The layer-by-layer deposition method to prepare multilayers of polyelectrolytes of alternating charge
has been followed in situ by means of optical reflectometry experiments. It turns out that in solutions
containing both polyelectrolyte and appropriate salts up to a certain concentration, the regular build up
of multilayers is modified and becomes an adsorption/redissolution process. We explain this by taking into
account (i) that during the regular multilayer formation process the macromolecules cannot equilibrate,
(ii) that the added salt plasticizes the multilayer to a state where the molecules are sufficiently mobile
to enable them to equilibrate between the layer and the surrounding solution, and (iii) that the presence
of excess polyelectrolyte brings the system to a one-phase region of the polyelectrolyte complex phase
diagram, implying that polyelectrolyte complexes must dissolve under these conditions.
With the aim to gain insight into the possible applicability of protein-filled polyelectrolyte complex micelles under physiological salt conditions, we studied the behavior of these micelles as a function of salt concentration. The micelles form by electrostatically driven co-assembly from strong cationic block copolymers poly(2-methyl vinyl pyridinium) 41 -block-poly(ethylene oxide) 205 , weak anionic homopolymers poly(acrylic acid) 139 , and negatively charged lipase molecules. The formation and disintegration of these micelles were studied with dynamic light scattering (DLS), by means of composition and salt titrations, respectively. The latter measurements revealed differences between disintegration of lipase-filled and normal polyelectrolyte complex micelles. These data, together with small angle neutron scattering (SANS) measurements provide indications that lipase is gradually released with increasing salt concentration. From the SANS data a linear relation between the intensity at q ¼ 0 and the volume of the cores of the micelles at different salt concentrations was derived, indicating a loss of volume of the micelles due to the release of lipase molecules. It was estimated that beyond 0.12 M NaCl all lipase molecules are released.
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