Skip to main navigation Skip to search Skip to main content

Intracellular delivery of biologically-active fungal metabolite gliotoxin using magnetic nanoparticles

  • Laura Comas
  • , Esther Polo
  • , M. Pilar Domingo
  • , Yulán Hernández
  • , Maykel Arias
  • , Patricia Esteban
  • , Luis Martínez-Lostao
  • , Julián Pardo
  • , Jesús Martínez de la Fuente
  • , Eva M. Gálvez
  • Instituto de Carboquímica (ICB-CSIC)
  • Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS)
  • Instituto de Investigaciones Sanitarias de Aragón (IIS Aragón)
  • CSIC-Universidad de Zaragoza
  • Hospital Clinico Lozano Blesa
  • Fundación Araid

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Gliotoxin (GT), a secondary metabolite produced by Aspergillus molds, has been proposed as a potential anti-tumor agent. Here we have developed a nanoparticle approach to enhance delivery of GT in tumor cells and establish a basis for its potential use as therapeutical drug. GT bound to magnetic nanoparticles (MNPs) retained a high anti-tumor activity, correlating with efficient intracellular delivery, which was increased in the presence of glucose. Our results show that the attachment of GT to MNPs by covalent bonding enhances intracellular GT delivery without affecting its biological activity. This finding represents the first step to use this potent anti-tumor agent in the treatment of cancer.

Original languageEnglish
Article number1092
JournalMaterials
Volume12
Issue number7
DOIs
StatePublished - 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cancer cells
  • Drug delivery
  • Gliotoxin
  • Magnetic nanoparticles
  • Therapeutic

Fingerprint

Dive into the research topics of 'Intracellular delivery of biologically-active fungal metabolite gliotoxin using magnetic nanoparticles'. Together they form a unique fingerprint.

Cite this