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Updated: Mar 3, 2026

The Lambda Select cII Mutation Detection System
Published on: April 26, 2018
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.
Abstract:
Current nontarget effect-directed analysis of complex samples for mutagens is hampered by matrix effects, associated cytotoxicity, diffusion effects, insufficient sensitivity, and a lack of selectivity. Non-target analysis may overlook highly potent, unknown mutagens at trace levels. To overcome these limitations, a duplex planar Ames mutagenicity-cytotoxicity bioassay was developed to sensitively and selectively detect individual mutagens and cytotoxic compounds with or without metabolic activation. Key innovations included high-throughput testing of samples, either directly or as raw extracts, separated in parallel by planar chromatography, substance zone fixation to prevent diffusion during long incubation times, integration of the human versus rat liver S9 enzyme systems for metabolic de/activation, and use of a tetrazolium salt substrate that provides a dual end-point read-out. Compared to the state of the art, time to result was reduced 5-fold, manual work was reduced 330-fold, and costs for nearly plastic-free consumables were reduced 651-fold. The selective, sensitive, and quantitative unmasking of previously unknown mutagens and cytotoxica was shown for highly complex samples, such as teas, cosmetics, skin care creams, and perfumes. An exemplary daily exposure to 11.5 g of skin care products exceeded the half-maximal effective mutagenicity dose by at least 4 orders of magnitude. Using the open-source and sustainable 2LabsToGo-Eco, the new duplex planar bioassay method can be applied worldwide to serve as a valuable tool for hazard minimization and to support regulatory safety and risk assessments, industrial quality control, and drug development.
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.
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