Contact lens and the method of manufacturing thereof

Claim 2

A contact lens consisting of a carrier optical portion and a hydrophilic supporting portion which mediates the contact of the lens with an eye surface, wherein both portions are made from different materials; the supporting portion is divided into at least two independent pieces which protrude above the concave side of the lens and lead from the lens circumference towards the center of said lens which is left free, with gaps being left between individual pieces of the supporting portion; the supporting portion being made from a water-swelling synthetic crosslinked hydrogel which has, in the state of full swelling with physiological saline, a swelling capacity of about 40 to 95 percent; the carrier optical portion being made from a transparent material having a modulus of elasticity at least about twice that of the modulus of elasticity of the supporting portion; and the supporting portion forming a gap of at least 0.01 mm between the eye surface and the uncovered carrier portion of the lens.

Claim 3

A contact lens according to claim 1, wherein said carrier optical portion is preferably produced from poly-(HEMA) or poly (methyl methacrylate).

Claim 4

A contact lens according to claim 1, wherein the longitudinal axes of the individual pieces of said supporting portion are coincidently deflected from the radius of the lens.

Claim 5

A contact lens according to claim 2, wherein the individual pieces of said supporting portion have a bow shape, the angle of deflection being larger at the lens circumference than in the part directed towards center of the lens.

Claim 6

A process for the production of a contact lens having a carrier optical portion and a hydrophilic supporting portion comprising forming a carrier optical lens portion having a concave lower side and a concave exterior side, said carrier optical portion being made of a transparent material having a modulus of elasticity at least about twice that of the modulus of elasticity of the supporting portion, forming on the concave side of said carrier portion the hydrophilic supporting portion comprising at least two independent pieces, by applying to said concave side a cross-linkable solution of a hydrophilic monomer or polymer which, when crosslinked, forms a gel having, in the full state of swelling with physiological saline, a swelling capacity of about 40 to 90 percent, allowing the solvent to evaporate, cross-linking said monomer or polymer, resulting in a hydrophilic supporting portion which is comprised of a different material than the carrier optical portion, storing the resulting lens in physiological saline, and sterilizing the lens, the crosslinkable solution being applied to form protrusions above the concave side of the lens leading from the lens circumference towards, but not including, the center of said lens, each of said protrusions having gaps therebetween, the protrusions being permanently joined on one side thereof to the concave side of said carrier optical portion, the opposite side of said protrusions forming an eye surface designed for resting, in use, on the surface of an eye, the crosslinkable solution being applied in sufficient thickness to result in a gap of at least 0.01 mm between the eye surface and the interior concave surface of the carrier portion.

Claim 7

A process for the production of a contact lens having a carrier optical portion and a hydrophilic supporting portion comprising forming a carrier optical lens portion having a concave lower side and a concave exterior side, said carrier optical portion being made of a transparent material having a modulus of elasticity at least about twice that of the modulus of elasticity of the supporting portion, forming on the concave side of said carrier portion the hydrophilic supporting portion comprising at least two independent pieces, by applying to said concave side a cross-linkable solution of a hydrophilic monomer or polymer which, when crosslinked, forms a gel having, in the full state of swelling with physiological saline, a swelling capacity of about 40 to 90 percent, allowing the solvent to evaporate, cross-linking said monomer or polymer, resulting in a hydrophilic supporting portion which is comprised of a different material than the carrier optical portion, storing the resulting lens in physiological saline, and sterilizing the lens, the crosslinkable solution being applied to form protrusions above the concave side of the lens leading from the lens circumference towards, but not including, the center of said lens, each of said protrusions having gaps therebetween, the protrusions being permanently joined on one side thereof to the concave side of said carrier optical portion, the opposite side of said protrusions forming an eye surface designed for resting, in use, on the surface of an eye, the crosslinkable solution being applied in sufficient thickness to result in a gap of at least 0.01 mm between the eye surface and the interior concave surface of the carrier portion.

Claim 8

The process according to claim 5, wherein said solvent is preferably methanol or ethanol.

Claim 9

The process according to claim 5, wherein the solution of a crosslinkable hydrophilic monomer or polymer is applied on the concave side of a lens by painting or spraying.

Claim 10

The process according to claim 5, wherein the solution of a crosslinkable polymer :s applied on the lower surface of the lens by serigraphy.

Claim 11

The process according to claim 5, wherein a copolymer of glycol methacrylate with glycol dimethacrylate soluble in methanol or ethanol is used as the hydrophilic crosslinkable polymer, where glycol is understood as a mono-, di-, or triethylene glycol.

Claim 12

The process according to claim 5, wherein the crosslinking is carried out by the evaporation of a solvent and reaction with a crosslinking agent at about 40 to 100° C.

Claim 13

The process according to claim 10., wherein the crosslinking agent is glycol monomethacrylate with initiatory liberating free radicals.

Claim 14

The process according to claim 11, wherein said crosslinking agent is preferably 2,2-azo-bisisobutyronitrile.

Claim 15

The process according to claim 10, wherein an anhydride of dicarboxylic acid is used as a crosslinking agent.

Claim 16

The process according to claim 10, wherein an acid condensation catalyst is used as a crosslinking agent.

Claim 17

The process according to claim 14, wherein said acid condensation catalyst is a multivalent metal halide.

Claim 18

The process according to claim 15, wherein said multivalent metal halide is preferably zinc dichloride.

Claim 19

The process according to claim 5, wherein the carrier optical portion of the lens is produced from a hydrophilic crosslinked gel, the solution of a crosslinkable hydrophilic monomer or polymer being applied on the lower surface of the carrier portion after it has been dried at least in part, and the monomer being polymerized either by means of an initiator added in advance or by the additional irradiation with rays, for example, short-wave rays.

Claim 20

The process according to claim 17, wherein said initiator is preferably 2,2-azo-bis-isobutyronitrile.

Claim 21

The process according to claim 5, wherein the pieces of the protruding supporting portion of the lens are formed on the lower surface of the lens by the action of chemical reagents which increase the local swelling capacity of the original material to about 40 to 95 percent.

Claim 22

The process according to claim 19, wherein said reagent is selected from the group consisting of an at least 5% solution of alkaline hydroxide, an at least 10% solution of ammonium hydroxide, a solution of hydrogen chloride in an at least 50% aqueous solution of zinc dichloride having a pH up to 1.5, an at least 70% solution of sulfuric acid, an at least 96% solution of phosphoric acid, and mixtures of mutually compatible agents from this group used as the reagent to locally increase the swelling capacity of the organic material of the carrier optical part.

Claim 23

The process according to claim 20, wherein said reagent contains glycerol.