High-Throughput Testing for Unknown Mutagens and Cytotoxica via Duplex Planar Ames-Cytotoxicity Bioassay Including

Katharina Schmidtmann1, Ann-Cathrin Kayser1, Gertrud E Morlock1

  • 1Chair of Food Science, Institute of Nutritional Science, Justus Liebig University Giessen, Heinrich-Buff-Ring 26-32, Giessen 35392, Germany.

Analytical Chemistry
|March 2, 2026
PubMed

Insights

A new duplex planar bioassay detects mutagens and cytotoxic compounds in complex samples. This method enhances sensitivity and selectivity, reducing time, labor, and costs for improved safety assessments.

Area of Science:

  • Environmental Chemistry
  • Toxicology
  • Biotechnology

Background:

  • Nontarget effect-directed analysis for mutagens faces challenges like matrix effects, cytotoxicity, and low sensitivity.
  • Existing methods may miss potent, unknown mutagens at trace levels in complex mixtures.

Purpose of the Study:

  • To develop a sensitive and selective duplex planar Ames mutagenicity-cytotoxicity bioassay for detecting individual mutagens and cytotoxic compounds.
  • To overcome limitations of current methods, including matrix effects and diffusion issues.

Main Methods:

  • Utilized a duplex planar Ames bioassay with high-throughput testing and parallel planar chromatography.
  • Implemented substance zone fixation to prevent diffusion and integrated human/rat liver S9 systems for metabolic activation.
  • Employed a tetrazolium salt substrate for dual end-point read-out.

Main Results:

  • Achieved a 5-fold reduction in time to result, a 330-fold reduction in manual labor, and a 651-fold cost reduction.
  • Successfully detected and quantified unknown mutagens and cytotoxins in complex samples like teas, cosmetics, and perfumes.
  • Demonstrated that exemplary daily exposure to skincare products significantly exceeded mutagenicity thresholds.

Conclusions:

  • The developed bioassay offers selective, sensitive, and quantitative detection of mutagens and cytotoxins in complex matrices.
  • This open-source, sustainable method provides a valuable tool for hazard minimization, regulatory safety assessment, and quality control.
  • The assay is applicable worldwide, supporting drug development and risk assessment processes.