| abstract |
A pharmacological agent-lipid solution preparation comprising a lipophilic pharmacological agent, a desalted charged lipid and an aqueous-miscible lipid solvent such that upon introduction into an aqueous medium a suspension of lipid aggregates associated with the pharmacological agent are formed, the suspension exhibiting a stability of at least about 0.25 to 6 hours or longer without sedimentation. The preparations may contain an immunomodulator, an antifungal, anti-inflammatory, antineoplastic agent or hormone, and may be in unit (oral) dosage form including tablets, capsules, dragees or troches. |