Membranes (Aug 2020)

A Reevaluation of Chitosan-Decorated Nanoparticles to Cross the Blood-Brain Barrier

  • Hernán Cortés,
  • Sergio Alcalá-Alcalá,
  • Isaac H. Caballero-Florán,
  • Sergio A. Bernal-Chávez,
  • Arturo Ávalos-Fuentes,
  • Maykel González-Torres,
  • Manuel González-Del Carmen,
  • Gabriela Figueroa-González,
  • Octavio D. Reyes-Hernández,
  • Benjamín Floran,
  • María L. Del Prado-Audelo,
  • Gerardo Leyva-Gómez

DOI
https://doi.org/10.3390/membranes10090212
Journal volume & issue
Vol. 10, no. 9
p. 212

Abstract

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The blood-brain barrier (BBB) is a sophisticated and very selective dynamic interface composed of endothelial cells expressing enzymes, transport systems, and receptors that regulate the passage of nutrients, ions, oxygen, and other essential molecules to the brain, regulating its homeostasis. Moreover, the BBB performs a vital function in protecting the brain from pathogens and other dangerous agents in the blood circulation. Despite its crucial role, this barrier represents a difficult obstacle for the treatment of brain diseases because many therapeutic agents cannot cross it. Thus, different strategies based on nanoparticles have been explored in recent years. Concerning this, chitosan-decorated nanoparticles have demonstrated enormous potential for drug delivery across the BBB and treatment of Alzheimer’s disease, Parkinson’s disease, gliomas, cerebral ischemia, and schizophrenia. Our main objective was to highlight the high potential of chitosan adsorption to improve the penetrability through the BBB of nanoformulations for diseases of CNS. Therefore, we describe the BBB structure and function, as well as the routes of chitosan for crossing it. Moreover, we define the methods of decoration of nanoparticles with chitosan and provide numerous examples of their potential utilization in a variety of brain diseases. Lastly, we discuss future directions, mentioning the need for extensive characterization of proposed nanoformulations and clinical trials for evaluation of their efficacy.

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