PhD

dissertationDrug delivery development and optimization require understanding of the roles of lipid phase on partitioning, permeation pathways, and barrier functions of bilayers on a molecular level. Quantitative contributions of lipid phase and chemical structure remain unknown for most biological membranes of pharmaceutical interest. Current investigations ascertained contributions of bilayer packing phases to solute partitioning into and permeation across lipid bilayers, an objective most effectively addressed with model bilayers of defined structure, composition, and phase. Well-characterized large unilamellar liposomes modeled different bilayer phases composed of tilted gel and liquid-crystalline dipalmitoylphosphatidylcholine and distearoyl-phosphatidylcholine, interdigitated gel and liquid-crystalline dihexadecylphosphatidyl-choline, and liquid-crystalline cholesterol-containing phases of these phospholipids. Variations in polar headgroup spacings versus acyl chain mobilities were exploited to systematically probe aspects of phospholipid bilayer packing phase that determine the bilayer's barrier function. Bilayer lipid composition strongly influenced the number of bilayers, average size, size distribution, and stability of liposomes extruded through a constant pore size polycarbonate filter. Liposome surface areas and internal volumes were calculated using diameters, number of bilayers/liposome, bilayer thicknesses, and headgroup surface areas. These variables and solute efflux were used to calculate permeability. Thus, effects of differing liposome sizes on permeation were differentiated. Quantitative permeabilities for hydrophilic nonelectrolytes ranging from thiourea to sucrose represented the first obtained for well-characterized large unilamellar liposomes. Permeability trends with varying solute size/hydrophilicity suggested selectivity to hydrophilicity dominated over molecular volume for the solutes studied. Gel phases were established to have different barrier properties than liquid-crystalline phases, with selectivity differing for different gel phases. Each bilayer phase studied possessed an overall diffusional barrier more lipophilic than an octanol environment. Contributions to lipophilic solute partitioning included both polar headgroup/interfacial and acyl chain bilayer structural regions. However, partitioning barriers for even fairly lipophilic molecules were not the same barriers as those for diffusion. Through systematic evaluation of permeabilities as a function of bilayer phase, the primary diffusional barrier was established to be within acyl chain regions, with a smaller but significant contribution by the polar headgroup spacing that has not been previously reported in the literature