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Related Experiment Video

Updated: Jun 10, 2026

Generation of Genetically Modified Organotypic Skin Cultures Using Devitalized Human Dermis
09:16

Generation of Genetically Modified Organotypic Skin Cultures Using Devitalized Human Dermis

Published on: December 14, 2015

In vitro dermal toxicology using skin organ cultures.

A A Rutten1, J J van de Sandt

  • 1TNO Food and Nutrition Research, Department of Biological Toxicology, PO Box 360, 3700 AJ Zeist, The Netherlands.

Toxicology in Vitro : an International Journal Published in Association with BIBRA
|August 10, 2010
PubMed
Summary

This study developed a novel in vitro skin model for toxicity testing, reducing animal use. The model effectively assessed dermal toxicity, percutaneous absorption, and metabolism of various compounds.

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Area of Science:

  • Toxicology
  • Dermatology
  • In Vitro Models

Background:

  • Need for reliable, cost-effective in vitro alternatives to animal testing for skin toxicity.
  • Current methods lack quantitative endpoints and may cause animal discomfort.

Purpose of the Study:

  • Develop and validate an in vitro model using cultured full-thickness skin from multiple species.
  • Investigate dermal toxicity, percutaneous absorption, and biotransformation of applied compounds.

Main Methods:

  • Cultured full-thickness skin from rabbit, pig, and human.
  • Topical application of test compounds.
  • Assessed cytotoxicity (MTT assay), inflammatory mediator release (HETE's), percutaneous absorption, and metabolism.

Main Results:

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Last Updated: Jun 10, 2026

Generation of Genetically Modified Organotypic Skin Cultures Using Devitalized Human Dermis
09:16

Generation of Genetically Modified Organotypic Skin Cultures Using Devitalized Human Dermis

Published on: December 14, 2015

Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding
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Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding

Published on: August 22, 2016

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  • MTT conversion inhibition correlated with irritant dose, indicating cytotoxicity.
  • Release of 12-HETE (pro-inflammatory) and 15-HETE (anti-inflammatory) observed.
  • Percutaneous absorption varied by species (pig > human ≈ rabbit); extensive cutaneous metabolism occurred.

Conclusions:

  • The developed in vitro skin model provides a viable alternative for assessing dermal toxicity, absorption, and metabolism.
  • The model demonstrates dose-dependent cytotoxicity and inflammatory mediator release, with potential for repair assessment.
  • Species-specific differences in absorption and metabolism highlight the model's utility in comparative studies.