Interactions of liposomes and hydrophobically-modified poly-(N-isopropylacrylamides): an attempt to model the...

The interactions of small unilamellar vesicles (SUV) and water-soluble copolymers were studied by fluorescence spectroscopy, differential scanning calorimetry (DSC) and quasi-elastic light scattering (QELS). The anchoring onto liposomal bilayer membranes of copolymers of N-isopropylacrylamide, N-(2-(1-naphthyl)ethyl)-N-n-octadecylacrylamide and or N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide (0.5 mol% of the octadecylacrylamide comonomer) was monitored by non-radiative energy transfer between excited naphthalene and pyrene. The anchoring process occurred on zwitterionic lecithin liposomes and on negatively charged phosphatidic acid liposomes, whether the bilayer was in the crystalline or the liquid-crystalline phase. Insertion of the copolymer octadecyl groups within crystalline bilayers was attributed to the presence of packing defects. Aqueous solutions of poly-(N-isopropylacrylamide) and of its hydrophobically-modified copolymers exhibit a lower critical solution temperature (LCST). The coil to globule collapse of the polymer chains which is known to occur as the aqueous solution is heated through the LCST, also took place when the copolymers were anchored onto vesicular bilayers. The copolymers remained anchored during this collapse and the liposomes were not destroyed. The process was thermo-reversible. Detailed aspects of the reversibility of the phenomenon depended on the relative values of the phase transition temperatures of the liposomes and of the polymer LCST.