Novel Supramolecular Nanoparticles Derived from Cucurbit[7]uril and Zwitterionic Surfactants

J. Fernández-Rosas, Marcia Pessêgo, Angel Acuña, Carlos Vázquez-Vázquez, Javier Montenegro, Mercedes Parajó, Pedro Rodríguez-Dafonte, Faruk Nome, Luis Garcia-Rio

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Binding constants, log K ≈ 6.6 M-1, and NMR characterization of the complexes formed by sulfobetaines and cucurbit[7]uril (CB7) support the electrostatic interaction as the major driving force. This very strong binding motif is cross-linked by additional CB7 molecules, resulting in the formation of supramolecular nanoparticles (SNPs) with an average diameter of 172 nm and a negative surface potential. The time course evolution of the particle size and the surface potential suggests the very fast formation of an amorphous aggregate that absorbs an additional amount of sulfobetaine. These aggregates afford very stable (more than 2 weeks) nanoparticles in an aqueous dispersion. The reversibility of the sulfobetaine/CB7 host/guest complexes allows SNP disaggregation by adding a competitive guest as shown by treatment with tetraethylammonium chloride. The addition of this competitive cation triggers a SNP-to-micelle transition. The potential application of these nanoparticles as drug delivery vehicles was investigated by using carboxyfluorescein. These experiments revealed that upon externally induced disruption of the SNPs (by tetraethylammonium chloride) the fluorescent dye was trapped in micellar aggregates that can be further disrupted by cyclodextrin addition.

Original languageEnglish
Pages (from-to)3485-3493
Number of pages9
JournalLangmuir
Volume34
Issue number11
DOIs
Publication statusPublished - 20 Mar 2018

Fingerprint Dive into the research topics of 'Novel Supramolecular Nanoparticles Derived from Cucurbit[7]uril and Zwitterionic Surfactants'. Together they form a unique fingerprint.

Cite this