EP1817627A1 - Methods for reducing corneal staining in contact lens wearers - Google Patents

Methods for reducing corneal staining in contact lens wearers

Info

Publication number
EP1817627A1
EP1817627A1 EP04810854A EP04810854A EP1817627A1 EP 1817627 A1 EP1817627 A1 EP 1817627A1 EP 04810854 A EP04810854 A EP 04810854A EP 04810854 A EP04810854 A EP 04810854A EP 1817627 A1 EP1817627 A1 EP 1817627A1
Authority
EP
European Patent Office
Prior art keywords
lens
lenses
methods
silicone
curves
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP04810854A
Other languages
German (de)
English (en)
French (fr)
Inventor
Philippe F. Jubin
Sheila B. Hickson-Curran
Susan W. Neadle
William F. Jones
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Johnson and Johnson Vision Care Inc
Original Assignee
Johnson and Johnson Vision Care Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Johnson and Johnson Vision Care Inc filed Critical Johnson and Johnson Vision Care Inc
Publication of EP1817627A1 publication Critical patent/EP1817627A1/en
Ceased legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02CSPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C7/00Optical parts
    • G02C7/02Lenses; Lens systems ; Methods of designing lenses
    • G02C7/04Contact lenses for the eyes
    • GPHYSICS
    • G02OPTICS
    • G02CSPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
    • G02C7/00Optical parts
    • G02C7/02Lenses; Lens systems ; Methods of designing lenses
    • G02C7/04Contact lenses for the eyes
    • G02C7/048Means for stabilising the orientation of lenses in the eye

Definitions

  • the invention relates to contact lenses.
  • the invention provides lenses in which the occurrence of corneal staining in the lens wearer is reduced.
  • contact lenses for the correction of visual acuity, for cosmetic purposes, or both is well known.
  • Soft contact lenses which lenses generally are manufactured from materials including, without limitation, hydragels and silicone hydrogels.
  • a portion of the soft contact lens overlies the wearer's cornea.
  • Corneal cell damage that is observable by corneal staining, or upon instillation of a diagnostic dye onto the corneal surface, may occur in soft contact lens wearers.
  • stainingT sulting from mechanical chaffing of the lens on the cornea.
  • Such staining is considered a precursor to corneal tissue splitting.
  • Such damage has been observed in wear-er's of lathe cut lenses, lenses made from materials having a Young's modulus of 40 psi or greater, lenses with a single back surface curve, and lenses in which the center thickness, the peripheral thickness profile, or cross-sectional thickness, or both is greater than about 0.1 mm.
  • corneal cell damage has been observed in wearer's of lenses having certain geometries on their front or back surfaces.
  • Particularly problematic geometries are those in which junctions between zones on the front or back surface of the lens creates surface discontinuities in the mid-peripheral area of the lens.
  • mid-peripheral area is meant the non-optical area, outside of the optical zone, between the lens' geometric center and the lens edge, which area overlies the cornea when the lens is on-eye.
  • this area will have a radius of between about 3.5 and 6.5 mm from the lens' geometric center.
  • corneal cell damage can result from lenses having areas over which the thickness profile is non-constant.
  • Corneal staining due to mechanical chaffing is most commonly found in the superior region of the cornea, or the area of the cornea above the pupil, and in the inferior region, or region below the pupil. Thus, the cell damage is most likely to appear in the areas of the cornea that underlie the upper or lower eyelid.
  • the incidence of corneal staining varies from lens to lens based on the material and design of the lens, but can be as high as 50 % of lens wearers. Therefore, a need exists for lens designs in which the incidence of corneal staining is reduced or eliminated.
  • Figure 1 is a magnified, cross-sectional view of a lens of the invention.
  • Figure 2 is a magnified plan view of the front surface of the lens of Figure 1.
  • the invention provides methods, and lenses produced by such methods, for reducing the incidence of corneal staining in lens wearers. It is believed that corneal staining resulting from mechanical chaffing is most frequently the result of peak pressure on the cornea, meaning that an area of the cornea experiences a higher force imposed by an area of the lens, relative to the adjacent areas of the cornea. Most frequently, these areas of peak pressure occur under the lens wearer's eyelids. Such peak pressure is the result of one or more of the lens' thickness profiles, or cross-sectional thickness, material modulus, and junctions between the zones on the lens' surfaces.
  • the invention provides a contact lens comprising, consisting essentially of, or consisting of at least one surface comprising a design wherein a peak pressure is reduced.
  • One lens design of the invention provides an iso-thickness vertical profile.
  • iso-thickness vertical profile is meant that the radial thickness of the lens' mid- peripheral area as measured between the front and back lens surfaces and along a direction orthogonal to the back surface, is distributed evenly along any meridian within 45 degrees of the vertical meridian (the 90-270 degree axis) of the lens.
  • the iso-thickness vertical profile creates an area around the vertical meridian of the lens in which the cross-sectional thickness of the lens' mid-peripheral area is constant.
  • Figure 1 depicts lens 10 embodying this design. Mid-peripheral areas 11 are shown at the superior (top) and inferior (bottom) portions of the lens in which areas iso-thickness vertical profiles are used.
  • Figure 2 depicts a plan view of the lens showing the superior-lying area 11.
  • the iso-thickness vertical profile may be achieved by offsetting the back surface periphery with the front surface periphery to form the desired profile.
  • Such a profile may be obtained by any number of design methods including, without limitation, incorporating off-axis bevel curves or using multiple peripheral zones. Additionally, the design methods of United States Patent No. 6,595,640 may be used, which patent is incorporated herein in its entirety.
  • the junctions between the various zones on one or both of the lens' surfaces may be smoothed so as to eliminate slope discontinuities on the back surface. More specifically, in this embodiment the junction between curves -on the back surface are such that the first order derivatives, i.e., the slopes of the curves at the junction, are equal. Any number of methods maybe used to obtain the smoothed junctions including, without limitation, blending two consecutive zones using conventional mathematical techniques.
  • the lenses of the invention preferably are rotationally stabilized to maintain their on-eye orientation.
  • Suitable rotational stabilization includes prism stabilization including, without limitation, decentering of the lens' front surface relative to the back surface, prismatic balancing, thickening of the lower lens edge, supporting the lens on the lower eyelid, forming depressions or elevations on the lens' surface away from the 90 degree meridian, and truncating the lens edge.
  • the lens maybe dynamically stabilized.
  • Dynamic stabilization includes reducing the thickness of the lens' outer surface at two symmetrically lying regions, thickening two regions in the horizontal center axis, and thinning, or slabbing off, top and bottom zones on the lens.
  • the areas of stabilization are located in the lens' periphery meaning the non-optical portion of the lens surrounding the optic zone, but excluding the lens edge or outermost portion of the lens relative to the geometric center.
  • the invention may be used in designing single vision, multifocal and toric lenses. Additionally, the invention may be used in designing lenses made from any suitable contact lens material. However, the invention may have its greatest utility in lenses that are either or boht rotationally stabilized by use of areas of different thicknesses in the lens' periphery and lenses made from high modulus material, or materials having a Young's modulus of about 40 psi, preferably about 60 psi, or greater.
  • Exemplary high modulus lens materials include, without limitation hydrogels including, without limitation, etafilcon A.
  • the invention is used in lenses made of silicone hydrogels meaning a material containing one or more silicone- containing components and one or more hydrophilic components, such as galyfilcon.
  • the one or more silicone-containing components and one or more hydrophilic components can be any of the known components used in the prior art to make silicone hydrogels.
  • the terms "silicone-containing component” and “hydrophilic component” are not mutually exclusive, in that, the silicone-containing component can be somewhat hydrophilic and the hydrophilic component can contain some silicone.
  • a silicone-containing component is one that contains at least one [ — Si — O — Si] group, in a monomer, macromer or prepolymer.
  • the Si and attached O are present in the silicone-contaim ' ng component in an amount greater than 20 weight percent, and more preferably greater than 30 weight percent of the total molecular weight of the silicone-containing component.
  • Useful silicone- containing components preferably comprise polymerizable functional groups such as acrylate, methacrylate, acrylamide, methacrylamide, N-vinyl lactam, N-vinylamide, and styryl functional groups. Examples of silicone-containing components which are useful in this invention may be found in U.S. Pat. Nos.
  • suitable silicone-containing monomers are polysiloxanylalkyl(meth)acrylic monomers including, without limitation, methacryloxypropyl tris(trimethylsiloxy) silane, pentamethyldisiloxanyl methylmethacrylate, and methyldi(trimethylsiloxy)methacryloxymethyl silane.
  • silicone-containing components is a poly(organosiloxane) prepolymer such as a, ⁇ -bismethacryloxypropyl poly- dimethylsiloxane.
  • a poly(organosiloxane) prepolymer such as a, ⁇ -bismethacryloxypropyl poly- dimethylsiloxane.
  • mPDMS monoomethacryloxypropyl terminated mo ⁇ o-n-butyl terminated polydimethylsiloxane.
  • Another useful class of silicone containing components is a poly(organosiloxane) prepolymer such as a, ⁇ -bismethacryloxypropyl poly- dimethylsiloxane.
  • mPDMS monoomethacryloxypropyl terminated mo ⁇ o-n-butyl terminated polydimethylsiloxane.
  • silicone-containing vinyl carbonate or vinyl carbamate monomers including, without limitation, l,3-bis[4-(vinyloxycarbonyloxy)but-l-yl]tetramethyl- isiloxane 3-(vinyloxycarbonylthio) propyl- ⁇ tris (trimethylsiloxysilane]; 3- [tris(trimethylsiloxy)silyl] propyl allyl carbamate; 3-[tris(trimethylsiloxy)wilyl] propyl vinyl carbamate; trimethylsilylethyl vinyl carbonate; and trimethylsilylmethyl vinyl carbonate.
  • Hydrophilic components include those which are capable of providing at least about 20% and preferably at least about 25% water content to the resulting lens when combined with the remaining reactive components. Suitable hydrophilic components may be present in amounts between about 10 to about 60 weight% based upon the weight of all reactive components. About 15 to about 50 weight % and more preferably between about 20 to about 40 weight %.
  • the hydrophilic monomers that may be used to make the polymers of this invention have at least one polymerizable double bond and at least one hydrophilic functional group.
  • polymerizable double bonds examples include acrylic, methacrylic, acrylamido, methacrylamido, fumaric, maleic, styryl, isopropenylphenyl, 0-vinylcarbonate, O- vinylcarbamate, allylic, O-vinylacetyl and N-vinyllactam and N-vinylamido double bonds.
  • hydrophilic monomers may themselves be used as crosslmking agents.
  • DMA N,N-dimethylacrylamide
  • 2- hydroxyethyl acrylate glycerol methacrylate
  • 2-hydroxyethyl methacrylamide polyethyleneglycol monomethacrylate
  • methacrylic acid acrylic acid and mixtures thereof.
  • Hydrophilic vinyl-containing monomers which may be incorporated into the hydro gels of the present invention include monomers such as N- vinyl lactams (e.g. N-vinyl pyrrolidone (NVP)), N-vinyl-N-methyl acetamide, N-vinyl-N-ethyl acetamide, N-vinyl-N-ethyl formamide, N-vinyl formamide, N-2-hydroxyethyl vinyl carbamate, N-carboxy- ⁇ -alanine N-vinyl ester, with NVP being preferred.
  • NVP N-vinyl lactams
  • examples include polyethylene glycol with one or more of the terminal hydroxyl groups replaced with a functional group containing a polymerizable double bond.
  • Examples include polyethylene glycol reacted with one or more molar equivalents of an end-capping group such as isocyanatoethyl methacrylate ("IEM”), methacrylic anhydride, methacryloyl chloride, vinylbenzoyl chloride, or the like, to produce a polyethylene polyol having one or more terminal polymerizable olefmic groups bonded to the polyethylene polyol through linking moieties such as carbamate or ester groups.
  • IEM isocyanatoethyl methacrylate
  • methacrylic anhydride methacryloyl chloride
  • vinylbenzoyl chloride vinylbenzoyl chloride
  • hydrophilic vinyl carbonate or vinyl carbamate monomers disclosed in U.S. Pat. No.5,070,215
  • hydrophilic oxazolone monomers disclosed in U.S. Pat. No. 4,190,277.
  • Other suitable hydrophilic monomers will be apparent to one skilled in the art.
  • More preferred hydrophilic monomers which may be incorporated into the polymer of the present invention include hydrophilic monomers such as N,N-dimethyl acrylamide (DMA), 2- hydroxyethyl acrylate, glycerol methacrylate, 2-hydroxyethyl methacrylamide, N- vinylpyrrolidone (NVP), and polyethyleneglycol monomethacrylate.
  • Most preferred hydrophilic monomers include DMA, NVP and mixtures thereof.
  • Curing of the lens material may be carried out by any convenient method.
  • the material may be deposited within a mold and cured by thermal, irradiation, chemical, electromagnetic radiation curing and the like and combinations thereof.
  • molding is carried out using ultraviolet light or using the full spectrum of visible light. More specifically, the precise conditions suitable for curing the lens material will depend on the material selected and the lens to be formed. Suitable processes are disclosed in U.S. Patents Nos. 4,495,313, 4,680,336, 4,889,664, 5,039,459, and 5,540,410 incorporated herein in their entireties by reference.
  • the contact lenses of the invention may be formed by any convenient method.
  • One such method uses a lathe to produce mold inserts.
  • the mold inserts in turn are used to form molds.
  • a suitable lens material is placed between the molds followed by compression and curing of the resin to form the lenses of the invention.
  • any other number of known methods may be used to produce the lenses of the invention.

Landscapes

  • Health & Medical Sciences (AREA)
  • Ophthalmology & Optometry (AREA)
  • Physics & Mathematics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Eyeglasses (AREA)
  • Lenses (AREA)
EP04810854A 2004-11-12 2004-11-12 Methods for reducing corneal staining in contact lens wearers Ceased EP1817627A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2004/037836 WO2006054970A1 (en) 2004-11-12 2004-11-12 Methods for reducing corneal staining in contact lens wearers

Publications (1)

Publication Number Publication Date
EP1817627A1 true EP1817627A1 (en) 2007-08-15

Family

ID=34959619

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04810854A Ceased EP1817627A1 (en) 2004-11-12 2004-11-12 Methods for reducing corneal staining in contact lens wearers

Country Status (7)

Country Link
EP (1) EP1817627A1 (pt)
JP (1) JP4855412B2 (pt)
CN (1) CN101151569B (pt)
AU (1) AU2004324989A1 (pt)
BR (1) BRPI0419181B1 (pt)
CA (1) CA2587322C (pt)
WO (1) WO2006054970A1 (pt)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0889348A1 (fr) * 1997-07-03 1999-01-07 Gérard Muller Procédé de fabrication d'une lentille de contact à correct

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5020898A (en) * 1990-01-29 1991-06-04 Schering Corporation Contact lens for correction of astigmatism
US5650838A (en) * 1995-05-04 1997-07-22 Johnson & Johnson Vision Products, Inc. Programmable smooth junctions on lenses
US6467903B1 (en) * 2000-03-31 2002-10-22 Ocular Sciences, Inc. Contact lens having a uniform horizontal thickness profile
JP5051808B2 (ja) * 2000-12-11 2012-10-17 東レ株式会社 プラスチック成形品、およびそれからなるコンタクトレンズ
WO2003087920A1 (fr) * 2002-04-12 2003-10-23 Menicon Co., Ltd. Lentille de contact et procede de production de lentille de contact
AU2003902102A0 (en) * 2003-05-02 2003-05-22 The Institute For Eye Research Contact lens

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0889348A1 (fr) * 1997-07-03 1999-01-07 Gérard Muller Procédé de fabrication d'une lentille de contact à correct

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2006054970A1 *

Also Published As

Publication number Publication date
BRPI0419181B1 (pt) 2017-03-28
CA2587322C (en) 2014-01-14
WO2006054970A1 (en) 2006-05-26
CN101151569B (zh) 2013-11-20
BRPI0419181A (pt) 2007-12-18
CN101151569A (zh) 2008-03-26
AU2004324989A1 (en) 2006-05-26
JP4855412B2 (ja) 2012-01-18
CA2587322A1 (en) 2006-05-26
JP2008520002A (ja) 2008-06-12

Similar Documents

Publication Publication Date Title
CA2618648C (en) Contact lenses and methods for reducing conjunctival pressure in contact lens wearers
CA2536147C (en) Rotationally stabilized contact lenses
KR101489170B1 (ko) 근시 진행의 예방을 위한 안과 렌즈
US6899425B2 (en) Multifocal ophthalmic lenses
CA2431059A1 (en) Dynamically stabilized contact lenses
AU2010319453A1 (en) Ophthalmic lenses for prevention of myopia progression
KR20070009585A (ko) 하이브리드 콘택트렌즈 시스템 및 방법
US7036930B2 (en) Methods for reducing corneal staining in contact lens wearers
US20170261766A1 (en) Contact lens with flexible center and rigid periphery
WO2009094368A1 (en) Contact lens
CA2587322C (en) Methods for reducing corneal staining in contact lens wearers
AU2012202279B2 (en) Methods for reducing corneal staining in contact lens wearers
CN103543539B (zh) 一种减少接触透镜佩戴者的角膜污染的方法
KR20070102668A (ko) 콘택트 렌즈 착용자의 각막 오염을 감소시키는 방법
US20100053548A1 (en) Toric Contact Lenses

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20070604

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB IE IT

RIN1 Information on inventor provided before grant (corrected)

Inventor name: JONES, WILLIAM F.,

Inventor name: HICKSON-CURRAN, SHEILA B.,

Inventor name: NEADLE, SUSAN W.,

Inventor name: JUBIN, PHILIPPE F.,

RIN1 Information on inventor provided before grant (corrected)

Inventor name: NEADLE, SUSAN W.,

Inventor name: HICKSON-CURRAN, SHEILA B.,

Inventor name: JUBIN, PHILIPPE F.,

Inventor name: JONES, WILLIAM F.,

DAX Request for extension of the european patent (deleted)
RBV Designated contracting states (corrected)

Designated state(s): DE FR GB IE IT

REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 1107412

Country of ref document: HK

17Q First examination report despatched

Effective date: 20081216

REG Reference to a national code

Ref country code: DE

Ref legal event code: R003

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20180701