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In this study, nanocarriers based on self-assembled nystatin and pillar[5]arene were proposed. It was shown that pillar[5]arene with a terpene moiety is capable of targeted delivery of the natural antifungal drug nystatin to the cell membrane of opportunistic fungi (Candida sp.). A water-soluble pillar[5]arene containing a farnesyl moiety was synthesized for the first time. The membranotropic properties of the synthesized pillar[5]arene were demonstrated using the model lipid systems DPPC and DPPC : POPG. The formation of associates between pillar[5]arene and nystatin was confirmed by 2D DOSY, 1H–1H NOESY spectroscopy, and molecular dynamics. UV spectroscopy revealed that pillar[5]arene interacts with nystatin in a 1 : 2 stoichiometry. Dynamic light scattering and transmission electron microscopy showed that pillar[5]arene and nystatin form a stable monodisperse system with spherical-shaped associates. This study revealed that the pillar[5]arene/nystatin system exhibits more effective antifungal activity against clinical isolates of Candida sp. and Saccharomyces cerevisiae compared to free nystatin or pillar[5]arene. These findings represent a promising approach for the discovery of new membrane-targeting nanocarriers for the treatment of fungal diseases.

Graphical abstract: Combined antifungal nanocarriers based on self-assembled nystatin and pillar[5]arene with a terpene moiety

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