PART 1 - DIRECT MEASUREMENT OF DEPLETION ATTRACTION AND THIN-FILM VISCOSITY BETWEEN LIPID BILAYERS IN AQUEOUS POLYETHYLENE-GLYCOL SOLUTIONS

Citation
Tl. Kuhl et al., PART 1 - DIRECT MEASUREMENT OF DEPLETION ATTRACTION AND THIN-FILM VISCOSITY BETWEEN LIPID BILAYERS IN AQUEOUS POLYETHYLENE-GLYCOL SOLUTIONS, Macromolecules, 31(23), 1998, pp. 8250-8257
Citations number
49
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00249297
Volume
31
Issue
23
Year of publication
1998
Pages
8250 - 8257
Database
ISI
SICI code
0024-9297(1998)31:23<8250:P1-DMO>2.0.ZU;2-#
Abstract
Using the surface forces apparatus, we have measured the static and hy drodynamic forces between two substrate supported lipid bilayers in wa ter and semidilute aqueous solutions of 8000 MW poly(ethylene glycol) (PEG), a neutral polymer for which water is a good solvent. At small s eparations (D < R-F, Flory radius), an enhanced adhesion due to deplet ion attraction was measured. Conversely, at larger separations we foun d a repulsive barrier, which is not predicted by mean-field theories. Dynamic measurements of the viscosity as a function of film thickness reflected the same pattern of behavior as exhibited in the static forc e experiments: Thus, in the absence of polymer, the shear plane was at the lipid-water interface, while in the 8000 MW polymer solution the viscosity decreased as a function of decreasing surface separation due to a polymer-depleted layer of lower viscosity at the bilayer surface . We discuss our results in terms of depletion attraction, depletion s tabilization, thin film lubrication, the effective viscosity in thin f ilms, and the possibility of polymer aggregates in PEG solutions. The crossover from depletion attraction to adsorption and repulsion with i ncreasing MW is addressed in part 2 of this work.