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Intracellular Delivery of Biologically-Active Fungal Metabolite Gliotoxin Using Magnetic Nanoparticles.
Comas, Laura; Polo, Esther; Domingo, M Pilar; Hernández, Yulán; Arias, Maykel; Esteban, Patricia; Martínez-Lostao, Luis; Pardo, Julián; Martínez de la Fuente, Jesús; Gálvez, Eva M.
Affiliation
  • Comas L; Instituto de Carboquímica (ICB-CSIC), 50018 Zaragoza, Spain. lcomasc@hotmail.com.
  • Polo E; Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS), Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain. epolo82@gmail.com.
  • Domingo MP; Instituto de Carboquímica (ICB-CSIC), 50018 Zaragoza, Spain. mpdomingo@icb.csic.es.
  • Hernández Y; Pontificia Universidad Católica del Peru, Departamento de Ciencias - Sección Química, Lima 1761, Peru. yhernandez@pucp.pe.
  • Arias M; Instituto de Carboquímica (ICB-CSIC), 50018 Zaragoza, Spain. maykelariascabrero@gmail.com.
  • Esteban P; Instituto de Carboquímica (ICB-CSIC), 50018 Zaragoza, Spain. patri.estb@gmail.com.
  • Martínez-Lostao L; Instituto de Investigaciones Sanitarias de Aragón (IIS), 50009 Zaragoza, Spain. lumartin@unizar.es.
  • Pardo J; Departamento de Microbiología, Medicina Preventiva y Salud Pública, Universidad de Zaragoza, 50009 Zaragoza, Spain. lumartin@unizar.es.
  • Martínez de la Fuente J; Servicio de Inmunologia, Hospital Clinico Lozano Blesa, 50009 Zaragoza, Spain. lumartin@unizar.es.
  • Gálvez EM; Instituto de Nanociencia de Aragón, Universidad de Zaragoza, 50018 Zaragoza, Spain. lumartin@unizar.es.
Materials (Basel) ; 12(7)2019 04 02.
Article in En | MEDLINE | ID: mdl-30987007
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.
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