2. Academic Validation
  3. Doxorubicin-Loaded Physalis Mottle Virus Particles Function as a pH-Responsive Prodrug Enabling Cancer Therapy

Doxorubicin-Loaded Physalis Mottle Virus Particles Function as a pH-Responsive Prodrug Enabling Cancer Therapy

  • Biotechnol J. 2020 Dec;15(12):e2000077. doi: 10.1002/biot.202000077.
He Hu 1,  Nicole F Steinmetz 1 2 3 4 5
Affiliations

Affiliations

  • 1 Department of NanoEngineering, University of California San Diego, 9500 Gilman Dr., La Jolla, CA, 92039, USA.
  • 2 Department of Bioengineering, University of California San Diego, 9500 Gilman Dr., La Jolla, CA, 92039, USA.
  • 3 Department of Radiology, University of California San Diego, 9500 Gilman Dr., La Jolla, CA, 92039, USA.
  • 4 Center for Nano-ImmunoEngineering, University of California San Diego, 9500 Gilman Dr., La Jolla, CA, 92039, USA.
  • 5 Moores Cancer Center, University of California San Diego, 9500 Gilman Dr., La Jolla, CA, 92039, USA.
PMID: 32918857 DOI: 10.1002/biot.202000077
Abstract

The controlled release of drugs using nanoparticle-based delivery vehicles is a promising strategy to improve the safety and efficacy of chemotherapy. A simple, scalable, and reproducible strategy is developed to synthesize a drug delivery system (DDS) by loading 6-maleimidocaproyl-hydrazone doxorubicin (DOX-EMCH) into the empty core of virus-like particles (VLPs) derived from Physalis mottle virus (PhMV) via a combination of chemical conjugation to cysteine residues and π-π stacking interactions with the anchored doxorubicin molecule. The DOX-EMCH prodrug features an acid-sensitive hydrazine linker that triggers the release of doxorubicin in the slightly acidic extracellular tumor microenvironment or acidic endosomal or lysosomal compartments following cellular uptake. The VLP external surface is coated with polyethylene glycol (PEG) to prevent non-specific uptake and improve biocompatibility. The DOX-PhMV-PEG particles are stable in vitro and show greater efficacy in vivo compared to free doxorubicin in a breast tumor mouse model (using MDA-MB-231 cells and nude mice): 92% of the tumor-bearing mice treated with DOX-PhMV-PEG are completely cured compared to 27% of those treated with free doxorubicin under the same conditions, representing a 3.4-fold improvement. These results lay a foundation for the further development of this biological drug delivery system for a new generation of chemotherapy products.

Keywords

doxorubicin; nanomedicine; pH sensitivity; tumor microenvironment; virus-like particle.

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