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Extracellular vesicles versus synthetic nanoparticles for drug delivery

Cell-released biological nanoparticles, that is, extracellular vesicles (EVs), are emerging drug carriers with high complexity. EV-based drug delivery exploits intrinsic mechanisms for molecular transport in the body. Integrating EV biology and manufacturing with clinical insights from synthetic nanoparticles is likely to substantially advance the field of drug delivery.

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Fig. 1: Characteristics of free drugs, clinically approved synthetic nanoparticles and extracellular vesicles.

References

  1. Wolfram, J. & Ferrari, M. Clinical cancer nanomedicine. Nano Today 25, 85–89 (2019).

    Article  CAS  Google Scholar 

  2. van Niel, G., D’Angelo, G. & Raposo, G. Shedding light on the cell biology of extracellular vesicles. Nat. Rev. Mol. Cell Biol. 19, 213–228 (2018).

    Article  Google Scholar 

  3. Walker, S. et al. Extracellular vesicle-based drug delivery systems for cancer treatment. Theranostics 9, 8001–8017 (2019).

    Article  CAS  Google Scholar 

  4. Luo, W. et al. Spatial and temporal tracking of cardiac exosomes in mouse using a nano-luciferase-CD63 fusion protein. Commun. Biol. 3, 114 (2020).

    Article  CAS  Google Scholar 

  5. Reshke, R. et al. Reduction of the therapeutic dose of silencing RNA by packaging it in extracellular vesicles via a pre-microRNA backbone. Nat. Biomed. Eng. 4, 52–68 (2020).

    Article  CAS  Google Scholar 

  6. Elsharkasy, O. M. et al. Extracellular vesicles as drug delivery systems: why and how? Adv. Drug Deliv. Rev. 159, 332–343 (2020).

    Article  CAS  Google Scholar 

  7. Witwer, K. W. et al. Defining mesenchymal stromal cell (MSC)-derived small extracellular vesicles for therapeutic applications. J. Extracell. Vesicles 8, 1609206 (2019).

    Article  CAS  Google Scholar 

  8. Gimona, M., Pachler, K., Laner-Plamberger, S., Schallmoser, K. & Rohde, E. Manufacturing of human extracellular vesicle-based therapeutics for clinical use. Int. J. Mol. Sci. 18, 1190 (2017).

    Article  Google Scholar 

  9. Busatto, S. et al. Lipoprotein-based drug delivery. Adv. Drug Deliv. Rev. 159, 377–390 (2020).

    Article  CAS  Google Scholar 

  10. Laggner, M. et al. Reproducibility of GMP-compliant production of therapeutic stressed peripheral blood mononuclear cell-derived secretomes, a novel class of biological medicinal products. Stem Cell. Res. Ther. 11, 9 (2020).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work is partially supported by the Mayo Clinic Center for Regenerative Medicine in Florida (J.W.), the National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), United States under award numbers R21AI152318 (J.W.) and R01AI144997 (K.W.W.), and the NIH Common Fund through the Office of Strategic Coordination/Office of the NIH Director under award number UG3CA241694 (K.W.W.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.

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Correspondence to Kenneth W. Witwer or Joy Wolfram.

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Witwer, K.W., Wolfram, J. Extracellular vesicles versus synthetic nanoparticles for drug delivery. Nat Rev Mater 6, 103–106 (2021). https://doi.org/10.1038/s41578-020-00277-6

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