4.8 Article

Natural Killer Cell Membrane-Cloaked Virus-Mimicking Nanogenerator with NIR-Triggered Shape Reversal and •C/•OH Storm for Synergistic Thermodynamic-Chemodynamic Therapy

Journal

ADVANCED SCIENCE
Volume 9, Issue 5, Pages -

Publisher

WILEY
DOI: 10.1002/advs.202103498

Keywords

immune escape; NIR-triggered shape reversal; natural killer cell membrane; thermodynamic-chemodynamic therapy; virus-mimicking nanogenerators

Funding

  1. National Natural Science Foundation of China [61727823, 82001950, 62005284]
  2. China Postdoctoral Science Foundation [2020M671928]
  3. Mengchao Hepatobiliary Hospital of Fujian Medical University [QDZJ-2019-003]

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A virus-mimicking nanogenerator is designed for synergistic thermodynamic-chemodynamic therapy, encapsulating AIPH precursor and cloaked with NK cell membrane for enhanced tumor accumulation. The nanogenerator can be activated by NIR and GSH to generate radicals for oxidative stress-based anticancer therapy.
Free radical-based anticancer modality has been widely applied to cancer therapies. However, it still faces challenges of low delivery efficiency and poor selectivity of free radical generation specifically toward tumors. Herein, a virus-mimicking hollow mesoporous disulfide-bridged organosilica is designed to encapsulate center dot C precursor 2, 2'-azobis[2-(2-imidazolin-2-yl) propane] dihydrochloride (AIPH), which is then enclosed by tannic acid (TA)/Fe-III photothermal assembly and further cloaked by natural killer (NK) cell membrane to achieve synergistic thermodynamic-chemodynamic therapy. The nanogenerator can first evade immune surveillance via NK cell membrane cloaking mechanism to strongly accumulate in tumors. Interestingly, the NIR laser-induced heat can trigger NK cell membrane rupture for shape reversal to expose a virus-like surface to amplify the cellular uptake, and simultaneously break the azo bonds of AIPH for in situ controlled center dot C generation. Then upon glutathione (GSH) triggering, the nanogenerator disintegrates via disulfide-thiol exchange and efficiently generates center dot OH by lysosomal pH-initiated TA-Fe-III reaction; notably, the consumption of GSH can amplify oxidative stress to enhance free radical therapy by weakening the self-defense mechanism of tumor cells. It is envisioned that the NK cell membrane-cloaked virus-mimicking and NIR/GSH sequentially activated center dot C/center dot OH radical nanogenerator can provide a promising strategy for oxidative stress-based anticancer therapy.

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