Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
  • C07F7/02—Silicon compounds
  • C07F7/08—Compounds having one or more C—Si linkages
  • C07F7/0834—Compounds having one or more O-Si linkage
  • C07F7/0838—Compounds with one or more Si-O-Si sequences
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
  • G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
  • G02B1/041—Lenses
  • G02B1/043—Contact lenses
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
  • A61L27/14—Macromolecular materials
  • A61L27/18—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
  • A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
  • A61L27/52—Hydrogels or hydrocolloids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
  • C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
  • C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
  • C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
  • C08F290/068—Polysiloxanes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L2430/00—Materials or treatment for tissue regeneration
  • A61L2430/16—Materials or treatment for tissue regeneration for reconstruction of eye parts, e.g. intraocular lens, cornea

Definitions

• the present invention relates to materials useful in the manufacture of biocompatible medical devices. More particularly, the present invention relates to elastomeric, expandable hydrogel compositions, which are soft and foldable both in the unhydrated and hydrated states, useful in the manufacture of ophthalmic devices.
• intraocular lens lOL
• an intraocular lens is implanted within an eye at the time of surgically removing the diseased or damaged natural lens, such as, for example, in the case of cataracts.
• the preferred material for fabricating such intraocular lens implants was poly(methyl methacrylate), which is a rigid, glassy polymer.
• Softer, more flexible IOL implants have gained in popularity in more recent years due to their ability to be compressed, folded, rolled or otherwise deformed. Such softer IOL implants may be deformed prior to insertion thereof through an incision in the cornea of an eye. Following insertion of the IOL in an eye, the IOL returns to its original pre-deformed shape due to the memory characteristics of the soft material. Softer, more flexible IOL implants as just described may be implanted into an eye through an incision that is much smaller, i.e., less than 4.0 mm, than that necessary for more rigid lOLs, i.e., 5.5 to 7.0 mm.
• a larger incision is necessary for more rigid IOL implants because the lens must be inserted through an incision in the cornea slightly larger than the diameter of the inflexible IOL optic portion. Accordingly, more rigid IOL implants have become less popular in the market because larger incisions have been found to be associated with an increased incidence of postoperative complications, such as induced astigmatism.
• hydrophilic acrylics In general, high water content hydrophilic acrylics, or "hydrogels,” have relatively low refractive indices, making them less desirable than other materials with respect to minimal incision size. Low refractive index materials require a thicker IOL optic portion to achieve a given refractive power. Silicone materials may have a higher refractive index than high-water content hydrogels, but tend to unfold explosively after being placed in the eye in a folded position. Explosive unfolding can potentially damage the corneal endothelium and/or rupture the natural lens capsule and associated zonules. Low glass transition temperature hydrophobic acrylic materials are desirable because they typically have a high refractive index and unfold more slowly and more controllably than silicone materials.
• Soft, foldable, high refractive index, elastomeric, expandable hydrogel compositions of the present invention are produced through the polymerization or copolymerization of one or more fluoro side-chain methacrylate end-capped silicone monomers with varying concentrations of a hydrophilic monomer.
• the subject silicone monomers are synthesized through a multi-step reaction scheme.
• the hydrogel compositions produced from the fluoro side-chain methacrylate end-capped silicone monomers and hydrophilic monomers have ideal physical properties for the manufacture of ophthalmic devices including a reduced friction "TeflonTM-like" (E. I. DuPont de Nemours and Company, Wilmington, Delaware) surface in the dry state.
• the hydrogel compositions of the present invention are likewise transparent, of relatively high strength for durability during surgical manipulations, of relatively high elongation, of relatively high refractive index and are biocompatible.
• the subject hydrogel compositions are particularly well suited for use as intraocular lens (lOLs) implants because the presence of fluoro groups in the material prevents self adherence when the IOL is folded for implantation.
• the subject hydrogel compositions are likewise well suited for use as contact lenses, keratoprostheses, corneal rings, corneal inlays and the like.
• Preferred fluoro side-chain methacrylate end-capped silicone monomers for use in preparing the hydrogel compositions of present invention have the generalized structure represented by Formula 1 below,
• R is selected from the group consisting of hydrogen and fluorine; R 1 is an activated unsaturated polymerizable group; x is an integer less than 51 ; y is an integer less than 101 ; z is an integer less than 21 ; and q is an integer less than 11. Accordingly, it is an object of the present invention to provide transparent, hydrogel compositions having desirable physical characteristics for the manufacture of ophthalmic devices.
• Another object of the present invention is to provide hydrogel compositions of relatively high refractive index.
• Another object of the present invention is to provide hydrogel compositions suitable for use in the manufacture of intraocular lens implants.
• Another object of the present invention is to provide hydrogel compositions that are biocompatible.
• Another object of the present invention is to provide hydrogel compositions suitable for use as contact lens materials.
• Still another object of the present invention is to provide hydrogel compositions that are economical to produce.
• the present invention relates to novel fluoro side-chain methacrylate end- capped silicone monomers synthesized through a multi-step reaction scheme.
• the subject fluoro side-chain methacrylate end-capped silicone monomers are useful in the production of biocompatible hydrogel compositions.
• the subject hydrogel compositions have particularly desirable physical properties.
• the subject hydrogel compositions have a relatively high refractive index of approximately 1.35 or greater in the hydrated state and a
• the fluoro side-chain methacrylate end-capped silicone monomers of the present invention are generally represented by Formula 1 below:
• R is selected from the group consisting of hydrogen and fluorine; Ri is an activated unsaturated polymerizable group selected from the group consisting of methacrylates, methacrylamides, vinyl carbamates and maleonates; x is an integer less than 51 ; y is an integer less than 101 ; z is an integer less than 21 ; and q is an integer less than 11.
• monomers of the present invention include for example but are not limited to methacrylate end-capped polymethylsiloxanes containing varying mole percentages of trifluoropropyl, 3-(2,2,3,3-tetrafluoropropoxy)propyl, 3- (2,2,3,3,4,4,5,5-octafluoropentoxy)propyl and 3-i2,2,3,3,4A,5,5 ⁇ ,6,7 - dodecafluorotridecoxy)propyl side-chains.
• Fluoro side-chain methacrylate end-capped silicone monomers of the present invention may be synthesized through a multi-step ring opening/hydrosilation reaction scheme as represented in Scheme 1 below:
• One or more fluoro side-chain methacrylate end-capped silicone monomers of the present invention produced as described above is preferably copolymerized with one or more hydrophilic monomers in accordance with the present invention to produce a hydrogel composition useful in the manufacture of ophthalmic medical devices.
• hydrophilic monomers useful for copolymerization with one or more fluoro side-chain methacrylate end-capped silicone monomers of the present invention include for example but are not limited to N,N- dimethylacrylamide, acrylamide, acrylic acic, 2-hydroxyethyl methacrylate, glyceryl methacrylate, N-vinylpyrrolidone, diacetone acrylamide, 2-acrylamido-2- methylpropanesulfonic acid and its salts, 2-(meth)acryloyloxyethylsulfonic acid and its salts, 3-(meth)acryloyloxypropylsulfonic acid and its salts, styrenesulfonic acid and its salts, carboxystyrene and its salts, 3-(meth)acrylamidopropyl-N,N- dimethylamine and its salts, 2-(meth)acryloylethyl-N,N-dimethylamine and its salts and methacrylic acid
• High water content hydrogel compositions of 15 percent or higher water content by volume, of the present invention having ideal physical characteristics for use in the manufacture of ophthalmic devices are described herein.
• one or more fluoro side-chain methacrylate end-capped silicone monomers of the present invention are copolymerized with one or more hydrophilic monomers to form crosslinked three-dimensional networks.
• one or more crosslinking agents may be added in quantities less than 10 percent weight per volume (WA ) to the fluoro side-chain methacrylate end-capped silicone monomer(s), if desired, prior to copolymerization thereof.
• crosslinking agents include but are not limited to diacrylates and dimethacrylates of tetraethylene glycol, triethylene glycol, butylene glycol, neopentyl glycol, hexane-1 ,6-diol, thio-diethylene glycol and ethylene glycol, poly(ethylene glycol), trimethylolpropane triacrylate, N,N'- dihydroxyethylene bisacrylamide, diallyl phthalate, triallyl cyanurate, divinylbenzene; ethylene glycol divinyl ether, N,N'-methylene-bis- (meth)acrylamide, divinylbenzene and divinylsulfone.
• fluoro side-chain methacrylate end-capped silicone monomers within the scope of the present invention may optionally have one or more strengthening agents added thereto prior to copolymerization thereof, preferably in quantities of less than about 80 weight percent but more typically from about 20 to about 60 weight percent.
• suitable strengthening agents are described in U.S. Patent Nos. 4,327,203, 4,355,147 and 5,270,418, each incorporated herein in its entirety by reference. Specific examples, not intended to be limiting, of such strengthening agents include cycloalkyl acrylates and methacrylates, such as for example tert-butylcyclohexyl methacrylate and isopropylcyclopentyl acrylate.
• One or more ultraviolet light absorbers may optionally be added to the subject fluoro side-chain methacrylate end-capped silicone monomers prior to copolymerization thereof in quantities typically less than 2 percent W ⁇ Suitable ultraviolet light absorbers for use in the present invention include for
• ⁇ -(4-benzotriazoyl-3-hydroxyphenoxy)ethyl acrylate is the preferred ultraviolet light absorber.
• the fluoro side-chain methacrylate end-capped silicone monomers of the present invention may be readily cured in cast shapes, as discussed in more detail below, by one or more conventional methods. Such methods include for example but are not limited to ultraviolet light polymerization, visible light polymerization, microwave polymerization, thermal polymerization, free radical thermal polymerization or combinations thereof.
• One or more suitable free radical thermal polymerization initiators may be added to the monomers of the present invention.
• suitable free radical thermal polymerization initiators include for example but are not limited to organic peroxides, such as acetyl peroxide, lauroyl peroxide, decanoyl peroxide, stearoyl peroxide, benzoyl peroxide, tert-butyl peroxypivalate, peroxydicarbonate, and the like.
• organic peroxides such as acetyl peroxide, lauroyl peroxide, decanoyl peroxide, stearoyl peroxide, benzoyl peroxide, tert-butyl peroxypivalate, peroxydicarbonate, and the like.
• an initiator is employed in a concentration of approximately 0.01 to 1 percent by weight of the total monomer mixture.
• Representative ultraviolet light initiators include those known in the field such as for example but not limited to benzoin methyl ether, benzoin ethyl ether, DarocurTM 1173, 1164, 2273, 1116, 2959, 3331 (EM Industries) and IrgacurTM 651 and 184 (Ciba-Geigy, Basel, Switzerland).
• the hydrogel compositions of the present invention are of relatively high refractive index and relatively high expansion.
• the hydrogel compositions of the present invention with the desirable physical properties noted above are particularly useful in the manufacture of ophthalmic devices such as but not limited to relatively thin, foldable intraocular lens implants, contact lenses and corneal inlays.
• lOLs having relatively thin optic portions are critical in enabling a surgeon to minimize surgical incision size. Keeping the surgical incision size to a minimum reduces intraoperative trauma and postoperative complications.
• a relatively thin IOL optic portion is also critical for accommodating certain anatomical locations in the eye such as the anterior chamber and the ciliary sulcus.
• lOLs may be placed in the anterior chamber for increasing visual acuity in either aphakic or phakic eyes, or placed in the ciliary sulcus for increasing visual acuity in phakic eyes.
• the hydrogel compositions of the present invention are particularly well suited for the manufacture of intraocular lenses due to the same remaining soft and flexible with a reduced friction surface in an unhydrated state. Intraocular lenses manufactured from the subject hydrogel compositions are ideally suited for small incision cataract surgery.
• the hydrogel compositions of the present invention have the flexibility required to allow implants manufactured from the same to be folded or deformed in the unhydrated state for insertion into an eye through the smallest possible surgical incision, i.e., 3.0 mm or smaller. It is unexpected that the subject hydrogel compositions could possess the ideal physical properties described herein.
• the physical properties of the subject polymeric compositions are ideal because lenses made therefrom do not adhere when rolled or folded as would be done for purposes of implantation within an eye, unlike non-fluorinated siloxanes, and possesses excellent recovery characteristics. Also, the surface of reduced friction characteristics aids in surgical implantation when using a cartridge inserter or similar surgical device.
• Ophthalmic devices such as but not limited to lOLs manufactured using the hydrogel compositions of the present invention can be of any design capable of being rolled or folded for implantation through a relatively small surgical incision, i.e., 3.0 mm or less.
• ophthalmic devices such as lOLs typically comprise an optic portion and one or more haptic portions.
• the optic portion reflects light onto the retina and the permanently attached haptic portions hold the optic portion in proper alignment within an eye.
• the haptic portions may be integrally formed with the optic portion in a one-piece design or attached by staking, adhesives or other methods known to those skilled in the art in a multipiece design.
• the subject ophthalmic devices such as for example lOLs, may be manufactured to have an optic portion and haptic portions made of the same or differing materials.
• both the optic portion and the haptic portions of the lOLs are made of one or more hydrogel compositions of the present invention.
• the IOL optic portion and haptic portions may be manufactured from differing materials and/or differing hydrogel compositions of the present invention, such as described in U.S. Patent Numbers 5, 217,491 and 5,326,506, each incorporated herein in its entirety by reference.
• the disks are lathed or machined into lOLs at low temperatures below the glass transition temperature(s) of the material(s).
• the lOLs, whether molded or machined/lathed, are then cleaned, polished, packaged and sterilized by customary methods known to those skilled in the art.
• the hydrogel compositions of the present invention are also suitable for use in the manufacture of other ophthalmic devices such as but not limited to contact lenses, keratoprostheses, capsular bag extension rings, corneal inlays, corneal rings or like devices.
• lOLs manufactured using the unique hydrogel compositions of the present invention are used as customary in the field of ophthalmology. For example, in a surgical procedure, an incision is placed in the cornea of an eye. Most commonly, through the corneal incision the natural lens of the eye is removed (aphakic application) such as in the case of a cataractous natural lens. An IOL is then inserted into the anterior chamber, posterior chamber or lens capsule of the eye prior to closing the incision.
• the subject ophthalmic devices may be used in accordance with other surgical procedures known to those skilled in the field of ophthalmology.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Polymers & Plastics (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Dermatology (AREA)
• Physics & Mathematics (AREA)
• Transplantation (AREA)
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• Public Health (AREA)
• Veterinary Medicine (AREA)
• Dispersion Chemistry (AREA)
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• Optics & Photonics (AREA)
• Materials For Medical Uses (AREA)
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• Macromonomer-Based Addition Polymer (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

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• 2002
  • 2002-09-18 US US10/246,242 patent/US20040054026A1/en not_active Abandoned
• 2003
  • 2003-09-10 EP EP03797898A patent/EP1546225A1/en not_active Withdrawn
  • 2003-09-10 CA CA002499504A patent/CA2499504A1/en not_active Abandoned
  • 2003-09-10 JP JP2004537764A patent/JP2005539128A/ja active Pending
  • 2003-09-10 AU AU2003266026A patent/AU2003266026A1/en not_active Abandoned
  • 2003-09-10 CN CNA038221853A patent/CN1681862A/zh active Pending
  • 2003-09-10 WO PCT/US2003/028442 patent/WO2004026928A1/en not_active Ceased
  • 2003-09-17 TW TW092125635A patent/TWI258488B/zh not_active IP Right Cessation
  • 2003-09-18 AR ARP030103379A patent/AR041294A1/es not_active Application Discontinuation
• 2005
  • 2005-03-17 KR KR1020057004547A patent/KR20050057384A/ko not_active Withdrawn

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