June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
PRGF-Endoret enhances stromal wound healing after additive surgery in deep stroma for 7 days
Author Affiliations & Notes
  • Lucia Ibares-Frias
    Universidad de Valladolid, Grupo de Técnicas Ópticas de Diagnóstico, Valladolid, Spain
    Universidad de Valladolid, Hospital Clínico Universitario de Valladolid, Valladolid, Spain
  • Patricia Gallego
    Histology & Molecular Biology, University of Valladolid, Valladolid, Spain
    Universidad de Valladolid, Grupo de Técnicas Ópticas de Diagnóstico, Valladolid, Spain
  • Roberto Cantalapiedra
    Histology & Molecular Biology, University of Valladolid, Valladolid, Spain
  • Gorka Orive
    Biotechnology, BTI, Vitoria, Spain
  • Jesus Merayo-Lloves
    Universidad de Valladolid, Grupo de Técnicas Ópticas de Diagnóstico, Valladolid, Spain
    Universidad de Oviedo, Fundación de Investigación Oftalmológica, Oviedo, Spain
  • Carmen Martínez-García
    Histology & Molecular Biology, University of Valladolid, Valladolid, Spain
    Universidad de Valladolid, Grupo de Técnicas Ópticas de Diagnóstico, Valladolid, Spain
  • Footnotes
    Commercial Relationships Lucia Ibares-Frias, None; Patricia Gallego, None; Roberto Cantalapiedra, None; Gorka Orive, BTI (E); Jesus Merayo-Lloves, None; Carmen Martínez-García, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 712. doi:
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      Lucia Ibares-Frias, Patricia Gallego, Roberto Cantalapiedra, Gorka Orive, Jesus Merayo-Lloves, Carmen Martínez-García, Grupo de Técnicas Ópticas de diagnóstico; PRGF-Endoret enhances stromal wound healing after additive surgery in deep stroma for 7 days. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):712.

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

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Abstract

Purpose: To compare clinical and histological outcomes after intracorneal ring segment (ICRS) implantation with and without plasma rich in growth factors (PRGF-Endoret) covering the segment

Methods: We performed surgery for this study on hens as an animal model. We used 36 eyes which were randomly divided into two groups. In the first group we implanted one segment per eye by a manual technique. In the second group we implanted the ICRS immersed in PRGF. Hens were also separated into 3 groups (48 hours, 7 days, and 1month) regarding the time they were killed and then corneal tissue was fixed for histological analysis and immunofluorescency studies. Clinical examination and measurements of the refractive error were carried out with a specific device at different time points. Quantitative measurements of the histological preparations were also performed. SPSS 20 Statistical software was used. An independent T Student Test or Mann-Whitney U test was used to compare means of measurements in both groups. A p value less than 0.05 was considered to be statistically significant.

Results: In the ICRS-PRGF group more deposits were found at 7 days, later there were no clinical differences. Histologically corneal thickness at 48 hours was thinner in the ICRS-PRGF group. At 7 days in the PRGF group there were double the number of cells around the segment compared with the ICRS group. These cells had different morphologies resembling fibroblast and immature cells. TUNEL positive cells in ICRS-PRGF group appeared for more than 7 days at the same time and BrdU positive cells were found which is indicative of cell exchange.

Conclusions: Our results indicated that PRGF-Endoret in clinical and histological response after implantation of ICRS in an experimental animal model enhances proliferation and apoptosis of cells for 7 days after administration.

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