4.8 Article

2D Core/Shell-Structured Mesoporous Silicene@Silica for Targeted and Synergistic NIR-II-Induced Photothermal Ablation and Hypoxia-Activated Chemotherapy of Tumor

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 24, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202102043

关键词

AQ4N; hypoxia‐ activated prodrugs; mesoporous silica; silicene; synergistic treatments

资金

  1. National Key R&D Program of China [2016YFA0203700]
  2. National Natural Science Foundation of China [51672303, 81725008, 81771836, 81671695, 81901753]
  3. Excellent Young Scientist Foundation of NSFC [51722211]
  4. Fundamental Research Funds for the Central Universities [22120190021, 22120190137]
  5. Program of Shanghai Subject Chief Scientist [18XD1404300]

向作者/读者索取更多资源

A multifunctional theranostic nanoplatform composed of silicene and silica with mesoporous structure stores drug molecules and generates heat therapy, providing a synergistic cancer treatment approach.
Silicene nanosheets, the emerging 2D nanomaterial, as the third topology of silicon-composed materials with distinct physicochemical properties, is a desirable candidate for photothermal-conversion nanoagent (PTA) and drug-delivery nanosystems. Inspired by the individual physiochemical properties and structure features of mesoporous silica and 2D silicene, a distinctive 2D core/shell-structured multifunctional silicon-composed theranostic nanoplatform (Silicene@Silica) is constructed by coating a mesoporous silica layer onto the surface of 2D silicene nanosheets. The well-defined mesopores originating from mesoporous silica shell provide the reservoirs for guest drug molecules and the core of silicene produces heat shock upon NIR-II laser irradiation, aiming to induce the synergistic cancer-therapeutic modality. Importantly, when AQ4N, hypoxia-activated prodrug, is introduced into this system, this nanoplatform (Silicene@Silica-AQ4N) exhibits tumor microenvironment (TME)-responsive and synergistic hyperthermia-augmented therapeutic bioactivity. Such a nanoplatform can amplify the hypoxia of TME by destroying the tumor microcirculation and then further efficiently activate AQ4N, a DNA affinity agent and topoisomerase II inhibitor. The results reveal that this multifunctional theranostic nanoplatform can efficiently eliminate tumors without recurrence.

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