Nanoparticle-based co-delivery of siRNA and paclitaxel for dual-targeting of glioblastoma

Nanomedicine (Lond). 2020 Jun;15(14):1391-1409. doi: 10.2217/nnm-2020-0066. Epub 2020 Jun 4.

Abstract

Aim: To explore the therapeutic effect of nanoparticle-based dual-targeting delivery of antitumor agents for glioblastoma treatment. Materials & methods: A hepatitis B core protein-virus-like particle (VLP)-based dual-targeting delivery system was designed with the primary brain targeting peptide TGN for blood-brain barrier penetration and tumor vascular preferred ligand RGD (arginine-glycine-aspartic acid) for glioblastoma targeting. Chemo- and gene-therapeutic agents of paclitaxel and siRNA were co-packaged inside the vehicle. Results: The results demonstrated efficient delivery of the packaged agents to invasive tumor sites. The combination of chemo- and gene-therapies demonstrated synergistic antitumor effects through enhancing necrosis and apoptosis, as well as being able to inhibit tumor invasion with minimal cytotoxicity. Conclusion: Our hepatitis B core-VLP-based dual-targeting delivery of chemo- and gene-therapeutic agents possesses a synergistic antitumor effect for glioblastoma therapy.

Keywords: RNA interference; brain tumor targeting; chemotherapy; synergistic efficiency; virus-like particle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Drug Delivery Systems
  • Glioblastoma* / drug therapy
  • Glioblastoma* / genetics
  • Humans
  • Nanoparticles*
  • Paclitaxel / therapeutic use
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / therapeutic use

Substances

  • RNA, Small Interfering
  • Paclitaxel