Exosomes as New Generation Vehicles for Drug Delivery: Biomedical Applications and Future Perspectives

Molecules. 2022 Oct 27;27(21):7289. doi: 10.3390/molecules27217289.

Abstract

Currently, particular interest among the scientific community is focused on exploring the use of exosomes for several pharmaceutical and biomedical applications. This is due to the identification of the role of exosomes as an excellent intercellular communicator by delivering the requisite cargo comprising of functional proteins, metabolites and nucleic acids. Exosomes are the smallest extracellular vesicles (EV) with sizes ranging from 30-100 nm and are derived from endosomes. Exosomes have similar surface morphology to cells and act as a signal transduction channel between cells. They encompass different biomolecules, such as proteins, nucleic acids and lipids, thus rendering them naturally as an attractive drug delivery vehicle. Like the other advanced drug delivery systems, such as polymeric nanoparticles and liposomes to encapsulate drug substances, exosomes also gained much attention in enhancing therapeutic activity. Exosomes present many advantages, such as compatibility with living tissues, low toxicity, extended blood circulation, capability to pass contents from one cell to another, non-immunogenic and special targeting of various cells, making them an excellent therapeutic carrier. Exosome-based molecules for drug delivery are still in the early stages of research and clinical trials. The problems and clinical transition issues related to exosome-based drugs need to be overcome using advanced tools for better understanding and systemic evaluation of exosomes. In this current review, we summarize the most up-to-date knowledge about the complex biological journey of exosomes from biogenesis and secretion, isolation techniques, characterization, loading methods, pharmaceutical and therapeutic applications, challenges and future perspectives of exosomes.

Keywords: biogenesis; drug delivery; exosomes; isolation; therapeutic applications.

Publication types

  • Review

MeSH terms

  • Drug Delivery Systems / methods
  • Excipients
  • Exosomes* / metabolism
  • Extracellular Vesicles*
  • Liposomes / metabolism
  • Nucleic Acids* / metabolism

Substances

  • Liposomes
  • Excipients
  • Nucleic Acids

Grants and funding

This research received no external funding.