INSERTION MATERIALS WITH HIGH OXYGEN PERMEABILITY AND HIGH REFRACTIVE INDEX

Abstract

The invention relates generally to an insert intended to be embedded in a silicone hydrogel contact lens. The insert is made of crosslinked materials that are rigid in the dry state at room temperature (approximately 22°C to approximately 26°C), have high oxygen permeability and a high refractive index in the fully hydrated state, and can be softened at temperatures above 32°C. Such materials are useful in the manufacture of embedded contact lens inserts for correcting corneal astigmatism, presbyopia, and color blindness, and for imparting photochromic characteristics to the lenses. The invention also relates to a method for manufacturing embedded silicone hydrogel contact lenses comprising an insert of the invention, and embedded silicone hydrogel contact lenses comprising an insert of the invention.

Description

INSERTION MATERIALS WITH HIGH OXYGEN PERMEABILITY AND HIGH REFRACTIVE INDEX The present invention relates generally to a crosslinked polymeric material that has high oxygen permeability and a high refractive index and is useful for manufacturing soft or rigid inserts for embedded contact lenses. Furthermore, the present invention provides a method for producing inserts made of a crosslinked polymeric material of the invention. BACKGROUND In recent years, it has been proposed that various inserts can be incorporated into hydrogel contact lenses for various purposes, e.g., for corneal health, vision correction, diagnosis, etc. See, e.g., U.S. Patent Nos. 4268132, 4401371, 5098546, 5156726, 6851805, 7490936, 7883207, 8154804, 8215770, 8348424, 8874182, 9176332, 9618773, 10203521, and 10209534; and U.S. Patent Application Publications Nos. 20040141150, 20040212779, 2008 / 0208335, 2009 / 0091818, 20090244477, 2010 / 0072643, 2010 / 0076553, 20110157544, 2012 / 0120365, 2012 / 0140167, 2012 / 0234453, 2014 / 0276481 and 2015 / 0145155. The inserts are typically made of a non-hydrogel material that cannot absorb water, is non-swelling in water, has low oxygen permeability, and a relatively low refractive index. High oxygen permeability is required in an insert to minimize adverse effects on corneal health. A high refractive index is desirable to provide higher optical performance to embedded contact lenses. Therefore, it is desirable to have inserts made of a material with high oxygen permeability and a high refractive index. SUMMARY OF THE INVENTION In one aspect, the invention provides an insert intended to be embedded in a silicone hydrogel contact lens. The insert comprises a crosslinked polymeric material comprising: (1) repeating units of at least one polymerizable material containing polysiloxane, wherein said at least one polymerizable material containing polysiloxane comprises at least one polysiloxane vinyl monomer and / or at least one polysiloxane vinyl crosslinker; (2) repeating units of at least one aryl acrylic monomer;and (3) repeating units of at least one vinyl crosslinking agent, wherein the sum of the amounts of components (1) and (2) is at least approximately 70% by weight of the total weight of the crosslinked polymeric material, wherein the crosslinked polymeric material in the dry state has an upper glass transition temperature greater than approximately 30°C, wherein the crosslinked polymeric material has a water content of less than approximately 5% by weight, an oxygen permeability of at least approximately 60 Barrer and a refractive index of at least approximately 1.40. In another aspect, the invention provides a method for the production of embedded silicone hydrogel contact lenses, each of which comprises an insertion of the invention. In a further aspect, the invention provides an embedded silicone hydrogel contact lens comprising an insertion of the invention therein. L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ These and other aspects of the invention will become apparent from the following description of currently preferred embodiments. The detailed description is merely illustrative of the invention and does not limit its scope, which is defined by the appended claims and their equivalents. As will be obvious to a person skilled in the art, many variations and modifications of the invention can be made without departing from the spirit or scope of the novel concepts disclosed herein. DETAILED DESCRIPTION OF THE EMBODIMENTS OF THE INVENTION Unless otherwise defined, all technical and scientific terms and expressions used herein have the same meaning as those commonly understood by a person skilled in the art to which the present invention pertains. Generally, the nomenclature used herein and the laboratory procedures are well known and commonly employed in the art. These procedures employ conventional methods, such as those provided in the art and various general references. When a term is given in the singular, the inventors also consider the plural form of that term. The nomenclature used herein and the laboratory procedures described below are those well known and commonly employed in the art. The term approximately, as used herein in this application, means that a number, referred to as approximately, comprises the stated number plus or minus 1-10% of that stated number. The term "contact lens" refers to a structure that can be placed on or inside the eye of a wearer. A contact lens can correct, improve, or alter a user's vision, but this is not necessarily the case. A contact lens can be made of any suitable material known to the art or subsequently developed, and can be a soft lens, a hard lens, or an embedded lens. A hydrogel contact lens refers to a contact lens comprising a hydrogel core material. A hydrogel core material may be a non-silicone hydrogel material or preferably a silicone hydrogel material. A silicone hydrogel contact lens refers to a contact lens comprising a silicone hydrogel core material. A hydrogel or hydrogel material refers to a cross-linked polymeric material that has three-dimensional polymer networks (i.e., a polymer matrix), is insoluble in water, but can contain at least 10% by weight of water in its polymer matrix when fully hydrated (or equilibrated). A silicone hydrogel or SiHy refers to a silicone-containing hydrogel obtained by copolymerizing a polymerizable composition comprising at least one silicone-containing monomer or at least one silicone-containing macromer or at least one crosslinkable silicone-containing prepolymer. A siloxane, which is often also described as a silicone, refers to a molecule that has at least one -Si-O-Si- moiety where each Si atom carries two organic groups as substituents. LJCL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ As used in this application, the expression non-silicone hydrogel refers to a hydrogel that is theoretically free of silicone. An embedded silicone hydrogel contact lens refers to a silicone hydrogel contact lens comprising at least one insert made of a material other than a hydrogel and embedded within the silicone hydrogel material as the main lens material in the contact lens. An insert refers to any three-dimensional article made of a non-hydrogel material and having dimensions of at least 5 micrometers, but small enough to be embedded in a silicone hydrogel contact lens. According to the invention, a non-hydrogel material can be any material capable of absorbing less than 5% (preferably about 4% or less, more preferably about 3% or less, even more preferably about 2% or less) by weight of water when fully hydrated. According to the invention, an insert of the invention has a thickness less than any thickness of a silicone hydrogel contact lens embedded in the region where the insert is embedded. An insert can be any object having any geometric shape and can have any desired function. Examples of preferred inserts include, without limitation, thin rigid discs for providing rigid-center optics for astigmatism masking, such as a rigid gas permeable (RGP) contact lens, multifocal lens inserts, photochromic inserts, cosmetic inserts having colored patterns printed thereon, etc. The term hydrophilic, as used herein, describes a material or part thereof that will associate more readily with water than with lipids. The expression room temperature refers to a temperature of approximately 22 °C to approximately 26 °C. The term soluble, in reference to a compound or material in a solvent, means that the compound or material can be dissolved in the solvent to provide a solution with a concentration of at least approximately 0.5% by weight at room temperature (i.e., a temperature of approximately 22°C to approximately 26°C). The term insoluble, in reference to a compound or material in a solvent, means that the compound or material can be dissolved in the solvent to provide a solution with a concentration of less than approximately 0.01% by weight at room temperature (as defined above). A vinyl monomer refers to a compound that has a single ethylenically saturated group, is soluble in a solvent, and can be polymerized actinically or thermally. As used in this application, the term ethylenically unsaturated group is used herein in a broad sense and is intended to encompass any group containing at least one >C=C< group. Examples of ethylenically unsaturated groups include, but are not limited to, L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ O ch3o (met)acryloyl (cC=CH2y / 0c ch=ch2^a|¡|Oi vinyl, styrene or other groups containing C=C. An acrylic monomer refers to a vinyl monomer that has a single (meth)acryloyl group. Examples of acrylic monomers include (meth)acryloxy [or (meth)acryloyloxy] monomers and (meth)acrylamido monomers. A (meth)acryloxy monomer or (meth)acryloxy monomer refers to a vinyl or CH3O monomer that has a single -OCC=CH2 group. A (meth)acrylamide monomer refers to a vinyl monomer that has a single CH3Q group -nr°-cc=ch2 or-nr°-c-ch=ch2 in e| What is H or C1-C4 alkyl. The expression aryl acrylic monomer refers to an acrylic monomer that has at least one aromatic ring. A (meth)acryloxy monomer or (meth)acryloyloxy monomer refers to a vinyl or CH3O monomer that has a single -occ=CH2 ooc-CH=CH2 group A (meth)acrylamide monomer refers to a vinyl monomer that has a single CH3Q group -nr°-cc=ch2 or-nr°-c-ch=ch2θηθ| qUeR° is H or C1-C4 alkyl. The term (meth)acrylamide refers to methacrylamide and / or acrylamide. The term (meth)acrylate refers to methacrylate and / or acrylate. An N-vinyl amide monomer refers to an amide compound that has a vinyl group (—CH=CH2) that is directly attached to the nitrogen atom of the amide group. An ene monomer refers to a vinyl monomer that has a single ene group. A hydrophilic vinyl monomer, a hydrophilic acrylic monomer, a hydrophilic (meth)acryloxy monomer, or a hydrophilic (meth)acrylamide monomer, as used herein, refers, respectively, to a vinyl monomer, an acrylic monomer, a (meth)acryloxy monomer, or a (meth)acrylamide monomer, which typically produces a homopolymer that is soluble in water or can absorb at least 10 percent by weight of water. A hydrophobic vinyl monomer, a hydrophobic acrylic monomer, a hydrophobic (meth)acryloxy monomer, or a hydrophobic (meth)acrylamide monomer, as used herein, refers, respectively, to a vinyl monomer, an acrylic monomer, a (meth)acryloxy monomer, or a (meth)acrylamide monomer, which typically produces a homopolymer that is insoluble in water and can absorb less than 10% by weight of water. As used in this application, the term vinyl crosslinker refers to an organic compound having at least two ethylenically unsaturated groups. A vinyl crosslinking agent refers to a vinyl crosslinker having a molecular weight of 700 Da or less. The term terminal (meth)acryloyl group refers to a (meth)acryloyl group at one of the two ends of the main chain (or structure) of an organic compound, as a person knowledgeable in the subject knows. L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ As used herein, the term "actinic curing," in reference to the curing, crosslinking, or polymerization of a polymerizable composition, prepolymer, or material, means that the curing (e.g., crosslinking and / or polymerization) is carried out by actinic irradiation, such as UV / visible irradiation, ionizing radiation (e.g., gamma-ray or X-ray irradiation), microwave irradiation, and the like. Actinic or thermal curing methods are well known to a person skilled in the art. As used in this application, the term polymer means a material formed by the polymerization / crosslinking of one or more monomers or macromers or prepolymers or combinations thereof. A macromer or prepolymer refers to a compound or polymer that contains ethylenically unsaturated groups and has a number average molecular weight greater than 700 Da. As used in this application, the term "molecular weight of a polymeric material (including monomeric or macromeric materials)" refers to the number-average molecular weight, unless specifically stated otherwise or unless the test conditions indicate otherwise. A person skilled in this art knows how to determine the molecular weight of a polymer by known methods, for example, GPC (gel permeation chromatography) with one or more of a refractive index detector, a low-angle laser light scattering detector, a multi-angle laser light scattering detector, a differential viscometer detector, a UV detector, and an infrared (IR) detector; MALDI-TOF MS (array-assisted desorption / ionization time-of-flight mass spectrometry); en1H NMR (proton nuclear magnetic resonance) spectroscopy, etc. A polysiloxane segment or polydiorganosiloxane segment refers indistinctly to Rsi Rsi •-Si-0--Si— SN r a polymer chain segment (i.e., a divalent radical) of S2 S2 wherein SN is an integer that is 3 or higher and each of Rsi and Rsz are independently selected from each other from the group consisting of: C1-C10 alkyl; phenyl; C1-C4 alkyl-substituted phenyl; C1-C4 alkoxy-substituted phenyl; Ci-Ce phenyl-alkyl; C1-C10 fluoroalkyl; C1-C10 fluoroether; aryl; Ci-Cis aryl-alkyl; -alc(OC2H4)yi-OR° (where ale is an Oi-Oβ alkylene diradical, R° is H or C1-C4 alkyl and γ1 is an integer from 1 to 10); a C2-C4 organic radical having at least one functional group selected from the group consisting of a hydroxyl group (-OH), carboxyl group (-COOH), amino group (-NRniRni), amino linkages of -NRni-, amide linkages of -CONRni-, amide of -CONRniRni, urethane linkages of -OCONH and a C1-C4 alkoxy group, or a linear hydrophilic polymer chain, wherein Rni and Rni are independently of each other hydrogen or a C1-C15 alkyl;and a photochromic organic radical having a photochromic group.; A vinyl polysiloxane monomer refers to a compound comprising at least one polysiloxane segment and a single ethylenically unsaturated group. A polydiorganosiloxane vinyl crosslinker or polysiloxane vinyl crosslinker refers to L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ interchangeably to a compound comprising at least one polysiloxane segment and at least two ethylenically unsaturated groups. A linear polydiorganosiloxane vinyl crosslinker or linear polysiloxane vinyl crosslinker refers interchangeably to a compound comprising a main chain that includes at least one polysiloxane segment and terminates with an ethylenically unsaturated group at each of the two ends of the main chain. A long-chain polydiorganosiloxane vinyl crosslinker or long-chain polysiloxane vinyl crosslinker refers interchangeably to a compound comprising at least two ethylenically unsaturated groups and at least two polysiloxane segments, each pair of which is linked by a divalent radical. The term fluid, as used herein, indicates that a material can flow like a liquid. As used in this application, the term transparent, with reference to a polymerizable composition, means that the polymerizable composition is a transparent liquid mixture or solution (i.e., having a light transmissibility of 85% or greater, preferably 90% or greater, in the range between 400 and 700 nm). The term monovalent radical refers to an organic radical obtained by removing a hydrogen atom from an organic compound and bonding it to another group in that organic compound. Examples include, but are not limited to, alkyl (by removing a hydrogen atom from an alkane), alkoxy (or alkoxyl) (by removing a hydrogen atom from the hydroxyl group of an alkyl alcohol), thiyl (by removing a hydrogen atom from the thiol group of an alkylthiol), cycloalkyl (by removing a hydrogen atom from a cycloalkane), cycloheteroalkyl (by removing a hydrogen atom from a cycloheteroalkane), aryl (by removing a hydrogen atom from an aromatic ring of an aromatic hydrocarbon), heteroaryl (by removing a hydrogen atom from any ring atom), amino (by removing a hydrogen atom from an amine), and so on. The term divalent radical refers to an organic radical obtained by removing two hydrogen atoms from an organic compound and forming two bonds with two other groups in that organic compound. For example, a divalent alkylene (i.e., alkylenyl) radical is obtained by removing two hydrogen atoms from an alkane, and a divalent cycloalkylene (i.e., cycloalkylenyl) radical is obtained by removing two hydrogen atoms from a cyclic ring. In this application, the term substituted, with reference to an alkyl or alkylenyl, means that the alkyl or alkylenyl comprises at least one substituent that replaces a hydrogen atom of the alkyl or alkylenyl and is selected from the group consisting of hydroxyl (OH), carboxyl (-COOH), -NHi, sulfhydryl (-SH), C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio (alkyl sulfide), C1-C4 acylamino, C1-C4 alkylamino, C1-C4 dialkylamino and combinations thereof. A free radical initiator can be either a photoinitiator or a thermal initiator. A photoinitiator refers to a chemical that initiates the crosslinking / polymerization reaction of L / CL ίη / ZZΖΠZ / E / YΙΛΙ free radicals by using light. A thermal initiator refers to a chemical that initiates the free radical crosslinking / polymerization reaction by using thermal energy. The intrinsic oxygen permeability, Dk, of a material is the rate at which oxygen will pass through it. Oxygen permeability is conventionally expressed in units of barre, where barre is defined as [(cm3 of oxygen) (mm) / (cm2)(s)(mm Hg)] x 1010. The oxygen transmissibility, Dk / t, of an insert or material is the rate at which oxygen will pass through a specific insert or material with an average thickness of t [in mm] in the area being measured. Oxygen transmissibility is conventionally expressed in units of swabs / mm, where swabs / mm is defined as [(cm³ of oxygen) / (cm²)(s)(mm Hg)] x 10⁹. Oxygen permeability can be measured according to the procedures described in Example 1. The term modulus or elastic modulus, when referring to a contact lens or a material, means the tensile modulus or Young's modulus, which is a measure of the stiffness of a contact lens or a material. The modulus can be measured according to the procedures described in Example 1. An unprocessed state refers to an insert obtained by casting a polymerizable composition into a mold and which has not undergone any post-molding extraction and / or hydration processes (i.e., it has not been in contact with water or any organic solvent or any liquid after molding). In general, the invention relates to crosslinked materials that are rigid in the dry state at room temperature (approximately 22°C to approximately 26°C), have high oxygen permeability and a high refractive index in the fully hydrated state, and can be softened at temperatures above 32°C. Such materials are useful in the manufacture of inserts in embedded contact lenses for correcting corneal astigmatism, presbyopia, and color blindness, and for imparting photochromic characteristics to lenses. The present invention is based in part on the finding that, when a polymerizable composition for making inserts comprises (1) at least one aryl acrylic monomer and (2) at least one polymerizable material containing silicone, as the two main components (i.e., in a combination constituting at least approximately 70% by weight with respect to the total weight of all polymerizable materials) and at least one vinyl crosslinking agent, insert materials can be obtained that have high oxygen permeability and a high refractive index and are rigid in the dry (unprocessed) state at room temperature.It is believed that by incorporating polymerizable components containing silicone (e.g., vinyl monomer and / or crosslinker) into a polymerizable composition for the manufacture of insert materials (crosslinked polymeric materials), the resulting insert materials can have high oxygen permeability. However, such insert materials are softer and more sticky at room temperature, so there are manufacturing and handling problems associated with this softness and stickiness. It would be very difficult to open the molds and remove the cast-molded inserts from the molds in an unprocessed state (i.e., dry demolding and lens peeling). It has been found that by incorporating an aryl acrylic monomer and / or a crosslinker into the polymerizable composition... L / CL ίη / ZZΖΠZ / E / YΙΛΙ In the manufacture of inserts, the resulting insert materials can have a higher glass transition temperature (e.g., greater than 32 °C) and are thus rigid in the dry (i.e., unprocessed) state at room temperature. Due to their rigidity in the dry state at room temperature, the manufacturing and handling problems associated with the softness and stickiness of an insert material can be significantly reduced or eliminated. The present invention is also based in part on the discovery that, by varying the ratio of the two types of polymerizable components, as well as the amount of a vinyl crosslinker, an insert material can be obtained that has a desired set of properties, such as oxygen permeability, refractive index, and elastic modulus, suitable for embedded contact lenses for different applications. The performance of the embedded contact lenses can be optimized for a given application. In one aspect, the present invention provides an insert intended to be embedded in a silicone hydrogel contact lens, comprising a crosslinked polymeric material comprising: (1) repeating units of at least one polymerizable silicone-containing material (or component); (2) repeating units of at least one aryl acrylic monomer; and (3) repeating units of at least one vinyl crosslinking agent, wherein the sum of the amounts of components (1) and (2) is at least approximately 70% by weight (preferably from approximately 75% to approximately 99% by weight, more preferably from approximately 80% to approximately 98% by weight, even more preferably from approximately 85% to 98% by weight) with respect to the total weight of the crosslinked polymeric material.wherein the crosslinked polymeric material in the dry state has a glass transition temperature greater than approximately 28 °C (preferably approximately 30 °C or more, more preferably approximately 32 °C or more), wherein the crosslinked polymeric material has a water content of less than approximately 5% by weight (preferably approximately 4% by weight or less, more preferably approximately 3% by weight or less, even more preferably approximately 2% by weight or less), an oxygen permeability of at least approximately 60 Barrer (preferably at least approximately 70 Barrer, more preferably at least approximately 80 Barrer, even more preferably at least approximately 90 Barrer) and a refractive index of at least approximately 1.45 (preferably at least 1.47, more preferably at least 1.49, even more preferably at least 1.51). It is understood that the weight percentages of each of the crosslinked polymeric material components of an insert of the invention can be obtained based on the weight percentages of their corresponding polymerizable component (material) in a polymerizable composition for the manufacture of the insert. According to the invention, a polymerizable material (or component) containing silicone can be a silicone-containing vinyl monomer, a polysiloxane vinyl crosslinker, or combinations thereof. According to the invention, a vinyl monomer containing silicone can be any L / CL ίη / ZZΖΠZ / E / YΙΛΙ vinyl monomer containing silicone known to a person skilled in the art. Examples of preferred silicone-containing vinyl monomers include, without limitation, vinyl monomers each having a bis(trialkylsilyloxy)alkyl group or a tris(trialkylsilyloxy)silyl group, vinyl monomers of polysiloxane, 3-methacryloxypropylpentamethyldisiloxane, f-butyldimethylsiloxyethyl vinyl carbonate, trimethylsilylethyl vinyl carbonate, and trimethylsilylmethyl vinyl carbonate, and combinations thereof. The preferred vinyl polysiloxane monomers, including those of Formula (M1), are described later in this application and can be obtained from commercial suppliers (e.g., Shin-Etsu, Gelest, etc.); prepared according to the procedures described in the patents, e.g., U.S. Patent No.° 5070215, 6166236, 6867245, 8415405, 8475529, 8614261 and 9217813; prepare by the reaction of a (meth)acrylamide or a hydroxyalkyl (meth)acrylate or a (meth)acryloxypolyethylene glycol with a mono-epoxypropyloxypropyl polydimethylsiloxane; prepare by the reaction of a glycidyl (meth)acrylate with a mono-carbinol-terminated polydimethylsiloxane, a mono-aminopropyl-terminated polydimethylsiloxane or a monoethylaminopropyl-terminated polydimethylsiloxane; or prepare by the reaction of an ethyl isocyanato (meth)acrylate with a mono-carbinol-terminated polydimethylsiloxane according to coupling reactions well known to a person skilled in the art. The preferred silicone-containing vinyl monomers, each having either a bis(trialkylsilyloxy)alkylsilyl group or a tris(trialkylsilyloxy)silyl group, including those of Formula (M2), are described later in this application and can be obtained from commercial suppliers (e.g., Shin-Etsu, Gelest, etc.) or prepared according to the procedures described in U.S. Patent Nos. 5070215, 6166236, 7214809, 8475529, 8658748, 9097840, 9103965, and 9475827. In the invention, any suitable polysiloxane vinyl crosslinker may be used. Examples of preferred polysiloxane vinyl crosslinkers are di(meth)acryloyl-terminated polydimethylsiloxanes; divinyl carbonate-terminated polydimethylsiloxanes; divinyl carbamate-terminated polydimethylsiloxane; N,N,N',N'-tetraquis(3-methacryloxy-2-hydroxypropyl)-alpha,omega-bis-3-aminopropyl-polydimethylsiloxane; the polysiloxane-containing macromer selected from the group consisting of Macromer A, Macromer B, Macromer O, and Macromer D described in U.S. Patent 5,760,100; and the polysiloxane-containing macromers disclosed in U.S. Patent No. 4,136,250. 4153641, 4182822, 4189546, 4343927, 4254248, 4355147, 4276402, 4327203, 4341889, 4486577, 4543398, 4605712, 4661575, 4684538, 4703097, 4833218, 4837289, 4954586, 4954587, 5010141, 5034461, 5070170, 5079319, 5039761, 5346946, 5358995, 5387632, 5416132, 5451617, 5486579, 5962548, 5981675, 6039913 and 6762264; the polysiloxane-containing macromers disclosed in U.S. Patent Nos. 4259467, 4260725 and 4261875. One class of preferred polysiloxane vinyl crosslinkers are di-(meth)acryloyloxy-terminated polysiloxane vinyl crosslinkers, each having dimethylsiloxane units and hydrolyzed siloxane units, each having a methyl substituent and a monovalent C4-C40 organic radical substituent having 2 to 6 hydroxyl groups, more preferably a polysiloxane vinyl crosslinker of Formula (G), which are described later in this application and can be prepared L / CL Ln / Zznz / E / YIAI according to the procedures disclosed in U.S. Patent No. 10081697. Another class of preferred polysiloxane vinyl crosslinkers are vinyl crosslinkers comprising each a single polydiorganosiloxane segment and two terminal (meth)acryloyl groups, which can be obtained from commercial suppliers; prepared by the reaction of a glycidyl (meth)acryloyl chloride of (meth)acrylate with a di-amino-terminated polydimethylsiloxane or a di-hydroxyl-terminated polydimethylsiloxane; prepared by the reaction of an ethyl isocyanato (meth)acrylate with di-hydroxyl-terminated polydimethylsiloxanes prepared by the reaction of an amino-containing acrylic monomer with a di-carboxyl-terminated polydimethylsiloxane in the presence of a coupling agent (a carbodiimide); prepared by the reaction of a carboxyl-containing acrylic monomer with a di-amino-terminated polydimethylsiloxane in the presence of a coupling agent (a carbodiimide);or prepare by reacting a hydroxyl-containing acrylic monomer with a di-hydroxy-terminated polydisiloxane in the presence of a diisocyanate or di-epoxy coupling agent. Other preferred classes of polysiloxane vinyl crosslinkers are the long-chain polysiloxane vinyl crosslinkers having, each, at least two polydiorganosiloxane segments connected by a linker between each pair of polydiorganosiloxane segments and two terminal ethylenically unsaturated groups, which can be prepared according to the procedures described in U.S. Patent Nos. 5034461, 5416132, 5449729, 5760100, 7423074, 8529057, 8835525, 8993651, 10301451 and 10465047. According to the invention, an aryl vinyl monomer is a vinyl monomer of Formula (I) L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ or (H) Say Ai RbRc^ R / Re' Rhzr.zw2 'w(II) where Ai is H or CH3 (preferably H); B1 is (CH2)mi or [O(CH2)2]zi where m1 is 2-6 and z1 is 110; Y1 is a direct bond, O, S or NR' where R' is H, CH3, Cn H2n+i where n'=1 -10, ¡SO-OC3H7, CeHs or CH2C6H5; Ra, Rb, Rc, Rd, Re, Rr, Rg, Rh and R¡ are independently of each other H, C1-C12 alkyl or C1C12 alkoxy (preferably all H); w1 is 0-6, provided that m1+w1<8; w2 is an integer from 1 to 3; and Di is H, Cl, Br, C1-C4 alkyl, C1-C4 alkoxy, CeHs or CH2C6H5. Examples of aryl acrylic monomers of Formula (I) include, but are not limited to: 2-ethylphenoxy acrylate; 2-ethylphenoxy methacrylate; phenyl acrylate; phenyl methacrylate; benzyl acrylate; benzyl methacrylate; 2-phenylethyl acrylate; 2-phenylethyl methacrylate; 3-phenylpropyl acrylate; 3-phenylpropyl methacrylate; 4-phenylbutyl acrylate; 4-phenylbutyl methacrylate; 4-methylphenyl acrylate; 4-methylphenyl methacrylate; 4-methylbenzyl acrylate; 4-methylbenzyl methacrylate; 2-(2-methylphenyl)ethyl acrylate; 2-(2-methylphenyl)ethyl methacrylate; 2-(3-methylphenyl)ethyl acrylate; 2-(3-methylphenyl)ethyl methacrylate; 2-(4-methylphenyl)ethyl acrylate; 2-(4-methylphenyl)ethyl methacrylate; 2-(4propylphenyl)ethyl acrylate; 2-(4-propylphenyl)ethyl methacrylate; 2-(4-(1-methylethyl)phenyl)ethyl acrylate; 2(4-(1-methylethyl)phenyl)ethyl methacrylate; 2-(4-methoxyphenyl)ethyl acrylate; 2-(4-methoxyphenyl)ethyl methacrylate;2-(4-cyclohexylphenyl)ethyl acrylate; 2-(4-cyclohexylphenyl)ethyl methacrylate; 2-(2-chlorophenyl)ethyl acrylate; 2-(2-chlorophenyl)ethyl methacrylate; 2-(3-chlorophenyl)ethyl acrylate; 2-(3-chlorophenyl)ethyl methacrylate; 2-(4-chlorophenyl)ethyl acrylate; 2-(4-chlorophenyl)ethyl methacrylate; 2-(4-bromophenyl)ethyl acrylate; 2-(4-bromophenyl)ethyl methacrylate; 2-(3-phenylphenyl)ethyl acrylate; 2-(3-phenylphenyl)ethyl methacrylate; 2-(4-phenylphenyl)ethyl acrylate; 2-(4-phenylphenyl)ethyl methacrylate; 2-(4-benzylphenyl)ethyl acrylate; 2-(4-benzylphenyl)ethyl methacrylate; 2-(phenylthio)ethyl acrylate; 2-(phenylthio)ethyl methacrylate; 2-benzyloxyethyl acrylate; 3-benzyloxypropyl acrylate; 2-benzyloxyethyl methacrylate; 3-benzyloxypropyl methacrylate; 2-[2-(benzyloxy)ethoxy]ethyl acrylate; 2-[2-(benzyloxy)ethoxy]ethyl methacrylate;or combinations thereof. The aryl acrylic monomers of Formula (I) listed above can be obtained from commercial suppliers or, alternatively, can be prepared according to methods known in the art. The preferred aryl acrylic monomers of Formula (I) are those in which Bi is OCH2CH2, (OCH2CH2)2, (OCH2CH2)3 or (CH2)mi in which m1 is 2-5, Y1 is a direct bond or O, w1 is 0 or 1 and Di is H. The most preferred are 2-phenylethyl acrylate; 3-phenylpropyl acrylate; 4-phenylbutyl acrylate; 5-phenylpentyl acrylate; 2-benzyloxyethyl acrylate; 3-benzyloxypropyl acrylate; 2-[2(benzyloxy)ethoxy]ethyl acrylate; and their corresponding methacrylates. Aryl acrylic monomers of Formula (II) can be prepared from monofunctional polyphenyl ethers (i.e., those having one functional group, such as hydroxyl, amino, or carboxyl groups). Generally, a monofunctional OH-terminated poly(phenyl ether) is reacted with a (meth)acrylic acid derivative (such as acryloyl chloride, methacryloyl chloride, methacrylic anhydride, or an alkyl isocyanato acrylate or methacrylate) under coupling reaction conditions known to a person skilled in the art. Monoamine-terminated, monocarboxylic acid-terminated polyphenyl ethers are functionalized in a similar manner using suitable (meth)acrylic acid derivatives. Monofunctional terminated polyphenyl ethers can be prepared according to the procedures described in the literature (J. Org. Chem., 1960, 25 (9), pp. 1590-1595).Experimental procedures for the preparation of aryl acrylic monomers of Formula (II) can be found in U.S. Patent No. 10064977. In the invention, any suitable vinyl crosslinking agent may be used. Examples of preferred vinyl crosslinking agents include, without limitation: ethylene glycol dimethacrylate; ethylene glycol diacrylate; 1,3-propanediol dimethacrylate; 1,3-propanediol dimethacrylate; 2,3-propanediol dimethacrylate; 2,3-propanediol dimethacrylate; 1,4-butanediol dimethacrylate; 1,4-butanediol dimethacrylate; 1,5-pentanediol dimethacrylate; 1,5-pentanediol dimethacrylate; 1,6-hexanediol dimethacrylate; 1,6-hexanediol dimethacrylate; diethylene glycol dimethacrylate; diethylene glycol dimethacrylate; triethylene glycol dimethacrylate; triethylene glycol diacrylate; tetraethylene glycol dimethacrylate; tetraethylene glycol diacrylate; allyl methacrylate; allyl acrylate; N,N'-methyleneb¡s(acrylamide); N,N'-met¡lenobis(methacrylam¡da); N,N'-ethylenebis(acrylamide); N,N'-ethylenebis(methacrylamide); Ν,Ν'-hexamethylenebisacrylamide; Ν,Ν'-hexamethylenebismethacrylamide; L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ pentaerythritol triacrylate; pentaerythritol trimethacrylate; trimethyloylpropane triacrylate; trimethyloylpropane trimethacrylate; tris(2-hydroxyethyl)isocyanurate triacrylate; tris(2-hydroxyethyl)isocyanurate trimethacrylate; 1,3,5-triacryloxylhexahydro-1,3,5-triazine; 1,3,5-trimethacryloxylhexahydro-1,3,5-triazine; pentaerythritol tetraacrylate; pentaerythritol tetramethacrylate; di(trimethylpropane) tetraacrylate; di(trimethyloylpropane) tetramethacrylate; an aryl crosslinking agent (e.g., divinylbenzene, 2-methyl-1,4-divinylbenzene, bis(4-vinylphenyl)methane, 1,2-bis(4-vinylphenyl)ethane, etc.) or combinations thereof. According to the invention, the amount of the vinyl crosslinking agent is from approximately 1% to approximately 30% by weight, preferably from approximately 1% to approximately 25% by weight, more preferably from approximately 2% to approximately 20% by weight, even more preferably from approximately 2% to approximately 15% by weight. The insert materials of the present invention are prepared by conventional polymerization methods. For example, a polymerizable composition can be prepared by mixing all the polymerizable materials, as described above, in the desired proportions, together with any other polymerizable material, such as a UV-absorbing vinyl monomer, a high-energy UV / violet (HEVL) absorbing vinyl monomer, a polymerizable photochromic compound, and a conventional thermal initiator (or photoinitiator), in the presence or preferably in the absence of a non-reactive organic solvent (i.e., a non-reactive diluent).The polymerizable composition can then be introduced into a mold of the desired shape and polymerization can be carried out thermally (i.e., by heating) or photochemically (i.e., by actinic radiation, e.g., UV radiation and / or visible radiation) to activate the initiator. In the invention, any thermal polymerization initiator may be used. Suitable thermal polymerization initiators are known to those skilled in the art, and these include, for example, peroxides, hydroperoxides, azo-bis(alkylnitriles or cycloalkylnitriles), persulfates, percarbonates, or mixtures thereof. Examples of preferred thermal polymerization initiators include, without limitation, benzoyl peroxide, α-butyl peroxide, β-amyl peroxybenzoate, 2,2-bis(β-butylperoxy)butane, 1,1-bis(β-butylperoxycyclohexane, 2,5-bis(β-butylperoxy)-2,5-dimethylhexane, 2,5-bis(β-butylperoxy)-2,5-dimethyl-3-hexyne, bis(β-(β-butylperoxy)-1-methylethyl)benzene, 1,1-bis(β-butylperoxy)-3,3,5-trimethylcyclohexane, dibutyl-diperoxyphthalate, β-butyl hydroperoxide, β-butyl peracetate, β-butyl peroxybenzoate, isopropyl butylperoxycarbonate, acetyl peroxide, lauroyl peroxide, decanoyl peroxide, dicetyl peroxydicarbonate,di(4-i-butylcyclohexyl) peroxydicarbonate (Perkadox 16S), di(2-ethylhexyl) peroxydicarbonate, i-butyl peroxypivalate (Lupersol 11), i-butyl peroxy-2-ethylhexanoate (Trigonox 21-C50), 2,4-pentanedione peroxide, dicumyl peroxide, peracetic acid, potassium persulfate, sodium persulfate, ammonium persulfate, 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitryl) (VAZO 33), 2,2'-azobis[2-(2-imidazolin-2-i)propane dihydrochloride] (VAZO 44), 2,2'-azobis(2-amidenopropane) dihydrochloride (VAZO 50), 2,2'-azobis(2,4-dimethylvaleronitrile) (VAZO 52), 2,2'-azobis(isobutyronitrile) (VAZO 64 or AIBN), 2,2'-azobis-2-methylbutyronitrile (VAZO 67), 1,1-azobis(1-cyclohexanecarbonitrile) (VAZO, L7CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ 88); 2,2'-azobis(2-cyclopropylpropionitrile), 2,2'-azobis(methylisobutyrate), 4,4'-azobis(4-cyanovaleric acid) and combinations thereof. Preferably, the thermal initiator is 2,2'-azobis(isobutyronitrile) (AIBN or VAZO 64). Suitable photoinitiators include benzoin methyl ether, dietoxyacetophenone, a benzoylphosphine oxide, 1-hydroxycyclohexylphenyl ketone, and the Darocur and Irgacur types, preferably Darocur 1173® and Darocur 2959®, germanium-based Norrish type I photoinitiators (e.g., those described in US patent 7,605,190). Examples of benzoylphosphine initiators include 2,4,6-trimethylbenzoyldiphenylphosphine oxide; bis-(2,6-dichlorobenzoyl)-4-N-propylphenylphosphine oxide; and bis-(2,6-dichlorobenzoyl)-4-N-butylphenylphosphine oxide. Reactive photoinitiators that can be incorporated, for example, into a macromer or used as a special monomer are also suitable. Examples of reactive photoinitiators are those disclosed in document EP 632 329. Any suitable UV-absorbing vinyl monomer and UV / HEVL-absorbing vinyl monomer can be used in a polymerizable composition for the preparation of a preformed SÍHy contact lens of the invention. Examples of preferred UV-absorbing and UV / HEVL-absorbing vinyl monomers include, but are not limited to: 2-(2-hydroxy-5-vinylphenyl)-2H-benzotriazole, 2-(2-hydroxy-5-acryloxyphenyl)-2H-benzotriazole, 2-(2-hydroxy-3-methacrylamide-5-tert-octylphenyl)benzotriazole, 2-(2'-hydroxy-5'-methacrylamide-phenyl)-5-chlorobenzotriazole, 2-(2'-hydroxy-5'-methacrylamide-phenyl)-5-methoxybenzotriazole, 2-(2'-hydroxy-5'-methacrylamide-5-butylphenyl)-5-chlorobenzotriazole, 2-(2'-hydroxy¡-5'methacryloxypropylphen¡l)benzotrázole, 2-hydroxy¡-5-methoxy-3-(5-(trifluoromethyl)-2 / - / benzo[d][1,2,3]triazol-2-yl)benzyl methacrylate (WL-1), 2-hydroxy¡-5-methoxy-3-(5-methoxy¡-2 / - / benzo[d][1,2,3]triazol-2-yl)benzyl (WL-5), 3-(5-fluoro-2 / - / -benzo[d][1,2,3]triazol-2-yl)-2-hydroxy5-methoxybenzyl (WL-2), methacrylate of 3-(2 / 7-benzo[d][1,2,3]triazol-2-yl)-2-h¡droxy-5-methoxybenzyl (WL-3), methacrylate of 3-(5-chloro-2 / 7-benzo[d][1,2,3]triazol-2-yl)-2-hydroxy-5-methox¡benz¡lo (WL-4), methacrylate of 2hydroxy-5-methoxy¡-3-(5-methyl-2 / 7-benzo[d][1,2,3]triazol-2-ylbenzyl) (WL-6), 2-hydroxy-5-methyl-3(5-(trifIuoromethyl)-2 / 7-benzo[d][ 1,2,3]triazol-2-¡l)benzol methacrylate (WL-7), 4-allyl-2-(5-chloro-2 / 7-benzo[d][1,2,3]triazol-2yl)-6-methoxyphenol (WL-8), 2-{2'-h¡drox¡-3'-terc-5'[3-(4-v¡n¡lbenzyloxy)propox¡]phen¡l}-5-methoxy-2 / 7-benzotr¡azole, phenol, 2-(5-chloro-2 / - / -benzotr¡azol-2-1-methyl-1, methylene yl)-4-ethenyl- (UVAM), 2-[2'-h hydroxy-5'-(2methacryloxyethyl)phenyl)]-2H-benzotriazole (ester of 2-[3-(2H-benzotriazol-2-¡l)-4-h¡droxyphenyl]ethyl acid, 2-bloc-normal, Norpec- 2-{2'-h¡drox¡-3'-terc-but¡l-5'-[3'-metacr¡lo¡lo¡lox¡propoxy]phen¡l}-2 / 7-benzot¡azole,2{2'-h¡drox¡-3'-terc-butyl-5'-[3'-methacryloyloxypropox¡]phen¡l}-5-methoxy-2 / 7-benzotr¡azole (UV13), 2-{2'-hydrox¡-3'terc-butyl-5'-[3'-metacr¡lo¡lox¡propox¡]phen¡l}-5-chloro-2 / 7-benzotriazole (UV28), 2-[2'-hydroxy-3'-terc-butyl-5'-(3'acr¡lo¡lox¡propoxy)phenyl]-5-trifluorometh¡l-2 / 7-benzotr¡azole (UV23), 2-(2'-h¡drox¡-5-methacrylamidophenyl-trizol-trizol (UV26), 2-(3-allyl-2-h¡drox¡-5-met¡lphenyl)-2 / - / -benzotriazole (UV9), 2-(2-hydroxy-3-metal¡l-5methylphenyl)-2 / - / -benzotriazole (UV12), 2-3,-in-butyl-2'-hydroxy¡-5'-(3-dimethylvinylsilylpropoxy)-2'-hydroxy-phenyl)-5methoxybenzotriazole (UV15), 2-(2'-hydroxy-5'-methacr¡lo¡lpropyl-3'-ferc-but¡l-phen¡l)-5-methoxy-2 / 7-benzotriazole (UV16), 2-(2'-hydroxy-5'-acr¡loylprop¡l-3'-ierc-but¡l-phen¡l)-5-methoxy-2 / 7-benzotr¡azole (UV16A), ester of 3-[3terc-butyl-5-(5-chlorobenzotr¡azol-2-¡l)-4-hydroxy¡phenyl]-propyl of 2-methylacrylic acid (16-100, CAS no. 96478-15-8), methacrylate of 2-(3-(tert-butyl)-4-h¡drox¡-5-(5-methoxy¡-2 / 7-benzo[d][1,2,3]triazol-2-yl)phenoxy¡)et¡lo, LJCL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ (16-102), phenol, 2-(5-chloro-2 / - / -benzotriazol-2-yl)-6-methoxy¡-4-(2-propen-1-yl) (CAS No. 1260141-20-5), 2[2-hydroxy¡-5-[3-(methacrylo¡lox¡)prop¡l]-3-ferc-but¡lfen¡l]-5-chloro-2 / - / -benzotráazole, phenol, 2-(5-ethenyl-2 / - / benzotriazol-2-yl)-4-methyl-, homopolymer (9CI) (CAS No. 83063-87-0). According to the invention, the polymerizable composition comprises from approximately 0.1% to approximately 3.0%, preferably from approximately 0.2% to approximately 2.5%, more preferably from approximately 0.3% to approximately 2.0%, by weight of one or more UV-absorbing vinyl monomers, relative to the amount of all polymerizable components in the polymerizable composition. Examples of preferred photochromic vinyl monomers include polymerizable naphthopyrans, polymerizable benzopyrans, polymerizable indenonaphthopyrans, polymerizable phenanthropyrans, polymerizable spiro(benzyndole)naphthopyrans, polymerizable spiro(indoline)benzopyrans, polymerizable spiro(indoline)naphthopyrans, polymerizable spiro(indoline)quinopyrans, polymerizable spiro(indoline)pyrans, polymerizable naphthoxazines, polymerizable spirobenzopyrans, polymerizable spirobenzothiopyrans, polymerizable naphtacenediones, polymerizable spirooxazines, polymerizable spiro(indoline)naphthoxazines. polymerizable spiro(indoline)pyridobenzoxazines, polymerizable spiro(benzyndoline)pyridobenzoxazines, polymerizable spiro(benzyndoline)naphthoxazines, polymerizable spiro(indoline)benzoxazines, polymerizable diarylethene and combinations thereof, as disclosed in U.S. patents N.° 4929693, 5166345 6017121, 7556750, 7584630, 7999989, 8158037, 8697770, 8741188, 9052438, 9097916, 9465234, 9904074, 10197707, 6019914, 6113814, 6149841,6296785 y 6348604. Once the insertion materials of the present invention have cured, they are extracted in a suitable solvent to remove as much as possible of the unreacted material components. Examples of suitable solvents include acetone, methanol, cyclohexane, tetrahydrofuran, tripropylene glycol methyl ether, dipropylene glycol methyl ether, ethylene glycol n-butyl ether, ketones (e.g., acetone, methyl ethyl ketone, etc.), diethylene glycol n-butyl ether, diethylene glycol methyl ether, ethylene glycol phenyl ether, propylene glycol methyl ether, propylene glycol methyl ether acetate, dipropylene glycol methyl ether acetate, propylene glycol n-propyl ether, dipropylene glycol n-propyl ether, tripropylene glycol n-butyl ether, propylene glycol n-butyl ether, dipropylene glycol n-butyl ether, tripropylene glycol n-butyl ether, propylene glycol phenyl ether. dipropylene glycol dimethyl ether, polyethylene glycols, polypropylene glycols, ethyl acetate,butyl acetate, amyl acetate, methyl lactate, ethyl lactate, propyl lactate, methylene chloride, 2-butanol, 1-propanol, 2-propanol, menthol, cyclohexanol, cyclopentanol and exonorborneol, 2-pentanol, 3-pentanol, 2-hexanol, 3-hexanol, 3-methyl-2-butanol, 2-heptanol, 2-octanol, 2-nonanol, 2-decanol, 3-octanol, norborneol, ferric-butanol, tert-amyl alcohol, 2-methyl-2-pentanol, 2,3-dimethyl-2-butanol, 3-methyl-3-pentanol, 1-methylcyclohexanol, 2-methyl-2-hexanol, 3,7-dimethyl-3-octanol, 1-chloro-2-methyl-2-propanol, 2methyl-2-heptanol, 2-methyl-2-octanol, 2-2-methyl-2-nonanol, 2-methyl-2-decanol, 3-methyl-3-hexanol, 3-methyl-3heptanol, 4-methyl-4-heptanol, 3-methyl-3-octanol, 4-methyl-4-octanol, 3-methyl-3-nonanol, 4-methyl-4-nonanol, 3methyl-3-octanol, 3-ethyl-3-hexanol, 3-methyl-3-heptanol, 4-ethyl-4-heptanol, 4-propyl-4-heptanol, 4-isopropyl-4heptanol, 2,4-dimethyl-2-pentanol, 1-methylcyclopentanol, 1 -ethylcyclopentanol, 1 -ethylcyclopentanol, 3-hydroxy¡-3L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ methyl-1-butene,4-hydroxy-4-methyl-1-cyclopentanol, 2-phenyl-2-propanol, 2-methoxy-2-methyl-2-propanol, 2,3,4-trimethyl-3-pentanol, 3,7-dimethyl-3-octanol, 2-phenyl-2-butanol, 2-methyl-1-phenyl-2-propanol and 3-ethyl-3-pentanol, 1-ethoxy-2-propanol, 1-methyl-2-propanol, t-amyl alcohol, isopropanol, 1-methyl-2-pyrrolidone, N,N-dimethylpropionamide, dimethylformamide, dimethylacetamide, dimethylpropionamide, N-methylpyrrolidone and mixtures thereof. The most commonly used organic solvents include, but are not limited to, methanol, ethanol, 1-propanol, isopropanol, sec-butanol, tert-butyl alcohol, tert-amyl alcohol, acetone, methyl ethyl ketone, methyl isopropyl ketone, methyl propyl ketone, ethyl acetate, heptane, methylhexane (various isomers), methylcyclohexane, dimethylcyclopentane (various isomers), 2,2,4-trimethylpentane, and mixtures thereof. An insertion material of the invention can be used particularly in the manufacture of embedded silicone hydrogel contact lenses. The invention also provides a method for producing embedded silicone hydrogel contact lenses, the method of the invention comprising the steps of: (1) obtaining a silicone hydrogel lens-forming composition (i.e., a silicone hydrogel lens formulation or a polymerizable composition for forming silicone hydrogel contact lenses); (2) obtaining an insert, wherein the insert is made of a crosslinked polymeric material of the invention, as described above, wherein the disc is made of a rigid gas-permeable material;(3) obtaining a lens mold, wherein the lens mold comprises a male mold half having a first molding surface and a female mold half having a second molding surface, wherein the male and female mold halves are configured to receive each other such that a mold cavity is formed between the first and second molding surfaces when the mold is closed; (4) in no particular order, placing the insert of the invention, as described above, in a specified position in the lens mold and introducing the silicone hydrogel lens-forming composition into the lens mold, wherein the insert is immersed in the silicone hydrogel lens-forming composition in the lens mold; (5) curing the silicone hydrogel lens-forming composition in the lens mold to form an unprocessed embedded silicone hydrogel contact lens;(6) separating the lens mold obtained in step (5) into male and female mold halves, with the raw embedded silicone hydrogel contact lens adhered onto one of the lens-adhered mold half halves; (7) removing the raw embedded silicone hydrogel contact lens from the lens-adhered mold half before the raw embedded silicone hydrogel contact lens comes into contact with water or any other liquid; and (8) subjecting the raw embedded silicone hydrogel contact lens to post-molding processes, including a hydration process and one or more distinct processes selected from the group consisting of extraction, surface treatment, packaging, sterilization, and combinations thereof. According to the invention, a silicone hydrogel lens forming composition comprises at least one polymerizable material (or component) containing silicone and at least one hydrophilic vinyl monomer. Any polymerizable material (or component) containing silicone described above is L / CL ίη / ZZΖΠZ / E / YΙΛΙ can be used in the formation of a silicone hydrogel lens forming composition. In the invention, any hydrophilic vinyl monomer may be used. Examples of preferred hydrophilic vinyl monomers are alkyl (meth)acrylamides (as described later in this application), hydroxyl-containing acrylic monomers (as described later), amino-containing acrylic monomers (as described later in this application), carboxyl-containing acrylic monomers (as described later in this application), N-vinylamide monomers (as described later in this application), and methylene-containing pyrrolidone monomers (i.e., pyrrolidone derivatives each having a methylene group attached to the pyrrolidone ring at position 3 or 5) (as described later in this application).acrylic monomers having a C1-C4 alkoxyethoxy group (as described later in this application), vinyl ether monomers (as described later in this application), allyl ether monomers (as described later in this application), vinyl monomers containing phosphorylcholine (as described later in this application), N-2-hydroxyethylvinyl carbamate, N-carboxyvinyl-p-alanine (VINAL), N-carboxyvinyl-a-alanine, and combinations thereof. A silicone hydrogel lens-forming composition may also further comprise at least one hydrophobic vinyl monomer, at least one non-silicone vinyl crosslinker, or combinations thereof. According to the invention, the present invention may contain any hydrophobic vinyl monomer. Examples of preferred hydrophobic vinyl monomers include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, isopropyl (meth)acrylate, cyclohexyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl valerate, styrene, chloroprene, vinyl chloride, vinylidene chloride, (meth)acrylonitrile, 1-butene, butadiene, vinyl toluene, vinyl ethyl ether, perfluorohexylethyl thiocarbonylaminoethyl methacrylate, isobornyl (meth)acrylate, trifluoroethyl (meth)acrylate, hexafluoroisopropyl (meth)acrylate, hexafluorobutyl (meth)acrylate, and combinations thereof. According to the invention, any non-silicone vinyl crosslinking agent may be used. Examples of preferred non-silicone vinyl crosslinking agents are described later in this application. A silicone hydrogel lens-forming composition may also comprise other necessary components known to a person skilled in the art, for example, such as initiators that are free radicals (e.g., thermal polymerization initiators, photoinitiators) (as described above in this application), a UV / HEVL absorbing vinyl monomer (as described above in this application), a staining agent for visibility (e.g., reactive dyes, polymerizable dyes, pigments) (as described above in this application), antimicrobial agents (e.g., preferably silver nanoparticles), a bioactive agent, leachable polymeric wetting agents (e.g., L / CL ίΠ / ZZΖηZ / E / YΙΛΙ non-polymerizable hydrophilic polymers, etc.), leachable tear stabilizing agents (e.g., phospholipids, monoglycerides, diglycerides, triglycerides, glycolipids, glyceroglycolipids, sphingolipids, sphingoglycolipids, etc.) and mixtures thereof, as known to a person skilled in the art. A silicone hydrogel lens-forming composition (SiHy lens formulation) may be a solvent-free, transparent liquid prepared by mixing all polymerizable components (or materials) and one other necessary component (or materials), or a solution prepared by dissolving all desirable components (or materials) in any suitable solvent, such as a mixture of water and one or more water-miscible organic solvents, an organic solvent, or a mixture of one or more organic solvents, as known to a person skilled in the art. The term solvent refers to a chemical that cannot participate in the free-radical polymerization reaction (any of those solvents described above in this application). A solventless SiHy lens formulation (silicone hydrogel lens forming composition) typically comprises at least one blended vinyl monomer as a reactive solvent for dissolving all other polymerizable components of the solventless SiHy lens formulation. Examples of preferred blended vinyl monomers are described later in this application. Preferably, methyl methacrylate is used as the blended vinyl monomer in the preparation of a solventless SiHy lens formulation. Numerous SiHy lens formulations (silicone hydrogel lens-forming compositions) have been described in numerous patents and patent applications published up to the filing date of this application and have been used to produce commercial SiHy contact lenses. Examples of commercial SiHy contact lenses include, but are not limited to, asmofilcon A, balafilcon A, comfilcon A, delefilcon A, efrofilcon A, enfilcon A, fanfilcon A, galyfilcon A, lotrafilcon A, lotrafilcon B, narafilcon A, narafilcon B, senofilcon A, senofilcon B, senofilcon C, smafilcon A, somofilcon A, and stenfilcon A. A silicone hydrogel lens-forming composition (SiHy lens formulation) can be prepared by dissolving / mixing all desirable components (materials) and, optionally, one or more organic solvents (described above), according to any known technique. According to the invention, the silicone hydrogel lens-forming composition is suitable for forming a silicone hydrogel material having a water content of approximately 20% to approximately 70% (preferably approximately 20% to approximately 65%, more preferably approximately 25% to approximately 65%, and even more preferably approximately 30% to approximately 60%) by weight when fully hydrated. The polymerizable composition may comprise: (a) approximately 20% to approximately 79% (preferably approximately 20% to approximately 75%, more preferably approximately 25% to approximately 70%, and even more preferably approximately 30% to approximately 65%) by weight of LJCL iP / ZZΖ / E / YILI less a silicone-containing vinyl monomer and / or at least one silicone-containing vinyl crosslinker; (b) from 20% to approximately 79% (preferably from approximately 20% to approximately 75%, more preferably from approximately 25% to approximately 70%, even more preferably from approximately 30% to approximately 65%) by weight of the hydrophilic vinyl monomer; (c) from 0 to approximately 2.5% (preferably from 0 to approximately 2.0%, more preferably from 0 to approximately 1.5%, even more preferably from approximately 0 to approximately 1.0%) by weight of the non-silicone vinyl crosslinker; (d) from approximately 0.05% to approximately 2.0% (preferably from approximately 0.1% to approximately 2.0%, more preferably from approximately 0.2% to approximately 1.5%, even more preferably from approximately 0.3% to approximately 1.(e) 0 to approximately 15% (preferably 0 to approximately 14%, more preferably approximately 2% to approximately 13%, even more preferably approximately 4% to approximately 12%) by weight of the blending vinyl monomer; and (f) 0 to approximately 3.0%, preferably approximately 0.1% to approximately 2.5%, more preferably approximately 0.2% to approximately 2.0%, by weight of the UV-absorbing vinyl monomer and / or the UV / HEVL-absorbing vinyl monomer, with respect to the total amount of the polymerizable composition, provided that the sum of the amounts of the polymerizable materials (a) to (f) and other unlisted components is 100%.Preferably, the sum of the amounts of polymerizable materials (a) and (b) is at least 70% (preferably at least 75%, more preferably at least 80%, even more preferably 85%) by weight with respect to the total amount of all polymerizable materials in the polymerizable composition. Lens molds for the manufacture of contact lenses, including SiHy contact lenses, are well known to anyone skilled in the art and are used, for example, in slip molding or centrifugal casting. For instance, a mold (for slip molding) generally comprises at least two mold sections (or parts) or mold halves, namely the first and second mold halves. The first mold half defines a first molding (or optical) surface, and the second mold half defines a second molding (or optical) surface. The first and second mold halves are configured to receive each other such that a lens forming cavity is created between the first and second molding surfaces. The molding surface of a mold half is the surface that forms the mold cavity and is in direct contact with the polymerizable composition. The methods for manufacturing mold sections for the slip molding of a contact lens are generally well known to those skilled in the art. The process of the present invention is not limited to any particular mold-forming method. In fact, any mold-forming method may be used in the present invention. The first and second mold halves can be formed by various techniques, such as injection molding or turning. Examples of suitable processes for forming the mold halves are disclosed in L / CL ίη / 77Π7 / Ε / ΥΙΛΙ US Patent No. 4444711; 4460534; 5843346 and 5894002. Virtually all materials known to the art can be used to make molds for manufacturing contact lenses. For example, polymeric materials such as polyethylene, polypropylene, polystyrene, PMMA, Topas® COC grade 8007-S10 (a transparent amorphous copolymer of ethylene and norbornene, from Ticona GmbH of Frankfurt, Germany and Summit, New Jersey), or similar materials can be used. Other materials that allow UV light transmission, such as quartz crystal and sapphire, could also be used. According to the invention, the insert can be placed in the mold, and the silicone hydrogel lens-forming composition can be introduced (dispensed) into a cavity formed by a mold using any technique known to a person skilled in the art. In a preferred embodiment, an insert is placed on the molding surface of a female mold half in a specified position; a specified quantity of a silicone hydrogel lens-forming composition is then dispensed into the female mold half with the insert on it by means of a dispensing device, and the male mold half is then placed on top and the mold is closed.As the mold closes, any excess lens-forming material that has not polymerized is pressed into an overflow provided in the female mold half (or, alternatively, the male mold half) and the insert is immersed in the silicone hydrogel lens-forming composition in the mold. After the insert of the invention is placed in the mold and the silicone hydrogel lens forming composition is dispensed into the mold, the closed mold containing the silicone hydrogel lens forming composition is then cured (i.e., polymerized) thermally or actinically (but preferably thermally initiated) to form an unprocessed embedded silicone hydrogel contact lens. The actinic polymerization of the silicone hydrogel lens-forming composition in the mold can be carried out by irradiating the closed mold with the silicone hydrogel lens-forming composition in it with visible or UV light, according to any technique known to a person skilled in the art. The thermal polymerization of the silicone hydrogel lens-forming composition in the mold can be conveniently carried out in an oven at a temperature of 25 to 120 °C, and preferably 40 to 100 °C, as anyone skilled in the art knows. The reaction time can vary within a wide range, but is conveniently, for example, from 1 to 24 hours, or preferably from 2 to 12 hours. It is advantageous to pre-degas the silicone hydrogel lens-forming composition and carry out the copolymerization reaction in an inert atmosphere, for example, in a nitrogen or argon atmosphere. In a preferred embodiment, after the silicone hydrogel lens-forming composition is cured in the molds in the oven to form raw embedded silicone hydrogel contact lenses, the oven temperature is increased to a post-cure temperature of approximately 105°C or higher (preferably at least approximately 110°C, plus L / CL ίΠ / ZZΖηZ / E / YΙΛΙ preferably at least approximately 115 °C, even more preferably at least approximately 120 °C) and the flow rate of nitrogen gas through the furnace is increased to a second flow rate that is at least approximately 1.5 times (preferably at least approximately 2.0 times, more preferably at least approximately 3.0 times, even more preferably at least approximately 4.0 times) the first flow rate. The post-curing treatment stage is carried out by heating the lens mold with the unprocessed silicone hydrogel contact lens embedded within it in the oven at the post-curing temperature with the nitrogen gas flow through the oven at the second flow rate for at least approximately 30 minutes (preferably at least approximately 60 minutes, more preferably at least approximately 90 minutes, even more preferably at least approximately 120 minutes). After the curing stage and, optionally, the post-curing stage, the following steps are carried out: opening the mold (i.e., separating the male mold half from the female mold half with the raw embedded silicone hydrogel contact lens attached to one of the male and female mold halves) and peeling the lens (i.e., removing the raw embedded silicone hydrogel contact lens from the mold half attached to the lens). After peeling off the raw embedded silicone hydrogel contact lens, it is typically extracted using an extraction medium such as those well known to a person skilled in the art. A liquid extraction medium is any solvent capable of dissolving the diluent(s), unpolymerized polymerizable materials, and oligomers in the raw embedded silicone hydrogel contact lens. In the invention, water, any organic solvent known to a person skilled in the art, or a mixture thereof may be used. Preferably, the organic solvents used as a liquid extraction medium are water, a buffered saline solution, a C1-C3 alkyl alcohol, 1,2-propylene glycol, a polyethylene glycol having a number-average molecular weight of approximately 400 Da or less, an Oi-Ce alkyl alcohol, or combinations thereof. The extracted silicone hydrogel-embedded contact lens can then be hydrated using any method known to a person skilled in the art. The hydrated embedded silicone hydrogel contact lens can also be subjected to additional processes, such as, for example, a surface treatment, packaging in lens containers with a packaging solution that is well known to a person skilled in the art, sterilization, such as autoclave sterilization at a temperature of 118 to 124 °C for at least approximately 30 minutes, and the like. Lens containers are well known to a person skilled in the art for autoclaving and storing a soft contact lens. In the invention, any lens container may be used. Preferably, a lens container is a blister-type container comprising a base and a lid, wherein the lid is sealed to the base so as to be separable, and wherein the base includes a cavity for receiving a sterile packaging solution and the contact lens. L / CL Ln / Zznz / E / YIAI Lenses are packaged in individual containers, sealed, and sterilized (for example, by autoclaving at approximately 120°C or higher for at least 30 minutes under pressure) before being dispensed to users. A person skilled in the art will have a thorough understanding of how to seal and sterilize lens containers. In a further aspect, the invention provides an embedded silicone hydrogel contact lens, comprising a silicone hydrogel material and an insert of the invention (as described above in this application) therein, wherein the silicone hydrogel material is a crosslinked material having a polymer matrix and comprising (a) repeating units of at least one silicone-containing vinyl monomer and / or at least one silicone-containing vinyl crosslinker and (b) repeating units of at least one hydrophilic vinyl monomer, wherein the embedded silicone hydrogel contact lens in the fully hydrated state has a water content of approximately 15% to approximately 70% (preferably approximately 15% to approximately 65%, more preferably approximately 20% to approximately 65%).even more preferably from approximately 25% to approximately 60%) by weight of water when fully hydrated. All the various embodiments, including preferred embodiments of polymerizable compositions, silicone-containing vinyl monomers, silicone-containing vinyl crosslinkers, hydrophilic vinyl monomers, non-silicone vinyl crosslinkers, hydrophobic vinyl monomers, UV / HEVL absorption vinyl monomers, blending vinyl monomers, inserts, RGP discs, non-reactive polymeric diluents, water swelling degrees of unprocessed embedded silicone hydrogel contact lenses, and equilibrium water contents of embedded silicone hydrogel contact lenses, can be incorporated into these two aspects of the invention. Although various embodiments of the invention have been described using specific terms or expressions, devices, and methods, such description is for illustrative purposes only. The words used are descriptive rather than limiting. As will be evident to a person skilled in the art, those skilled in the art may make many variations and modifications of the invention without departing from the spirit or scope of the novel concepts disclosed. Furthermore, it should be understood that aspects of the various embodiments of the invention may be interchanged, either in whole or in part, or combined in any way and / or used together, as illustrated below: 1. An insert intended to be embedded in a silicone hydrogel contact lens, comprising a crosslinked polymeric material, comprising: (1) repeating units of said at least one polymerizable material containing silicone; (2) repeating units of at least one aryl acrylic monomer; and (3) repeating units of at least one vinyl crosslinking agent, wherein the sum of the amounts of components (1) and (2) of the crosslinked polymeric material is at least approximately 70% by weight of the total weight of the polymeric material L / CL ίη / ZZΖΠZ / E / YΙΛΙ crosslinked, wherein the crosslinked polymeric material in the dry state has a glass transition temperature greater than approximately 28 °C, wherein the crosslinked polymeric material in the fully hydrated state has a water content of less than approximately 5% by weight, an oxygen permeability of at least approximately 60 Barrer and a refractive index of at least approximately 1.45. 2. The insertion of embodiment 1, wherein the sum of the quantities of components (1) and (2) of the crosslinked polymeric material is approximately 75% to approximately 99% by weight, with respect to the total weight of the crosslinked polymeric material. 3. The insertion of embodiment 1, wherein the sum of the quantities of components (1) and (2) of the crosslinked polymeric material is approximately 80% to approximately 98% by weight, with respect to the total weight of the crosslinked polymeric material. 4. The insertion of embodiment 1, wherein the sum of the quantities of components (1) and (2) of the crosslinked polymeric material is approximately 85% to 98% by weight, with respect to the total weight of the crosslinked polymeric material. 5. The insertion of any one of embodiments 1 to 4, wherein the amount of component (2) of the crosslinked polymeric material is approximately 25% to approximately 50% by weight, with respect to the total weight of the crosslinked polymeric material. 6. The insertion of any one of embodiments 1 to 5, wherein the crosslinked polymeric material in the dry state has a glass transition temperature of approximately 30 °C or higher. 7. The insertion of any one of embodiments 1 to 5, wherein the crosslinked polymeric material in the dry state has a glass transition temperature of approximately 32 °C or higher. 8. The insertion of any one of embodiments 1 to 7, wherein the crosslinked polymeric material in a fully hydrated state has a water content of approximately 4% by weight or less. 9. The insertion of any one of embodiments 1 to 7, wherein the crosslinked polymeric material in a fully hydrated state has a water content of approximately 3% by weight or less. 10. The insertion of any one of embodiments 1 to 7, wherein the crosslinked polymeric material in a fully hydrated state has a water content of approximately 2% by weight or less. 11. The insertion of any one of embodiments 1 to 10, wherein the crosslinked polymeric material in a fully hydrated state has an oxygen permeability of at least approximately 70 Barrer. 12. The insertion of any one of embodiments 1 to 10, wherein the crosslinked polymeric material in a fully hydrated state has an oxygen permeability of at least approximately 80 Barrer. 13. The insertion of any one of embodiments 1 to 10, wherein the crosslinked polymeric material in the fully hydrated state has an oxygen permeability of at least L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ approximately 90 Sweep. 14. The insertion of any one of embodiments 1 to 13, wherein the crosslinked polymeric material in the fully hydrated state has a refractive index of at least approximately 1.47. 15. The insertion of any one of embodiments 1 to 13, wherein the crosslinked polymeric material in a fully hydrated state has a refractive index of at least 1.49. 16. The insertion of any one of embodiments 1 to 13, wherein the crosslinked polymeric material in the fully hydrated state has a refractive index of at least approximately 1.51. 17. The insertion of any one of embodiments 1 to 16, wherein said at least one aryl acrylic monomer is a vinyl monomer of Formula (I) or (II) L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ where Ai is H or CH3 (preferably H); B1 is (CH2)mi or [O(CH2)2]zi where m1 is 2-6 and z1 is 1-10; Y1 is a direct bond, O, S or NR' in which R' is H, CH3, Cn H2n+i in which n'=1 -10, ¡S0-OC3H7, CeHs or CH2C6H5; Ra, Rb, Re, Rd, Re, Rf, Rg, Rh and Ri are independently of each other H, C1-C12 alkyl or C1-C12 alkoxy (preferably they are all H); w1 is 0-6, whenever m1+w1<8; w2 is an integer from 1 to 3; and Di is H, Cl, Br, C1-C4 alkyl, C1-C4 alkoxy, CeHs or CH2C6H5. 18. The insertion of any one of embodiments 1 to 16, wherein said at least one aryl acrylic monomer comprises at least one vinyl monomer selected from the group consisting of 2-ethylphenoxy acrylate; 2-ethylphenoxy methacrylate; phenyl acrylate; phenyl methacrylate; benzyl acrylate; benzyl methacrylate; 2-phenylethyl acrylate; 2-phenylethyl methacrylate; 3-phenylpropyl acrylate; 3-phenylpropyl methacrylate; 4-phenylbutyl acrylate; 4-phenylbutyl methacrylate; 4-methylphenyl acrylate; 4-methylphenyl methacrylate; 4-methylbenzyl acrylate; 4-methylbenzyl methacrylate; 2-(2-methylphenyl)ethyl acrylate; 2-(2-methylphenyl)ethyl methacrylate; 2-(3-methylphenyl)ethyl acrylate; 2-(3-methylphenyl)ethyl methacrylate; 2-(4-methylphenyl)ethyl acrylate; 2-(4-methylphenyl)ethyl methacrylate; 2-(4-propylphenyl)ethyl acrylate; 2-(4-propylphenyl)ethyl methacrylate; 2-(4-(1-methylethyl)phenyl)ethyl acrylate;2(4-(1-methylethyl)phenyl)ethyl methacrylate; 2-(4-methoxyphenyl)ethyl acrylate; 2-(4-methoxyphenyl)ethyl methacrylate; 2(4-cyclohexylphenyl)ethyl acrylate; 2-(4-cyclohexylphenyl)ethyl methacrylate; 2-(2-chlorophenyl)ethyl acrylate; 2-(2-chlorophenyl)ethyl methacrylate; 2-(3-chlorophenyl)ethyl acrylate; 2-(3-chlorophenyl)ethyl methacrylate; 2-(4-chlorophenyl)ethyl acrylate; 2-(4-chlorophenyl)ethyl methacrylate; 2-(4-bromophenyl)ethyl acrylate; 2-(4-bromophenyl)ethyl methacrylate; 2-(3-phenylphenyl)ethyl acrylate; 2-(3-phenylphenyl)ethyl methacrylate; 2-(4-phenylphenyl)ethyl acrylate; 2-(4-phenylphenyl)ethyl methacrylate; 2-(4-benzylphenyl)ethyl acrylate; 2-(4-benzylphenyl)ethyl methacrylate; 2-(phenylthio)ethyl acrylate; 2-(phenylthio)ethyl methacrylate; 2-benzyloxyethyl acrylate; 3-benzyloxypropyl acrylate; 2-benzyloxyethyl methacrylate; 3-benzyloxypropyl methacrylate; 2-[2(benzyloxy)ethoxy]ethyl acrylate;2-[2-(benzyloxy)ethoxy]ethyl methacrylate and combinations thereof.; 26. The insertion of any one of embodiments 1 to 24, wherein said at least one polymerizable material containing silicone comprises a vinyl monomer of Formula (M1) or (M2)rmo O , CH3. CH3 H2C = C—(o) C-XMo-LM14-Si-Ol— Si--Rt1(MI) ' CH3Ail ¿h3 7X Rmo O j^o Si-CH3) H2C=C—(o)---C-Xmo-Lmi-S¡ CH3(M2)aMl1 \Rt2 / 3-rl L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ in which: 3mi is zero or 1; Rmo is H or methyl; Xmo is O or NRmi; Lmi is a divalent radical of _i ._y_i -(C2H4O)—¡-CONH-LMí'— -{c2H4o)-í-Lm1— C2-C8 alkylene or a radical of Lm1 Xm1 Lm1,1, -LM1'-NHCOo4c2H4o)^-LM1- -CH2 <H(OH)CH2-Xmi4c2H4o)^-Lm1J5 — I '-Y '-OH -CH / OHLCH -C1 -1 — ~(G2H4O)v, CH2-CH(OH)*CH2”O-Lfy|i lMi xMi ch2ch(oh) ch2o lm1 o'V1 2.Lmi-es un rad¡ca| divalente de alquileno C2-C8 que tiene un grupo hidroxilo o ninguno; Lmi es un radical divalente de alquileno Cs-Cs que tiene un grupo hidroxilo o ninguno; Xmi es O, NRmi, NHCOO, OCONH, CONRmi o NRmiCO; Rmi es H o un alquilo C1-C4 que tiene de 0 a 2 grupos hidroxilo; Rti y Rt2 son independientemente entre sí un alquilo Oí-Ce; Xm-Γ es O o NR1; v1 es un número entero de 1 a 30; m2 es un número entero de 0 a 30; n1 es un número entero de 3 a 40; y r1 es un número entero de 2 o 3. 27. The listing of a list of designs 1 to 24, where I say at least one polymerizable material that contains silicone includes (meth)acrylate of tr¡s(trimethylsilyloxy)silylpropyl, [3(met)acr¡lox¡-2-h¡drox¡prop¡lox¡]prop¡lb¡s(tr¡met¡ls¡lox¡)met¡ls¡lano, [3-(met)acrylox¡-2- h¡drox¡prop¡lox¡]prop¡lbis(tr¡met¡ls¡lox¡)but¡ls¡lano, 3-(met)acr¡loxi-2-(2-h¡drox¡etox¡)prop¡lox¡)propylbis(tr¡met¡ls¡lox¡)methylsilane, 3-(meth)acr¡loxi-2-hidroxypropyloxi)propyltris(trimethylsiloxy)silane, N-[tr¡s(trimethylsiloxi)silylpropyl]-(meth)acrylamida, N-(2-hidroxi-3-(3-(bis(tr¡methylsiloxi)methylsilyl)propyloxi)propyl)2-methyl (meth)acrylam¡da, N-(2-hidroxi-3-(3-(bis(trimethylsyloxy)methylsilyl)propyloxy)-propyl) (meth)acrylamida, N-(2hidroxy-3-(3-(tris(trimethylsilyloxi)silyl)propyloxi)propyl)-2-methyl acrylamida, N-(2-hidrox¡-3-(3(tr¡s(tr¡methyls¡l¡loxi)silyl)prop¡lox¡)prop¡l) (meth)acrylamida, N-[tr¡s(dimethylprop¡lsilox¡)s¡l¡lpropyl]-(meth)acr¡lam¡da,N-[tris(dimethylphenylsiloxy)-silylpropyl] (meth)acrylamide, N-[tns(dimethylethylsiloxy)-s¡l¡lprop¡l] (meth)acrylamide, N,Nbis[2-h¡droxy-3-(3-(bis(trimethylsilyloxy)methylsilyl)-methyl-propyl-2)] (meth)acrylamide, N,N-bis[2-hydroxy¡-3(3-(b¡s(tr¡methylsilyloxy)met¡ls¡l)propyloxy)-propyl] (meth)acrylamide, N,N-bis[2-hydroxy¡-3-(3(tris(tr¡met¡lsilyloxy)silyl)propylox¡)-propyl]-2-methyl (meth)acrylamide, N,N-bis[2-hydroxy¡-3-(3(tr¡s(trimet¡lsilyl)-propyl)-propyl) (meth)acrylamide, N-[2-hydroxy-3-(3-(t-butyl¡meth¡lsilyl)prop¡lox¡)-prop¡l]2-methyl (meth)acrylamide, N-[2-hydroxy-3-(3-(i-butyldimethylsilyl)propyloxy)-propylamide,) N,N-bis[2hydroxy-3-(3-(t-butyld¡methylsilyl)propyloxy)propyl]-2-methyl (meth)acnlamide, carbamate of N-2-(meth)acryloxyethylO(methyl-bis-trimet¡ls¡l¡lox¡-3-propyl)silyl carbonate 3-(trimeth¡ls¡l¡l)prop¡lv¡n¡l, 3-(vinyloxycarbonylthio)-propyltris(tr¡met¡ls¡loxy)silane, 3-[tris(tr¡methylsiloxy)s¡lyl]prop¡ln¡l,3-[tris(trimethylsiloxy)sil]propyl carbamate, 3-[tris(trimethylsiloxy)sil]propyl vinyl carbonate or a combination thereof. 28. The insertion of any one of embodiments 1 to 24, wherein said at least one polymerizable silicone-containing material comprises polydimethylsiloxane terminated in c(meth)acryloxypropyl terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-(meth)acryloxy-2-hydroxypropyloxypropyl terminated in C1-C4 ω-alkyl, α-(2-hydroxyyl-methacryloxypropyloxypropyl)-ω-alkyl C1-C4-decamethylpentasiloxane, polydimethylsiloxane terminated in α-[3-(meth)acryloxyethoxy-2-hydroxypropyloxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxypropyloxy-2-hydroxypropyloxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in a-[3(meth)acryloxy¡soprop¡lox¡-2-h¡drox¡prop¡lox¡propílo] terminated in ω-C1-C4 alkyl, polydimethylsiloxane terminated in a-[3-(meth)acrylox¡ethylamino-2-hydroxy¡prop¡lox¡propyl] terminated in ωC1-C4alkyl,polydimethylsiloxane terminated in α-[3-(meth)acryloxypropylamine-2-hydroxypropyloxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxy-butylamine-2-hydroxypropyloxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy(polyethyleneoxy)-2-hydroxypropyloxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyloxy-ethoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyl-N-ethylaminepropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropylaminopropyl] terminated in C1-C4 ωalkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyloxy-(polyethyleneoxy)propyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-(meth)acryloaminopropyloxypropyl terminated in C1-C4 ω-alkyl,polydimethylsiloxane terminated in aN-methyl-(meth)acryloylamidopropyloxpropyl terminated in ω-alkyl C1-C4, polydimethylsiloxane terminated in q-[3-(meth)acrylamidoetoxi-2-hdroxpropyloxpropyl] terminated in ω-alkyl C1-C4, polidimethylsiloxane terminated in c-[3-(met)acr¡lam¡doprop¡lox¡-2hidroxypropiloxypropilo] terminating in ω-alquilo C1-C4, polidimethylsiloxane terminating in c-[3(met)acr¡lamido¡soprop¡lox¡-2-h¡drox¡prop¡lox¡prop¡lo] terminated in ω-alquilo C1-C4, polidimetilsiloxano terminado en a-[3-(met)acrilam¡dobutiloxy-2-h¡drox¡prop¡lox¡prop¡lo] terminado en ω-alquilo C1-C4, polidimetilsiloxano terminado en a-[3-(met)acrilo¡lamido-2-h¡drox¡prop¡lox¡prop¡lo] terminado en ω-alquilo C1-C4, polidimetilsiloxano terminado en a-[3-[N-metil-(met)acr¡lo¡lamido]-2-hidroxiprop¡lox¡prop¡lo] terminado en ω-alquilo C1-C4, N-metil-N'qpropiltetraídimetilsiloxOdimetilbutilsilanoXmeflacnlamida, N-(2,3d¡h¡drox¡propane)-N'-(prop¡ltetra(d¡methylsiloxy)dimeth¡lbut¡ls¡lane)(meth)acr¡lam¡da,(meth)acrylolamidopropyltetra(dimethylsiloxy)dimethylbutylsilane, q-vinyl carbonate terminated with C1-C4 ω-alkyl, q-vinyl carbamate terminated with C1-C4 ω-alkyl, or a mixture thereof. 29. The insertion of any one of embodiments 1 to 28, wherein said at least one polymerizable silicone-containing material comprises at least one vinyl polysiloxane crosslinking first. 30. The insertion of embodiment 29, wherein said at least one first polysiloxane vinyl crosslinker comprises: (1) a vinyl crosslinker comprising a single segment of L / CL ίΠ / ZZΖηZ / E / YΙΛΙ polydiorganosiloxane and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups, vinylcarbamate groups; and / or (2) a long-chain polysiloxane vinyl crosslinker comprising at least two polydiorganosiloxane segments and a covalent linker between each pair of polydiorganosiloxane segments and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups and vinylcarbamate groups. 31. La inserción de la realización 29 o 30, en donde dicho al menos un primer reticulante vinílico de polisiloxano comprende polidimetilsiloxano terminado en a,üj-b¡s[3-(met)acrilam¡doprop¡lo], polidimetilsiloxano terminado en a,a)-bis[3-(met)acnlox¡propilo], polidimetilsiloxano terminado en a,u)-bis[3(met)acrilox¡-2-h¡drox¡prop¡lox¡prop¡lo], polidimetilsiloxano terminado en a,üJ-bis[3-(met)acr¡loxietox¡-2- L / CL ίη / 77Π7 / Ε / ΥΙΛΙ nitroxypropyloxypropyl], polydimethylsiloxane terminated in a,m-bis[3-(meth)acryloxypropyloxy-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,(Ob¡s[3-(meth)acryloxy-¡isopropyloxy-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a^-bis[3-(meth)acryloxybutyloxy-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,(jo-bis[3-(meth)acryl¡lamidoethoxy¡-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,u-bis[3-(meth)acrylamidopropyloxy-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a^-bis[3-(meth)acrylamidoisopropyloxy-2 nitroxypropyloxypropyl], polydimethylsiloxane terminated in a,ub¡s[3-(meth)acrylamidobutyl¡lox¡-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,(jL>-bis[3-(meth)acryloxyethyl¡amino-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,üj-bis[3-(meth)acryloxypropyl¡amino-2 hydroxypropyloxypropyl], polydimethylsiloxane terminated in a,oj-bis[3-(meth)acryloxybutyl¡amino-2 hydroxypropyloxypropyl],polydimethylsiloxane terminated in a,co-bis[(meth)acrylamidoethylamino-2-hydroxypropyloxy-propyl], polydimethylsiloxane terminated in a, <jj-bis[3-(met)acrilam¡dopropilamino-2 hidroxipropiloxipropilo], polidimetilsiloxano terminado en a,cü-bis[3-(met)acr¡lam¡do-butilamino-2 nidroxipropiloxipropilo], a^-bis[(met)acriloxi-2-h¡droxipropiloxethoxypropyl], a,cü-b¡s[(meth)acryloxy-2-hydroxy¡prop¡lN-ethyllam¡noprop¡l], polydimethylsiloxane terminated α,ωb¡s[(meth)acryloxy-2-hydroxyprop¡lox¡-(polyethyleneoxy)propyl], polydimethylsiloxane terminated in α,ωb¡s[(meth)acryloxyethylamino-carbonyloxy¡-(polyethylenex¡)propyl] or combinations thereof. 32. The insertion of any one of embodiments 1 to 31, wherein the insertion has a modulus greater than 20 MPa at room temperature. 33. The insertion of any one of embodiments 1 to 31, wherein the insertion has a modulus greater than 30 MPa at room temperature. 34. The insertion of any one of embodiments 1 to 31, wherein the insertion has a modulus greater than 40 MPa at room temperature. 35. The insertion of any one of embodiments 1 to 31, wherein the insertion has a modulus greater than 50 MPa at room temperature. 36. A method for the production of an embedded silicone hydrogel contact lens, comprising the steps of: (1) obtain a silicone hydrogel lens forming composition; (2) obtain an insertion of any one of the realizations 1 to 35; (3) obtaining a lens mold, wherein the lens mold comprises a male mold half having a first molding surface and a female mold half having a second molding surface, wherein the male and female mold halves are configured to receive each other in such a way that a mold cavity is formed between the first and second molding surfaces when the mold is closed; (4) in no particular order, placing the insert of the invention, as described above, in a specified position in the lens mold and introducing the silicone hydrogel lens forming composition into the lens mold, wherein the insert is immersed in the silicone hydrogel lens forming composition in the lens mold; (5) curing the silicone hydrogel lens forming composition in the lens mold to form an unprocessed embedded silicone hydrogel contact lens comprising a silicone hydrogel material and the embedded insert within the silicone hydrogel material; (6) separating the lens mold obtained in step (5) into male and female mold halves, with the raw embedded silicone hydrogel contact lens adhered onto one mold half attached to the lens that is one of the male and female mold halves; (7) removing the raw embedded silicone hydrogel contact lens from the mold half bonded to the lens before the raw embedded silicone hydrogel contact lens comes into contact with water or any liquid; and (8) subjecting the raw embedded silicone hydrogel contact lens to post-molding processes, including a hydration process and one or more different processes selected from the group consisting of extraction, surface treatment, packaging, sterilization and combinations thereof. 37. An embedded silicone hydrogel contact lens, comprising: a silicone hydrogel material; and an insertion of any one of embodiments 1 to 35 within the silicone hydrogel material, wherein the silicone hydrogel material is a crosslinked material having a polymer matrix and comprising (a) repeating units of at least one second silicone-containing vinyl monomer and / or at least one second silicone-containing vinyl crosslinker and (b) repeating units of at least one hydrophilic vinyl monomer, wherein the embedded silicone hydrogel contact lens in the fully hydrated state has a water content of approximately 15% to approximately 70% by weight of water when fully hydrated. 38. The method of embodiment 36 or the embedded silicone hydrogel contact lens of claim 37, wherein the silicone hydrogel material comprises repeating units of at least one silicone-containing vinyl monomer selected from the group consisting of a vinyl monomer having a bis(trialkylsiloxy)alkyl group, a vinyl monomer having a group L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ tris(tr¡alkyls¡l¡loxy)silyl, a polysiloxane vinyl monomer, 3-methacryloxypropylpentamethyldisiloxane, f-butyldimethylsiloxyethyl vinylcarbonate, trimethylsilylethyl vinylcarbonate and trimethylsilylmethyl and combinations thereof. 39. The method of embodiment 36 or 38 or the embedded silicone hydrogel contact lens of embodiment 37 or 38, wherein the silicone hydrogel material comprises repeating units of at least one second silicone-containing vinyl monomer of Formula (M1) or (M2) Rmo or / ch3. ch3 H2C = C—(o)--C-Xmo-Lmi—f-Si-Oí—Si--Rt1(Mí)aM1' CH3¿1 ch3( 'H3\ Rmo 9 LO-SÍ-CHs ) h2c=c—(o)---C-Xmo-Lm1-Si ch3(M2) 'aMi iRt2 / 3-rl in the que: aMi is cero o 1; Rmo es H or methyl; Xmo es O o NRmi; Lmi is a divalent radical of _i _i -(CoH^krCONH-LMj'- -(c2H4o)-rLM1— alquilene C2-C8o a radical of the mixmilmi ;2 4'viM,2 4 / vi mi -Lm1'-NHCOO-(C2H4O)^-Lm1- -CH2-CH(OH)CH2-Xmi4c2H4o)^Lmí'—i '-y '-ch -ch / ohvch -o-ι (θ2Η4θ)νι LMi XM1 CH2CH(OH) CH2O LM1 02 4'vi;|_M1·is a divalent Cz-Cs alkylene radical having one hydroxyl group or none; Lmi is a divalent C3-C8 alkylene radical having one hydroxyl group or none; Xmi is O, NRmi, NHCOO, OCONH, CONRmi or NRmiCO; Rmi is H or a C1-C4 alkyl having 0 to 2 hydroxyl groups; Rn and Rt2 are independently of each other a Ci-Ce alkyl; Xmi' is O or NR1; v1 is an integer from 1 to 30; m2 is an integer from 0 to 30; n1 is an integer from 3 to 40; and r1 is an integer from 2 or 3. 40. The method of any one of embodiments 36, 38 and 39 or the silicone hydrogel contact lens embedded in any one of embodiments 37-39, wherein the silicone hydrogel material comprises tris(trimethylsilyloxy)silylpropyl (meth)acrylate, [3-(meth)acryloxy-2-hydroxypropyloxy]propylbis(trimethylsiloxy)methylsilane, [3-(meth)acryloxy-2-hydroxypropyloxy]propylbis(trimethylsiloxy)butylsilane, 3-(meth)acryloxy-2-(2-hydroxyethoxy)propyloxy)propylbis(trimethylsiloxy)methylsilane, 3-(meth)acryloxy-2-hydroxypropyloxy)propyltris(trimethylsiloxy)silane, N-[tris(trimethylsiloxy)silylpropyl]-(meth)acrylamide, N-(2-hydroxy-3-(3-(bis(trimethylsilyloxy)methylsilyl)propyloxy)propyl)2-methyl(meth)acrylamide, N-(2-hydroxy-3-(3-(bis(trimethylsilyloxy)methylsilyl)propyloxy)-propyl)(meth)acrylamide, N-(2hydroxy¡-3-(3-(tr¡s(trimethylsilyloxy)silyl)propyloxy)propyl)-2-methylacrylamide, N-(2-hydroxy-3-(3(tris(trimethylsilyloxy)silyl)propyloxy)propyl)(meth)acrylamide,N-[tr¡s(dimethylpropylsiloxy)silylpropyl]-(meth)acrylam¡da, N-[tris(dimethylphenylsiloxy)-silylpropyl](meth)acrylamide, N-[tris(dimethylethylsiloxy¡)-sil¡lpropyl](meth)acrylamide, N,Nbis[2-hydroxy-3-(3-(b¡s(trimethylsilyloxy)methyls¡l¡l)-propyloxy)propyl]-2-met¡l(meth)acrylamide, N,N-bis[2-hydroxy¡-3(3-(b¡s(tr¡methyls¡l¡lox¡)meth¡ls¡l¡l)propylox¡)-propyl](meth)acrylamide, N,N-bis[2-hydroxy¡-3-(3(trimeth) ls¡l¡lox¡)sil¡l)prop¡lox¡)-prop¡l]-2-met¡l(meth)acrylam¡da, N,N-bis[2-hydroxy¡-3-(3(tr¡s(tr¡meth¡ls¡l¡l¡lox¡)s¡lil)-propyloxy)prop¡l](meth)acrylamide, N-[2-hydroxy-3-(3-(f-butyldimethylsilyl)-propyl)) L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ 2-methyl(meth)acrylamide, N-[2-hydroxy-3-(3-(β-butyldimethylsilyl)propyloxy)propyl](meth)acrylamide, N,N-bis[2-hydroxy-3-(3-(f-butyldimethylsilyl)propyloxy)propyl]-2-methyl(meth)acrylamide, N-2-(meth)acryloxyethyl(1O)(methyl-bis-trimethylsilyl-3-propyl)silyl carbamate, 3-(trimethylsilyl)propylvinyl carbonate, 3-(vinyloxycarbonylthio)-propyltris(trmethylsilyloxy)silane, 3-[tris(trimethylsilyl)silyl]propylvinyl carbamate, 3[tris(tr¡methylsiloxy)silyl]propylalyl, vinylcarbonate de 3-[tris(trimethylsiloxy)syl¡l]propyl or a combination of the same. 41. The method of any one of embodiments 36 and 38-40 or the silicone hydrogel contact lens embedded in any one of embodiments 37-40, wherein the silicone hydrogel material comprises C1-C4 ωalkyl-terminated α-(meth)acryloxypropyl polydimethylsiloxane, C1-C4 ω-terminated α-(meth)acryloxy-2-hydroxypropyloxypropyl polydimethylsiloxane, C1-C4 ω-terminated α-(2-hydroxy-methacryloxypropyloxypropyl)-ω-alkyl α-C1-C4-decamethylpentasiloxane, C1-C4 ω-terminated α-[3-(meth)acryloxyethoxy-2-hydroxypropyloxypropyl]-terminated α-[3-(meth)acryloxyethoxy-2-hydroxypropyloxypropyl]-terminated α-C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxy-propoxy-2-hydroxypropoxypropyl] terminated in C1-C4 ωalkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxyisopropyloxy-2-hydroxypropoxypropyl] terminated in C1-C4 ωalkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxybutoxy-2-hydroxypropyloxypropyl] terminated in C1-C4 ωalkyl,polydimethylsiloxane terminated in α-[3(meth)acryloxyethylamine-2-hydroxypropoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxypropylamine-2-hydroxypropoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[3-(meth)acryloxy-butylamine-2-hydroxypropoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-(meth)acryloxy(polyethyleneoxy)-2-hydroxypropoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropoxy-ethoxypropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyl-N-ethylaminopropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyl-aminopropyl] terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-[(meth)acryloxy-2-hydroxypropyloxy(polyethyleneoxy)propyl] terminated in C1-C4 ω-alkyl,a(meth)acryloylamidopropyloxypropyl terminated polydimethylsiloxane ω-C1-C4 alkyl terminated, ω-C1-C4 alkyl terminated aN-methyl(meth)acryloylamidopropyloxypropyl terminated polydimethylsiloxane, a-[3(meth)acrylamidoethoxy-2-hydroxy¡prop¡loxy-propyl] terminated in ω-C1-C4 alkyl, polydimethylsiloxane terminated in a-[3-(meth)acrylam¡doisoprop¡lox¡-2-hydrox¡prop¡lox¡propílo] terminated in ω-alkyl C1-C4, polydimethylsiloxane terminated in α-[3-(meth)acrylamide butyloxy-2-hydroxypropyloxypropyl] terminated in ωalkyl C1-C4, polydimethylsiloxane terminated in α-[3-(meth)acrylolamido-2-hydroxypropyloxypropyl] terminated in ωalkyl C1-C4, polydimethylsiloxane terminated in α-[3-[N-methyl-(meth)acrylolamido]-2-hydroxypropyloxypropyl] terminated in ωalkyl C1-C4, N-methyl-N1(propyltetra(dimethylsiloxy)dimethylbutylsilane)(meth)acrylamide, N-(2,3-dihydroxypropane)-N'(propyltetra(dimethylsiloxy)dimethylbutylsilane)(meth)acrylamide, (meth)acrylamide propyltetra(dimethylsiloxy)dimethylbutylsilane, polydimethylsiloxanes terminated in α-vinyl carbonate terminated in C1-C4 ω-alkyl, polydimethylsiloxane terminated in α-vinyl carbamate, LJCL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ in ω-C1-C4 alkyl or a mixture thereof. 42. The method of any one of embodiments 36 and 38-41 or the silicone hydrogel contact lens embedded in any one of embodiments 37-41, wherein the silicone hydrogel material comprises repeating units of at least one second polysiloxane vinyl crosslinker. 43. El método o la lente de contacto de hidrogel de silicona embebida de la realización 42, en donde dicho al menos un segundo reticulante vinílico de polisiloxano comprende un polidimetilsiloxano terminado en di-(met)acriloílo, un polidimetilsiloxano terminado en di-carbonato de vinilo; un polidimetilsiloxano terminado en di-carbamato de vinilo; N,N,N',N'-tetraqu¡s(3-metacr¡loxi-2-h¡drox¡prop¡l)alfa,omega-bis-3-am¡noprop¡l-pol¡d¡metils¡loxano o una combinación de los mismos. 44. The method or contact lens of silicone hydrogel embedded in the implementation 42, where I say at least a second vinyl cross-linker of polysiloxane includes a vinyl cross-linker of Formula (III) Rio O CH3 1 CH3» 1 R13 » CH3 OR|q H2C=c—C-Xd-Rn-Si-OT-Si-oj-í-Si-OI— Si—R|2-X01-CC=CH2(|||) CH3' CH3 / dA ¿H3 / d2 ¿H3en la que: d1 is an integer from 30 to 500 and d2 is an integer from 1 to 75, provided that d2 / d1 is from approximately 0.035 to approximately 0.15 (preferably from approximately 0.040 to approximately 0.12, even more preferably from approximately 0.045 to approximately 0.10); X01 is O or NRin in which Rin is hydrogen or C1-C10 alkyl; Rio is hydrogen or methyl; R11 and R12 are independently of each other a substituted or unsubstituted C1-C10 divalent alkylene radical or a -R14-O-R15- divalent radical wherein Rw and Ris are independently of each other a substituted or unsubstituted C1-C10 divalent alkylene radical; R13 is a monovalent radical of any one of the formulas (Illa) to (lile) R|6 4CH2)^O-CH2)—C-CH.-Xh-R^O^ (Illa) OH —^°η24——X|2-ri84oh) , (Hib) CH2OH —(-ch2Vo-ch2-c-ch2oh (|IIc) R|9 L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ R|6 —(-CH2)--fo-CH2)—C-CH2-OH (Ule) k1 is zero or 1; m1 is an integer from 2 to 4; m2 is an integer from 1 to 5; m3 is an integer from 3 to 6; m4 is an integer from 2 to 5; Laughs is hydrogen or methyl; Ri7 is a C2-C6 hydrocarbon radical that has valences (m2+1); Ria is a C2-C6 hydrocarbon radical that has valences (m4+1); R19 is ethyl or hydroxymethyl; Rno is not methyl or hydromethyl; R111 is hydroxyl or methoxy; X11 is an -S- sulfur bond or a -NR112- tertiary amino bond wherein R112 is C1-C1 alkyl, hydroxyethyl, hydroxypropyl, or 2,3-dihydroxypropyl; and OO X12 is an amide bond of-nrm3-c—oC-NRh3-en e| queri13 is hydrogen or C1C10 alkyl. 45. The method or the silicone hydrogel contact lens embedded in any one of embodiments 42 to 44, wherein said at least one second polysiloxane vinyl crosslinker comprises: (1) a vinyl crosslinker comprising a single polydiorganosiloxane segment and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups, vinylcarbamate groups; and / or (2) a long-chain polysiloxane vinyl crosslinker comprising at least two polydiorganosiloxane segments and a covalent linker between each pair of polydiorganosiloxane segments and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups, and vinylcarbamate groups. 46. ​​The method or the silicone hydrogel contact lens embedded in any one of embodiments 42 to 45, wherein said at least one second vinyl polysiloxane crosslinker comprises α,ω-bis[3-(meth)acryloxypropyl]-terminated polydimethylsiloxane, α,ω-bis[3-(meth)acryloxypropyl]-terminated polydimethylsiloxane, α,ω-bis[3-(meth)acryloxy-2-hydroxypropyloxypropyl]-terminated polydimethylsiloxane, α,ω-bis[3-(meth)acryloxy-2-hydroxypropyloxypropyl]-terminated polydimethylsiloxane, <jj-bis[3-(met)acriloxipropiloxi-2-hidrox¡propiloxiprop¡lo], polidimetilsiloxano terminado en a,(o-b¡s[3-(met)acr¡loxi-isoprop¡loxi-2-hidrox¡prop¡loxiprop¡lo], α,ω-bisis-L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ (meth)acryloxibutyloxi-2-hidrox¡propilox¡propilo], polidimethylsiloxano terminated in a,io-bis[3- (met)acr¡lam¡doetoxi-2-hidrox¡prop¡lox¡propilo], polidimethylsiloxano terminado in a,m-bis[3- (met)acr¡lamidopropiloxi-2-hidrox¡propiloxipropilo], polidimethylsiloxano terminated in a,co-bis[3- (meth)acrylam¡do¡soprop¡lox¡-2-hidrox¡prop¡lox¡prop¡lo], polidimethylsiloxano terminado in a,(o-bis[3- (meth)acrylam¡dobut¡lox¡-2-h¡drox¡prop¡lox¡prop¡lo], polydimethylsiloxane terminated in a,üj-bis[3- (meth)acrilox¡etilam¡no-2-h¡drox¡prop¡lox¡propilo], polidimethylsiloxane terminated in a,m-bis[3- (met)acr¡lox¡prop¡lamino-2-h¡drox¡prop¡lox¡prop¡lo], polydimethylsiloxane terminated in a,co-bis[3- (meth)acryloxybutylamino-2-hidroxypropyloxypropilo], polydimethylsiloxane terminated in α,ωb¡s[(meth)acrylamidoethylam¡no-2-h¡droxipropylox¡-propilo], polydimethylsiloxane terminated in a,co-bis[3(meth)acrylam¡doprop¡lam¡no-2-h¡drox¡prop¡lox¡prop¡lo], polidimethylsiloxano terminado en a^-bis[3(meth)acrylam¡do-but¡lam¡no-2-h¡drox¡prop¡lox¡prop¡lo], polidimethylsiloxane terminado en α,ωbis[(meth)acriloxi-2-hidroxipropiloxi-etoxipropilo], polydimethylsiloxane terminated in a^-bis[(meth)acriloxi-2hidroxipropyl-N-ethylaminopropyl], a^-bis[(meth)acriloxi-2-hidroxipropyl-aminopropyl]-polydimethylsiloxane, polidimethylsiloxane terminated in a^-b¡s[(meth)acryloxi-2-h¡drox¡prop¡loxi-(pol¡ethyleneox¡)prop¡lo], L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ polidimethylsiloxano terminado en a,Lü-bis[(met)acr¡lox¡et¡lamino-carbonilox¡-etox¡propilo], polidimethylsiloxano terminado en a,wb¡s[(met)acr¡loxiet¡lam¡no-carbon¡lox¡-(pol¡et¡lenox¡)prop¡lo] or combinations of the same. 47. The method of any one of embodiments 36 and 38-46 or the silicone hydrogel contact lens embedded in any one of embodiments 37-46, wherein the silicone hydrogel material comprises repeating units of at least one hydrophilic vinyl monomer. 48. The method or the embedded silicone hydrogel contact lens of embodiment 47, wherein said at least one hydrophilic vinyl monomer comprises: (1) an alkyl(meth)acrylamide selected from the group consisting of (meth)acrylamide, N,Ndimethyl(meth)acrylamide, N-ethyl(meth)acrylamide, N,Ndiethyl(meth)acrylamide, N-propyl(meth)acrylamide, N-isopropyl(meth)acrylamide, N-3-methoxypropyl(meth)acrylamide and combinations thereof; (2) an acrylic monomer containing hydroxyl selected from the group consisting of N-2-hydroxyethyl(meth)acrylamide, N,Nbis(hydroxyethyl)(meth)acrylamide, N-3-hydroxypropyl(meth)acrylamide, N-2-hydroxypropyl(meth)acrylamide, N-2,3-dihydroxypropyl(meth)acrylamide, A / -tris(hydroxymethyl)methyl(meth)acrylamide, 2-hydroxyethyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, glycerol methacrylate (GMA), diethylene glycol (meth)acrylate, tri(ethylene glycol)methacrylate, tetra(ethylene glycol)methacrylate,(meth)acrylate of poly(ethylene glycol) having a number average molecular weight up to 1,500, ethyl(meth)acrylamide of poly(ethylene glycol) having a number average molecular weight up to 1,500 and combinations thereof; (3) an acrylic monomer containing carboxyl selected from the group consisting of 2-(meth)acrylamidoglycolic acid, (meth)acrylic acid, ethylacrylic acid, 3-(meth)acrylamidopropionic acid, 5-(meth)acrylamidopentanoic acid, 4-(meth)acrylamidobutanoic acid, 3-(meth)acrylamido-2-methylbutanoic acid, 3-(meth)acrylamido-3-methylbutanoic acid, 2-(meth)acrylamido-2-methyl-3,3-dimethylbutanoic acid, 3-(meth)acrylamidohexanoic acid, 4-(meth)acrylamido-3,3-dimethylhexanoic acid and combinations thereof; (4) an amino-containing acrylic monomer selected from the group consisting of N-2-aminoethyl(meth)acrylamide, N-2-methylaminoethyl(meth)acrylamide, N-2-ethylaminoethyl(meth)acrylamide, N-2-dimethylaminoethyl(meth)acrylamide, N-3-aminopropyl(meth)acrylamide,N3-methylaminopropyl(meth)acrylamide, N-3-dimethylaminopropyl(meth)acrylamide, 2-aminoethyl (meth)acrylate, 2-methylaminoethyl (meth)acrylate, 2-ethylaminoethyl (meth)acrylate, 3-aminopropyl (meth)acrylate, 3-methylaminopropyl (meth)acrylate, 3-ethylaminopropyl (meth)acrylate, 3-amino-2-hydroxypropyl (meth)acrylate, trimethylammonium 2-hydroxypropyl (meth)acrylate hydrochloride, dimethylaminoethyl (meth)acrylate and combinations thereof; (5) an N-vinylamide monomer selected from the group consisting of N-vinylpyrrolidone (also known as N-vinyl-2-pyrrolidone), N-vinyl-3-methyl-2-pyrrolidone, N-vinyl-4-methyl-2-pyrrolidone, N-vinyl-5-methyl-2-pyrrolidone, N-vinyl-6-methyl-2-pyrrolidone, N-vinyl-3-ethyl-2-pyrrolidone, N-vinyl-4,5-dimethyl-2-pyrrolidone, N-vinyl-5,5-dimethyl-2-pyrrolidone, N-vinyl-3,3,5-trimethyl-2-pyrrolidone, N-vinylpiperidone (also known as N-vinyl-2-piperidone), N-vinyl-3-methyl-2-piperidone, N-vinyl-4-methyl-2-piperidone,N-vinyl-5-methyl-2-piperidone, N-vinyl-6-methyl-2-piperidone, N-vinyl-6-ethyl-2-piperidone, N-vinyl-3,5-dimethyl-2-piperidone, Nvinyl-4,4-dimethyl-2-piperidone, N-vinylcaprolactam (also known as N-vinyl-2-caprolactam), N-vinyl-3-methyl-2-caprolactam, Nvinyl-4-methyl-2-caprolactam, Nvinyl-7-methyl-2-caprolactam, N-vinyl-7-ethyl-2-caprolactam, N-vinyl-3,5-dimethyl-2-caprolactam, N-vinyl-4,6dimethyl-2-caprolactam, N-vinyl-3,5,7-trimethyl-2-caprolactam, N-vinyl-N-methylacetamide, N-vinylformamide, N-vinylacetamide, N-vinylisopropylamide, N-vinyl-N-ethylacetamide, N-vinyl-N-ethylformamide and mixtures thereof; (6) a methylene-containing pyrrolidone monomer selected from the group consisting of 1-methyl-3-methylene-2-pyrrolidone, 1-ethyl-3-methylene-2-pyrrolidone, 1-methyl-5-methylene-2-pyrrolidone, 1-ethyl-5-methylene-2-pyrrolidone, 5-methyl-3-methylene-2-pyrrolidone, 5-ethyl-3-methylene-2-pyrrolidone, 1-n-propyl-3-methylene-2-pyrrolidone, 1-n-propyl-5-methylene-2-pyrrolidone,1-isopropyl-3-methylene-2-pyrrolidone, 1-isopropyl-5-methylene-2-pyrrolidone, 1-n-butyl-3-methylene-2-pyrrolidone, 1-tert-butyl-3-methylene-2-pyrrolidone and combinations thereof; (7) an acrylic monomer having a C1-C4 alkoxyethoxy group and selected from the group consisting of ethylene glycol (meth)methyl ether (meth)acrylate, di(ethylene glycol)methyl ether (meth)acrylate, tri(ethylene glycol)methyl ether (meth)acrylate, tetra(ethylene glycol)methyl ether (meth)acrylate, C1-C4-poly(ethylene glycol) alkoxy (meth)acrylate having a number-average molecular weight up to 1,500, methoxy-poly(ethylene glycol) ethyl(meth)acrylamide having a number-average molecular weight up to 1,500 and combinations thereof; (8) a vinyl ether monomer selected from the group consisting of ethylene glycol monovinyl ether, di(ethylene glycol) monovinyl ether, tri(ethylene glycol) monovinyl ether, tetra(ethylene glycol) monovinyl ether, poly(ethylene glycol) monovinyl ether,(9) ethylene glycol methyl vinyl ether, d(ethylene glycol) methyl vinyl ether, tri(ethylene glycol) methyl vinyl ether, tetra(ethylene glycol) methyl vinyl ether, poly(ethylene glycol) methyl vinyl ether and combinations thereof; (1) an allyl ether monomer selected from the group consisting of ethylene glycol monoallyl ether, di(ethylene glycol) monoallyl ether, tri(ethylene glycol) monoallyl ether, tetra(ethylene glycol) monoallyl ether, poly(ethylene glycol) monoallyl ether, ethylene glycol methylallyl ether, di(ethylene glycol) methylallyl ether, tri(ethylene glycol) methylallyl ether, tetra(ethylene glycol) methylallyl ether, poly(ethylene glycol) methylallyl ether and combinations thereof; (10) a phosphorylcholine-containing vinyl monomer selected from the group consisting of (meth)acryloyloxyethylphosphorylcholine, (meth)acryloyloxypropylphosphorylcholine, 4-((meth)acrylo¡lox¡)but¡l-2'-(trimethylammon¡o)ethylphosphate, 2-[(meth)acryloylamno]ethyl-2'-(trimethylammonium)-ethylphosphate,3-[(meth)acryloylamine]propyl-2'-(trimethylamonium)ethylphosphate, 4-[(meth)acryloylamine]butyl-2'(trimethylamonium)ethylphosphate, 5-((meth)acryloyloxy)pentyl-2'-(trimethylamonium)ethylphosphate, 6-((meth)acryloyloxy)hexyl-2'(trimethylamonium)ethylphosphate, 2-((meth)acryloyloxy)ethyl-2'-(triethylamonium)ethylphosphate, 2-((meth)acryloyloxy)ethyl-2'(tripropylamonium)ethylphosphate, 2-((meth)acryloyloxy)ethyl-2'-(tributylammonium)ethylphosphate, 2-((meth)acryloylox)propyl-2'(trimethylamonium)-ethylphosphate, 2-((meth)acryloyloxy)butyl-2'-(trimethylamonium)ethylphosphate, 2-((meth)acryloylox)pentyl-2'(trimethylamonium)ethylphosphate, 2-(meth)acryloylox)hexyl-2'-(trimethylamonium)ethylphosphate, 2-(vinylox)ethyl-2'(trimethylamonium)ethylphosphate, 2-(aliloxy)et¡l-2'-(tr¡met¡lamonio)ethylphosphate, 2-(vinyloxycarbonyl)et¡l-2', L / CL ίη / ZZΖΠZΖ / E / YΙΛΙ (trimethylammonium)ethyl phosphate, 2-(allyloxycarbonyl)ethyl-2'-(trimethylammonium)-ethyl phosphate, 2-(vinylcarbonylamino)ethyl-2'-(trimethylammonium)ethyl phosphate, 2-(allyloxycarbonammonium)ethyl-2'-(trimethylammonium)ethyl phosphate, 2-(butenoyloxy)ethyl-2'-(trimethylammonium)ethyl phosphate and combinations thereof; (11) allyl alcohol; (12) N-2-hydroxyethyl vinylcarbamate; (13) N-carboxyvinyl-p-alanine (VINAL); (14) N-carboxyvinyl-a-alanine; (15) or combinations thereof. 49. The method or the embedded silicone hydrogel contact lens of embodiment 47 or 48, wherein said at least one hydrophilic vinyl monomer comprises N-vinylpyrrolidone, N-vinyl-N-methylacetamide or combinations thereof. 50. The method or silicone hydrogel contact lens embedded in any one of embodiments 47 to 49, wherein said at least one hydrophilic vinyl monomer comprises N,N-dimethyl(meth)acrylamide. 51. The method or the silicone hydrogel contact lens embedded in any one of embodiments 47 to 50, wherein said at least one hydrophilic vinyl monomer comprises N-2-hydroxyethyl(meth)acrylamide, N,N-bis(hydroxyethyl)(meth)acrylamide, N-3-hydroxypropyl(meth)acrylamide, N-2-hydroxypropyl(meth)acrylamide, N-2,3-dihydroxypropyl(meth)acrylamide, N-tr(hydroxymethyl)methyl(meth)acrylamide, 2-hydroxyethyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, glycerol methacrylate (GMA), di(ethylene glycol)methacrylate, (meth)acrylate of tri(ethylene glycol), tetra(ethylene glycol) (meth)acrylate, poly(ethylene glycol) (meth)acrylate having a number average molecular weight up to 1,500, poly(ethylene glycol) ethyl(meth)acrylamide having a number average molecular weight up to 1,500 or combinations thereof. 52. The method of any one of embodiments 36 and 38-51 or the silicone hydrogel contact lens embedded in any one of embodiments 37-51, wherein the silicone hydrogel material comprises repeating units of at least one non-silicone vinyl crosslinking agent. 53. El método o la lente de contacto de hidrogel de silicone embebida de la realización 52, en donde dicho al menos un agente de reticulación vinílico no de silicone comprende di-(met)acrilato de ethyleneglicol, di-(met)acrilato de diethyleneglicol, di-(met)acrilato de triethyleneglicol, di-(met)acrilato de tetraethyleneglicol, di-(met)acrilato de glicerol, di-(met)acrilato de 1,3-propanodiol, di-(met)acrilato de 1,3butanodiol, di-(met)acrilato de 1,4-butanodiol, di-(met)acrilato de 1,3-diglicerolato de glicerol, d¡(met)acrilato de ethylenebis[ox¡(2-hidroxypropane-1,3-diyl)], bis[2-(meth)acryloxietyl]phosphate, trimethylolpropane d¡(meth)acrylate and 3,4-bis[(meth)acryloyl]tetrahydrofuran, diacrylamida, dimethacrylamida, N,Nd¡(meth)acryloyl-N-met¡lam¡na, N,N-di(meth)acr¡lo¡lN-et¡lamina, N,N'-met¡lenobis(meth)acrylamida, N,N'ethylenobis(met)acr¡lam¡da, N,N'-dih¡drox¡et¡lenob¡s(met)acr¡lam¡da, N,N'-propylenobis(met)acr¡lam¡da, N,N'2-hidrox¡prop¡lenobis(meth)acrylam¡da, N,N'-2,3-dihydroxybutylenebis(meth)acrylamide, 1,3-bis(meth)acrylamidopropane-2-yl dihydrogen phosphate, piperazinediacrylamide, tetraethylene glycol divinyl ether, triethylene glycol divinyl ether, diethylene glycol divinyl ether, ethylene glycol divinyl ether, trialyl isocyanurate, trialyl cyanurate, trimethylpropane trimethacrylate, pentaerythritol tetramethacrylate, bisphenol A dimethacrylate, allyl methacrylate, allyl acrylate, N-allyl methacrylamide, N-allyl acrylamide or combinations thereof. L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ 54. The method of any one of embodiments 36 and 38-53 or the silicone hydrogel contact lens embedded in any one of embodiments 37-53, wherein the silicone hydrogel material comprises repeating units of at least one blending vinyl monomer. 55. The method or the embedded silicone hydrogel contact lens of embodiment 54, wherein said at least one blending vinyl monomer comprises C1-C10 alkyl (meth)acrylate, cyclopentyl acrylate, cyclohexyl methacrylate, cyclohexyl acrylate, isobornyl (meth)acrylate, styrene, 4,6-trimethylstyrene (TMS), i-butylstyrene (TBS), trifluoroethyl (meth)acrylate, hexafluoroisopropyl (meth)acrylate, hexafluorobutyl (meth)acrylate, or combinations thereof. The foregoing disclosure will enable a person skilled in the art to implement the invention. Various modifications, variations, and combinations of the embodiments described herein are possible. To enable the reader to better understand the specific embodiments and their advantages, reference to the following examples is suggested. The description and examples are intended to be illustrative. Example 1 Oxygen permeability measurements Unless otherwise specified, the oxygen transmissibility (Dk / t), intrinsic (or edge-corrected) oxygen permeability (Dk1 or Dkc) of an insert and insert material are determined according to the procedures described in ISO 18369-4. Equilibrium water content The equilibrium water content (EWC) of contact lenses is determined as follows. The amount of water (expressed as a weight percentage) present in a hydrated hydrogel contact lens, fully equilibrated in saline solution, is determined at room temperature. The lenses are quickly stacked and transferred to an aluminum pan on an analytical balance after drying the lenses on a cloth. The number of lenses for each sample pan is typically five (5). The hydrated weight of the lenses is recorded along with the pan. The pan is covered with aluminum foil. The pans are placed in a laboratory oven at 100 ± 2 °C to dry for 16–18 hours. The pan and lenses are removed from the oven and cooled in a desiccator for at least 30 minutes. One pan is removed from the desiccator, and the aluminum foil is discarded. The pan and the dried lens sample are weighed on an analytical balance. This is repeated for all pans.The wet and dry weight of the lens samples can be calculated by subtracting the weight of the empty weighing pan. refractive index The refractive index (RI) of the inserts is determined using a Reichert Abbe Mark III laboratory transmission refractometer at 25 °C. The inserts are fully equilibrated in PBS saline solution before measurement. Elastic modulus The storage modulus (Young's modulus) of the insertions is determined using a DMA The insert was cut into a 3.08 mm wide strip using a Precision Concept dry lens cutter. Five thickness values ​​were measured within a 6.5 mm reference length. The strip was mounted in the instrument using metal clamps. A temperature rise test was applied to the insert at a linear rate of 2 °C / minute from 10 °C to 50 °C. The material's response to the temperature rise was monitored at a constant frequency of 1 Hz, a constant amplitude of 0.5% strain, and a sampling rate of 10.0 pts / s. The storage modulus (Ej), loss modulus (E'j), and tan δ data were calculated using TRIOS software. The elastic modulus of a silicone hydrogel material or contact lens is determined using an MTS Insight instrument. The contact lens is first cut into a 3.12 mm wide strip using a Precision Concept two-stage cutter. Five thickness values ​​are measured within a 6.5 mm reference length. The strip is mounted in the instrument's grippers and immersed in PBS (phosphate-buffered saline) at a temperature controlled to 21 ± 2 °C. Typically, a 5 N load cell is used for the test. A constant force and velocity are applied to the sample until it breaks. Force and displacement data are collected using TestWorks software. The TestWorks software calculates the elastic modulus value, which is the slope or tangent of the stress-strain curve near zero elongation, in the elastic deformation region. Glass transition temperature The glass transition temperature (Tg) of the insertion is defined as the maximum of tan δ from the dynamic temperature rise test, as described above. Delamination The embedded silicone hydrogel contact lenses are examined for possible delamination, either using an Optimec instrument or optical coherence tomography (OCT). Regardless of the evaluation method, contact lenses are analyzed for a minimum of 12 hours at room temperature after the autoclave process and before the delamination study. After the required analysis time is completed, the fully hydrated contact lens is placed in a V-shaped grid mount of an Optimec instrument (model JCF, OPTIMEC England). Once the contact lens has settled under the influence of gravity, the front view of the lens is carefully inspected for any signs of circular patterns. Delamination appears as circular patterns in the Optimec image. An OCT (spectral-domain optical coherence tomography, model Telesto-II, from Thorlabs) could also be used to study delamination. OCT allows for non-invasive imaging of the contact lens to obtain a high-resolution cross-sectional image. To this end, after meeting the minimum analysis requirements, the contact lens is removed from its blister pack and immersed in a PBS solution for a minimum of 30 minutes to reach equilibrium. Next, approximately 1 / 2% of a V-block cuvette will be filled with a freshly prepared PBS solution, and the contact lens will be transferred to the cuvette using a cotton swab. The lens will be allowed to float freely to the V-shape at the bottom of the cuvette, and the entire contact lens will be scanned in 10-degree increments. Delamination appears as an air pocket at the insertion-support interval on OCT images. Chemicals In the following examples, the following abbreviations are used: PEMA represents phenylethyl methacrylate; PEA represents phenylethyl acrylate; BzA represents benzyl acrylate; BzMA represents benzyl methacrylate; PVV represents vinylmethyl-terminated phenylmethylsiloxane-vinylphenylsiloxane copolymer (PVV-3522, 800-1,500 Da, from Gelest); PMV represents vinyl-terminated polyphenylmethylsiloxane (PMV-9925, 2,000-3,000 Da, from Gelest); TBEC represents 2-ethylhexyl tert-butylperoxycarbonate; PETA represents pentaerythritol tetraacrylate; TrisMA represents 3-[tris(trimethylsiloxane)silyl]propyl methacrylate; HFIPMA represents hexafluoroisopropyl methacrylate; NPGDMA represents neopentyl glycol dimethacrylate; TrisAm represents N-[tr¡s(trimethylsiloxy)-silylpropyl]acrylamide; D6 represents monobutyl-terminated monomethacryloxypropyl-terminated polydimethylsiloxane (Gelest MW 600 to 800 g / mol);D9 represents monobutyl-terminated monomethacryloxypropyl polydimethylsiloxane (MW ~ 984 g / mol of Shin-Etsu); Betacon represents a dimethacrylate-terminated extended-chain polydimethylsiloxane (Mn ~ 5,000 g / mol), having two polydimethylsiloxane (PDMS) segments separated by a perfluoropolyether (PFPE) by means of diurethane linkages between the PDMS and PFPE segments and two urethane linkages, each located between a terminal methacrylate group and a PDMS segment, prepared according to a method similar to that described in Example B-1 of U.S. Patent No. 5760100; BDDA represents 1,4-butanediol diacrylate; NVP represents N-vinylpyrrolidone; DMA represents N,N-dimethylacrylamide; MMA represents methyl methacrylate; TEGDMA represents triethylene glycol dimethacrylate; EGDMA represents ethylene glycol methyl ether methacrylate; AMA represents allyl methacrylate; AIBN represents 2,2'-azobis(isobutyrontrilo);Vazo-64 represents 2,2'-dimethyl-2,2'-azodipropiononitrile; V88 represents 1,T-azobis(cyanocyclohexane) which has a half-life of 10 hours at a temperature of 88 °C; Norbloc is Aldrich's 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate; RB247 is reagent blue 247; TAA represents tert-amyl alcohol; PrOH represents 1-propanol; IPA represents isopropanol; PPG represents poly(propylene glycol); EGBE represents ethylene glycol butyl ether; PBS represents a phosphate-buffered saline solution having a pH of 7.2±0.2 at 25°C and containing approximately 0.044 wt% of NaH2PO4-H2O, approximately 0.388 wt% of Na2HPO4-2H2O and approximately 0.79 wt% of NaCl and wt% represents the weight percent; the H4 macromer represents a di-methacryloyloxypropyl terminated polysiloxane (Mn ~ 11.3K12.3K g / mol, OH content ~ 1.82-2.01 mequiv. / g) of Formula (A) shown below;The macromer H1 represents a di-methacryloyloxypropyl terminated polysiloxane (Mn ~ 8,000 g / mol, OH content ~ 1.8-2.0 mequiv. / g) of Formula (A) shown below.; L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ (TO) L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ Example 2 Polymerizable Composition Polymerizable compositions are prepared for the manufacture of inserts, just as the control lens formulation is prepared at room temperature in air, by mixing all the components (materials) in their desired quantities (parts by weight units) to obtain the composition shown in Tables 1-3. Table 1 polymerizable composition number ABC PEMA 57.5 57.5 57.5 D6 40 40 40 BDDA 3 5 10 AIBN 1 1 1 TOTALS 101.5 103.5 108.5 Dry Lens Peel Ability after 2 s of cold air treatment 2 s of cold air treatment IR 1.53 1.52 1.50 DK 113 107 108 Modulus (MPa) 2.4 5.8 22 Table 2 Polymerizable Composition No. DEFGH PEMA 57.5 57.5 57.5 57.5 57.5 Component 40 containing Si Tris-MA D6 D9 R11 Betacon BDDA 3 3 3 - AIBN 1 1 1 1 1 IR 1.50 1.50 1.50 1.50 1.50 DK 93 113 110 96 108 Modulus (MPa) 28 2.4 2.6 20.3 10 Table 3 Polymerizable Composition No. Formulation No. Monomer EF 57.5 GH aryl acrylic PEA PEMA BzA BzMA D6 40 40 40 D6 BDDA 3 3 3 3 AIBN 1 1 1 1 IR 1.50 1.53 1.50 1.54 Modulus (MPa) 0.6 Cast-molded inserts 2.4 1.8 30 L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ A polymerizable composition is purged with nitrogen at room temperature for 30 to 35 minutes. The N2-purged composition is then placed into polypropylene molds, which are sealed and placed in an oven. The oven is configured as follows: a nitrogen supply is connected to the oven via a high-capacity flow controller that can regulate the nitrogen flow rate through the oven; vacuum pumps are connected to the oven's exhaust line to control the oven's differential pressure. The polymerizable compositions in the molds are thermally cured in the oven under the following conditions: an increase from ambient temperature to 55 °C at a rate of approximately 7 °C / minute; a holding at 55 °C for approximately 30 minutes; an increase from 55 °C to 80 °C at a rate of approximately 7 °C / minute; a holding at 55 °C for approximately 30 minutes; an increase from 80 °C to 100 °C at a rate of approximately 7 °C / minute; and a holding at 100 °C for approximately 30 minutes. The molds are then opened and the molded inserts are removed. The inserts are then extracted and hydrated as follows. First, the inserts are extracted with PrOH for approximately 3 hours, immersed twice in deionized water for approximately 10 minutes, and then immersed in PBS for at least one hour before the assay. The test results and observations of the dry lens peelability are shown in Tables 1-3. The insert modules are also tested at various temperatures. The results are shown in Table 4. Table 4 Temperature Increase Storage Module of Inserts [MPa] Temperature [°C] ABC 15 124.0 42.3 186.0 20 65.3 36.8 85.1 25 31.8 22.5 50.0 30 11.3 10.7 45.8 35 4.7 5.3 22.3 37 2.7 4.2 16.6 Thickness (pm) 87 110 97 Tg (at maximum of tan δ)(°C) 31.6 21.0 / 35.2 28.7 / 41.9 L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ Example 3 Preparation of the inserts Polymerizable compositions (i.e., insert formulations) for the manufacture of rigid or soft hydrophobic inserts are prepared at room temperature in air by mixing all components (materials) in their desired quantities (parts by weight units) to obtain the composition shown below: Insertion formulation 1 (rigid): 62 parts by weight of PEMA; 27 parts by weight of D6; 10 parts by weight of BDDA; 1 part by weight of VAZO-64. Insertion formulation 2 (semi-rigid): 89 parts by weight units of BzA; 10 parts by weight units of BDDA; 1 part by weight unit of VAZO-64. Insertion formulation 3 (soft): 29 parts by weight units of Betacon; 17 parts by weight units of Tris-MA; 28 parts by weight units of DMA; 25 parts by weight units of EGBE and 0.5 parts by weight units of VAZO-64. A previously prepared polymerizable composition is purged with nitrogen at room temperature for 30 to 35 minutes. The N2-purged polymerizable composition is then placed into polypropylene molds, which are closed and placed in an oven. The oven is configured as follows: a nitrogen supply is connected to the oven via a high-capacity flow controller that can regulate the nitrogen flow rate through the oven; vacuum pumps are connected to the oven's exhaust line to control the oven's differential pressure. The polymerizable compositions in the molds are thermally cured in the oven under the following conditions: an increase from ambient temperature to 55°C at a rate of approximately 7°C / minute; a holding at 55°C for approximately 30–40 minutes; an increase from 55°C to 80°C at a rate of approximately 7°C / minute; a holding at 55°C for approximately 30–40 minutes; an increase from 80°C to 100°C at a rate of approximately 7°C / minute; and a holding at 100°C for approximately 30–40 minutes. The molds are then opened and the molded inserts are removed. Optionally, the inserts can be extracted and hydrated as follows. First, the inserts are extracted with ProOH for approximately 3 hours, immersed twice in deionized water for approximately 10 minutes, and then immersed in PBS for at least one hour before the assay. Extraction of the inserts has been found to be unnecessary. The properties of the insertions are indicated in Table 5. L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ Table 5 Insertion 1 Insertion 2 Insertion 3 Module (MPa) 22 8 0.9 IR 1.53 1.55 1.41 Preparation of embedded SiHy contact lenses Four SiHy lens formulations are prepared at room temperature in air by mixing all components (materials) in their desired quantities (parts by weight units) to obtain the composition shown below: SiHy 1 Lens Formulation: 40 parts by weight of CE-PDMS (Mn -10.5K Daltons); 28 parts by weight of TrisAm; 32 parts by weight of DMA; 5 parts by weight of PrOH; 0.5 parts by weight of VAZO-64. SiHy 2 Lens Formulation: 55 parts by weight of H1; 24 parts by weight of DMA; 25 parts by weight of EGBE; 1 part by weight of VAZO-64. SiHy 3 Lens Formulation: 57 parts by weight of H1; 22 parts by weight of DMA; 30 parts by weight of EGBE; 1 part by weight of VAZO-64. SiHy 4 Lens Formulation: 40 parts by weight of H1; 15 parts by weight of MMA; 20 parts by weight of DMA; 28 parts by weight of EGBE; 1 part by weight of VAZO-64. Cast-molded contact lenses are prepared as follows. A previously prepared insert is placed in the central region of the molding surface of a female mold half (made of polypropylene) that preferably has three or more points distributed in a circle with a diameter sufficient to accommodate the insert. To fix the position of the insert on the molding surface, a quantity of a previously prepared SiHy lens formulation is dispensed into the female mold half to immerse the insert. A male polypropylene mold half is then placed over the female mold half, and the mold is securely closed. The closed mold, containing an insert immersed in a SiHy lens formulation, is heat-cured in an oven under the following conditions: heating from room temperature to 55°C at a rate of approximately 7°C / minute; holding at 55°C for approximately 30–40 minutes; heating from 55°C to 80°C at a rate of approximately 7°C / minute; holding at 55°C for approximately 30–40 minutes; heating from 80°C to 100°C at a rate of approximately 7°C / minute; and holding at 100°C for approximately 30–40 minutes. The molds are then opened, and the molded inserts are removed. The lens molds, each containing a molded, unprocessed silicone hydrogel contact lens, are opened mechanically. The molded, unprocessed, embedded silicone hydrogel contact lens adheres to the male or female mold halves. The molded, unprocessed, embedded silicone hydrogel contact lenses adhered to the male mold halves are peeled off using an ultrasonic unit; the molded, unprocessed, embedded silicone hydrogel contact lenses adhered to the female mold halves are peeled off manually from the female mold halves attached to the lens. Unwound, raw embedded silicone hydrogel contact lenses can be extracted with a 50:50 mixture of propylene glycol and water. Preferably, unfolded, raw embedded silicone hydrogel contact lenses are subjected to the following extraction / hydration, coating, and autoclave sterilization processes, as described below. The raw embedded silicone hydrogel contact lenses are immersed in a bath containing deionized water or an aqueous solution of Tween 80 (500 PPM) for approximately 60 minutes, then in a bath containing an aqueous solution of polyacrylic acid (PAA, PM 450K) with a concentration of approximately 0.1% by weight at 40°C for approximately 120 minutes; then in a bath containing a PBS solution at room temperature for approximately 60 minutes; packaged / sealed in polypropylene lens packaging wraps (or blisters) (one lens per wrap) with 0.65 ml of a coating packaging saline solution in the package prepared according to the procedure described in Example 19 of US8480227; and finally, autoclaved for approximately 45 minutes at 121°C. The resulting embedded SiHy contact lenses each have a hydrogel coating and are examined for delamination according to the procedures described in Example 1. The results are reported in Table 6. L / CL ίη / ΖΖΠΖ / Ε / ΥΙΛΙ Table 6 Embedded SiHy contact lenses Formulation No. 1 1 1 4 4 4 3 2 SiHy lens Formulation No. 1 2 3 1 2 3 1 1 insertion Delamination Yes Yes Yes No No No No No All publications, patents, and patent application publications cited earlier in this application are incorporated herein in their entirety by reference.

Claims

1. An insert intended to be embedded in a silicone hydrogel contact lens, comprising a crosslinked polymeric material, comprising: (1) repeating units of said at least one polymerizable material containing silicone; (2) repeating units of at least one acrylic monomer; and (3) repeating units of at least one vinyl crosslinking agent, wherein the sum of the amounts of components (1) and (2) of the crosslinked polymer material is at least approximately 70% by weight of the total weight of the crosslinked polymer material, wherein the crosslinked polymer material in the dry state has a glass transition temperature greater than approximately 28°C, wherein the crosslinked polymer material in the fully hydrated state has a water content less than approximately 5% by weight, an oxygen permeability of at least approximately 60 Barrer and a refractive index of at least approximately 1.

45.

2. The insertion of claim 1, wherein said at least one aryl acrylic monomer is a vinyl monomer of Formula (I) or (II) L / CL ίΠ / ZZΖηZ / E / YΙΛΙ wherein Ai is H or CH3 (preferably H); B1 is (CH2)mi or [O(CH2)2]zi whereinm1 is 2-6 and z1 is 1-10; Y1 is a direct bond, O, S or NR' in which R' is H, CH3, Cn H2n+i in which n'=1-10, ¡S0-OC3H7, CeHs or CH2C6H5; Ra, Rb, Rc, Rd, Re, Rf, Rg, Rh and R¡ are independently of each other H, C1-C12 alkyl or C1-C12 alkoxy (preferably all H); w1 is 0-6, provided that m1+w1<8; w2 is an integer from 1 to 3; and Di is H, Cl, Br, C1-C4 alkyl, C1-C4 alkoxy, CeHs or CH2C6H5.

3. The insertion of claim 1 or 2, wherein said at least one vinyl crosslinking agent comprises ethylene glycol dimethacrylate; ethylene glycol diacrylate; 1,3-propanediol diacrylate; 1,3-propanediol dimethacrylate; 2,3-propanediol diacrylate; 2,3-propanediol dimethacrylate; 1,4-butanediol dimethacrylate; 1,4-butanediol diacrylate; 1,5-pentanediol dimethacrylate; 1,5-pentanediol diacrylate; 1,6-hexanediol dimethacrylate; 1,6-hexanediol diacrylate; diethylene glycol dimethacrylate; diethylene glycol diacrylate; triethylene glycol dimethacrylate;triethylene glycol diacrylate; tetraethylene glycol dimethacrylate; tetraethylene glycol diacrylate; allyl methacrylate; allyl acrylate; N,N'-methylene bis(methacrylamide); N,N'-ethylene bis(acrylamide); N,N'-ethylene bis(methacrylamide); N,N'-hexamethylene bis(methacrylamide); N,N'-hexamethylene bismethacrylamide; pentaerythritol triacrylate; pentaerythritol trimethacrylate; trimethyloylpropane triacrylate; trimethyloylpropane trimethacrylate; tris(2-hydroxyethyl)isocyanurate triacrylate; tris(2-h¡drox¡ethyl)¡soc¡anurate trimethacrylate; 1,3,5-triachlox¡lhexahidro-1,3,5-triazine; 1,3,5-tr¡metacr¡loxilhexahidro-1,3,5-triazine; pentaerythritol tetraacrylate; pentaerythritol tetramethacrylate; tetraacrylate of di(trimethyloylpropane); di(trimethylpropane) tetramethacrylate; an aryl crosslinking agent (for example, divinylbenceno, 2-methyl-1,4divinylbenceno, bis(4-vinylphenyl)methane, 1,2-bis(4-vinylphenyl)ethane, etc.) or combinations of the same.

4. Theinsertion of any one of claims 1 to 3, wherein said at least one polymerizable material containing silicone comprises a vinyl monomer having a bis(trialkylsilyloxy)alkylsilyl group, a vinyl monomer having a tris(trialkylsilyloxy)silyl group, a vinyl monomer of polysiloxane, 3-methacryloxypropylpentamethyldisiloxane, t-butyldimethylsiloxyethyl vinylcarbonate, trimethylsilylethyl vinylcarbonate and trimethylsilylmethyl vinylcarbonate or combinations thereof.

5. The insertion of any one of claims 1 to 3, wherein said at least one polymerizable material containing silicone comprises a vinyl monomer of Formula (M1) or (M2) Rmo or , ch3 x ch3 H2C=C—(o)--C-Xm0-Lm14-S¡-o)—Si--Rt1 (Mí) aM1 \CH3 / nlCH3 / ch3 Rm° or Vo S|-ch3 ) h2c=c—(o)---c-xM0-LM1-Si CH3 (M2) aMl \ ( Rt2)3_rl L / CL ίΠ / ZZΖηZ� / E / YΙΛΙ wherein: am is zero or 1; Rmo is H or methyl; Xmo is O or NRmi; Lmi is a divalent radical of _i ·_γ _।-(c2h4o)—¡-CONH-Lm1alkylene O2-O3 or a divalent radical of Lm1 Xm1 Lm1 -ÍC^O^Lm / '— -Lmi'-NHCOO-ÍC^O^Lmi- -CH2-CH(OH)CH2-Xm14c2H4o)^Lmí'— I '-Y '-OH -CHÍOH1TH -0-1 “(C2H4O)rT·CH2CH(OH)'CH2*OLm-| LM1 XM1 CH2 CH(OH) CH2 O Lm1 o 4 4 / vi · Lmi' is a divalent radical of C2-C8 alkylene having a hydroxyl group or none; Lmi is a divalent radical of Cs-Cs alkylene having a hydroxyl group or none; Xmi is O, NRmi, NHCOO, OCONH, CONRmi, or NRmiCO; Rmi is H or a C1-C4 alkyl having from 0 to 2 hydroxyl groups; Rti and Rt2 are independently of each other a C1-C2 alkyl; Xmi' is O or NR1; v1 is an integer from 1 to 30; m2 is an integer from 0 to 30; n1 is an integer from 3 to 40; and r1 is an integer from 2 or 3.

6. The insertion of any one of claims 1 to 5, wherein said at least one polymerizable silicone-containing material comprises at least one first polysiloxane vinyl crosslinker.

7. The insertion of claim 6, wherein said at least oneless a first polysiloxane vinyl crosslinker comprising: (1) a vinyl crosslinker comprising a single polydiorganosiloxane segment and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups, vinylcarbamate groups; and / or (2) a long-chain polysiloxane vinyl crosslinker comprising at least two polydiorganosiloxane segments and a covalent linker between each pair of polydiorganosiloxane segments and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamino groups, vinyl carbonate groups, and vinylcarbamate groups.

8. An embedded silicone hydrogel contact lens, comprising: a silicone hydrogel material; and an insertion of any one of claims 1 to 7 within the silicone hydrogel material, wherein the hydrogel material ofSilicone is a crosslinked material having a polymer matrix and comprising (a) repeating units of at least one second silicone-containing vinyl monomer and / or at least one second silicone-containing vinyl crosslinker and (b) repeating units of at least one hydrophilic vinyl monomer, wherein the fully hydrated, embedded silicone hydrogel contact lens has a water content of approximately 15% to approximately 70% by weight when fully hydrated.

9. The embedded silicone hydrogel contact lens of claim 8, wherein the silicone hydrogel material comprises repeating units of at least one silicone-containing vinyl monomer selected from the group consisting of a vinyl monomer having a bis(trialkylsilyloxy)alkylsilyl group, a vinyl monomer having a tris(trialkylsilyloxy)silyl group, a polysiloxane vinyl monomer,3-methacryloxypropylpentamethyldisiloxane, vinylcarbonate de f-butyldimethylsiloxyethyl, vinylcarbonate de trimethylsilylethyl and vinylcarbonate de trimethylsilylmethyl and combinations of the same.

10. La lente de contacto de hidrogel de silicona embebida de la reivindicación 8 o 9, en donde el material de hidrogel de silicona comprende unidades de repetición de al menos un monómero vinílico que contiene silicone de Fórmula (M1) o (M2) Rmo o , ch3 , ch3 H2c=c—(o)--C-XM0-LM1—fS¡-o]—Si--Rt1 (MI) \¿H3 / nl¿H3 ( ·Η3 \ Rmo O ^O-Si-CH3) h2c=c—(o)---C-XM0-LM1-S¡ CH3 (M2) aMl X \ CRt2)3-rl L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ in which: aMi es cero or 1; Rmo es H or methyl; Xmo es O o NRmi; Lmi is a divalent radical of alquilene C2-C8 or a divalent radical of -lmi -xmi—lmi - , -(c2H4O)-j-CONH LM1 -{c2H40)?rLM1— -LmY-NHCOO-ÍCzH^^Lm / '- -CH2-CH(OH)-CH2-Xm1'-(c2H4o)^-Lm1— i '-x '-ΓΉ -(ΉίΠΗνΓΗ -0-1 CH2“CH(OH)'CH2”O“Lmi LM1 rad¡ca|. divalent to the C2-C8 aquilene which holds ahydroxyl group or none; Lmi is a C3-C8 divalent alkylene radical having a hydroxyl group or none; Xmi is O, NRmi, NHCOO, OCONH, CONRmi or NRmiCO; Rmi is H or a C1-C4 alkyl having from O to 2 hydroxyl groups; Rn and Rt2 are independently of each other a Ci-Ce alkyl; Xmi' is O or NR1; v1 is an integer from 1 to 30; m2 is an integer from 0 to 30; n1 is an integer from 3 to 40; and r1 is an integer from 2 or 3.

11. The silicone hydrogel contact lens embedded in any one of claims 5 to 10, wherein the silicone hydrogel material comprises repeating units of at least one second polysiloxane vinyl crosslinker.

12. The embedded silicone hydrogel contact lens of claim 11, wherein said at least one second polysiloxane vinyl crosslinker comprises a vinyl crosslinker of Formula (IH) Rio O CH3, CH3 vi ri3 x CH3 or R|0 H2C=¿—C-XorRirSi-O-í-Si-oj-í-Si-ol—Si—R|2-XorC-C=CH2 (|||) CH3 ' CH3 / dACH3 / d2 ?H3 wherein: d1 is an integer from 30 to 500 and d2 is an integer from 1 to 75, provided that d2 / d1 is from approximately 0.035 to approximately 0.15 (preferably from approximately 0.040 to approximately 0.12, even more preferably from approximately 0.045 to approximately 0.10); X01 is O or NRin wherein Rin is hydrogen or C1-C10 alkyl; Rio is hydrogen or methyl; Rn and R12 are independently of each other a substituted or unsubstituted C1-C10 divalent alkylene radical or a divalent -R14-O-R15- radical wherein R14 and Ris are independently of each other a substituted or unsubstituted C1-C10 divalent alkylene radical; R13 is a monovalent radical of any one of the Formulas (Illa) a (lile) RI6 4CH2)sFr(°-CH2)—CG^-Xh-R^Oh)^ (Illa) OH ~(-CH2)^-XI2-R|84oh) (lllb) ' 'mj ' 'm4 ch2oh —^CH2 )gO-CH2-C-CH2OH (lllc) R|9 or Rno -(CH2^-O-<__VOH (|||d) R111 OH R|6 —(·ΟΗ2)--fo-CH2)—C-CH2-OH (Ule) ^ÓH k1 is zero or 1; m1 is an integer from 2 to 4; m2 isan integer from 1 to 5; m3 is an integer from 3 to 6; m4 is an integer from 2 to 5; R1 is hydrogen or methyl; R17 is a Ca-Ce hydrocarbon radical having valences (m2+1); Ris is a C2-C6 hydrocarbon radical having valences (m4+1); R19 is ethyl or hydroxymethyl; Rno is methyl or hydromethyl; R111 is hydroxyl or methoxy; Xn is an -S- sulfur bond or a -NRn2- tertiary amino bond wherein R112 is C1-C1 alkyl, hydroxyethyl, hydroxypropyl, or 2,3-dihydroxypropyl; and OO X12 is an amide linkage of -NRn3-c— 0 -C-NR|13- in θ| qUe ph3 is hydrogen or CiC10 alkyl.

13. The silicone hydrogel embedded contact lens of claim 11 or 12, wherein said at least a second polysiloxane vinyl crosslinker comprises: (1) a vinyl crosslinker comprising a single polydiorganosiloxane segment and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, groups(meth)acryloylamine, vinyl carbonate groups, vinylcarbamate groups; and / or (2) a long-chain polysiloxane vinyl crosslinker comprising at least two polydiorganosiloxane segments and a covalent linker between each pair of polydiorganosiloxane segments and two ethylenically unsaturated terminal groups selected from the group consisting of (meth)acryloyloxy groups, (meth)acryloylamine groups, vinyl carbonate groups, and vinylcarbamate groups.

14. The silicone hydrogel contact lens embedded in any one of claims 8 to 13, wherein said at least one hydrophilic vinyl monomer comprises: (1) an alkyl(meth)acrylamide selected from the group consisting of (meth)acrylamide, N,N-dimethyl(meth)acrylamide, N-ethyl(meth)acrylamide, N,N-diethyl(meth)acrylamide, N-propyl(meth)acrylamide, N-isopropyl(meth)acrylamide, N-3-methoxypropyl(meth)acrylamide and combinations thereof; (2) a hydroxyl-containing acrylic monomer selected from the group thatIt consists of N-2-hydroxyethyl(meth)acrylamide, N,Nbis(hydroxyethyl)(meth)acrylamide, N-3-hydroxypropyl(meth)acrylamide, N-2-hydroxypropyl(meth)acrylamide, N-2,3-dihydroxypropyl(meth)acrylamide, A / -tris(hydroxymethyl)methyl(meth)acrylamide, 2-hydroxyethyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, glycerol methacrylate (GMA), di(ethylene glycol)methacrylate, tri(ethylene glycol)methacrylate, tetra(ethylene glycol)methacrylate, poly(ethylene glycol)methacrylate, which has a number-average molecular weight of up to 1,500, (3) poly(ethylene glycol) ethyl(meth)acrylamide having a number-average molecular weight of up to 1,500 and combinations thereof; (4) an acrylic monomer containing carboxyl selected from the group consisting of 2-(meth)acrylamidoglycolic acid, (meth)acrylic acid, ethylacrylic acid, 3-(meth)acrylamidopropionic acid, 5-(meth)acrylamidopentanoic acid, 4-(meth)acrylamidobutanoic acid,3(meth)acrylamido-2-methylbutanoic acid, 3-(meth)acrylamido-3-methylbutanoic acid, 2-(meth)acrylamido-2-methyl-3,3-dimethylbutanoic acid, 3-(meth)acrylamidohexanoic acid, 4-(meth)acrylamido-3,3-dimethylhexanoic acid and combinations thereof; (4) an amino-containing acrylic monomer selected from the group consisting of N-2-aminoethyl(meth)acrylamide, N-2-methylaminoethyl(meth)acrylamide, N-2-ethylaminoethyl(meth)acrylamide, N-2-dimethylaminoethyl(meth)acrylamide, N-3-aminopropyl(meth)acrylamide, N-3-methylaminopropyl(meth)acrylamide, N-3-dimethylaminopropyl(meth)acrylamide, 2-aminoethyl (meth)acrylate, 2-methylaminoethyl (meth)acrylate, 2-ethylaminoethyl (meth)acrylate, 3-aminopropyl (meth)acrylate, 3-methylaminopropyl (meth)acrylate, 3-ethylaminopropyl (meth)acrylate, (meth)acrylate of 3-amino-2-hydroxypropyl, trimethylammonium (meth)acrylate hydrochloride, dimethylaminoethyl (meth)acrylate and combinations thereof; (5) a monomer ofN-vinylamide selected from the group consisting of N-vinylpyrrolidone (also known as N-vinyl-2-pyrrolidone), N-vinyl-3-methyl-2-pyrrolidone, N-vinyl-4-methyl-2-pyrrolidone, N-vinyl-5-methyl-2-pyrrolidone, N-vinyl-6-methyl-2-pyrrolidone, N-vinyl-3-ethyl-2-pyrrolidone, N-vinyl-4,5-dimethyl-2-pyrrolidone, N-vinyl-5,5-dimethyl-2-pyrrolidone, N-vinyl-3,3,5-trimethyl-2-pyrrolidone, N-vinylpiperidone (also known as N-vinyl-2-piperidone), N-vinyl-3-methyl-2-piperidone, N-vinyl-4-methyl-2-piperidone, N-vinyl-5-methyl-2-piperidone, N-vinyl-6-methyl-2-piperidone, N-vinyl-6-ethyl-2-piperidone, N-vinyl-3,5-dimethyl-2-piperidone, N-vinyl-4,4-dimethyl-2-piperidone, N-vinylcaprolactam (also known as N-vinyl-2-caprolactam), N-vinyl-3-methyl-2-caprolactam, N-vinyl-4-methyl-2-caprolactam, N-vinyl-7-methyl-2-caprolactam, N-vinyl-7-ethyl-2-caprolactam, N-vinyl-3,5-dimethyl-2-caprolactam, N-vinyl-4,6dimethyl-2-caprolactam, N-vinyl-3,5,7-trimethyl-2-caprolactam, N-vinyl-N-methylacetamide,N-vinylformamide, N-vinylacetamide, N-vinylisopropylamide, N-vinyl-N-ethylacetamide, N-vinyl-N-ethylformamide and mixtures thereof; (6) a methylene-containing pyrrolidone monomer selected from the group consisting of 1-methyl-3-methylene-2-pyrrolidone, 1-ethyl-3-methylene-2-pyrrolidone, 1-methyl-5-methylene-2-pyrrolidone, 1-ethyl-5-methylene-2-pyrrolidone, 5-methyl-3-methylene-2-pyrrolidone, 5-ethyl-3-methylene-2-pyrrolidone, 1-n-propyl-3-methylene-2-pyrrolidone, 1-n-propyl-5-methylene-2-pyrrolidone, 1-isopropyl-3-methylene-2-pyrrolidone, 1-isopropyl-5-methylene-2-pyrrolidone, 1-n-butyl-3-methylene-2-pyrrolidone, 1-tert-butyl-3-methylene-2-pyrrolidone and combinations thereof; (7) an acrylic monomer having a C1-C4 alkoxyethoxy group and selected from the group consisting of ethylene glycol (meth)-methyl ether, di(ethylene glycol)-methyl ether, tri(ethylene glycol)-methyl ether, tetra(ethylene glycol)-methyl ether, alkoxy (meth)-methyl ether(8) a vinyl ether monomer selected from the group consisting of ethylene glycol monovinyl ether, di(ethylene glycol) monovinyl ether, tri(ethylene glycol) monovinyl ether, tetra(ethylene glycol) monovinyl ether, poly(ethylene glycol) monovinyl ether, ethylene glycol methyl vinyl ether, di(ethylene glycol) methyl vinyl ether, tri(ethylene glycol) methyl vinyl ether, tetra(ethylene glycol) methyl vinyl ether, poly(ethylene glycol) methyl vinyl ether, and combinations thereof; (9) an allyl ether monomer selected from the group consisting of ethylene glycol monoallyl ether, di(ethylene glycol) monoallyl ether, tri(ethylene glycol) monoallyl ether, tetra(ethylene glycol) monoallyl ether, poly(ethylene glycol) monoallyl ether, ethylene glycol methylallyl ether, methylallyl ether ofdi(ethylene glycol), tri(ethylene glycol) methylallyl ether, tetra(ethylene glycol) methylallyl ether, poly(ethylene glycol) methylallyl ether and combinations thereof; (10) a vinyl monomer containing phosphorylcholine selected from the group consisting of (meth)acryloyloxyethylphosphorylcholine, (meth)acryloyloxypropylphosphorylcholine, 4-((meth)acryloyloxy)butyl-2'-(trimethylammonium)ethyl phosphate, 2-[(meth)acryloylamino]ethyl-2'-(trimethylammonium)-ethyl phosphate, 3-[(meth)acryloylamino]propyl-2'-(trimethylammonium)-ethyl phosphate, 4-[(meth)acryloylamino]butyl-2'-(trimethylammonium)-ethyl phosphate, 5-((meth)acryloyloxy)pentyl-2'-(trimethylammonium)ethyl phosphate, 6-((meth)acryloyloxy)hexyl-2'-(trimethylammonium)-ethyl phosphate, 2-((meth)acryloyloxy)ethyl-2'-(triethylammonium)ethylphosphate, 2-((meth)acryloyloxy)ethyl-2'(tripropylammonium)ethylphosphate, 2-((meth)acryloyloxy)ethyl-2'-(tributylammonium)ethylphosphate, 2-((meth)acryloyloxy)propyl-2'(trimethylammonium)-ethylphosphate, 2-((meth)acryloyloxy)butyl-2'-(trimethylammonium)ethylphosphate,2-((meth)acryloyloxy)pentyl-2'(trimethylammonio)ethylphosphate, 2-((meth)acryloyloxy)hexyl-2'-(trimethylammonium)ethylphosphate, 2-(vinyloxy)ethyl-2' L / CL ίΠ / ΖΖηΖ / Ε / ΥΙΛΙ (trimethylammonium)ethylphosphate, 2-(allyloxy)ethyl-2'-(trimethylammonium)ethylphosphate, 2-(vinyloxycarbon¡l)ethyl-2'(trimethylammonium)ethylphosphate, 2-(allyloxycarbonyl)ethyl-2'-(trimethylammonium)-ethylphosphate, 2-(vinylcarbonylamno)ethyl-2'(trimethyllammonium)ethylphosphate, 2-(allyloxycarbonylamino)ethyl-2'-(trimethylammonium)ethylphosphate, 2-(butenoyloxy)ethyl-2'-(trimethylammonium)ethylphosphate and combinations thereof; (11) allyl alcohol; (12) N-2-hydroxyethyl vinylcarbamate; (13) N-carboxyvinyl-p-alanine (VINAL); (14) N-carboxyvinyl-a-alanine; (15) or combinations thereof.

15. The silicone hydrogel contact lens embedded with any one of claims 8 to 14, wherein the silicone hydrogel material comprises repeating units of at least one non-silicone vinyl crosslinking agent.

16. The hydrogel contact lensde siliconea embebida de la reivindicación 15, en donde dicho al menos un agente de reticulación vinílico no de silicone comprende di-(met)acrilato de ethyleneglicol, di-(met)acrilato de diethyleneglicol, di-(met)acrilato de triethyleneglicol, di-(met)acrilato de tetraethyleneglicol, di(met)acrilato de glicerol, di-(met)acrilato de 1,3-propanodiol, di-(met)acrilato de 1,3-butanodiol, d¡(met)acrilato de 1,4-butanodiol, di-(met)acrilato de 1,3-diglicerolato de glicerol, di-(met)acrilato de etilenobis[ox¡(2-hidroxipropano-1,3-diilo)], fosfato de bis[2-(meth)acrylox¡et¡lo], di-(meth)acrylate of trimethylolpropane and 3,4-bis[(meth)acrylo¡l]tetrahydrofuran, diacrylamida, dimethacrylam¡na, N,N-di(meth)acrylo¡lN-methylamine, N,Nd¡(meth)acryloyl-N-ethylam¡na, N,N'-met¡lenob¡s(met)acrylam¡da, N,N'ethylenob¡s(met)acr¡lamida, N,N'-dih¡droxiet¡lenob¡s(met)acr¡lamida, N,N'-propylenobis(meth)acrylamida, N,N'2-hidrox¡prop¡lenobis(met)acr¡lam¡da, N,N'-2,3-dih¡drox¡butylenob¡s(met)acr¡lam¡da, dihydrogen phosphate de1,3-bis(meth)acrylamidopropane-2-yl, piperazinediacrylamide, tetraethylene glycol divinyl ether, triethylene glycol divinyl ether, diethylene glycol divinyl ether, ethylene glycol divinyl ether, trialyl isocyanurate, trialyl cyanurate, trimethylpropane trimethacrylate, pentaerythritol tetramethacrylate, bisphenol A dimethacrylate, allyl methacrylate, allyl acrylate, N-allyl methacrylamide, N-allyl acrylamide, or combinations thereof.

17. The silicone hydrogel contact lens embedded with any one of claims 8 to 16, wherein the silicone hydrogel material comprises repeating units of at least one blending vinyl monomer.

18. The silicone hydrogel-embedded contact lens of claim 17, wherein said at least one vinyl blending monomer comprises C1-C10 alkyl (meth)acrylate, cyclopentyl acrylate, cyclohexyl methacrylate, cyclohexyl acrylate, isobornyl (meth)acrylate, styrene, 4,6-trimethylstyrene (TMS),f-butylstyrene (TBS), trifluoroethyl (meth)acrylate, hexafluoroisopropyl (meth)acrylate, hexafluorobutyl (meth)acrylate or combinations thereof.