光热治疗
肿瘤微环境
光动力疗法
材料科学
体内
荧光寿命成像显微镜
荧光
临床前影像学
吲哚青绿
纳米技术
适体
癌症研究
生物物理学
化学
医学
病理
肿瘤细胞
生物
分子生物学
有机化学
生物技术
物理
量子力学
作者
Yudong Sun,Yifei Wang,Yaqi Liu,Benrui Weng,Huiran Yang,Zhouxuan Xiang,Jiabing Ran,Huimin Wang,Changying Yang
标识
DOI:10.1021/acsami.1c17642
摘要
Intrinsic tumor microenvironment (TME)-related therapeutic resistance and nontumor-specific imaging have limited the application of imaging-guided cancer therapy. Herein, a TME-responsive MnO2-based nanoplatform coupled with turn-on and always-on fluorescence probes was designed through a facile biomineralization method for imaging-guided photodynamic/chemodynamic/photothermal therapy (PDT/CDT/PTT). After the tumor-targeting delivery of the AuNCs@MnO2-ICG@AS1411 (AMIT) nanoplatform via aptamer AS1411, the TME-responsive dissociation of MnO2 generated sufficient O2 and Mn2+ with the consumption of GSH for improving PDT efficacy and Fenton-like reaction-mediated CDT. Simultaneously, the released small-sized ICG and AuNCs facilitated PDT and PTT efficacy via the deep tumor penetration. Moreover, the turn-on fluorescence of AuNCs revealed the real-time TME-responsive MnO2 degradation process, and the always-on ICG fluorescence enabled the in situ monitoring of the payload distribution in vitro and in vivo. The AMIT NPs also provided magnetic resonance and thermal imaging guidance for the enhanced PDT, CDT, and PTT. Therefore, this all-in-one nanosystem provides a simple and versatile strategy for multiple imaging-guided theranostic applications.
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