May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
In vitro Evaluation of New Methods to Remove Lens Epithelial Cells During Cataract Surgery to Prevent Posterior Capsule Opacification
Author Affiliations & Notes
  • U.B. Kottler
    Department Ophthalmology, University Erlangen–Nurnberg, Erlangen, Germany
  • T. Dietrich
    Department Ophthalmology, University Erlangen–Nurnberg, Erlangen, Germany
  • U. Schlötzer–Schrehardt
    Department Ophthalmology, University Erlangen–Nurnberg, Erlangen, Germany
  • K. Blüthner
    Department Ophthalmology, University Erlangen–Nurnberg, Erlangen, Germany
  • F.E. Kruse
    Department Ophthalmology, University Erlangen–Nurnberg, Erlangen, Germany
  • Footnotes
    Commercial Relationships  U.B. Kottler, None; T. Dietrich, None; U. Schlötzer–Schrehardt, None; K. Blüthner, None; F.E. Kruse, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 2862. doi:
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      U.B. Kottler, T. Dietrich, U. Schlötzer–Schrehardt, K. Blüthner, F.E. Kruse; In vitro Evaluation of New Methods to Remove Lens Epithelial Cells During Cataract Surgery to Prevent Posterior Capsule Opacification . Invest. Ophthalmol. Vis. Sci. 2005;46(13):2862.

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

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Abstract

Abstract: : Purpose: The proliferation of lens epithelial cells (LEC) remaining in the equatorial region of the lens capsule after cataract surgery is known to be responsible for formation of posterior capsule opacification (PCO). The SCI system (Sealed Capsule Irrigation) offers the opportunity to seal the capsular bag after capsulorrhexis and to apply toxic or antiproliferative substances. In vivo, distilled water appears to reduce capsule fibrosis and opacification, but dose–response curves have not been established. Methods: Bovine LEC were cultured in black 96–well–plates until confluence and were exposed to distilled water, hyperosmolar solutions and ethanol at different concentrations and different time periods, ranging from 1 to 60 minutes. Cell survival was quantified using the LIVE/DEAD viability/cytotoxicity kit (Molecular probes). Potential damage to the lens capsule was analyzed by electron microscopy after treatment with various modalities. Results: Initially, we tested the clinically feasible time interval of up to 4 minutes. After exposure to distilled water, the cells showed a mortality rate of 15,1% after 4 minutes. The maximum mortality rate of 23,2% was reached after 24 minutes in distilled water without any further increase with time. Three molar sodium chloride was the most effective hyperosmolar salt solution resulting in a mortality rate of 68,2% after 2 minutes. Exposure to 45% ethanol resulted in a mortality rate of 95,7% after 1 minute. Ultrastructurally, there were no alterations of lens capsules after exposure to any of the tested substances. Conclusions: The presumed reduction of the PCO rate in humans and animal models after intraoperative exposure to distilled water does not seem to be based on an immediate cytotoxic action. In contrast, hyperosmolar salt solutions or ethanol have an immediate cytotoxic effect on LEC in vitro and may be suitable agents for clinical applications.

Keywords: posterior capsular opacification (PCO) • cell death/apoptosis • pathology: experimental 
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