EP0865615A1 - Methods of manufacturing contact lenses - Google Patents
Methods of manufacturing contact lensesInfo
- Publication number
- EP0865615A1 EP0865615A1 EP96939249A EP96939249A EP0865615A1 EP 0865615 A1 EP0865615 A1 EP 0865615A1 EP 96939249 A EP96939249 A EP 96939249A EP 96939249 A EP96939249 A EP 96939249A EP 0865615 A1 EP0865615 A1 EP 0865615A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lens
- oxygen
- contact lens
- polymerizable material
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/26—Mixtures of macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C39/00—Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor
- B29C39/22—Component parts, details or accessories; Auxiliary operations
- B29C39/42—Casting under special conditions, e.g. vacuum
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5003—Polyethers having heteroatoms other than oxygen having halogens
- C08G18/5015—Polyethers having heteroatoms other than oxygen having halogens having fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/61—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8108—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group
- C08G18/8116—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group esters of acrylic or alkylacrylic acid having only one isocyanate or isothiocyanate group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
- C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
- C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
- C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2011/00—Optical elements, e.g. lenses, prisms
- B29L2011/0016—Lenses
- B29L2011/0041—Contact lenses
Definitions
- This invention relates broadly to methods of forming polymeric articles (e.g. lenses) and polymeric materials, especially those useful in optic and ophthalmic arts.
- this invention relates to methods of forming polymeric materials useful in the manufacture of contact lenses.
- this invention relates to methods of manufacturing contact lenses having a high water, ion and gas permeability which are useful as extended-wear contact lenses.
- biocompatible depends on the particular application for which the polymer is designed.
- a biocompatible lens may be generally defined as one which will not substantially damage the surrounding ocular tissue and ocular fluid during the time period of contact.
- ophthalmically compatible more appropriately describes the biocompatibility requirements of ophthalmic lenses.
- One ophthalmic compatibility requirement for contact lenses is that the lens must allow oxygen to reach the cornea in an amount which is sufficient for long-term cornea! health.
- the contact lens must allow oxygen from the surrounding air to reach the cornea because the cornea does not receive oxygen from the blood supply like other tissue. If sufficient oxygen does not reach the cornea, corneal swelling occurs. Extended periods of oxygen deprivation causes the undesirable growth of blood vessels in the cornea.
- Soft contact lenses conform closely to the shape of the eye, so oxygen cannot easily circumvent the lens. Thus, soft contact lenses must allow oxygen to diffuse through the lens to reach the cornea.
- Another ophthalmic compatibility requirement for soft contact lenses is that the lens must not strongly adhere to the eye. Clearly, the consumer must be able to easily remove the lens from the eye for disinfecting, cleaning, or disposal.
- the lens must also be able to move on the eye in order to encourage tear flow between the lens and the eye. Tear flow between the lens and eye allows for debris, such as foreign particulates or dead epithelial cells, to be swept from beneath the lens and, ultimately, out of the tear fluid. Thus, a contact lens must not adhere to the eye so strongly that adequate movement of the lens on the eye is inhibited.
- RGP gas permeable
- HEMA 2-hydroxyethyl methacrylate
- polysiloxanes are typically highly lipophilic.
- the properties (e.g., lipophilicity, glass transition temperature, mechanical properties) of known polysiloxanes has resulted in contact lenses which adhere to the eye, inhibiting the necessary lens movement.
- polysiloxane lipophilicity promotes adhesion to the lens of lipids and proteins in the tear fluid, causing a haze which interferes with vision through the lens.
- European Patent Application No. 0 687 550 A2 describes a method of manufacu ⁇ ng contact lenses which requires degassing both concave (front surface) and convex (base curve surface) mold halves.
- This application states that the level of oxygen at the reactive monomer/mold interface must be controlled to approximately 300 times less than the concentration of oxygen in air (3x10 3 moles/liter). The reduction of oxygen in the molds is accomplished in order to achieve reduced defects and high speed, high volume manufacturing operations
- U.S. Patent No. 5,435,943 teaches a process for manufacturing an ophthalmic lens including a step of degassing monomer by drawing and maintaining a subsatmoshe ⁇ c pressure about the exterior of a tube through which the monomer is pumped.
- the objectives of the process include reducing the amount of nitrogen in the monomer as well as reducing the amount of oxygen in the monomer.
- PCT Application No. WO 96/11782 discloses a method of improving the surface characteristics of cast molded contact lenses This surface-altering method involves the removal of oxygen from the plastic mold pieces prior to casting the lenses.
- An object of this invention is to provide a method of manufacturing a contact lens having good on-eye movement while exhibiting sufficient oxygen permeability for extended wear periods of a week or more
- An object of the invention is to provide a method of forming a material having a balance of oxygen permeability, ion permeability, on-eye movement and tear exchange, all of which are sufficient for corneal health and wearer comfort during extended periods of continuous wear.
- One embodiment of the invention is a method of producing a contact lens having a balance of high oxygen transmissibility and good on-eye movement. The method includes the steps of:
- Another embodiment is a contact lens formed by the above-described process.
- One embodiment of the present invention is a method of forming an ophthaimically compatible, transparent lens suited to extended periods of continuous contact with ocular tissue and tear fluids.
- a particularly preferred embodiment of the invention is a method of forming an extended-wear vision correction lens suited for safe and comfortable long term wear without removal.
- an "ophthalmic lens” refers to lenses which are placed in intimate contact with the eye or tear fluid, such as contact lenses for vision correction (e.g., spherical, toric, bifocal), contact lenses for modification of eye color, ophthalmic drug delivery devices, ocular tissue protective devices (e.g., ophthalmic healing promoting lenses), and the like.
- a particularly preferred ophthalmic lens is an extended-wear contact lens, especially extended-wear contact lenses for vision correction.
- oxygen transmissibility of a lens is the rate at which oxygen will pass through a specific ophthalmic lens.
- Oxygen transmissibility, Dk t is conventionally expressed in units of barrers/mm, where t is the average thickness of the material [in units of mm] over the area being measured and "barrer" is defined as:
- Oxygen permeability is the rate at which oxygen will pass through a material. Oxygen permeability is conventionally expressed in units of barrers, where "barrer” is defined as:
- a “macromer”, as used herein, refers to a polymerizable material which has a molecular weight of at least about 800 grams/mol.
- the term “macromer”, as used herein, also encompasses oligomers.
- a “monomer”, as used herein refers to a polymerizable material which has a molecular weight of less than about 800 grams/mol.
- phase refers to a region of substantially uniform composition which is a distinct and physically separate portion of a heterogeneous polymeric material.
- phase does not imply that the material described is a chemically pure substance, but merely that certain bulk properties differ significantly from the properties of another phase within the material.
- an ionoperm phase refers to a region composed of essentially only ionoperm polymer (and water, when hydrated), while an oxyperm phase refers to a region composed of essentially only oxyperm polymer.
- a “continuous phase”, as used herein, refers to a region of substantially uniform composition which forms a continuous pathway from one surface of an article to another surface of an article.
- Co-continuous phases refers to at least two regions, each of substantially uniform composition which differs from the other, and each of which forms a continuous pathway from one surface of an article to another surface of an article.
- an ophthalmic lens having co-continuous phases of oxyperm polymer and ionoperm polymer will have two continuous pathways or sets of continuous pathways extending from the inner surface of the lens to the outer surface of the lens.
- Morphology refers to the structure and relationship of the phases of a material.
- Optically compatible refers to a material or surface of a material which may be in intimate contact with the ocular environment for an extended period of time without significantly damaging the ocular environment and without significant user discomfort.
- an ophthalmically compatible contact lens will not produce significant corneal swelling, will adequately move on the eye with blinking to promote adequate tear exchange, will not have substantial amounts of lipid adsorption, and will not cause substantial wearer discomfort during the prescribed period of wear.
- Optacular environment refers to ocular fluids (e.g., tear fluid) and ocular tissue (e.g., the cornea) which may come into intimate contact with a contact lens used for vision correction, drug delivery, wound healing, eye color modification, or other ophthalmic applications.
- ocular fluids e.g., tear fluid
- ocular tissue e.g., the cornea
- Hydrophilic describes a material or portion thereof which will more readily associate with water than with lipids.
- a “hydrophilic surface” refers to a surface which is more hydrophilic and lipophobic than the bulk or core material of an article.
- an ophthalmic lens having a hydrophilic surface describes a lens having a core material having a certain hydrophilicity surrounded, at least in part, by a surface which is more hydrophilic than the core.
- the "outer surface” of a lens refers to the surface of the lens which faces away from the eye during wear.
- the outer surface which is typically substantially convex, may also be referred to as the front curve of the lens.
- the “inner surface” of a lens refers to the surface of the lens which faces towards the eye during wear.
- the inner surface which is typically substantially concave, may also be referred to as the base curve of the lens.
- 'TRIS refers to 3-methacryloxypropylths(trimethylsiloxy) silane, which is represented by CAS No. 17096-07-0.
- 'TRIS also includes dimers of 3- methacryloxypropyltris(trimethylsiloxy) silane.
- Molecular weight of a polymeric material refers to the number-average molecular weight unless otherwise specifically noted or unless testing conditions indicate otherwise.
- Polymerization refers to both crosslinking and conventional polymerization processes (e.g., free radical polymerization). Polymerization includes all polymerization and/or crosslinking processes regardless of the means by which the polymerization is initiated or terminated.
- the removal of oxygen from the process of copolymerizing a siloxane- and/or fluorine- containing acrylate macromer with one or more acrylamide or pyrrolidone monomers results in a contact lens having the extraordinary balance of characteristics necessary for a true extended wear lens, namely high oxygen transmissibility and good on-eye movement.
- the siloxane- and/or fluorine-containing acrylate macromers include a wide range of materials which may be polymerized to form a polymer displaying a relatively high oxygen diffusion rate therethrough. In addition, these materials must be relatively ophthalmically compatible after polymerization. Macromers having dialkyl siloxane groups, especially dimethyl siloxanes, are particularly preferred. These macromers are broadly referred to as poly(dimethyl siloxanes) (also, PDMS). Examples of suitable siloxane-containing macromers include, without limitation thereto, the Materials A, B, and C as described hereinafter.
- the oxygen transmissibility (Dk t) of the lens is preferably at least 70 barrers/mm, more preferably at least 75 barrers/mm, and most preferably at least 87 barrers/mm.
- the lens center thickness is typically more than about 30 microns, preferably about 30 to about 200 microns, more preferably about 40 to about 150 microns, even more preferably about 50 to about 120 microns, and most preferably about 60 to about 100 microns.
- the oxygen transmissibility of the extended-wear lens from the outer surface to the inner surface must be sufficient to prevent any substantial corneal swelling during the period of extended wear. It is known that the cornea swells approximately 3% to 4% during overnight periods of sleep when the eyelids are closed, as a result of oxygen deprivation. It is also known that wearing a typical contact lens, such as ACUVUE (Johnson & Johnson), for a period of about 8 hours (overnight wear) causes corneal swelling of about 11%. However, a preferred extended-wear contact lens will produce, after wear of about 24 hours, including normal sleep periods, corneal swelling of less than about 8%, more preferably less than about 6%, and most preferably less than about 4%.
- ACUVUE Johnson & Johnson
- a preferred extended-wear contact lens will produce, after wear of about 7 days, including normal sleep periods, corneal swelling of less than about 10%, more preferably less than about 7%, and most preferably less than about 5%.
- the extended-wear lens must have oxyperm polymer in an amount sufficient to produce oxygen diffusion pathways from the outer surface to the inner surface of the lens which are sufficient to yield the above properties relating to corneal swelling.
- the extended-wear lens has a continuous phase of oxyperm polymer extending from the outer surface to the inner surface of the lens.
- the acrylamides and pyrrolidones include a wide range of materials which may be copolymerized with the siloxane- and/or fluorine-containing acrylate macromer to form a polymer displaying a relatively high ion diffusion rate therethrough. In addition, these materials must be relatively ophthalmically compatible after polymerization. These materials include, without limitation thereto, acrylamide, methacrylamide, and dimethyiacrylamide; N- vinyl pyrrolidones such as N-vinyl-2-pyrrolidone; and the like and mixtures thereof. Other acrylamides and pyrrolidones are disclosed in the specific embodiments of Materials A-C, described below.
- the ratios of siloxane- and/or fluorine-containing acrylate macromers to acrylamide or pyrrolidone monomers may vary substantially, depending on the selected balance of oxygen permeability and ion permeability for the chosen end-use of the molded polymeric article.
- the volumetric ratio of siloxane- and/or fluorine-containing acrylate macromers to acrylamide or pyrrolidone monomers (including water) in the fully hydrated lens is about 40 to about 60 to about 60 to about 40.
- weight percentages based on the total weight of the lens, will be defined because weight percentages are more conveniently utilized in lens fab ⁇ cation.
- the ratio of macromer to monomer will be about 60 to about 85 weight percent siloxane- and/or fluorine-containing acrylate macromers and about 15 to about 40 weight percent acrylamide or pyrrolidone monomers in the prepolymerization mixture, based on total polymerizable material weight. More preferably, the prepolymerization mixture will contain about 70 to about 82 weight percent siloxane- and/or fluorine-containing acrylate macromers and about 18 to about 30 weight percent acrylamide or pyrrolidone monomers, based on total polymerizable material weight.
- a wide variety of additional polymerizable materials may be included in the mixture prior to polymerization.
- Cross-linking agents such as ethylene glycol dimethacrylate (EGDMA)
- EGDMA ethylene glycol dimethacrylate
- Antimicrobial polymerizable materials such as poly(quaternary ammonium) salts may be added to inhibit microbial growth on the lens material.
- additional ionoperm monomers or macromers and oxyperm polymerizable materials may be added to adjust the oxygen permeability and ion permeability of the final molded article.
- An especially advantageous polymerizable material is TRIS, which may act both to increase oxygen permeability and to improve the modulus of elasticity.
- a siioxane-containing monomer having a carbon chain length of less than 20 carbon atoms preferably TRIS.
- a preferred polymerizable material comprises:
- a further preferred prepolymerization mixture will include (a) about 30 to 60 weight percent siloxane- and/or fluorine-containing acrylate macromers , (b) about 20 to 40 weight percent acrylamide or pyrrolidone monomers, and (c) about 1 to 35 weight percent TRIS, based on the total lens weight. More preferably, the amount of TRIS is about 10 to 33 weight percent, based on the total prepolymerization mixture weight.
- the prepolymerization mixture includes less than about 5 weight percent cross-linking agent, based on the total prepolymerization mixture weight. More preferably, the prepolymerization mixture includes less than about 2 weight percent cross ⁇ linking agent, based on the total prepolymerization mixture weight. Even more preferably, the prepolymerization mixture includes substantially no cross-linking agent. In a particularly preferred embodiment, the prepolymerization mixture includes no added cross-linking agent.
- the lens material is that the lens allow a high visible light transmission from the outer to inner surface of the lens.
- a lens morphology which includes large phase separated regions will reduce visible light transmission and cause substantial undesirable image distortion, thereby destroying the value of the lens as a vision correction device.
- the lens must have a morphology which allows at least about 80%, more preferably about 90%, visible light transmission and does not produce any significant undesirable image distortion.
- the lens material has at least two phases: the phases including at least one oxyperm phase (i.e. a phase having a high oxygen transmissibility) and at least one ionoperm phase (i.e. a phase having a high ion permeability). While there may be two distinct phases, it is believed that there may be a transition phase, or interphase, in which the material composition and the material properties are a blend of those of the oxyperm and ionoperm materials.
- the glass transition temperature (Tg) of the oxyperm phase is less than about -115° Celsius.
- Oxygen will diffuse predominantly through the oxyperm polymer, while the ionoperm polymer provides a higher barrier to oxygen diffusion.
- ions will diffuse well through the ionoperm polymer, but the oxyperm polymer provides a higher resistance to ion diffusion.
- one homogeneous oxyperm/ionoperm phase will provide undesirable resistance to both oxygen and ion diffusion, while two separate oxyperm and ionoperm phases will provide low resistance pathways for transmission of both oxygen and ions or water.
- the ideal extended-wear lens has a pathway or series of pathways from the outer surface to the inner surface for transmission of oxygen therethrough, and an analogous continuous pathway or series of pathways for transmission of water or ions therethrough.
- the lens has two co-continuous phases, one an oxyperm phase and the other an ionoperm phase, allowing for permeation of water or ions and oxygen between the front and base curves of the lens.
- the preferred bulk water content of the hydrated lens will be a function of the lens material properties.
- the material properties are dependent on the prepolymerization macromers and monomers and polymerization conditions. Accordingly, while general ranges for bulk water content are offered for a better understanding of the invention, the invention is not generally limited to specific bulk water contents.
- One method of measuring the water content of a lens formed in accordance with the present invention is as follows. First the lens is thoroughly hydrated in a physiological saline solution, such that the water in the lens is in equilibrium with the surrounding water. Next the lens is gently blotted between two lint-free blotting cloths to remove surface moisture. The lens is quickly placed on an aluminum weighing pan and the first wet weight, W 1( is measured. Next, the aluminum pan with lens is placed in a oven at 36°C for a period of at least 24 hours. After heat treating, the pan with lens is removed, placed in a desiccator, and allowed to cool to room temperature (about 22°C).
- the pan with lens is weighed again to determine the dry weight, W d .
- the lens is re-equilibrated in physiological saline solution and a second wet weight W 2 is determined thereon.
- the wet weights (Wi and W 2 ) are averaged to yield an average wet weight, W w .
- the bulk water content is determined by the following equation:
- Percent water content (W w - W d ) / W w x 100
- a preferred lens bulk water content is less than about 32 weight percent. More preferably, the lens has a water content of about 10 to 30 weight percent, based on the total lens weight. A particularly preferred lens water content is about 15 to about 25 weight percent.
- the ion permeability through the lens correlates well with on-eye movement, and furthermore, that the presence of oxygen in polymerization of certain material reduces ion permeability.
- on-eye movement of the lens is required to ensure good tear exchange, and ultimately, to ensure good corneal health. While the invention is not bound by theory presented herein, it may be useful to discuss some theory for a better understanding of ways to practice the invention.
- water permeability is an exceptionally important feature for an extended- wear lens which includes oxyperm polymers such as those disclosed herein.
- Siioxane- containing oxyperm materials tend to adhere strongly to the eye, thereby stopping on-eye movement.
- the ability to pass water through the lens is believed to allow a siioxane- containing polymeric lens to move on the eye, where the movement occurs via forces exerted by water being squeezed out of the lens.
- the water permeability of the lens is also believed important in replenishing lens water content once pressure is removed. Further, the permeability of ions is believed to be directly proportional to the permeability of water. Thus, ion permeability is a predictor of on-eye movement.
- the present innovative extended-wear contact lenses provide a balance between the relatively high oxygen permeability (and associated high binding capacity) of oxyperm materials with the low binding capacity (high on-eye movement) of ionoperm materials. It is believed that this is accomplished by providing a plurality of continuous ion transmission pathways for ion and water movement through the lens.
- ions may move through the lens via these ion pathways by a number of means.
- ions may diffuse through the lens because of concentration differences from one surface to another.
- Ions may also be forced through the ion pathways by the mechanical action of blinking, with the concomittent compression forces on the lens essentially squeezing water out of the lens.
- the charge nature of the surfaces may provide an electromotive force which drives ion permeation through the lens. At times, one of these driving forces may be larger than the others, while at other times the relative magnitude may reverse.
- the water permeability of a lens may be determined from the rate of water permeation through the lens, from one surface to another surface.
- the water permeability of a lens may be determined by positioning a lens between two reservoirs holding solutions having known, and different, initial concentrations of radiolabeled water (e.g., tritiated water), and then measuring concentration of radiolabeled water in the "receiving" reservoir (the reservoir towards which the net flow of radiolabeled water is positive) as a function of time.
- radiolabeled water e.g., tritiated water
- the relative ion permeability of a lens may be determined from the rate of ion permeation through the lens, from one surface to another surface.
- the rate of ion permeation may be determined by positioning a lens between two reservoirs holding solutions having known, and different, initial ion concentrations, and then measuring conductivity in the "receiving" reservoir (the reservoir towards which the net flow of ions is positive) as a function of time.
- concentration of ions such as sodium
- Ions are believed to be transmitted through a lens, from inner to outer surfaces and vice versa, primarily by the diffusion of ions through water pathways in the lens. Ion permeability through a lens is believed to be directly proportional to water permeability through a lens.
- lonoflux Technique is a preferred method for determining the ion permeability of a lens. This technique may be used to determine the likelihood of adequate on-eye movement.
- the "lonoflux Technique” involves the use of a conductometer (LF 2000/C, catalog no. 300105,ticianlich-Technische psychologyen GmbH (WTW), Germany), an electrode equipped with a temperature sensor (LR 01 T, catalog no. 302 520, WTW), a donor chamber containing a salt solution, a receiving chamber containing about 60 ml of deionized water, a stir bar and a thermostat.
- the donor chamber is specially designed for sealing a contact lens thereto, so that the donor solution does not pass around the lens (i.e., ions may only pass through the lens).
- the donor chamber is composed of a glass tube which is threaded at the end which is immersed in the receiving solution.
- the glass tube includes a centrally located hole of about 9 mm in diameter.
- a lid which is threaded to mate with the glass tube, holds a lens-retaining member which includes a centrally located hole of about 8 mm in diameter.
- the lens-retaining member includes a male portion adapted to mate with and seal the edges of the inner (concave) surface of a lens and a female portion adapted to mate with and seal the edges of the outer (convex) surface of a lens.
- the lens to be measured is placed in the lens-retaining member, between the male and female portions.
- the male and female portions include flexible sealing rings which are positioned between the lens and the respective male or female portion.
- the lens-retaining member is placed in the threaded lid.
- the lid is screwed onto the glass tube to define the donor chamber.
- the donor chamber is filled with 16 ml of 0.1 molar NaCl solution.
- the receiving chamber is filled with 60 ml of deionized water.
- the leads of the conductivity meter are immersed in the deionized water of the receiving chamber and a stir bar is added to the receiving chamber.
- the receiving chamber is placed in a thermostat and the temperature is held at about 35°C. Finally, the donor chamber is immersed in the receiving chamber.
- A area of lens exposed [mm 2 ]
- An lonoflux Diffusion Coefficient of greater than about 6.4 x 10 "6 mm 2 /min is preferred for achieving sufficient on-eye movement. More preferably, the lonoflux Diffusion Coefficient is greater than about 2.6 x 10 mm /min, while most preferably, the lonoflux Diffusion Coefficient is greater than about 1.5 x 10 " * mm 2 /min. It must be emphasized that the lonoflux Diffusion Coefficient correlates with ion permeability through the lens, and thereby is a predictor of on-eye movement.
- lonoton Measurement Technique is another preferred method for determining the relative ion permeability of a lens.
- the technique is based on measurement of the diffusion of sodium chloride through a lens.
- the "lonoton Technique” involves the use of a pH meter (Beckman, VWR catalog no. BK123142), a VSC-1 Diffusion Cell Drive Console (Crown-Bio, Somerville, NJ), a DCB- 100B Diffusion Cell (Crown-Bio), and a 6 cm sodium ion-specific electrode (Microelectronics, Londonderry, NH, catalog no. MI-414P).
- the technique is not limited to the aforementioned instruments or materials; equivalent instruments or materials may be used.
- a contact lens is mounted onto an orifice of the DCB-100B cell chamber, the donor chamber.
- the connecting cell chamber (receptor chamber) is placed against the cell chamber containing the contact lens and tightly clamped on the clamp holder supplied with the VSC-1 Drive Console.
- a phosphate-buffered saline (PBS, Mediatech catalog no. 21-031-LV) is placed into the receptor side of the cell chamber. Stir bars are added to each cell chamber.
- the 6 cm electrode is placed into the PBS saline receptor side. After the electrode has equilibrated in the PBS saline, the pH meter is placed in the mV function to establish the 0 mV point.
- PBS which has been saturated with sodium chloride is added to the donor chamber.
- the millivolt signal is recorded at 5, 10, 15, 30, 60, 120, and 180 minute intervals.
- the millivolt signal is converted to a sodium ion concentration by a standard curve of sodium ion concentration vs. millivolt signal.
- the lonoton Ion Permeability Coefficient, P is then determined in accordance with the following equation:
- C(t) concentration of sodium ions at time t in the receiving cell
- C(0) initial concentration of sodium ions in donor cell
- A membrane area, i.e., lens area exposed to cells
- V volume of cell compartment (3.0 ml)
- d average lens thickness in the area exposed
- the average thickness of the lens in the exposed test area may be determined by averaging a number of readings, e.g., 10 readings, with a low-pressure thickness- measuring instrument, such as a Mitotoya micrometer VL-50, or equivalents thereof.
- the lonoton Ion Permeability Coefficient, P having units of cm 2 /second, may be determined from the slope of a plot of time (t) v. In( 1 - 2C(t)/C(0) ) x (-2At / Vd).
- lonoton Ion Permeability Coefficient, P of greater than about 0.2 x 10 "6 cm 2 /sec is preferred, while greater than about 0.3 x 10 "6 cm 2 /sec is more preferred and greater than about 0.4 x 10 '6 cm 2 /sec is most preferred. It must be emphasized that the lonoton Ion Permeability Coefficient correlates with ion permeability through the lens, and thereby is a predictor of on-eye movement.
- Hydrodell Water Permeability Technique The following technique, referred to herein as the "Hydrodell Technique", is a preferred method for determining the water permeability of a lens. This technique may be used to determine the likelihood of adequate on-eye movement.
- the Hydrodell Technique involves the measurement of the rate of transfer of the radiolabeled solutes THO ( 3 H-HO or tritiated water) and 14 C-glucose across the contact lens using a two-chamber apparatus. 14 C-glucose is used in this measurement technique to reveal any leak in the system during testing.
- the lens is mounted between chambers, which are stirred at a controllable rate. Chamber I contains a solution with a high concentration of labeled solute. Chamber II, the "receiving chamber", contains an identical solution but without the labeled solute. Samples of the solution in chambers I and II are taken at intervals over the test period. The radioactivity in the samples is measured. The permeability of the lens is calculated from the measured radioactivity, the sample times, the chamber volumes and the lens area exposed to the solutions. A more detailed description of the Hydrodell Technique follows.
- Dulbecco's phosphate buffered saline is prepared by first dissolving, sequentially, about 160 g sodium chloride (NaCl), about 4 grams potassium chloride (KCl), about 23 grams disodium hydrogen orthophosphate (Na 2 HP0 4 ), about 4 grams potassium dihydrogen orthophosphate (KH 2 PO ), and about 10 grams sodium azide in a liter of reverse-osmosis (MilliQ) water. Then, the pH is adjusted to about 7.3 by adding appropriate amounts of HCl. Finally, the buffer solution is diluted to 1 :20 (50 ml buffer solution with 950 mi reverse-osmosis water), and allowed to degas either in a screw-capped container ovemight or under vacuum.
- a Cold Glucose buffer solution is prepared by adding about 0.1 grams D-glucose to one liter of DPBS, followed by sterilization via filtration through a 0.2 ⁇ l millipore filter and storage at 4°C until use.
- the Chamber I solution is prepared by adding about 6 ⁇ l THO (TR53, 1.0 mCi/ml activity, available from Amersham Australia, located in North Ryde NSW Australia) and about 16 ⁇ l 14 C-glucose (in ethanol, available from Amersham Australia) to about 12 ml of the Cold Glucose buffer solution. Preferably, this solution is used within about 24 hours of preparation.
- the Chamber II solution is DPBS.
- the chambers have a volume sufficient to hold about 12 ml of solution during testing. While the exact shape of the chambers is not critical, both chambers have rectangular cross-sections for ease of construction.
- the chambers may be made from a variety of water-proof rigid materials, preferably clear (e.g., acrylic plates, FX Plastics, Marrickville NSW Australia) so that samples may be observed during testing.
- Each chamber has a circular aperture of about 7 mm diameter appropriate for mounting a lens between the chambers for contact with solutions held within the chambers.
- Some affixing means such as a set of mounting bolts, are necessary to securely affix one chamber to the other with the lens mounted in between.
- a test contact lens is mounted symmetrically over the aperture of Chamber II. Folds and wrinkles are manually removed from the lens. Chamber I is positioned adjacent the aperture and mounted lens of Chamber II, and the chambers are secured to one another using mounting bolts.
- the final sample time, t f is usually at about 50 minutes for high water content lenses and about 120 minutes for low water content lenses, although these times are not critical.
- one sample of about 1.0 ml volume is pipetted from Chamber II and one 1.0 ml aliquot of DPBS is added to Chamber II to restore the volume.
- the sample is placed into a plastic counting tube with about 4 ml Ultima GoldTM cocktail.
- one sample of about 1.0 ml volume is pipetted from Chamber II and one 1.0 ml aliquot of DPBS is added to Chamber II to restore the volume.
- Each sample is placed into a plastic counting tube with about 4 ml Ultima GoldTM cocktail.
- the activity of the samples are measured by liquid scintillation counting, or other appropriate technique.
- Liquid scintillation counting may be advantageously accomplished by using protocol number 6 for 3 H/ 1 C on a Tri-Carb Liquid Scintillation Analyzer (1900TR, available from Packard Instrument Co.).
- b t measured activity of blank sample in channel 1
- b 2 measured activity of blank sample in channel 2
- S'n measured activity of standard 3 H sample in channel 1
- S' 12 measured activity of standard 14 C sample in channel 2
- S' 2 measured activity of standard 3 H sample in channel 1
- S' 22 measured activity of standard 14 C sample in channel 2
- y ! measured activity of test sample (both 3 H and 14 C) in channel 1
- y 2 measured activity of test sample (both 3 H and 14 C) in channel 2
- Vn is the volume of Chamber II
- Cn(t 2 ) is the concentration of 3 H in Chamber II at time t 2
- cn(t ⁇ ) is the concentration of 3 H in Chamber II at time ti
- A is the area of lens exposure
- Ci is the average concentration of 3 H in Chamber I over the time period ti to t 2
- di is the average concentration of 3 H in Chamber II over the time period ti to t 2 .
- the ophthalmic lenses of one embodiment of the present invention have a Hydrodell Water Permeability Coefficient of greater than about 0.2 x 10 "6 cm 2 /sec.
- the ophthalmic lenses in a preferred embodiment of the invention have Hydrodell Water Permeability Coefficient of greater than about 0.3 x 10 "6 cm /sec.
- the ophthalmic lenses in a preferred embodiment of the invention have Hydrodell Water Permeability Coefficient of greater than about 0.4 x 10 "6 cm 2 /sec.
- the cornea receives oxygen primarily from the corneal surface which is exposed to the environment, in contrast to other tissues which receives oxygen from blood flow.
- an ophthalmic lens which may be worn on the eye for extended periods of time must allow sufficient oxygen to permeate through the lens to the cornea to sustain corneal health.
- One result of the cornea receiving an inadequate amount of oxygen is that the cornea will swell.
- the oxygen transmissibility of the present ophthalmic lenses is sufficient to prevent any clinically significant amount of corneal swelling from occurring.
- a preferred ophthalmic lens material will have an oxygen transmissibility, Dk/t, of at least 70 ( (ccmm 33 ooxxyyggeenn))((mmmm))//mmmm--ccmm 22 xx ((sseecc//mmmm HHgg)) xx 1100 ""99 oorr [[bbaarrrreenrs/mm], more preferably at least 75 barrers/mm, and most preferably at least 87 barrers/mm.
- the oxygen permeability of a lens and oxygen transmissibility of a lens material may be determined by the following technique.
- Oxygen fluxes (J) are measured at 34 C in a wet cell (i.e., gas streams are maintained at about 100% relative humidity) using a Dk1000 instrument (available from Applied Design and Development Co., Norcross, Georgia), or similar analytical instrument.
- the barometric pressure surrounding the system ⁇ measured' ' s measured.
- the thickness (t) of the lens in the area being exposed for testing is determined by measuring about 10 locations with a Mitotoya micrometer VL-50, or similar instrument, and averaging the measurements.
- the oxygen concentration in the nitrogen stream i.e., oxygen which diffuses through the lens
- the oxygen permeability of the lens material, D ⁇ is determined from the following formula:
- the oxygen transmissibility (D k /t) of the material may be calculated by dividing the oxygen permeability (D k ) by the average thickness (t) of the lens.
- the Material "A” macromer is defined by formula (l):
- each P 1 f independently of the others, is a free-radical-polymerizable group
- each Y, independently of the others, is -CONHCOO-, -CONHCONH-, -OCONHCO-, -NHCONHCO-, -NHCO-, -CONH-, -NHCONH-, -COO-, -OCO-, -NHCOO- or -OCONH-
- m and p, independently of one another, are 0 or 1
- each L, independently of the others, is a divalent radical of an organic compound having up to 20 carbon atoms
- each X, independently of the others is -NHCO-, -CONH-, -NHCONH-, -COO-, -OCO-,
- Q is a bivalent polymer fragment consisting of the segments:
- each Z independently of the others, is a divalent radical having up to 12 carbon atoms or Z is a bond;
- each E independently of the others, is -(OCH 2 CH 2 ) q -, where q has a value of from 0 to 2, and where the link -Z-E- represents the sequence -Z-(OCH 2 CH 2 ) q -; and k is 0 or 1 ;
- n is an integer from 5 to 100;
- Alk is alkylene having up to 20 carbon atoms
- radicals R i, R 2 , R 3 and R 4 independently of one another, are alkyl and
- radicals R i, R 2 , R 3 and R independently of one another, are alkenyl, aryl or cyanoalkyt;
- the number of segments (b) in the polymer fragment Q is preferably greater than or equal to the number of segments (a).
- the ratio between the number of segments (a) and (b) in the polymer fragment Q is preferably 3:4, 2:3, 1 :2 or 1 :1.
- the molar ratio between the number of segments (a) and (b) in the polymer fragment Q is more preferably 2:3, 1 :2 or 1 :1.
- the mean molecular weight of the polymer fragment Q is in the range of about 1000 to about 20000, preferably in the range of about 3000 to about 15000, particularly preferably in the range of about 5000 to about 12000.
- the total number of segments (a) and (b) in the polymer fragment Q is preferably in the range of 2 to about 11 , particularly preferably in the range of 2 to about 9, and in particular in the range of 2 to about 7.
- the smallest polymer unit Q is preferably composed of one perfluoro segment (a), one siloxane segment (b) and one segment (c).
- the polymer fragment Q is terminated at each end by a siloxane segment (b).
- compositions in a bivalent polymer fragment Q always correspond above and below to a mean statistical composition. This means that, for example, even individual block copolymer radicals containing identical recurring units are included, so long as the final mean statistical composition is as specified.
- X is preferably -NHCONH-, -NHCOO- or -OCONH-, particularly preferably -NHCOO- or -OCONH-.
- the X 2 -R-X 2 segment is preferably a radical derived from a diisocyanate, where each X 2 , independently of the other, is -NHCONH-, -NHCOO- or -OCONH-, in particular -NHCOO- or -OCONH-.
- Z is preferably a bond, lower alkylene or -CONH-arylene, in which the -CO- moiety is linked to a CF 2 group.
- Z is particularly preferably lower alkylene, in particular methylene.
- q is preferably 0, 1 , 1.5 or 2, particularly preferably 0 or 1.5.
- the perfluoroalkoxy units OCF 2 and OCF 2 CF 2 with the indices x and y in segment (a) can either have a random distribution or be in the form of blocks in a chain.
- the sum of the indices x+y is preferably a number in the range of 10 to 25, particularly preferably of 10 to 15.
- the ratio x:y is preferably in the range of 0.5 to 1.5, in particular in the range of 0.7 to 1.1.
- a free-radical-polymerizable group P i is, for example, alkenyl, alkenylaryl or alkenylarylenealkyl having up to 20 carbon atoms.
- alkenyl are vinyl, allyl, 1-propen-2-yl, 1-buten-2-, -3- and -4-yl, 2-buten-3-yl, and the isomers of pentenyl, hexenyl, octenyl, decenyl and undecenyl.
- alkenylaryl are vinylphenyl, vinylnaphthyl or allylphenyl.
- An example of alkenylarylenealkyl is o-, m-, or p-vinylbenzyl.
- Pi is preferably alkenyl or alkenylaryl having up to 12 carbon atoms, particularly preferably alkenyl having up to 8 carbon atoms, in particular alkenyl having up to 4 carbon atoms.
- Y is preferably -COO-, -OCO-, -NHCONH-, -NHCOO-, -OCONH-, -NHCO- or -CONH-, parti ⁇ cularly preferably -COO-, -OCO-, NHCO- or -CONH-, and in particular, -COO- or -OCO-.
- the indices, m and p are not simultaneously zero. If p is zero, m is preferably 1.
- L is preferably alkylene, arylene, a saturated bivalent cycloaliphatic group having 6 to 20 carbon atoms, arylenealkylene, alkylenearylene, alkylenearylenealkylene or arylenealkylenearylene.
- L is a divalent radical having up to 12 carbon atoms, particularly preferably a divalent radical having up to 8 carbon atoms.
- L is furthermore alkylene or arylene having up to 12 carbon atoms.
- a particularly preferred embodiment of L is lower alkylene, in particular lower alkylene having up to 4 carbon atoms.
- the divalent radical R is, for example, alkylene, arylene, alkylenearylene, arylenealkylene or arylenealkylenearylene having up to 20 carbon atoms, a saturated bivalent cycloaliphatic group having 6 to 20 carbon atoms or cycloalkylenealkylenecycloalkylene having 7 to 20 carbon atoms.
- R is alkylene, arylene, alkylenearylene, arylenealkylene or arylenealkylenearylene having up to 14 carbon atoms or a saturated divalent cycloaliphatic group having 6 to 14 carbon atoms. In a particularly preferred embodiment, R is alkylene or arylene having up to 12 carbon atoms or a saturated bivalent cycloaliphatic group having 6 to 14 carbon atoms.
- R is alkylene or arylene having up to 10 carbon atoms or a saturated bivalent cycloaliphatic group having 6 to 10 carbon atoms.
- n is an integer from 5 to 70, particularly preferably 10 to 50, in particular 14 to 28.
- R 1t R 2 , R 3 and R are, independently of one another, lower alkyl having up to 8 carbon atoms, particularly preferably lower alkyl having up to 4carbon atoms, especially lower alkyl having up to 2 carbon atoms.
- R R 2 , R 3 and R 4 is methyl.
- radicals R 1 , R 2 , R 3 and R are, independently of one another, lower alkenyl, unsubstituted or lower alkyl- or lower alkoxy-substituted phenyl or cyano(lower alkyl).
- Arylene is preferably phenylene or naphthylene, which is unsubstituted or substituted by lower alkyl or lower alkoxy, in particular 1 ,3-phenylene, 1 ,4-phenylene or methyl-1 ,4- phenylene, 1 ,5-naphthylene or 1 ,8-naphthylene.
- Aryl is a carbocyclic aromatic radical which is unsubstituted or substituted preferably by lower alkyl or lower alkoxy. Examples are phenyl, tolyl, xylyl, methoxyphenyl, t- butoxyphenyl, naphthyl and phenanthryl.
- a saturated bivalent cycloaliphatic group is preferably cycloalkylene, for example cyclohexylene or cyclohexylene(lower alkylene), for example cyclohexylenemethylene, which is unsubstituted or substituted by one or more lower alkyl groups, for example methyi groups, for example trimethylcyclohexylenemethylene, for example the bivalent isophorone radical.
- radicals and compounds denotes, in particular, radicals or compounds having up to 8 carbon atoms, preferably having up to 4 carbon atoms.
- Lower alkyl has, in particular, up to 8 carbon atoms, preferably up to 4 carbon atoms, and is, for example, methyl, ethyl, propyl, butyl, tert-butyl, pentyl, hexyl or isohexyl.
- Alkylene has up to 12 carbon atoms and can be straight-chain or branched. Suitable examples are decylene, octylene, hexylene, pentylene, butylene, propylene, ethylene, methylene, 2-propylene, 2-butylene, 3-pentylene, and the like.
- Lower alkylene is alkylene having up to 8 carbon atoms, particularly preferably up to 4 carbon atoms. Particularly preferred meanings of lower alkylene are propylene, ethylene and methylene.
- the arylene unit in alkylenearylene or arylenealkylene is preferably phenylene, unsubstituted or substituted by lower alkyl or lower alkoxy, and the alkylene unit therein is preferably lower alkylene, such as methylene or ethylene, in particular methylene. These radicals are therefore preferably phenylenemethylene or methylenephenylene.
- Lower alkoxy has, in particular, up to 8 carbon atoms, preferably up to 4 carbon atoms, and is, for example, methoxy, ethoxy, propoxy, butoxy, tert-butoxy or hexyloxy.
- Arylenealkylenearylene is preferably phenylene(lower alkylene)phenylene having up to 8, in particular up to 4, carbon atoms in the alkylene unit, for example phenyleneethylenephenylene or phenylenemethylenephenylene.
- the macromers of the formula (I) can be prepared by processes known per se, for example as follows:
- X 3 is -OH, -NH 2 , -COOH, -COCI, -NCO or -COOR 5
- -COOR 5 is generally an activated ester in which R 5 is alkyl or aryl which is unsubstituted or substituted by halogen or cyano, and the variables Z, E, k, x and y are as defined above, is preferably reacted with two equivalents of a bifunctional radical of formula (V):
- R is as defined above and X is a functional radical which is coreactive with an X 3 and is preferably -OH-, -NH 2 , COOH, -COCI, -COOR 5 or -NCO; in the presence or absence of a suitable catalyst, where the reaction of X 3 with X gives a group X 2 ; after which a reactive derivative of formula (VI):
- Y 2 is a functional radical which is coreactive with X 3 and is preferably -OH, -NH 2 , -COOH, -COCI, -COOR 5 , -CONCO or -NCO, and the variables are as defined above, and in which Xi is formed from the reaction of X 3 with X 4 and Y is formed from the reaction of Y 2 with X 3 .
- Fomblin derivatives of the formula (IV) are commercially available, including, for example, Fomblin ZDISOC, in which the radical -Z-X 3 in the formula (IV) is CONH-C 6 H 3 (CH 3 )-NCO; Fomblin ZDEAL, in which the radical Z-X 3 in the formula (IV) is -COOR ; and Fomblin ZDIAC, in which the radical -Z-X 3 in the formula (IV) is -COOH.
- Bifunctional radicals having a substitution pattern as per formula (V) exist in large numbers and are commercially available. Examples include, without limitation thereto: diisocyanates, such as isophorone diisocyanate and 2,2,4-tr ⁇ methylhexane 1 ,6-d ⁇ socyanate; diols, such as glycol and cyclohexane-1 ,2-d ⁇ ol; dicarboxylic acids, such as adipic acid and maleic acid; diamines, such as ethylenediamine and hexamethylenediamine, diesters, such as diethyl phthalate and dibutyl malonate; derivatives containing various functional groups, such as 2- aminoethanol, monomethyl malonate, glycolic acid, salicylic acid, glycine and glycine methyl ester.
- diisocyanates such as isophorone diisocyanate and 2,2,4-tr ⁇ methylhexane 1 ,6-d ⁇ socyanate
- diols
- bifunctional derivatives of the formula (V) which have different reactivities irrespective of the nature of their functional radicals 4 .
- this is achieved, for example, through different steric requirements in the direct vicinity of a radical X 4 .
- examples thereof are isophorone diisocyanate, 2,2,4- tnmethylhexane 1 ,6-d ⁇ socyanate and toluene 2,4-d ⁇ socyanate.
- the advantage of using bifunctional derivatives of formula (V) of different reactivity is that the chain length of polymer Q (number of segments (a), (b) and (c)) is easily adjustable and controllable.
- ⁇ , ⁇ -subst ⁇ tuted siloxanes of formula (VII) are likewise commercially available, for example ⁇ , ⁇ -hydroxypropyl-terminated polydimethylsiloxane KF6001 from Shin-Etsu.
- the novel compounds can be prepared in the presence or absence of a solvent. It is advantageous to use a substantially inert solvent, i.e., one which does not participate in the reaction Suitable examples thereof are ethers, such as tetrahydrofuran (THF), diethyl ether, diethylene glycol dimethyl ether or dioxane, halogenated hydrocarbons, such as chloroform or methylene chloride, bipolar aprotic solvents, such as acetonitrile, acetone, dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), hydrocarbons, such as hexane, petroleum ether, toluene or xylene, and furthermore pyridine or N-methylmorphoiine.
- ethers such as tetrahydrofuran (THF), diethyl ether, diethylene glycol dimethyl ether or dioxane
- halogenated hydrocarbons such as chloroform or methylene chloride
- the reactants are advantageously employed in stoichiometric amounts.
- the reaction temperature can be, for example, from -30 e C to 150°C, preferably from 0 s to room temperature.
- the reaction times are in the range of about 15 minutes to 7 days, preferably about 12 hours. If necessary, the reaction is carried out under argon or nitrogen as protective gas.
- a suitable catalyst for example, dibutyltin dilaurate (DBTDL), is advantageously added.
- DBTDL dibutyltin dilaurate
- the present Material "A” furthermore relates to a polymer comprising a product of the polymerization of at least one compound of formula (I) as defined above and, if desired, at least one vinylic comonomer (a).
- the proportion by weight of a compound of formula (I) is in the range of 100 to 0.5%, in particular in the range of 80 to 10%, preferably in the range of 70 to 30%, based on the total polymer.
- comonomer (a) is absent and the polymer is a homopolymer.
- a comonomer (a) present in the novel polymer can be hydrophilic or hydrophobic or a mixture thereof. Suitable comonomers are, in particular, those which are usually used in the production of contact lenses and biomedical materials.
- a hydrophobic comonomer (a) is taken to mean a monomer which typically gives a homopolymer which is insoluble in water and can absorb less than 10% by weight of water.
- a hydrophilic comonomer (a) is taken to mean a monomer which typically gives a homopolymer which is soluble in water or can absorb at least 10% by weight of water.
- Suitable hydrophobic comonomers (a) are, without limitation thereto, C rC ⁇ ⁇ alkyl and C 3 -C 18 cycloalkyl acrylates and methacrylates, C 3 -C ⁇ ealkylacrylamides and -methacrylamides, acrylonitrile, methacrylonitrile, vinyl C ⁇ -C ⁇ 8 alkanoates, C 2 -C ⁇ 8 alkenes, C 2 -C ⁇ 8 haloalkenes, styrene, (lower alkyl)styrene, lower alkyl vinyl ethers, C 2 -C ⁇ 0 perfluoroalkyl acrylates and methacrylates and correspondingly partially fluorinated acrylates and methacrylates, C 3 -C ⁇ 2 perfluoroalkylethyl- thiocarbonylaminoethyl acrylates and methacrylates, acryloxy- and methacryloxyalkyl- siloxanes, N
- hydrophobic comonomers (a) are methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl acrylate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, styrene, chloroprene, vinyl chloride, vinylidene chloride, acrylonitrile, 1-butene, butadiene, methacrylonitrile, vinyltoluene, vinyl ethyl ether, perfluorohexylethylthiocarbonylaminoethyl methacrylate, isobornyl methacrylate, trifluoroethyl methacrylate, hexafluoroisopropyl methacrylate, hexa
- hydrophobic comonomers (a) are methyl methacrylate, TRIS and acrylonitrile.
- Suitable hydrophilic comonomers (a) are, without this being an exhaustive list, hydroxyl- substituted lower alkyl acrylates and methacrylates, acrylamide, methacrylamide, (lower alkyl)acrylamides and -methacrylamides, ethoxylated acrylates and methacrylates, hydroxyl- substituted (lower alkyl)acrylamides and -methacrylamides, hydroxyl-substituted lower alkyl vinyl ethers, sodium vinylsulfonate, sodium styrenesulfonate, 2-acrylamido-2- methylpropanesulfonic acid, N-vinylpyrrole, N-vinyl-2-pyrrolidone, 2-vinyloxazoline, 2-vinyl- 4,4'-dialkyloxazolin-5-one, 2- and 4-vinylpyridine, vinylically unsaturated carboxylic acids having a total of 3 to 5 carbon atoms, amino(lower alkyl)- (where
- hydrophilic comonomers (a) are hydroxyethyl methacrylate (HEMA), hydroxyethyl acrylate, hydroxypropyl acrylate, trimethylammonium 2-hydroxy propylmethacrylate hydrochloride (Blemer® QA, for example from Nippon Oil), dimethylaminoethyl methacrylate (DMAEMA), dimethylaminoethylmethacrylamide, acrylamide, methacrylamide, N,N-dimethylacrylamide (DMA), allyl alcohol, vinylpyridine, glycerol methacrylate, N-(1 ,1-dimethyl-3-oxobutyl)acrylamide, N-vinyl-2-pyrrolidone (NVP), acrylic acid, methacrylic acid and the like.
- HEMA hydroxyethyl methacrylate
- DMAEMA dimethylaminoethyl methacrylate
- DMA dimethylaminoethylmethacrylamide
- Preferred hydrophilic comonomers (a) are trimethylammonium 2-hydroxy propylmethacrylate hydrochloride, 2-hydroxyethyl methacrylate, dimethylaminoethyl methacrylate, trimethylammonium 2-hydroxypropylmethacrylate hydrochloride, N,N- dimethylacrylamide and N-vinyl-2-pyrrolidone.
- novel polymers are synthesized in a manner known per se from the corresponding monomers (the term monomer here also including a macromer according to the definition of the formula (I)) by a polymerization reaction customary to the person skilled in the art.
- a mixture of the abovementioned monomers is warmed with addition of a free- radical former.
- free-radical formers are azoisobutyronitrile (AIBN), potassium peroxodisulfate, dibenzoyl peroxide, hydrogen peroxide and sodium percarbonate. If, for example, said compounds are warmed, free radicals form with homolysis, and can then initiate, for example, a polymerization.
- a polymerization reaction can particularly preferably be carried out using a photoinitiator.
- photoinitiator which can initiate free-radical polymerization and/or crosslinking by using light.
- suitable photoinitiators are, in particular, benzoin methyl ether, 1-hydroxycyclohexylphenyl ketone, Darocur and Irgacur products, preferably Darocur® 1173 and Irgacur® 2959.
- reactive photoinitiators which can be incorporated, for example, into a macromer, or can be used as a specific comonomer (a).
- the photopolymerization can then be initiated by actinic radiation, for example light, in particular UV light having a suitable wavelength.
- actinic radiation for example light, in particular UV light having a suitable wavelength.
- the spectral requirements can, if necessary, be controlled appropriately by addition of suitable photosensitizers.
- a polymerization can be carried out in the presence or absence of a solvent.
- Suitable solvents are in principle all solvents which dissolve the monomers used, for example water, alcohols, such as lower alkanols, for example ethanol or methanol, furthermore carboxamides, such as dimethylformamide, dipolar aprotic solvents, such as dimethyl sulfoxide or methyl ethyl ketone, ketones, for example acetone or cyclohexanone, hydrocarbons, for example toluene, ethers, for example THF, dimethoxyethane or dioxane, halogenated hydrocarbons, for example trichloroethane, and also mixtures of suitable solvents, for example mixtures of water and an alcohol, for example a water/ethanol or water/methanol mixture.
- a polymer network can, if desired, be reinforced by addition of a crosslinking agent, for example a polyunsaturated comonomer (b).
- a crosslinking agent for example a polyunsaturated comonomer (b).
- the term crosslinked polymers is used.
- the invention therefore, furthermore relates to a crosslinked polymer comprising the product of the polymerization of a macromer of the formula (I), if desired with at least one vinylic comonomer (a) and with at least one comonomer (b).
- Examples of typical comonomers (b) are allyl (meth)acrylate, lower alkylene glycol di(meth)acrylate, poly(lower alkylene) glycol di(meth)acrylate, lower alkylene di(meth)acrylate, divinyl ether, divinyl sulfone, di- and trivinylbenzene, trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, bisphenol A di(meth)acrylate, methylenebis(meth)acrylamide, triallyl phthalate and diallyl phthalate.
- the amount of comonomer (b) used is expressed in a proportion by weight based on the total polymer and is in the range from 20 to 0.05%, in particular in the range from 10 to 0.1%, preferably in the range from 2 to 0.1%.
- Material "B” polymers are formed by polymerizing polymerizable macromers which contain free hydroxyl groups. Macromers which are built up, for example, from an amino-alkylated polysiloxane which is derivatized with at least one polyol component containing an unsaturated polymerizable side chain are disclosed. Polymers can be prepared on the one hand from the macromers according to the invention by homopolymerization. The macromers mentioned furthermore can be mixed and polymerized with one or more hydrophilic and/or hydrophobic comonomers. A special property of the macromers according to the invention is that they function as the element which controls microphase separation between selected hydrophilic and hydrophobic components in a crosslinked end product.
- the hydrophilic/hydrophobic microphase separation is in the region of less than 300nm.
- the macromers are preferably crosslinked at the phase boundaries between, for example, an acrylate comonomer on the one hand and an unsaturated polymerizable side chain of polyols bonded to polysiloxane on the other hand, by covalent bonds and additionally by reversible physical interactions, for example hydrogen bridges. These are formed, for example, by numerous amide or urethane groups.
- the continuous siloxane phase which exists in the phase composite has the effect of producing a surprisingly high permeability to oxygen.
- the present embodiment of the invention relates to a macromer comprising at least one segment of the formula (I):
- (b) is a polyol segment which contains at least 4 C atoms
- Z is a segment (c) or a group Xi
- (c) is defined as X 2 -R-X 2 , wherein
- R is a bivalent radical of an organic compound having up to 20 C atoms and each X 2 independently of the other is a bivalent radical which contains at least one carbonyl group,
- Xi is defined as X 2 .
- Pr is a group which can be polymerized by free radicals
- Y and X 3 independently of one another are a bivalent radical which contains at least one carbonyl group; k is 0 or 1 ; and
- L is a bond or a divalent radical having up to 20 C atoms of an organic compound.
- a polysiloxane segment (a) is derived from a compound of the formula (III): in which n is an integer from 5 to 500;
- radicals R 1, R 2 , R 3 , R 4 , R 5 and R 6 independently of one another are alkyl and 0.2-75% of the radicals R 1 , R 2 , R 3 , R , R 5 and R 6 independently of one another are partly fluorinated alkyl, aminoalkyl, alkenyl, aryl, cyanoalkyi, alk-NH-alk-NH 2 or alk-(OCH 2 ) m -(OCH 2 ) p -OR 7 ,
- R 7 is hydrogen or lower alkyl, alk is alkylene, and m and p independently of one another are an integer from 0 to 10, one molecule containing at least one primary amino or hydroxyl group.
- alkylenoxy groups -(OCH 2 CH 2 ) m and -(OCH 2 ) p in the siloxane of the formula (HI) are either distributed randomly in a ligand alk-(OCH 2 CH 2 ) m -(OCH 2 ) p -OR 7 or are distributed as blocks in a chain.
- a polysiloxane segment (a) is linked a total of 1-50 times, preferably 2-30 times, and in particular 4-10 times, via a group Z with a segment (b) or another segment (a), Z in an a-Z-a sequence always being a segment (c).
- the linkage site in a segment (a) with a group Z is an amino or hydroxyl group reduced by one hydrogen.
- a polysiloxane segment is derived from a compound of the formula (III) in which the radicals Ri, R 2 , R 3 , R 4 , R5 and R 6 are a total of 1-50 times, more preferably 2-30 times, and in particular 4-10 times, independently either terminally or pendently aminoalkyl or hydroxyalkyl, the other variables being as defined above.
- a polysiloxane segment is derived from a compound of the formula (III) in which 95-29% of the radicals R 1 ( R 2 , R 3 , R 4 , R 5 and R 6 independently of one another are alkyl and 5-71 % of the radicals R 1 , R 2 , R 3 , R , R 5 and R 6 independently of one another are partly fluorinated alkyl, aminoalkyl, alkenyl, aryl, cyanoalkyi, alk-NH-alk-NH 2 or alk-(OCH 2 CH 2 ) m -(OCH 2 ) p -OR 7 , and in which the variables are as defined above.
- n is an integer from 5 to 400, more preferably 10 to 250 and particularly preferably 12 to 125.
- the two terminal radicals R, and R 6 are aminoalkyl or hydroxyalkyl, the other variables being as defined above.
- radicals R 4 and R 5 are 1-50 times, more preferably 2-30 times and in particular 4-10 times pendently aminoalkyl or hydroxyalkyl and the other variables are as defined above.
- radicals Ri, R 2 , R 3 , R 4 , R 5 and R 6 are a total of 1-50 times, more preferably 2-30 times and in particular 4-10 times, independently both terminally and pendently aminoalkyl or hydroxyalkyl and the other variables are as defined above.
- Xi is a bivalent group which contains at least one carbonyl group.
- a carbonyl group mentioned is flanked in any manner, if appropriate, by -O-, -CONH-, -NHCO- or -NH-.
- Examples of bivalent groups Z are typically carbonyls, esters, amides, urethanes, ureas or carbonates.
- Xi is preferably an ester, amide, urethane or urea group, in particular an ester or amide group.
- X 2 is defined in the same way as Xi and is preferably an ester, amide, urethane, carbonate or urea group, more preferably an ester, amide, urethane or urea group and in particular an amide, urethane or urea group.
- a polyol segment b is preferably understood as meaning a polyol derived from a carbohydrate, carbohydrate monolactone or carbohydrate dilactone.
- a carbohydrate is understood as meaning a mono-, di-, tri-, tetra-, oligo- or polysaccharide.
- a carbohydrate lactone is understood as meaning the lactone of an aldonic or uronic acid.
- An aldonic or uronic acid is, for example, a carboxylic acid formed by oxidation of a mono-, di-, tri-, tetra-, oligo- or polysaccharide.
- aldonic acid lactones are gluconolactone, galactonolactone, lactobionolactone or maltoheptaonolactone;
- examples of uronic acid lactones are glucuronic acid lactone, mannuronic acid lactone or iduronic acid lactone.
- An example of a carbohydrate dilactone is D-glucaro-1 ,4:6,3-dilactone.
- a carbohydrate lactone reacts, for example, with a primary amino group or a hydroxyl group of segment (a) to form a covalent amide or ester bond of the type X
- Such linkages are the constituent of a further preferred embodiment of macromers according to the invention.
- Such macromers have an alternating distribution of segments of type (a) and (b) which are interrupted by Xi.
- This embodiment of the invention preferably relates to a macromer of the formula (IV):
- An embodiment of the invention furthermore preferably relates to a macromer according to formula (V):
- polysiloxane segment (a) contains q pendent ligands, x is 0, 1 or 2, q has an average numerical value of 1-20, preferably 1-10, and in particular 1-5, and the segments (b) in a macromer according to the formula (V) are linked in total (per molecule) with up to 20, preferably with up to 15, and in particular with up to 6 polymerizable segments (d).
- An embodiment of the invention furthermore preferably relates to a macromer according to formula (VI): in which a linear sequence is present, is 0, 1 or 2, q has an average numerical value of 1-20, preferably 1 -10, and in particular 1-5, and the segments (b) in a macromer according to the formula (VI) are linked in total (per molecule) with up to 20, preferably with up to 15, and in particular with up to 6 polymerizable segments (d).
- An embodiment of the invention furthermore very preferably relates to a macromer according to formula (VII):
- x is 0, 1 or 2
- the average number of segments (d) per molecule of the formula (VII) is preferably in the range from 2 to 5, and very preferably is in the range from 3 to 4.
- a polyol segment (b) is derived from a polyol which carries no lactone group if the group Z is a segment (c).
- polyols are a 1 ,2-polyol, for example the reduced monosaccharides, for example mannitol, glucitol, sorbitol or iditol, a 1 ,3-polyol, for example polyvinyl alcohol (PVA), which is derived from partly or completely hydrolysed polyvinyl acetate, and furthermore amino-terminal PVA telomers, aminopolyols, aminocyclodextrins, aminomono-, -di-, -tri-, -oligo- or -polysaccharides or cyclodextrin derivatives, for example hydroxypropylcyclodextrin.
- PVA polyvinyl alcohol
- a segment (b) carries at least one vinylic polymerizable segment (d), a linkage of a segment (d) via the bivalent radical X 3 thereof to an amino or hydroxyl group, of a segment (b), reduced by a hydrogen atom being intended.
- a vinylic polymerizable segment (d) is incorporated either terminally or pendently preferably 1-20 times, more preferably 2-15 times, and in particular 2-6 times, per macromer molecule according to the invention.
- a vinylic polymerizable segment (d) is inco ⁇ orated terminally and also pendently as desired (as a terminal/pendent mixture) preferably 1-20 times, more preferably 2-15 times and in particular 2-6 times, per macromer molecule according to the invention.
- a group Pi which can be polymerized by free radicals is, for example, alkenyl, alkenylaryl or alkenylarylenealkyl having up to 20 C atoms.
- alkenyl are vinyl, allyl, 1-propen- 2-yl, 1-buten-2- or -3- or -4-yl, 2-buten-3-yl and the isomers of pentenyl, hexenyl, octenyl, decenyl or undecenyl.
- alkenylaryl are vinylphenyl, vinylnaphthyl or allylphenyl.
- An example of alkenylarylenealkyl is vinylbenzyl.
- Pi is preferably alkenyl or alkenylaryl having up to 12 C atoms, more preferably alkenyl having up to 8C atoms and in particular alkenyl having up to 4 C atoms.
- L is preferably alkylene, arylene, a saturated bivalent cycloaliphatic group having 6 to 20 carbon atoms, arylenealkylene, alkylenearylene, alkylenearylenealkylene or arylenealkylenearylene. In a preferred meaning, L furthermore is preferably a bond.
- L is a divalent radical having up to 12 C atoms, and more preferably a divalent radical having up to 8 C atoms.
- L furthermore is alkylene or arylene having up to 12 C atoms.
- a very preferred meaning of L is lower alkylene, in particular lower alkylene having up to 4C atoms.
- Y is preferably a carbonyl, ester, amide or urethane group, in particular a carbonyl, ester or amide group, and very preferably a carbonyl group. ln another preferred meaning, Y is absent, i.e., k is 0.
- X 3 is a urethane, urea, ester, amide or carbonate group, more preferably a urethane, urea, ester or amide group, and in particular a urethane or urea group.
- a vinylic polymerizable segment (d) is derived, for example, from acrylic acid, methacrylic acid, methacryloyl chloride, 2-isocyanatoethyl methacrylate (IEM), allyl isocyanate, vinyl isocyanate, the isomeric vinylbenzyl isocyanates or adducts of hydroxyethyl methacrylate (HEMA) and 2,4-tolylene diisocyanate (TDI) or isophorone diisocyanate (IPDI), in particular the 1 :1 adduct.
- HEMA hydroxyethyl methacrylate
- TDI 2,4-tolylene diisocyanate
- IPDI isophorone diisocyanate
- the invention furthermore preferably relates to a macromer in which a segment (d) is incorporated either terminally or pendently or as a terminal/pendent mixture 5 times.
- the invention furthermore preferably relates to a macromer in which a segment (d) is incorporated terminally 5 times.
- the diradical R is, for example, alkylene, arylene, alkylenearylene, arylenealkylene or arylenealkylenearylene having up to 20 carbon atoms, a saturated bivalent cycloaliphatic group having 6 to 20 carbon atoms or cycloalkylenealkylenecycloalkylene having 7 to 20 carbon atoms.
- R is alkylene, arylene, alkylenearylene, arylenealkylene or arylenealkylenearylene having up to 14 carbon atoms or a saturated bivalent cycloaliphatic group having 6 to 14 carbon atoms.
- R is alkylene, arylene, alkylenearylene or arylenealkylene having up to 14 carbon atoms, or a saturated bivalent cycloaliphatic group having 6 to 14 carbon atoms.
- R is alkylene or arylene having up to 12 carbon atoms, or a saturated bivalent cycloaliphatic group having 6 to 14 carbon atoms.
- R is alkylene or arylene having up to 10 carbon atoms, or is a saturated bivalent cycloaliphatic group having 6 to10 carbon atoms.
- a segment (c) is derived from a diisocyanate, for example from hexane 1 ,6-diisocyanate, 2,2,4-trimethylhexane 1 ,6-diisocyanate, tetramethylene diisocyanate, phenylene 1 ,4-diisocyanate, toluene 2,4-diisocyanate, toluene 2,6- diisocyanate, m- or p-tetramethylxylene diisocyanate, isophorone diisocyanate or cyclohexane 1 ,4-diisocyanate.
- segment (c) is furthermore derived from a diisocyanate in which the isocyanate groups have different reactivities.
- the different reactivity is influenced, in particular, by the spatial requirements and/or electron density in the neighbourhood of an isocyanate group.
- the average molecular weight of a macromer according to the invention is preferably in the range from about 300 to about 30,000, very preferably in the range from about 500 to about 20,000, more preferably in the range from about 800 to about 12,000, and particularly preferably in the range from about 1000 to about 10,000.
- a preferred embodiment of the macromer has a segment sequence of the formula (VIII):
- a preferred embodiment of the macromer has a segment sequence of formula (IX):
- sequence (c-a)-(Z-b)t hangs pendently r times on the segment (a) and may or may not be terminated by a segment (b);
- r is an integer from 1 to 10, preferably from 1 to 7, and in particular from 1 to 3;
- t is 0 or 1 , and is preferably 1 ;
- Z is a segment (c) or a group X i; and the above preferences apply to the total number of segments (d), which are preferably bonded to a segment (b).
- Another preferred embodiment of the macromer has a segment sequence of formula (X):
- s is an integer from 1 to 10, preferably from 1 to 7, and in particular from 1 to 3;
- B is a segment (a) or (b); and the above preferences apply to the number of segments (d), which are bonded to a segment (b).
- Another preferred embodiment of the macromer has a segment sequence of the formula (XI):
- the total sum of segments (a) and (b) or, where appropriate, (a) and (b) and (c) is in a range from 2 to 50, preferably 3 to 30, and in particular in the range from 3 to 12.
- Alkyl has up to 20 carbon atoms and can be straight-chain or branched. Suitable examples include dodecyl, octyl, hexyl, pentyl, butyl, propyl, ethyl, methyl, 2-propyl, 2-butyl or 3-pentyl.
- Arylene is preferably phenylene or naphthylene, which is unsubstituted or substituted by lower alkyl or lower alkoxy, in particular 1 ,3-phenylene, 1 ,4-phenylene or methyl-1 ,4- phenylene; or 1 ,5-naphthylene or 1 ,8-naphthylene.
- Aryl is a carbocyclic aromatic radical, which is unsubstituted or substituted by preferably lower alkyl or lower alkoxy. Examples are phenyl, toluyl, xylyl, methoxyphenyl, t- butoxyphenyl, naphthyl or phenanthryl.
- a saturated bivalent cycloaliphatic group is preferably cycloalkylene, for example cyclohexylene or cyclohexylene-lower alkylene, for example cyclohexylenemethylene, which is unsubstituted or substituted by one or more lower alkyl groups, for example methyl groups, for example trimethylcyclohexylenemethylene, for example the bivalent isophorone radical.
- lower in the context of this invention in connection with radicals and compounds, unless defined otherwise, means, in particular, radicals or compounds having up to 8 carbon atoms, preferably having up to 4 carbon atoms.
- Lower alkyl has, in particular, up to 8 carbon atoms, preferably up to 4 carbon atoms, and is, for example, methyl, ethyl, propyl, butyl, tert-butyl, pentyl, hexyl or isohexyl.
- Alkylene has up to 12 carbon atoms and can be straight-chain or branched. Suitable examples include decylene, octylene, hexylene, pentylene, butylene, propylene, ethylene, methylene, 2-propylene, 2-butylene or 3-pentylene.
- Lower alkylene is alkylene having up to 8, and particularly preferably having up to 4 carbon atoms. Particularly preferred examples of lower alkylenes are propylene, ethylene and methylene.
- the arylene unit of alkylenearylene or arylenealkylene is preferably phenylene, which is unsubstituted or substituted by lower alkyl or lower alkoxy, and the alkylene unit of this is preferably lower alkylene, such as methylene or ethylene, in particular methylene.
- Such radicals are therefore preferably phenylenemethylene or methylenephenylene.
- Lower alkoxy has, in particular, up to 8 carbon atoms, preferably up to 4 carbon atoms, and is, for example, methoxy, ethoxy, propoxy, butoxy, tert-butoxy or hexyloxy.
- Partly fluorinated alkyl is understood as meaning alkyl in which up to 90%, preferably up to 70%, and in particular up to 50%, of the hydrogens are replaced by fluorine.
- Arylenealkylenearylene is preferably phenylene-lower alkylene-phenylene having up to 8, and in particular having up to 4 carbon atoms in the alkylene unit, for example phenylenethylenephenylene or phenylenemethylenephenylene.
- a monosaccharide in the context of the present invention is understood as meaning an aldopentose, aldohexose, aldotetrose, ketopentose or ketohexose.
- Examples of an aldopentose are D-ribose, D-arabinose, D-xylose or D-lyose; examples of an aldohexose are D-allose, D-altrose, D-glucose, D-mannose, D-gulose, D-idose, D- galactose, D-talose, L-fucose or L-rhamnose; examples of a ketopentose are D-ribulose or D-xylulose; examples of a tetrose are D-erythrose or threose; and examples of a ketohexose are D-psicose, D-fructose, D-sorbose or D-tagatose.
- Examples of a disaccharide are trehalose, maltose, somaltose, cellobiose, gentiobiose, saccharose, lactose, chitobiose, N,N-diacetylchitobiose, palatinose or sucrose.
- Raffinose, panose or maltotriose may be mentioned as an example of a trisaccharide.
- Examples of an oligosaccharide are maltotetraose, maltohexaose, chitoheptaose and furthermore cyclic oligosaccharides, such as cyclodextrins.
- Cyclodextrins contain 6 to 8 identical units of ⁇ -1 ,4-glucose. Some examples are ⁇ -, ⁇ -and ⁇ -cyclodextrin, derivatives of such cyclodextrins, for example hydroxypropylcyclodextrins, and branched cyclodextrins.
- the macromers according to this embodiment of invention can be prepared by processes known per se, for example as follows.
- a polysiloxane containing at least one primary amino- or hydroxyalkyl group is reacted with a carbohydrate lactone, an amide or ester bond being formed and a compound of the formula (Xlla) or (Xllb) being formed:
- X 4 is a group which is coreactive with a hydroxyl or amino group of segment (a), an X 2 group of a segment (c) being formed from such a reaction, where X is preferably -COOH, -COOR 10 , -COCI or -NCO, in which R 10 is alkyl, or aryl which is unsubstituted or substituted by lower alkyl or lower alkoxy, and R is as defined above, after which this intermediate is reacted with a polyol which carries no lactone group to give a compound of the formula (XVI):
- s is an integer from 1 to 10, preferably from 1 to 7, and in particular from 1 to 3;
- B is a segment (a) or (b); and the above preferences apply to the number of segments (d) which are bonded to a segment (b).
- r is an integer from 1 to 10, preferably from 1 to 7, and in particular from 1 to 3;
- t is 0 or 1 , and is preferably 1 ;
- Another process starts from a carbohydrate lactone which is reacted in a first step with a compound of the formula (XIII), the lactone function being retained, after which the intermediate is reacted with a polysiloxane containing at least one amino or hydroxyl group to give a compound of the formula (IV) or (V):
- the present embodiment of the invention furthermore relates to the intermediates which are novel and which occur during synthesis of the macromers according to the invention.
- the invention therefore furthermore relates to a compound of the formula (Xlla):
- (b) is derived from a carbohydrate dilactone.
- An embodiment of the invention furthermore relates to a compound of the formula (Xllb): a-(Z-b) q (Xllb) in which Z, (b) and q are as defined and preferred above, but with the proviso that a segment (a) is derived from a compound of the formula (III):
- n is an integer from 5 to 500;
- R 1 f R 2 , R 3 , R 4 , Rs and R 6 independently of one another are alkyl and 0.2 - 75 % of the radicals R ⁇ , R 2 , R 3 , R 4 , Rs and R 6 independently of one another are partly fluorinated alkyl, aminoalkyl, alkenyl, aryl, cyanoalkyi, alk-NH-Alk-NH 2 or alk- (OCH 2 CH 2 ) m -(OCH 2 )p-OR 7 in which R 7 is hydrogen or lower alkyl, alk is alkylene and m and p independently of one another are an integer from 0 to 10, one molecule containing at least one primary amino or hydroxyl group and at least one partly fluorinated alkyl group.
- the invention furthermore relates to a compound of the formula (XVI): b-c- ⁇ a-c ⁇ s -b (XVI) in which a segment (b) is derived from a polyol which carries no lactone and the other variables are as defined and preferred above.
- An embodiment of the invention furthermore relates to a compound of the formula (XVII): b-Z-a- ⁇ c-a ⁇ r -Z-b (XVII) in which a segment (b) is derived from a polyol which carries no lactone and the other variables are as defined and preferred above.
- a siloxane (a) containing at least one primary amino or hydroxyl group is, for example, commercially obtainable. Examples are KF-6002, KF-8003, X-22-161C (Shin Etsu) or GP4 (Genesee). Other siloxanes can be synthesized with the aid of published processes.
- a polyol (b) required for the synthesis is as a rule commercially obtainable. Examples are gluconolactone or lactobionolactone. Otherwise, they can be synthesized with the aid of a published process.
- the compounds according to the invention can be prepared in the presence or absence of a solvent. A solvent which is largely inert, i.e., does not participate in the reaction, is advantageously used.
- ethers such as tetrahydrofuran (THF), 1 ,2-dimethoxyethane, diethylene glycol dimethyl ether or dioxane, halogenated hydrocarbons, such as chloroform or methylene chloride, bipolar aprotic solvents, such as acetonitrile, acetone, dimethylformamide (DMF) or dimethyl sulfoxide (DMSO), hydrocarbons, such as toluene or xylene, and furthermore pyridine or N-methylmorpholine.
- THF tetrahydrofuran
- 1 ,2-dimethoxyethane diethylene glycol dimethyl ether or dioxane
- halogenated hydrocarbons such as chloroform or methylene chloride
- bipolar aprotic solvents such as acetonitrile, acetone, dimethylformamide (DMF) or dimethyl sulfoxide (DMSO)
- hydrocarbons such as toluene or x
- the reactants are advantageously employed in stoichiometric amounts for the preparation of the compounds according to the invention.
- the reaction temperature can be, for example, from -30°C to 150°C. The range from 0°C to 40°C is a preferred temperature range.
- the reaction times here are in the range from about 15 minutes to 7 days, preferably in the region of about 12 hours. If necessary, the reaction is carried out under argon or nitrogen as an inert gas.
- a suitable catalyst is advantageously added for urethane- forming reactions, for example dibutyltin dilaurate (DBTDL).
- DBTDL dibutyltin dilaurate
- the present invention furthermore relates to a polymer comprising a polymerization product of at least one macromer according to the invention as defined above and, if appropriate, at least one vinylic comonomer (a).
- the preferred composition of a polymer according to the invention comprises a weight content, with respect to the total polymer, of a macromer according to the invention in the range from 100 to 0.5%, in particular in the range from 80 to 10%, and preferably in the range from 70 to 30%.
- comonomer (a) is absent and the polymer is preferably a homopolymer.
- a comonomer (a) which is contained in a polymer according to the invention can be hydrophilic or hydrophobic or a mixture of both. Suitable comonomers include, in particular, those which are usually used for the preparation of contact lenses and biomedical materials.
- a hydrophobic comonomer (a) is understood as meaning monomers which typically give, as a homopolymer, polymers which are water-insoluble and can absorb less than 10% by weight of water.
- hydrophilic comonomer (a) is understood as meaning a monomer which typically gives, as a homopolymer, a polymer which is water-soluble or can absorb at least 10% by weight of water.
- Suitable hydrophobic comonomers (a) include, without this list being exhaustive, C ⁇ -C ⁇ 8 alkyl and C 3 -C ⁇ 8 cycloalkyl acrylates and methacrylates, C 3 -C ⁇ 8 alkylacrylamides and - methacrylamides, acrylonitrile, methacrylonitrile, vinyl C C ⁇ 8 alkanoates, C 2 -C ⁇ 8 alkenes, C 2 - C 18 haloalkenes, styrene, lower alkyl styrene, lower alkyl vinyl ethers, C 2 -C ⁇ 0 perfluoroalkyl acrylates and methacrylates or correspondingly partly fluorinated acrylates and methacrylates, C 3 -C 12 perfluoroalkyl-ethyl-thiocarbonylaminoethyl acrylates and methacrylates, acryloxy- and methacryloxy-alkylsiloxanes, N-vin
- Preferred comonomers are, for example, acrylonitrile, C rC alkyl esters of vinylically unsaturated carboxylic acids having 3 to 5 carbon atoms, or vinyl esters of carboxylic acids having up to 5 carbon atoms.
- hydrophobic comonomers (a) include methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, isobutyl acrylate (IBA), isooctyl acrylate (OA), isodecyl acrylate (DA), cyclohexyl acrylate, 2-ethylhexyl acrylate (EHA), methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl acrylate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, styrene, chloroprene, vinyl chloride, vinylidene chloride, acrylonitrile, 1-butene, butadiene, methacrylonitrile, vinyl toluene, vinyl ethyl ether, perfluorohexylethylthiocarbonylaminoethyl methacrylate, isoborn
- hydrophobic comonomers (a) are methyl methacrylate, IBA, HFBA, HFBMA, OA, EHA, DA, TRIS and acrylonitrile.
- Suitable hydrophilic comonomers (a) include, without this list being conclusive, hydroxyl- substituted lower alkyl acrylates and methacrylates, acrylamide, methacrylamide, lower alkylacrylamides and -methacrylamides, ethoxylated acrylates and methacrylates, hydroxyl- substituted lower alkylacrylamides and -methacrylamides, hydroxyl-substituted lower alkyl vinyl ethers, sodium vinylsulfonate, sodium styrenesulfonate, 2-acrylamido-2- methylpropanesulfonic acid, N-vinylpyrrole, N-vinyl-2-pyrrolidone, 2-vinyloxazoline, 2-vinyl- 4,4'-dialkyloxazolin
- Preferred comonomers are, for example, N-vinyl-2-pyrrolidone, acrylamide, methacrylamide, hydroxyl- substituted lower alkyl acrylates and methacrylates, hydroxyl-substituted lower alkylacrylamides and -methacrylamides and vinylically unsaturated carboxylic acids having a total of 3 to 5 carbon atoms.
- hydrophilic comonomers (a) include hydroxyethyl methacrylate (HEMA), hydroxyethyl acrylate, hydroxypropyl acrylate, trimethylammonium-2-hydroxypropyl methacrylate hydrochloride (Blemer®QA, for example from Nippon Oil), dimethylaminoethyl meth acrylate (DMAEMA), dimethylaminoethyl methacrylamide, acrylamide, methacrylamide, N,N-dimethylacrylamide (DMA), allyl alcohol, vinylpyridine, glycerol methacrylate, N-(1 ,1-dimethyl-3-oxobutyl)acrylamide, N-vinyl-2-pyrrolidone (NVP), acrylic acid, methacrylic acid and the like.
- HEMA hydroxyethyl methacrylate
- DMAEMA dimethylaminoethyl meth acrylate
- DMA dimethylaminoethyl methacrylamide
- Preferred hydrophilic comonomers (a) are 2-hydroxyethyl methacrylate, dimethylaminoethyl methacrylate, trimethylammonium-2-hydroxypropyl methacrylate hydrochloride, N,N- dimethylacrylamide and N-vinyl-2-pyrrolidone.
- the polymers according to the invention are built up in a manner known per se from the corresponding monomers (the term monomers here also including a macromer according to the invention) by a polymerization reaction with which the expert is familiar.
- a mixture of the abovementioned monomers is heated, with the addition of an agent which forms free radicals.
- an agent which forms free radicals is, for example, azoisobutyronitrile (AIBN), potassium peroxodisulfate, dibenzoyl peroxide, hydrogen peroxide or sodium percarbonate. If the compounds mentioned are heated, for example, free radicals are then formed, by homolysis, and can then, for example, initiate a polymerization.
- a polymerization reaction can particularly preferably be carried out using a photoinitiator.
- Photopolymerization is the term used in this case.
- a photoinitiator which can initiate free radical polymerization and/or crosslinking by the use of light is suitably added. Examples of this are familiar to the expert, and specifically, suitable photoinitiators are benzoin methyl ether, 1 -hydroxycyclohexyl phenyl ketone and Darocur and Irgacur types, preferably Darocur 1173® and Darocur 2959® .
- Reactive photoinitiators which can be incorporated, for example, into a macromer or can be used as a special comonomer (a) are also suitable.
- the photopolymerization can then be triggered off by actinic radiation, for example light, in particular UV light of a suitable wavelength.
- actinic radiation for example light, in particular UV light of a suitable wavelength.
- the spectral requirements can be controlled accordingly, if appropriate, by addition of suitable photosensitizers.
- Suitable solvents are in principle all solvents which dissolve the monomers used, for example water, alcohols, such as lower alkanols, for example ethanol or methanol, and furthermore carboxylic acid amides, such as dimethylformamide, dipolar aprotic solvents, such as dimethyl sulfoxide or methyl ethyl ketone, ketones, for example actone or cyclohexanone, hydrocarbons, for example toluene, ethers, for example THF, dimethoxyethane or dioxane, and halogenated hydrocarbons, for example trichloroethane, and also mixtures of suitable solvents, for example mixtures of water with an alcohol, for example a water/ethanol or a water/methanol mixture.
- suitable solvents for example mixtures of water with an alcohol, for example a water/ethanol or a water/methanol mixture.
- a polymer network can be intensified by addition of a so-called crosslinking agent, for example a polyunsaturated comonomer (b).
- the invention furthermore relates to a polymer comprising the polymerization product of a macromer according to the invention with, if appropriate, at least one vinylic comonomer (a) and with at least one comonomer (b).
- Examples of typical comonomers (b) are, for example, allyl(meth)acrylate, lower alkylene glycol di(meth)acrylate, poly lower alkylene glycol di(meth)acrylate, lower alkylene di(meth)acrylate, divinyl ether, divinyl sulfone, di- or trivinylbenzene, trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, bisphenol A di(meth)acrylate, methylenebis(meth)acrylamide, triallyl phthalate or diallyl phthalate.
- the amount of comonomer (b) used is expressed in the weight content with respect to the total polymer and is in the range from 20 to 0.05 %, in particular in the range from 10 to 0.1%, and preferably in the range from 2 to 0.1%.
- siioxane-containing macromer which is formed from a poly(dialkylsiloxane) dialkoxyalkanol having the following structure:
- n is an integer from about 5 to about 500, preferably about 20 to 200, more preferably about 20 to 100; the radicals R 1 f R 2 , R 3 , and R , independently of one another, are lower alkylene, preferably
- C ⁇ -C 6 alkylene more preferably C C 3 alkylene, wherein in a preferred embodiment, the total number of carbon atoms in R ⁇ and R 2 or in R 3 and R is greater than 4;
- Rs, Re, 7, and R 8 independently of one another, are lower alkyl, preferably C r C 6 alkyl, more preferably C C 3 alkyl.
- ACRYLATE is selected from acrylates and methacrylates
- LINK is selected from urethanes and diurethane linkages
- ALK - O - ALK is as defined above (R O-R 2 or R 3 -0-R 4 )
- PDAS is a poly(dialkylsiloxane).
- a Material "C" macromer may be prepared by reacting isophorone diisocyanate, 2-hydroxyethyl (meth)acrylate and a poly(dialkylsiloxane) dialkoxyalkanol in the presence of a catalyst.
- a preferred Material "C” macromer may be prepared by reacting a slight excess of isocyanatoalkyl methacrylate, especially isocyanatoethyl methacrylate (IEM), with a poly(dialkylsiloxane) dialkoxyalkanol, preferably poly(dimethylsiloxane) dipropoxyethanol, in the presence of a catalyst, especially an organotin catalyst such as dibutyltin dilaurate (DBTL).
- DBTL dibutyltin dilaurate
- R 9 and Rn are alkylene; preferably C ⁇ -6 alkylene, more preferably ethylene; R 10 and R 12 are methyl or hydrogen.
- the Material "C” prepolymer mixture may be formed by mixing the aforementioned siioxane- containing macromer with one or more hydrophilic monomers and a thermoinitiator or a photoinitiator such as Darocur® 1173.
- a solvent such as hexanol, is preferably added to homogenize the mixture.
- an appropriate amount of TRIS is added to lower the modulus of elasticity to a desired level.
- the ionoperm monomer or monomers may be selected from any of the aforementioned ionoperm or hydrophilic monomers.
- the ionoperm monomer is selected from the group consisting of acrylates, methacrylates, acrylamides, methacrylamides and mixtures thereof. More preferably, the ionoperm monomers are selected from dimethylacrylamide (DMA) and methacrylic acid (MAA).
- DMA dimethylacrylamide
- MAA methacrylic acid
- a preferred Material “C” prepolymer mixture in weight percentages based on total mixture weight, includes about 35 to 60% Material “C” macromer; about 6 to 25% TRIS; about 15 to 35% ionoperm monomer; about 0.1 to 1% photoinitiator; and about 10 to 20% solvent.
- a particularly preferred Material "C” prepolymer mixture in weight percentages based on total mixture weight, includes the following: about 44 to 50% Material "C” macromer; about 10 to 12% TRIS; about 22 to 26% dimethylacrylamide; about 0 to 1% methacrylic acid; about 0.2 to 0.6% photoinitiator; and about 10 to 20% solvent.
- the prepolymer mixture may be formed into lenses and other ophthalmic devices by any of a number of techniques known in the art and disclosed herein.
- the prepolymer mixture is conveyed into a concave half of a lens mold, the convex mold half is mated with the concave mold half, and an appropriate amount of radiation is applied to initiate polymerization. While ultraviolet (UV) radiation is preferred, a number of other energy sources known in the art and disclosed herein may also be used.
- UV radiation ultraviolet
- the Material "C” ophthalmic lens is preferably a polymerization product of the following macromeric and monomeric components, based on total weight of polymerizable material:
- the Material "C'ophthalmic lens is more preferably a polymerization product of the following macromeric and monomeric components, based on total weight of polymerizable material:
- the Material "C” ophthalmic lens is a polymerization product of the following macromeric and monomeric components, based on total weight of polymerizable material:
- the ophthalmic lenses of the present invention have a surface which is biocompatible with ocular tissue and ocular fluids during the desired extended period of contact.
- the ophthalmic lenses of the present invention include a core material, as defined above, surrounded, at least in part, by a surface which is more hydrophilic and lipophobic than the core material.
- a hydrophilic surface is desirable in order to enhance the compatibility of the lens with the ocular tissues and tear fluids.
- surface hydrophilicity increases, undesirable attraction and adherence of lipids and proteinaceous matter typically decreases.
- There are factors other than surface hydrophilicity such as immunological response, which may contribute to deposit accumulation on the lens.
- lipids and proteinaceous matter causes haze on the lens, thereby reducing visual clarity. Proteinaceous deposits may also cause other problems, such as irritation to the eye. After extended periods of continuous or intermittent wear, the lens must be removed from the eye for cleaning, i.e., deposit removal. Therefore, increased surface hydrophilicity, and concomittent reductions in deposits of biological matter, allows increased wear time.
- “Surface treatment processes”, as used herein, refers to processes to render a surface more ophthalmically compatible, in which, by means of contact with a vapor or liquid, and/or by means of application of an energy source (1) a coating is applied to the surface of an article, (2) chemical species are adsorbed onto the surface of an article, (3) the chemical nature (e.g., electrostatic charge) of chemical groups on the surface of an article are altered, or (4) the surface properties of an article are otherwise modified.
- the lens may be coated with a layer of a hydrophilic polymeric material.
- hydrophilic groups may be grafted onto the surface of the lens, thereby producing a monolayer of hydrophilic material.
- These coating or grafting processes may be effected by a number of processes, including without limitation thereto, exposing the lens to plasma gas or immersing the lens in a monomeric solution under appropriate conditions.
- Another set of methods of altering the surface properties of a lens involves treatment prior to polymerization to form the lens.
- the mold may be treated with a plasma (i.e., an ionized gas), a static electrical charge, irradiation, or other energy source, thereby causing the prepolymerzation mixture immediately adjacent the mold surface to differ in composition from the core of the prepolymerization mixture.
- a plasma i.e., an ionized gas
- static electrical charge i.e., irradiation, or other energy source
- a preferred class of surface treatment processes are plasma processes, in which an ionized gas is applied to the surface of an article.
- Plasma gases and processing conditions are described more fully in U.S. Patent Nos. 4,312,575 and 4,632,844, which are incorporated herein by reference.
- the plasma gas is preferably a mixture of lower alkanes and nitrogen, oxygen or an inert gas.
- the lens is plasma treated in the presence of a mixture of (a) a C 1 - 6 alkane and (b) a gas selected from the group consisting of nitrogen, argon, oxygen, and mixtures thereof.
- the lens is plasma treated in the presence of a mixture of methane and air.
- ophthalmic moldings in addition to contact lenses, include without limitation thereto, contact lenses for vision correction, contact lenses for eye color modification, ophthalmic drug delivery devices, ophthalmic wound healing devices, and the like.
- a specific embodiment of the invention is directed to contact lenses which comprise a novel polymer or polymeric network formed by a novel polymerization process.
- Such contact lenses have a range of unusual and extremely advantageous properties. Amongst these properties are, for example, their excellent compatibility with the human cornea (if necessary after suitable surface treatment (coating)) and with tear fluid, which is based on a balanced ratio between ion or water permeability, oxygen transmissibility and mechanical and adsorptive properties. This balance of desirable properties results in high comfort and the absence of irritation and allergenic effects.
- the novel contact lenses Owing to their favorable permeability properties with respect to various salts, nutrients, water and diverse other components of tear fluid and gases (C0 2 and 0 2 ), the novel contact lenses have no effect, or virtually no effect, on the natural metabolic processes in the cornea. In contrast to many other siioxane- containing contact lenses, the present innovative extended-wear lenses have chemical and mechanical properties and ion permeability sufficient to avoid the undesired binding effect. Furthermore, the novel contact lenses have high dimensional stability and shelf life.
- the high oxygen permeability is required to prevent corneal swelling, thereby reducing the likelihood of ocular damage and wearer discomfort during periods of extended wear.
- the high ion permeability enables the lens to move on the eye such that corneal health is not substantially altered and wearer comfort is acceptable during a period of extended, continuous contact with ocular tissue and ocular fluids.
- the preferred extended-wear contact lenses of the present invention are those which are comfortable over the period of extended wear. If the lens diameter is too small, the eyelids will not cover any portion of the lens when the eye is open. Thus, the eyelids will contact the edge of the lens each time the eyelid is closed. This repeated eyelid-lens interaction typically causes irritation, wearer discomfort, and lens dislodgement. Accordingly, the preferred contact lens diameters are those which are sufficiently large to minimize eyelid- lens interaction and the associated irritation.
- the contact lens has a diameter of about 12 to about 16 millimeters, more preferably about 13 to 15 mm, and most preferably about 13.5 to 14.8 mm.
- the above-described ophthalmic lenses have special utility as extended-wear contact lenses.
- Contact lenses having sufficient oxygen and water transmission rates from inner (base curve) to outer (front curve) surface may be continuously worn for long periods of time without substantial corneal swelling or wearer discomfort.
- the method of wear includes (a) applying the lens to the eye and (b) allowing the lens to remain in intimate contact with the eye and tear fluids for a period of at least 24 hours without substantial adverse impact on corneal health or wearer comfort.
- a preferred method includes additional steps of (c) removing the lens from the ocular environment; (d) treating the lens (i.e., disinfecting or cleaning the lens); (e) re-applying the lens to the eye; and (f) allowing the lens to remain in intimate contact with the eye and tear fluids for a period of at least an additional 24 hours without substantial adverse impact on corneal health or wearer comfort.
- the lens is worn for a continuous period of at least four (4) days without substantial corneal swelling or wearer discomfort. In another preferred embodiment, the lens is worn for a continuous period of at least seven (7) days without substantial corneal swelling or wearer discomfort. In another preferred embodiment, the lens is worn for a continuous period of at least 14 days without substantial corneal swelling or wearer discomfort. In yet another preferred embodiment, the lens is worn for a continuous period of at least 30 days without substantial corneal swelling or wearer discomfort.
- oxygen is rigorously removed from the polymerizable material, rigorously removed from the mold halves used to shape the lens, and rigorously removed from the casting environment.
- one or more of these steps may be omitted, or a rigorous removal of oxygen may not be required.
- the mold halves may be determined that, for a particular siloxane- and/or fluorine-containing acrylate macromer and acrylamide monomer mixture, degassing of the mold halves does not substantially increase the ion permeability (and, hence, on-eye movement) of the resultant contact lens.
- molds having a relatively low oxygen permeability are used (e.g., polypropylene molds), the rigorous removal of oxygen may not be required.
- the ophthalmic lens may be manufactured by thoroughly mixing the siloxane- and/or fluorine-containing acrylate macromer and acrylamide or pyrrolidone monomer, degassing the mixture, applying an appropriate amount of the mixture to a lens mold cavity, sealing the mold and initiating polymerization.
- the siloxane- and/or fluorine-containing acrylate macromer and acrylamide or pyrrolidone monomer may be degassed separately, and subsequently mixed in an atmosphere which is oxygen-free or substantially oxygen-free.
- Photoinitiators such as those commercially available photoinitiators disclosed above, may be added to the prepolymerization mixture to aid in initiating polymerization.
- Polymerization may be initiated by a number of well known techniques, which, depending on the polymerizable material, may include application of radiation such as microwave, thermal, e-beam and ultraviolet.
- a preferred method of initiating polymerization is by application of ultraviolet radiation.
- Suitable gases in which the polymerization may be conducted and which are readily commercially available include, without limitation thereto, nitrogen and carbon dioxide.
- the polymerizable materials are copolymerized advantageously in an atmosphere having less than about 500 ppm oxygen. More preferably, the atmosphere surrounding the polymerizable material contains less than about 200 ppm oxygen. Even more preferably, the surrounding atmosphere contains less than about 100 ppm oxygen or particularly less than about 50 ppm oxygen, while the most preferred oxygen content is less than about 20 ppm.
- the prepolymer mixture must be rigorously degassed prior to polymerization. The degassing may be accomplished by a number of techniques known in the art.
- One technique for degassing the prepolymer mixture involves the use of a series of freezing and thawing steps which are repeated until the appropriate gas concentration level is achieved in the prepolymer mixture.
- This freeze/thaw method involves cooling the prepolymer mixture until the mixture solidifies, applying a vacuum to the solidified prepolymer mixture, discontinuing the vacuum, and thawing the prepolymer mixture until the mixture is again in liquid form. While this degassing technique is advantageous in a laboratory setting, other degassing techniques known in the art may be more advantageous for commercial lens manufacturing processes.
- Another means of degassing polymerizable material is to pass an inert gas through the polymerizable material, thereby replacing dissolved oxygen with the inert gas. Yet another means is to merely apply a vacuum to the polymerizable material, in order to cause the dissolved oxygen to convert to a gaseous phase because of reduced pressure. Similarly, oxygen may be removed from the polymerizable material by placing the polymerizable material in a chamber adjacent to an evacuated chamber, the chambers being separated from each other by a semipermeable membrane.
- the aforementioned processes may be operated in batch, semi-batch or continuous manners, and a variety of commercial equipment available for degassing of solutions and solvents may be easily applied to the present application by a person having ordinary skill in the art.
- An exemplary means for degassing polymerizable material is to pass the polymerizable mixture through a gas-permeable, liquid-impermeable membrane or tube while reducing the pressure outside the membrane or tube, e.g., to a subatmospheric pressure, such that the presssure differential between the inside and outside of the membrane or tube drives dissolved oxygen out of the polymerizable material.
- Suitable gas-permeable membranes and tubes are well known in the art.
- European Patent Application 376 638 and U.S. Patent No. 5,123,937 issued to Shibata, et al. teach methods for degassing various solvents using gas-permeable tubes.
- the concentration of oxygen dissolved in the polymerizable mixture is preferably less than about 500 ppm. More preferably, the free oxygen concentration in the polymerizable mixture is less than about 200 ppm. Even more preferably, the free oxygen concentration in the polymerizable mixture is less than about 100 ppm, while a most preferred level is below 20 ppm.
- a preferred technique is to merely store the lens molds in an environment having no oxygen, or substantially no oxygen, for a sufficient period of time to achieve substantial equilibration.
- the lens molds are stored in an inert substantially oxygen-free atmosphere, e.g., nitrogen or carbon dioxide, prior to use.
- a preferred method of degassing molds is to subject the mold halves to an inert atmosphere having an oxygen concentration of less than 100 ppm for a period of at least 4 hours.
- a more preferred method involves exposing the molds halves to an inert atmosphere having an oxygen concentration of less than 50 ppm for a period of at least 6 hours.
- the lens mold halves are exposed to an inert atmosphere having an oxygen concentration of less than 20 ppm for a period of at least 8 hours.
- the lens is formed by the following steps: (1) the polymerizable mixture is degassed, (2) oxygen is rigorously removed from the lens mold halves, (3) a lens mold half is filled with the prepolymer mixture, (4) the mold halves are affixed to one another in an environment substantially free of oxygen, and (5) the polymerization is initiated in an environment substantially free of oxygen to form the lens, where the lens mold halves are formed from a material having a low oxygen permeability.
- steps (4)-(5) may occur in the presence of oxygen.
- An essential feature of the manufacturing methods of the present innovative lenses is that a balance of high oxygen permeability and high ion permeability is achieved. Manufacturing techniques and conditions which result in lowering either the oxygen permeability or the ion permeability below levels sufficient to maintain good corneal health and on-eye movement during periods of extended wear are unacceptable to produce the innovative extended-wear contact lenses of the present invention.
- the manufacturing method produces a contact lens having a Dk/t of at least 70 barrers/mm and a lonoton Ion Permeability Coefficient of at least 0.2 x 10 "6 cm 2 /sec. More preferably, the manufacturing method produces a contact lens having a Dk/t of at least 75 barrers/mm and a lonoton Ion Permeability Coefficient of at least 0.3 x 10 "6 cm 2 /sec.
- the manufacturing method preferably provides a contact lens having a Dk/t of at least 87 barrers/mm and a lonoton Ion Permeability Coefficient of at least 0.4 x 10 6 cm 2 /sec.
- a preferred process for the manufacture of a contact lens comprises:
- Examples A-C are arranged in accordance with the materials defined above. Thus, Examples A-1 , A-2, etc. relate to Material “A” as defined above, Examples B-1 , B-2, etc. relate to Material “B” as defined above, and Examples C-1, C-2, etc. relate to Material “C”. Temperatures are stated in degrees Celsius unless otherwise specified. Examples E, F and G are directed to demonstrating a correlation between on-eye movement and the lonoton Ion Permeability Coefficient, the lonoflux Ion Permeability Coefficient, and the Hydrodell Water Permeability Coefficient, respectively.
- Examples I and J are directed to showing the correlation of oxygen content in the polymerizable material and/or molds with ion permeability.
- EXAMPLE A-1 Macromer synthesis 51.5g (50 mmol) of the perfluoropolyether Fomblin® ZDOL (from Ausimont S.p.A, Milan) having a mean molecular weight of 1030 g/mol and containing 1.96meq/g of hydroxyl groups according to end-group titration is introduced into a three-neck flask together with 50mg of dibutyltin dilaurate. The flask contents are evacuated to about 20 mbar with stirring and subsequently decompressed with argon. This operation is repeated twice. 22.2g (0.1 mol) of freshly distilled isophorone diisocyanate kept under argon are subsequently added in a counterstream of argon.
- 202g of the ⁇ , ⁇ -hydroxypropyl-term ⁇ nated polydimethylsiloxane KF-6001 from Shin-Etsu having a mean molecular weight of 2000g/mol (1.00meq/g of hydroxyl groups according to titration) are introduced into a flask.
- the flask contents are evacuated to approx 0.1 mbar and decompressed with argon. This operation is repeated twice.
- the degassed siloxane is dissolved in 202ml of freshly distilled toluene kept under argon, and 10Omg of dibutyltin dilaurate (DBTDL) are added.
- DBTDL dibutyltin dilaurate
- the macromer prepared in this way is completely colourless and clear. It can be stored in air at room temperature for several months in the absence of light without any change in molecular weight.
- EXAMPLE A-2 Macromer synthesis The first step of the macromer synthesis described under Example A-1 is repeated. An isocyanate titration of the perfluoropolyether reacted with IPDI gives a content of 1.33meq/g of NCO (theory 1.35meq/g).
- a second step 87.1 g of the ⁇ , ⁇ -hydroxypropyl-terminated polydimethylsiloxane TegomerH-Si2111 (Th. Goldschmidt AG, Essen) having a mean molecular weight of 890g/mol (2.25meq/g of hydroxyl groups according to titration) are dissolved in 87ml of toluene. After the reaction has been carried out as indicated under A-1 and the solvent has been removed, a hydroxyl group content of 0.66meq/g is determined by microtitration (theory 0.60meq/g). The resultant intermediate is in turn reacted with a stoichiometric amount of isocyanatoethyl methacrylate.
- the macromer prepared in this way is completely colourless and clear and has a long shelf life.
- a stoichiometric amount of Tegomer Hi-Si2111 and toluene are again added.
- a hydroxyl group content of 0.63meq/g is determined by microtitration (theory 0.58meq/g).
- the resultant intermediate is in turn reacted with a stoichiometric amount of isocyanatoethyl methacrylate.
- Microtitration then no longer shows any isocyanate groups (detection limit 0.01 meq/g). 0.55meq/g of methacryl groups are found (theory 0.51 meq/g).
- the macromer prepared in this way is completely colourless and clear and has a long shelf life.
- EXAMPLE A-4 Macromer synthesis The first step of the macromer synthesis described under Example A-1 is repeated, but 5.0 g of Fomblin/ZDOL and 2.18 g of IPDI are employed. When the reaction is complete, microtitration shows an isocyanate group content of 1.31 meq/g of hydroxyl groups (theory 1.36 meq/g).
- Example A-1 The second step of the synthesis described under Example A-1 is likewise carried out analogously, the stoichiometric ratio between isocyanate-terminated perfluoropolyether and hydroxypropyl-terminated polysiloxane being 2:3. After the reaction has been completed and the solvent has been removed, microtitration shows a content of 0.2meq/g of hydroxyl groups (theory 0.18meq/g).
- Example A-1 The third step of the synthesis described under Example A-1 is likewise carried out analogously, lEM being employed in a precisely stoichiometric ratio. After the reaction, free isocyanate groups can no longer be detected (detection limit 0.01 meq/g). 0.19meq/g of methacryl groups are found (theory 0.19meq/g).
- EXAMPLE A-5 Production of contact lenses 13.0g of macromer from Example A-1 are dissolved in 5.6g of ethanol (Fluka, puriss. p.a.) (70% by weight solution). After complete homogenization of the solution, 5.2g of 3- tris(trimethylsiloxy)silylpropyl methacrylate (TRIS from Shin-Etsu, product No. KF-2801), 7.8g of freshly distilled dimethylacrylamide (DMA) and 160mg of photoinitiator Darocur® 1173 (Ciba) are added.
- TIS trimethylsiloxy)silylpropyl methacrylate
- This solution is filtered through a Teflon membrane having a pore width of 0.45mm under an argon pressure of from 1 to 2 atm
- the filtered solution is frozen in a flask in liquid nitrogen, the flask is evacuated under a high vacuum, and the solution is returned to room temperature with the flask sealed This degassing operation is repeated twice.
- the flask containing the macromer/comonomer solution is then transferred into a glove box with an inert-gas atmosphere, where the solution is pipetted into dust-free contact-lens moulds made from polypropylene.
- the moulds are closed, and the polymerization reaction is effected by UV irradiation (15mW/cm 2 , 5m ⁇ n.), with simultaneous crosslinking
- the moulds are then opened and placed in ethanol, causing the resultant lenses to swell out of the moulds.
- the lenses are extracted for 24 hours with constantly replenished distilled dichloromethane and subsequently dried in a high vacuum
- the dried lenses are equilibrated in phosphate-buffered physiological saline solution in autoclave- resistant vials and then autoclaved at 120°C for 30minut.es. All physical data measurements are carried out on autoclaved lenses.
- the lenses produced in this way are characterized by the following values: oxygen permeability (Dk) 77 barrer (determined by the "wet” method described below), water content of the equilibrated lenses 32 percent by weight, elongation at break at 35°C 360%, modulus of elasticity 30°C 0.5MPa (measured using a Minimat from Polymer Laboratories, UK).
- the oxygen permeability of a material is determined by the coulometnc method. To this end, pre-autoclaved lenses are clamped in a holder and then covered on the upper side with a 2cm layer of water. A gas mixture comp ⁇ sing 21% of oxygen and 79% of nitrogen is passed continuously through the water layer with swirling. The oxygen which diffuses through the lens is measured using a coulometnc detector. The reference values are those measured on commercially available contact lenses using this method. C ⁇ basoft (CIBA- Vision, HEMA lens) gives a measurement of approx. 7-10 barrer, and Excelens 9 / (CIBA- Vision, PVA lens) gives a measurement of approx 22 barrer. Unfortunately, the oxygen permeability of, for example, contact lenses is frequently given in the literature as a straight Dk value without further definition and frequently without giving any reference material. These are usually values determined on dry material (dry measurement).
- a comparative measurement of the oxygen permeability of polymer A-5 shows the differences: a) "wet” measurement: 77 barrer b) dry measurement: 158 barrer
- EXAMPLE A-7 The process described under Example A-5 for the production of contact lenses is repeated, but the mixture of comonomers has the following composition (in percent by weight): 55 % of macromer from Example A-1
- EXAMPLE A-8 Analogously to EXAMPLE A-5 (in weight percent): 40 % of macromer from Example A-1 30 % of TRIS 30 % of DMA
- EXAMPLE A-9 The process described under A-5 for the production of contact lenses is repeated, but a 70% by weight solution of the macromer in toluene is used instead of the 75% by weight solution in ethanol described above.
- the mixture of comonomers has the following composition (in per cent by weight):
- EXAMPLE A-11 About 10.0 grams of macromer from Example A-1 are dissolved in 3.3 grams of ethanol (Fluka, puriss. p.a.). After complete homogenization of the solution, about 4.0 grams of 3- tris(trimethylsiloxy)silylpropyl methacrylate (TRIS, from Shin-Etsu, product no. KF-2801), about 5.9 g. freshly distilled dimethylacrylamide (DMA), about 0.1 g. Blemer® QA (a methacrylate having quaternary ammonium substituents, Linz Chemie) and about 100 mg of photoinitiator Darocur® 1173 (Ciba) are added. The solution is filtered through a TEFLON membrane having a pore width of 0.45 mm under an argon pressure of from about 1 to 2 atm.
- TMS tris(trimethylsiloxy)silylpropyl methacrylate
- DMA dimethylacrylamide
- Blemer® QA a me
- the filtered solution is frozen in a flask in liquid nitrogen, the flask is evacuated under a high vacuum, and the solution is returned to room temperature with the flask sealed. This degassing operation is repeated twice.
- the flask containing the macromer/comonomer solution is then transferred into a glove box with an inert gas atmosphere, where the solution is pipetted into dust-free, polypropylene contact lens molds.
- the molds are closed, and the polymerization reaction is effected by UV irradiation, with simultaneous crosslinking.
- the molds are then opened and placed in isopropyl alcohol, causing the resultant lenses to swell out of the molds.
- the lenses are extracted for about 24 hours with nearly continuous replenishing of isopropyl alcohol. Subsequently, the lenses are dried under high vacuum.
- the dried contact lenses are equilibrated in autoclave-resistant vials in phosphate-buffered physiological saline solution, and then autoclaved for 30 minutes at about 120 °C. Physical measurement data for the autoclaved lens is presented below:
- EXAMPLE A-12 Lenses are prepared in accordance with the procedures described in Example A-1 1 , but are subsequent surface treated as follows.
- the dried lenses are transferred into a plasma coating apparatus wherein they are surface treated in a methane/"air" mixture ("air”, as used here, denotes 79% nitrogen and 21% oxygen) for a period of about 5 minutes.
- air as used here, denotes 79% nitrogen and 21% oxygen
- the apparatus and plasma treatment process have been disclosed by H. Yasuda in "Plasma Polymerization", Academic Press, Orlando, Florida (1985), pages 319 forward.
- the plasma-treated contact lenses are equilibrated in autoclave-resistant vials in phosphate-buffered physiological saline solution, and then autoclaved for 30 minutes at about 120°C. Physical measurement data for the plasma-coated autoclaved lens is presented below:
- Lenses are prepared in accordance with the procedures described in Example A-5, but the mixture of comonomers has the following composition, in weight percentages:
- EXAMPLE A-14 Lenses are prepared in accordance with the procedures described in Example A-6, with the same comonomer composition, but the comonomers are dispensed into dust-free contact lens molds in ambient air atmosphere.
- the amino-functionalized polydimethylsiloxane employed for the synthesis (X-22-161-C, Shin Etsu, JP) was finely dispersed in acetonitrile, extracted and then subjected to molecular distillation.
- X-22-161-C and KF 8003 are products from Shin Etsu (Japan), PS813 is a product from
- Petrarch-H Is, GP4 and GP6 are products from Genesee.
- EXAMPLE B-8 The reaction is carried out in accordance with Example B-1 , but instead of D(+)gluconic acid d-lactone, 75mmol of lactobionic acid 1 ,5-lactone, suspended in 50 ml of absolute THF, are added dropwise to a solution of amino-functionalized polydimethylsiloxane (X-22-161-C) in 180 ml of absolute THF and 20 ml of DMSO (pure, 99%). Titration of the amino groups with perchloric acid indicates a reaction conversion of 99% ( ⁇ 0.01 meq of NH 2 /g).
- a colourless optically clear macromer is obtained.
- EXAMPLE B-9 and B-10 The reactions are carried out analogously to Example B-1. However, the catalyst necessary for addition of the isocyanate onto the hydroxyl groups is varied. Instead of DBTDL, catalytic amounts of 1 ,4-diazabicyclo[2.2.2]octane (DABCO) or 4-dimethylamino-pyridine (DMAP) are added and the reaction is continued as described under Example B-1. In both cases, an optically clear, colourless rubber-elastic macromer results in a manner corresponding to Example B-1.
- DBTDL 1 ,4-diazabicyclo[2.2.2]octane
- DMAP 4-dimethylamino-pyridine
- EXAMPLE B-11 The reaction is carried out analogously to Example B-1.
- 0.1 mol of lactobionic acid 1 ,5-lactone is suspended in 50 ml of absolute THF and the suspension is added dropwise to a solution of amino-functionalized polydimethylsiloxane (KF-8003) in 180 ml of absolute THF and 20 ml of DMSO (pure, 99%).
- the reaction time is increased to about 48 hours.
- a residual content of 0.07meq of NH 2 /g can be detected, and is reacted completely by addition of the corresponding molar amount of D(+)gluconic acid d-lactone to the reaction solution.
- the colourless highly transparent product has a residual content of amino groups of ⁇ 0.01 meq/g.
- EXAMPLE B-12 52.09 g (9.78 mmol) of purified amino-functionalized polydimethylsiloxane (X-22-161-C, Shin Etsu JP), dissolved in 110 ml of absolute THF, are initially introduced into the reaction vessel under an inert gas atmosphere, and 1.14g (6.52 mmol) of D-glucaro-1 ,4:6,3- dilactone, dissolved in 20 ml of absolute THF, are added. The reaction solution is stirred at room temperature for 15 hours and then worked up in a manner corresponding to Example B-1. The amine content is 0.134meq/g. The terminal amino groups of the resulting penta- block macromer are reacted with gluconolactone in the following reaction step.
- purified amino-functionalized polydimethylsiloxane X-22-161-C, Shin Etsu JP
- EXAMPLE B-13 Preparation of an amino- and perfluoroalkyl-functionalized polydimethylsiloxane: 3.0 ml of absolute toluene are added to 15 g of poly(dimethylsiloxane-co- methylhydrosiloxane) [Bayer Silopren U-230; 10,000 g/mol; 2.3mmol of Si-H/g], and 1.72 g (9.2mmol) of allylphthalimide [CAS Reg. No. 5428-09-1] are then added. The mixture is frozen several times and the flask evacuated and then brought to room temperature again. The flask is then let down with argon.
- the resulting macromer is clear and viscous.
- the amino group content is 78.6% of theory.
- the total yield of macromer after the chromatographic purification is 75%.
- EXAMPLE B-14 Before the polymerization, the acrylates employed, isobutyl acrylate (IBA), N.N- dimethylacrylamide (DMA) and 3-methacryloyloxypropyl-tris(trimethylsilyloxy)silane (TRIS) are each freed from inhibitors by distillation. 0.32g (2.76mmol) of IBA, 0.80g (8.1 mmol) of DMA and 1.44g (3.4mmol) of TRIS are weighed into a 50ml round-bottomed flask and the flask is flushed with N2 for half an hour, while cooling with ice.
- IBA isobutyl acrylate
- DMA N.N- dimethylacrylamide
- TRIS 3-methacryloyloxypropyl-tris(trimethylsilyloxy)silane
- the mixture is then irradiated with a UV-A mercury high pressure lamp in a nitrogen atmosphere in a UV oven equipped for this for 5 minutes.
- the lamps (5 each of the brand TLK40W/10R, Philips) are above and below the holder inserted.
- the irradiation intensity is 14.5mW/cm 2 .
- the polypropylene mould is opened and the finished discs or lenses are removed by soaking by means of a solvent mixture of methylene chloride and ethanol (2:3).
- the lenses and discs are extracted in ethanol at room temperature in special polypropylene cages for 48 hours and then dried at 40°C under 10Pa (0.1 mbar) for 24 hours (autoclaving at 120°C, 30 minutes).
- the discs show an E modulus of 1 .1MPa, a permeability to oxygen of 183 barrier and a hardness (Shore A) of 53.
- EXAMPLE B-15 to B-19 Further polymers are prepared in a manner corresponding to Example B-14 (composition in percentages by weight). Table B-ll shows examples B-15 to B-19 and the properties of the resulting materials measured on discs. TABLE B-ll
- TRIS 3-Methacryloyloxypropyl-tris(trimethylsilyloxy)silane
- DMEA 2-Dimethylaminoethyl acrylate
- EXAMPLE B-20 Uncoated contact lens A contact lens is prepared in a manner corresponding to Example B-14, using the Example B-3 macromer, with the following composition in percentages by weight:
- the lens has a Dk of about 94 and a water content of about 20.0 weight percent.
- the results are presented in TABLE B-lll for comparision with coated lens properties.
- EXAMPLE B-21 Plasma-treated contact lens Dried lenses prepared in accordance with the procedures described in Example B-20 are transferred into a plasma coating apparatus where the lenses are surface treated in a methane/"air" mixture ("air”, as used here, denotes 79% nitrogen and 21% oxygen).
- air as used here, denotes 79% nitrogen and 21% oxygen.
- the apparatus and plasma treatment process have been disclosed by H. Yasuda in "Plasma Polymerization", Academic Press, Orlando, Florida (1985), pages 319 forward.
- the dried plasma-treated contact lenses are equilibrated in autoclave-resistant vials in phosphate-buffered physiological saline solution, and then autoclaved for 30 minutes at about 120°C.
- the plasma-treated autoclaved lens has a Dk [barrer] of 90 and a water content of 21.5%. The results are presented in TABLE B-lll for comparision with coated lens properties.
- Example B-22 The synthesis of this polymer corresponds to Example B-14 with the following comonomer composition: Example B-3 macromer/TRIS/DMA: 32.8%/32.6%/34.2% (in percentages by weight) and an addition of 0.4% by weight of trimethylammonium-2-hydroxypropyl methacrylate hydrochloride (Blemer® QA, Nippon Oil Corp.).
- the polymer has a modulus of 0.9MPa and a permeability to oxygen of 82 barrer.
- the water content is 25.1 % (after 30 minutes' autoclaving at 120°C).
- Example B-16 has a water content of 20% with a very similar comonomer composition (no addition of Blemer® QA).
- Example B-23 The polymer is prepared analogously to Example B-14, but the polymerization is carried out in bulk, which means without addition of ethanol.
- the composition of the comonomers and the material properties of the polymer synthesized, measured on discs is given below.
- NDP 1-vinyl-2-pyrrolidone
- AN acrylonitrile
- EXAMPLE B-24 The polymerization is carried out in accordance with Example B-14 but with the following changed comonomer composition: macromer of Example B-7/IBA/TRIS 20%/19%/60% and 1% (in percentages by weight) of bis(3-methacryloyloxypropyl)tetra methyldisiloxane.
- IBA is isobutylacrylate
- DMA is N,N-Dimethylacrylamide
- TRIS is 3-methacryloyloxypropyl-tris(trimethylsiloxy) silane
- HFBA 2,2-3,4,4,4-hexafluorbutylester
- EXAMPLE B-28 The polymerization is carried out in accordance with Example B-14 but with the following changed comonomer composition: macromer of Example B-1/DMA/TRIS 33.3% / 33.3% / 33.3%. An optically clear polymer is obtained.
- EXAMPLE C-1 Macromer Synthesis In a dry box under nitrogen atmosphere, about 200 grams of dry PDMS dipropoxyethanol (Shin-Etsu) is added to a container. Isocyanatoethyl methacrylate (IEM) in an amount equal to about 2 moles per mole PDMS dialkanol is added to the container. About 0.1 weight percent dibutyltin dilaurate (DBTL) catalyst, based on PDMS dialkanol weight, is added to the container along with a stir bar. The container is immersed in an oil bath atop a stir plate, and secured in place with a clamp. A stream of UPC air at about 2 psig is passed over the mixture.
- IEM Isocyanatoethyl methacrylate
- DBTL dibutyltin dilaurate
- the mixture is agitated at room temperature (about 22°C) for about 24 hours.
- An iterative procedure follows in which the mixture is analyzed for isocyanate content and IEM is added if the PDMS dialkoxyalkanol has not been completely reacted.
- the mixture is stirred about 24 hours more.
- the macromer produced is a siioxane-containing macromer.
- a prepolymerization mixture is prepared by mixing about 56 grams of the macromer from Example C-1 , about 14 grams of TRIS, about 29 grams N,N-dimethylacrylamide (DMA), about 1 gram methacrylic acid, about 0.5 grams Darocur® 1173 photoinitiator, and about 20 grams hexanol. The mixture is agitated for about 20 minutes at room temperature.
- DMA N,N-dimethylacrylamide
- DMA N,N-dimethylacrylamide
- Darocur® 1173 photoinitiator about 20 grams hexanol.
- the mixture is degassed via a series of freezing and thawing steps.
- the container is placed in a liquid nitrogen bath until the mixture solidifies.
- a vacuum is applied to the container at a pressure of about 200 millitorr or less for about 5 minutes.
- the container is placed in a bath of room temperature water until the mixture is liquid again. This process is performed a total of three times.
- the mixture is then polymerized to form contact lenses.
- the prepolymerization mixture is poured into polypropylene contact lens molds in a nitrogen atmosphere.
- the polymerization is effected by applying UV radiation (about 4-6 mW/cm 2 ) for a period of about 15 minutes.
- the resulting fully hydrated contact lens has a water content of about 23%.
- the lens has a Dk of about 115 barrers and a modulus of elasticity of about 2 MPa.
- Lens fabrication A contact lens is prepared in accordance with the procedure described in Example C-2, with the difference being that the composition is about 50% macromer of Example C-1 , about 20% TRIS and about 30% DMA.
- the resulting fully hydrated contact lens has a water content of about 20%.
- the lens has a Dk of about 118 barrers and a modulus of elasticity of about 1.8 Mpa.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the cured lens has an equilibrium water content of about 26 weight percent. No coating is applied to the surface.
- the lonoton Ion Permeability Coefficient of the lens is - 0.063 x 10 '3 cm 2 /sec. Clinical examination shows that the lens does not move on the human eye. See Table E for a summary of the results.
- a contact lens is prepared substantially in accordance with the procedure described in Example A-12.
- the prepolymerization mixture Prior to polymerization, the prepolymerization mixture is degassed by cooling the prepolymer mixture with liquid nitrogen until the mixture solidifies and is near liquid nitrogen temperature, then applying a vacuum (about 0.1 mm Hg) to the solidified prepolymer mixture, discontinuing the vacuum, and thawing the prepolymer mixture until the mixture is again in liquid form This degassing procedure is performed a total of three times on the prepolymerization mixture.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the cured lens has an equilibrium water content of about 30 weight percent.
- the lens is plasma treated for about 3 minutes in an atmosphere of methane and air at a 2:1 CH :a ⁇ r volume:volume ratio.
- the working pressure of the gas is about 50 millitorr.
- the plasma treatment is accomplished in a Plasma Polymerization Apparatus LCVD-20- 400A (Plasmacarb, Bedford, Massachusetts).
- the lonoton Ion Permeability Coefficient of the lens is 0.50 x 10 3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- EXAMPLE E-3 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-12. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens
- the cured lens has an equilibrium water content of about 30 weight percent.
- the lens is plasma treated for about 5 minutes in an atmosphere of methane and air at a 2:1 CH :a ⁇ r volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 0.47 x 10 3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- a contact lens is prepared substantially in accordance with the procedure described in Example A-12 Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2. The prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens. The cured lens has an equilibrium water content of about 30 weight percent. Subsequent to curing, the lens is plasma treated for about 7.5 minutes in an atmosphere of methane and air at a 2:1 CH 4 :air volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 0.35 x 10 "3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- EXAMPLE E-5 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-1 1. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the cured lens has an equilibrium water content of about 30 weight percent.
- the lens is not subsequently coated.
- the lonoton Ion Permeability Coefficient of the lens is 1.1 x 10 "3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- EXAMPLE E-6 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-21 . Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the lens is plasma treated for about 5 minutes in an atmosphere of methane and air at a 2:1 CH 4 :air volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 2.9 x 10 "3 cm 2 /sec.
- Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- EXAMPLE E-7 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-21. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens. Subsequent to curing, the lens is plasma treated for about 7.5 minutes in an atmosphere of methane and air at a 2:1 CH 4 :air volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 0.25 x 10 "3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- EXAMPLE E-8 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-20. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in an air atmosphere to form the contact lens. Subsequent to curing, the lens is not surface treated.
- a contact lens is prepared substantially in accordance with the procedure described in Example C-2. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2. The prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens. Subsequent to curing, the lens is not surface treated.
- the lonoton Ion Permeability Coefficient of the lens is 1.4 x 10 ⁇ 3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- a contact lens is prepared substantially in accordance with the procedure described in Example C-2.
- the prepolymerization mixture Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the lens is plasma treated for about 7.5 minutes in an atmosphere of methane and air at a 2:1 CH 4 :air volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 0.61 x 10 '3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- a contact lens is prepared substantially in accordance with the procedure described in Example C-2.
- the prepolymerization mixture Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2.
- the prepolymer mixture is cured in a nitrogen atmosphere to form the contact lens.
- the lens is plasma treated for about 5 minutes in an atmosphere of methane and air at a 2:1 CH 4 :air volume ratio.
- the lonoton Ion Permeability Coefficient of the lens is 1.5 x 10 3 cm 2 /sec. Clinical examination shows that the lens moves on the human eye. See Table E for a summary of the results.
- a contact lens is prepared substantially in accordance with the procedure described in Example C-2. Prior to polymerization, the prepolymerization mixture is degassed by the repeated freeze/thaw procedure of Example E-2. The prepolymer mixture is cured in an air atmosphere to form the contact lens. Subsequent to curing, the lens is not surface treated.
- the lonoton Ion Permeability Coefficient of the lens is -0.001 x 10 "3 cm 2 /sec. Clinical examination shows that the lens does not move on the human eye. See Table E for a summary of the results.
- a contact lens preferably has an lonoton Ion Permeability Coefficient greater than about 0.008 x 10 '3 cm 2 /sec, more preferably greater than about 0.25 x 10 "3 cm 2 /sec.
- EXAMPLE F-1 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-25. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 0 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone (PVP) in accordance with the following procedure, using a glass plasma reactor equipped with an external ring electrode and a 27.13 MHz radio frequency (RF) generator for the generation of an inductively-coupled, cold glow discharge plasma. Highly purified argon is used as a plasma gas and as a carrier gas for N-vinylpyrrolidone (NVP) monomer feed. The NVP feed line is located about 10 cm below the glow zone.
- PVP polyvinylpyrrolidone
- the contact lens is placed in the 20 cm diameter plasma reactor at a position about 15 cm below the plasma glow zone.
- the reactor is then evacuated for about 30 minutes to about 0.009 mbar.
- the plasma gas flow is set to 20 seem (standard cubic centimeters)
- the glow discharge is started at a pressure of about 0.15 mbar and maintained for about one minute at a power of about 170 Watts (in order to clean and activate the lens surface).
- the argon carrier gas flow for the NVP monomer is also set to 10 seem.
- the temperature of the NVP source (with the carrier gas bubbling through the liquid NVP) is held at about 40°C.
- the lenses are treated for about 10 minutes with a pulsing glow discharge plasma (1 ⁇ sec. on, 3 ⁇ sec. off) at about 0.35 mbar pressure and about 150 Watts power.
- the reactor After interrupting the glow discharge and the carrier gas flow, the reactor is continuously purged with a 20 seem argon stream at a pressure of about 0.009 mbar for about 30 minutes, in order to remove residual monomer and activated species.
- the PVP coated contact lenses thus produced are highly wettable and show the following dynamic contact angles, measured with a KRUESS (Hamburg, Germany) K-12 instrument:
- EXAMPLE F-2 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-26. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 2.8 x 10 "7 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens does not move on the eye. See Table F for a summary of the results.
- EXAMPLE F-3 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-27. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 9.3 x 10 "7 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens does not move on the eye. See Table F for a summary of the results.
- EXAMPLE F-4 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-18. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 2.6 x 10 "6 mm 2 /min.
- Example F-1 the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- EXAMPLE F-5 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-16. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 1.3 x 10 '5 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results. EXAMPLE F-6 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-19. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 2.7 x 10 "5 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- EXAMPLE F-7 Material B A contact lens is prepared substantially in accordance with the procedure described in Example B-17. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 7.8 x 10 "6 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- EXAMPLE F-8 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-13. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 1.5 x 10 '6 mm 2 /min.
- Example F-1 the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens does not move on the eye. See Table F for a summary of the results.
- EXAMPLE F-9 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-14. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 1.1 x 10 ⁇ mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens does not move on the eye. See Table F for a summary of the results. EXAMPLE F-10 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-7. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 3.8 x 10 "6 mm z /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- EXAMPLE F-11 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-6. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 8.5 x 10 "6 mm 2 /min. Subsequent to ion permeability measurements, the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- EXAMPLE F-12 Material A A contact lens is prepared substantially in accordance with the procedure described in Example A-5. Prior to surface treatment, the lonoflux Ion Permeability Coefficient is determined to be about 7.1 x 10 "5 mm 2 /min.
- Example F-1 the lens surface is coated with polyvinylpyrrolidone as in Example F-1. Clinical tests show that the lens moves on the eye. See Table F for a summary of the results.
- a contact lens preferably has an lonoflux Ion Permeability Coefficient greater than about 1.5 x 10* mm 2 /min., more preferably greater than about
- EXAMPLE G-1 A contact lens is prepared substantially in accordance with the procedure described in Example A-5.
- the Hydrodell Water Permeability Coefficient is determined to be about 1.09 x 10 "6 cm 2 /second. Clinical tests show that the lens moves on the eye. See Table G for a summary of the results.
- EXAMPLE G-2 A contact lens is prepared substantially in accordance with the procedure described in Example A-6. The lens is surface treated in a plasma gas in accordance with the procedure described in Example F-1. The Hydrodell Water Permeability Coefficient is determined to be about 0.27 x 10* cm 2 /second. Clinical tests show that the lens moves on the eye. See Table G for a summary of the results.
- EXAMPLE G-3 A contact lens is prepared substantially in accordance with the procedure described in Example B-19. The lens is surface treated in a plasma gas in accordance with the procedure described in Example F-1. The Hydrodell Water Permeability Coefficient is determined to be about 0.37 x 10* cm 2 /second. Clinical tests show that the lens moves on the eye. See Table G for a summary of the results.
- EXAMPLE G-4 A contact lens is prepared substantially in accordance with the procedure described in Example C-2.
- the Hydrodell Water Permeability Coefficient is determined to be about 1.26 x 10* cm 2 /second. Clinical tests show that the lens moves on the eye. See Table G for a summary of the results.
- EXAMPLE G-5 A contact lens is prepared substantially in accordance with the procedure described in Example B-14.
- the Hydrodell Water Permeability Coefficient is determined to be about 0.08 x 10* cm 2 /second. Clinical tests show that the lens does not move on the eye. See Table G for a summary of the results.
- a contact lens preferably has a Hydrodell Water Permeability Coefficient greater than about 0.08 x 10* cm 2 /sec, more preferably greater than 0.27 x 10* cm 2 /sec.
- a polymerizable mixture containing about 25 weight percent Material B macromer, about 25% TRIS and about 25% dimethylacrylamide (DMA) is prepared with about 25% ethanol solvent and Darocur 1173 photoinitiator.
- the polymerizable mixture is subjected to a freeze-thaw process in order to remove oxygen before polymerization.
- the freeze-thaw process is accomplished by (a) cooling the prepolymer mixture in a container by applying liquid nitrogen until the mixture solidifies, (b) applying a vacuum (about 0.1 mm Hg) to the solidified polymerizable material, (c) discontinuing the vacuum, (d) sealing the container, and (e) thawing the prepolymer mixture until the mixture is again in liquid form. This cycle is performed a total of three times on the polymerizable material.
- a glove box is prepared by evacuating and then filling with nitrogen.
- the degassed polymerizable mixture is then introduced into the front curve mold half in a glove box.
- the base curve mold half is mated with the front curve mold half.
- the polymerizable mixture is cured in a glove box by applying 15 mW ultraviolet light for a period of about 5 minutes.
- This process yields a contact lens having an oxygen transmissibility of 87 barrers/mm and an lonoflux Diffusion Coefficient of 3.5 x 10 " mm 2 /min. See Table I for comparative results.
- EXAMPLE I-2 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1. The degassed mixture is cast into a contact lens in accordance with the glove box procedure of Example 1-1 by applying 8 mW ultraviolet light for a period of about 20 minutes. This process yields a contact lens having an oxygen transmissibility of 104 barrers/mm and an lonoflux Diffusion Coefficient of 3.5 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE I-3 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1. The degassed mixture is cast into a contact lens in accordance with the glove box procedure of Example 1-1 by applying 8 mW ultraviolet light for a period of about 10 minutes. This process yields a contact lens having an oxygen transmissibility of 95 barrers/mm and an lonoflux Diffusion Coefficient of 4.1 x 10 " mm 2 /min. See Table I for comparative results.
- EXAMPLE I-4 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes. This process yields a contact lens having an oxygen transmissibility of 97 barrers/mm and an lonoflux Diffusion Coefficient of 2.0 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE I-5 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes. This process yields a contact lens having an oxygen transmissibility of 85 barrers/mm and an lonoflux Diffusion Coefficient of 2.2 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE I-6 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 15 mW ultraviolet light for a period of about 5 minutes. This process yields a contact lens having an oxygen transmissibility of 93 barrers/mm and an lonoflux Diffusion Coefficient of 1.9 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE 1-7 A polymerizable mixture is prepared as in Example 1-1. The mixture is subjected to a freeze-thaw degassing process as in Example 1-1.
- the degassed mixture is cast into a contact lens in ambient atmosphere by applying 15 mW ultraviolet light for a period of about 10 minutes.
- This process yields a contact lens having an oxygen transmissibility of 96 barrers/mm and an lonoflux Diffusion Coefficient of 1.6 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE I-8 A polymerizable mixture is prepared as in Example 1-1. The mixture is degassed by applying a vacuum via the conventional laboratory technique of tap water aspiration for a period of about 20 minutes. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes.
- This process yields a contact lens having an oxygen transmissibility of 94 barrers/mm and aann lloonnooflux Diffusion Coefficient of 1.6 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE I-9 A polymerizable mixture is prepared as in Example 1-1.
- the mixture is degassed by applying a vacuum via the conventional laboratory technique of tap water aspiration for a period of about 20 minutes.
- the degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes. This process yields a contact lens having an oxygen transmissibility of 94 barrers/mm and an lonoflux Diffusion Coefficient of 1.3 x 10 "4 mm /min. See Table I for comparative results.
- EXAMPLE 1-10 A polymerizable mixture is prepared as in Example 1-1. The mixture is degassed by applying a vacuum via the conventional laboratory technique of tap water aspiration for a period of about 20 minutes. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 60 minutes. This process yields a contact lens having an oxygen transmissibility of 96 barrers/mm and an lonoflux Diffusion Coefficient of 0.9 x 10 "4 mm 2 /min. See Table I for comparative results.
- EXAMPLE 1-1 1 A polymerizable mixture is prepared as in Example 1-1. The mixture is degassed by bubbling nitrogen through the mixture for a period of about 30 minutes.
- the degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes. This process yields a contact lens having an oxygen transmissibility of 91 barrers/mm and an lonoflux Diffusion Coefficient of 1.6 x 10 " mm 2 /min. See Table I for comparative results.
- EXAMPLE 1-12 A polymerizable mixture is prepared as in Example 1-1. The mixture is degassed by bubbling nitrogen through the mixture for a period of about 30 minutes. The degassed mixture is cast into a contact lens in ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes. This process yields a contact lens having an oxygen transmissibility of 94 barrers/mm and an lonoflux Diffusion Coefficient of 1.1 x 10 "4 mm 2 /min. See Table I for comparative results.
- Table I shows that a freeze-thaw degassing procedure produces a higher lonoflux Diffusion Coefficient than the aspirator or nitrogen purge techniques.
- the freeze-thaw technique is more rigorous, and produces a mixture having a lower oxygen concentration. Accordingly, lower oxygen concentrations in the polymerizable mixture result in higher ion permeability in the cured contact lens. Furthermore, the correlation between ion permeability and on-eye movement was established in prior Examples. Thus, a lower oxygen concentration in the polymerizable mixture produces a contact lens having a better on-eye movement.
- the glove box curing technique produced a high ion permeability, and hence better on-eye movement, than the atmosphere curing techniques. Accordingly, in order to produce a lens having a balance of high oxygen permeability and good on-eye movement, it is highly preferred to polymerize a siioxane-containing methacrylate macromer with an acrylamide monomer in the absence or substantial absence of oxygen.
- EXAMPLE J-1 A polymerizable mixture containing about 50 weight percent Material A macromer, about 20% TRIS, about 25.5% dimethylacrylamide (DMA), and about 0.5% BLEMER QA, is prepared, with all percentages based on total polymerizable mixture weight. Ethanol is added as a solvent at about 22.4% and about 0.5% Darocur 1173 is added as a photoinitiator, with percentages based on total mixture weight.
- DMA dimethylacrylamide
- Example 1-1 The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1.
- the degassed mixture is cast into a contact lens in accordance with the glove box procedure of Example 1-1 by applying 15 mW ultraviolet light for a period of about 5 minutes.
- This freeze-thaw/glove box process yields a contact lens having an oxygen transmissibility of 96 barrers/mm and an lonoflux Diffusion Coefficient of 3.5 x 10 "4 mm 2 /min. See Table J for comparative results.
- EXAMPLE J-2 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in accordance with the glove box procedure of Example 1-1 by applying 8 mW ultraviolet light for a period of about 20 minutes. This freeze-thaw/glove box process yields a contact lens having an oxygen transmissibility of 116 barrers/mm and an lonoflux Diffusion Coefficient of 4.1 x 10 "4 mm 2 /m ⁇ n. See Table J for comparative results.
- EXAMPLE J-3 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in accordance with the glove box procedure of Example 1-1 by applying 8 mW ultraviolet light for a period of about 10 minutes.
- This freeze-thaw/glove box process yields a contact lens having an oxygen transmissibility of 1 18 barrers/mm and an lonoflux Diffusion Coefficient of 3.8 x 10 "4 mm 2 /m ⁇ n. See Table J for comparative results.
- EXAMPLE J-4 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes. This process yields a contact lens having an oxygen transmissibility of 111 barrers/mm and an lonoflux Diffuston Coefficient of 0.06 x 10 "4 mm 2 /m ⁇ n. See Table J for comparative results.
- EXAMPLE J-5 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes. This process yields a contact lens having an oxygen transmissibility of 114 barrers/mm and an lonoflux Diffusion Coefficient of 0.09 x 10 "4 mm 2 /m ⁇ n. See Table J for comparative results.
- EXAMPLE J-6 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 15 mW ultraviolet light for a period of about 5 minutes. This process yields a contact lens having an lonoflux Diffusion Coefficient of 0.25 x 10 '4 mm 2 /min. See Table J for comparative results.
- EXAMPLE J-7 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a freeze-thaw degassing process as described in Example 1-1. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 15 mW ultraviolet light for a period of about 10 minutes.
- This process yields a contact lens having an oxygen transmissibility of 90 barrers/mm and an lonoflux Diffusion Coefficient of 0.47 x 10 "4 mm 2 /min. See Table J for comparative results.
- EXAMPLE J-8 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to an aspirator degassing process as described in Example I-8. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes. This process yields a contact lens having an oxygen transmissibility of 98 barrers/mm and an lonoflux Diffusion Coefficient of 0.31 x 10 "4 mm 2 /min. See Table J for comparative results.
- EXAMPLE J-9 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to an aspirator degassing process as described in Example I-8. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes.
- This process yields a contact lens having an oxygen transmissibility of 93 barrers/mm and an lonoflux Diffusion Coefficient of 0.31 x 10 "4 mm 2 /min. See Table J for comparative results.
- EXAMPLE J-10 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to an aspirator degassing process as described in Example I-8. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 60 minutes This process yields a contact lens having an oxygen transmissibility of 95 barrers/mm and an lonoflux Diffusion Coefficient of 0.19 x 10 "4 mm 2 /m ⁇ n See Table J for comparative results
- EXAMPLE J-11 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a nitrogen bubbling degassing process as desc ⁇ bed in Example I-8. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 15 minutes
- EXAMPLE J-12 A polymerizable mixture is prepared as in Example J-1. The mixture is subjected to a nitrogen bubbling degassing process as described in Example I-8. The degassed mixture is cast into a contact lens in an ambient atmosphere by applying 8 mW ultraviolet light for a period of about 30 minutes. This process yields a contact lens having an oxygen transmissibility of 118 barrers/mm and an lonoflux Diffusion Coefficient of 0.16 x 10 "4 mm /m ⁇ n. See Table J for comparative results.
- Table J shows that a freeze-thaw degassing procedure produces a higher lonoflux Diffusion Coefficient than the aspirator or nitrogen purge techniques. As with Table I, this data further illustrates that a lower oxygen concentration in the polymerizable mixture produces a contact lens having a better on-eye movement.
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Abstract
Description
Claims
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US569816 | 1995-12-08 | ||
US08569816 US5760100B1 (en) | 1994-09-06 | 1995-12-08 | Extended wear ophthalmic lens |
US2773696P | 1996-10-03 | 1996-10-03 | |
PCT/IB1996/001368 WO1997022019A1 (en) | 1995-12-08 | 1996-12-06 | Methods of manufacturing contact lenses |
US27736 | 2001-12-19 |
Publications (1)
Publication Number | Publication Date |
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EP0865615A1 true EP0865615A1 (en) | 1998-09-23 |
Family
ID=26702828
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96939249A Withdrawn EP0865615A1 (en) | 1995-12-08 | 1996-12-06 | Methods of manufacturing contact lenses |
Country Status (5)
Country | Link |
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EP (1) | EP0865615A1 (en) |
JP (1) | JP2000501853A (en) |
AU (1) | AU7637396A (en) |
CA (1) | CA2238650A1 (en) |
WO (1) | WO1997022019A1 (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU9629098A (en) * | 1997-10-02 | 1999-04-27 | Novartis Ag | Ophthalmic lens production process |
JPH11228643A (en) | 1998-02-17 | 1999-08-24 | Menicon Co Ltd | Material for eye lens and its production |
AR024237A1 (en) * | 1998-12-21 | 2002-09-25 | Novartis Ag | AMPHIFILIC BLOCK COPOLYMERS, PROCEDURE AND PRECURSORS FOR THEIR PREPARATION, AND MOLDED ARTICLE OBTAINABLE FROM THE SAME |
JP2001201723A (en) * | 2000-01-18 | 2001-07-27 | Asahi Kasei Aimii Kk | Soft contact lens for continuous wearing |
JP3929014B2 (en) * | 2000-02-24 | 2007-06-13 | Hoyaヘルスケア株式会社 | Contact lens material comprising a macromer having a polysiloxane structure in the side chain |
US6926965B2 (en) * | 2002-09-11 | 2005-08-09 | Novartis Ag | LbL-coated medical device and method for making the same |
US8470906B2 (en) * | 2008-09-30 | 2013-06-25 | Johnson & Johnson Vision Care, Inc. | Ionic silicone hydrogels having improved hydrolytic stability |
US20130203812A1 (en) | 2008-09-30 | 2013-08-08 | Johnson & Johnson Vision Care, Inc. | Ionic silicone hydrogels comprising pharmaceutical and/or nutriceutical components and having improved hydrolytic stability |
TWI459071B (en) | 2011-09-02 | 2014-11-01 | Benq Materials Corp | Material for contact lenses, method for manufacturing contact lenses and contact lenses obtained thereby |
JP6037454B2 (en) * | 2013-11-15 | 2016-12-07 | 信越化学工業株式会社 | Monomers for ophthalmic device manufacturing |
WO2018095837A1 (en) * | 2016-11-23 | 2018-05-31 | Atheneum Optical Sciences, Llc | Three-dimensional printing of optical devices |
US11029538B2 (en) | 2017-10-25 | 2021-06-08 | Coopervision International Limited | Contact lenses having an ion-impermeable portion and related methods |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5010141A (en) * | 1989-10-25 | 1991-04-23 | Ciba-Geigy Corporation | Reactive silicone and/or fluorine containing hydrophilic prepolymers and polymers thereof |
AU643495B2 (en) * | 1989-12-29 | 1993-11-18 | Hoya Corporation | Contact lens material and contact lens |
DE69121179T2 (en) * | 1990-12-20 | 1997-01-30 | Ciba Geigy Ag | Poly (alkylene oxide) block copolymers and contact lenses containing fluoride and / or silicone |
US5194556A (en) * | 1991-01-09 | 1993-03-16 | Ciba-Geigy Corporation | Rigid contact lenses with improved oxygen permeability |
JP3335216B2 (en) * | 1992-06-29 | 2002-10-15 | 株式会社メニコン | Ophthalmic lens materials |
-
1996
- 1996-12-06 CA CA 2238650 patent/CA2238650A1/en not_active Abandoned
- 1996-12-06 EP EP96939249A patent/EP0865615A1/en not_active Withdrawn
- 1996-12-06 AU AU76373/96A patent/AU7637396A/en not_active Abandoned
- 1996-12-06 WO PCT/IB1996/001368 patent/WO1997022019A1/en not_active Application Discontinuation
- 1996-12-06 JP JP9521892A patent/JP2000501853A/en active Pending
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See references of WO9722019A1 * |
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Publication number | Publication date |
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JP2000501853A (en) | 2000-02-15 |
AU7637396A (en) | 1997-07-03 |
CA2238650A1 (en) | 1997-06-19 |
WO1997022019A1 (en) | 1997-06-19 |
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