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Hazard screening of colloidal silica nanomaterials with varying degrees of silane surface functionalization: a safe-by-design case study

Ruijter, Nienke; Zanoni, Ilaria; Persson, Daniel; Arts, Josje; Carriere, Marie; Guiot, Arnaud; Persson, Michael; Katsumiti, Alberto; Marshall, Jessica; Boyles, Matthew; Cassee, Flemming R.; Braakhuis, Hedwig

Authors

Nienke Ruijter

Ilaria Zanoni

Daniel Persson

Josje Arts

Marie Carriere

Arnaud Guiot

Michael Persson

Alberto Katsumiti

Jessica Marshall

Flemming R. Cassee

Hedwig Braakhuis



Abstract

Background: The Safe and Sustainable by Design (SSbD) concept facilitates the design of safer and more sustainable chemicals and materials and is a crucial approach towards reaching the goals set out in the European Green Deal. It is critical that suitable guidance is provided on how to use new approach methodologies (NAMs) to fill hazard data gaps for nanomaterials (NMs) to facilitate SSbD decisions. Here, we showcase a nano-specific in vitro SSbD case study. The five colloidal silica nanoforms (SiO2-NFs) under investigation in this study are surface modified with varying amounts of glycerolpropyl-organosilane groups. In this study, we use a simple yet comprehensive in vitro test battery along with thorough particle characterization to investigate the effect of surface silanization on in vitro toxicity to inform SSbD decisions. Results: Cytotoxic, pro-inflammatory and oxidative stress responses in A549, dTHP-1, and BEAS-2B cells after exposure to SiO2-NFs submerged and at the air-liquid interface (ALI) decreased with increasing silane surface modification. None of the SiO2-NFs showed surface reactivity or haemolytic potential. Deposition assessment using inductively coupled plasma – optical emission spectrometry (ICP-OES) revealed that increasing silane surface modification decreased particle settling. The two SiO2-NFs with the highest amount of surface silanization did not reach the cells in a submerged exposure setting, and they were therefore only tested at the ALI. Identical dose-response curves were observed for both the submerged testing and testing at the ALI for the SiO2-NFs without and with low/intermediate surface functionalization, again showing a decrease in effects with increasing surface functionalization. Conclusion: We show that in vitro toxicity assays provide valuable information for SSbD decision making. In vitro cytotoxic, pro-inflammatory and oxidative stress responses can be reduced with increasing surface silane functionalization. The reduced deposition efficiency with increasing silane functionalization, however, highlights that thorough characterization of particle behaviour in cell culture medium should always be performed for SSbD hazard testing. The amount of silane required to reduce toxicity is important information for the future production of safer SiO2-NFs and nano-enabled products. Exposure, functionality, and sustainability remain to be investigated to draw full SSbD conclusions.

Citation

Ruijter, N., Zanoni, I., Persson, D., Arts, J., Carriere, M., Guiot, A., Persson, M., Katsumiti, A., Marshall, J., Boyles, M., Cassee, F. R., & Braakhuis, H. (2025). Hazard screening of colloidal silica nanomaterials with varying degrees of silane surface functionalization: a safe-by-design case study. Particle and fibre toxicology, 22(1), Article 15. https://doi.org/10.1186/s12989-025-00629-6

Journal Article Type Article
Acceptance Date Apr 29, 2025
Online Publication Date May 26, 2025
Publication Date 2025
Deposit Date Jun 2, 2025
Publicly Available Date Jun 2, 2025
Journal Particle and Fibre Toxicology
Print ISSN 1743-8977
Publisher BMC
Peer Reviewed Peer Reviewed
Volume 22
Issue 1
Article Number 15
DOI https://doi.org/10.1186/s12989-025-00629-6
Keywords In vitro, SSbD, Silane, SiO2-NF, Silica, Nanomaterials
Public URL http://researchrepository.napier.ac.uk/Output/4521878

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Publisher Licence URL
http://creativecommons.org/licenses/by-nc-nd/4.0/

Copyright Statement
This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.





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