Giant unilamellar vesicles (diameter of a few tens of micrometers) are commonly produced by hydration of a dried lipidic film. After addition of the aqueous solution, two major protocols are used: (i) the gentle hydration method where the vesicles spontaneously form and (ii) the electroformation method where an ac electric field is applied. Electroformation is known to improve the rate of unilamellarity of the vesicles though it imposes more restricting conditions for the lipidic composition of the vesicles. Here we further characterize these methods by using fluorescence microscopy. It enables not only a sensitive detection of the defects but also an evaluation of the quantity of lipids in these defects. A classification of the defects is proposed and statistics of their relative importance in regard to both methods and lipid composition are presented: it shows for example that 80% of the vesicles obtained by electroformation from 98% 1,2-Dioleoyl-sn-Glycero-3-Phosphocholine are devoid of significant defects against only 40% of the vesicles with the gentle hydration method. It is also shown that the presence of too many negatively charged lipids does not favor the formation of unilamellar vesicles with both methods. For the gentle hydration, we checked if the negatively charged lipids were inserted in the vesicles membrane in the same proportion as that of the lipid mixture from which they are formed. The constant incorporation of a negatively charged labeled lipid despite an increasing presence of negatively charged 1,2-Dioleoyl-sn-Glycero-3-[Phospho-l-Serine] tends to confirm that the composition of vesicles is indeed close to that of the initial mixture.

Inverse micelles of surfactant AOT at low water contents are studied. From RMN measurements the molar fraction of bound water was obtained. Ultrasonic measurements, which depend on the compressibility, permit to determine the internal radius (water radius) of the micelles. With both results, the size of the bound water layer in this system was found around 0.3 nm. Correlated changes in the FT‐IR absorption spectra give us information about the interaction between water and the polar head of AOT. Multilamellar vesicles, at different concentrations, of phospholipid DPPC, studied by DSC and FT‐IR present a sub‐zero transition near −40°C. This transition is attributed to the interstitial water, i.e. the water confined between two DPPC bilayers. These results emphasize the peculiar properties of the bound water in such systems.

Fluorescence recovery after pattern photobleaching is used to measure the self-diffusion of surfactant molecules, along cylinders and perpendicular to their main axis in an oriented hexagonal lyotropic phase. Unexpectedly, while the motion along cylinders is diffusive, a superdiffusive behavior is observed in the direction perpendicular to the cylinder axis. Moreover, varying the lattice parameter, we found that the perpendicular diffusion time is governed only by the number of cylinders to cross, providing experimental evidence for superdiffusion with a bounded step length.

Oil-in-water emulsions are currently being investigated to facilitate the transport of viscous heavy oils. The behavior of these emulsions is largely controlled by the interfaces between oil drops and water. The surface-active components of crude oil, such as asphaltenes and naphthenic acids, compete among themselves at these interfaces and also with possibly added synthetic surfactant emulsifier. Here, we present a study of dynamic interfacial tension of interfaces between water and a model oil (toluene) in which variable amounts of asphaltenes are solubilized. We show that pH has a strong influence on interfacial properties of asphaltenes at the oil/water interface. At high or low pH, asphaltenes functional groups become charged, enhancing its surface activity. The influence of lower-molecular-weight surface-active species, such as the natural naphthenic acids contained in maltenes (crude oil without asphaltenes), has been investigated, and an interaction between asphaltenes and maltenes that facilitates molecular arrangement at the interface was detected. Several micropipette experiments, in which micrometric drops have been manipulated, are also described and indicate that very little coalescence of water droplets is observed at high or low pH. The microscopic properties of the interface and the macroscopic behavior of the emulsion are determined to be correlated.

Among the various molecular interactions used to construct supramolecular self-assembling systems, homoliganded metallic NTA-Ni-NTA complexes have received little attention despite their considerable potential applications, such as the connection of different biochemical functions. The stability of this complex is investigated here by using two concordant nanotechniques (surface forces apparatus and vesicle micromanipulation) that allow direct measurements of adhesion energies due to the chelation of nickel ions by nitrilotriacetate (NTA) groups grafted on surfaces. We show that two NTA groups can share a nickel ion, and that the association of a Ni-NTA complex with an NTA group has a molecular binding energy of 1.4 kcal/mol. Binding measurements in bulk by isothermal titration calorimetry experiments give the same value and, furthermore, indicate that the Ni-NTA chelation bond is about five times stronger than the NTA-Ni-NTA one. This first direct proof and quantification of the simultaneous chelation of a nickel ion by two NTA groups sheds new light on association dynamics involving chelation processes and offers perspectives for the development of new supramolecular assemblies and anchoring strategies.