Lamellar-to-cubic phase change in phospholipid bilayer systems incorporated with block copolymers: DMPC and PEO-PPO-PEO (P85).

We have used small-angle X-ray scattering and calorimetric methods to investigate the temperature-dependent phase behavior of ternary systems of phospholipid (DMPC), amphiphilic PEO-PPO-PEO block copolymer (Pluronics P85), and water. It is shown that a relatively small amount of block copolymers ( approximately 3 wt %) results in a lamellar-to-cubic phase transition. Still, both the bilayer-characteristic main transition, associated with chain melting, and the pretransition, associated with in-plane modulations, are preserved for copolymer concentrations up to 50-70 wt %, indicating the preservation of a bilayer type of lipid organization also within the cubic phase. The main transition splits up into two transitions upon the addition of copolymers, one resembling the high cooperativity of the main transition and one broad transition which may reflect complex formation with the copolymers. Parallel studies incorporating poly(ethylene glycol) into the DMPC multilamellar vesicles do not give analogous structural changes. It is concluded that the major effect on the molecular scale of adding PEO-PPO-PEO block copolymers is not only due to the hydration of the membrane but also due to the incorporation of the PPO block into the bilayer structure.