December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Laser in Situ Keratomileusis (LASIK) in Human Corneas: A New Organ Culture Model
Author Affiliations & Notes
  • SG Priglinger
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • C-A May
    Dept of Anatomy Friedrich Alexander University Erlangen Germany
  • AS Neubauer
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • CS Alge
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • AJ Mueller
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • K Ludwig
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • U Welge-Lüßen
    Dept of Ophthalmology Ludwig-Maximilians University Muenchen Germany
  • Footnotes
    Commercial Relationships   S.G. Priglinger, None; C. May, None; A.S. Neubauer, None; C.S. Alge, None; A.J. Mueller, None; K. Ludwig, None; U. Welge-Lüßen, None.
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 2082. doi:
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    • Get Citation

      SG Priglinger, C-A May, AS Neubauer, CS Alge, AJ Mueller, K Ludwig, U Welge-Lüßen; Laser in Situ Keratomileusis (LASIK) in Human Corneas: A New Organ Culture Model . Invest. Ophthalmol. Vis. Sci. 2002;43(13):2082.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To establish an in vitro model of laser in situ keratomileusis (LASIK) in human donor eyes and to test its validity in comparison with animal models. Methods: LASIK was performed on 20 organ cultured human cornea discs. The excimer laser ablations performed ranged from 0 - 12 diopters. The corneas were maintained in culture for up to 6 months and were then investigated with light and transmission electron microscopy. In addition, corneal sections were immunohistochemically stained for collagen type III, laminin and fibronectin. Results: Ultrastructural investigations in the peripheral cornea revealed a disarrangement of collagen fibers indicating scar formation. These findings were not observed in the central area. Immunohistochemical staining for fibronectin and collagen type III was detected over the entire stromal incision interface, whereas laminin staining was related to the ingrowth of epithelial cells. Conclusion: The morphological changes following LASIK in an organ culture model can simulate the in vivo situation. The model thus appears useful for further morphological investigations and for developing methods to detect LASIK in potential human donor corneas.

Keywords: 548 refractive surgery: LASIK • 370 cornea: basic science • 631 wound healing 
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