Abstract

Introduction: Cochleates are  cylindrical lipid structures that are more stable against oxidation and temperature than liposomes.  Our research is formulation of  cochleates for oral delivery of insulin as a model protein drug. Protein drugs are softer from environmental degradation and poor oral absorption; therefore any carrier system for their oral delivery must have protection against enzymes and absorption  enhancing ability.

Methods and Results: In this study, liposomes with different proportion of lipids (DPPC and DMPC) and cholesterol were prepared by film hydration method and converted to cochleates by hydrogel method with CaCl₂ and MgCl₂. Microscopically observation of structures was carried out by phase-contrast microscope and Scanning Electron Microscope (SEM). Physicochemical characteristics of these structures were evaluated by measuring size distribution  using with  laser light scattering technique, entrapment efficiency percentage, investigation of release profile, and stability of selected cochleates. HPLC method  was used for analytical evaluation of entrapped and released insulin.Best formulation of liposomes contains 70% of lipid and 30% of cholesterol. According to microscopic size distribution, cochleates with CaCl₂ bridges were better. The size of vesicles was less than 6 µm. Insulin entrapment efficiency of cochleates with DPPC was more than DMPC type. Between 60-70% of encochleated insulin released after 2-4 hours in a buffer with pH 6.8.

Conclusions:The results shows that cochleates can be suitable oral delivery systems for insulin.