Ultrastructural Analysis of Rehydrated Human Donor Corneas After Air-Drying and Dissection by Femtosecond Laser

Purpose: To evaluate the efficiency of femtosecond laser (FSL) incision of rehydrated human donor corneas after air-drying and its effects on corneal structure. Methods: We compared the rehydrated and fresh-preserved corneas by microscopy following Victus-Tecnolas FSL treatment for straight-edge anterior lamellar keratoplasty (ALK). The corneas were dehydrated at room temperature under a laminar-flow hood. Results: To obtain the horizontal cut in rehydrated corneas, we increased the FSL pulse energy to 1.2 μJ from 0.80 μJ applied for the fresh corneas and obtained a clear-cut separation of the lamellar lenticule cap from the corneal bed. Light microscopy showed regular arrangement of stromal collagen lamellae, with spaces in between the fibers in the corneal stroma in the fresh and the rehydrated corneas, but the uppermost epithelial layers in the rehydrated corneas were lost. Transmission electron microscopy (TEM) revealed no signs of thermal or mechanical damage to the corneal structure. The epithelial basal membrane and Bowman's layer maintained their integrity. The epithelial basal layer and cells were separated by large spaces due to junction alteration in the rehydrated corneas. There were gaps between the lamellar layers in the stroma, especially in the rehydrated corneas. Keratocytes displayed normal structure in the fresh corneas but were devoid of microorganules in the rehydrated corneas. Minor irregularities were observed in the vertical incision and the horizontal stroma appeared smooth on scanning electron microscopy. Conclusion: The corneal stroma of rehydrated corneas maintained morphology and integrity, while corneal cellular components were generally altered. When corneas are intended for FSL-assisted ALK, effective stromal bed incision is best achieved at a laser power higher than that currently adopted for fresh corneas.

[1]  D. Ponzin,et al.  Gram stain and addition of amphotericin B to improve the microbial safety of human donor corneas , 2021, Cell and Tissue Banking.

[2]  D. Ponzin,et al.  Corneal transplantation during the COVID-19 pandemic: An operational guide , 2021, European journal of ophthalmology.

[3]  G. Virgili,et al.  Effect of COVID-19-related lockdown on ophthalmic practice in Italy: A report from 39 institutional centers , 2021, European journal of ophthalmology.

[4]  G. Marchini,et al.  Femtosecond Laser-Assisted Big-Bubble Deep Anterior Lamellar Keratoplasty , 2021, Clinical ophthalmology.

[5]  J. Mehta,et al.  Femtolaser-assisted keratoplasty: Surgical outcomes and benefits , 2020 .

[6]  S. Chaurasia,et al.  A review of long-term corneal preservation techniques: Relevance and renewed interests in the COVID-19 era , 2020, Indian journal of ophthalmology.

[7]  H. Dua,et al.  Lamellar keratoplasty techniques , 2018, Indian journal of ophthalmology.

[8]  P. Gain,et al.  Comparison of four methods of surface roughness assessment of corneal stromal bed after lamellar cutting. , 2017, Biomedical optics express.

[9]  Kerri L. Colman,et al.  The effect of repeated freeze‐thaw cycles on human muscle tissue visualized by postmortem computed tomography (PMCT) , 2017, Clinical anatomy.

[10]  Neeti Gupta,et al.  Use of glycerol-preserved corneas for corneal transplants , 2017, Indian journal of ophthalmology.

[11]  R. Tandon,et al.  Long-term preservation of donor corneas in glycerol for keratoplasty: exploring new protocols , 2015, British Journal of Ophthalmology.

[12]  A. Russo,et al.  Long-Term Dehydrated Donor Lamella Survival in Anterior Keratoplasty: Keratocyte Migration and Repopulation of Corneal Stroma , 2015, Cornea.

[13]  N. Marsit,et al.  Substantiation of 25 kGy radiation sterilization dose for banked air dried amniotic membrane and evaluation of personnel skill in influencing finished product bioburden , 2014, Cell and Tissue Banking.

[14]  D. Peyrot,et al.  Wavelength optimization in femtosecond laser corneal surgery. , 2013, Investigative ophthalmology & visual science.

[15]  A. Chao,et al.  Eye preservation tectonic graft using glycerol-preserved donor cornea , 2012, Eye.

[16]  W. Stark,et al.  The Intraoperative Impression and Postoperative Outcomes of Gamma-Irradiated Corneas in Corneal and Glaucoma Patch Surgery , 2011, Cornea.

[17]  A. Russo,et al.  Deep anterior lamellar keratoplasty with dehydrated, 4 °C-stored, and rehydrated lenticules. , 2011, European journal of ophthalmology.

[18]  W. Armitage,et al.  Preservation of Human Cornea , 2011, Transfusion Medicine and Hemotherapy.

[19]  E. Pels,et al.  Organ culture preservation for corneal tissue. Technical and quality aspects. , 2009, Developments in ophthalmology.

[20]  L. Sousa,et al.  Light and Transmission Electronic Microscopy Evaluation of Lyophilized Corneas , 2008, Cornea.

[21]  J. Mehta,et al.  Future Directions in Lamellar Corneal Transplantation , 2007, Cornea.

[22]  J. M. Villalba,et al.  Keratocyte injury in human corneas cryopreserved under standard conditions , 2004, Cell and Tissue Banking.

[23]  J. Kirwan,et al.  Deep lamellar keratoplasty with lyophilised tissue in the management of keratoconus , 2001, The British journal of ophthalmology.

[24]  M. D. Merindano,et al.  Long-Term Cryopreservation of Human Donor Corneas , 1996, European journal of ophthalmology.

[25]  C. Sheard,et al.  Deep lamellar keratoplasty on air with lyophilised tissue. , 1992, The British journal of ophthalmology.

[26]  I. Fazzari [Stroma]. , 2020, Rassegna clinico-scientifica.