Methods and apparatuses for sealing ophthalmic lens packages

Abstract

Methods and apparatuses for the treatment of ophthalmic lens packages prior to sealing are described herein.

Description

RELATED APPLICATIONS

This application is a non-provisional filing of U.S. Ser. No. 60/672,192, filed on Apr. 15, 2005, a provisional patent application.

This invention related to methods and apparatuses used for the treatment of ophthalmic lens packages prior to sealing those packages.

BACKGROUND

Contact lenses have been used commercially to improve vision since the 1950s. The first contact lenses were made of hard materials, glass and hard plastics. Later developments in the field gave rise to soft contact lenses, based upon hydrogels, which are extremely popular today. The ophthalmic lenses are often packaged in individual packages, commonly known as blister packs. Typical blister packs consist of a plastic bowl that is covered with a laminate foil to contain the lens. See, U.S. Pat. Nos. D458,023; 5,467,868; and 5,656,362 all of which are hereby incorporated by reference in their entirety. Due to the comfort and popularity of these lenses, which are manufactured on a large scale by automated processes that include sealing ophthalmic lenses in a primary package and sterilizing those lenses. See, U.S. Pat. Nos. 6,054,090; 6,018,931; 5,696,686; 5,577,367; 5,488,815, and US Pat. App. Nos. 2004/0112008, 2005/0013729 all of which are hereby incorporated by reference in their entirety.

Even though theses methods are useful, problems can occur with the hermetic sealing of an ophthalmic lens in its blister pack under certain conditions. For example when ophthalmic lenses are packaged with aqueous solutions and heated to an elevated temperature in order to sterilize the package, steam is formed. This steam may interfere with the hermetic sealing of the blister to the laminate foil and form channels of unsealed areas or wrinkles in the laminated foil. Both of these conditions are undesirable in a product that must be delivered to consumer or an eye-care practitioner for ultimate use in an eye. This problem is heightened when the aqueous solution is in contact with the areas of the package that forms the hermetic seal between the plastic bowl and its cover. Such poorly sealed packages are typically discarded and lenses that are otherwise useable will be discarded. Therefore it would be useful to find methods of preventing poorly sealed packages in a manufacturing environment. This need is met by the following invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 Illustrates an ophthalmic lens package

FIG. 2 Illustrates a member of the invention attached to a support

FIG. 3 Illustrates an image of a contact lens manufacturing line

FIG. 4 Illustrates a perspective view of a member of the invention

DETAILED DESCRIPTION OF THE INVENTION

This invention includes a method of treating an ophthalmic lens package containing an ophthalmic lens and a packaging liquid prior to sealing said package with a cover comprising, consisting essentially of, or consisting of removing said packaging liquid from the sealing portion of said package. As used herein “ophthalmic lens” refers to a device that resides in or on the eye. These devices can provide optical correction or may be cosmetic. The term ophthalmic lens includes but is not limited to soft contact lenses, intraocular lenses, overlay lenses, ocular inserts, and optical inserts. Preferred lenses of the invention are soft contact lenses are made from silicone elastomers or hydrogels, which include but are not limited to silicone hydrogels, and fluorohydrogels. Soft contact lens formulations are disclosed in U.S. Pat. No. 5,710,302, WO 9421698, EP 406161, JP 2000016905, U.S. Pat. No. 5,998,498, U.S. patent application Ser. No. 09/532,943, U.S. Pat. No. 6,087,415, U.S. Pat. No. 5,760,100, U.S. Pat. No. 5,776,999, U.S. Pat. No. 5,789,461, U.S. Pat. No. 5,849,811, U.S. Pat. No. 5,965,631, and silicone hydrogels as prepared in U.S. Pat. No. 5,998,498, U.S. patent application Ser. No. 09/532,943, a continuation-in-part of U.S. patent application Ser. No. 09/532,943, filed on Aug. 30, 2000, U.S. Pat. App. No. 60/318,536, entitled Biomedical Devices Containing Internal wetting Agents,” filed on Sep. 10, 2001 and its non-provisional counterpart of the same title, U.S. Ser. No. 10/236,538, filed on Sep. 6, 2002, U.S. Pat. No. 6,087,415, U.S. Pat. No. 5,760,100, U.S. Pat. No. 5,776, 999, U.S. Pat. No. 5,789,461, U.S. Pat. No. 5,849,811, and U.S. Pat. No. 5,965,631. These patents and patent applications as well as all other patents and patent applications disclosed in this application are hereby incorporated by reference in their entirety. The particularly preferred lenses of the inventions are etafilcon A, galifilcon A, senofilcon A, lenefilcon A, lotrfilcon A, lotrifilcon B, balifilcon A, polymacon, genfilcon A, lenefilcon A, bafilcon, acofilcon A acquafilcon A, alofilcon A alphafilcon A, amifilcon A, astifilcon A, atalafilcon A, bisfilcon A bufilcon A, crofilcon A, cyclofilcon A, darfilcon A deltafilcon A, deltafilcon B, dimefilcon A, drooxifilcon A, epsifilcon A, esterifilcon A, focofilcon A, galyfilcon A, govafilcon A, hefilcon A hefilcon B, hefilcon D, hilafilcon A, hilafilcon B, hixoifilcon A, hioxifilcon B, hioxifilcon C, hydrofilcon A, licryfilcon A, licryfilcon B, lidofilcon B, lidofilcon A, mafilcon A, mesifilcon A, methafilcon B, mipafilcon A, nelfilcon A, netrafilcon A, ocufilcon A, ocufilcon B, ocufilcon C, ocufilcon D, ocufilcon E, ofilcon A, omafilcon A, oxyfilcon A, pentafilcon A, perfilcon A, pevafilcon A, phemfilcon A, silafilcon A, siloxyfilcon A, tefilcon A, tetrafilcon A, trifilcon A, vifilcon A, or xylofilcon A. More particularly preferred lenses of the invention are etafilcon A, genfilcon A, galifilcon A, senofilcon A, lenefilcon A, lotrfilcon A, lotrifilcon B, and balifilcon A. The most particularly preferred lenses are galifilcon A and senofilcon A.

As used herein, “ophthalmic lens package” refers to any receptacle that houses an ophthalmic lens and a packaging liquid. The preferred ophthalmic lens package is the hard or plastic portion of a blister package. See, U.S. Pat. Nos. 4,691,820; 5,054,610; 5,337,888; 5,375,698; 5,409,104; 5,467,868; 5,515,964; 5,609,246; 5,695,049; 5,704,468; 5,711,416; 5,722,536; 5,573,108; 5,823,327; 5,704,468; 5,983,608; 6,029,808; 6,044,966; and 6,401,915 for examples of such packaging, all of which are hereby incorporated by reference in their entirety. One example of an ophthalmic lens package is illustrated in FIG. 1. Such ophthalmic lens packaging 9, typically has a substantially planar first surface 10 and a cavity 11 for holding the lens and the liquid. The particularly preferred ophthalmic lens packaging is made of polypropylene. The “sealing portion” of the ophthalmic lens package is the area that is hermetically sealed to the cover. Typically the hermetic seal is formed by a process that heat seals the cover to the sealing portion. Sealing portions may be any area on the substantially planar first surface 10. Preferably the sealing portion 12, is a raised above the substantially planar first surface and circumferentially surrounds the cavity 11. As used herein “cover” refers to flexible materials that may be hermetically sealed to the ophthalmic lens package. The preferred cover is a flexible laminate made of aluminum sandwiched between one or more polymers. See U.S. Pat. Nos. 6,054,090 and 5,467,868, which are hereby incorporated by reference in their entirety.

As used herein, “packaging liquid” refers to solutions that are used to wash, swell, store, sterilize, or hydrate ophthalmic lenses. Examples of liquids include but are not limited to water, deionized water, organic solutions, aqueous salt solutions, alcohols such as methanol, ethanol, isopropanol, t-amyl alcohol, methylene chloride, hexane, and diluents that are used in the production of ophthalmic lenses. Preferred diluents include organic solvents, water or mixtures hereof. Preferred organic solvents include alcohols, methylene chloride, hexanes, diols, triols, polyols and polyalkylene glycols. Examples include but are not limited to glycerin, diols such as ethylene glycol or diethylene glycol; boric acid esters of polyols such as those described in U.S. Pat. Nos. 4,680,336; 4,889,664 and 5,039,459; polyvinylpyrrolidone; ethoxylated alkyl glucoside; ethoxylated bisphenol A; polyethylene glycol; mixtures of propoxylated and ethoxylated alkyl glucoside; single phase mixture of ethoxylated or propoxylated alkyl glucoside and C₂-₁₂ dihydric alcohol; adducts of ε-caprolactone and C₂-₆ alkanediols and triols; ethoxylated C₃-₆ alkanetriol; and mixtures of these as described in U.S. Pat. Nos. 5.457,140; 5,490,059, 5,490,960; 5,498,379; 5,594,043; 5,684,058; 5,736,409; 5,910,519, all of the aforementioned patents are hereby incorporated by reference in their entirety. Diluents can also be selected from the group having a combination of a defined viscosity and Hanson cohesion parameter as described in U.S. Pat. No. 4,680,336, which is hereby incorporated by reference in its entirety. The preferred liquids are aqueous salt solutions, water, and deionized water. The most preferred liquids are aqueous salt solutions, particularly, borate buffered saline solution and deionized water. Processing aids may be added to the liquids including surfactants such as Tween, methylcellulose, hydroxypropylmethylcellulose, carboxycellulose and the like, antibacterial agents, such as silver nitrates, borates and the like.

As used herein “removing” refers to any method of moving packaging liquid from the sealing portion of the ophthalmic lens package, which includes but is not limited to applying a vacuum to (pulling air past), blowing compressed air at, the sealing portion. The preferred method of removing the liquid is by applying a vacuum to the sealing portion.

Further the invention includes an apparatus for removing packaging liquid from a sealing portion of an ophthalmic lens package comprising

a means for applying a vacuum,

a support mounted on an ophthalmic lens manufacturing line,

a member attached to said support,

• • wherein said member comprises a first surface, and a second surface,
  • wherein said first surface comprises at least one first aperture, that extends through said member to at least one second aperture located on said second surface,
  • wherein said at least one first aperture is removably attached to said means for applying a vacuum
  • wherein said manufacturing line comprises at least one ophthalmic lens package comprising a sealing portion and a means for moving said ophthalmic lens package through said manufacturing line
  • wherein said sealing portion of said ophthalmic lens package is no more than about 2 mm below an area of said second surface when said ophthalmic lens package moves through said manufacturing line.

As used herein “means for applying a vacuum” include but are not limited to a vacuum pump. The preferred vacuum pump runs at a 4 to 8 cubic feet per minute (cfm). The amount of air that is pulled by the vacuum pump through each of second apertures 23, can be calculated by known methods using the velocity of the vacuum pump, the diameter (or area) of the apertures. The most preferred vacuum pump is manufactured by a GAST, Model 1023. Referring to FIG. 2, support, 13 is a removably mounted on a stationary structure of a ophthalmic lens manufacturing line (not shown). Member 17 is attached to support 13 at the third surface 18 and the fourth surface 19 (not shown). The first surface 20 of member 17 has three first apertures 21. It is preferred that the diameter of each first apertures 21 is about 4.0 mm to about 5.9 mm, more preferably about 5 mm. It is preferred that the number of first apertures 21 vary, from at least one to about 5, most preferably about three. The second surface 22 has several second apertures 23. It is preferred that the diameter of each said second apertures is about 0.75 mm to about 1.5 mm, more preferably about 1.0 mm. It is preferred that the number of second apertures 23 is about at least one to about at least 30, more preferably about 15 to about 25, most preferably about 20. Member 17 may be made from a variety of materials, including but not limited to derin, Teflon, aluminum, stanless steel, and chelated polyether ethyl ketone (“PEEK”) It is preferred that member 17 is made from aluminum.

FIG. 3 illustrates support, 13 removably mounted on a stationary structure of an ophthalmic lens manufacturing line via bolt 24. The ophthalmic lens packages 14 move along rails in the direction of arrow 15. Packages 14 contain an ophthalmic lens and a small amount of deionized water (not shown). Packages 14, have a raised sealing portion 25 surrounding the cavity 26. In the depicted embodiment packages 14 travel through the line in carriers 16. Vacuum tubing 27 is attached to the first aperture 21 (not shown) and vacuum is applied using the vacuum pump. Member 17 is pivotally mounted to support 13 at the third surface 18 (not shown) and fourth surface 19 of member 17. Member 17 is attached to support 13 at a height that allows the area of second surface 22 that surrounds second apertures 23 to contact or be no more that about 2 mm above the portion of the package that is to be heat sealed. More preferably this height is set to allow the area of second surface 22 to contact, or to be no more that about 0.5 mm above the portion of the package that is to be heat sealed. As depicted in FIG. 3, the area of second surface 22 (not shown) surrounding second apertures 23 (not shown) contacts sealing portion 25 as the package moves through the manufacturing line. When the vacuum pump is engaged, deionized water remaining on the sealing portion 25 from upstream processes is substantially removed when the apertured area of second surface 22 contacts sealing portion 25.

FIG. 4 is a perspective drawing of member 17 pivotally attached to support 13 at bolts 28. Three first apertures 21 extend from first surface 20 through member 17 and is shown in phantom by the dashed lines ( - - - ) 21a Apertures 21a extend though to a central channel 29, shown in phantom by the dashed lines ( - - - ), is perpendicular to the apertures 21a and connects all first apertures 21. Central channel 29 extends though apertures 23 and terminates on second surface 22. Preferably the each of apertures 21a have a diameter of about 4.5 mm to about 5.5, mm, more preferably about 5.1 mm. Preferably central channel 29, has a diameter of about 5 mm to about 7 mm, more preferably about 6.7 mm

In order to illustrate the invention the following examples are included. These examples do not limit the invention. They are meant only to suggest a method of practicing the invention. Those knowledgeable in the production of lenses as well as other specialties may find other methods of practicing the invention. However, those methods are deemed to be within the scope of this invention.

EXAMPLE 1

Galifilcon A contact lenses were prepared substantially as described in example 49 U.S. Pat. No. 6,822,016. The lenses were hydrated and placed into blister packages, as illustrated in U.S. Pat. No. D458,023. 500 microliters of 50 ppm methyl cellulose in aqueous saline solution was added to each package and de-ionized water droplets were added to the sealing portion of the packages. An aluminum laminate foil consisting of aluminum sandwiched between layers of polyester printing materials and oriented polypropylene (materials used to seal Acuvue® Advance™ Brand Contact Lenses). The packages were heat sealed and examined for the presence of channels in the laminate foil. Of 411 packages produced, 354 packages contained channels (86.13%)

This experiment was repeated except that the filled packages were passed under a manifold containing holes on one end and connected to a vacuum device on the other end, which operates at 4 cfm. Packages passed under the manifold on their way to the heat sealing station and were sealed and examined for channels in the same manner as above. Of 1084 packages tested, zero packages contained channels (0.00%).

Claims

1. A method of treating an ophthalmic lens package containing an ophthalmic lens and a packaging liquid prior to sealing said package with a cover comprising removing said packaging liquid from the sealing portion of said package.

2. The method of claim 1 wherein vacuum is applied to the sealing portion of said package.

3. The method of claim 2 wherein the vacuum is applied by a vacuum running at an air flow rate of about 4 to about 8 cfm.

4. The method of claim 1 wherein the ophthalmic lens is a contact lens.

5. An apparatus for removing packaging liquid from a sealing portion of an ophthalmic lens package comprising

a means for applying a vacuum,

a support mounted on an ophthalmic lens manufacturing line,

a member attached to said support, wherein said member comprises a first surface, and a second surface, wherein said first surface comprises at least one first aperture, that extends through said member to at least one second aperture located on said second surface, wherein said at least one first aperture is removably attached to said means for applying a vacuum wherein said manufacturing line comprises at least one ophthalmic lens package comprising a sealing portion and a means for moving said ophthalmic lens package through said manufacturing line wherein said sealing portion of said ophthalmic lens package is no more than about 2 mm below an area of said second surface when said ophthalmic lens package moves through said manufacturing line.

6. The apparatus of claim 5 wherein said area of said second surface surrounds said at least one second aperture.

7. The apparatus of claim 5 wherein said sealing portions comprises a raised sealing ring.

8. The apparatus of claim 5 wherein said sealing portion of said ophthalmic lens package contacts said area of said second surface when said ophthalmic lens package moves through said manufacturing line.

9. The apparatus of claim 8 wherein said sealing portion of said ophthalmic lens package comprises a raised sealing ring

10. The apparatus of claim 5 wherein said member further comprises a third surface and a second surface wherein said is pivotally attached to said support on said third surface and said fourth surface.

11. The apparatus of claim 5 comprising at least three first apertures.

12. The apparatus of claim 5 comprising at least twenty second apertures

13. The apparatus of claim 8 comprising at least three first apertures.

14. The apparatus of claim 8 comprising at least twenty second apertures.

15. The apparatus of claim 12 wherein each of said first apertures is about 5 mm.

16. The apparatus of claim 13 wherein each of said second apertures is about 1 mm

17. The apparatus of claim 5 wherein said member comprises aluminum.