CA1270119B - Polymeric scrub - Google Patents
Polymeric scrubInfo
- Publication number
- CA1270119B CA1270119B CA615,525A CA615525A CA1270119B CA 1270119 B CA1270119 B CA 1270119B CA 615525 A CA615525 A CA 615525A CA 1270119 B CA1270119 B CA 1270119B
- Authority
- CA
- Canada
- Prior art keywords
- nylon
- range
- particulate polymer
- cellulose
- recited
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- 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
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0013—Liquid compositions with insoluble particles in suspension
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Eyeglasses (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Surface Treatment Of Optical Elements (AREA)
Abstract
POLYMERIC SCRUB
ABSTRACT
Soft and hard contact lenses are freed from deposits by rubbing them with a particulate organic polymer with a carrier, the polymer having a particular size in the range from about one micron to about 600 microns and a Rockwell hardness in the range of from about R30 to about M105, or a shore hardness in the range from about A15 to about D100.
ABSTRACT
Soft and hard contact lenses are freed from deposits by rubbing them with a particulate organic polymer with a carrier, the polymer having a particular size in the range from about one micron to about 600 microns and a Rockwell hardness in the range of from about R30 to about M105, or a shore hardness in the range from about A15 to about D100.
Description
~270~3 POLYMER I C SCRUB
This invention relates to a cleansing composition for optical surfaces such as contact lenses and similar optic apparatuses.
Cleansing compositions containing various abrasive materials have been used in the past. The abradant material is added to the compo~ition to increase the effectiveness o~ the composition in removing undesired matter from the surface being cleaned. ~eretofore the abradants, even when in fine particle form, were harsh and had a tendency to scratch optical surfaces.
Efficient cleaning of optical surfaces without damaging them when such surfaces become encrusted with foreign matter sometimes presents difficult problems.
Contact lenses that have developéd heavy proteinaceous or other encrustations present particularly difficult cleaning problems. Encrustations that form on contact lenses may be proteinaceous in nature or may be lipids or other ma~erials foreign to the eye such as lady's mascara which usually is a soap or wax in gelatin.
Success in wearing and properly using contact lenses is a function of maintaining them in a clean condition without the buildup of foreign matter, particularly encrustations which physically or chemically attach to the lens surface. Buildup of such material is gradual, but will ultimately render the lens opaque. Even before the lens becomes opaque, however, the presence of encrustations on the lens causes the wearer of the lens increased discomfort and irritation. Hard contact lenses may ble buffed to remove encrustations, but such a process requires skill and is not easily done by the user at home without the considerable danger o scratching the lens. The surface of a soft contact lens is particularly prone to develop encrustations and presents particularly difficult cleaning problems since ,~
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soft contact lenses cannot be cleaned except by professionals and then only with limited success.
` Many different solutions have been formulated for cleaning contact lenses. The compositions, however, are primarily directed to disinfecting lenses and generally do not remove encrustations. Those compositions that have been formulated for the purpose of removing encrustations have met with limited success.
Soft contact lenses may be divided into two broad categories, namely, hydrophilic and hydrophobic lenses. Hydrophobic contact lenses are usually based on elastic and flexible silicone rubber (polysiloxane), and are generally made from cross-linked dimethyl polysiloxane.
Hydrophilic soft contact lenses are a hydrated gel, and the ability to absorb water results in swelling to a transparent soft mass of good mechanical strength which is very comfortable to the wearer. Hydrated gel lenses can contain: hydroxyethylmethacrylate (HEMA) or its analogs, ethylene-glycol dimethacrylate (EGMA) or its analogs, polymethylmethacrylate (PMMA) or its analogs, polyvinylpyrrolidone (PVP) or its analogs, monomers, inhibitors, traces of catalysts and water.
Hydrophilic groups of these plastic lenses attract and hold large amounts of water in the gel. These virtues, however, lead to difficulties in cleaning and sterilizing the lenses.
Hydrophilic ~oft lenses may be disinfected by chemical treatment or by boiling. As indicated, neitber procedure is entirely successful in remoYing encrustations. Some chemicals are ineffective in removing proteins, others in removing lipids. Boiling may even denature proteinaceous material on the lenses thereby atta~hing encrustations all the more firmly to the lenses. United States Patent No. 3~91D,296 to ..
::.: : ..:
- , . .. . . . .. ..
7~:~L19 Karageozian et al., discusses a method for removing proteinaceous deposits from contact lenses with the use of a protease, however, lenses may become encrusted and contaminated with other deleterious materials such as lipids which protease enzyme will not remove.
The highly hydrophobic nature of the contact lenses based upon silicone rubber interferes with their uniform and effective cleaning United States Patent No. 4,127,423 to Rankin discus~;es a method of cleansing encrusted soft contact lenses including silicone lenses, with aqueous solutions of sodium silicates. Deionized water is required and boiling is required when the lenses are heavily encrusted.
United States Patent No. 3,954,644 to Krezanoski et al. discusses a contact lens cleaning, storing and wetting solution. The solution discussed contains a poly(oxyethylene)-poly(oxypropylene) block copolymer which is the primary wetting and cleaning agent of the composition. Elimina~ion of encrustations from the surface of the lens i5 not discussed.
A need exists, therefore, for a cleansing composition which can remove foreign deposits and encrustations from both hard and soft surfaces without adversely affecting the surfaces thereof. More particularly, a need exists for a cleansing composition which can clean and remove foreign deposits from both soft and hard contact lenses, and particularly from soft contact lenses.
In accordance with the present invention, the use of particulate organic polymers or polysiloxane having particle sizes between one and six hundred microns suspended in a suitable carrier unexpectedly provides a composition which can clean, without damage, soft or delic:ate surfaces including hard or soft contact lenses.
To provide a cleansing composition, the :- ,., . ., - . . ..
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, : . .
:- :
- ., . :
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particulate polymer is mixed with a carrier containing a thickening agent such as Carbopol (a registered trademark of B.F. Goodrich Chemical Co.), cellulose or polyethylene glycol with a molecular weight distribution of 400 to 4000 to form a suspension. The carrier can be any ocular compatible composition in which the polymeric particulates remain in suspension. Most generally the carrier is water to which various optional ingredients may be added. The end product may be a fluid or may be a thixotropic ointment or gel. A surfactant such as Pluronic, (a registered ~rademark of Wyanclotte Chemicals Co.), Tween, (a registered trademark of Atlas Powder Company) or tyloxapol may optionally be added to the cleaning composition to increase its effectiveness.
Thimerosal (a product of Eli Lilly & Co.), sorbic acid, or ethylenediamintetraacetic acid (EDTA), as preservatives or bactericides, sodium chloride, and purified water may be optionally employed as is known in the art to provide a sterile, buffered, isotonic cleansing composition for contact lenses.
According to the present invention, a suspension is prepared containing a particulate organic polymer or polysiloxane of a particle size of one to six hundred microns and forming 1 to 25 percent by weight of the suspension, a surfactant, and a sufficient amount of a thickener to give the suspension a viscosity of between about 150 and about 1500 cps. The thickener keeps the polymeric particles in suspension and any viscosity suspension that will accomplish this result may be used. The polymeric particles are preferably spherical, have a particle size range preferably between about twenty and about one hundred microns, and preferably form 5 to 20 percent by weight o~ the suspension. A particle ~ize above and below the twenty to one hundred micron range will function; however, the smaller sized particles will take longer to complete ; . .:
. .
.
. .
, ~27(~
their cleaning function and larger particles will feel gritty to the user.
Nylon 6 which has the formula (CH2 CH2 CH2 CH2 CH2 C-NH), Nylon 11, which has the formula (CH2 (CH2)8-CH2CN), Nylon 12~
which has the formula (CH2 (CH2)9 CH2 C-NH) or mixtures thereof with Rockwell hardnesses of R80-83, R-108, and R-106, respectively, and particle size ranges of 1 to 80 microns, 1 to 80 microns, and 20 to 45 microns, respectively, all may be used a~ polymeric particulates. Nylon 11 is a preferred polymer.
Polyethylene glycol is a preferred thickener in amounts of between about 20 and about 80 percent by weight of the suspension, preferably between about 25 and about 50 percent by weight. The following polymers with their hardnesses as indicated -in TABLE 1 will serve as a suitable particulate polymer.
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TABLE I
SUITABLE PARTICULATE POLYMERS*
POLYMER SHORE ROCKWELL
ARDNESS HARDNESS
5 acrylonitrile-butadiene- R75-115 styrene acetal M94 polymethylmethacrylate (PMMA) M85-105 methylmethacrylate/styrene 10 copolymer ~75 ethyl cellulose R50-115 cellulose acetate butyrate R30-115 cellulose acetate R85-120 polytetrafluoroethylene D50-55 15 polychlorotrifluorethylene R75-95 modified poolyethylene-tetrafluoroethylene (PE-TFE) RS0 ionomer (copolymers of ethylene) D50-65 20 fluoro ethylene polymer (FEP) fluoroplastic D50-65 .. ~.. ... ~. . .
:~L270iL1~
Nylon 6 R80-83 Nylon 6/6 Nylon 11 R108 Nylon 12 R106 5 polyutadiene R40 polyarylether R117 polycarbonate M70 P~T polyester M68-78 polyethylene R50 10 polypropylene R80 polysulfone R88 silicone A15-65 *ASTM test method D735 applies to the Rockwell Hardness figure given, and ASTM test method D22450 applies to the Shore Hardness figures given.
Pluronic F-127 is a preferred surfactant and is an ethylene oxide-propylene oxide-propylene glycol condensation product sold by Wyandotte Chemical Corporation. The surfactant as a 20~ gel by wei~ht in purified water is optionally added to the suspension in an amount of between about 5 to 15 percent by weight of the suspension, preferably between about B and about 12 percent by weight.
.
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, :~;Z7~19 The particulate polymer, the polyethylene glycol and Pluronic F-127, as a 20% gel in purified water, may be mixed with thimerosal, sorbic acid, EDTA, sodium chloride, and purified water to provide a sterile isotonic cleaning suspension.
To prepare a cleansing suspension polyethylene glycol having a molecular weight range form 400 to 4,000 is melted by suspending a suitable sized eon~ainer, such as a beaker, containing the glycol in hot water. When the polyethylene glycol is completely melted, the beaker is removed from the heat source. The Pluronic F-127 is added with stirring until the mixture is cooled to room temp~rature. Upon cooling the particulate polymer is added with stirring. The optional salts and preservative are then added together with the required amount of water to provide a cleansing suspension of the desired viscosity.
For a clearer understanding of the invention, specific examples are set forth below. These examples are merely illustrative, and are not to be understood as limiting the scope and underlying principles of the invention in any way~ In the following Examples the particulate polymer, which is commercially purchased, has a range of particle sizes. A certain percentage of the substance may have a particle size below 5 or even 1 micron. Hence, the particle sizes expressed in the Examples will be set forth as a range from between 0 and a size at the larger end of the range.
EXAMPLE I
A mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400 was melted and thoroughly mixed. With stirring 20 grams of a 20~ gel in purified water of Pluronic F-127 was added to the polyethylene glycol mix. The resulting mixture was sitrred until cooled to :-. '.. ' :
': . :, . ' .
lZ70~19 room temperature. Upon cooling 10 grams of Natural (10/15) ES ~which is a trademark of Rislan Corporation and is Nylon-ll electrostatic extrude of a particle size range between 0 to 44 microns) was added with stirring to the polyethylene glycol and Pluronic* mixture. With stirring 15 ml of purified water was added to the mixture and stirring was continued until a smooth suspension was formed.
EXAMPLE II
As in Example I, 25 grains of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 grams of Polymer H0050/80 (which is a trademark of Rislan Corporation and is Nylon-ll of a particle size range between 0 to 80 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. With stirring 10 ml of purified water was added to the mixture and stirring was continued until a smooth suspension was formed.
EXAMPLE III
As in Example I, 35 grams of Pluronic F-127 20 gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams o~ polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 grams of French-Naturelle ES
(which is a trademark of Rislan Corporation and is Nylon-ll electrostatic extrude of a particle size range between 0 to 80 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. Stirring of the mixture was continued until a smooth suspension was formed.
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EXAMPLE IV
As in Example I, 35 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol oi a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 gràms of CAB 381-20 (which is a trademark of Eastman Chemical Co. and is cellulose acetate butyrate of a particle size range between 0 to 120 microns) was added to the polyethylene glycol and Pluronic mixture. Stirring of the mixture was continued until a smooth suspension was formedd EXAMPLE V
As in Example I, 25 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. ~he resulting mixture was stirred until cooled to room temperature, whereupon 12.5 grams of Naturell Fine (which is a trademark of Rislan Corporation and is Nylon-ll of a particle size range between 0 to 45 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. With constant agitation 0.02 grams of a 1.0~ aqueous solution of thimero~al and 0.9 grams of sodium chloride were mixed into the glycol-Pluronic-Naturell Fine mixture to form the cleaning composition. After addition of the thimerosal and sodium chloride, with continued stirring purified water was added to bring the total weight of the composition to 100 grams and a smooth suspension was formed.
EXAMPLE VI
As in Example I, 25 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 ' . .
- ' .: . - ' :` "'' ' -... . . .
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grams of polyethylene glycol of a molecular wei~ht of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10.0 grams of polyethylene F-N500 (which is a product of S. Industrial Chemicals and is low density polyethylene of a particle size of less than 20 microns~ was added with stirring to the polyethylene glycol and Pluronic mixture. 'With constant a~itation 0.02 grams of an aqueous solution of thimerosal and 0.9 grams of sodium chloride were mixed into the glycol-Pluronic- polyethylene mixture to form the cleaning composition. After the addition of the thimerosal and sodium cnloride, with continuous stirring purified water was added to bring the total weight of the composition to 100 grams and a smooth suspension was formed.
EXAMPLE VII
In a beaker 0.8 grams of hydroxy ethyl cellulose having a molecular weight of approximately 15,000 and 0.5 grams Tween 21 is dispersed into about 40 ml of purified water. The mixture then is sterilized by autoclaving at 121C under a pressure of 18 psi for 1/2 hour. In another beaker 0.6 gram sodium chloride, 0.2 gram boric acid, 0~1 gram EDTA-disodium, 0.25 gram sodium borate qs to pH 7.6 and 0.4 ml of a 1.0% aqueous solution of thimerosal is dissolved and mixed with constant agitation into 40 ml of purified water. This mixture is then pressure filtered into the first mixture using a sterile millipore setup fitted with a 0.2 micron filter. The two mixtures are then homogeneously mixed.
10 grams of French Naturelle beads, sterilized at 121C at 18 psi for 1/2 hour, are added to the homogeneous mixture with constant agitation. With continuous stirring purified water was added to the latter mixture to bring the total weight of the ~, ' ~' . . '. : -: ` :
~LZ7~9 composition to 100 ~rams and to form a smooth suspension.
EXAMPLE VIII
A mixture of 30 grams of polyethylene glycol of a molecular weight of approximately 4000, and 40 grams of polyethylene glycol of a molecular weight of approximately 400 was melted in a beaker by suspending the beaker into hot water. After the polyethylene glycol was completely melted, it was thoroughly mixed with a glass rod to form a smooth ointment base. T~e ointment base was transferred onto a porcelain tile and was mixed with a spatula with 15 grams of Natural ES
(10/15) to form an ointment. With continued stirring purified water was incorporated into the ointment to bring the total weight of the composition to 100 grams and to soften and smooth the resulting cleansing ointment.
EXAMPLE IX
A mixture of 50 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of 400 was melted and mixed as in Example VIII. After mixing and melting, as in Example VIII, the glycol mixture was mixed with 10 grams of Natural ES and further mixed with purifiPd water to bring the total weight of the composition to 100 grams and to provide a soft smooth cleansing ointment.
EXAMPLE X
A mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of 400 was melted and mixed as in Example VII. After mixing and melting, 25 grams of a 20% ~el in purified water of Pluronic F-127 and 10 grams of polymer ~0050/80 were added and mixed into the polyethylene glycol to provide an ointment. With continued mixing purified waker was incorporated into the ointment to bring the total weight .. .. . ...
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of the composition to 100 grams and to soften and smooth the resulting cleansing ointment.
A study was designed to determine the non-abrasive nature of the polymeric cleaner formulation.
Five unused lenses of each of the six brands of contact lenses were selected for the non-abrasive test.
The six brands of contact lenses selected were:
Polycon - Syntex Tesicon - Uricon TRESOFT - Alcon Laboratories, Inc.
Silicon - Wohlk CAB - Danker Wohlk PMMA - Standard Hard Lenses Prior to starting the study to determine the non-abrasive nature of the polymeric cleaner formulations, all the lenses were viewed through the Bausch & Lomb Optical Microscope under 40X magnification for scratches and/or cuts on lens surface. It was noted that almost all types of lenses had some surface scratches.
Each brand of lenses was then cycled through a cleaning regimen. The lens was rubbed with 2 to 3 drops of polymeric cleaner of Example VIII in the palm of ~he hand with the index finger for a total of 20 seconds and rinsed with normal saline. This procedure was repeated for a total of fifty cycles on each lens. The lenses were viewed for scratches after 5, 10, 20, 30, 40 and 50 cleaning cycles using the Bausch & Lomb Optical Microscope under 20X and lOOX magnifications.
Photographs were taken.
The lens photographs indicate no sign of new cuts and/or scratches on the lens surfaces under study.
The efficacy of polymeric cleaner was determined on laboratory deposited as well as human worn soft contact lenses.
In the laboratory, soft contact lenses were ~I.Z7~
soiled with artificial deposition model solution, containing 0005 percent by weight lysozyme 3X protein and 0.05% percent by weight mucin type 2 in isotonic solution to pH 7Ø The deposition of clean lenses involved heating the lenses with a 5ml of deposition model solution in stoppered glass vial for one hour at 92C. The above procedure was repeated two times with fresh depositions model solution to obtain heavier deposits of protein on the lens surfaceO
The deposited lens was then rubbed with 2 to 3 drops of the polymer cleaner of Example VIII in the palm of the hand with the index finger for a total of 20 seconds (both sides of the lens) and rinsed with normal saline. Depending on the extent of protein deposit on the lens, one to two applicatons of polymeric cleaner of Example VIII was needed to clean the protein from ~he lens.
In another efficacy study, human worn soft contact lenses having protein encrustations were collected and cleaning efficacy of the polymeric cleaner was determined following a similar cleaning regimen as described above. Six sets of human worn lenses were used for the efficacy study and all the lenses were effectively cleaned, and the protein encrustations were removed.
- ~ ...
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This invention relates to a cleansing composition for optical surfaces such as contact lenses and similar optic apparatuses.
Cleansing compositions containing various abrasive materials have been used in the past. The abradant material is added to the compo~ition to increase the effectiveness o~ the composition in removing undesired matter from the surface being cleaned. ~eretofore the abradants, even when in fine particle form, were harsh and had a tendency to scratch optical surfaces.
Efficient cleaning of optical surfaces without damaging them when such surfaces become encrusted with foreign matter sometimes presents difficult problems.
Contact lenses that have developéd heavy proteinaceous or other encrustations present particularly difficult cleaning problems. Encrustations that form on contact lenses may be proteinaceous in nature or may be lipids or other ma~erials foreign to the eye such as lady's mascara which usually is a soap or wax in gelatin.
Success in wearing and properly using contact lenses is a function of maintaining them in a clean condition without the buildup of foreign matter, particularly encrustations which physically or chemically attach to the lens surface. Buildup of such material is gradual, but will ultimately render the lens opaque. Even before the lens becomes opaque, however, the presence of encrustations on the lens causes the wearer of the lens increased discomfort and irritation. Hard contact lenses may ble buffed to remove encrustations, but such a process requires skill and is not easily done by the user at home without the considerable danger o scratching the lens. The surface of a soft contact lens is particularly prone to develop encrustations and presents particularly difficult cleaning problems since ,~
." . ...
.. ~ ..., ,... ;., .
~Z7()~
soft contact lenses cannot be cleaned except by professionals and then only with limited success.
` Many different solutions have been formulated for cleaning contact lenses. The compositions, however, are primarily directed to disinfecting lenses and generally do not remove encrustations. Those compositions that have been formulated for the purpose of removing encrustations have met with limited success.
Soft contact lenses may be divided into two broad categories, namely, hydrophilic and hydrophobic lenses. Hydrophobic contact lenses are usually based on elastic and flexible silicone rubber (polysiloxane), and are generally made from cross-linked dimethyl polysiloxane.
Hydrophilic soft contact lenses are a hydrated gel, and the ability to absorb water results in swelling to a transparent soft mass of good mechanical strength which is very comfortable to the wearer. Hydrated gel lenses can contain: hydroxyethylmethacrylate (HEMA) or its analogs, ethylene-glycol dimethacrylate (EGMA) or its analogs, polymethylmethacrylate (PMMA) or its analogs, polyvinylpyrrolidone (PVP) or its analogs, monomers, inhibitors, traces of catalysts and water.
Hydrophilic groups of these plastic lenses attract and hold large amounts of water in the gel. These virtues, however, lead to difficulties in cleaning and sterilizing the lenses.
Hydrophilic ~oft lenses may be disinfected by chemical treatment or by boiling. As indicated, neitber procedure is entirely successful in remoYing encrustations. Some chemicals are ineffective in removing proteins, others in removing lipids. Boiling may even denature proteinaceous material on the lenses thereby atta~hing encrustations all the more firmly to the lenses. United States Patent No. 3~91D,296 to ..
::.: : ..:
- , . .. . . . .. ..
7~:~L19 Karageozian et al., discusses a method for removing proteinaceous deposits from contact lenses with the use of a protease, however, lenses may become encrusted and contaminated with other deleterious materials such as lipids which protease enzyme will not remove.
The highly hydrophobic nature of the contact lenses based upon silicone rubber interferes with their uniform and effective cleaning United States Patent No. 4,127,423 to Rankin discus~;es a method of cleansing encrusted soft contact lenses including silicone lenses, with aqueous solutions of sodium silicates. Deionized water is required and boiling is required when the lenses are heavily encrusted.
United States Patent No. 3,954,644 to Krezanoski et al. discusses a contact lens cleaning, storing and wetting solution. The solution discussed contains a poly(oxyethylene)-poly(oxypropylene) block copolymer which is the primary wetting and cleaning agent of the composition. Elimina~ion of encrustations from the surface of the lens i5 not discussed.
A need exists, therefore, for a cleansing composition which can remove foreign deposits and encrustations from both hard and soft surfaces without adversely affecting the surfaces thereof. More particularly, a need exists for a cleansing composition which can clean and remove foreign deposits from both soft and hard contact lenses, and particularly from soft contact lenses.
In accordance with the present invention, the use of particulate organic polymers or polysiloxane having particle sizes between one and six hundred microns suspended in a suitable carrier unexpectedly provides a composition which can clean, without damage, soft or delic:ate surfaces including hard or soft contact lenses.
To provide a cleansing composition, the :- ,., . ., - . . ..
, ' , --.' '.:
, : . .
:- :
- ., . :
. . , ~27~
particulate polymer is mixed with a carrier containing a thickening agent such as Carbopol (a registered trademark of B.F. Goodrich Chemical Co.), cellulose or polyethylene glycol with a molecular weight distribution of 400 to 4000 to form a suspension. The carrier can be any ocular compatible composition in which the polymeric particulates remain in suspension. Most generally the carrier is water to which various optional ingredients may be added. The end product may be a fluid or may be a thixotropic ointment or gel. A surfactant such as Pluronic, (a registered ~rademark of Wyanclotte Chemicals Co.), Tween, (a registered trademark of Atlas Powder Company) or tyloxapol may optionally be added to the cleaning composition to increase its effectiveness.
Thimerosal (a product of Eli Lilly & Co.), sorbic acid, or ethylenediamintetraacetic acid (EDTA), as preservatives or bactericides, sodium chloride, and purified water may be optionally employed as is known in the art to provide a sterile, buffered, isotonic cleansing composition for contact lenses.
According to the present invention, a suspension is prepared containing a particulate organic polymer or polysiloxane of a particle size of one to six hundred microns and forming 1 to 25 percent by weight of the suspension, a surfactant, and a sufficient amount of a thickener to give the suspension a viscosity of between about 150 and about 1500 cps. The thickener keeps the polymeric particles in suspension and any viscosity suspension that will accomplish this result may be used. The polymeric particles are preferably spherical, have a particle size range preferably between about twenty and about one hundred microns, and preferably form 5 to 20 percent by weight o~ the suspension. A particle ~ize above and below the twenty to one hundred micron range will function; however, the smaller sized particles will take longer to complete ; . .:
. .
.
. .
, ~27(~
their cleaning function and larger particles will feel gritty to the user.
Nylon 6 which has the formula (CH2 CH2 CH2 CH2 CH2 C-NH), Nylon 11, which has the formula (CH2 (CH2)8-CH2CN), Nylon 12~
which has the formula (CH2 (CH2)9 CH2 C-NH) or mixtures thereof with Rockwell hardnesses of R80-83, R-108, and R-106, respectively, and particle size ranges of 1 to 80 microns, 1 to 80 microns, and 20 to 45 microns, respectively, all may be used a~ polymeric particulates. Nylon 11 is a preferred polymer.
Polyethylene glycol is a preferred thickener in amounts of between about 20 and about 80 percent by weight of the suspension, preferably between about 25 and about 50 percent by weight. The following polymers with their hardnesses as indicated -in TABLE 1 will serve as a suitable particulate polymer.
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TABLE I
SUITABLE PARTICULATE POLYMERS*
POLYMER SHORE ROCKWELL
ARDNESS HARDNESS
5 acrylonitrile-butadiene- R75-115 styrene acetal M94 polymethylmethacrylate (PMMA) M85-105 methylmethacrylate/styrene 10 copolymer ~75 ethyl cellulose R50-115 cellulose acetate butyrate R30-115 cellulose acetate R85-120 polytetrafluoroethylene D50-55 15 polychlorotrifluorethylene R75-95 modified poolyethylene-tetrafluoroethylene (PE-TFE) RS0 ionomer (copolymers of ethylene) D50-65 20 fluoro ethylene polymer (FEP) fluoroplastic D50-65 .. ~.. ... ~. . .
:~L270iL1~
Nylon 6 R80-83 Nylon 6/6 Nylon 11 R108 Nylon 12 R106 5 polyutadiene R40 polyarylether R117 polycarbonate M70 P~T polyester M68-78 polyethylene R50 10 polypropylene R80 polysulfone R88 silicone A15-65 *ASTM test method D735 applies to the Rockwell Hardness figure given, and ASTM test method D22450 applies to the Shore Hardness figures given.
Pluronic F-127 is a preferred surfactant and is an ethylene oxide-propylene oxide-propylene glycol condensation product sold by Wyandotte Chemical Corporation. The surfactant as a 20~ gel by wei~ht in purified water is optionally added to the suspension in an amount of between about 5 to 15 percent by weight of the suspension, preferably between about B and about 12 percent by weight.
.
- .; ....
`'; ` ~ ' . : ' :
, :~;Z7~19 The particulate polymer, the polyethylene glycol and Pluronic F-127, as a 20% gel in purified water, may be mixed with thimerosal, sorbic acid, EDTA, sodium chloride, and purified water to provide a sterile isotonic cleaning suspension.
To prepare a cleansing suspension polyethylene glycol having a molecular weight range form 400 to 4,000 is melted by suspending a suitable sized eon~ainer, such as a beaker, containing the glycol in hot water. When the polyethylene glycol is completely melted, the beaker is removed from the heat source. The Pluronic F-127 is added with stirring until the mixture is cooled to room temp~rature. Upon cooling the particulate polymer is added with stirring. The optional salts and preservative are then added together with the required amount of water to provide a cleansing suspension of the desired viscosity.
For a clearer understanding of the invention, specific examples are set forth below. These examples are merely illustrative, and are not to be understood as limiting the scope and underlying principles of the invention in any way~ In the following Examples the particulate polymer, which is commercially purchased, has a range of particle sizes. A certain percentage of the substance may have a particle size below 5 or even 1 micron. Hence, the particle sizes expressed in the Examples will be set forth as a range from between 0 and a size at the larger end of the range.
EXAMPLE I
A mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400 was melted and thoroughly mixed. With stirring 20 grams of a 20~ gel in purified water of Pluronic F-127 was added to the polyethylene glycol mix. The resulting mixture was sitrred until cooled to :-. '.. ' :
': . :, . ' .
lZ70~19 room temperature. Upon cooling 10 grams of Natural (10/15) ES ~which is a trademark of Rislan Corporation and is Nylon-ll electrostatic extrude of a particle size range between 0 to 44 microns) was added with stirring to the polyethylene glycol and Pluronic* mixture. With stirring 15 ml of purified water was added to the mixture and stirring was continued until a smooth suspension was formed.
EXAMPLE II
As in Example I, 25 grains of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 grams of Polymer H0050/80 (which is a trademark of Rislan Corporation and is Nylon-ll of a particle size range between 0 to 80 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. With stirring 10 ml of purified water was added to the mixture and stirring was continued until a smooth suspension was formed.
EXAMPLE III
As in Example I, 35 grams of Pluronic F-127 20 gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams o~ polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 grams of French-Naturelle ES
(which is a trademark of Rislan Corporation and is Nylon-ll electrostatic extrude of a particle size range between 0 to 80 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. Stirring of the mixture was continued until a smooth suspension was formed.
' :
",;
- ~Z~
EXAMPLE IV
As in Example I, 35 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol oi a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10 gràms of CAB 381-20 (which is a trademark of Eastman Chemical Co. and is cellulose acetate butyrate of a particle size range between 0 to 120 microns) was added to the polyethylene glycol and Pluronic mixture. Stirring of the mixture was continued until a smooth suspension was formedd EXAMPLE V
As in Example I, 25 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. ~he resulting mixture was stirred until cooled to room temperature, whereupon 12.5 grams of Naturell Fine (which is a trademark of Rislan Corporation and is Nylon-ll of a particle size range between 0 to 45 microns) was added with stirring to the polyethylene glycol and Pluronic mixture. With constant agitation 0.02 grams of a 1.0~ aqueous solution of thimero~al and 0.9 grams of sodium chloride were mixed into the glycol-Pluronic-Naturell Fine mixture to form the cleaning composition. After addition of the thimerosal and sodium chloride, with continued stirring purified water was added to bring the total weight of the composition to 100 grams and a smooth suspension was formed.
EXAMPLE VI
As in Example I, 25 grams of Pluronic F-127 20%
gel was added with stirring to a melted mixture of 25 ' . .
- ' .: . - ' :` "'' ' -... . . .
lZ7~
grams of polyethylene glycol of a molecular wei~ht of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of approximately 400. The resulting mixture was stirred until cooled to room temperature, whereupon 10.0 grams of polyethylene F-N500 (which is a product of S. Industrial Chemicals and is low density polyethylene of a particle size of less than 20 microns~ was added with stirring to the polyethylene glycol and Pluronic mixture. 'With constant a~itation 0.02 grams of an aqueous solution of thimerosal and 0.9 grams of sodium chloride were mixed into the glycol-Pluronic- polyethylene mixture to form the cleaning composition. After the addition of the thimerosal and sodium cnloride, with continuous stirring purified water was added to bring the total weight of the composition to 100 grams and a smooth suspension was formed.
EXAMPLE VII
In a beaker 0.8 grams of hydroxy ethyl cellulose having a molecular weight of approximately 15,000 and 0.5 grams Tween 21 is dispersed into about 40 ml of purified water. The mixture then is sterilized by autoclaving at 121C under a pressure of 18 psi for 1/2 hour. In another beaker 0.6 gram sodium chloride, 0.2 gram boric acid, 0~1 gram EDTA-disodium, 0.25 gram sodium borate qs to pH 7.6 and 0.4 ml of a 1.0% aqueous solution of thimerosal is dissolved and mixed with constant agitation into 40 ml of purified water. This mixture is then pressure filtered into the first mixture using a sterile millipore setup fitted with a 0.2 micron filter. The two mixtures are then homogeneously mixed.
10 grams of French Naturelle beads, sterilized at 121C at 18 psi for 1/2 hour, are added to the homogeneous mixture with constant agitation. With continuous stirring purified water was added to the latter mixture to bring the total weight of the ~, ' ~' . . '. : -: ` :
~LZ7~9 composition to 100 ~rams and to form a smooth suspension.
EXAMPLE VIII
A mixture of 30 grams of polyethylene glycol of a molecular weight of approximately 4000, and 40 grams of polyethylene glycol of a molecular weight of approximately 400 was melted in a beaker by suspending the beaker into hot water. After the polyethylene glycol was completely melted, it was thoroughly mixed with a glass rod to form a smooth ointment base. T~e ointment base was transferred onto a porcelain tile and was mixed with a spatula with 15 grams of Natural ES
(10/15) to form an ointment. With continued stirring purified water was incorporated into the ointment to bring the total weight of the composition to 100 grams and to soften and smooth the resulting cleansing ointment.
EXAMPLE IX
A mixture of 50 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of 400 was melted and mixed as in Example VIII. After mixing and melting, as in Example VIII, the glycol mixture was mixed with 10 grams of Natural ES and further mixed with purifiPd water to bring the total weight of the composition to 100 grams and to provide a soft smooth cleansing ointment.
EXAMPLE X
A mixture of 25 grams of polyethylene glycol of a molecular weight of approximately 4000, and 30 grams of polyethylene glycol of a molecular weight of 400 was melted and mixed as in Example VII. After mixing and melting, 25 grams of a 20% ~el in purified water of Pluronic F-127 and 10 grams of polymer ~0050/80 were added and mixed into the polyethylene glycol to provide an ointment. With continued mixing purified waker was incorporated into the ointment to bring the total weight .. .. . ...
. : ' ` ' , ~ ' ~ 1 , :'~ .~ ' .
.
:. .: . , ~Z7~
of the composition to 100 grams and to soften and smooth the resulting cleansing ointment.
A study was designed to determine the non-abrasive nature of the polymeric cleaner formulation.
Five unused lenses of each of the six brands of contact lenses were selected for the non-abrasive test.
The six brands of contact lenses selected were:
Polycon - Syntex Tesicon - Uricon TRESOFT - Alcon Laboratories, Inc.
Silicon - Wohlk CAB - Danker Wohlk PMMA - Standard Hard Lenses Prior to starting the study to determine the non-abrasive nature of the polymeric cleaner formulations, all the lenses were viewed through the Bausch & Lomb Optical Microscope under 40X magnification for scratches and/or cuts on lens surface. It was noted that almost all types of lenses had some surface scratches.
Each brand of lenses was then cycled through a cleaning regimen. The lens was rubbed with 2 to 3 drops of polymeric cleaner of Example VIII in the palm of ~he hand with the index finger for a total of 20 seconds and rinsed with normal saline. This procedure was repeated for a total of fifty cycles on each lens. The lenses were viewed for scratches after 5, 10, 20, 30, 40 and 50 cleaning cycles using the Bausch & Lomb Optical Microscope under 20X and lOOX magnifications.
Photographs were taken.
The lens photographs indicate no sign of new cuts and/or scratches on the lens surfaces under study.
The efficacy of polymeric cleaner was determined on laboratory deposited as well as human worn soft contact lenses.
In the laboratory, soft contact lenses were ~I.Z7~
soiled with artificial deposition model solution, containing 0005 percent by weight lysozyme 3X protein and 0.05% percent by weight mucin type 2 in isotonic solution to pH 7Ø The deposition of clean lenses involved heating the lenses with a 5ml of deposition model solution in stoppered glass vial for one hour at 92C. The above procedure was repeated two times with fresh depositions model solution to obtain heavier deposits of protein on the lens surfaceO
The deposited lens was then rubbed with 2 to 3 drops of the polymer cleaner of Example VIII in the palm of the hand with the index finger for a total of 20 seconds (both sides of the lens) and rinsed with normal saline. Depending on the extent of protein deposit on the lens, one to two applicatons of polymeric cleaner of Example VIII was needed to clean the protein from ~he lens.
In another efficacy study, human worn soft contact lenses having protein encrustations were collected and cleaning efficacy of the polymeric cleaner was determined following a similar cleaning regimen as described above. Six sets of human worn lenses were used for the efficacy study and all the lenses were effectively cleaned, and the protein encrustations were removed.
- ~ ...
, .. :,...... . -.
Claims (9)
1. A cleansing composition for cleaning optical surfaces, comprising: a particulate polymer selected from the group consisting of cellulose-acetate-butyrate, polyethylene, acrylonitrile-butadiene-styrene, acetal, polymethylmethacrylate, methylmethacrylate/styrene copolymer, ethyl cellulose, cellulose acetate, cellulose acetate butyrate polychlorotrifluoroethylene, modified polyethylene-tetrafluoroethylene, nylon 6, nylon 6/6, nylon 11, nylon 12, polybutadiene, polyarylether, poly-carbonate, polybutylene terephthalate polyester, polypropylene, polysulfone, polytetraflourethylene, ionomer, fluoroethylene polymer, polysiloxane polymers and mixtures thereof, wherein said particulate polymer has a particle size in the range of from about one micron to about six hundred microns and a Rockwell hardness in the range of from about R30 to about M105 or a Shore hardness in the range from about A15 to about D100; and a carrier having a viscosity sufficient to keep said particulate polymer in suspension.
2. A cleansing composition as recited in claim 1, wherein said carrier is compatible with ocular tissue.
3. A cleansing composition as recited in claim 1, wherein said carrier, comprises: water and a thickener, wherein said thickener is selected from the group consisting of polyethylene glycol, Carbopol*, cellulose and mixtures thereof.
4. A cleansing composition as recited in claim 1, 2 or 3, wherein said particulate polymer has a Rockwell hardness in the range from about R30 to about M105.
5. A cleansing composition as recited in claim 1, 2 or 3, wherein said particulate polymer has a Shore hardness in the range from about A15 to about D100.
6. A cleansing composition as recited in claim 1, 2 or 3, wherein said particulate polymer is selected from the group consisting of cellulose-acetate-butyrate, polyethylene, acrylonitrile-butadiene-styrene, acetal, polymethylmethacrylate, methylmethacrylate/-styrene copolymer, ethyl cellulose, cellulose acetate, cellulose acetate butyrate polychlorotrifluoroethylene, modified polyethylene-tetrafluoroethylene, nylon 6, nylon 6/6, nylon 11, nylon 12, polybutadiene, polyaryl-ether, polycarbonate, polybutylene terephthalate polyester, polypropylene, polysulfone and mixtures thereof, and wherein said particulate polymer has a Rockwell hardness in the range from about R30 to about M105.
7. A cleansing composition as recited in claim 1, 2 or 3, wherein said particulate polymer is selected from the group consisting of polytetraflourethylene, ionomer, fluoroethylene polymer, polysiloxane polymers and mixtures thereof, and wherein said particulate polymer has a Shore hardness in the range from about A15 to about D100.
8. A method for cleansing a contact lens, comprising: rubbing the contact lens with a composition, comprising a particulate polymer selected from the group consisting of cellulose-acetate-butyrate, polyethylene, acrylonitrile-butadiene-styrene, acetal, polymethylmeth-acrylate, methylmethacrylate/styrene copolymer, ethyl cellulose, cellulose acetate, cellulose acetate butyrate polychlorotrifluoroethylene, modified polyethylene-tetrafluoroethylene, nylon 6, nylon 6/6, nylon 11, nylon 12, polybutadiene, polyarylether, polycarbonate, polybutylene terephthalate polyester, polypropylene, polysulfone, polytetraflourethylene, ionomer, fluoro-ethylene polymer, polysiloxane polymers and mixtures thereof, wherein said particulate polymer has a particle size in the range of from about one micron to about six hundred microns and a Rockwell hardness in the range of from about R30 to about M105 or a Shore hardness in the range from about A15 to about D100; and a carrier having a viscosity sufficient to keep said particulate polymer in suspension.
9. A method as recited in claim 8, wherein said carrier is compatible with ocular tissue.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25586181A | 1981-04-20 | 1981-04-20 | |
| US255,861 | 1981-04-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1270119B true CA1270119B (en) | 1990-06-12 |
Family
ID=22970167
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000401225A Expired CA1195127A (en) | 1981-04-20 | 1982-04-19 | Polymeric scrub |
| CA615,525A Expired - Lifetime CA1270119B (en) | 1981-04-20 | 1989-10-13 | Polymeric scrub |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000401225A Expired CA1195127A (en) | 1981-04-20 | 1982-04-19 | Polymeric scrub |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0063472B1 (en) |
| JP (1) | JPS57192922A (en) |
| AT (1) | ATE32270T1 (en) |
| AU (1) | AU559965B2 (en) |
| BR (1) | BR8202239A (en) |
| CA (2) | CA1195127A (en) |
| DE (1) | DE3278049D1 (en) |
| MX (1) | MX166498B (en) |
| ZA (1) | ZA822496B (en) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4481126A (en) * | 1982-07-26 | 1984-11-06 | The Procter & Gamble Company | No rinse liquid car cleaner with solid polymers |
| US4693840A (en) * | 1982-07-26 | 1987-09-15 | The Procter & Gamble Company | No rinse liquid car cleaner with solid polymers |
| US4533399A (en) * | 1983-04-12 | 1985-08-06 | Minnesota Mining And Manufacturing Company | Contact lens cleaning method |
| US4678698A (en) * | 1983-04-12 | 1987-07-07 | Minnesota Mining And Manufacturing Company | Contact lens cleaning article |
| US4622258A (en) * | 1983-04-12 | 1986-11-11 | Minnesota Mining And Manufacturing Company | Contact lens cleaning article |
| JPS60159721A (en) * | 1984-01-31 | 1985-08-21 | Nippon Contact Lens Seizo Kk | Cleaner for contact lens |
| US4655957A (en) * | 1984-06-25 | 1987-04-07 | Bausch & Lomb Incorporated | Contact lens cleaning composition with polymeric beads |
| AT380897B (en) * | 1984-12-10 | 1986-07-25 | Koller Anton | MIXTURE FOR THE CARE AND CLEANING OF CONTACT LENSES |
| GB2188744B (en) * | 1986-04-01 | 1989-11-15 | Donald James Highgate | Contact lens cleaners |
| AU1156288A (en) * | 1986-12-24 | 1988-07-27 | Alcon Laboratories, Inc. | Contact lens cleaning composition and method of use |
| DE3852571T2 (en) * | 1987-05-28 | 1995-08-17 | Colgate Palmolive Co | Detergent composition for hard surfaces. |
| JPH01177014A (en) * | 1987-12-28 | 1989-07-13 | Tome Sangyo Kk | Detergent for contact lens |
| US4855067A (en) * | 1988-05-10 | 1989-08-08 | Colgate-Palmolive Company | Household cleaning composition |
| JPH01293314A (en) * | 1988-05-20 | 1989-11-27 | Daicel Chem Ind Ltd | Cleaning agent for contact lens |
| EP0394456B1 (en) * | 1988-06-18 | 1994-03-23 | Tomei Sangyo Kabushiki Kaisha | Detergent for contact lens and method for washing contact lens |
| US4968447A (en) * | 1988-08-11 | 1990-11-06 | Gage Products Company | Cleaning composition and method |
| JPH0633415B2 (en) * | 1988-12-02 | 1994-05-02 | 花王株式会社 | Skin cleanser composition |
| US5128058A (en) * | 1989-05-31 | 1992-07-07 | Hoya Corporation | Contact lens cleaner containing a microcapsular polishing agent |
| US5017238A (en) * | 1989-08-30 | 1991-05-21 | Dow Corning Corporation | Aqueous cleaning dispersions using adsorptive polymeric powder and method of using |
| US5037485A (en) * | 1989-09-14 | 1991-08-06 | Dow Corning Corporation | Method of cleaning surfaces |
| CA2039378A1 (en) * | 1990-04-03 | 1991-10-04 | Toyoyasu Tanaka | Contact lens cleaning instrument |
| DE19808054C2 (en) * | 1998-02-26 | 2002-06-13 | Boehme Chem Fab Kg | Object for cleaning surfaces |
| GB0004898D0 (en) | 2000-03-02 | 2000-04-19 | Ici Plc | Extrusion process |
| US20050272619A1 (en) * | 2004-06-07 | 2005-12-08 | Borgonjon Patrice M L | Detergent composition |
| JP4896650B2 (en) * | 2006-09-29 | 2012-03-14 | 株式会社コーセー | Novel water-soluble scrub agent and oil-based skin cleansing agent containing the scrub agent |
| DE102012222263A1 (en) * | 2012-12-05 | 2014-06-05 | Henkel Ag & Co. Kgaa | Removal of greasy soiling |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1295611A (en) * | 1970-07-16 | 1972-11-08 | ||
| US3884826A (en) * | 1973-07-20 | 1975-05-20 | Barnes Hind Pharm Inc | Thixotropic cleaning agent for hard contact lenses |
| US4048122A (en) * | 1976-01-23 | 1977-09-13 | Barnes-Hind Pharmaceuticals, Inc. | Cleaning agents for contact lenses |
| CA1152843A (en) * | 1979-06-25 | 1983-08-30 | Polymer Technology Corporation | Abrasive-containing contact lens cleaning materials |
-
1982
- 1982-04-13 ZA ZA822496A patent/ZA822496B/en unknown
- 1982-04-14 AU AU82587/82A patent/AU559965B2/en not_active Expired - Fee Related
- 1982-04-15 DE DE8282301936T patent/DE3278049D1/en not_active Expired
- 1982-04-15 AT AT82301936T patent/ATE32270T1/en not_active IP Right Cessation
- 1982-04-15 EP EP82301936A patent/EP0063472B1/en not_active Expired
- 1982-04-19 MX MX192307A patent/MX166498B/en unknown
- 1982-04-19 CA CA000401225A patent/CA1195127A/en not_active Expired
- 1982-04-19 BR BR8202239A patent/BR8202239A/en not_active IP Right Cessation
- 1982-04-20 JP JP57066174A patent/JPS57192922A/en active Granted
-
1989
- 1989-10-13 CA CA615,525A patent/CA1270119B/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE3278049D1 (en) | 1988-03-03 |
| ATE32270T1 (en) | 1988-02-15 |
| JPS632091B2 (en) | 1988-01-16 |
| EP0063472B1 (en) | 1988-01-27 |
| EP0063472A3 (en) | 1983-05-04 |
| AU559965B2 (en) | 1987-03-26 |
| BR8202239A (en) | 1983-03-29 |
| AU590848B2 (en) | 1989-11-16 |
| AU7372387A (en) | 1987-10-08 |
| CA1195127A (en) | 1985-10-15 |
| EP0063472A2 (en) | 1982-10-27 |
| ZA822496B (en) | 1983-02-23 |
| MX166498B (en) | 1993-01-12 |
| AU8258782A (en) | 1982-10-28 |
| JPS57192922A (en) | 1982-11-27 |
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Legal Events
| Date | Code | Title | Description |
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| NARE | Reissued | ||
| MKEX | Expiry |