4.8 Article

Macrophage-mediated tumor homing of hyaluronic acid nanogels loaded with polypyrrole and anticancer drug for targeted combinational photothermo-chemotherapy

Journal

THERANOSTICS
Volume 11, Issue 14, Pages 7057-7071

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/thno.60427

Keywords

macrophages; hyaluronic acid nanogels; polypyrrole; tumor homing property; photothermochemotherapy

Funding

  1. National Natural Science Foundation of China [81761148028, 21773026]
  2. Science and Technology Commission of Shanghai Municipality [19410740200, 19XD1400100, 20520710300, 20DZ2254900]
  3. Shanghai Education Commission through the Shanghai Leading Talents Program
  4. Fundamental Research Funds for the Central Universities and Graduate Student Innovation Fund of Donghua University [CUSF-DH-D-2020062]

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The study developed a novel nanosystem integrated with macrophages for tumor therapy. By encapsulating hyaluronic acid nanogels with polypyrrole photothermal agent and anticancer drug doxorubicin, tumor homing and combination photothermo-chemotherapy were achieved. The results showed that the hybrid nanosystem has good targeting capability and enhanced antitumor therapy effect.
Rationale: Development of nanosystems that can be integrated with macrophages (MAs), an emerging carrier system, for effective tumor therapy remains to be challenging. We report here the development of MAs specifically loaded with hyaluronic acid (HA) nanogels (NGs) encapsulated with a photothermal agent of polypyrrole (PPy) and anticancer drug doxorubicin (DOX) (HA/DOX@PPy NGs) for tumor homing and combination photothermo-chemotherapy. Methods: Cystamine dihydrochloride-crosslinked HA NGs were first prepared through a double emulsification method, then loaded with PPy via an in-situ oxidization polymerization and physically encapsulated with DOX. The created HA/DOX@PPy NGs were well characterized and subjected to be endocytosed by MAs (MAs-NGs). The MAs-mediated tumor-homing property, phenotype changes and photothermal performance of MAs-NGs were investigated in vitro, and a subcutaneous tumor model was also established to confirm their targeting capability and enhanced antitumor therapy effect in vivo. Results: The generated hybrid NGs possess a size around 77 nm and good colloidal stability, and can be specifically endocytosed by MAs without appreciably affecting their normal biofunctionalities. In particular, NG-loaded MAs display excellent in-vitro cancer cell and in-vivo tumor homing property. Systemic administration of the MAs-NGs leads to the significant inhibition of a subcutaneous tumor model through combination photothermo-chemotherapy under laser irradiation. Conclusions: The developed hybrid HA-based NG nanosystem incorporated with PPy and DOX fully integrates the coordination and heating property of PPy to regulate the optimized DOX release in the tumor region with the assistance of MA-mediated tumor homing, providing a promising cell therapy strategy for enhanced antitumor therapy.

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