6533b7d4fe1ef96bd1261dd0

RESEARCH PRODUCT

Dual drug-loaded halloysite hybrid-based glycocluster for sustained release of hydrophobic molecules

Renato NotoConcetta BaiamonteCarla GiordanoGiuseppe PizzolantiSerena RielaFilippo ParisiJosé L. Jiménez BlancoP. Lo MeoMarina MassaroGiuseppe LazzaraStefana Milioto

subject

Hydrodynamic radiusGeneral Chemical Engineering02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteNanomaterialsSettore MED/13 - EndocrinologiaFluorescence microscopeSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationbiologyCyclodextrinLectinGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesMembraneBiochemistrychemistryDrug deliveryengineeringbiology.proteinBiophysicshalloysite nanotubes glycocluster effect cyclodextrin curcumin and silibinin0210 nano-technology

description

A dual drug-loaded HNT–CD glycocluster delivery system based on halloysite nanotubes and carbohydrate functionalized cyclodextrin was developed by a green protocol using solvent-free microwave irradiation. The nanohybrid was employed for concurrent load and release of silibinin and curcumin. The new delivery system was characterized by means of TGA, FT-IR spectroscopy, SEM and DLS. These techniques confirm the successful loading of the two drugs in the system. SEM and DLS measurements highlighted that the nanomaterial preserves a tubular structure with an average hydrodynamic radius of ca. 200 nm. The release of the drugs from the HNT glycocluster was investigated by means of UV-vis spectroscopy at two different pH values simulanting the typical physiological conditions of either gastric or intestinal fluids. Enzyme-linked lectin assays (ELLA) demonstrated that highly mannoside–cyclodextrins HNT entities display high affinity towards mannose selective ConA lectin. Biological assays showed that the new drug delivery system exhibits anti-proliferative activity against the investigated cell lines. Fluorescence microscopy confirmed ELLA results and it showed a high propensity of this drug delivery system to cross cell membranes and to penetrate into the cell nucleus. The results revealed that the synthesized multicavity system is a material of suitable size and nanoarchitecture to transport drugs into living cells. Spanish Ministerio de Economia y Competitividad (SAF2013-44021-R)

10.1039/c6ra14657khttp://hdl.handle.net/10447/204537