Abstract

In this paper, we report the development of the novel self-assembling systems based on oppositely charged Pillar[5]arenes and surfactants for encapsulation of diagnostic dye DAPI. For this purpose, the aggregation behavior of synthesized macrocycles and surfactants in the presence of Pillar[5]arenes functionalized by carboxy and ammonium terminal groups was studied. It has been demonstrated that by varying the molar ratio in Pillar[5]arene-surfactant systems, it is possible to obtain various types of supramolecular systems: host–guest complexes at equimolar ratio of Pillar[5]arene-surfactant and interpolyelectrolyte complexes (IPECs) are self-assembled materials formed in aqueous medium by two oppositely charged polyelectrolytes (macrocycle and surfactant micelles). It has been suggested that interaction of Pillar[5]arenes with surfactants is predominantly driven by cooperative electrostatic interactions. Synthesized stoichiometric and non-stoichiometric IPECs specifically interact with DAPI. UV-vis, luminescent spectroscopy and molecular docking data show the structural feature of dye-loaded IPEC and key role of the electrostatic, π–π-stacking, cation–π interactions in their formation. Such a strategy for the design of supramolecular Pillar[5]arene-surfactant systems will lead to a synergistic interaction of the two components and will allow specific interaction with the third component (drug or fluorescent tag), which will certainly be in demand in pharmaceuticals and biomedical diagnostics.

Highlights

  • It was shown that by varying the molar ratio in Pillar[5]arene-surfactant systems, it is possible to obtain various types of nanosystems: (1) host-guest complexes at equimolar ratio of Pillar[5]arene-surfactant and (2) interpolyelectrolyte complexes (IPECs), are self-assembled materials formed in aqueous medium by two oppositely charged polyelectrolytes

  • It has been suggested that interaction of Pillar[5]arenes with surfactants is predominantly driven by cooperative electrostatic interactions

  • Synthesized stoichiometric and non-stoichiometric IPECs interact with a third component, imaging system agent, 40,6-diamidino-2-phenylindole (DAPI)

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Summary

Introduction

Pillar[5]arenes are capable of forming complexes with various biologically significant substrates using their hydrophobic macrocyclic cavity or substituents on both rims of the macrocycle [6,7,8,9,10]. Directed functionalization of Pillar[5]arenes allows one to control such important properties of molecules as bioavailability and water solubility [11,12,13,14,15]. The ability of water-soluble macrocycles, by analogy with non-macrocyclic surfactants, to form various types of associates such as liposomes [36,37,38], micelles [39,40,41], and liquid crystals [42,43], etc., is well known

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