Back to Search Start Over

Functionalization using biocompatible carboxylated cyclodextrins of iron-based nanoMIL-100

Authors :
Fondo Nacional de Desarrollo Científico y Tecnológico (Chile)
Ministerio de Ciencia, Innovación y Universidades (España)
Centre National de la Recherche Scientifique (France)
Generalitat Valenciana
Carmona, Thais
Marco, J.F.
Giménez-Marqués, Mónica
Cañón-Mancisidor, W.
Gutiérrez-Cutiño, M.
Hermosilla-Ibáñez, P.
Perez, Edwin G.
Mínguez Espallargas, Guillermo
Venegas-Yazigi, D.
Fondo Nacional de Desarrollo Científico y Tecnológico (Chile)
Ministerio de Ciencia, Innovación y Universidades (España)
Centre National de la Recherche Scientifique (France)
Generalitat Valenciana
Carmona, Thais
Marco, J.F.
Giménez-Marqués, Mónica
Cañón-Mancisidor, W.
Gutiérrez-Cutiño, M.
Hermosilla-Ibáñez, P.
Perez, Edwin G.
Mínguez Espallargas, Guillermo
Venegas-Yazigi, D.
Publication Year :
2021

Abstract

Here we report the first example of nanoMIL-100 particles modified with monomeric cyclodextrin derivatives of different length by exploiting strong interactions between non-saturated iron trimers at the external surface and carboxylate functionalities located at the end of biocompatible and flexible linkers of cyclodextrins. The main results revealed that, after the functionalization, the cyclodextrins are selectively located at the external surfaces covering the nanoparticles. Z potential measurements show that this functionalization induced changes respect to the bare nanoMIL-100 particles, however, the presence of the cyclodextrins does not modify the size neither porosity of the nanoparticles. The amount of cyclodextrins attached, investigated by thermogravimetry, increases with the length of the linker between CD cavity and nanoparticle surface, reaching up a 9 % wt. Auger spectroscopy suggested a clear predominant sp character after the functionalizations (vs. sp predominance in the unmodified nanoMIL-100). This study supposes the creation of an alternative family of hybrids based on carboxylated monomeric cyclodextrins.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1293836745
Document Type :
Electronic Resource