Patent Application
20070043140
The present invention relates to a process for the mitigation of symptoms of contact lens related dry eye.
Soft contact lenses have been available since the 1980s. While there are many people who can successfully wear contact lenses, there are a number of people who can wear contact lenses for only short periods of time due to contact lens related dry eye (“CLRDE”). Symptoms of this disorder include thin and/or unstable tear films, corneal staining and subjective symptoms such as ocular discomfort, burning/stinging and dryness. Contact lens wear may trigger the onset of these symptoms or may exacerbate the symptoms. People with CLRDE generally can comfortably wear contact lenses only for limited periods of time (less than 6 hours and in some cases less than four hours).
There are many eye drops for the treatment of CLRDE. Because the eye drops are readily washed from the eye by blinking and the normal functioning of the eye, they provide only temporary relief and must be frequently reapplied. Currently, there is one contact lens, PROCLEAR®, commercially available from Cooper Vision, which is FDA approved and marketed for contact lens wearers with CLRDE. However, many patients with CLRDE symptoms who wear PROCLEAR are still unable to comfortably wear their lenses for an entire day. Accordingly, there remains a need in the art for a contact lens which can extend the comfortable wear time of contact lens wearers displaying CLRDE symptoms.
The present invention relates to a method for the mitigation of symptoms of contact lens related dry eye comprising contacting the surface of the eye of a patient in need of relief of contact lens related dry eye with a contact lens comprising a modulus of less than about 120 psi and at least about 5 weight % of at least one lubricious polymer.
The present invention relates to a method for the mitigation of symptoms of contact lens related dry eye comprising contacting the surface of the eye of a patient in need of relief of contact lens related dry eye with a contact lens comprising senofilcon A.
As used herein “contact lens related dry eye” (“CLRDE”) is a disorder marked by at least one objective clinical symptom and at least one subjective symptom. Clinical symptoms are selected from (a) a tear film break up time (“TFBUT”) of less than about 10 seconds in at least one eye; (b) a fluorescein staining score ≧3 on a scale of 0-15 in at least one eye; (c) a lissamine green staining score ≧3 on a scale of 0-18 in at least one eye; or (d) a tear meniscus grade of ‘abnormal’ in at least one eye. Subjective symptoms are determined via patient feedback and include (a) ≧about 2 hour difference between average daily contact lens wear time and average daily comfortable contact lens wear time and (b) a rating of frequent or constant feelings of dryness, burning, stinging or discomfort during lens wear. CLRDE sign includes both excessive tear evaporation and Non-Sjogren's aqueous tear deficiency. Excessive tear evaporation is a disorder marked by a TFBUT of about 10 seconds or less in at least one eye or a TFBUT of 10 seconds or less in at least one eye as well as conjunctival or corneal staining of about 3 or greater on the NEI scale. Non-Sjogren's aqueous tear deficiency tear meniscus is a disorder marked by a grade of ‘abnormal’ in at least one eye or a tear meniscus grade of ‘abnormal’ in at least one eye as well as conjunctival or corneal staining of 3 or greater on the NEI scale.
As used herein “contact lens” includes ophthalmic devices that reside on the eye. The contact lenses can provide optical correction, vision enhancement, wound care, drug delivery, diagnostic functionality or cosmetic enhancement or effect or a combination of these properties. Accordingly, the contact lenses of the present invention can be spherical, toric, bifocal, may contain cosmetic tints, opaque cosmetic patterns, combinations thereof and the like.
It has been surprisingly found that contact lenses comprising a modulus of less than about 120 psi and at least about 5% of at least one lubricious polymer provide superior comfort than ACUVUE® ONE DAY brand contact lenses to people with CLRDE. The contact lenses of the present invention display superior overall comfort throughout wear, and at the end of the day. The lenses of the present invention were found, in clinical trials, to be significantly more comfortable than ACUVUE® ONE DAY brand contact lenses, which is recognized in the industry as lenses which are among the most comfortable commercially available lenses. The lenses of the present invention were also found to be significantly more comfortable during computer usage. Wearers also reported a significant preference for the lenses of the present invention compared to ACUVUE® ONE DAY brand contact lenses when asked which lenses made their eyes feel moist. By significant, we mean a preference rating of at least 1.5 to 1 in a double masked, clinical trial with at least about 20 patients completing the trial and wearing lenses for at least 8 hours per day in a daily disposable modality for at least one week. End of day comfort data was collected at the end of the week of wear and at least 8 hours after lens insertion. The questionnaires allowed participants the following choices: preferred the test lens, preferred the control lens, preferred both lenses or preferred neither lens. Ratings were generated using all responses indicating a preference between the lenses. ACUVUE® ONE DAY brand contact lenses are soft hydrogel contact lenses made from etafilcon A and commercially available from Johnson & Johnson Vision Care, Inc.
Applicants believe that the contact lenses of the present invention provide superior comfort than ACUVUE® ONE DAY brand contact lenses in people having CLRDE because they support a stable tear film when viewed via a tear interferometer.
Tear film interferometry is based upon well-established optical principles. Tear interferometry uses specular reflectance to generate visible interference patterns which give detailed information of the topography of the tear layer overlaying a contact lens. The intereference patterns are created by using two images of the same source. Specifically, two interfering beams are used, the reflected beam from the front surface of the tear film and the reflected beam from the rear surface of the tear film. The two beams originate from the same lights source 1. When the two reflected beams are combined at a common focus, the result is a series of light and dark interference fringes. These fringes are analogous to the contour lines on a topographical map and the contour interval constant in this case is dependent upon the wavelength of the incident light. Each fringe represents a location on the tear film of consistent film thickness. Moving to an adjacent line or fringe will represent a change in tear film thickness equal to the contour interval. The configuration of the tear interferometer used in the examples is described in Example 3. General descriptions of tear interferometry may also be found in U.S. Pat. No. 4,747,683 and Optometry and Vision Science, M. Doane, Vol. 66, No. 6 pages 383-388.
By stable tear film we mean a tear film of at least moderate thickness and displaying a break up time of at least about 3 seconds when viewed with a tear interferometer. Generally, the thickness of the tear film may be evaluated by the number of fringes visible, the more fringes visible via tear interferometry, the thicker the tear film over the lens. If few fringes, or partial fringes are seen, that usually indicates a very thin tear film and a poorly wetting contact lens in that individual's eye. Rapidly moving fringes indicate that the tear film is rapidly thinning.
It is believed that the incorporation of at least one lubricious polymer provides the lenses of the present invention with the unique stable tear film and smoothness upon dehydration observed via tear interferometry. Suitable lubricious polymers include non-reactive hydrophilic polymers which may be incorporated into the monomer mixture to form an interpenetrating network and reactive hydrophilic polymers. Suitable lubricious polymers have a weight average molecular weight of at least about 50,000 Daltons, and in some embodiments greater than about 100,000 Daltons. The molecular weight of the lubricious polymers may be determined via gel permeation chromatography (GPC) using a ViscoGEL GMPWXL Column with a 20/80 methanol/water ratio with a flow rate 1.0 ml/min. at 30° C.
In addition to the average molecular weight specified above, lubricious polymers also possess, when polymerized and crosslinked to minor amount, a water content of at least about 70%, preferably at least about 80%. For lubricious polymers which are free radical reactive, a “minor amount” of crosslinking may be effected by polymerizing the monomer(s) from which the polymer is formed with a small amount (such as about 7.5 mmol/100 gram of polymer) of crosslinker (for example, EGDMA). Methods for forming crosslinked polymers which are not free radical reactive will be apparent to those of skill in the art from the disclosure contained herein.
Alternatively, the suitability of a polymer for use as a lubricious polymer may be determined by mixing 10 wt % of the monomer from which the polymer is formed in water at room temperature. Monomers that are soluble under these conditions may be used to form lubricious polymers for use in the contact lenses of the present invention. Specific examples of lubricious polymers include high molecular weight hydrophilic polymers and copolymers of polyamides, polylactones, polyimides, polylactams and functionalized polyamides, polylactones, polyimides, polylactams, such as DMA functionalized by copolymerizing DMA with a lesser molar amount of a hydroxyl-functional monomer such as HEMA, and then reacting the hydroxyl groups of the resulting copolymer with materials containing radical polymerizable groups, such as isocyanatoethylmethacrylate or methacryloyl chloride. Hydrophilic polymers or prepolymers made from DMA or n-vinyl pyrrolidone with glycidyl methacrylate may also be used. The glycidyl methacrylate ring can be opened to give a diol which may be used in conjunction with other hydrophilic prepolymers in a mixed system. Specific examples of lubricious polymers include but are not limited to poly-N-vinyl pyrrolidone, poly(N-vinyl-N-methylacetamide), poly-N-vinyl-2-piperidone, poly-N-vinyl-2-caprolactam, poly-N-vinyl-3-methyl-2-caprolactam, poly-N-vinyl-3-methyl-2-piperidone, poly-N-vinyl-4-methyl-2-piperidone, poly-N-vinyl-4-methyl-2-caprolactam, poly-N-vinyl-3-ethyl-2-pyrrolidone, and poly-N-vinyl-4,5-dimethyl-2-pyrrolidone, polyvinylimidazole, poly-N-N-dimethylacrylamide, polyvinyl alcohol, polyethylene oxide, poly 2 ethyl oxazoline, heparin polysaccharides, polysaccharides, mixtures and copolymers (including block or random, branched, multichain, comb-shaped or star shaped) thereof where poly-N-vinylpyrrolidone (PVP), poly(N-vinyl-N-methylacetamide) (PVMA) are particularly preferred. Copolymers might also be used such as graft copolymers of PVP or amphiphilic copolymers having hydrophilic and hydrophobic blocks such as those disclosed in U.S. Ser. No. 10/954,560. The lubricious polymer may be incorporated into the lens polymer without chemical bonding, such as is disclosed in US2003/162,862 and US2003/125,498 or may be copolymerized into the lens matrix or coated onto the contact lens, by any known method such as premold spin casting, as disclosed, for example, in US2003/052,424, grafting, soaking the lens in a polymeric solution as disclosed in US2002/006,521 and U.S. Pat. No. 6,478,423, and the like. The foregoing patents and applications, and all others referenced herein, are hereby incorporated herein by reference.
When the lubricious polymer is incorporated into the lens polymer, the lubricious polymer may also comprise polyacrylic acid. However, when the lubricious polymer is coated onto the lens, the lubricious polymer is not polyacrylic acid or poly(N,N-dimethylacrylamide).
Alternatively, the lubricious polymer may be a reactive polymer having a molecular weight as low as 2000. Suitable low molecular weight polymers are disclosed in U.S. Ser. No. 10/954559.
In yet another embodiment, precursors of the lubricious polymers, such as the monomers from which they are formed, may be incorporated into the monomer mix, which is then cured using conditions to form lubricious polymers having the molecular weights disclosed above.
The lenses of the present invention may be made from any known lens materials so long as the lens comprises at least about 5% of at least one lubricious polymer and a modulus of less than about 120 psi. In some embodiments the lens comprises between about 5 and about 20 weight% lubricious polymer, based upon all the components used to make the lens.
The modulus is less than about 120 psi, in some embodiments less than about 100 psi, and in some embodiments between about 40 and 100 psi.
Suitable lens materials include hydrophilic components, silicone containing components and combinations thereof.
The term components includes monomers, macromers and prepolymers. “Monomer” refers to lower molecular weight compounds that can be polymerized to higher molecular weight compounds, polymers, macromers, or prepolymers. The term “macromer” as used herein refers to a high molecular weight polymerizable compound. Prepolymers are partially polymerized monomers or monomers which are capable of further polymerization.
A “silicone-containing component” is one that contains at least two [—Si—O—] repeating units in a monomer, macromer or prepolymer. Preferably, the total Si and attached O are present in the silicone-containing 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. 3,808,178; 4,120,570; 4,136,250; 4,153,641; 4,740,533; 5,034,461 and 5,070,215, and EP080539. These references disclose many examples of olefinic silicone-containing components.
While almost any silicone containing component may be included, in order to provide the lenses of the present invention with the desired modulus, the majority of the mass fraction of the silicone components used in the lens formulation should contain only one polymerizable functional group (“monofunctional silicone containing component”). In silicone containing lenses, to insure the desired balance of oxygen transmissibility and modulus it is preferred that all components having more than one polymerizable functional groups (“multifunctional components”) make up no more than 10 mmol/100 g of the reactive components, and preferably no more than 7 mmol/100 g of the reactive components. Suitable monofunctional silicone containing components include polysiloxanylalkyl(meth)acrylic monomers of Formula I:
wherein: R denotes H or lower alkyl; X denotes O or NR4; each R4 independently denotes hydrogen or methyl,
each R1—R3 independently denotes a lower alkyl radical or a phenyl radical, and
n is 1 or 3 to 10.
Mono-functional polydimethylsiloxanes (mPDMS) may also be used. Suitable mPDMS compounds include Structure II:
where b=0 to 100, where it is understood that b is a distribution having a mode equal to a stated value, preferably 4 to 16, more preferably 8 to 10; R58 is a monovalent group containing at least one ethylenically unsaturated moiety, preferably a monovalent group containing a styryl, vinyl, or methacrylate moiety, more preferably a methacrylate moiety; each R59 is independently a monovalent alkyl, or aryl group, which may be further substituted with alcohol, amine, ketone, carboxylic acid or ether groups, preferably unsubstituted monovalent alkyl or aryl groups, more preferably methyl; R60 is a monovalent alkyl, or aryl group, which may be further substituted with alcohol, amine, ketone, carboxylic acid or ether groups, preferably unsubstituted monovalent alkyl or aryl groups, preferably a C1-10 aliphatic or aromatic group which may include hetero atoms, more preferably C3-8 alkyl groups, most preferably butyl; and R61 is independently alkyl or aromatic, preferably ethyl, methyl, benzyl, phenyl, or a monovalent siloxane chain comprising from 1 to 100 repeating Si—O units. Examples of suitable mPDMS compounds include 3-methacryloxy-2-hydroxypropyloxy)propylbis(trimethylsiloxy)methylsilane, monomethacryloxypropyl terminated mono-n-butyl terminated polydimethylsiloxane, methacryloxypropylpentamethyl disiloxane, combinations thereof and the like.
Examples of polysiloxanylalkyl (meth)acrylic monomers include methacryloxypropyl tris(trimethylsiloxy) silane, pentamethyldisiloxanyl methylmethacrylate, and methyldi(trimethylsiloxy)methacryloxymethyl silane. Methacryloxypropyl tris(trimethylsiloxy)silane is the most preferred.
In some embodiments monofunctional polydimethylsiloxanes may be preferred, as they lower not only modulus, but also tan δ, while bulky silicones, such as those containing at least one branching trimethylsiloxy group will increase tan δ. Accordingly, at least about 30 and preferably at least about 60 weight% of all the silicone components should be non-bulky silicone containing compounds such as polydimethylsiloxanes.
In one embodiment, where a silicone hydrogel lens is desired, the lens of the present invention will be made from a reactive mixture comprising at least about 20 and preferably between about 20 and 70% wt silicone containing components based on total weight of reactive monomer components from which the polymer is made.
In addition to the monofunctional silicone containing components, multifunctional silicone containing components and/or bulky silicone containing compounds may also be included in amounts which do not impart an undesirably high modulus and/or tan δ.
One class of silicone-containing components is a poly(organosiloxane) prepolymer represented by formula III:
wherein each A independently denotes an activated unsaturated group, such as an ester or amide of an acrylic or a methacrylic acid or an alkyl or aryl group (providing that at least one A comprises an activated unsaturated group capable of undergoing radical polymerization); each of R5, R6, R7 and R8 are independently selected from the group consisting of a monovalent hydrocarbon radical or a halogen substituted monovalent hydrocarbon radical having 1 to 18 carbon atoms which may have ether linkages between carbon atoms;
R9 denotes a divalent hydrocarbon radical having from 1 to 22 carbon atoms, and
m is 0 or an integer greater than or equal to 1, and preferable 5 to 400, and more preferably 10 to 300. One specific example is α, ω-bismethacryloxypropyl polydimethylsiloxane.
Another useful class of silicone containing components includes silicone containing vinyl carbonate or vinyl carbamate monomers of the following formula:
wherein: Y denotes O, S, or NH; RSi denotes a silicone-containing organic radical; R denotes
hydrogen or methyl; d is 1, 2, 3 or 4; and q is 0 or 1. Suitable silicone-containing organic radicals RSi include the following:
Wherein p is 1 to 6; R10 denotes an alkyl radical or a fluoroalkyl radical having 1 to 6 carbon atoms; e is 0 to 200; q′ is 1, 2, 3 or 4; and s is 0, 1, 2, 3, 4 or5.
The silicone-containing vinyl carbonate or vinyl carbamate monomers specifically include: 1,3-bis[4-(vinyloxycarbonyloxy)but-1-yl]tetramethyl-disiloxane; 3-(vinyloxycarbonylthio) propyl-[tris (trimethylsiloxy)silane]; 3-[tris(trimethylsiloxy)silyl]propyl allyl carbamate; 3-[tris(trimethylsiloxy)silyl]propyl vinyl carbamate; trimethylsilylethyl vinyl carbonate; trimethylsilylmethyl vinyl carbonate, and
Another class of silicone-containing components includes polyurethane macromers of the following formulae:
(*D*A*D*G)a *D*D*E1;
E(*D*G*D*A)a *D*G*D*E1 or;
E(*D*A*D*G)a *D*A*D*E1 Formulae IV-VI
wherein:
D denotes an alkyl diradical, an alkyl cycloalkyl diradical, a cycloalkyl diradical, an aryl diradical or an alkylaryl diradical having 6 to 30 carbon atoms,
G denotes an alkyl diradical, a cycloalkyl diradical, an alkyl cycloalkyl diradical, an aryl diradical or an alkylaryl diradical having 1 to 40 carbon atoms and which may contain ether, thio or amine linkages in the main chain;
denotes a urethane or ureido linkage;
ais at least 1;
A denotes a divalent polymeric radical of formula:
Formula VII
R11 independently denotes an alkyl or fluoro-substituted alkyl group having 1 to 10 carbon atoms which may contain ether linkages between carbon atoms; y is at least 1; and p provides a moiety weight of 400 to 10,000; each of E and E1 independently denotes a polymerizable unsaturated organic radical represented by formula:
wherein: R12 is hydrogen or methyl; R13 is hydrogen, an alkyl radical having 1 to 6 carbon atoms, or a —CO—Y—R15 radical wherein Y is —O—, Y—S—or —NH—; R14 is a divalent radical having 1 to 12 carbon atoms; X denotes —CO—or —OCO—; Z denotes —O— or —NH—; Ar denotes an aromatic radical having 6 to 30 carbon atoms; w is 0 to 6; x is 0 or 1; y is 0 or 1; and z is 0 or 1.
A preferred silicone-containing component is a polyurethane macromer represented by the following formula:
wherein R16 is a diradical of a diisocyanate after removal of the isocyanate group, such as the diradical of isophorone diisocyanate. Another suitable silicone containing macromer is compound of formula X (in which x+y is a number in the range of 10 to 30) formed by the reaction of fluoroether, hydroxy-terminated polydimethylsiloxane, isophorone diisocyanate and isocyanatoethylmethacrylate.
Other silicone containing components suitable for use in this invention include those described is WO 96/31792 such as macromers containing polysiloxane, polyalkylene ether, diisocyanate, polyfluorinated hydrocarbon, polyfluorinated ether and polysaccharide groups. U.S. Pat. Nos. 5,321,108; 5,387,662 and 5,539,016 describe polysiloxanes with a polar fluorinated graft or side group having a hydrogen atom attached to a terminal difluoro-substituted carbon atom. US 2002/0016383 describe hydrophilic siloxanyl methacrylates containing ether and siloxanyl linkanges and crosslinkable monomers containing polyether and polysiloxanyl groups. Any of the foregoing polysiloxanes can also be used as the silicone containing component in this invention.
Hydrophilic monomers are also included in the reactive components used to make the contact lenses of the present invention. The hydrophilic monomers used to make the contact lenses of this invention can be any of the known hydrophilic monomers disclosed in the prior art to make hydrogels.
The preferred hydrophilic monomers used to make the polymer of this invention may be either acrylic- or vinyl-containing. Such hydrophilic monomers may themselves be used as crosslinking agents, however, where hydrophilic monomers having more than one polymerizable functional group are used, their concentration should be limited as discussed above to provide a contact lens having the desired modulus. The term “vinyl-type” or “vinyl-containing” monomers refer to monomers containing the vinyl grouping (—CH═CH2) and are generally highly reactive. Such hydrophilic vinyl-containing monomers are known to polymerize relatively easily.
“Acrylic-type” or “acrylic-containing” monomers are those monomers containing the acrylic group: (CH2═CRCOX) wherein R is H or CH3, and X is O or N, which are also known to polymerize readily, such as N,N-dimethyl acrylamide (DMA), 2-hydroxyethyl methacrylate (HEMA), glycerol methacrylate, 2-hydroxyethyl methacrylamide, polyethyleneglycol monomethacrylate, methacrylic acid and acrylic acid.
Hydrophilic vinyl-containing monomers which may be incorporated into the silicone hydrogels of the present invention include monomers such as N-vinyl amides, N-vinyl lactams (e.g. NVP), N-vinyl-N-methyl acetamide, N-vinyl-N-ethyl acetamide, N-vinyl-N-ethyl formamide, N-vinyl formamide, with NVP being preferred.
Other hydrophilic monomers that can be employed in the invention include polyoxyethylene polyols having one or more of the terminal hydroxyl groups replaced with a functional group containing a polymerizable double bond. Examples include polyethylene glycol, ethoxylated alkyl glucoside, and ethoxylated bisphenol A reacted with one or more molar equivalents of an end-capping group such as isocyanatoethyl methacrylate (“IEM”), methacrylic anhydride, methacryloylchloride, vinylbenzoyl chloride, or the like, to produce a polyethylene polyol having one or more terminal polymerizable olefinic groups bonded to the polyethylene polyol through linking moieties such as carbamate or ester groups.
Still further examples are the hydrophilic vinyl carbonate or vinyl carbamate monomers disclosed in U.S. Pat. No. 5,070,215, and the hydrophilic oxazolone monomers disclosed in U.S. Pat. No. 4,910,277. Other suitable hydrophilic monomers will be apparent to one skilled in the art.
In one embodiment the hydrophilic comprises at least one hydrophilic monomer such as DMA, HEMA, glycerol methacrylate, 2-hydroxyethyl methacrylamide, NVP, N-vinyl-N-methyl acrylamide, polyethyleneglycol monomethacrylate, methacrylic acid and acrylic acid with DMA being the most preferred.
The hydrophilic monomers may be present in a wide range of amounts, depending upon the specific balance of properties desired. For silicone hydrogel lenses, amounts of hydrophilic monomer up to about 50 and preferably between about 5 and about 50 weight %, based upon all components in the reactive components are acceptable. For example, in one embodiment lenses of the present invention comprise a water content of at least about 30%, and in another embodiment between about 30 and about 50%. For these embodiments, the hydrophilic monomer may be included in amounts between about 20 and about 50 weight %.
In another embodiment, the contact lens of the present invention is a hydrophilic lens and is formed from lens components comprising primarily or only hydrophilic components and the lubricious polymer. In these embodiments the hydrophilic components are present in amounts from about 70 to about 95 weight percent, and in some embodiments from about 80 to about 95 weight %.
Additionally contact lenses of the present invention may have water contents of at least about 30%, and preferably between about 30 and about 50%. The contact lenses of the present invention may also display advancing contact angles of less than about 80° and in some embodiments less than about 70° as measured using a Wilhelmy dynamic contact angle balance.
In one embodiment, it has been surprisingly found that contact lenses made from senofilcon A provide relief from CLRDE symptoms when worn by patients with CLRDE. Senofilcon A is a polymer formed from the following reactive components: 3-methacryloxy-2-hydroxypropyloxy)propylbis(trimethylsiloxy)methylsilane (SiMAA), monomethacryloxypropyl terminated mono-n-butyl terminated polydimethylsiloxane (mPDMS), N,N-dimethyl acrylamide (DMA), 2-hydroxyethyl methacrylate (HEMA), poly-N-vinyl pyrrolidone (PVP), a UV absorber and a visibility tint.
The contact lenses of the present invention may be used for the temporary relief or mitigation of subjective CLRDE symptoms such as dryness, burning, stinging and discomfort. Relief or mitigation of symptoms may be clinically measured via a clinical study. For example, in the study patients wear a control lenses and the senofilcon A lenses for a predetermined period of time and are asked about CLRDE symptoms such as ocular discomfort, dryness, burning and stinging. If the control lens is a lens approved for use for the treatment of CLRDE, like Proclear Compatibles, the test lens would only need subjective scores equivalent to Proclear Compatibles to be considered useful for the relief or mitigation of CLRDE symptoms. If the control lens is a conventional lens, the test lens would need subjective scores better than the control to be considered useful for the relief or mitigation of CLRDE symptoms. Accordingly, as used herein, temporary relief or mitigation of CLRDE symptoms means a clinically measurable dimunition of at least one CLRDE symptom, such as dryness, burning, stinging or discomfort as measured in a masked, clinical trial with at least about 10 patients completing the trial and wearing lenses for at least about 8 hours per day on average for at least one week. Preferably the clinical trial is a double-masked trial with at least about 20 patients completing the trial and wearing lenses for at least about 8 hours on average per day for at least one week.
The duration of contact (or wear time) will vary depending on the individual patient. However, because the symptomatic benefit is provided by the lens itself and not an additive that elutes from the lens, the benefits derived from using the lenses in accordance with the present invention extend throughout the entire wear time. Suitable wear times include up to about 8 hours, up to about 12 hours, up to about 24 hours, up to a week and for some patients up to a month of continuous wear.
The lenses may be worn continuously or may be worn only during waking hours. If the lenses are worn during waking hours only, the lenses may be cleaned and stored using any conventional cleaning and/or storing solution.
Tear film break-up (TFBUT) time was measured as follows. Five (5) μl of non-preserved, 2% sodium fluorescein was instilled into the right of a clinical patient using a micropipette. The patient was instructed to blink 2 times without squeezing his/her eyelids together, then stare straight ahead. Immediately after the second blink and within 30 seconds of fluorescein instillation, the right eye was observed through a slit lamp and the time was measured for the first sign of disruption of the tear film. The measurement was immediately repeated on the right eye. If the recorded TFBUT measurements were less than 10 seconds and greater than 2 seconds apart, a third measurement was taken. The measurements were averaged. The procedure was repeated for the left eye.
Fluorescein staining is measured by instilling 5 microliters of 2% fluorescein solution into the inferior conjunctival cul-de-sac. The patient is instructed to blink several times. After 5 minutes the eye is evaluated using a slit lamp. The staining is rated in each of five regions using a 0-3 scale extracted from the 1995 NEI workshop on Dry Eye (Section 11.1) (0=None, 1=Discrete, countable, 2=Moderate, coalescent, Uncountable, 3=Confluent). The cumulative sum of the regional scores is reported.
Lissamine green staining score is measured by instilling 10 microliters of lissamine green into the inferior cul-de-sac a drop of each eye. The patient is instructed to blink several times. After 5 minutes the eye is evaluated using a slit lamp. The staining is rated in each of six regions using a 0-3 scale extracted from the 1995 NEI workshop on Dry Eye (Section 11.1) (0=None, 1=Discrete, countable, 2=Moderate, coalescent, Uncountable, 3=Confluent). The cumulative sum of the regional scores is reported.
The tear meniscus is evaluated by observing the eye using a slit lamp and a diffuse/specular reflection illumination source under low to moderate magnification. A normal tear film produced a specular reflection off the upper edge of the lower lid tear prism which appeared to float well above the lower lid as the slit lamp light source is moved from one side to the other. An abnormal tear film (low tear volume) produced a lower lid tear prism reflection which was absent or appeared immediately adjacent to the lid margin. The reflex will followed an irregular path across the lid margin as the light beam was moved from side to side.
Senofilcon A lenses were made as disclosed in WO03/022321 (Example 1) and clinically evaluated against ACUVUE® ONE DAY brand contact lenses (etafilcon A). The clinical evaluation was a single masked (patient), randomized, bilateral cross-over study with twenty-eight patients completing the study. Only patients who reported dry eye symptoms with their own contacts using the following eligibility criteria were recruited.
Selection of Replacement Frequency. ICLC Vol. 19, May/June 1992 pp 104-120. (where 0=not dry at all; 168=severely dry)
The lenses were worn in a daily disposable mode (lenses thrown out each night) for a period of one week. After one week of wear for each lens, the patients were asked to rate which lens they preferred for initial comfort, end of day comfort, overall comfort and dryness. Table 1 shows the preference data.
Senofilcon A lenses were made as disclosed in WO03/022321 (Example 1) and clinically evaluated against Proclear Compatibles® (omafilcon A) contact lenses. The clinical evaluation was a double masked, randomized, bilateral cross-over study with 54 patients completing the study. Only patients meeting the following criteria were enrolled:
Sixty-three percent (63%) of the enrolled patients were classified as having evaporative tear deficiency and thirty-seven percent (37%) were classified as having both evaporative tear deficiency and aqueous tear deficiency. The lenses were worn in a daily wear mode (nightly removal) for a period of one month using ReNu Multi-Plus Multi-Purpose Solution. Both lens types were replaced after 2 weeks of lens wear. After two and four weeks of wear for each lens, the patients were asked to rate the lenses for ocular discomfort and visual acuity. At each visit the senofilcon A lenses were rated as good or better than the Proclear Compatibles® lenses on both ocular discomfort (0.6 2 weeks and 0.7 after four weeks in the cohort population on a 4 point scale:0=no discomfort, 4=severe discomfort) and visual acuity (average of 0.0 on logMar scale for both senofilcon A and Proclear Compatibles® at the 4-week follow-up visit).
Those of ordinary skill in the art will recognize that many modifications and variations of the present invention may be implemented. The foregoing description and the following claims are intended to cover all such modifications and variations.
A tear interferometer, as shown in
Ten subjects wore each of lenses listed above for 8-hour periods. All subjects wore each of the three lenses. Interferometric examinations were made on each subject at 30-minutes and 8-hour wearing times. The subjects wore the same lens type in both eyes during each wearing period. During the exams, the subjects were asked to blink normally for about 20-30 seconds, then to keep their lids open for an extended period (10 seconds or more) without blinking. The tear film thickness, time to dry (time it took for the contact lens to become dry when withholding blinks), and recovery (recovery from dryness to a wet surface) were evaluated. Based upon the evaluation the lenses were rated on a scale of 1-5 (5 being the best overall performance). The results are shown in the Table below.
Representative examples of the interferometric images which were collected are shown in
Even after 10 seconds the ACUVUE OASYS brand contact lens did not display dark pits or crevasses. A strong fringe pattern was observed after a single blink.
This patent application claims priority of a provisional application, U.S. Ser. No. 60/650,656, which was filed on Feb. 7, 2005. This patent application is a continuation-in-part of U.S. Ser. No. 11/036669, which claimed priority from provisional application U.S. Ser. No. 60/537369, filed on Jan. 17, 2003 and was a continuation-in-part of U.S. Ser. No. 10/236,538, and U.S. Ser. No. 10/236,762, both of which were filed on Sep. 6, 2002, and both of which claim the priority of provisional application Ser. No. 60/318,536, filed on Sep. 10, 2001; and also a continuation-in-part of U.S. Ser. No. 09/652,817, filed on Aug. 30, 2000, which is a continuation-in-part of U.S. Ser. No. 09/532,943, filed on Mar. 22, 2000, which is a continuation-in-part of U.S. Ser. No. 09/414,365, filed on Oct. 7,1999, which is a continuation-in-part of U.S. Ser. No. 09/033,347, filed on Mar. 2, 1998, now issued as U.S. Pat. No. 5,998,498.
| Number | Date | Country | |
|---|---|---|---|
| 60650656 | Feb 2005 | US | |
| 60537369 | Jan 2004 | US | |
| 60318536 | Sep 2001 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11036669 | Jan 2005 | US |
| Child | 11347973 | Feb 2006 | US |
| Parent | 10236538 | Sep 2002 | US |
| Child | 11347973 | Feb 2006 | US |
| Parent | 10236762 | Sep 2002 | US |
| Child | 11347973 | Feb 2006 | US |
| Parent | 09652817 | Aug 2000 | US |
| Child | 11347973 | Feb 2006 | US |
| Parent | 09532943 | Mar 2000 | US |
| Child | 09652817 | Aug 2000 | US |
| Parent | 09414365 | Oct 1999 | US |
| Child | 09532943 | Mar 2000 | US |
| Parent | 09033347 | Mar 1998 | US |
| Child | 09414365 | Oct 1999 | US |
