2017
DOI: 10.1016/j.cis.2017.04.012
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Probing the threshold of membrane damage and cytotoxicity effects induced by silica nanoparticles in Escherichia coli bacteria

Abstract: The engineering of nanomaterials, because of their specific properties, is increasingly being developed for commercial purposes over the past decades, to enhance diagnosis, cosmetics properties as well as sensing efficiency. However, the understanding of their fate and thus their interactions at the cellular level with bio-organisms remains elusive. Here, we investigate the size- and charge-dependence of the damages induced by silica nanoparticles (SiO-NPs) on Gram-negative Escherichia coli bacteria. We show a… Show more

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Cited by 29 publications
(29 citation statements)
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“…Then, such a treatment induces the opposite effect of that observed for SiO 2 NPs 100 nm (Q1 = 0.4 MPa, Q3 = 1.6 MPa). SiO 2 NPs 4 nm induced a significant decrease in cell elasticity, in good agreement with the morphological and membrane damage previously shown [17].…”
Section: Comparative Analysissupporting
confidence: 90%
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“…Then, such a treatment induces the opposite effect of that observed for SiO 2 NPs 100 nm (Q1 = 0.4 MPa, Q3 = 1.6 MPa). SiO 2 NPs 4 nm induced a significant decrease in cell elasticity, in good agreement with the morphological and membrane damage previously shown [17].…”
Section: Comparative Analysissupporting
confidence: 90%
“…Many studies have focused on the well known antibacterial activity of metal oxide and silver NPs, coping with the charge and size dependency of their interactions without addressing their impact on the mechanical properties of cells [16,28,81]. In our pre vious work, we had shown the existence of a critical diameter (50 nm < U c < 80 nm) below which SiO 2 NPs induce morphological and membrane structural damages eventually leading to the E. coli cell lysis [17]. Here, by combining AFM imaging with spec troscopy mode, we also quantitatively demonstrate that such a toxicity is statistically correlated with modifications in the E. coli elasticity.…”
Section: Resultsmentioning
confidence: 86%
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“…cells was analyzed underwater with a multimode AFM (Asylum Research, MFP‐3D) using silicon probes in the Scanasyst mode. To avoid the effect of air drying on the cell surface topography, we recorded the AFM images of samples directly in deionized water . For underwater imaging, the collected samples were resuspended in the deionized water, pipetted onto a cleaned culture dish of the polystyrene (60 mm in diameter), and then flushed with deionized water to remove loose cells.…”
Section: Methodsmentioning
confidence: 99%