Skip to main content

Research Repository

Advanced Search

Pan-European inter-laboratory studies on a panel of in vitro cytotoxicity and pro-inflammation assays for nanoparticles

Piret, Jean-Pascal; Bondarenko, Olesja M.; Boyles, Matthew S. P.; Himly, Martin; Ribeiro, Ana R.; Benetti, Federico; Smal, Caroline; Lima, Braulio; Potthoff, Annegret; Simion, Monica; Dumortier, Elise; Leite, Paulo Emilio C.; Balottin, Luciene Bottentuit; Granjeiro, José Mauro; Ivask, Angela; Kahru, Anne; Radauer-Preiml, Isabella; Tischler, Ulrike; Duschl, Albert; Saout, Christelle; Anguissola, Sergio; Haase, Andrea; Jacobs, An; Nelissen, Inge; Misra, Superb K.; Toussaint, Olivier

Authors

Jean-Pascal Piret

Olesja M. Bondarenko

Martin Himly

Ana R. Ribeiro

Federico Benetti

Caroline Smal

Braulio Lima

Annegret Potthoff

Monica Simion

Elise Dumortier

Paulo Emilio C. Leite

Luciene Bottentuit Balottin

José Mauro Granjeiro

Angela Ivask

Anne Kahru

Isabella Radauer-Preiml

Ulrike Tischler

Albert Duschl

Christelle Saout

Sergio Anguissola

Andrea Haase

An Jacobs

Inge Nelissen

Superb K. Misra

Olivier Toussaint



Abstract

The rapid development of nanotechnologies and increased production and use of nanomaterials raise concerns about their potential toxic effects for human health and environment. To evaluate the biological effects of nanomaterials, a set of reliable and reproducible methods and development of standard operating procedures (SOPs) is required. In the framework of the European FP7 NanoValid project, three different cell viability assays (MTS, ATP content, and caspase-3/7 activity) with different readouts (absorbance, luminescence and fluorescence) and two immune assays (ELISA of pro-inflammatory cytokines IL1-β and TNF-α) were evaluated by inter-laboratory comparison. The aim was to determine the suitability and reliability of these assays for nanosafety assessment. Studies on silver and copper oxide nanoparticles (NPs) were performed, and SOPs for particle handling, cell culture, and in vitro assays were established or adapted. These SOPs give precise descriptions of assay procedures, cell culture/seeding conditions, NPs/positive control preparation and dilutions, experimental well plate preparation, and evaluation of NPs interference. The following conclusions can be highlighted from the pan-European inter-laboratory studies: Testing of NPs interference with the toxicity assays should always be conducted. Interference tests should be designed as close as possible to the cell exposure conditions. ATP and MTS assays gave consistent toxicity results with low inter-laboratory variability using Ag and CuO NPs and different cell lines and therefore, could be recommended for further validation and standardization. High inter-laboratory variability was observed for Caspase 3/7 assay and ELISA for IL1-β and TNF-α measurements.

Journal Article Type Article
Acceptance Date Nov 24, 2016
Online Publication Date Dec 10, 2016
Publication Date 2017-06
Deposit Date Oct 13, 2023
Print ISSN 0340-5761
Electronic ISSN 1432-0738
Publisher Springer
Peer Reviewed Peer Reviewed
Volume 91
Issue 6
Pages 2315-2330
DOI https://doi.org/10.1007/s00204-016-1897-2
Keywords Inter-laboratory studies, Standard operating procedures, Interference, In vitro assays, Nanoparticles