Ionic liquids (ILs) attract significant
attention as novel solvents
for drug delivery systems because of their ability to solubilize poorly
soluble drugs and tune the physiological properties of active pharmaceutical
ingredients. For the next generation of IL-based drug delivery systems,
biocompatibility is a high priority. In the current study, choline–fatty
acids ([Cho][FA]) were used as a biocompatible IL to mediate the dissolution
of a water-soluble antigen peptide in an oil-based skin penetration
enhancer. Among the candidate fatty acids (C8, C10, C12, C14, C16,
C18:0, and C18:1), C18:1 was selected because of its low cytotoxicity
and mediation of skin permeability for an antigen peptide. Using IL[Cho][C18:1]
and an oil-based penetration enhancer, the flux of transdermal delivery
of the peptide increased 28-fold compared with delivery using an aqueous
vehicle. Furthermore, the IL-mediated transcutaneous vaccination succeeded
in suppressing tumor growth in vivo compared to injection. The skin
irritation produced by this formulation was tested using an in vitro
3D constructed skin tissue model and an in vivo histological study,
which concluded that the formulation did not cause skin irritation.
The results suggest that biocompatible IL-mediated dissolution in
an oil-based skin penetration enhancer is a promising strategy for
transdermal drug delivery.