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Flash drug release from nanoparticles accumulated in the targeted blood vessels facilitates the tumour treatment

Author

Listed:
  • Ivan V. Zelepukin

    (Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences
    National Research Nuclear University MEPhI (Moscow Engineering Physics Institute))

  • Olga Yu. Griaznova

    (Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences
    National Research Nuclear University MEPhI (Moscow Engineering Physics Institute))

  • Konstantin G. Shevchenko

    (Institute of Cytology of the Russian Academy of Sciences
    Chumakov Federal Scientific Center for Research and Development of Immunobiological Drugs of the Russian Academy of Sciences)

  • Andrey V. Ivanov

    (Sechenov First Moscow State Medical University (Sechenov University))

  • Ekaterina V. Baidyuk

    (Institute of Cytology of the Russian Academy of Sciences)

  • Natalia B. Serejnikova

    (Sechenov First Moscow State Medical University (Sechenov University))

  • Artur B. Volovetskiy

    (Sechenov First Moscow State Medical University (Sechenov University))

  • Sergey M. Deyev

    (Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences
    National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)
    Sechenov First Moscow State Medical University (Sechenov University))

  • Andrei V. Zvyagin

    (Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences
    National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)
    Sechenov First Moscow State Medical University (Sechenov University)
    Macquarie University)

Abstract

Tumour microenvironment hinders nanoparticle transport deep into the tissue precluding thorough treatment of solid tumours and metastatic nodes. We introduce an anticancer drug delivery concept termed FlaRE (Flash Release in Endothelium), which represents alternative to the existing approaches based on enhanced permeability and retention effect. This approach relies on enhanced drug-loaded nanocarrier accumulation in vessels of the target tumour or metastasised organ, followed by a rapid release of encapsulated drug within tens of minutes. It leads to a gradient-driven permeation of the drug to the target tissue. This pharmaceutical delivery approach is predicted by theoretical modelling and validated experimentally using rationally designed MIL-101(Fe) metal-organic frameworks. Doxorubicin-loaded MIL-101 nanoparticles get swiftly trapped in the vasculature of the metastasised lungs, disassemble in the blood vessels within 15 minutes and release drug, which rapidly impregnates the organ. A significant improvement of the therapeutic outcome is demonstrated in animal models of early and late-stage B16-F1 melanoma metastases with 11-fold and 4.3-fold decrease of pulmonary melanoma nodes, respectively.

Suggested Citation

  • Ivan V. Zelepukin & Olga Yu. Griaznova & Konstantin G. Shevchenko & Andrey V. Ivanov & Ekaterina V. Baidyuk & Natalia B. Serejnikova & Artur B. Volovetskiy & Sergey M. Deyev & Andrei V. Zvyagin, 2022. "Flash drug release from nanoparticles accumulated in the targeted blood vessels facilitates the tumour treatment," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34718-3
    DOI: 10.1038/s41467-022-34718-3
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    References listed on IDEAS

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    1. Jacob S. Brenner & Daniel C. Pan & Jacob W. Myerson & Oscar A. Marcos-Contreras & Carlos H. Villa & Priyal Patel & Hugh Hekierski & Shampa Chatterjee & Jian-Qin Tao & Hamideh Parhiz & Kartik Bhamidipa, 2018. "Red blood cell-hitchhiking boosts delivery of nanocarriers to chosen organs by orders of magnitude," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
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    Cited by:

    1. Ivan V. Zelepukin & Konstantin G. Shevchenko & Sergey M. Deyev, 2024. "Rediscovery of mononuclear phagocyte system blockade for nanoparticle drug delivery," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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