April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
The Cross-Linked Biopolymer Hyaluronic Acid as Artificial Vitreous Substitute
Author Affiliations & Notes
  • C. Frank
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • M. S. Spitzer
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • S. Henke-Fahle
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • E. Yoeruek
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • K. U. Bartz-Schmidt
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • P. Szurman
    Ophthalmology, University Eye Hospital Tuebingen, Tuebingen, Germany
  • Footnotes
    Commercial Relationships  C. Frank, None; M.S. Spitzer, None; S. Henke-Fahle, None; E. Yoeruek, None; K.U. Bartz-Schmidt, None; P. Szurman, None.
  • Footnotes
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Investigative Ophthalmology & Visual Science April 2009, Vol.50, 4445. doi:
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      C. Frank, M. S. Spitzer, S. Henke-Fahle, E. Yoeruek, K. U. Bartz-Schmidt, P. Szurman; The Cross-Linked Biopolymer Hyaluronic Acid as Artificial Vitreous Substitute. Invest. Ophthalmol. Vis. Sci. 2009;50(13):4445.

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

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Abstract

Purpose: : Aim of the study was to create an artificial vitreous substitute by cross-linking the biopolymer hyaluronic acid in order to obtain a clear, biocompatible, antiproliferative, anti-adhesive, three-dimensional hydrogel that does not change refraction.

Methods: : Different hydrogels were assembled by cross-linking hyaluronic acid either with hydrazides or by photopolymerization with UV light. To quantify the degradation of the hydrogels the release of free hyaluronic acid was measured photometrically by means of the degradation product uronic acid. Furthermore, various cell culture methods were used to monitor the in vitro effects of the hydrogels on retinal pigment epithelium cells (RPE cells).

Results: : The hydrogels were all clear and transparent, three-dimensional and rubber-like. Quantification of the degradation products revealed that only a small release occurred during the observation period of one month. No toxicity and induction of apoptosis in RPE cells was found.

Keywords: vitreous substitutes • vitreoretinal surgery • glycoconjugates/glycoproteins 
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