The rising incidence of fungal infections, compounded by the emergence of severe antifungal resistance, has resulted in an urgent need for innovative antifungal therapies. We developed an antifungal protein-based formulation as a topical antifungal agent by combining an artificial lipidated chitin-binding domain of antifungal chitinase (LysM-lipid) with recently developed ionic liquid-in-oil microemulsion formulations (MEFs). Our findings demonstrated that the lipid moieties attached to LysM and the MEFs effectively disrupted the integrity of the stratum corneum in a mouse skin model, thereby enhancing the skin permeability of the LysM-lipids. Among the MEFs incorporating LysM modified with lauric (C12), myristic (C14), and palmitic (C16) acids, the LysM-C14-loaded MEF emerged as the most promising candidate, exhibiting potent antifungal activity against Trichoderma viride growing actively beneath the skin. The stability of the MEFs was investigated after a 28 day storage period at room temperature, and both LysM-C14- and LysM-C16-loaded MEFs retained comparable antifungal activity with that of the freshly prepared MEFs. These results highlight the considerable potential of LysM-lipid-loaded MEFs as effective topical antifungal agents.
Keywords: antifungal reagent; chitin-binding domain; microbial transglutaminase; microemulsions; surface-active ionic liquids.