Cell Membrane Fragment-Wrapped Parenteral Nanoemulsions: A New Drug Delivery Tool to Target Gliomas

Author:

Dianzani Chiara1ORCID,Bozza Annalisa1,Bordano Valentina1ORCID,Cangemi Luigi1,Ferraris Chiara1,Foglietta Federica1ORCID,Monge Chiara1ORCID,Gallicchio Margherita1,Pizzimenti Stefania2ORCID,Marini Elisabetta1ORCID,Muntoni Elisabetta1ORCID,Valsania Maria Carmen34,Battaglia Luigi14ORCID

Affiliation:

1. Department of Drug Science and Technology, University of Turin, via Pietro Giuria 9, 10124 Turin, Italy

2. Department of Clinical and Biological Sciences, University of Turin, Corso Raffaello 30, 10124 Turin, Italy

3. Department of Chemistry, University of Turin, Via Quarello 15/a, 10135 Turin, Italy

4. Nanostructured Interfaces and Surfaces (NIS) Interdepartmental Centre, University of Turin, 10124 Turin, Italy

Abstract

Poor prognosis in high-grade gliomas is mainly due to fatal relapse after surgical resection in the absence of efficient chemotherapy, which is severely hampered by the blood–brain barrier. However, the leaky blood–brain–tumour barrier forms upon tumour growth and vascularization, allowing targeted nanocarrier-mediated drug delivery. The homotypic targeting ability of cell-membrane fragments obtained from cancer cells means that these fragments can be exploited to this aim. In this experimental work, injectable nanoemulsions, which have a long history of safe clinic usage, have been wrapped in glioma-cell membrane fragments via co-extrusion to give targeted, homogeneously sized, sterile formulations. These systems were then loaded with three different chemotherapeutics, in the form of hydrophobic ion pairs that can be released into the target site thanks to interactions with physiological components. The numerous assays performed in two-dimensional (2D) and three-dimensional (3D) cell models demonstrate that the proposed approach is a versatile drug-delivery platform with chemo-tactic properties towards glioma cells, with adhesive interactions between the target cell and the cell membrane fragments most likely being responsible for the effect. This approach’s promising translational perspectives towards personalized nanomedicine mean that further in vivo studies are foreseen for the future.

Funder

Compagnia di San Paolo

University of Turin

Publisher

MDPI AG

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