4.6 Article

Biodegradable nanoparticles combining cancer cell targeting and anti-angiogenic activity for synergistic chemotherapy in epithelial cancer

期刊

DRUG DELIVERY AND TRANSLATIONAL RESEARCH
卷 12, 期 10, 页码 2488-2500

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s13346-021-01090-6

关键词

Polymeric nanoparticles; Anti-angiogenic peptides; Folate targeting; Tumor spheroids; Xenografted zebrafish embryos

资金

  1. Italian Association for Cancer Research [15764]
  2. Regione Campania-POR Campania FESR 2014/2020 Combattere la resistenza tumorale: piattaforma integrata multidisciplinare per un approccio tecnologico innovativo alle oncoterapie-Campania Oncoterapie [B61G18000470007]
  3. Department of Biology, University of Padova (PRIDseed 2018 Grant)

向作者/读者索取更多资源

This study proposes a biodegradable nanoplatform that combines anti-angiogenic activity and targeting of cancer cells to enhance the anticancer effect of docetaxel (DTX). The nanoparticles (NPs) developed in this study showed good size, stability, and the ability to effectively deliver DTX. In various in vitro and in vivo experiments, the NPs exhibited promising therapeutic outcomes and reduced systemic toxicity. Overall, this research emphasizes the importance of nanotechnology in cancer treatment.
A biodegradable engineered nanoplatform combining anti-angiogenic activity and targeting of cancer cells to improve the anticancer activity of docetaxel (DTX) is here proposed. Indeed, we have developed biodegradable nanoparticles (NPs) of poly(ethylene glycol)-poly(epsilon-caprolactone), exposing on the surface both folate motifs (Fol) for recognition in cells overexpressing Folate receptor-alpha (FR alpha) and the anti-angiogenic hexapeptide aFLT1. NPs showed a size around 100 nm, the exposure of 60% of Fol moieties on the surface, and the ability to entrap DTX and sustain its release with time. NPs were stable in simulated biological fluids and slightly interacted with Fetal Bovine serum, especially in the formulation decorated with Fol and aFLT1. The presence of Fol on NPs did not impair the anti-angiogenic activity of aFLT1, as assessed by in vitro tube formation assay in HUVEC endothelial cells. In both 2D and 3D KB cell cultures in vitro, the cytotoxicity of DTX loaded in NPs was not significantly affected by Fol/aFLT1 double decoration compared to free DTX. Remarkably, NPs distributed differently in 3D multicellular spheroids of FR alpha-positive KB cancer cells depending on the type of ligand displayed on the surface. In particular, NPs unmodified on the surface were randomly distributed in the spheroid, whereas the presence of Fol promoted the accumulation in the outer rims of the spheroid. Finally, NPs with Fol and aFLT1 gave a uniform distribution throughout the spheroid structure. When tested in zebrafish embryos xenografted with KB cells, NPs displaying Fol/aFLT1 reduced DTX systemic toxicity and inhibited the growth of the tumor mass and associated vasculature synergistically. Overall, nanotechnology offers excellent ground for combining therapeutic concepts in cancer, paving the way to novel multifunctional nanopharmaceuticals decorated with bioactive elements that can significantly improve therapeutic outcomes.

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