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Cédric Lorthioir

Publications and source records attributed to Cédric Lorthioir.

2 recordsLinked to original sources

Nanostructure of PEGDA-PEG hydrogel membranes and how it controls their permeability

The spacial heterogeneity of hydrogels composed of PEGDA and added polymer chains is expected to play a crucial role on their transport properties which can be exploited in filtration or tissue engineering. However little is known about the arrangement of the polymer chains in the matrix and the length scales of these heterogeneities. Here we combine solid-state NMR and Small Angle Neutron Scattering to unravel the structure and dynamics of PEGDA hydrogels containing added PEG chains of various concentrations. Our results show that the samples present heterogeneities in both the PEGDA and PEG concentrations and suggest that the PEG chains entangle with the PEGDA network. When plotting the sample permeability, K, as a function the specific surface of the PEGDA heterogeneities we obtain a master curve, showing that the heterogeneity of the PEGDA matrix controls the permeability of the sample. Moreover the scaling K ___ V/S suggests a structure composed of facetted PEGDA/PEG heterogeneities separated by a network of aqueous thin and flattened films in which the water can permeate.

cond-mat.soft↗

Topological connection between vesicles and nanotubes in single-molecule lipid membranes driven by head-tail interactions

Lipid nanotube-vesicle networks are important channels for intercellular communication and transport of matter. Experimentally observed in neighboring mammalian cells, but also reproduced in model membrane systems, a broad consensus exists on their formation and stability. Lipid membranes must be composed of at least two molecular components, each stabilizing low (generally a phospholipid) and high curvatures. Strong anisotropy or enhanced conical shape of the second amphiphile is crucial for the formation of nanotunnels. Anisotropic driving forces generally favor nanotube protrusions from vesicles. In the present work, we report the unique case of topologically-connected nanotubes-vesicles obtained in the absence of directional forces, in single-molecule membranes, composed of an anisotropic bolaform glucolipid, above its melting temperature, Tm. Cryo-TEM and fluorescence confocal microscopy show the interconnection between vesicles and nanotubes in a single-phase region, between 60{\textdegree} and 90{\textdegree}C under diluted conditions. Solid-state NMR demonstrates that the glucolipid can assume two distinct configurations, head-head and head-tail. These arrangements, seemingly of comparable energy above the Tm, could explain the existence and stability of the topologically-connected vesicles and nanotubes, which are generally not observed for classical single-molecule phospholipid-based membranes above their Tm.

cond-mat.soft↗