化学
光动力疗法
DNA
核仁素
药物输送
适体
癌细胞
阿霉素
体内
药品
紫杉醇
癌症研究
光敏剂
生物物理学
靶向给药
癌症
组合化学
化疗
生物化学
药理学
分子生物学
生物
光化学
有机化学
细胞质
核仁
生物技术
遗传学
作者
Qiu-Ge Zhao,Yunjie Zhou,Dongxiao Cao,An‐Na Tang,De‐Ming Kong
标识
DOI:10.1021/acs.jmedchem.3c01479
摘要
A DNA-functionalized porphyrinic MOF (porMOF) drug delivery system was successfully constructed. porMOF as a photosensitizer and drug delivery carrier can integrate photodynamic therapy (PDT) and chemotherapy. Via the strong coordination interaction between the zirconium cluster of porMOF and the terminal phosphate group of DNA, the stable modification of the DNA layer on the porMOF surface is achieved. Meanwhile, the introduction of C/G-rich base pairs into the DNA double-stranded structure provides more binding sites of chemotherapeutic drug doxorubicin (DOX). AS1411, an aptamer of nucleolin proteins that are overexpressed by cancer cells, is introduced in the double-stranded terminal, which can endow the nanosystem with the ability to selectively recognize cancer cells. C-rich sequences in DNA double strands form an i-motif structure under acidic conditions to promote the highly efficient release of DOX in cancer cells. In vitro and in vivo experiments demonstrate that the synergistic PDT/chemotherapy modality achieves highly efficient cancer cell killing and tumor ablation without undesirable side effects.
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