EP2152503A1 - Ophthalmic lens mold surface energy differential - Google Patents
Ophthalmic lens mold surface energy differentialInfo
- Publication number
- EP2152503A1 EP2152503A1 EP08746429A EP08746429A EP2152503A1 EP 2152503 A1 EP2152503 A1 EP 2152503A1 EP 08746429 A EP08746429 A EP 08746429A EP 08746429 A EP08746429 A EP 08746429A EP 2152503 A1 EP2152503 A1 EP 2152503A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mold
- lens
- mold part
- thermal plastic
- surface energy
- 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- Withdrawn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
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000000654 additive Substances 0.000 claims abstract description 26
- 230000000996 additive effect Effects 0.000 claims abstract description 17
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 50
- 238000009472 formulation Methods 0.000 claims description 24
- 239000000017 hydrogel Substances 0.000 claims description 14
- 239000000088 plastic resin Substances 0.000 claims description 10
- 229920006109 alicyclic polymer Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 229920000098 polyolefin Polymers 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 230000005855 radiation Effects 0.000 claims description 5
- 230000000977 initiatory effect Effects 0.000 claims description 4
- 238000000465 moulding Methods 0.000 claims description 4
- UURVHRGPGCBHIC-UHFFFAOYSA-N 3-(ethenoxycarbonylamino)propanoic acid 4-[[[[[[[[[[[[[[[[[[[[[[[[[[[4-ethenoxycarbonyloxybutyl(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]butyl ethenyl carbonate 1-ethenylpyrrolidin-2-one ethenyl N-[3-tris(trimethylsilyloxy)silylpropyl]carbamate Chemical compound C=CN1CCCC1=O.OC(=O)CCNC(=O)OC=C.C[Si](C)(C)O[Si](CCCNC(=O)OC=C)(O[Si](C)(C)C)O[Si](C)(C)C.C[Si](C)(CCCCOC(=O)OC=C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)CCCCOC(=O)OC=C UURVHRGPGCBHIC-UHFFFAOYSA-N 0.000 claims description 3
- ZOPSJJCUEOEROC-NSQCPRBHSA-N 3-[[butyl(dimethyl)silyl]oxy-dimethylsilyl]propyl 2-methylprop-2-enoate;n,n-dimethylprop-2-enamide;1-ethenylpyrrolidin-2-one;2-hydroxyethyl 2-methylprop-2-enoate;[(2r)-2-hydroxy-3-[3-[methyl-bis(trimethylsilyloxy)silyl]propoxy]propyl] 2-methylprop-2-enoat Chemical compound CN(C)C(=O)C=C.C=CN1CCCC1=O.CC(=C)C(=O)OCCO.CC(=C)C(=O)OCCOC(=O)C(C)=C.CCCC[Si](C)(C)O[Si](C)(C)CCCOC(=O)C(C)=C.CC(=C)C(=O)OC[C@H](O)COCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C ZOPSJJCUEOEROC-NSQCPRBHSA-N 0.000 claims description 3
- 229920001616 Polymacon Polymers 0.000 claims description 3
- 239000002736 nonionic surfactant Substances 0.000 claims description 3
- NLAIHECABDOZBR-UHFFFAOYSA-M sodium 2,2-bis(2-methylprop-2-enoyloxymethyl)butyl 2-methylprop-2-enoate 2-hydroxyethyl 2-methylprop-2-enoate 2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O.CC(=C)C(=O)OCCO.CCC(COC(=O)C(C)=C)(COC(=O)C(C)=C)COC(=O)C(C)=C NLAIHECABDOZBR-UHFFFAOYSA-M 0.000 claims description 3
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 2
- 229920001971 elastomer Polymers 0.000 claims 9
- 239000000806 elastomer Substances 0.000 claims 9
- 239000004033 plastic Substances 0.000 claims 9
- 239000000155 melt Substances 0.000 claims 2
- VCLWNCAUAKTVII-UHFFFAOYSA-N C=C.CC=C.C=CC1=CC=CC=C1 Chemical group C=C.CC=C.C=CC1=CC=CC=C1 VCLWNCAUAKTVII-UHFFFAOYSA-N 0.000 claims 1
- 229920001400 block copolymer Polymers 0.000 claims 1
- 238000000151 deposition Methods 0.000 claims 1
- 229920006132 styrene block copolymer Polymers 0.000 claims 1
- 230000008569 process Effects 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- -1 and lotrafilcon A Chemical compound 0.000 description 29
- 239000000463 material Substances 0.000 description 26
- 239000004743 Polypropylene Substances 0.000 description 17
- 229920001155 polypropylene Polymers 0.000 description 13
- 239000000178 monomer Substances 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 7
- 125000002837 carbocyclic group Chemical group 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 5
- 125000003368 amide group Chemical group 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000013329 compounding Methods 0.000 description 4
- 230000036571 hydration Effects 0.000 description 4
- 238000006703 hydration reaction Methods 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 description 4
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000012937 correction Methods 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 229920002397 thermoplastic olefin Polymers 0.000 description 3
- 239000004713 Cyclic olefin copolymer Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 238000012876 topography Methods 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- 240000000015 Iris germanica Species 0.000 description 1
- 206010052143 Ocular discomfort Diseases 0.000 description 1
- 241000245032 Trillium Species 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical class [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007516 diamond turning Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000004384 eye physiology Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical class C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000003698 laser cutting Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002847 norbornane derivatives Chemical class 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007152 ring opening metathesis polymerisation reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00009—Production of simple or compound lenses
- B29D11/00038—Production of contact lenses
- B29D11/00125—Auxiliary operations, e.g. removing oxygen from the mould, conveying moulds from a storage to the production line in an inert atmosphere
- B29D11/00192—Demoulding, e.g. separating lenses from mould halves
-
- 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
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/38—Moulds or cores; Details thereof or accessories therefor characterised by the material or the manufacturing process
Definitions
- This invention describes molds and ophthalmic lenses formed with the molds and a surface energy differential therebetween.
- contact lenses can be used to improve vision.
- Various contact lenses have been commercially produced for many years. Early designs of contact lenses were fashioned from hard materials. Although these lenses are still currently used in some applications, they are not suitable for all patients due to their poor comfort and relatively low permeability to oxygen. Later developments in the field gave rise to soft contact lenses based upon hydrogels.
- Hydrogel contact lenses are popular and often more comfortable to wear than contact lenses made of hard materials.
- Malleable soft contact lenses made from hydrogels can be manufactured by forming a lens in a multi-part mold where the combined parts form a topography consistent with the desired final lens.
- Ophthalmic lenses are often made by cast molding, in which a monomer material is deposited in a cavity defined between optical surfaces of opposing mold parts.
- Multi-part molds used to fashion hydrogels into a useful article, such as an ophthalmic lens can include for example, a first mold part with a convex portion that corresponds with a back curve of an ophthalmic lens and a second mold part with a concave portion that corresponds with a front curve of the ophthalmic lens.
- an uncured hydrogel lens formulation is placed between a front curve mold part and a back curve mold part. The mold parts are brought together to shape the lens formulation according to desired lens parameters.
- a lens edge was formed about the perimeter of the formed lens by compression of an edge formed into the mold parts which penetrates the lens formulation and incises it into a lens portion and an excess ring portion.
- the lens formulation was subsequently cured, for example by exposure to heat and light, thereby forming a lens.
- mold portions are separated and the lens remains adhered to one of the mold portions.
- the lens and the excess polymer ring must be separated and the excess polymer ring discarded.
- lens damage may occur. Damage can include, for example: edge chips and tears; holes; lens delamination or pulls; lenses adhering to a wrong mold part, optical distortion; and surface marks.
- the present invention includes improved molds and processes useful in the creation of an ophthalmic lens.
- a mold material can be used with one or more additives which reduce the surface tension of the mold material and increase a differential between one or both mold parts and the lens formed therebetween.
- a lens forming mixture is cured in a cavity of a desired shape formed by two or more mold parts. At least one of the mold parts is molded from a material with a differential in surface energy between a mold used to form an ophthalmic lens and the ophthalmic lens formed.
- Embodiments can include at least one of the mold parts being transparent to polymerization initiating radiation such that a polymerizable lens forming mixture can be deposited in the cavity and the mold part and polymerizable composition can be exposed to polymerization initiating radiation.
- Embodiments can also include methods of producing an ophthalmic lens by dispensing an uncured lens formulation onto a surface of a mold part with a surface tension less than 30 mN/m.
- the lens can include, for example, a silicone hydrogel formulation or a hydrogel formulation.
- Specific examples can include a lens formed from: acquafilcon A, balafilcon A, and lotrafilcon A, etafilcon A, genfilcon A, lenefilcon A, polymacon and galyfilcon A, and senofilcon A.
- FIG. 1 illustrates a mold assembly according to some embodiments of the present invention.
- FIG. 2 illustrates a flow chart of exemplary steps that can be executed while implementing some embodiments of the present to create a mold part.
- FIG. 3 illustrates a flow chart of exemplary steps that can be executed while implementing some embodiments of the present to create an ophthalmic lens.
- FIG. 4 illustrates a chart with exemplary data indicating surface energy qualities of molds fashioned from thermoplastic resins and compounds of thermoplastic resins.
- FIG. 5 illustrates a chart with lens release time data as it relates to different mold part materials.
- the present invention includes molds and methods for making an ophthalmic lens.
- at least one part of a multi-part mold that is used in the manufacture of an ophthalmic lens is injection molded from a thermal plastic resin (hereinafter referred to as "TPR") compounded with an additive to reduce the surface energy of the mold material.
- TPR thermal plastic resin
- selection of mold part materials and monomers which result in an increased surface energy differential between monomers or cured lenses and FC molds facilitates silicone hydrogel easy lens release during aqueous hydration.
- surface energy differential or "delta" can defined as Surface Energy of Monomer or Cured Lens - Surface Energy of Mold Part.
- preferred embodiments include a surface energy of delta between a front curve mold part and a lens that is greater than 0.
- the mechanisms of adhesion are generally the result of surface energy related parameters relating to the two surfaces that are in contact.
- use of mold materials with low surface energy, such as, for example, ⁇ 30 mN/m or less, as front curve (FC) reduces adhesive force or adhesion energy between cured lens and FC mold, and, therefore, facilitate easier and faster silicone hydrogel lens release during aqueous hydration.
- FC mold materials with lower surface energy can be successfully obtained by compounding PP with selective additives, such as Siloxane MB50-001 and Trilwet A.
- ophthalmic lens molds comprising TPR and additive blends result in a mold surface energy of an uncoated ophthalmic lens mold of about 30 mN/m or less.
- Methods of the present invention therefore include fashioning an ophthalmic lens from a mold with one or more mold part having an uncoated surface energy of about 30 mN/m or less.
- One or both mold parts utilized to form an ophthalmic lens is injection molded from a TPR with an additive or other mechanism to reduce the surface energy of the mold part to less than 30mN/m.
- Injection molding apparatus will typically include precision tooling that has been machined from a metal, such as, for example, brass, stainless steel or nickel or some combination thereof.
- tooling is fashioned in a desired shape and machined or polished to achieve precision surface quality. The precision surface in turn increases the quality of a mold part injection molded therefrom.
- mold parts are fashioned from a thermoplastic polyolefin with an additive to produce single use cast molds with a surface energy of less than 30 mN/m which reduces the adhesive force between a cured lens and mold parts used to fashion the lens and is therefore conducive to the manufacture of ophthalmic lenses.
- Advantages of utilizing molds comprising a thermoplastic polyolefin material with an additive which results in a surface energy of less than 30mN/m include a diminished number of lens defects, such as holes, chips and tears resulting from demold; and also improved release from a mold part in which it is formed.
- lens refers to any ophthalmic device that resides in or on the eye. These devices can provide optical correction or may be cosmetic.
- the term lens can refer to a contact lens, intraocular lens, overlay lens, ocular insert, optical insert or other similar device through which vision is corrected or modified, or through which eye physiology is cosmetically enhanced (e.g. iris color) without impeding vision.
- the term "lens forming mixture” refers to a mixture of materials that can react, or be cured, to form an ophthalmic lens. Such a mixture can include polymerizable components (monomers), additives such as UV blockers and tints, photoinitiators or catalysts, and other additives one might desire in an ophthalmic lens such as a contact or intraocular lens.
- a preferred lens type can include a lens that is made from silicone elastomers or hydrogels, such as, for example, silicone hydrogels, fluorohydrogels, including those comprising silicone/hydrophilic macromers, silicone based monomers, initiators and additives.
- silicone elastomers or hydrogels such as, for example, silicone hydrogels, fluorohydrogels, including those comprising silicone/hydrophilic macromers, silicone based monomers, initiators and additives.
- some preferred lens types can also include etafilcon A, genifilcon A, lenefilcon A, polymacon, acquafilcon A, balafilcon A, lotrafilcon A, galyfilcon A, senofilcon A, silicone hydrogels.
- a diagram of an exemplary mold for an ophthalmic lens is illustrated.
- the terms "mold” and “mold assembly” refer to a form 100 having a cavity 105 into which a lens forming mixture can be dispensed such that upon reaction or cure of the lens forming mixture (not illustrated), an ophthalmic lens of a desired shape is produced.
- the molds and mold assemblies 100 of this invention are made up of more than one "mold parts" or "mold pieces" 101-102.
- the mold parts 101-102 can be brought together such that a cavity 105 is formed between the mold parts 101-102 in which a lens can be formed. This combination of mold parts 101-102 is preferably temporary. Upon formation of the lens, the mold parts 101-102 can again be separated for removal of the lens.
- At least one mold part 101-102 has at least a portion of its surface 103-104 in contact with the lens forming mixture such that upon reaction or cure of the lens forming mixture that surface 103-104 provides a desired shape and form to the portion of the lens with which it is in contact.
- the same is true of at least one other mold part 101-102.
- a mold assembly 100 is formed from two parts 101-102, a female concave piece (front piece) 102 and a male convex piece (back piece) 101 with a cavity formed between them.
- the portion of the concave surface 104 which makes contact with lens forming mixture has the curvature of the front curve of an ophthalmic lens to be produced in the mold assembly 100 and is sufficiently smooth and formed such that the surface of a ophthalmic lens formed by polymerization of the lens forming mixture which is in contact with the concave surface 104 is optically acceptable.
- the front mold piece 102 can also have an annular flange integral with and surrounding circular circumferential edge 108 and extends from it in a plane normal to the axis and extending from the flange (not shown).
- the back mold piece 101 has a central curved section with a concave surface 106, convex surface 103 and circular circumferential edge 107, wherein the portion of the convex surface 103 in contact with the lens forming mixture has the curvature of the back curve of a ophthalmic lens to be produced in the mold assembly 100 and is sufficiently smooth and formed such that the surface of a ophthalmic lens formed by reaction or cure of the lens forming mixture in contact with the back surface 103 is optically acceptable.
- the inner concave surface 104 of the front mold half 102 defines the outer surface of the ophthalmic lens
- the outer convex surface 103 of the base mold half 101 defines the inner surface of the ophthalmic lens.
- molds 100 can include two mold parts 101-102 as described above, wherein one or both of the front curve part 102 and the back curve part 101 of the mold 100 comprises a thermoplastic polyolefin compound with a surface energy of less than 30mN/m.
- Blended mold material resins can be obtained, for example, using different compounding methods, including hand blending, single screw compounding, twin screw and/or multiple screw compounding.
- Preferred embodiments of a mold material include a polyolefin; cyclic olefins; and cyclic olefin copolymers; including, in some embodiments polyolefins and COCs.
- Additives that may be compounded with the preferred mold materials include: a) Siloxanes including a class of organosilicon compounds with empirical formula R ⁇ SiO, where R is an organic group; b) non-ionic surfactants such as: alkyl ethoxylates and glycerol monostearate; and
- Siloxanes can include [SiO(CH 3 ) 2 ] n (dimethylsiloxane) and [SiO(C6H 5 ) 2 ] n
- Siloxane orgaosilicon compounds can include both organic and inorganic chemical compounds.
- Organic side chains can confer hydrophobic properties and an -Si-O-Si-O- backbone is inorganic.
- Glycerol monostearate can include a lipophilic non-ionic surfactant with HLB of 3.6 - 4.2 and a chemical formula of CH3(CH2)16COOCH2CHOHCH2OH.
- Polyvinylpyrrolidone can include a nonionic powder with the chemical formula (C 6 H 9 NO) x
- additives that decrease the surface energy of a mold material predominantly made up of one or more of: polyolefin; cyclic olefins; and cyclic olefin copolymers; include:
- Glycerol Monostearate from SparTech, Inc.
- PVP K-90 from International Specialty Products.
- Preferred embodiments can also include a polyolefin of one or more of: polypropylene, polystyrene, polyethylene, polymethyl methacrylate, and modified polyolefins.
- Thermoplastics that can be compounded with an additive can include, for example, one or more of: polypropylene, polystyrene and alicyclic polymers.
- the thermoplastic resin can include an alicyclic polymer which refers to compounds having at least one saturated carbocyclic ring therein.
- the saturated carbocyclic rings may be substituted with one or more members of the group consisting of hydrogen, Ci-ioalkyl, halogen, hydroxyl, Ci-ioalkoxycarbonyl, Ci-ioalkoxy, cyano, amido, imido, silyl, and substituted Ci_ioalkyl where the substituents are selected from one or more members of the group consisting of halogen, hydroxyl, Ci-ioalkoxycarbonyl, Ci-ioalkoxy, cyano, amido, imido, and silyl.
- alicyclic polymers include but are not limited to polymerizable cyclobutanes, cyclopentanes, cyclohexanes, cycloheptanes, cyclooctanes, biscyclobutanes, biscyclopentanes, biscyclohexanes, biscycloheptanes, biscyclooctanes, and norbornanes. It is preferred that the at least two alicyclic polymers be polymerized by ring opening metathesis followed by hydrogenation. Since co-polymers are costly, it is preferable that the molds made from these co-polymers may be used several times to prepare lenses instead of once which is typical. For the preferred molds of the invention, they may be used more than once to produce lenses.
- examples of alicyclic polymer containing saturated carbocyclic rings include but are not limited to the following structures
- R . 1 - 6 are independently selected from one or more members of the group consisting of hydrogen, Ci-ioalkyl, halogen, hydroxyl, Ci-ioalkoxycarbonyl, Ci-ioalkoxy, cyano, amido, imido, silyl, and substituted Ci_ioalkyl where the substituents selected from one or more members of the group consisting of halogen, hydroxyl, Ci_ioalkoxycarbonyl, Ci_ioalkoxy, cyano, amido, imido and silyl.
- R 1"6 may be taken together to form an unsaturated bond, a carbocyclic ring, a carbocyclic ring containing one or more unsaturated bonds, or an aromatic ring.
- the preferred R 1"6 is selected from the group consisting of Ci-ioalkyl and substituted Ci-ioalkyl where the substituents are selected from the group consisting of halogen, hydroxyl, Ci-ioalkoxycarbonyl, Ci-ioalkoxy, cyano, amido, imido and silyl.
- the alicyclic co-polymers consist of at least two different alicyclic polymer s.
- the preferred alicyclic co-polymers contain two or three different alicyclic polymer s, selected from the group consisting of
- the particularly preferred alicyclic co-polymer contains two different alicyclic momoners where the generic structure of the saturated carbocyclic rings of the alicyclic
- polymers are of the formula R x -R 4 are Ci_ioalkyl.
- the surface energy of the alicyclic co-polymer is between 30 and 45 dynes/cm at 25 0 C.
- a preferred alicyclic co-polymer contains two different alicyclic polymers and is sold by Zeon Chemicals L.P. under the trade name ZEONOR. There are several different grades of ZEONOR. Various grades may have glass transition temperatures ranging from 105 0 C to 160 0 C. A specifically preferred material is ZEONOR 1060R, which according the to the manufacturer, ZEON Chemicals L.P.
- MFR melt flow rate
- Other mold materials that may combined with one or more additives to provide a surface energy of less then 30mN/m and used to form an ophthalmic lens mold include, for example, Zieglar-Natta polypropylene resins (sometimes referred to as znPP).
- Zieglar-Natta polypropylene resins sometimes referred to as znPP.
- PP 9544 MED is a clarified random copolymer for clean molding as per FDA regulation 21 CFR (c)3.2 made available by ExxonMobile Chemical Company.
- PP 9544 MED is a random copolymer (znPP) with ethylene group (hereinafter 9544 MED).
- Other exemplary Zieglar-Natta polypropylene resins include: Atofina Polypropylene 3761 and Atofina Polypropylene 3620 WZ.
- the molds of the invention may contain polymers such as polypropylene, polyethylene, polystyrene, polymethyl methacrylate, modified polyolefins containing an alicyclic moiety in the main chain and cyclic polyolefins, such as, for example Zeonor and EOD 00-11 by Atofina Corporation.
- polymers such as polypropylene, polyethylene, polystyrene, polymethyl methacrylate, modified polyolefins containing an alicyclic moiety in the main chain and cyclic polyolefins, such as, for example Zeonor and EOD 00-11 by Atofina Corporation.
- a blend of the alicyclic co-polymers and polypropylene metalocene catalyst process with nucleation, such as ATOFINA EOD 00-11®
- This blend can be used on either or both mold halves, where it is preferred that this blend is used on the back curve and the front curve consists of the alicyclic co-pol
- molds 100 injection molding is utilized according to known techniques, however, embodiments can also include molds fashioned by other techniques including, for example: lathing, diamond turning, or laser cutting.
- lenses are formed on at least one surface of both mold parts 101-102.
- one surface of the lenses may be formed from a mold part 101-102 and the other lens surface can be formed using a lathing method, or other methods.
- lens forming surface means a surface 103-104 that is used to mold a lens.
- any such surface 103-104 can have an optical quality surface finish, which indicates that it is sufficiently smooth and formed so that a lens surface fashioned by the polymerization of a lens forming material in contact with the molding surface is optically acceptable.
- the lens forming surface 103-104 can have a geometry that is necessary to impart to the lens surface the desired optical characteristics, including without limitation, spherical, aspherical and cylinder power, wave front aberration correction, corneal topography correction and the like as well as any combinations thereof.
- a flowchart illustrates exemplary steps that may be used to implement the present invention.
- a resin including a TPE and an additive for reducing the surface energy of the TPE is plasticized and prepared for use in an injection molding process. Injection molding techniques are well known and preparation typically involves heating resin pellets beyond a melting point.
- the plasticized resin is injected into an injection mold shaped in a fashion suitable for creating an ophthalmic lens mold part 101-102.
- the injection mold is typically placed in a pack and hold status for an appropriate amount of time, which can depend, for example upon the resin utilized and the shape and size of the mold part.
- the formed mold part 101-102 is allowed to cool and at 205, the mold part 101-102 can be ejected, or otherwise removed from the injection mold.
- some embodiments of the present invention include methods of making an ophthalmic lens comprising, consisting essentially of, or consisting of the following steps.
- one or more mold parts 101-102 are created which comprise, consist essentially of, or consist of, including a TPR compounded with an additive for reducing the surface energy of the TPE.
- an uncured lens formulation is dispensed onto the one or more mold parts 101-102 and at 303, the lens formulation is cured under suitable conditions. Additional steps can include, for example, hydrating a cured lens until it releases from a mold part 101-102 and leaching acute ocular discomfort agents from the lens.
- the term "uncured” refers to the physical state of a lens formulation prior to final curing of the lens formulation to make the lens.
- lens formulations can contain mixtures of monomers which are cured only once.
- Other embodiments can include partially cured lens formulations that contain monomers, partially cured monomers, macromers and other components.
- the phrase "curing under suitable conditions" refers to any suitable method of curing lens formulations, such as using light, heat, and the appropriate catalysts to produce a cured lens.
- Light can include, in some specific examples, ultra violet light. Curing can include any exposure of the lens forming mixture to an actinic radiation sufficient to case the lens forming mixture to polymerize.
- a graph 400 is provided which illustrates surface energy characteristics of mold materials, in including some molds fashioned from a compound including a TPR and an additive for reducing the surface energy of a mold formed from the TPE. Data associated with the chart 400 is included herein as Table 1.
- a graph 500 illustrates how those materials with reduced mold surface energy facilitate improved release of lenses from the mold parts with the reduced surface energy, wherein the reduced surface energy resulted in a faster release time of a lens from a FC mold part.
- a mold part material with a relatively higher surface energy such as Zeonor 1060R which has surface energy of 43.39mN/m, required a significantly longer time to release an ophthalmic lens formed therein.
- the ophthalmic lenses formed in Zeonor 1060R mold parts required 79 seconds to release at 90 0 C and 170 seconds at 70 0 C.
- mold parts 101-102 fashioned from a thermal plastic resin compounded with an additive to provide an increase in a delta of the surface energy of the mold part and an ophthalmic lens formed therein.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Ophthalmology & Optometry (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Eyeglasses (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91307807P | 2007-04-20 | 2007-04-20 | |
| US11/753,198 US20080290534A1 (en) | 2007-05-24 | 2007-05-24 | Ophthalmic lens mold surface energy differential |
| PCT/US2008/061004 WO2008131329A1 (en) | 2007-04-20 | 2008-04-21 | Ophthalmic lens mold surface energy differential |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2152503A1 true EP2152503A1 (en) | 2010-02-17 |
Family
ID=39671408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP08746429A Withdrawn EP2152503A1 (en) | 2007-04-20 | 2008-04-21 | Ophthalmic lens mold surface energy differential |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP2152503A1 (en) |
| JP (1) | JP2010524729A (en) |
| KR (1) | KR20100017185A (en) |
| AR (1) | AR066116A1 (en) |
| AU (1) | AU2008242679A1 (en) |
| BR (1) | BRPI0810237A2 (en) |
| CA (1) | CA2684870A1 (en) |
| RU (1) | RU2009142845A (en) |
| TW (1) | TW200912424A (en) |
| WO (1) | WO2008131329A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090146329A1 (en) * | 2007-12-06 | 2009-06-11 | Changhong Yin | Lens release |
| CN104115053B (en) * | 2011-12-23 | 2016-04-20 | 庄臣及庄臣视力保护公司 | Comprise the variable optical Ophthalmoligic instrument of liquid crystal cell |
| US10386653B2 (en) | 2012-12-21 | 2019-08-20 | Johnson & Johnson Vision Care, Inc. | Variable optic ophthalmic device including liquid crystal elements |
| MY203315A (en) * | 2014-12-17 | 2024-06-24 | Dsm Ip Assets Bv | Plastic material for industrial former |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6551531B1 (en) * | 2000-03-22 | 2003-04-22 | Johnson & Johnson Vision Care, Inc. | Molds for making ophthalmic devices |
| US7320587B2 (en) * | 2005-08-09 | 2008-01-22 | Cooper Vision, Inc. | Contact lens molds and systems and methods for producing same |
-
2008
- 2008-04-18 TW TW097114043A patent/TW200912424A/en unknown
- 2008-04-18 AR ARP080101612A patent/AR066116A1/en unknown
- 2008-04-21 RU RU2009142845/05A patent/RU2009142845A/en not_active Application Discontinuation
- 2008-04-21 WO PCT/US2008/061004 patent/WO2008131329A1/en not_active Ceased
- 2008-04-21 JP JP2010504307A patent/JP2010524729A/en active Pending
- 2008-04-21 EP EP08746429A patent/EP2152503A1/en not_active Withdrawn
- 2008-04-21 CA CA002684870A patent/CA2684870A1/en not_active Abandoned
- 2008-04-21 AU AU2008242679A patent/AU2008242679A1/en not_active Abandoned
- 2008-04-21 KR KR1020097024210A patent/KR20100017185A/en not_active Withdrawn
- 2008-04-21 BR BRPI0810237-6A2A patent/BRPI0810237A2/en not_active Application Discontinuation
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2008131329A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100017185A (en) | 2010-02-16 |
| AR066116A1 (en) | 2009-07-22 |
| TW200912424A (en) | 2009-03-16 |
| RU2009142845A (en) | 2011-05-27 |
| JP2010524729A (en) | 2010-07-22 |
| AU2008242679A1 (en) | 2008-10-30 |
| CA2684870A1 (en) | 2008-10-30 |
| WO2008131329A1 (en) | 2008-10-30 |
| BRPI0810237A2 (en) | 2014-10-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20080290534A1 (en) | Ophthalmic lens mold surface energy differential | |
| JP6010832B2 (en) | Ophthalmic device mold and related methods | |
| EP2136987A1 (en) | Molds with thermoplastic elastomers for producing ophthlmic lenses | |
| JP5236653B2 (en) | Removal of excess polymer ring during ophthalmic lens manufacturing | |
| EP1857246A1 (en) | Biomedical device mold | |
| WO2007146365A2 (en) | Decreased lens delamination during ophthalmic lens manufacture | |
| EP1629960B1 (en) | Method and Molds for producing ophthalmic lenses & xA; | |
| WO2008131329A1 (en) | Ophthalmic lens mold surface energy differential | |
| TW200824881A (en) | Electrostatic charge during ophthalmic lens manufacture | |
| CN101663158A (en) | Ophthalmic lens mold surface energy differential | |
| US20090146329A1 (en) | Lens release | |
| HK1088579A (en) | Molds for producing ophthalmic lenses | |
| HK1087067B (en) | Method and molds for producing ophthalmic lenses & xa | |
| HK1110270A (en) | Biomedical device mold |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20091120 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: AL BA MK RS |
|
| DAX | Request for extension of the european patent (deleted) | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1140450 Country of ref document: HK |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
| 18W | Application withdrawn |
Effective date: 20101111 |
|
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: WD Ref document number: 1140450 Country of ref document: HK |