Aqueous-phase synthesis of upconversion metal-organic frameworks for ATP-responsive in situ imaging and targeted combinational cancer therapy

被引:20
作者
Yang, Lin [1 ]
Zhu, Shuaidong [1 ]
He, Zhimei [1 ]
Li, Xiangli [1 ]
Chen, Jiangning [1 ]
Bi, Sai [2 ]
Zhu, Jun-Jie [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Sch Life Sci, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
[2] Qingdao Univ, Coll Chem & Chem Engn, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金;
关键词
Upconversion nanoparticles; Metal-organic frameworks; ATP response; In situ imaging; Targeted combinational therapy; EMBEDDING ENZYMES; NANOPARTICLES;
D O I
10.1016/j.cclet.2021.07.007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, the nanoscaled ATP-responsive upconversion metal-organic frameworks (UCMOFs) are aqueous-phase synthesized for co-delivery of therapeutic protein cytochrome c (Cyt c) and chemodrugs doxorubicin (DOX), achieving targeted combinational therapy of human cervical cancer. The UCMOFs are rationally fabricated by growing ZIF-90 on mesoporous silica-coated upconversion nanoparticles (UCNPs), in which the ZIF-90 layer attenuates the upconversion luminescence (UCL) and the rigid frameworks increase the stability of encapsulated proteins. Once the UCMOF@DOX/Cyt c are internalized into HeLa cells via specific recognition of sgc8 aptamers, the intracellular ATP triggers the dissolution of ZIF-90 into Zn2+, which facilitates not only the release of Cyt c and DOX but also the restoration of UCL for real-time monitoring of drug release. It has been demonstrated that the therapeutic efficacy is greatly improved by the combination of caspase-mediated apoptosis activated by Cyt c (protein therapeutics), DNA fragmentation induced by DOX (chemotherapy), and Zn2+-promoted generation of reactive oxygen species (ROS) (oxidative stress). Overall, our proposed multifunctional UCMOFs provide an effective platform for targeted combinational cancer therapy and in situ imaging, which hold great promise in biomedical and clinical applications. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:314 / 319
页数:6
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