gms | German Medical Science

25th Annual Meeting of the German Retina Society

German Retina Society

01.06. - 02.06.2012, Münster

Evaluating retinal toxicity of a new heavy intraocular dye using the model of perfused and isolated retinal cultures of human origin

Meeting Abstract

  • Kai Januschowski - Universitäts-Augenklinik Tübingen
  • S. Mueller - Universitäts-Augenklinik Tübingen
  • M.S. Spitzer - Universitäts-Augenklinik Tübingen
  • C. Schramm - Universitäts-Augenklinik Tübingen
  • K.-U. Bartz-Schmidt - Universitäts-Augenklinik Tübingen
  • P. Szurman - Universitäts-Augenklinik Tübingen

German Retina Society. 25th Annual Conference of the German Retina Society. Münster, 01.-02.06.2012. Düsseldorf: German Medical Science GMS Publishing House; 2012. Doc12rg56

doi: 10.3205/12rg56, urn:nbn:de:0183-12rg569

This is the English version of the article.
The German version can be found at: http://www.egms.de/de/meetings/rg2012/12rg56.shtml

Published: May 30, 2012

© 2012 Januschowski et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en). You are free: to Share – to copy, distribute and transmit the work, provided the original author and source are credited.


Outline

Text

Background: During vitreoretinal surgery vital dyes such as Brilliant Blue (BBG) are used to visualize anatomical structures. By adding deuteriumoxide (D2O) many surgeons try to create a dye mixture heavier than water to facilitate staining of the inner limiting membrane (ILM) without preceding fluid-air exchange. However, the intraocular use of D2O is critical. This study investigated the effect of 0.4 ml BBG (Brilliant Peel™ 0.25 mg/ml, Fluoron, Ulm, Germany) mixed with 0.13 ml/ml D2O on retinal function of a pseudo in vivo model using human whole mount cultures.

Methods: Human retinas were isolated and superfused with an oxygen saturated nutrient solution before the electroretinogram (ERG) was recorded. BBG mixed with 0.13 ml/ml D2O was applied epiretinally for a staining period of 60 seconds. ERG-recovery was monitored for 75 minutes. For obtaining a-waves1 mM aspartate was added to the nutrient solution.

Results: Reductions of the a- and b-wave amplitude were found directly after exposure with BBG in all test series. These effects on the electroretinogram were rapidly and completely reversible within the recovery time for all exposure times. Between the ERG-amplitudes no differences were found before and after dye application at the end of the washout.

Conclusions: The clinically used mixture of BBG and 0.13 ml/ml D2O seems to be safe for clinical use. Longer staining periods than 60 seconds were not tested.