June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Combining Iontophoresis and corneal collagen crosslinking: a basic science study on human corneas
Author Affiliations & Notes
  • Rita Mencucci
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Iacopo Paladini
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Eleonora Favuzza
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Ugo Menchini
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Mirca Marini
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Erica Sarchielli
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Barbara Gabriella Vannelli
    Ophthalmology, Eye Clinic University of Florence, Firenze, Italy
  • Footnotes
    Commercial Relationships Rita Mencucci, None; Iacopo Paladini, None; Eleonora Favuzza, None; Ugo Menchini, None; Mirca Marini, None; Erica Sarchielli, None; Barbara Gabriella Vannelli, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 5270. doi:
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      Rita Mencucci, Iacopo Paladini, Eleonora Favuzza, Ugo Menchini, Mirca Marini, Erica Sarchielli, Barbara Gabriella Vannelli; Combining Iontophoresis and corneal collagen crosslinking: a basic science study on human corneas. Invest. Ophthalmol. Vis. Sci. 2013;54(15):5270.

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

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Abstract

Purpose: To evaluate whether different UV-A treatment intensities on human corneas (ex vivo) soaked through iontophoresis procedure performed with a new hypotonic solution of riboflavin + enhancer, determine different morphological and biochemical response on the corneal tissue (epithelium, keratocytes, collagen and nerve fibers and endothelium).

Methods: Fifteen human cadaver corneas were divided in 3 different groups according to methods of soaking and UV-A intensity used: Group 1- four corneas, treated with the new riboflavin formulation using iontophoresis for 5 minutes and an irradiance power of 3 mW/cm2 for 30 minutes; Group 2 - four corneas treated with the new riboflavin formulation using iontophoresis for 5 minutes and an irradiance power of 10 mW/cm2 for 9 minutes; Group 3 - four corneas treated with the new riboflavin formulation using iontophoresis for 5 minutes without irradiance power; Group 4 - three untreated corneas utilized as control. All samples were prepared for immunohistochemical and biomolecular analysis using different markers as β catenin, connexin 43, CD34, vimentin/desmin and collagen I.

Results: Group 3 didn’t show corneal modifications and the appearance was similar to the control corneas. The crosslinking groups (Group 1 and Group 2) showed variable changes in the stroma, mainly due to keratocytes apoptosis and in relationship with the intensity of the treatment. No corneas showed signs of fibrosis with a negative Desmin-Vimentin staining. No endothelial damage was evidenced in the treated groups, nor nerve fiber alterations.

Conclusions: On the basis of this ex-vivo study, iontophoresis can be considered a potential delivery tool for riboflavin penetration in the corneal stroma. Variable morphological changes are related to different intensity of energy.

Keywords: 479 cornea: clinical science  
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