Evidence map›Paper›PMID 36136466›Full record

ArticleToxics2022

Incorporation of Metabolic Activation in the HPTLC-SOS-Umu-C Bioassay to Detect Low Levels of Genotoxic Chemicals in Food Contact Materials.

Emma Debon, Paul Rogeboz, Hélia Latado, Gertrud E Morlock, Daniel Meyer, Claudine Cottet-Fontannaz, Gabriele Scholz, Benoît Schilter, Maricel Marin-Kuan

Open access · goldAbstract read
In one paragraph

Article in Toxics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 27 citations in OpenAlex.

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  7. Effect-Directed Profiling ofMolecules (Basel, Switzerland) · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Emma DebonFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.
Paul RogebozFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.
Hélia LatadoFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.
Gertrud E MorlockInstitute of Nutritional Science, Chair of Food Science, and TransMIT Center of Effect-Directed Analysis, Justus Liebig University Giessen, 35392 Giessen, Germany.ORCID 0000-0001-9406-0351
Daniel MeyerInstitute of Nutritional Science, Chair of Food Science, and TransMIT Center of Effect-Directed Analysis, Justus Liebig University Giessen, 35392 Giessen, Germany.ORCID 0000-0002-1505-9529
Claudine Cottet-FontannazFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.
Gabriele ScholzFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.ORCID 0000-0001-5762-5165
Benoît SchilterFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.
Maricel Marin-KuanFood Safety Research Department, Société des Produits Nestlé SA-Nestlé Research, Vers-chez-les-Blanc, 1000 Lausanne, Switzerland.ORCID 0000-0002-8409-8820
Nestlé (Switzerland) · CHJustus-Liebig-Universität Gießen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The safety evaluation of food contact materials requires excluding mutagenicity and genotoxicity in migrates. Testing the migrates using in vitro bioassays has been proposed to address this challenge. To be fit for that purpose, bioassays must be capable of detecting very low, safety relevant concentrations of DNA-damaging substances. There is currently no bioassay compatible with such qualifications. High-performance thin-layer chromatography (HPTLC), coupled with the planar SOS Umu-C (p-Umu-C) bioassay, was suggested as a promising rapid test (~6 h) to detect the presence of low levels of mutagens/genotoxins in complex mixtures. The current study aimed at incorporating metabolic activation in this assay and testing it with a set of standard mutagens (4-nitroquinoline-

Indexed as

food contact materialhazard identificationin vitro genotoxicitylimit of biological detectionmetabolic activationplanar chromatography coupled with bioassay

Identifiers

PMID36136466
PMCPMC9500983
OpenAlexW4293771331

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.