Two-dimensional semiconductor heterojunction nanostructure for mutually synergistic sonodynamic and chemoreactive cancer nanotherapy

声动力疗法 肿瘤微环境 材料科学 肿瘤缺氧 异质结 纳米结构 纳米技术 癌症研究 化学 活性氧 肿瘤细胞 医学 光电子学 生物化学 内科学 放射治疗
作者
Yajun Zhou,Luodan Yu,Caihong Dong,Junping Liu,Bin Yang,Yu Chen,Zhongqian Hu
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:431: 134017-134017 被引量:25
标识
DOI:10.1016/j.cej.2021.134017
摘要

Ultrasound (US)-activated sonodynamic therapy (SDT) has been extensively explored as an effective therapeutic modality for cancer treatment due to its noninvasiveness, physical targeting and deep tissue penetration. However, the inorganic semiconductor sonosensitizer-enabled SDT still suffers from the low therapeutic efficacy because of tumor hypoxia and low separation efficiency of electrons (e−) and holes (h+) from the energy-band structure of these inorganic sonosensitizers. Herein, the two-dimensional (2D) TiO2@MnO2-x heterojunction nanostructure was rationally designed and engineered for simultaneously modulating the tumor hypoxic microenvironment and augmenting the therapeutic efficacy of SDT against tumor. The MnO2-x component was heterogeneously grown onto the surface of initially synthesized 2D TiO2 nanosheets (NSs), which not only acted as the catalysts for converting tumor-overexpressed hydrogen peroxide into oxygen and subsequently modulating the tumor hypoxia, but also catalyzed the Fenton reaction for the production of hydroxyl radicals. The heterojunction design of TiO2@MnO2-x nanostructure effectively augmented the SDT efficacy of TiO2-based sonosensitizers under ultrasound activation by facilitating the separation of e−/h+ pairs. The simultaneously endowed tumor-hypoxia alleviation and synergistic sono/chemodynamic tumor nanotherapy achieved the high tumor cell-killing effect and tumor-suppression efficiency, as systematically demonstrated both in vitro and in vivo. This work provides a distinct paradigm of the heterojunction semiconductor nanostructure design for improving the ultrasound-based nanotherapy and achieving high tumor-treatment efficacy.

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