|Publication number||US3700761 A|
|Publication date||Oct 24, 1972|
|Filing date||Nov 28, 1969|
|Priority date||Nov 28, 1969|
|Also published as||CA936300A, CA936300A1|
|Publication number||US 3700761 A, US 3700761A, US-A-3700761, US3700761 A, US3700761A|
|Inventors||Allan A Isen, Kenneth F O'driscoll|
|Original Assignee||Griffin Lab Inc|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (68), Classifications (27)|
|External Links: USPTO, USPTO Assignment, Espacenet|
[ Oct. 24, 1972 I54] FABRICATION OF SOFT PLASTIC CONTACT LENS BLANK  Inventors: Kenneth F. ODriscoll, Williamsville;
Allan A. Isen, Buffalo, both of N.Y.
 Assignee: Griffin Laboratories Incorporated,
221 Filed: Nov. 28, 1969 21 Appl.No.: 880,828
 US. Cl. ..264/1, 260/29.6 WB, 260/885,
Primary ExaminerRobert F. White Assistant Examiner-Allen M. Sokal Attorney-.Abraham A. Saffitz ABSTRACT Graft or block copolymers of hydroxy alkyl methacrylate esters and polyvinyl pyrrolidone are (I) cast in a shaping mold as a monomer-polymer dispersion, polymerized to a solid at -60 C. in the presence of low and medium temperature free radical initiators, (2) the solid taken out of the mold and heated to 90-120 C., and then post-polymerized by (3) radiation while dr y andby (4) hydrogen peroxide treatment to form hygroscopic, solid, shaped masses which may be cut in the dry state, after step (2), into contact lenses. The lenses may be equilibrated in the wet state by hydrating with normal saline solution. The lenses may be maintained by treatment with hydrogen peroxide. Steps (3) and (4) toughen the lens, increase its elasticity and its elastic recovery and improve its dimensional stability. From 20 to percent by weight of polyvinyl pyrrolidone imparts hygroscopic and unusual water-swelling characteristics while retaining elastic recovery. The water-swollen lens contains from 40-80 percent water, preferably from -55 percent, and in isotonic saline, the water content changes to about 5258 percent. As a result of the polyvinyl pyrrolidone incorporation, the lens is readily cleaned after use in the eye with dilute hydrogen peroxide to rid it of imbibed muco-protein, catalase and the like.
8 Claims, 8 Drawing Figures R EMOVE FROM CASTING FORM AND PLACE CYLINDER ON TRAY FOR REMOVAL 35 l/ I  Int. Cl. ..B29d 11/00  Field of Search ..264/1; 260/885  References Cited UNITED STATES PATENTS 3,462,385 8/ 1969 Barabas et al. ..260/885 X 3,468,832 9/1969 Barabas et al. ..260/885 X 3,417,054 12/1968 Merijan et al ..260/885 X 3,496,254 2/ 1970 Wichterle ..264/1 3,220,960 1 1/ 1965 Wichterle et al. ..264/ l FOREIGN PATENTS OR APPLICATIONS 2,021,154 7/1970 France 829,565 3/1960 Great Britain ..264/l HYDROXY ALKYL METHACRYLATE and POLYVINYL-PYRROLIDONE FORM LOW TEMPERATURE INITIATOR SLURRY MEDIUM TEMPERATURE INITIATOR STIR and DE-GAS FIRST STAGE CURING LOW TEMP. (40 C.)
CAST ON TEFLON SECOND STAGE CURING MEDIUM TEMP. (-115 C.)
BY ARBOR PRESS (FIG. 5)
CUT TO CURVATURE AND POLISH (FIG. 4a-4d) P'A'TENTEB B I 3.700.761
sum 1 0F 3 HYDROXY ALKYL METHACRYLATE and POLYVlNYL-PYRROLIDONE FORM LOWTEMPERATUREINITIATOR MEDIUM TEMPERATURE INITIATOR STIR and DE-GAS FIG. 1 T
FIRST STAGE cunme LOW TEMP. (40 c.) CAST 0N TEFLON SECOND STAGE CURING MEDIUM TEMP. (105-115, c.)
REMOVE FROM CASTING ON TRAY FOR REMOVAL BY ARBOR PRESS (FIG. 5)
CUT TO CURVATURE AND POLISH (FIG. 4a-4d) INVENTORS KENNETH F. O'DRISCOLL ALLAN A. ISEN ATTORNEY FORM AND PLACE CYLINDER PATENTEBUBI 24 I972 RADIATION HYDRATION AND ALKALINE SWELLING (SOFI'ENS LENS) OSMOTIC SWELLING TO MATCH SALINITY OF HUMAN TEARS (EXPANDS WET LENS) HARDENING BY HYDROGEN PEROXIDE TO TOUGHEN LENS SURFACE (CLEANTNG BY OXIDATION) EQUILIBRATION AND WASHING OUT PRODUCTS OF OXIDATION SHEET 2 0F 3 1% SODIUM BICARBONATE I DISSOLVED IN WATER at pH 8 for 2 20 hours 0.7 0.9% NaCl SOLUTION HEAT TO 200F for 4 12 hours WITH AT LEAST 3 CHANGES of SOLUTION 3% HYDROGEN PEROXIDE IN WATER I at pH 9 nd 0.6 0.9% SALINE for 4 hours INVENTORS KENNETH F.
O'DRISCOLL ALLAN A. ISEN NORMAL SALINE (0.9% NaCl, *1 BUFFER 3- 4% NaHCO gym ,q Thad-z pH 11 ATTORNEY P'A'rEmEnumz4 1912 3.700.761
SHEET 3 [IF 3 INVENTORS KENNETH F-. O'DRISCOLL ALLAN A. ISEN ATTORNEY F ABRllCATION OF SOFT PLASTIC CONTACT LENS BLANK BACKGROUND OF THE INVENTION 1. Field of the Invention The invention relates to a method of shaping and polymerizing, at low (4060 C.) and medium temperatures (90-l20 C.), a monomer-polymer dispersion by casting in a mold and continuing the polymerization after removal from the mold, the dispersion consisting preferably of 20 -45 percent of polymerized vinyl pyrrolidone and 80-55 percent of monomethacrylate ester of a glycol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, there being present no more than about 1 percent by weight of methacrylic acid and no more than 0.2 percent by weight of the dimethacrylate of the aforesaid glycols. Amounts of impurities in excess of these limits cause haze or cloudiness in the product, undue hardness of the casting after hydration, and lessen the amount of water which is absorbed by the hygroscopic solid polymerized product. The monomer is essentially pure hydroxy alkyl methacrylate ester.
An essential feature of the method of the present invention is the stagewise post-polymerization of the bulk polymerized solid casting after free radical initiation at low (40-60 C.) and medium (90-120 C.) temperatures by means of (a) polymerizing radiation'of the dry solid. The hydrogen peroxide treatment of the waterswollen product in an isotonic salt solution toughens the solid post-polymerized product into completely hydrated condition (swollen with from 45-80 percent water which is proportional to the polyvinyl pyrrolidone content).
2. Description of the Prior Art Fields US. Pat. No. 2,136,422 shows the bulk polymerization of ethylene glycol monomethacrylate with free radical initiator such as benzoyl peroxide at elevated temperatures in order to obtain a completely transparent, solid product which is cut and turned on a lathe to make a furniture leg or the like.
Armen et al. US. Pat. No. 3,086,956, in Example 7, shows polymerization of polyglycol monomethacrylate with polyvinyl pyrrolidone and ammonium persulfate initiator at pH 5 in the presence of water to provide a graft copolymer in the form of a turbid aqueous solution containing 19.7 percent solids.
Ackerman et al. US. Pat. No. 2,923,692 shows lightly cross-linked copolymers of esters of methacrylic acid and vinyl pyrrolidone (see column 7, line 32). The products of Ackerman et al. contain highly water-sensitive, cross-linked acrylic acid groups which can be neutralized with alkali to form a smooth, non-grainy mucilage after the product has been purified by washing, dried and then ground in a homogenizer or colloid mill.
The bulk polymerized ester of Fields, neutralized, hydrated, washed and ground by the method of Ackerman et al., would be expected to give a mucilage or glue. It has been found that before grinding, the product has limited hydration capacity (maximum of 20-30 percent) even with substantial amounts of acrylic or methacrylic acid being present in the interpolymer or copolymer. Commercial soft hydrophilic lenses made under the Trademark Sofiens, described in U.S. Pat. No. 3,408,429, are discussed more fully below.
Robinson US. Pat. No. 2,941,980 shows water-soluble polymers and copolymers of pyrrolidone with various monomers, such as acrylic acid, vinyl acetate and the like, and these water-soluble polymers are mixed with alkylated phenols serving as plasticizers to provide coatings for basis of metal, paper, glass, etc., to afford protection against water.
The accelerating effect of up to 1 percent of vinyl pyrrolidone on the polymerization of methacrylate esters is taught by Munday et al. US. Pat. No. 3,232,912, but the polymerized products which are produced are liquids or low-melting solids, useful as detergents in lubricating oils or as sludge dispersants in heating oils.
Copolymers of vinyl pyrrolidone and acrylic acid, as in Robinson, or graft polymers of polyglycol methacrylate with polyvinyl pyrrolidone, as in Armen et al., are not satisfactory as water-swollen, tough contact lens blanks. These products form low-strength films which, when wet with water, are easily distorted by tensile forces and exhibit poor recovery, inadequate elongation and inadequate toughness.
- One would not expect that graft polymers in proportions taught by Ackerman et al., Armen et al., Robinson or Munday et al. might be useful to form tough, transparent, water-swollen contact lenses, capable of being sterilized and cleaned with hydrogen peroxide.
SUMMARY OF THE INVENTION In general, the method converts a free radial initiated solid polymer containing polyvinyl pyrrolidone and polyhydroxy alkyl methacrylate to a highly permeable, soft, hydrated, shaped mass having improved toughness, elasticity and recovery by treating the dry solid mass with radiation to aid densification and thereafter hydrating the mass in saline solution and treating with hydrogen peroxide to cause further toughening by chemical interaction between the polyvinyl pyrrolidone and polymerized methacrylate.
In a preferred form, a tough, soft, hydrated, fluidpermeable contact lens cut from a hard blank is prepared by casting a composition consisting essentially of 20-45 percent of solid, high molecular weight polyvinyl pyrrolidone in a network of -5 5 percent of hydroxy ethylmethacrylate, hydroxy propylmethacrylate, or diethylene glycol monomethacrylate which may contain, as impurities, less than 1 percent of methacrylic acid, preferably not more than 0.2 percent, and up to 0.2 percent of ethylene glycol dimethacrylate. The polymerization of the bulk matrix and preformed polymer is carried out in stages, first in a casting mold and then outside of the mold, as follows:
1. In the open cylindrical casting mold with a lowtemperature peroxide, such as acetyl peroxide, disecondary butyl peroxy dicarbonate, cyclohexanone peroxide, etc., at 40-60 C. for a period of 4-24 hours;
. Out of the mold with a medium-temperature, free radical initiator, such as benzoyl peroxide, diethyl peroxide, asoisobutyronitrile, orthotolyl peroxide, etc., at a temperature of -l20 C. for a period of one-half to 2 hours;
3. Out of the mold as a shaped, hard, polymerized mass with actinic or high energy radiation, such as ultraviolet radiation, gamma radiation, etc., after the lens has been cut to size; and,
4. Finally with hydrogen peroxide in hydrated condition and in the presence of salt which produces the osmotic equivalent of normal saline solution, whereby the cut, water-swollen lens, containing from 40-80 percent water, preferably 50-60 percent water, is toughened in the wet condition.
Step (3) increases the toughness of the lens in hydrated condition, as measured by a bubble bursting test which blows compressed air against the lens to break or burst it and step (4) further increases the toughness of the water-swollen lens and aids in cleaning the lens of debris which accumulates thereon from the eye.
It was completely unexpected to find that a low methacrylic acid medium will provide a graft of hydroxy ethylmethacrylate which is formed with polyvinyl pyrrolidone and thereby provide castings from these materials in bulk which are tough, dimensionally-stable and uniformlyreproducible in hydrated, swollen form to contain from above 40 percent and preferably-5040 percent water in which the permeability of the hydrated product has been increased by post-polymerization treatment, first with radiation when dry and then with hydrogen peroxide in isotonic salt solution.
The function of polyvinyl pyrrolidone in responding to hydrogen peroxide treatment which, in the preferred embodiment of the invention, has a Fikentscher K value of from 30 to 90, appears to be a critical aspect of the new and unexpected properties of toughness, elastic recovery and elasticity developed by the graft copolymer with hydroxy alkyl acrylate.
Polyvinyl pyrrolidone is comparable to gelatin and albumen in respect to its high affinity for water and its low toxicity and general biochemical inertness. The polyvinyl pyrrolidone which is preferred for the present contact lens manufacture has a Fikentscher K value of 33, corresponding to a molecular weight between about 25,000 and 50,000, the number average molecular weight by osmosis being about 37,000 which is about half of that of bovine serum albumen. The carbonamide groups present in gelation are responsible for thread like structures in the hydration of gelatin emulsions which have been detected under the ultramicroscope in grainless photographic emulsions containing from 5-10 percent of gelatin in solutions adjusted to the isoelectric point. Surprisingly, electron microscope photographs of the hydrogen peroxidetreated lens structures of the present invention show no threads. Polyvinyl pyrrolidone imparts hygroscopic characteristics to the product is distributed in the matrix and takes part in chemical interaction with hydrogen peroxide. There appears to be increased permeability and diffusibility of solutes in water through the polymer membrane. This polymer membrane, used as a contact lens, can be cleaned with hydrogen peroxide to remove catalase deposited from tears and organic debris which tend to accumulate in the Wichterle hydrophilic contact lenses.
The hydrogen peroxide has the effect of clearing the lens of any catalase or of any other mucoprotein of the which not only sterilizes the lenses but maintains clarity, transparency and fluid permeability.
Accordingly, this treatment permits freedom from eye irritation and prevents the development of edema under the lens when the lens is worn continuously for 24 hours and longer.
The hydrated hydrogen peroxide-treated product of the present invention appears to possess significantly different properties from gelatin in its resistance to change by acids, alkalis and relatively high temperatures in the wet condition. Gelatin, being amphoteric, reacts with acid and alkali and reversibly dissolves on heating unless it is denatured and flocculated by overheating when wet. In contrast, the present product withstands boiling water for periods up to 72 hours without alteration of its desirable permeable characteristics. Although the chemical mechanism of alteration of carbonamide linkages by radiation and hydrogen peroxide polymerization is not fully understood, it is clear that a critical and significant enhancement of physical properties has been achieved and this could not be obtained by any other method.
BRIEF DESCRIPTION OF THE DRAWING In the fabrication of a soft, water-swollen, plastic contact lens from a hard, dry blank by the preferred method of the invention, a simple casting apparatus is used for shaping the blank and for polymerizing the blank which is illustrated in the attached drawing, in which:
FIG. 1 is a flow diagram showing mixing of ingredients, stirring, degassing, pouring into the mold and placing the filled mold into the oven for the first and second stage curings at low and medium temperatures, respectively, to produce a hard, transparent, shaped mass which is cut and polished;
FIG. 2 is a diagrammatic view showing the placement of male and female mold parts to shape the hard, transparent solid which is subsequently cut;
FIG. 3 is a flow diagram showing the manufacturing steps taken in a particularly preferred embodiment whereby radiation treatment, water-swelling in alkaline medium, osmotic swelling and hydrogen peroxide hardening are carried out to improve the physical properties and water permeability and to diminish osmotic swelling of the cut and polished lens;
FIGS. 40, 4b, 4c and 4d show stages in the cutting of the shaped mass ejected from the mold in FIG. 2 in achieving the finished lens; and,
FIG. 5 is a sectional view which shows the relation of the mold parts and the hard, transparent, shaped mass after one-stage curing and before ejection from the mold.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Example 1 To 120 parts of distilled hydroxyethylmethacrylate containing up to 0.2 percent of ethylene glycol dimethacrylate and less than 1 percent of methacrylic acid as impurities were added 40 parts of powdered polyvinyl pyrrolidone (Plasdone C Grade, supplied by GAF Corporation) having a Fikentscher K value of 33, number molecular weight of 37,000, molecular weight range of 25,00050,000 with the upper percent of K value distribution being 39 weight of the polymer and the lower 25 percent of K value distribution being 18.5 percent. This polymer, hereinafter termed PVP, is hygroscopic and had a moisture content of about 3 percent, but picked up 1 or 2 percent additional moisture from the atmosphere in the plant.
A 40 part portion of the liquid methacrylate, hereinafter termed HEMA, was mixed with catalyst, e.g. 0.2 grams of benzoyl peroxide in powdered form and 0.2 grams of di-secondary butyl peroxy dicarbonatc, available under the trade name of Lupersol 225 from Lucidol Chemical Corporation, Buffalo, New York.
The catalyst-liquid mixture, 40 parts, was added to the PVP-HEMA mixture, 120 parts, and was mixed carefully to provide 160 parts of monomer with 40 parts of polymer dispersion or slurry. These proportions cut down the shrinkage as compared with liquid HEMA alone. The amount of secondary butyl peroxy dicarbonate catalyst which is particularly effective at a temperature of 40-60 C. and of benzoyl peroxide catalyst which is particularly effective at a temperature of 90-120 C. is 0.2 part of each catalyst per 200 parts of liquid PVP mixture containing 160 parts of liquid monomer and 40 parts of PVP, e-.g. a proportion of about 0.1 percent for each of these catalysts. PVP was present in an amount of percent by weight of the dispersion The dispersion was de-aerated to permit air bubbles to escape, and the mold was filled in the manner shown diagrammatically in FIG. 1. The tray of molds was then placed in an air circulating oven for 20 hours at a temperature of 40 C. At the end of this time, the molds were removed from the oven and taken apart by using a small arbor press against the flat end of the Teflon core at the bottom of the mold unit. This forced the cast blank out of the other end of the sleeve. The cast blanks were placed on aluminum sheets and returned to the oven where they were post-cured at a temperature of 110 C. for 1% hours. When the trays were removed from the oven, the finished cast plastic blanks were a polymer consisting of PVP to which poly- HEMA had been grafted.
EXAMPLE 2 The casting procedure set out in Example 1 was carried out, but instead of using 20 percent by weight of PVP, 30 percent by weight was used. The lens made by the technique of Example 1 contained about 55 percent of water as measured in isotonic saline and resulted in a lens that came up to the exacting standards set for Example 1.
EXAMPLE 3 The process of Example 1 was repeated, except that diethylene glycol monomethacrylate was used with 25 percent by weight of PVP. This lens, too, met the standards set in Example 1.
EXAMPLE 4 The process of Example 1 was repeated except that instead of 20 percent of PVP, 35 percent by weight was used. The resulting lens came up to the standards set for Example 1.
EXAMPLE 5 A mixture of parts of hydroxy propyl methacrylate and 80 parts of HEMA was used for the monomer phase with 20 percent by weight of PVP and the process of Example 1 was repeated. The resulting lens came up to the high standards set for Example 1.
The water content of the lens made and tested in Example l was about 51 percent in water and about 49.5 percent in 0.9 percent saline solution. In contrast, the water content of poly-HEMA from which PVP has been excluded is about 38 percent and 36 percent. The water content of the remaining examples was substantially the same as that in Example 1. Generally, the main differences imparted by substituting propylene glycol monomethacrylate or diethylene glycol monomethacrylate is to lower the refractive index and to make the polymerized solid slightly more flexible.
If, in the foregoing examples, PVP is used in an amount less than 20 percent, the water uptake value of about 50-60 percent is not achieved in the hydrated water-swollen polymerized mass and the desired toughening and increase instrength are not achieved by subsequent hydrogen peroxide treatment.
If the low temperature initiator is omitted and polymerization is carried out at -l20 C. for onehalf to 2 hours, the solid product is not uniform in physical properties nor does it provide the toughening and improved strength necessary to come up to the desired standard. Without both low and medium temperature initiators, the improvement in permeability over the commercial Soflens made under the Wichterle patents is not achieved, nor is consistent reproducibility possible.
Accordingly, the critical two-stage initiation at temperatures of 4060 C. in the mold to form the solid rod and at 90-l20'C. out of the mold, in a tray in an oven, to harden the self-sustaining rod provides a rod of stock material of Shore A Hardness value between 70 and 90 which can be cut and polished into lenses by the familiar technique used with hard acrylic material. Even without further treatment, such lenses can be hydrated and water-swollen to surpass the performance of the presently commercially available hydrophilic lenses.
If more than 45 percent of PVP is used in the polymerized mass, the mass after hydration becomes excessively soft. Even after post-polymerization, the product cannot be toughened to match the high strength and elasticity values of the preferred examples above. Only in the range of 20-45 percent PVP can the present polymerized composition, free from crosslinker, match the strength properties of the commercial Soflens. The Soflens material does not possess the same high permeability rate of diffusion which in the present examples is from l-l5times that of the Soflens material.
MANUFACTURING THE LENS FROM THE BLANK The lenses are made by cutting and polishing the shaped masses in the hard state, as shown in the flow diagram of FIG. 1 and in the views of FIGS. 2, 4a-4d, and 5, so that they appear to be exactly like a hard acrylic contact lens.
The molding ingredients, comprising the mixture of hydroxy alkyl methacrylate, PVP, low and medium temperature initiators, cure in the first stage in the molds and in the second stage in the trays to produce hard, transparent, shaped, plano-concave cylinders .20, as illustrated in FIG. 2. The concave surface is formed by male mold member fitting into female'mold member 1 l. The interior surface of the female member 11 is coated with Teflon, as is the outer surface of the male member 10. After curing, the Shore A Hardness value of the shaped mass 20 is between about 80 and 90. Subsequent post-polymerization treatment increases the Shore A Hardness value by from 3 to 10 points. At higher PVP concentrations, lower initial Shore A Hardness values are obtained. Subsequent treatment, e.g., post-polymerization, by radiation causes a greater increase in Shore A Hardness at these higher PVP concentrations and this demonstrates that radiation is especially effective in post-polymerization of the PVP moiety in the product. Radiation also tends to cause slight embrittlement so that if is easier to cut the entire mass 20 before radiation treatment.
Because of the PVP content in the lens and the two stages of curing, there is no trace of unreacted material in the cast blank 20 and cut lenses which are formed by the steps shown in FIGS. 4a-4d have water-swelling characteristics far beyond the commercial hydrophilic lenses available in the prior art. The commercial Soflens, from the Bausch & Lomb Company, has a water uptake of 38 percent in comparison with a 50-55 percent water uptake for the cut lens of FIG. 4 herein, prior to radiation and hydrogen peroxide treatment. This combination of high hardness in the dry state and high water uptake in the wet state of the present lens blank material permits an entirely different and simpler manufacturing process to be carried out than with the Wichterle lens which must be cut when mounted on a support, as described in US. Pat. No. 3,361,858. The present material contains no cross-linker as is required in the lens composition of this patent and it is surprising that the substantially pure poly-HEMA matrix of the present invention, having a Shore A Hardness value close to 90, can be easily cut in the dry state to very small tolerances of about one one-hundredth mm. and thereafter can be hydrated to imbibe at least 50 percent more water than the prior art lens. This cutting in the dry state permits thinner edge sections to be produced and permits uniformity in lens manufacture which cannot be achieved in' the prior art manufacturing methods.
In the hard state, the index of refraction of the cast blank 20 is approximately 1.49. In the hydrated state, the index of refraction of the lens is approximately 1.39
to 1.40. The lenses become larger, thicker and flatter when they are changed to the soft state by hydration. In the cutting and polishing processing of the lenses, and additional reversal in shape occurs and they become somewhat steeper and slightly smaller in diameter. All of these changes are taken into account to produce the desired specifications of curvature and dimension in the hydrated state.
The lens blank 20 is a small cylinder with a concave curve at one end which must be optically finished and a small amount of stock is removed from this surface, e.g., a minimum amount of about 0.2 mm. in thickness and a maximum of 0.5 mm., the removal being symmetrical and from the entire surface.
The following are the steps in manufacturing after the low temperature and medium temperature cures of the blank 20. After the low temperature cure, the blank 20 is removed in the manner shown in FIG. 5 wherein ram 13 pushes against the planar surface of the blank STEP eject the blank from the female mold member 10. The blank is removed from the same end into which the dispersion or slurry was poured and this removal is completely different from that which is carried out in US. Pat. No. 3,361,858, wherein the lens is molded to size on a mount and is removed from the mount by immersing in water to swell it and allow it to be peeled from the mount. After this, the blank of the present invention is cured in the medium temperature stage on trays and the steps below are followed:
STEP 8c 1 CUTTING The cutting steps are shown diagrammatically in FIGS. 4a-4d. The dotted lines in FIG. 4a show removal of peripheral'or radial portions of the blank in order to cut the 180 arc down to about as shown in FIG. 4a and in FIG. 4b. The planar surface is then cut along the dotted line shown at the bottom of FIG. 4b in order to faciliate mounting the blank on a lathe, and this blank is shown in FIG. 4c. Where the chuck of the lathe can handle the form shown. in FIG. 4b, the planar cut shown in FIG. 40 is not required. The concave cut is made along the dotted line shown in FIG. 4c and cut lens is shown in FIG. 4d.
In the lens mad in accordance with the present invention, the flat surface on the back of the blank is faced off in the manner shown in FIGS. 4b and 4c and the center of the flat surface is tapped to make a pivot depression on a small jewelers lathe. The diameter of the blank was reduced in a Levin lathe to a size 0.1 mm. larger than the desired finished lens size (see FIG. 4a). The radius cut on the concave surface matched the surface.
STEP 2 POLISHING OF INNER OR BACK Surface SURFACE The base curve blank was then mounted on an optical polishing machine and it was polished against a brass lap coated with adhesive tape whose curve matched the base curve of the blank. In the polishing, the lens blank rocked back and forth on the polishing lap, and spun at the same time. Two polishing cycles were used, The first employed Snow Floss Compound, made by Johns Manville, mixed with odorless kerosene to the consistency of a thick paste. This rough polish procedure was used for 3 minutes. The finish polish was clone with U.S. Patent Grade of Zinc Oxide, made by Merck Pharmaceuticals, mixed with vaseline to form a paste. This cycle also lasted for 3 minutes. When the curve was finished, it was measured with a radiuscope for radius and quality to have a radius of curvature within plus or minus 0.4 mm. of the original lathe radius cut.
STEP 3 RADIUS CUTTING THE OUTER OR FRONT SURFACE The finished base curve was now mounted onto a brass or plastic chuck preparatory to radius cutting and polishing the front surface. This chuck has a finished, polished, convex surface which matches the base curve of the blank. The rear of the chuck fits into a collet of a small, high precision jewelers lathe made by Levin & Sons. The chuck was heated slightly, sufficiently to melt some mounting wax on the surface of the chuck. The finished base curve was pressed firmly onto this surface and was allowed to cool. The chuck was then mounted in a Levin lathe and its front surface was radius cut in two stages. In the first stage, rough cutting removed all of the stock. In the second stage, finish cutting produced a highly smooth radius cut and an exact center thickness. The thickness was measured by a regular plunger thickness gauge through the small diameter hole in the center of the chuck, which was also used for evaluating the optics as the lens was being finished. The front surface was then polished on an optical polishing machine. The chuck mounted on a vertical spindle and rotated as a polishing lap coated with adhesive tape rocked back and forth over the surface, spinning at the same time. The polish used was Snow Floss Compound mixed with odorless kerosene to the consistency of this paste. It required 3 minutes to complete the surface, and the optical quality was judged by removing the chuck from the spindle and viewing the optics in a lensometer through the hole in the chuck.
STEP 4 CUTTING THE LENTICULAR GROOVE ON MINUS LENSES On minus lenses, it is necessary to thin the edge by adding a minus lenticular cut to the peripheral region of the front of the lens. This is done with a single edge razor blade and polished with molefoam and the zinc oxide polishing solution. The width of this front lenticu- Iar region should not be greater than one-half of the diameter of the lens.
STEP 5 ADDING INSIDE BEVEL AND INSPECTION The lens was then removed from the chuck by heating the bottom of the chuck until the wax softened and the lens could be slid off the chuck easily, and was then cleaned in a test tube with Xylene which was put into an ultrasonic cleaner.
The finishing of the lens included the addition of a small flat bevel to the inside aspect of the edge approximately 0.3 mm. wide. This was put on by grinding against an emery sphere or a diamond impregnated lap, and polishing against a matching felt lap. Following this, the edge was rounded and polished against a polyurethane sponge saturated with the polish mixture or zinc oxide and odorless kerosene. The lens was then recleaned in Xylene in the ultrasonic cleaner. It was measured and inspected for base curve radius, optical value and quality, thickness and surface scratches.
STEP 6 IRRADIATION TREATMENT AS SHOWN IN FIG. 3
Irradiation is preferably carried out under an ultraviolet lamp which provides a high energy source in the spectral range of 2,000 to 4,000 Angstrom units, for at least one-half hour, preferably 2-4 hours. The bursting strength is increased from 7 p.s.i. gauge to 10.5-11.0 p.s.i. gauge, an increase of at least about 50 percent of the originalvalue and the hydrated lens loses practically none of its elasticity and rapid recovery. In
contrast, the commercial Sofiens, the lens of the prior art, does not improve under irradiation in its bursting strength. Therefore, it is clear that the PVP component in the original composition, as well as the unique two-step polymerizing procedure, 'e.g., the low temperature initiation and the medium temperature initiation referred to in FIG. 1, coact in a new way with irradiation treatment in the solid polymerized state to produce this new and unexpected result.
Utraviolet sources, such as the mercury vapor tube, a Xenon lamp, or a carbon arc tube, may be used.
Other irradiation sources which may be used are a cobalt 60 source which emits gamma radiation, spent reactor elements from a uranium pile which also emit gamma radiation, or high energy ionizing radiation from a commercially available source, e.g., Radiation Dynamics, Long Island, New York X-Rays may be used at exposure dosages of 10 roentgens for a period of 15 minutes to 1 hour. Gamma radiation dosage for postpolymerization treatment is preferably from about 5 to about megarads for 5 minutes to 1 hour. All treatments by irradiation are carried out'at room temperature.
In this irradiation treatment, as shown in FIG. 3, the hard finished lens was placed under a pure ultraviolet light for a period of 3% hours. The light source was 6 inches from the lens. The unit was covered to prevent light loss and the polymerization of poly-HEMA and PVP was completed in 2 hours. The light source was a 250 watt Spectraline utraviolet lamp.
STEP 7 NEUTRALIZATION, HYDRATION AND HYDROGEN PEROXIDE TREATMENT This step accomplished the neutralization and hydration of the lenses. Lenses were placed in a 0.8 percent saline bath mixed with sufficient bicarbonate of soda to produce a pH of 8. They remained in this bath for 2-20 hours. Each lens was held by a small flo-thru basket made of polypropylene. The lenses were then placed in a bath of normal saline at approximately 200 F. for 1 hour. The bath was then changed to fresh normal saline for a period of 3 hours and then changed again for an additional 4 hours. This boiling was done in a pressure cooker to which a condensing column had been added to prevent evaporation and to increase the concentration of the saline.
The lenses were then placed, for 4 hours, in a bath of 10 volume reagent grade hydrogen peroxide (3% H 0 to which had been added sufficient pure sodium chloride to produce the equivalent of a normal saline solution. This caused the lenses to shrink in size and become hypertonic. Following this, they were boiled in the pressure cooker in distilled water for 2 hours andagain in normal saline for 2 hours. See FIG. 3.
BURSTING STRENGTH OF THE LENS The post-polymerizaiton steps (6) and (7), irradiation and hydrogen peroxide, illustrated in FIG. 3 of the drawing, contribute to significant strengthening and toughening of the water-swollen lens and provide thereby advantages not available in any commercial lens of the soft hydrophilic type.
The hard cut lens resulting from the manufacturing operations shown in FIGS. 1 and 4a-4d can be tested for bursting strength by binding the edges about the opening of one-fourth inches pipe and measuring the air pressure required to burst the lens which has been boiled in water of 4 hours to hydrate it. This test carried out with the cut lens of FIGS. 1 and 4a-4d of the invention showed a bursting strength of 7 p.s.i. gauge pressure. This cut lens, based on poly-HEMA matrix containing 20 percent PVP, matched the bursting strength (7 p.s.i. gauge) of the centrifugally cast Soflens containing dimethacrylate cross-linker, thereby showing unexpected improvement in the absence of cross-linker and at almost 50 percent higher water content (52 percent uptake in the present lens against 37 percent in the *Soflens).
After irradiation and hydrogen peroxide treatment by the process of the invention, the bursting strength by the above mentioned test is increased from 10.5-11 p.s.i. up to 16-17 p.s.i., an increase of at least 250 percent based upon the original bursting strength and an increase of about 100 percent f the original value as compared with the 50 percent increase achieved by irradiation.
This enhancement of strength by hydrogen peroxide is uniquely based upon the PVP content since the commercial Soflens does not show such enhancement in bursting strength. Uniquely, both the irradiation and the hydrogen peroxide treatments are essential if the maximum bursting strength is to be achieved and if the other lens properties, e.g., controlled'elongation in lateral and vertical dimensions in water-swollen state,
are to be maintained.
These other lens properties, in Water-swollen state, will be more clearly visualized in comparison with the shape and dimensions of the hard lens shown in FIG. 4d. Upon immersing the lens in water at pH 8 after radiation (see Block 3, FIG. 3), the radius of curvature of the lens expands 26 percent, the core diameter expands 35 percent, and the thickness expands 23 percent. These values of anisotropic expansion do not change if the lens is immersed in saline (Block 4, FIG. 3). The water uptake is between 48 and 55 percent.
The hydrogen peroxide treatment accomplishes the most surprising improvements in the physical properties of the hydrated, water-swollen lens which facilitate maintenance and cleaning of the lens by the patient. By this treatment, there is accomplished, as mentioned above, an increase in bursting strength after irradiation of 10.5-11 p.s.i. up to 16-17 p.s.i., gauge pressure. If alkaline bicarbonate solution (1 percent) at pH 8 is repeatedly applied to the lens, a slight softening occurs and the bursting strength falls to about 12.5-13.5 p.s.i.
FLUID PERMEABILITY CHARACTERISTICS The fluid permeability of the lenses of Example 1 was studied and compared with the Bausch & Lomb Solfens, made by the process of Wichterle US. Pat. No. 3,408,429.
Individual vials of sterile fluorescein solution were made up various disodium fluorescein concentrations in 0.1M phosphate buffered saline at a pH of 7.4.
An objective slit lamp fluorophotometer measured fluorescein concentration in the lenses, in the interior segment of the eye, and in the solution. The fluorophotometer consists of a light sensing device built into the eye piece of the lamp and measures the fluorescein concentration in an area 0.08 mm. across. The instrument is accurate to within plus or minus 2 percent. The unknown is compared with a fresh, stable, standard fluorescein solution.
RESULTS OF IN VITRO STUDIES FULLY HYDRATED l. Uptake Fully hydrated lenses were placed in solutions of various fluorescein concentrations, were rinsed briefly after the test time in saline and were then mounted on the end of a glass test tube for measurement of the fluorescein concentration in the lens.
The lenses themselves absorb less than 3 percent of the emitted light and do not interfere with the test by reason of light absorption. The volume of the soaking solution is large in comparison to the lens volume.
Lenses fluoresced uniformly under the slit lamp after 90 seconds of soaking on a fluorescein (5 X 10 mg ./ml.) solution. Three distinct zones were observed in the Soflens lenses soaked for 30 minutes due to the fluorescein slowly diffusing to the interior of the lenses. The lenses of the present invention take up fluorescein quite rapidly; uptake is complete in about 2 hours. The Bausch & Lomb lenses (Soflens) take up fluorescein slowly and continue to do so for over 24 hours, reaching a final concentration approximately 2.3 times that in the lenses of the present invention.
2. Elution Studies After a 24 hour presoaking of the lenses in 5 X 10""mg./ml. fluorescein solution, they were placed in 4 cc. of buffered saline and the time rate of change of fluorescein concentration in the lenses and the eluting solutions were measured. At the end of 1 hour, the lenses of the present invention had released percent of the fluorescein into solution, while the Soflens lenses released 25 percent. Only after 8 hours did the Sofiens lenses release percent of the bound fluorescein.
After elution from each type of lens, it was determined that the Soflens lenses took up twice as much fluorescein as did the lenses of the present invention, on a weight basis.
The total uptake or fluorescein was linearly related to the concentration of the soaking solution over a 4,000-fold concentration range between 5 X 10- and 20 mg./ml. The present lenses were air dried, place in fluorescein solution and the uptake by the dried lenses was substantially identical to the fully hydrated lenses.
RESULTS OF THE VIVO STUDIES A young female who had worn both conventional and hydrophilic lenses without difficulty was studied. On the first day, she wore a lens of the present invention in one eye and no lens in the other. A single drop of sterile 2 percent fluorescein was instilled in each eye at 0, 2, 4, 6 and 11 hours. The corneal and anterior chamber concentrations were measured at 2, 4, 6 and 24 hours, each time removing the lens 10 minutes prior to measurement. ONe week later, the subject wore the Bausch & Lomb Soflens in one eye and a methyl methacrylate conventional hard lens in the other. Drops were instilled at O, 2 and 4 hours and measurements were made at 0, 2, 4 and 6 hours, at which time the Bausch & Lomb lens was removed, The corneal and anterior chamber concentrations of fluorescein are shown in Tables 1 and 2 below. The corneal and anterior chamber concentrations were higher with the lens of the present invention than with the other lenses. There was essentially no difference between using no. lens, standard methacrylate lens, or the Bausch & Lomb lens. At the end of 6 hours, the corneal and anterior chamber concentrations of fluorescein in the eye with the lens of the present invention were six to eight times that attained with any other mode of treatment. Furthermore, the lens of the present invention was able to maintain the fluorescein concentration in the ocular tissues for 24 hours despite the known rapid exit of fluorescein from the eye. It should be noted that the lens had not been presoaked in fluorescein prior to insertion.
In other studies, the present lenses were presoaked in solutions of 0.1 percent and 0.01 percent fluorescein and inserted into the right eyes of three rabbits. At the same time, a drop of the 0.01 percent solution was put into each of the left eyes. 90 minutes later, the lenses were removed, the eyes were irrigated with saline and the corneal and anterior chamber concentrations were determined. The lenses were the reinserted and the rabbits received one drop of the 0.01 percent solution in the left eye every 30 minutes for 2 additional hours. Saline solution was instilled into the right eye. The corneal and aqueous humor concentrations of fluorescein at l A and 3 Va hours are shown in Tables 3 and 4 below. The ocular concentrations attained with the presoaked lenses were four times higher than those attained with frequent drops. Increasing the concentration of the soaking solution ten-fold resulted in an 800 percent increase in the ocular concentrations. It took much less fluorescein to get the same ocular concentration if the fluorescein was permeated into a lens that if it was instilled topically.
TABLE 1 (All Values Are X l mg./ml.)
N 0 Lens Bausch and Lomb Lens Present Lens Time (hours) Methyl Meth acrylate TABLE2 Anterior Chamber Concentration of Fluorescein With Various Types of Contact Lenses in Place (All Values are X 10' mg./ml.)
Time Present Bausch and Methyl No (hours) Lens Lomb Lens Methacrylate Lens TABLE 3.
Corneal Fluorescein Concentration In Rabbits With Presoaked Lenses Of Present Invention (All VAlues are X l0' mg./ml.
(Number of Animals in Parenthesis) Lens Presoaked Lens Presoaked Fluorescein Concentration In Aqueous Humor Of Rabbits With Presoaked Lenses of the Present Invention (All Values are X l0' mg./ml.)
(Number of Animals in Parenthesis) Lens Presoaked Lens Presoaked Time in 0.1% in 0.01% Topical 0.01% (hours) Fluorescein Fluorescein Fluorescein OXYGEN PERMEABILITY STUDIES The lens of the present invention appears to permit higher transmission of oxygen than the commercially available hydrophilic lens and, as a consequence, is of value in permitting oxygen access across the lens to the cornea.
The lenses of the present invention, made by the twostage initiation process shown in FIG. 1 without the further steps of irradiation and hydrogen peroxide treatment, exhibit permeability and diffusion characteristics comparable to those pointed out in the studies above; and these lenses, cut from the polymerized rod, as shown in FIGS. 4a-4d, respond to hydrogen peroxide toughening and cleaning, althouth to a degree substantially less than the lenses which are made by the preferred method of the invention as shown in FIG. 3.
The diffusibility of solutes through the lenses made by the methods of FIGS. 1 and 3 is from about 6 toabout times as great as the diffusibility of the commercially available Soflens, this diffusibility being expressed as the rate of elution of a dilute tracer material through the lens. A comparative diffusion value is demonstrated where a dye is seen to completely diffuse in a few hours through the lens of the present invention, while such diffusion through the presently commercially available lenses takes 24 hours or longer.
The significance of such diffusion is demonstrated when the novel circular lens of our copending application, mentioned hereinabove, is placed in contact with the cornea, over the super-sensitive limbal area, with its thin flap or edge extending a few millimeters beyond the limbus, the limbal area of the lens defining a circular tear vesicle which is cut out from the material of the lens adjacent the flap. This novel lens vesicle provides a clear solution of liquid tears adjacent the cornea and osmotic pressure is created in a direction from the less dense tear liquid to the more dense liquid in the cornea to aid in bathing the eye. The semi-scleral flap is held to the scleral portion of the eye by capillary attraction. Tears can enter under the flap to replenish the vesicle well which is immediately adjacent the inner edge of the lens. Hypertonic eyedrops instilled into the eye stimulate the washing and cleaning function of the tears, and any medication in these eyedrops diffuses rapidly, in mere minutes, through the permeable structure of the lens.
The hydrogen peroxide treatment appears not only to toughen the lens and raise the bursting strength values, as mentioned above, from 16 p.s.i. gauge to 19-20 p.s.i. gauge, but it also opens and cleans the pores or microvoids in the lens material through which diffusion takes place. Therefore, hydrogen peroxide at 3 percent dilution constitutes a maintenance fluid which is used in conjunction with 1 percent sodium bicarbonate solution, the latter relaxing the pores and softening the lens to aid in cleaning and reducing the burstingstrength by 3 or 4 p.s.i. gauge units and the former reversing this decrease to bring the lens back to its maximum toughness after cleaning. Surprisingly, aging of the lens through normal use, e.g., wearing and cleaning, has been found to slightly increase the bursting strength value of the lens by 2 or 3 p.s.i. gauge. Whether the lens is a newly manufactured lens having a bursting strength of 16 p.s.i. gauge or an aged lens with bursting strength of 20 p.s.i. gauge, no difference is found in the corrective function of the lens or in its comfort.
The lenses of the present invention resist the substantial dimensional changes which ordinarily occur when different osmotic salt concentrations are applied. The anisotropic swelling and shrinking characteristics at 50-55 percent water uptake appear to provide a unique environment for resisting osmotic dimensional change which would cause the lens to shift its position or to flex in response to normal movement of the eyelid or illumination by strong light, irritation and the like.
If the lens is too stiff and insufiiciently hydrated, which is the case with the hydrophilic, highly crosslinked presently available commercial lens, the inside curve of the lens must be steeper than the curve of the cornea with a space under the lens in the central region 16 in order to shape the lens to the cornea. If is this space which flexes with each blink. The edge of the hydrophilic lens grabs the cornea at the sensitive limbal area.
The inadequate water uptake causes irritation and discomfort. Only by increasing the lens diameter and by providing a very thin, flexible edge can the presently available commercial lens to improved, but the liquid permeability is still insufficient and the optical tolerance can never be as good as in the present lens because the present lens is cut in the hard state with a greater degree of accuracy than can be obtained with the prior art lens which is cut in the soft state. Suprisingly, there is no dimensional change in the present lenses with small changes in hydration, while significant dimensional changes occur with the prior art lenses. Consequently, the fit is flatter and better with the present lens; the optical correction is more accurate; substantially no shifting occurs; and flexing by blinking is completely avoided. In the present lens, the elimination of flexing, the smoother optical finish, the flatter corneal curve, and the limbal tear vesicle make it possible to correct astigmatism in a manner far better than with any lens now available.
The chemical composition of the present hygroscopic lens, e. g.,' the critical PVP and I-IEMA content, combined with the critical method of two-step polymerization to permit precision grinding and uniformity, and the post-polymerization with radiation and hydrogen peroxide, provide precision fitting, maximum strength, elasticity and elastic recovery properties, all of which are essential to eye comfort when the lens is worn for long periods of time.
Instead of the polyvinyl pyrrolidone homopolymer, various lower alkyl derivatives thereof may bev employed. Such derivatives include:
3-methyl-N-vinyl-2-pyrrolidone 4-methyl-N-vinyl-2-pyrrolidone 3,3-dimethyl-N-vinyl-2-pyrrolidone 4-ethyl-Nrvinyl-2-pyrrolidone S-methyl-N-vinyl-2-pyrrolidone S-ethyl-N-vinyl-2-pyrrolidone and the like. These examples support any PVP having lower alkyl in the 3, 4 or 5 positions.
The composition also has utility as a liquid, hygroscopic coating material which strongly adheres to glass, plastic or metal when cured, after application, in two stages under the temperature condition shown in FIG. 1. The liquid slurry can be applied in a thickness .of l-lO mils onto a glass tumbler to provide a frost-free drinking glass for cold drinks, the glass being free from outside condensation. The coating may be applied to an automobile windshield to make it fog-free on the inside. The coating may be applied to the polycarbonate lenses used in ski goggles or to contact lenses made of CR-39 (polycarbonate) plastic.
The membrane composition may be cast as 'a desalination membrane and used to remove salt by reverse osmosis.
The membrane may be used as a germicide-carrying bandage for internal and external wounds. In the treatment of the eye, these drugs include pilocarpine, belladonna alkaloids, dibenzyline, hydergine, methacholine, carbachol, bethanechol, a sulfonamide and similar medicaments.
The precision fitting advantage of the lens of the present invention carries over to prevent liquid buildup behind the bandage when a medicament-carrying bandage is formed for the eyeball which extends over the scleral area under the lid. Edema which is encountered with hard, impermeable acrylic bandages is eliminated. The medicines are not concentrated in the present hydrated plastic membrane to cause osmotic swelling thereof, but are readily diffused to bathe the affected eye portion with the proper concentrations for therapeutic effectiveness. There is no dimensional change of the bandage when hypertonic concentrations of salts and medicines are applied to the eye, and this aids in the healing process.
The liquid slurry composition may be used to cast or coat an artificial eye, limb or appendage without shrinkage and to precise dimensions. In all of these uses, the coating, membrane, casting, etc. can be cleaned with hydrogen peroxide at an appropriate time.
Having thus disclosed the invention, what is claimed 1. A method of shaping and cutting a contact lens comprising:
l. mixing a slurry of 20 percent up to 45 percent of a solid, high molecular weight polyvinyl pyrrolidone of Fikentscher K value of 30-90 with 80-55 percent of monomethacrylate ester of a glycol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, there being present no more than about 1 percent by weight of methacrylic acid and no more than about 0.2 percent by weight of dimethacrylate of the aforesaid glycols and two free radical initiators, the first effective at a temperature of 4060 C. and the second at a temperature of 90-l20 C. to polymerize said mixture, each of said two free radical initiators being present in an amount of about 0.1 percent by weight of said slurry;
2. casting said slurry in an open cylindrical mold and polymerizing at a temperature of 4060 C. to form a hard, self-supporting mass which is hygroscopic and swells anisotropically in a water medium;
3. removing said mass and polymerizing at a temperature of 90120 C. to polymerize unreacted material from the polymerization with the first free radical initiator and to complete the hardening of said mass in its self-supporting condition outside of the mold; and,
4. cutting a lens from said mass;
5. subjecting said cut mass to polymerizing radiation for at least 5 minutes up to 4 hours to toughen said out mass in both the dry state and when swollen with water; and
6. neutralizing and hydrating said cut mass in saline solution.
2. A method of shaping and cutting a contact lens comprising:
1. mixing a slurry of 20 percent up to 45 percent of a solid, high molecular weight polyvinyl pyrrolidone of Fikentscher K value of 30-90 with 80-55 percent of monomethacrylate ester of a glycol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, there being present no more than about 1 percent by weight of methacrylic acid and no more than about 0.2 percent by weight of dimethacrylate of the aforesaid glycols and two free radical initiators, the first effective at a temperature of 40-60 C. and the second at a temperature of 90-120 C. to polymerize said mixture each of said two free radical initiators being present in an amount of about 0.1 percent by weight of said slurry;
2. casting said slurry in an opencylindricalmold and polymerizing at a temperature of 4060 C. to form a hard, self-supporting mass which is hygroscopic and swells anisotropically in a water medium;
3. removing said mass and polymerizing at a temperature of 90-l20 C. to polymerize unreacted material from the polymerization with the first free radical initiator and to complete the hardening. of said mass in its self-supporting condition outside of the mold;
. cutting a lens from said mass;
. subjecting said cut mass to polymerizing radiation for at least 5 minutes up to 4 hours to toughen said cut mass in both the dry state and when swollen with water;
6. neutralizing and hydrating said cut mass in saline solution; and,
7. treating said cut mass with dilute hydrogen peroxide.
3. The method of making a contact lens comprising:
i. casting a hard concave-planar cylinder consisting essentially of a reaction product of 20 percent up to 45 percent of a solid, high molecular weight polyvinyl pyrrolidone of Fikentscher K value of 30-90 with -55 percent of monomethacrylate ester of a glycol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol and dipropylene glycol, there being present no more than about 1 percent by weight of methacrylic acid and no more thanabout 0.2 percent by weight of dimethacrylate of the aforesaid LII-P glycols as impurities and two free radical initiators,
the first initiator polymerizing said cylinder at a temperature of 4 O-60 C. to form a self-supporting mass which is hygroscopic and which will swell anisotropically when placed in a water medium and the second initiator polymerizing said cylinder to polymerize unreacted material from the polymerization with the first free radical initiator, each of said two free radical initiators being present in an amount of about 0.1 percent by weight of said slurry at a temperature of l 20 C. to complete the hardening of the cylinder;
2. cutting away about 90-95 percent of the material from the planar face of the cylinder and from the circular outer periphery of the cylinder to leave the inner concave surface of the casting as the last surface to be cut as a lens blank having an arc .of about and in a diameter broad. enough to cover the cornea and at least several millimeters of the limbus;
3. cutting a bevel edge at the periphery of the lens blank to form a lens having a semi-scleral flap which is adapted to be lifted up by tears in the scleral portion of the eye adjacent the outer edge of the flap while simultaneously forming a circular tear vesicle in the interior edge of the bevel which is spaced inwardly from said flap and which provides a circular well for tears in the eye at the limbal area, while the inner central portion of the lens is relatively flat to contact the cornea without any tear layer therebetween.
4. subjecting said cut lens to polymerizing radiation for at least minutes up to 4 hours to toughen said cut lens in both the dry state and when swollen with water; and
5. neutralizing and hydrating said cut lens in saline solution.
4. The method as claimed in claim 3, wherein the lens blank is irradiated prior to cutting the bevel edge.
5. The method as claimed in claim 3, wherein the lens is irradiated after cutting the bevel edge of the lens blank.
6. The method as claimed in claim 3, wherein the center of the lens blank is cut and polished on both inner and outer surfaces to make its center thinner than the edges of the corneal section to thereby provide a minus correction.
7. The method as claimed in claim 3, wherein the lens blank is cut to make its corneal edges thinner than its center, to thereby provide a plus correction.
8. The method as claimed in claim 3, wherein the lens is cut and polished to besubstantially the same thickness at its center and at its corneal edges, to thereby provide zero correction and produce a lens useful as a corneal bandage through which eye medicaments may be diffused.
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3807398 *||Sep 19, 1972||Apr 30, 1974||B Grucza||Ocular implant|
|US3839304 *||Feb 12, 1973||Oct 1, 1974||American Optical Corp||Soft contact lens and method of production thereof|
|US3841598 *||Nov 27, 1973||Oct 15, 1974||B Grucza||A mold for casting a hydrophilic contact lens blank|
|US3894129 *||Mar 15, 1973||Jul 8, 1975||American Optical Corp||Method of manufacture of strain free contact lenses|
|US3901969 *||Sep 10, 1973||Aug 26, 1975||Union Corp||Sustained release of methantheline|
|US3912451 *||Mar 26, 1974||Oct 14, 1975||Warner Lambert Co||Method for removing hydrogen peroxide from soft contact lenses|
|US3916033 *||Dec 4, 1972||Oct 28, 1975||High Voltage Engineering Corp||Contact lens|
|US3959102 *||Oct 10, 1974||May 25, 1976||Essilor International (Compagnie Generale D'optique S.A.)||Method for preparing a crosslinked graft copolymer of silicone and polyvinylpyrrolidone for use as a contact lens, and a contact lens produced thereby|
|US3966847 *||Jan 4, 1974||Jun 29, 1976||Maurice Seiderman||Contact lens from hydrophilic gel polymers of polyvinylpyrrolidone and hydroxyalkyl methacrylate|
|US3979891 *||Mar 7, 1975||Sep 14, 1976||Patton Orvil D||Pneumatic fruit harvester|
|US3980084 *||Mar 3, 1975||Sep 14, 1976||Hydro Optics, Inc.||Ostomy gasket|
|US3983083 *||Dec 6, 1974||Sep 28, 1976||Japan Atomic Energy Research Institute||Soft contact lenses and process for preparation thereof|
|US4042552 *||Nov 14, 1975||Aug 16, 1977||Warner-Lambert Company||Composition for hydrophilic lens blank and method of casting|
|US4045547 *||Dec 17, 1975||Aug 30, 1977||Warner-Lambert Company||Fabrication of soft contact lens and composition therefor|
|US4063890 *||Apr 28, 1976||Dec 20, 1977||Baron Neville A||Method and apparatus for sterilizing and storing contact lenses|
|US4099859 *||Dec 27, 1976||Jul 11, 1978||High Voltage Engineering Corporation||Contact lens having a smooth surface layer of a hydrophilic polymer|
|US4123408 *||Nov 26, 1976||Oct 31, 1978||American Optical Corporation||Hydrogel contact lens|
|US4126138 *||May 16, 1977||Nov 21, 1978||Warner-Lambert Company||Soft contact lens|
|US4127638 *||Sep 13, 1976||Nov 28, 1978||American Optical Corporation||Process for casting polymer rods|
|US4189364 *||Jan 17, 1974||Feb 19, 1980||Hydroplastics, Inc.||Method for preparing hydrophilic polymers and polymer grafts including irradiation|
|US4212107 *||Jun 9, 1978||Jul 15, 1980||Orazio Mezzasalma||Lens measuring method and apparatus|
|US4260564 *||Aug 15, 1979||Apr 7, 1981||Intercast Europe S.P.A.||Process for the manufacture of spectacle lenses made of diglycol allyl carbonate or the like|
|US4300820 *||Oct 27, 1980||Nov 17, 1981||The Kendall Company||Water absorptive composition|
|US4330383 *||Jul 28, 1980||May 18, 1982||Polymer Technology Corporation||Dimensionally stable oxygen permeable hard contact lens material and method of manufacture|
|US4368310 *||Oct 23, 1981||Jan 11, 1983||Ppg Industries, Inc.||Method of polymerizing sheets|
|US4395496 *||Nov 16, 1981||Jul 26, 1983||Uco Optics, Inc.||Cured cellulose ester, method of curing same, and use thereof|
|US4550001 *||Mar 9, 1984||Oct 29, 1985||Japan Synthetic Rubber Co., Ltd.||Process for producing shaped articles having improved surfaces|
|US4562018 *||Jan 28, 1985||Dec 31, 1985||Neefe Charles W||Method of casting optical surfaces on lens blanks|
|US4585488 *||Dec 20, 1982||Apr 29, 1986||Ciba Vision Care Corporation||Method for disinfecting contact lenses|
|US4678838 *||Aug 4, 1986||Jul 7, 1987||Ciba-Geigy Corporation||Particulate hydroperoxidized poly-N-vinyl lactam, its preparation and use thereof|
|US4693446 *||Sep 20, 1985||Sep 15, 1987||Techna Vision, Inc.||Gasket for molding plastic lenses|
|US4729892 *||Mar 21, 1986||Mar 8, 1988||Ciba-Geigy Corporation||Use of cross-linked hydrogel materials as image contrast agents in proton nuclear magnetic resonance tomography and tissue phantom kits containing such materials|
|US4791175 *||Feb 17, 1987||Dec 13, 1988||Ciba-Geigy Corporation||Particulate hydroperoxidized poly-n-vinyl lactam, its preparation and use thereof|
|US4826889 *||Nov 7, 1986||May 2, 1989||Polymer Technology, Corp.||Dimensionally stable oxygen permeable hard contact lens material and method of manufacture|
|US4829126 *||Apr 13, 1987||May 9, 1989||Toyo Contact Lens Co., Ltd.||High water-absorptive soft contact lens|
|US4833196 *||Jul 25, 1988||May 23, 1989||Ciba-Geigy Corporation||Particulate hydroperoxidized poly-N-vinyl lactam, its preparation and use thereof|
|US4931228 *||Apr 5, 1989||Jun 5, 1990||Coastvision||Method of manufacturing soft contact lens buttons|
|US5058207 *||Nov 15, 1990||Oct 22, 1991||Winfried Altinger||Viewing window for heat protective clothing|
|US5094609 *||Apr 17, 1990||Mar 10, 1992||Vistakon, Inc.||Chamber for hydrating contact lenses|
|US5318853 *||Jul 22, 1992||Jun 7, 1994||Resikast Corporation||Adhesive polyester prepolymer which does not etch polycarbonate sheets, and method of preparing same|
|US5445890 *||Jun 6, 1994||Aug 29, 1995||Resikast Corporation||Bullet resistant glass/glass, glass/plastic, and plastic/plastic laminate composites|
|US6642333 *||Mar 24, 2003||Nov 4, 2003||Nippon Shokubai Co., Ltd.||Vinylpyrrolidone (co)polymer|
|US7187859||Dec 6, 2004||Mar 6, 2007||Paragon Vision Sciences, Inc.||Method and apparatus for manufacturing contact lenses|
|US7618142||Jun 12, 2007||Nov 17, 2009||Cooper Vision International Holding Company, Lp||Contact lenses|
|US7625084||Mar 20, 2008||Dec 1, 2009||Coopervision International Holding Company, Lp||Contact lens|
|US7628485||Dec 12, 2006||Dec 8, 2009||Coopervision International Holding Company, Lp||Contact lens having a uniform horizontal thickness profile|
|US7841716||Feb 10, 2006||Nov 30, 2010||Johnson & Johnson Vision Care, Inc.||Comfortable ophthalmic device and methods of its production|
|US8361355 *||Jan 20, 2011||Jan 29, 2013||Johnson & Johnson Vision Care, Inc.||Preparation of antimicrobial contact lenses with reduced haze using swelling agents|
|US8696115||Oct 4, 2010||Apr 15, 2014||Johnson & Johnson Vision Care, Inc.||Comfortable ophthalmic device and methods of its production|
|US8865681||Nov 14, 2007||Oct 21, 2014||Yissum Research Development Company of the Hebrew Unitersity of Jerusalem||Use of lipid conjugates in the treatment of diseases or disorders of the eye|
|US9052529||Mar 15, 2013||Jun 9, 2015||Johnson & Johnson Vision Care, Inc.||Comfortable ophthalmic device and methods of its production|
|US20040170666 *||May 14, 2002||Sep 2, 2004||Richard Keates||Eye coverings|
|US20060117919 *||Dec 6, 2004||Jun 8, 2006||Hank Stute||Method and apparatus for manufacturing contact lenses|
|US20060120705 *||Dec 6, 2004||Jun 8, 2006||Hank Stute||Method and apparatus for manufacturing contact lenses|
|US20070010595 *||Feb 10, 2006||Jan 11, 2007||Mccabe Kevin P||Comfortable ophthalmic device and methods of its production|
|US20080113002 *||Nov 14, 2007||May 15, 2008||Saul Yedgar||Contact lens compositions|
|US20080113935 *||Nov 14, 2007||May 15, 2008||Saul Yedgar||Use of lipid conjugates in the treatment of diseases or disorders of the eye|
|US20090051060 *||Mar 26, 2008||Feb 26, 2009||Yongcheng Li||Preparation of antimicrobial contact lenses with reduced haze using swelling agents|
|US20110111120 *||May 12, 2011||Yongcheng Li||Preparation of antimicrobial contact lenses with reduced haze using swelling agents|
|US20110130555 *||May 11, 2010||Jun 2, 2011||Saul Yedgar||Lipid-polymer conjugates, their preparation and uses thereof|
|USRE36302 *||Nov 16, 1995||Sep 14, 1999||Johnson & Johnson Vision Products, Inc.||Chamber for hydrating contact lenses|
|DE2411895A1 *||Mar 12, 1974||Sep 19, 1974||American Optical Corp||Verfahren zum herstellen eines spannungsfreien hydroskopischen festen polymerisats fuer haftglaeser|
|DE2443147A1 *||Sep 10, 1974||Apr 17, 1975||Flow Pharma Inc||Verfahren zur reinigung von kunststoffgegenstaenden|
|DE2740545A1 *||Sep 6, 1977||Mar 16, 1978||American Optical Corp||Verfahren zum giessen von polymerenstaeben|
|EP0453232A2 *||Apr 16, 1991||Oct 23, 1991||JOHNSON & JOHNSON VISION PRODUCTS, INC.||Chamber for hydrating contact lenses|
|EP0686488A2 *||Jun 9, 1995||Dec 13, 1995||JOHNSON & JOHNSON VISION PRODUCTS, INC.||Automated method and apparatus for hydrating soft contact lenses|
|EP0740998A2 *||Apr 30, 1996||Nov 6, 1996||JOHNSON & JOHNSON VISION PRODUCTS, INC.||Automated method and apparatus for hydrating soft contact lenses|
|WO2000024568A2 *||Oct 20, 1999||May 4, 2000||Bausch & Lomb||Method and apparatus for curing contact lenses|
|U.S. Classification||264/1.36, 525/283, 134/42, 134/2, 264/2.6, 351/159.2, 351/159.73|
|International Classification||A61L15/44, G02C13/00, A61L15/22, G02C7/04, B29D11/00, C08F271/02, C08F269/00, G02B1/04|
|Cooperative Classification||B29D11/00865, B29D11/00067, B29D11/00134, G02B1/043, B29D11/00, C08F271/02|
|European Classification||C08F271/02, G02B1/04B2, B29D11/00K, B29D11/00, B29D11/00C4Y2, B29D11/00C4D|