Eur. Phys. J. E 26, 225-234 (2008)
DOI: 10.1140/epje/i2007-10318-9

Confined diffusion of hydrophilic probes inserted in lyotropic lamellar phases

P. Moreau, D. van Effenterre, L. Navailles, F. Nallet and D. Roux

Centre de recherche Paul-Pascal, Université Bordeaux-1 CNRS, 115 avenue du Docteur-Schweitzer, F-33600, Pessac, France

navailles@crpp-bordeaux.cnrs.fr
nallet@crpp-bordeaux.cnrs.fr

Received 30 September 2007 / Published online 7 May 2008

Abstract

The dynamic behaviour of three hydrophilic probes (two dyes and one fluorescently-labelled protein) inserted in the water layers of lyotropic lamellar phases has been studied by confocal fluorescence recovery experiments. Two different, ionic (AOT/NaCl/ H₂O and non-ionic ( C₁₂E₅ /hexanol/ H₂O host systems were studied. The confinement effect has been carefully monitored using the swelling properties of the lamellar phases. In all cases, we measure the evolution of the probe diffusion coefficient in the layer plane D_⊥ versus the separation between the membranes d_w. Depending on the composition of the lamellar phase, this distance can be continuously adjusted from 500Å to about 20Å. For all systems, we observe a first regime, called dilute regime, where the diffusion coefficient decreases almost linearly with 1/d_w . In this regime, the Faxén theory for the friction coefficient of a spherical particle symmetrically dragged between two rigid walls can largely explain our results. More unexpectedly, when the membranes are non-ionic, and also quite flexible ( C₁₂E₅ /hexanol in water), we observe the existence of a second, concentrated (or confined) regime, where the diffusion coefficient is nearly constant and different from zero for membrane separations smaller than the particle size. This new regime can be heuristically explained by simple arguments taking into account the membrane fluidity.

PACS
82.70.-y - Disperse systems; complex fluids.
87.16.dj - Dynamics and fluctuations.
87.64.mk - Confocal.
82.56.Lz - Diffusion.

Correspondence: nallet@crpp-bordeaux.cnrs.fr


© EDP Sciences, Società Italiana di Fisica, Springer-Verlag 2008