A novel technology has been developed by which water-soluble substances ran
ging from simple inorganic salts to complex macromolecules, are solubilized
in the absence of water, into organic liquids. The resulting microphases a
re quite different from any that have been previously described in the lite
rature and can potentially be used for delivery of drugs and other material
s via a range of routes, including oral, topical, pulmonary, nasal and ocul
ar. The formulations are prepared using a liposomal methodology, and liposo
mes may also play a role in the ultimate delivery of the drug. This present
ation describes the manufacture and properties of the formulations, and pre
sents data for their use in delivering insulin and calcitonin in vivo, usin
g the juvenile pig model.