Abstract

Chemotherapeutics represent the standard treatment for a wide range of cancers. However, these agents also affect healthy cells, thus leading to severe off-target effects. Given the non-selectivity of the commonly used drugs, any increase in the selective tumor tissue uptake would represent a significant improvement in cancer therapy. Recently, the use of gene therapy to completely remove the lesion and avoid the toxicity of chemotherapeutics has become a tendency in oncotherapy. Ideally, the genetic material must be safely transferred from the site of administration to the target cells, without involving healthy tissues. This can be achieved by encapsulating genes into non-viral carriers and modifying their surface with ligands with high selectivity and affinity for a relevant receptor on the target cells. Hence, in this work we evaluate the use of terpolymer-based nanocapsules for the targeted delivery of DNA toward cancer cells. The surface of the nanocapsules is decorated with folic acid to actively target the folate receptors overexpressed on a variety of cancer cells. The nanocapsules demonstrate a good ability of encapsulating and releasing DNA. Moreover, the presence of the targeting moieties on the surface of the nanocapsules favors cell uptake, opening up the possibility of more effective therapies.

Highlights

  • Chemotherapy is the major therapeutic approach for the treatment of a wide range of cancers

  • In this study we evaluated our previously developed and fully characterized terpolymerbased nanoparticles [51] to be used for targeted DNA delivery, using folic acid as ligand to obtain active targeting toward cancer cells

  • The radical polymerization of the three monomers led to the formation of NCs directly in the reaction phase, with a monomer conversion around 100% for Butyl methacrylate (BMA) and (PEG)MEMA, and higher than 95% for DMAEMA

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Summary

Introduction

Chemotherapy is the major therapeutic approach for the treatment of a wide range of cancers. A major problem with such treatment is represented by side effects as the agents affect healthy tissues as well as cancerous cells [1,2,3]. Any selective increase in tumor tissue uptake would be a significant improvement in cancer therapy given the non-selectivity of the commonly used drugs [4]. Gene therapy has been acknowledged as major progress of modern medicine and a focus for oncotherapy research. In oncotherapy cancer cells can be modified with genes of cytotoxic or tumor suppressive proteins, or with a class of suicidal genes in combination with pro-drugs, all of which

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