Interactions between sub-10 nm iron and cerium oxide nanoparticles and 3T3 fibroblasts : the role of the coating and aggregation state
M. Safi, H. Sarrouj, O. Sandre, N. Mignet, J.-F. Berret

TL;DR
This study investigates how coating and aggregation influence the toxicity and cellular uptake of sub-10 nm iron and cerium oxide nanoparticles in fibroblasts, revealing coating-dependent biocompatibility and internalization behaviors.
Contribution
It provides new insights into how nanoparticle coatings and aggregation states affect cellular interactions and toxicity, informing safer nanomaterial design.
Findings
Most nanoparticles were biocompatible with fibroblasts.
Citrate-coated nanoceria showed higher cellular uptake.
Coating influences nanoparticle stability and internalization.
Abstract
Recent nanotoxicity studies revealed that the physico-chemical characteristics of engineered nanomaterials play an important role in the interactions with living cells. Here, we report on the toxicity and uptake of the cerium and iron oxide sub-10 nm nanoparticles by NIH/3T3 mouse fibroblasts. Coating strategies include low-molecular weight ligands (citric acid) and polymers (poly(acrylic acid), MW = 2000 g mol-1). Electrostatically adsorbed on the surfaces, the organic moieties provide a negatively charged coating in physiological conditions. We find that most particles were biocompatible, as exposed cells remained 100% viable relative to controls. Only the bare and the citrate-coated nanoceria exhibit a slight decrease of the mitochondrial activity for cerium concentrations above 5 mM (equivalent to 0.8 g L-1). We also observe that the citrate-coated particles are internalized by the…
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