Genotoxicity of synthetic amorphous silica nanoparticles in rats following short-term exposure. Part 1: Oral route

2014 ◽  
Vol 56 (2) ◽  
pp. 218-227 ◽  
Author(s):  
Adeline Tarantini ◽  
Sylvie Huet ◽  
Gérard Jarry ◽  
Rachelle Lanceleur ◽  
Martine Poul ◽  
...  
Author(s):  
João P. Vareda ◽  
Carlos A. García-González ◽  
Artur J. M. Valente ◽  
Rosana Simón-Vázquez ◽  
Marina Stipetic ◽  
...  

The toxicity and ecotoxicity effects, handling and disposal of synthetic amorphous silica nanoparticles and aerogels are reviewed and discussed.


2021 ◽  
pp. 074823372110105
Author(s):  
Roberta Tassinari ◽  
Andrea Martinelli ◽  
Mauro Valeri ◽  
Francesca Maranghi

Synthetic amorphous silica (SAS) nanomaterial – consisting of aggregates and agglomerates of primary silicon dioxide (SiO2) particles in the nanorange (<100 nm) – is commonly used as excipient in pharmaceuticals, in cosmetics and as food additive (E551). The available data suggest that SAS nanoparticles (NP) after intravenous (IV) exposure persist in liver and spleen; however, insufficient data exist to verify whether SAS may also induce adverse effects. The aim of the present study was to verify the potential long-term effects of SAS NP (NM-203) on spleen and liver as target organs following short-term exposure. Adult male and female Sprague-Dawley rats were treated by IV injection in the tail vein with a single (1-day) dose (SD) and repeated (5-day) doses (RD) of 20 mg/kg bw per day of SAS dispersed in sterile saline solution as vehicle. Histopathological examinations of target organs were performed after 90 days. Tissue biodistribution and full characterization of NM-203, primary particle size 13–45 nm, was performed within the framework of the Nanogenotox project. No mortality or general toxicity occurred; histopathological analysis showed splenomegaly in the RD group accompanied by inflammatory granulomas in both sexes. Granulomas were also present in liver parenchyma in the RD (both sexes) and SD groups (male only). The histopathological results indicated that SAS NP have the potential to persist and induce sex-specific chronic inflammatory lesions in spleen and liver upon short-term treatment. Overall, the data showed that the widespread use of silica in drugs might elicit chronic reactions in spleen and liver prompting to the need of further investigations on the safety of SAS NP.


2020 ◽  
Vol 5 (12) ◽  
pp. 886-909 ◽  
Author(s):  
Jonas G. Croissant ◽  
Kimberly S. Butler ◽  
Jeffrey I. Zink ◽  
C. Jeffrey Brinker

Author(s):  
Caroline Fontana ◽  
Anaïs Kirsch ◽  
Carole Seidel ◽  
Léa Marpeaux ◽  
Christian Darne ◽  
...  

2016 ◽  
Vol 1432 ◽  
pp. 92-100 ◽  
Author(s):  
Francisco Barahona ◽  
Isaac Ojea-Jimenez ◽  
Otmar Geiss ◽  
Douglas Gilliland ◽  
Josefa Barrero-Moreno

2017 ◽  
Vol 29 (12-14) ◽  
pp. 567-576 ◽  
Author(s):  
Jae Hoon Shin ◽  
KiSoo Jeon ◽  
Jin Kwon Kim ◽  
Younghun Kim ◽  
Mi Seong Jo ◽  
...  

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