1. Academic Validation
  2. A Novel Patient-Personalized Nanovector Based on Homotypic Recognition and Magnetic Hyperthermia for an Efficient Treatment of Glioblastoma Multiforme

A Novel Patient-Personalized Nanovector Based on Homotypic Recognition and Magnetic Hyperthermia for an Efficient Treatment of Glioblastoma Multiforme

  • Adv Healthc Mater. 2023 Apr 14;e2203120. doi: 10.1002/adhm.202203120.
Daniele De Pasquale 1 Carlotta Pucci 1 Andrea Desii 1 Attilio Marino 1 Doriana Debellis 2 Luca Leoncino 2 Mirko Prato 3 Stefania Moscato 4 Simone Amadio 1 Pietro Fiaschi 5 6 Alessandro Prior 5 Gianni Ciofani 1
Affiliations

Affiliations

  • 1 Smart Bio-Interfaces, Istituto Italiano di Tecnologia, Viale Rinaldo Piaggio 34, Pontedera, 56025, Italy.
  • 2 Electron Microscopy Facility, Istituto Italiano di Tecnologia, Via Morego 30, Genova, 16163, Italy.
  • 3 Materials Characterization Facility, Istituto Italiano di Tecnologia, Via Morego 30, Genova, 16163, Italy.
  • 4 Department of Clinical and Experimental Medicine, University of Pisa, Via Roma 55, Pisa, 56126, Italy.
  • 5 Department of Neurosurgery, IRCCS Ospedale Policlinico San Martino, Largo Rossana Benzi 10, Genova, 16132, Italy.
  • 6 Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genova, Largo Paolo Daneo 3, Genova, 16132, Italy.
Abstract

Glioblastoma multiforme (GBM) is the deadliest brain tumor, characterized by an extreme genotypic and phenotypic variability, besides a high infiltrative property in healthy tissues. Apart from very invasive surgical procedures, to date, there are no effective treatments, and life expectancy is very limited. In this work, we propose an innovative therapeutic approach based on lipid-based magnetic nanovectors, owning a dual therapeutic function: chemotherapy, thanks to an antineoplastic drug (regorafenib) loaded in the core, and localised magnetic hyperthermia, thanks to the presence of iron oxide nanoparticles, remotely activated by an alternating magnetic field. The drug has been selected based on ad hoc patient-specific screenings; moreover, the nanovector is decorated with cell membranes derived from patients' cells, aiming at increasing homotypic and personalized targeting. We demonstrated that this functionalization not only enhances the selectivity of the nanovectors towards patient-derived GBM cells, but also their blood-brain barrier in vitro crossing ability. The localised magnetic hyperthermia induces both thermal and oxidative intracellular stress, that lead to lysosomal membrane permeabilization and release of proteolytic Enzymes into the cytosol. Collected results show that hyperthermia and chemotherapy work in synergy to reduce GBM cell invasion properties, to induce intracellular damage and, eventually, to prompt cellular death. This article is protected by copyright. All rights reserved.

Keywords

glioblastoma; homotypic targeting; magnetic hyperthermia; personalized medicine.

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