Device for separating the epithelium layer from the surface of the cornea of an eye

Information

  • Patent Grant
  • 7708750
  • Patent Number
    7,708,750
  • Date Filed
    Wednesday, February 25, 2004
    21 years ago
  • Date Issued
    Tuesday, May 4, 2010
    15 years ago
Abstract
An automated mechanical device separates the epithelial layer of a cornea from the cornea. The device includes a separator such as a plate, wire or dull blade. The device can preserve a separated epithelial layer as a disk without rupturing the disk and without substantial epithelial cell loss. The epithelial layer is separated from the cornea without cutting the cornea.
Description
BACKGROUND

LASIK (Laser-Assisted In Situ Keratomileusis) is a surgical procedure intended to reduce a person's dependency on glasses or contact lenses. LASIK permanently changes the shape of the cornea, the clear covering of the front of the eye, using an excimer laser. A device, called a microkeratome, is used to cut a flap in the cornea. A hinge is left at one end of this flap. The flap is folded back revealing the stroma, the middlesection of the cornea. Pulses from a computer-controlled laser vaporize a portion of the stroma and the flap is replaced. It is important that the knife used during the LASIK procedure is sharp, otherwise the quality of the procedure and the healing time are poor. Additionally the knife has to be sharp in order to produce consistent and reproducible flaps. There are some complications related to the use of microkeratomes. The most common complication is the creation of an irregular flap, for example, a half flap, buttonhole, or total cup. These complications represent irregular incisions of the cornea, a situation that can permanently degrade visual performance.


Before LASIK, PRK (Photo-Refractive Keratectomy) was used to correct the curvature of the cornea. A physician could scrape away a superficial layer, e.g., the epithelium, of the cornea. After the superficial layer was removed, laser treatment was applied on to the exposed surface of the cornea. A problem existed, however, in that the healing period for the eye typically lasted for a week, much longer than the healing period of LASIK. Also, the patient experienced a lot of pain during healing. Typically in PRK a disposable contact lens is used to cover the treated area of the cornea and help reduce postoperative pain.


In another technique, LASEK (Laser Epithelial Keratomileusis) the epithelial layer is separated from the surface of the cornea in a manner that the separated epithelial layer can be preserved. First, the epithelium is treated with and alcohol solution to partially devitalize it. Once the exact surface area of treatment is determined, a few drops of a weak alcohol solution is applied to the surface of the cornea and allowed to stay in contact with the epithelium for a few seconds. This weak alcohol solution is then rinsed off the surface of the eye. The function of the weak alcohol solution is to loosen the epithelial layer (50 microns) and to allow it to be peeled back in a sheet of epithelial cells, thereby exposing the underlying cornea. This is not to be confused with LASIK, which actually uses a microkeratome instrument to create a flap of both epithelium and the front part of the stromal tissue measuring anywhere between 130 to 180 microns.


In LASEK, the epithelium-only layer is laid back in a similar fashion to LASIK, but consists of only epithelium, not corneal stroma. Once the epithelial cells have been laid out of the way, the laser is applied to the surface of the cornea in the exact same fashion as in PRK. Once the laser treatment has been completed, the epithelial layer is laid back into place and a soft contact lens is placed over the eye as in PRK. The epithelial cells, which were partly devitalized by the weak alcohol solution, are laid over the treatment area and may serve as a facilitator of new epithelium healing underneath. The alcohol-devitalized epithelium falls off the eye, similar to a scab, in 5-10 days. These devitalized epithelial cells do not become the new surface of the eye, but simply serve as a protective agent in addition to the contact lens to facilitate comfort and healing of the new underlying epithelium. Alcohol treatment of the epithelium results in a severe amount of epithelial cell loss, a fact that may render the epithelial disk not usable, due to the reduced durability and adhesion on to the cornea.


Thus, there is a need for an automated corneal epithelium separator that addresses the above problems by separating the epithelial layer as a whole in a mechanical way, not chemical.


BRIEF SUMMARY

To help correct an imperfect vision of a patient's eye, an automated mechanical device separates the epithelial layer from the cornea of a patient's eye from the cornea. After the epithelial layer is separated from the cornea, a laser is used to help correct imperfections in the cornea. Thereafter, the epithelial layer is placed back on the cornea to reduce the visual rehabilitation period and reduce postoperative pain.


In one aspect, the device includes a separator such as a plate, wire or dull blade. The device can preserve a separated epithelial layer as a disk without rupturing the disk and without substantial epithelial cell loss. The epithelial layer is separated from the cornea without cutting the cornea.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a diagram showing a side view of an eye and a cornea separator with a separator located in a first position according to the preferred embodiments.



FIG. 2 is a diagram showing a top view of the eye and the separator located in a first position according to the preferred embodiments.



FIG. 3 is a diagram showing a side view of the eye and the separator located in a second position according to the preferred embodiments.



FIG. 4 is a diagram showing a top view of the eye and the separator located in a second position according to the preferred embodiments.



FIG. 5 is a diagram showing a side view of the eye and the separator located in a third position according to the preferred embodiments.



FIG. 6 is a diagram showing a top view of the eye and the separator located in a third position according to the preferred embodiments.



FIG. 7 is a diagram showing a side view of the eye and the separator located in a fourth position according to the preferred embodiments.



FIG. 8 is a diagram showing a top view of the eye and the separator located in a fourth position according to the preferred embodiments.



FIG. 9 is a diagram showing a top view of the eye and the separator located in a fifth position according to the preferred embodiments, the separator is retracted after epithelial separation.



FIG. 10 is a diagram showing a top view of the eye with the separator removed.



FIG. 11 is a diagram showing a top view of the eye after ablations is performed with a laser.



FIG. 12 is a diagram showing a top view of the eye with the epithelium replaced on the eye.



FIG. 13. is a diagram showing a top view of the eye with the epithelium smoothly stretched into place.



FIG. 14 is a diagram showing a side view of the eye and the cornea separator device including a rotating drum.



FIG. 15 is a diagram showing a front view of the eye and the cornea separator device including the rotating drum.



FIG. 16 is a diagram showing a top view of the eye and the cornea separator device including the rotating drum.



FIG. 17 is a diagram showing a drum according to one embodiment.



FIG. 18 is a diagram showing a drum according to another embodiment.





DETAILED DESCRIPTION

To help correct an imperfect vision of a patient's eye, an automated mechanical device separates the epithelial layer from the cornea of a patient's eye from the cornea. A separator, such as a plate, wire or dull blade is used to separate the epithelial layer of the cornea from the basal membrane. In this way, the automated mechanical device can preserve the separated epithelial layer as a disk without rupturing the disk and without substantial epithelial cell loss, less than 5-10% loss, to ensure viability and stability of the epithelial disk after replacement on the surface of the cornea. After the epithelial layer is separated from the cornea, a laser is used to help correct imperfections in the cornea. Thereafter, the epithelial layer is placed back on the cornea to aid in the healing process of the eye.



FIG. 1 is a diagram showing a side view of an eye 10 of a patient and a cornea separator device 12. The cornea separator device 12 includes a separator 14, shown here in a first position located away from the eye 10. The separator 14 includes a device that can scrape the epithelium from the cornea such as a plate, a wire or a knife with a dull edge. The separator 14 removes an epithelium layer 16 located above a corneal surface 18 of the eye 10. The separator 14 is not sharp enough to excise corneal tissue during operation of the cornea separator device 12.


Referring also to FIG. 2, the cornea separator device 12 includes a ring 20 that sits on the eye 10 with its plane parallel to a limbus of the eye. The ring 20 includes an internal diameter 22 ranging from about 10 to about 12 mm and external diameter 24 from about 13 to about 16 mm and including a groove 26 (best seen in FIG. 15). The groove 26 is dimensioned wider than the internal diameter 22. A separator support 28 fits in the groove 26 to carry the separator 14 on a determined travel.


An oscillation device 30 provides motion and vibration to the separator 14. The oscillation device 30 can oscillate the separator 14 either transversely or longitudinally with frequency ranging from about 10 Hz to about 10 KHz. Electromagnetic or piezoelectric forces on the separator 14 can provide the oscillation, or external rotating or vibrating wires can provide the oscillation. To maintain the ring 20 on the eye 10, for example during oscillation, the ring 20 can include a circumferential groove 32 positioned on a side of the eye 10. Suction can be applied to the circumferential groove 32 to ensure stable mounting of the ring 20 to the eye 10.



FIGS. 3 and 4 are diagrams showing a side and a top view, respectively, of the eye 10 and the separator 14 located in a second position with respect to the eye. As the separator 14 travels to contact the eye 10, the corneal surface 18 is flattened. To accommodate the travel of the separator 14, the separator support 28 freely slides in the groove 26, for example, when driven by the oscillation device 30.



FIGS. 5 and 6 are diagrams showing a side and a top view of the eye 10 and the separator 14 located in a third position. As the separator 14 travels along the cornea 10, the epithelium layer 16 is separated from the cornea. The separator 14 separates the epithelium layer 16 without cutting the cornea 18.



FIGS. 7 and 8 are diagrams showing a side and a top view of the eye 10 and the separator 14 located in a fourth position. In one embodiment, the travel of the separator 14 is controlled to produce an epithelial disk 34 hinged at an edge 36 of the epithelial disk 34. In another embodiment the epithelial disk 34 is completely detached for the corneal surface 18, for example, as described below.



FIG. 9 is a diagram showing a top view of the eye 10 and the separator 14 located in a retracted position after the epithelial disk 34 as been formed. After the separator 14 is retracted, suction to the circumferential groove 32 is turned off and the cornea separator device 12 is removed from the eye 10. Referring also to FIG. 10, after the cornea separator device 12 is removed, a deepithelialized area 38 is exposed that corresponds to a shape and size of the area that the separator 14 contacted during travel.



FIG. 11 shows a top view of the eye 10 after laser ablation is performed. The laser ablation forms an irradiated area 40 on the eye 10. Referring to FIG. 12, thereafter, the epithelium disk 34 is replaced on the corneal surface 18 of the eye 10 to aid in the healing process. Referring to FIG. 13, once replaced on the corneal surface 18, the epithelium disk 34 is preferably smoothly stretched into place.



FIG. 14 is a diagram showing a side view of the eye 10 and the cornea separator device 12 including rotating drum 42. To rotate the drum 42, the cornea separator device 12 may include a rotating gear 44. The gear 44 could also be used to provide movement to the separator support 28. Referring also to FIGS. 15 and 16, front and top views, respectively, of the cornea separator device 12, the rotating gears 44 could be bilaterally placed on the separator support 28. The oscillating device 30 can provide for rotation of the gears 44 and the gears 44 can travel on rails, for example toothed rails, which run parallel to the groove 26.


Since a typical thickness of an epithelial disk 36 includes about 50 microns, to preserve an epithelial disk 36, a separated epithelial disk 36 is rolled onto the drum 42. The drum 42 can include a diameter ranging from about 3 to about 9 mm and a length of about 12 mm. Referring also to FIG. 17, in one embodiment, to maintain integrity of the epithelial disk 36, the drum 42 can be coated with a hydrating and/or a conditioning substrate. The hydrating and/or conditioning substrate can include, for example, HEMA contact lenses, tissue culture media, silicone and biocompatible hydrogels. The hydrating and/or conditioning substrate can be removed from the drum after the epithelial disk 36 attaches on to the drum. Thereafter, the epithelial disk 36 can be removed from the drum 46 and replaced on the corneal surface 16, as described above.



FIG. 18 shows another embodiment of the drum 42 includes apertures 46 and a connector 48 that connects to a suction source (not shown). By applying suction to the apertures 46 of the drum 42, the epithelial disk 36 can be rolled onto the drum 42. Thereafter, the epithelial disk 36 can be removed from the drum 46 and replaced on the corneal surface 16, as described above.


While the invention has been described above by reference to various embodiments, it will be understood that many changes and modifications can be made without departing from the scope of the invention. It is therefore intended that the foregoing detailed description be understood as an illustration of the presently preferred embodiments of the invention, and not as a definition of the invention. It is only the following claims, including all equivalents, which are intended to define the scope of this invention.

Claims
  • 1. An automated mechanical device to separate the epithelial layer of a cornea from the cornea, the device comprising: a separator, where said device can preserve the separated epithelial layer as a disk without rupturing said disk and without substantial epithelial cell loss;a ring configured to seat on the eye with its plane parallel to a limbus, and having an internal diameter ranging from about 10 to about 12 mm and external diameter from about 13 to about 16 mm including a groove, where said groove is wider than the internal diameter;a separator support that fits in said groove to carry the separator on a determined travel;an oscillation device that provides motion and vibration to the separator, wherein the separator oscillates with frequency ranging from about 10 Hz to about 10 KHz; androtating gears where a motion of the separator support is provided by the rotating gears placed on the support, where rotation to the gears is provided by said oscillating device and said rotating gears are traveling on toothed rails that are parallel to the groove.
  • 2. The device as claimed in claim 1 where said separator is not capable of excising corneal tissue during operation.
  • 3. The device as claimed in claim 1 where a travel of the separator is controlled to produce an epithelial disk hinged to the border of separation.
  • 4. The device as claimed in claim 1 where the ring includes a circumferential groove on the side of the eye and suction is applied to the circumferential groove to ensure stable mounting of the ring.
  • 5. The device as claimed in claim 1 where the ring includes a circumferential groove on the side contacting the eye and suction is applied to ensure stable mounting of the ring.
  • 6. The device as claimed in claim 1 where the separator oscillation is provided by electromagnetic forces on the separator.
  • 7. The device as claimed in claim 1 where the separator oscillation is provided by piezoelectric forces on the separator.
  • 8. The device as claimed in 1 where the separator oscillation is provided by external rotating or vibrating wires.
  • 9. The device as claimed in claim 1 where the separator support freely slides in the groove.
  • 10. The device as claimed in claim 9 where the separator support slides in the groove when driven by the oscillating device.
  • 11. The device as claimed in claim 1 further including a rotating drum configured so that the separated epithelial disk is rolled on the drum.
  • 12. The device as claimed in claim 11 wherein said drum includes a diameter ranging from about 3 to about 9 mm.
  • 13. The device as claimed in claim 12 where said drum is coated with at least one of a hydrating substrate and a conditioning substrate.
  • 14. The device as claimed in claim 13 where said at least one of the hydrating substrate and conditioning substrate is selected from the group consisting of HEMA contact lenses, tissue culture media, silicone and biocompatible hydrogels.
  • 15. The device as claimed in claim 13 where said hydrating and conditioning substrate can be removed from the drum after the epithelial disk attaches on to the drum.
  • 16. The device as claimed in claim 11 where said drum includes a hollow interior.
  • 17. The device as claimed in claim 16 where a surface of the drum includes holes.
  • 18. The device as claimed in claim 17 where said holes communicate with the hollow interior of the drum to connect to air suction through the hollow interior of said drum.
RELATED APPLICATION

This application is a Continuation of U.S. patent application Ser. No. 09/911,356, filed Jul. 23, 2001, now U.S. Pat. No. 7,156,859 entitled “Device for Separating the Epithelium Layer From the Surface of the Cornea of an Eye” which is hereby incorporated by reference herein.

US Referenced Citations (221)
Number Name Date Kind
2881500 Furness Apr 1959 A
4198132 Seger et al. Apr 1980 A
4346482 Tennant et al. Aug 1982 A
4381007 Doss Apr 1983 A
4414974 Dotson et al. Nov 1983 A
4417579 Soloviev et al. Nov 1983 A
4451254 Dinius et al. May 1984 A
4473076 Williams et al. Sep 1984 A
4501274 Skjaerpe Feb 1985 A
4576164 Richeson Mar 1986 A
4646720 Peyman et al. Mar 1987 A
4659584 Schlik Apr 1987 A
4662370 Hoffmann et al. May 1987 A
4662881 Nordan May 1987 A
4665914 Tanne May 1987 A
4676790 Kern Jun 1987 A
4688570 Kramer et al. Aug 1987 A
4715858 Lindstrom Dec 1987 A
4731079 Stoy Mar 1988 A
4770172 L'Esperance, Jr. Sep 1988 A
4773414 L'Esperance, Jr. Sep 1988 A
4775361 Jacques et al. Oct 1988 A
4793344 Cumming et al. Dec 1988 A
4798204 L'Esperance, Jr. Jan 1989 A
4838266 Koziol et al. Jun 1989 A
4840175 Peyman Jun 1989 A
4844060 Krumeich Jul 1989 A
4858324 Wiech, Jr. Aug 1989 A
4865033 Krumeich et al. Sep 1989 A
4884570 Krumeich et al. Dec 1989 A
4941093 Marshall et al. Jul 1990 A
4955894 Herman Sep 1990 A
5011498 Krumeich et al. Apr 1991 A
5063942 Kilmer et al. Nov 1991 A
5098444 Feaster Mar 1992 A
5108388 Trokel Apr 1992 A
5108412 Krumeich et al. Apr 1992 A
5133726 Ruiz et al. Jul 1992 A
5133747 Feaster Jul 1992 A
5163934 Munnerlyn Nov 1992 A
5163956 Liu et al. Nov 1992 A
5171318 Gibson et al. Dec 1992 A
5192316 Ting Mar 1993 A
5196027 Thompson et al. Mar 1993 A
5213720 Civerchia May 1993 A
5215104 Stenert Jun 1993 A
5269795 Arnott Dec 1993 A
5279611 McDonnell et al. Jan 1994 A
5292329 Werner Mar 1994 A
5308355 Dybbs May 1994 A
5312330 Klopotek May 1994 A
5312413 Eaton et al. May 1994 A
5318044 Kilmer et al. Jun 1994 A
5318047 Davenport et al. Jun 1994 A
5319424 Tomiyama Jun 1994 A
5323788 Silvestrini et al. Jun 1994 A
5368604 Kilmer et al. Nov 1994 A
5374515 Parenteau et al. Dec 1994 A
5376099 Ellis et al. Dec 1994 A
5395385 Kilmer et al. Mar 1995 A
5403335 Loomas et al. Apr 1995 A
5423801 Marshall et al. Jun 1995 A
5423843 Werner Jun 1995 A
5437658 Muller et al. Aug 1995 A
5458610 Feaster Oct 1995 A
5462739 Dan et al. Oct 1995 A
5464417 Eick Nov 1995 A
5490849 Smith Feb 1996 A
5492135 DeVore et al. Feb 1996 A
5496339 Koepnick Mar 1996 A
5505723 Muller Apr 1996 A
5522888 Civerchia Jun 1996 A
5549597 Shimmick et al. Aug 1996 A
5549599 Sumiya Aug 1996 A
5549632 Lai Aug 1996 A
5554155 Awh et al. Sep 1996 A
5556406 Gordon et al. Sep 1996 A
5569292 Schemberger et al. Oct 1996 A
5571124 Zelman Nov 1996 A
5599341 Mathis et al. Feb 1997 A
5603709 Johnson Feb 1997 A
5613965 Muller Mar 1997 A
5616139 Okamoto Apr 1997 A
5630810 Machat May 1997 A
5632757 Arnott May 1997 A
5634920 Hohla Jun 1997 A
5647865 Swinger Jul 1997 A
5649943 Amoils Jul 1997 A
5658303 Koepnick Aug 1997 A
5676679 Simon et al. Oct 1997 A
5685998 Shannon et al. Nov 1997 A
5690657 Koepnick Nov 1997 A
5699810 Pallikaris Dec 1997 A
5700274 Feaster Dec 1997 A
5711762 Trokel Jan 1998 A
5716633 Civerchia Feb 1998 A
5722427 Wakil et al. Mar 1998 A
5722971 Peyman Mar 1998 A
5735843 Trokel Apr 1998 A
5740803 Gray et al. Apr 1998 A
5741245 Cozean et al. Apr 1998 A
5766200 Mazurek et al. Jun 1998 A
5779696 Berry et al. Jul 1998 A
5779711 Kritzinger et al. Jul 1998 A
5779724 Werner Jul 1998 A
5782852 Foggia et al. Jul 1998 A
5795351 Clapham Aug 1998 A
5803923 Singh-Derewa et al. Sep 1998 A
5807380 Dishler Sep 1998 A
5807381 Lieberman Sep 1998 A
5827641 Parenteau et al. Oct 1998 A
5833701 Gordon Nov 1998 A
RE35974 Davenport et al. Dec 1998 E
5851213 Berleth et al. Dec 1998 A
5857995 Thomas et al. Jan 1999 A
RE36150 Gupta Mar 1999 E
5879363 Urich Mar 1999 A
5904678 Pop May 1999 A
5919185 Peyman Jul 1999 A
5934285 Kritzinger et al. Aug 1999 A
5941874 Hohla Aug 1999 A
5947987 Gordon et al. Sep 1999 A
5964748 Peyman Oct 1999 A
5970984 Wakil et al. Oct 1999 A
5975351 DeLacerda Nov 1999 A
5980543 Carriazo et al. Nov 1999 A
5984916 Lai Nov 1999 A
5989272 Barron et al. Nov 1999 A
5997559 Ziemer Dec 1999 A
6006756 Shadduck Dec 1999 A
6030376 Arashima et al. Feb 2000 A
6030398 Klopotek Feb 2000 A
6036683 Jean et al. Mar 2000 A
6045562 Amano et al. Apr 2000 A
6050999 Paraschac et al. Apr 2000 A
6059775 Nielson May 2000 A
6068625 Clapman May 2000 A
6068640 Gordon et al. May 2000 A
6071293 Krumeich Jun 2000 A
6079417 Fugo Jun 2000 A
6083236 Feingold Jul 2000 A
6099541 Klopotek Aug 2000 A
6110202 Barraquer et al. Aug 2000 A
6126668 Bair et al. Oct 2000 A
6129723 Anderson et al. Oct 2000 A
6132421 Clapham Oct 2000 A
6162210 Shadduck Dec 2000 A
6171336 Sawusch Jan 2001 B1
6187053 Minuth Feb 2001 B1
6203538 Peyman Mar 2001 B1
6203555 Amano Mar 2001 B1
6206900 Tabatabaei et al. Mar 2001 B1
6217571 Peyman Apr 2001 B1
6221067 Peyman Apr 2001 B1
6228025 Hipps et al. May 2001 B1
6231583 Lee May 2001 B1
6241721 Cozean et al. Jun 2001 B1
6254619 Garabet et al. Jul 2001 B1
6264648 Peyman Jul 2001 B1
6280435 Odrich et al. Aug 2001 B1
6280469 Terry et al. Aug 2001 B1
6280470 Peyman Aug 2001 B1
6293938 Muller et al. Sep 2001 B1
6302896 Carriazo et al. Oct 2001 B1
6306075 Shadduck Oct 2001 B1
6322216 Yee et al. Nov 2001 B1
6331177 Munnerlyn et al. Dec 2001 B1
6335006 Miller Jan 2002 B1
6350236 Hipps et al. Feb 2002 B1
6379370 Feinsod Apr 2002 B1
6391055 Ikada et al. May 2002 B1
6409345 Molebny et al. Jun 2002 B1
6436093 Ruiz et al. Aug 2002 B1
6451039 Richey, Jr. et al. Sep 2002 B1
6458141 Peyman Oct 2002 B1
6464692 Ruiz et al. Oct 2002 B1
6468206 Hipps et al. Oct 2002 B1
6468642 Bray et al. Oct 2002 B1
6482153 Hipps et al. Nov 2002 B1
6497701 Shimmick et al. Dec 2002 B2
6506198 Amano Jan 2003 B1
6530916 Shimmick Mar 2003 B1
6543453 Klima et al. Apr 2003 B1
6544286 Perez Apr 2003 B1
6551307 Peyman Apr 2003 B2
6589558 Pallikaris Jul 2003 B1
6599305 Feingold Jul 2003 B1
6607527 Ruiz et al. Aug 2003 B1
6623497 Feingold Sep 2003 B1
6626924 Klopotek Sep 2003 B1
6638271 Munnerlyn et al. Oct 2003 B2
6666855 Somani et al. Dec 2003 B2
6673062 Yee et al. Jan 2004 B2
6702807 Peyman Mar 2004 B2
6702832 Ross et al. Mar 2004 B2
6706036 Lai Mar 2004 B2
6730073 Bruce May 2004 B2
20010027314 Peyman Oct 2001 A1
20010053917 Lin et al. Dec 2001 A1
20020026101 Bookwalter Feb 2002 A1
20020026240 Pallikaris et al. Feb 2002 A1
20020052596 Pallikaris et al. May 2002 A1
20020052614 GeBauer May 2002 A1
20020077640 Metzger Jun 2002 A1
20020107508 Burnett Aug 2002 A1
20020116056 Kirk Aug 2002 A1
20020119141 Karageozian Aug 2002 A1
20020135736 Stark et al. Sep 2002 A1
20020138069 Peyman Sep 2002 A1
20030011745 Molebny et al. Jan 2003 A1
20030018347 Pallikaris et al. Jan 2003 A1
20030018348 Pallikaris et al. Jan 2003 A1
20030083743 Perez May 2003 A1
20030105521 Perez Jun 2003 A1
20030139755 Dybbs Jul 2003 A1
20030220653 Perez Nov 2003 A1
20040059361 Feingold Mar 2004 A1
20040073246 Aufure et al. Apr 2004 A1
20040097955 Feingold May 2004 A1
20040167555 Pallikaris et al. Aug 2004 A1
20040220599 Pallikaris et al. Nov 2004 A1
Foreign Referenced Citations (41)
Number Date Country
2355478 Feb 2002 CA
1259032 Jul 2000 CN
27 50 492 May 1979 DE
38 38 253 May 1990 DE
3838253 May 1990 DE
G93 15 396.1 Feb 1994 DE
297 14 266 Dec 1997 DE
297 12 339 Jan 1998 DE
298 05 538 Jul 1998 DE
298 10 603 Dec 1998 DE
198 47 089 May 2000 DE
201 07 259 Dec 2001 DE
201 15 585 Feb 2002 DE
100 51 215 May 2002 DE
101 19 477 Oct 2002 DE
200 23 239 Aug 2003 DE
202 04 635 Sep 2003 DE
102 14 917 Oct 2003 DE
102 32 169 Feb 2004 DE
0 659 955 Aug 1994 EP
0 659 955 81 Jan 1997 EP
0 873 735 Oct 1998 EP
0 956 840 Nov 1999 EP
0956 840 Nov 1999 EP
1 114 628 Jul 2001 EP
1 181 913 Feb 2002 EP
1 199 055 Apr 2002 EP
1 350 492 Oct 2003 EP
2 691 625 Dec 1993 FR
2000 245766 Sep 2000 JP
2002119532 Apr 2002 JP
WO 9417851 Aug 1994 WO
WO 9720529 Jun 1997 WO
WO 9853774 Dec 1998 WO
WO 0193791 Dec 2001 WO
WO 0197729 Dec 2001 WO
WO 0206883 Jan 2002 WO
WO 03009789 Feb 2003 WO
WO 03026542 Apr 2003 WO
WO 03061518 Jul 2003 WO
WO 2006017835 Feb 2006 WO
Related Publications (1)
Number Date Country
20040167555 A1 Aug 2004 US
Continuations (1)
Number Date Country
Parent 09911356 Jul 2001 US
Child 10786350 US