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We explore how a magnetic field breaks the symmetry of an initially spherical giant liposome filled with a magnetic colloid. The condition of rotational symmetry along the field axis leads either to a prolate or to an oblate ellipsoid. We demonstrate that an electrostatic interaction between the nanoparticles and the membrane triggers the shape transition. PACS numbers: 75.

Magnetic particles are very efficient Magnetic Resonance Imaging (MRI) contrast agents. In the recent years, chemists have unleashed their imagination to design multi-functional nanoprobes for biomedical applications including MRI contrast enhancement. This study is focused on the direct relationship between the size and magnetization of the particles and their nuclear magnetic resonance relaxation properties, which condition their efficiency. Experimental relaxation results with maghemite particles exhibiting a wide range of sizes and magnetizations are compared to previously published data and to well-established relaxation theories with a good agreement. This allows deriving the experimental master curve of the transverse relaxivity versus particle size and to predict the MRI contrast efficiency of any type of magnetic nanoparticles. This prediction only requires the knowledge of the size of the particles impermeable to water protons and the saturation magnetization of the corresponding volume. To predict the T2 relaxation efficiency of magnetic single crystals, the crystal size and magnetization obtained through a single Langevin fit of a magnetization curve is the only information needed. For contrast agents made of several magnetic cores assembled into various geometries (dilute fractal aggregates, dense spherical clusters, core-shell micelles, hollow vesicles), one needs to know a third parameter, namely the intra-aggregate volume fraction occupied by the magnetic materials relatively to the whole (hydrodynamic) sphere. Finally a calculation of the maximum achievable relaxation effect and the size needed to reach this maximum is performed for different cases: maghemite single crystals and dense clusters, core-shell particles (oxide layer around a metallic core) and zinc manganese ferrite crystals., Comment: 28 pages, 2 figures

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 cells in large amounts, typically 250 pg per cell after a 24 h incubation for iron oxide. In contrast, the polymer-coated particles are taken up at much lower rates (< 30 pg per cell). 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. In conclusion, we show that the uptake of nanomaterials by living cells depends on the coating of the particles and on its ability to preserve the colloidal nature of the dispersions., Comment: 9 figures, 2 tables

Water-soluble clusters made from 7 nm inorganic nanoparticles have been investigated by small-angle neutron scattering. The internal structure factor of the clusters was derived and exhibited a universal behavior as evidenced by a correlation hole at intermediate wave-vectors. Reverse Monte-Carlo calculations were performed to adjust the data and provided an accurate description of the clusters in terms of interparticle distance and volume fraction. Additional parameters influencing the microstructure were also investigated, including the nature and thickness of the nanoparticle adlayer., Comment: 5 pages, 4 figures, paper published in Physical Review E

A paradigm proposed recently by Boal et al. (A.K. Boal et al., Nature 404, 746-748, 2000) deals with the possibility to use inorganic nanoparticles as building blocks for the design and fabrication of colloidal and supracolloidal assemblies. It is anticipated that these constructs could be made of different shapes, patterns and functionalities and could constitute the components of future nanodevices including sensors, actuators or nanocircuits. Here we report a protocol that allowed us to fabricate such nanoparticle aggregates. The building blocks of the constructs were anionically coated iron oxide nanocrytals (superparamagnetic, size 7 nm) and cationic-neutral block copolymers. We have shown that the electrostatic interactions between charged species can be controlled by tuning the ionic strength of the dispersion. Under appropriate conditions, the control of electrostatics resulted in the elaboration of spherical or elongated aggregates at the micrometer length scale. The elongated aggregates were found to be rod-like, with diameters of a few hundred nanometers and lengths between 1 and 50 micrometers. In addition to their remarkable stiffness, the nanostructured rods were found to reorient along with an externally applied magnetic field, in agreement with the laws of superparamagnetism., Comment: 6 pages, 5 figures, appeared in Advanced materials in September 2008, reference

The attractive interactions between oppositely charged species (colloids, macromolecules etc) dispersed in water are strong, and the direct mixing of solutions containing such species generally yields to a precipitation, or to a phase separation. We have recently developed means to control the electrostatically-driven attractions between nanoparticles and polymers in water, and at the same time to preserve the stability of the dispersions. We give here an account of the formation of supracolloidal aggregates obtained by co-assembly of 7 nm particles with copolymers. Nanostructured rods of length comprised between 5 and 50 microns and diameter 500 nm were investigated. By application of a magnetic field, the rods were found to reorient along with the magnetic field lines. The kinetics of reorientation was investigated using step changes of the magnetic field of amplitude 90 degrees. From the various results obtained, among which an exponential decay of the tangent of the angle made between the rod and the field, we concluded that the rods are superparamagnetic., Comment: 12 pages - 452kB 7 - figures - 1 Table will be published in Journal of Physics : Condensed Matter

We report on the use of magnetic sedimentation as a means to determine the size distribution of dispersed magnetic particles. The particles investigated here are i) single anionic and cationic nanoparticles of diameter D = 7 nm and ii) nanoparticle clusters resulting from electrostatic complexation with polyelectrolytes and polyelectrolyte-neutral copolymers. A theoretical expression of the sedimentation concentration profiles at the steady state is proposed and it is found to describe accurately the experimental data. When compared to dynamic light scattering, vibrating sample magnetometry and cryogenic transmission electron microscopy, magnetic sedimentation exhibits a unique property : it provides the core size and core size distribution of nanoparticle aggregates., Comment: 9 pages - templated ACS - 7 figures - 1 table

We report on the electrostatic complexation between polyelectrolyte-neutral copolymers and oppositely charged 6 nm-crystalline nanoparticles. For two different dispersions of oxide nanoparticles, the electrostatic complexation gives rise to the formation of stable nanoparticle clusters in the range 20 - 100 nm. It is found that inside the clusters, the particles are pasted together by the polyelectrolyte blocks adsorbed on their surface. Cryo-transmission electronic microscopy allows to visualize the clusters and to determine the probability distributions functions in size and in aggregation number. The comparison between light scattering and cryo-microscopy results suggests the existence of a polymer brush around the clusters., Comment: 7 pages, 4 figures, to appear in JCIS