A few polyurethane (PUR) copolymers were recently considered as possible material in the drug delivery
systems domain. This study intends to obtain a transdermal carrier for lupeol. PUR nanocapsules were
synthesized by interfacial polycondensation combined with spontaneous emulsification. An organic phase
containing lysine diisocyanate ester in water-miscible solvent (acetone) and a homogeneous aqueous phase
formed by water, diols, polyether and a surfactant (Tween®20) were used in the synthesis. After the
optimization of the work procedure, was obtained around 600 nm size nanocapsules which were
characterized by pH, size and zeta potential measurements, SEM and DSC and no significant
modifications compared with an ethalon were reported