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Updated: Jun 9, 2026

A Reversible Silicon Oil-Induced Ocular Hypertension Model in Mice
09:03

A Reversible Silicon Oil-Induced Ocular Hypertension Model in Mice

Published on: November 15, 2019

The silicon microphysiometer for testing ocular toxicity in vitro.

P Catroux1, A Rougier, K G Dossou

  • 1L'Oreal Basic Research Center, 1 avenue E. Schueller, 93600 Aulnay-Sous-Bois, France.

Toxicology in Vitro : an International Journal Published in Association with BIBRA
|August 25, 2010
PubMed
Summary
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The silicon microphysiometer offers a reliable in vitro method for assessing ocular irritancy of water-soluble products. This cell-based assay shows high correlation with the in vivo Draize test, supporting its use as an alternative screening tool.

Area of Science:

  • Toxicology
  • Biomedical Engineering
  • Cell Biology

Background:

  • The Draize test is the standard for ocular irritancy assessment but involves animal testing.
  • There is a need for reliable in vitro alternatives to predict ocular irritation potential.
  • Silicon microphysiometry offers a novel approach to monitor cellular metabolic activity.

Purpose of the Study:

  • To evaluate the efficacy of the silicon microphysiometer for in vitro assessment of ocular irritancy.
  • To determine the correlation between silicon microphysiometer data and in vivo Draize test scores.
  • To assess the metabolic effects of various water-soluble ingredients and formulations on cultured cells.

Main Methods:

  • Utilized a silicon microphysiometer, a light-addressable potentiometric sensor, to monitor cellular metabolic rate.

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Last Updated: Jun 9, 2026

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Published on: November 15, 2019

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  • Exposed murine fibroblastic cells (L929 clone) to increasing concentrations of 53 products (surfactants and formulations).
  • Determined the MRD(50) (Metabolic Rate Decrease at 50%) and correlated it with historical Maximal Average Draize Scores (MAS).
  • Main Results:

    • The silicon microphysiometer effectively detected metabolic changes in cells exposed to test materials.
    • MRD(50) values varied widely across tested concentrations, indicating a broad range of sensitivities.
    • High linear (Pearson, r=0.91) and rank (Spearman, r=0.89) correlations were found between in vitro MRD(50) and in vivo MAS data.

    Conclusions:

    • The silicon microphysiometer method demonstrates a strong correlation with the Draize test for water-soluble substances.
    • This in vitro technique serves as a viable screening tool for predicting ocular irritation potential.
    • The study supports the adoption of this method as a cruelty-free alternative in product safety testing.