The role of the coating and aggregation state in the interactions between iron oxide nanoparticles and 3T3 fibroblasts

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 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). We find that most particles were biocompatible, as exposed cells remained 100% viable relative to controls. The strong uptake shown by the citrate-coated particles is related to the destabilization of the dispersions in the cell culture medium and their sedimentation down to the cell membranes.Comment: 5 pages 3 figure

Microrheology of viscoelastic solutions studied by magnetic rotational spectroscopy

Magnetic rotational spectroscopy is based on the use of magnetic micron-size wires for viscosity measurements. Submitted to a rotational magnetic field with increasing frequency, the wires undergo a hydrodynamic instability between a synchronous and an asynchronous regime. From a comparison between predictions and experiments, the static shear viscosity and elastic modulus of wormlike micellar solutions are here determined. The values agree with the determination by cone-and-plate rheometry.Comment: 6 pages, 4 figures, proceedings of the TNT2015 conference in Toulous

Rotational microrheology of Maxwell fluids using micron-sized wires

We demonstrate a simple method for rotational microrheology in complex fluids, using micrometric wires. The three-dimensional rotational Brownian motion of the wires suspended in Maxwell fluids is measured from their projection on the focal plane of a microscope. We analyze the mean-squared angular displacement of the wires of length between 1 and 40 microns. The viscoelastic properties of the suspending fluids are extracted from this analysis and found to be in good agreement with macrorheology data. Viscosities of simple and complex fluids between 0.01 and 30 Pa.s could be measured. As for the elastic modulus, values up to ~ 5 Pa could be determined. This simple technique, allowing for a broad range of probed length scales, opens new perspectives in microrheology of heterogeneous materials such as gels, glasses and cells.Comment: to appear in Soft Matte

Design and applications of a fluorescent labeling technique for lipid and surfactant preformed vesicles

International audienceAmphiphilic molecules such as surfactants, lipids and block copolymers can be assembled into bilayers and form vesicles. Fluorescent membrane labeling methods require the use of dye molecules that can be inserted in the bilayers at different stages of the synthesis. To our knowledge there is no generalized method for labeling preformed vesicles. Herein we develop a versatile protocol that is suitable to both surfactant and lipid preformed vesicles and requires no separation or purification steps. Based on the lipophilic carbocyanine green dye PKH67, the methodology is assessed on zwitterionic phosphatidylcholine vesicles. To demonstrate its versatility, it is applied to dispersions of anionic or cationic vesicles, such as a drug administrated to premature infants with respiratory distress syndrome, or a vesicle formulation used as a fabric softener for homecare applications. By means of fluorescence microscopy we then visualize the interaction mechanisms of nano-particles crossing live cell membranes and of surfactant adsorbing on cotton fabric. These results highlight the advantages of a membrane labeling technique that is simple and applicable to a large number of soft matter systems

Cerium oxide catalyzed disproportionation of hydrogen peroxide: a closer look at the reaction intermediate

Cerium oxide nanoparticles (CNPs) have recently gained increasing interest as redox enzyme-mimetics to scavenge the intracellular excess of reactive oxygen species, including hydrogen peroxide (H2O2). Despite the extensive exploration of CNP scavenging activity, there remains a notable knowledge gap regarding the fundamental mechanism underlying the CNP catalyzed disproportionation of H2O2. In this Letter, we present evidence demonstrating that H2O2 adsorption at CNP surface triggers the formation of stable intermediates known as ceriumperoxo complexes (Ce-O2 2-). The cerium-peroxo complexes can be resolved by Raman scattering and UV-Visible spectroscopy. We further demonstrate that the catalytic reactivity of CNPs in the H2O2 disproportionation reaction increases with the Ce(III) fraction. The developed approach using UV-Visible spectroscopy for the characterization of Ce-O2 2-complexes can potentially serve as a foundation for determining the catalytic reactivity of CNPs in the disproportionation of H2O2

Towards a better understanding on agglomeration mechanisms and thermodynamic properties of TiO2 nanoparticles interacting with natural organic matter

Interaction between engineered nanoparticles and natural organic matter is investigated by measuring the exchanged heat during binding process with isothermal titration calorimetry. TiO2 anatase nanoparticles and alginate are used as engineered nanoparticles and natural organic matter to get an insight into the thermodynamic association properties and mechanisms of adsorption and agglomeration. Changes of enthalpy, entropy and total free energy, reaction stoichiometry and affinity binding constant are determined or calculated at a pH value where the TiO2 nanoparticles surface charge is positive and the alginate exhibits a negative structural charge. Our results indicate that strong TiO2-alginate interactions are essentially entropy driven and enthalpically favorable with exothermic binding reactions. The reaction stoichiometry and entropy gain are also found dependent on the mixing order. Finally correlation is established between the binding enthalpy, the reaction stoichiometry and the zeta potential values determined by electrophoretic mobility measurements. From these results two types of agglomeration mechanisms are proposed depending on the mixing order. Addition of alginate in TiO2 dispersions is found to form agglomerates due to polymer bridging whereas addition of TiO2 in alginate promotes a more individually coating of the nanoparticles.Comment: 30 pages, 6 figures, 11 figures in S

A health concern regarding the protein corona, aggregation and disaggregation

Nanoparticle (NP)-protein complexes exhibit the correct identity of NP in biological media. Therefore, protein-NP interactions should be closely explored to understand and to modulate the nature of NPs in medical implementations. This review focuses mainly on the physicochemical parameters such as dimension, surface chemistry, the morphology of NPs and influence of medium pH on the formation of protein corona and conformational changes of adsorbed proteins by different kinds of methods. Also, the impact of protein corona on the colloidal stability of NPs is discussed. Uncontrolled protein attachment on NPs may bring unwanted impacts such as protein denaturation and aggregation. In contrast, controlled protein adsorption by optimal concentration, size, pH and surface modification of NPs may result in potential implementation of NPs as therapeutic agents especially for disaggregation of amyloid fibrils. Also, the effect of NPs-protein corona on reducing the cytotoxicity and clinical implications such as drug delivery, cancer therapy, imaging and diagnosis will be discussed. Validated correlative physicochemical parameters for NP-protein corona formation frequently derived from protein corona fingerprints of NPs which are more valid than the parameters obtained only on the base of NP features. This review may provide useful information regarding the potency as well as the adverse effects of NPs to predict their behavior in the in vivo experiments.Comment: 40 pages, 20 figure