Abstract |
A series of amphiphilic glycodendro[60] fullerene monoadducts were efficiently synthesized using the CuAAC "click chemistry" approach. These glycodendrofullerenes can self-assemble in aqueous media, in a process favoured through π-π interactions between the [60] fullerene moieties. This aggregation process leads to big and well-defined compact micelles with a uniform size and spherical-shape. The supramolecular aggregates were characterized using electronic microscopy (SEM and TEM), light scattering methods (DLS) and X-ray methodologies (SAXS and XRD). The antiviral efficiency of these aggregates has been tested in an experimental infection assay using Ebola virus glycoprotein (EboGP) pseudotyped viral particles on Jurkat cells overexpressing DC-SIGN and an improvement in the IC50 value with respect to other systems endowed with a higher number of carbohydrate ligands is observed.
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Authors | Antonio Muñoz , Beatriz M Illescas , Joanna Luczkowiak , Fátima Lasala , Renato Ribeiro-Viana , Javier Rojo , Rafael Delgado , Nazario Martín |
Journal | Journal of materials chemistry. B
(J Mater Chem B)
Vol. 5
Issue 32
Pg. 6566-6571
(Aug 28 2017)
ISSN: 2050-7518 [Electronic] England |
PMID | 32264418
(Publication Type: Journal Article)
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