Chitosan-Based Non-viral Gene and Drug Delivery Systems for Brain Cancer

Montserrat Lara-Velazquez1,2, Rawan Alkharboosh1,3,4, Emily S Norton1,3,4

  • 1Mayo Clinic Florida, Department of Neurosurgery, Jacksonville, FL, United States.

Frontiers in Neurology
|August 28, 2020
PubMed

Insights

Chitosan (CS) shows promise as a non-viral gene delivery system for brain tumors, overcoming the blood-brain barrier. This review explores CS-based nanostructures for targeted cancer therapy.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Oncology

Background:

  • Central nervous system (CNS) tumors represent a significant global health burden.
  • Current therapeutic strategies face challenges, particularly in penetrating the blood-brain barrier.
  • Gene therapy offers a promising avenue for targeted cancer treatment.

Purpose of the Study:

  • To review the application of chitosan (CS) as a non-viral gene delivery vehicle for brain tumors.
  • To highlight the advantages and challenges of CS-based delivery systems.
  • To assess the translational potential of CS strategies in clinical cancer studies.

Main Methods:

  • Review of existing literature on chitosan-based gene delivery for CNS tumors.
  • Evaluation of various CS-based nanostructures (nanocapsules, nanospheres, etc.).
  • Analysis of studies focusing on overcoming the blood-brain barrier.

Main Results:

  • Chitosan's properties (biodegradability, non-toxicity, nucleic acid protection) make it suitable for gene delivery.
  • CS-based nanostructures demonstrate potential for targeted drug delivery across the blood-brain barrier.
  • Evidence supports CS as an alternative gene delivery system for cancer treatment.

Conclusions:

  • Chitosan-based nanostructures offer a viable strategy for overcoming the blood-brain barrier in brain tumor gene therapy.
  • Further research and clinical studies are needed to fully realize the translational potential of CS delivery systems.
  • CS represents a promising natural-based polymer for advanced cancer therapeutics.