. wetting a contact lens comprising: (a) rubbing the contact lens with a solution comprising (i) a silicone polymer containing an alkyleneoxide side chain, (ii) a surface active agent having cleaning activity for contact lens deposits, and (iii) an antimicrobially effective amount of an antimicrobial agent, and rinsing the contact lens to remove contaminants; and
(b) subsequently treating the contact lens with said composition for sufficient time to disinfect the contact lens and to wet the surface thereof for insertion in the eye.
19. A method of wetting a contact lens comprising treating the contact lens with a composition comprising a silicone polymer containing an alkyleneoxide side chain.
20. The method of claim 19, wherein the composition is applied to the contact lens while worn in the eye.
PCT/US1994/006788 1993-06-18 1994-06-15 Composition for cleaning and wetting contact lenses WO1995000617A1 (en)

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BR9407263A BR9407263A (en) 1993-06-18 1994-06-15 Composition for treating a contact lens and methods for cleaning and wetting a contact lens and for cleaning disinfect and wetting a contact lens
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996000274A1 (en) * 1994-06-24 1996-01-04 Unilever Plc Glass and ceramic cleaning compositions
DE19752042A1 (en) * 1997-11-24 1999-07-29 Werra Papier Holding Gmbh Composition for cleaning high-value glass or similar materials, e.g. Spectacles or optical systems
WO2000060038A1 (en) * 1999-04-02 2000-10-12 Laboratoire Medidom S.A. A viscosity enhanced ophthalmic solution, having a detergent action on contact lenses
EP1794268A1 (en) * 2004-06-30 2007-06-13 Johnson and Johnson Vision Care, Inc. Solutions for ophthalmic lenses containing at least one silicone containing component
US9943622B2 (en) 2012-10-08 2018-04-17 Bausch & Lomb Incorporated Minimizing biological lipid deposits on contact lenses

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1071190A (en) * 1996-08-30 1998-03-17 Tomey Technol Corp Liquid agent for contact lens
US20030129083A1 (en) * 1997-11-26 2003-07-10 Advanced Medical Optics, Inc. Multi purpose contact lens care compositions including propylene glycol or glycerin
US6063745A (en) 1997-11-26 2000-05-16 Allergan Mutli-purpose contact lens care compositions
EP1034246B1 (en) 1997-11-26 2011-04-06 Abbott Medical Optics Inc. Use of hydroxypropyl methyl cellulose in a contact lens cleaning composition
US6369112B1 (en) * 1998-12-15 2002-04-09 Bausch & Lomb Incorporated Treatment of contact lenses with aqueous solution comprising a biguanide disinfectant stabilized by tyloxapol
DE60107461T2 (en) * 2000-10-24 2005-05-12 Bausch & Lomb Inc. USE OF CATIONIC POLYSACCHARIDES FOR THE PREVENTION OF BACTERIAL APPLICATIONS
US6634748B1 (en) * 2000-11-15 2003-10-21 Johnson & Johnson Vision Care, Inc. Methods of stabilizing silicone hydrogels against hydrolytic degradation
US6805836B2 (en) * 2000-12-15 2004-10-19 Bausch & Lomb Incorporated Prevention of preservative uptake into biomaterials
US6702983B2 (en) 2001-05-15 2004-03-09 Bausch & Lomb Incorporated Low ionic strength method and composition for reducing bacterial attachment to biomaterials
US20050202986A1 (en) * 2004-03-12 2005-09-15 Zhenze Hu Compositions for solubilizing lipids
WO2005123035A1 (en) * 2004-06-08 2005-12-29 Ocularis Pharma, Inc. Hydrophobic ophthalmic compositions and methods of use
US7858000B2 (en) * 2006-06-08 2010-12-28 Novartis Ag Method of making silicone hydrogel contact lenses
TWI441835B (en) 2006-07-12 2014-06-21 Novartis Ag Novel polymers
AR064286A1 (en) * 2006-12-13 2009-03-25 Quiceno Gomez Alexandra Lorena PRODUCTION OF OPHTHALMIC DEVICES BASED ON POLYMERIZATION BY PHOTOINDUCIDED SCALE GROWTH
US20080214421A1 (en) * 2007-02-19 2008-09-04 Fang Zhao Contact lens care composition
JP5643092B2 (en) 2007-08-31 2014-12-17 ノバルティス アーゲー Contact lens packaging solution
TWI551305B (en) 2007-08-31 2016-10-01 諾華公司 Use of a relatively-viscous packaging solution
JP2009096790A (en) * 2007-09-28 2009-05-07 Rohto Pharmaceut Co Ltd Contact lens fitting liquid for ameliorating eye strain and/or ameliorating blurred vision
US7837934B2 (en) * 2008-01-09 2010-11-23 Bausch & Lomb Incorporated Packaging solutions
US8173147B2 (en) * 2008-08-15 2012-05-08 Xttrium Laboratories, Inc. Gentle, non-irritating, non-alcoholic skin disinfectant
US20110114517A1 (en) * 2009-11-17 2011-05-19 Kasey Jon Minick Hydrogen peroxide solution and kit for disinfecting contact lenses
JP4976607B2 (en) * 2010-10-01 2012-07-18 株式会社シード Gel detergent for contact lenses
MY186090A (en) 2015-12-03 2021-06-21 Alcon Inc Contact lens packaging solutions
CN106010805A (en) * 2016-05-13 2016-10-12 郑海东 Contact lens packaging solution and preparing method thereof
CN106701352A (en) * 2016-12-02 2017-05-24 安徽长庚光学科技有限公司 Environment-friendly type efficient lens cleanser and preparation method thereof
CN112262204B (en) * 2018-06-19 2024-03-15 依视路国际公司 Economically optimized lens cleaning and stripping system
CN109851971B (en) * 2018-12-21 2022-05-06 江苏海伦隐形眼镜有限公司 Composite treatment fluid for improving surface hydrophilicity of silicon hydrogel and preparation and treatment methods thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3249550A (en) * 1964-05-27 1966-05-03 Dow Corning Glass cleaning compositions
FR2101735A5 (en) * 1970-07-16 1972-03-31 Dow Corning
US4048122A (en) * 1976-01-23 1977-09-13 Barnes-Hind Pharmaceuticals, Inc. Cleaning agents for contact lenses
JPS57168218A (en) * 1981-04-09 1982-10-16 Duskin Franchise Co Ltd Liquid lens cleaner
US4529535A (en) * 1982-06-01 1985-07-16 Sherman Laboratories, Inc. Soft contact lens wetting solution containing preservative system and method
US4613380A (en) * 1985-04-01 1986-09-23 Dow Corning Corporation Method for removing lipid deposits from contact lenses

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1034782A (en) * 1962-01-24 1966-07-06 Union Carbide Corp Organosilicon compositions
USB724600I5 (en) * 1968-04-26
US4409205A (en) * 1979-03-05 1983-10-11 Cooper Laboratories, Inc. Ophthalmic solution
US4820352A (en) * 1983-01-10 1989-04-11 Bausch & Lomb Incorporated Cleaning and conditioning solutions for contact lenses and methods of use
US5141665A (en) * 1987-03-31 1992-08-25 Sherman Laboratories, Inc. Cleaning, conditioning, storing and wetting system and method for rigid gas permeable contact lenses and other contact lenses
GB8812109D0 (en) * 1988-05-23 1988-06-29 Ifejika C Method for daily cleaning & protein deposit removal for contact lenses
GB9220339D0 (en) * 1992-09-25 1992-11-11 Johnson & Son Inc S C Improved fabric cleaning shampoo composition
EP0703965B1 (en) * 1993-06-18 1999-01-20 Polymer Technology Corporation Composition for cleaning and wetting contact lenses

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3249550A (en) * 1964-05-27 1966-05-03 Dow Corning Glass cleaning compositions
FR2101735A5 (en) * 1970-07-16 1972-03-31 Dow Corning
US4048122A (en) * 1976-01-23 1977-09-13 Barnes-Hind Pharmaceuticals, Inc. Cleaning agents for contact lenses
US4126587A (en) * 1976-01-23 1978-11-21 Barnes-Hind Pharmaceuticals, Inc. Cleaning agents for contact lenses
JPS57168218A (en) * 1981-04-09 1982-10-16 Duskin Franchise Co Ltd Liquid lens cleaner
US4529535A (en) * 1982-06-01 1985-07-16 Sherman Laboratories, Inc. Soft contact lens wetting solution containing preservative system and method
US4613380A (en) * 1985-04-01 1986-09-23 Dow Corning Corporation Method for removing lipid deposits from contact lenses

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 8247, Derwent World Patents Index; Class A97, AN 82-01144J *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996000274A1 (en) * 1994-06-24 1996-01-04 Unilever Plc Glass and ceramic cleaning compositions
DE19752042A1 (en) * 1997-11-24 1999-07-29 Werra Papier Holding Gmbh Composition for cleaning high-value glass or similar materials, e.g. Spectacles or optical systems
WO2000060038A1 (en) * 1999-04-02 2000-10-12 Laboratoire Medidom S.A. A viscosity enhanced ophthalmic solution, having a detergent action on contact lenses
US6528465B1 (en) 1999-04-02 2003-03-04 Laboratoire Medidom S.A. Viscosity enhanced ophthalmic solution, having a detergent action on contact lenses
EP1794268A1 (en) * 2004-06-30 2007-06-13 Johnson and Johnson Vision Care, Inc. Solutions for ophthalmic lenses containing at least one silicone containing component
EP1794268A4 (en) * 2004-06-30 2008-05-14 Johnson & Johnson Vision Care Solutions for ophthalmic lenses containing at least one silicone containing component
US9943622B2 (en) 2012-10-08 2018-04-17 Bausch & Lomb Incorporated Minimizing biological lipid deposits on contact lenses

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ES2144525T3 (en) 2000-06-16
EP0703967A1 (en) 1996-04-03
CN1081669C (en) 2002-03-27
DE69422813T2 (en) 2000-07-27
EP0703967B1 (en) 2000-01-26
DE69422813D1 (en) 2000-03-02
BR9407263A (en) 1996-10-01
CN1125463A (en) 1996-06-26
KR100341671B1 (en) 2002-11-30
US5500144A (en) 1996-03-19
AU684805B2 (en) 1998-01-08
AU7208294A (en) 1995-01-17

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