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M Chastellain

Publications and source records attributed to M Chastellain.

2 recordsLinked to original sources

Development of functionalized superparamagnetic iron oxide nanoparticles for interaction with human cancer cells.

Our goal is to develop, characterize and optimize functionalized super paramagnetic iron oxide nanoparticles (SPION) demonstrating the capacity to be internalized by human cancer cells. SPION (mean diameter 9nm) were coated with various ratios to iron oxide of either polyvinyl alcohol (PVA), carboxylate-functionalized PVA, thiol-functionalized PVA and amino-functionalized PVA (amino-PVA). The interaction with cells and cytotoxicity of the SPION preparations were determined using human melanoma cells. From the four functionalized SPION preparations, only the amino-PVA SPION demonstrated the capacity to interact with, and were not cytotoxic to, human melanoma cells. This interaction with melanoma cells was dependent on the amino-PVA to iron oxide ratio, was an active and saturable mechanism displayed by all cells in a culture. These functionalized SPION were characterized by transmission electron microscopy and electrophoretic mobility. The physical comportment of SPION changed at specific PVAs to iron oxide ratios, and this ratio corresponded to the ratio of optimal interaction with cells. In conclusion, the successful development of functionalized SPION displaying potential cellular uptake by human cancer cells depends both on the presence of amino groups on the coating shell of the nanoparticles and of its ratio to the amount of iron oxide.

Cell Line, Tumor↗

Particle size investigations of a multistep synthesis of PVA coated superparamagnetic nanoparticles.

Nanoscaled particles showing superparamagnetic behavior have been intensively studied in the past years for various applications. Nevertheless, the lack of well-defined particles remains an important problem. One of the major challenges is still the large-scale synthesis of particles with a narrow size distribution. The aim of this work is to synthesize and characterize ferrofluids throughout a multistep synthesis. The iron oxide nanoparticles are first obtained by classical coprecipitation in water, followed by a thermochemical treatment and centrifugation to obtain well-dispersed primary nanoparticles. Finally polyvinyl alcohol is grafted onto the particles to ensure colloidal stability of the ferrofluid at neutral pH. The different synthesis steps and intermediate and side products are described. A model is proposed for the stabilization mechanism.

Journal Article↗