4.8 Article

Biodegradable Mesoporous Silica Achieved via Carbon Nanodots-Incorporated Framework Swelling for Debris-Mediated Photothermal Synergistic Immunotherapy

期刊

NANO LETTERS
卷 19, 期 12, 页码 8409-8417

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.9b02448

关键词

Biodegradable silica; framework swelling enhanced photothermal effect; debris-mediated immunostimulation

资金

  1. National Natural Science Foundation of China [31922044, 81573002, 21675032, 81861138040, 81773280]
  2. Shanghai Pujiang Program [17PJD002]
  3. Natural Science Foundation of Shanghai [19ZR1471600]
  4. Fundamental Research Funds for the Central Universities
  5. Original Support Program of Fudan University [XM03180307]
  6. Minhang Hospital Collaboration Fund [RO-MY201802]
  7. DHU Distinguished Young Professor Program

向作者/读者索取更多资源

Incorporating carbon nanodots (CDs) into mesoporous silica framework for extensive biomedicine, especially for the desirable cancer immunotherapy, is considered to be an unexplored challenge. Herein, a hydrogen bond/electrostatic-assisted co-assembly strategy was smartly exploited to uniformly incorporate polymer-coated CDs into ordered framework of mesoporous silica nanoparticles (CD@MSNs). The obtained CD@MSN was not only biodegradable via the framework-incorporated CD-induced swelling but also capable of gathering dispersive CDs with enhanced photothermal effect and elevated targeting accumulation, which therefore can achieve photothermal imaging-guided photothermal therapy (PTT) in vitro and in vivo. Interestingly, benefiting from the biodegraded debris, it was found that CD@MSN-mediated PTT can synergistically achieve immune-mediated inhibition of tumor metastasis via stimulating the proliferation and activation of natural killer cells and macrophages with simultaneously up-regulating the secretion of corresponding cytokines (IFN-gamma and Granzyme B). This work proposed an unusual synthesis of biodegradable mesoporous silica and provided an innovative insight into the biodegradable nanoparticles-associated anticancer immunity.

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