纳米器件
脱氧核酶
化学
分子成像
纳米技术
光动力疗法
光敏剂
纳米颗粒
核酸
纳米医学
DNA
分子探针
生物物理学
核酸内切酶
劈开
医学影像学
光子上转换
临床诊断
内化
内窥镜
小分子
分子工程
作者
R. Li,Huanhuan He,J Feng,Luna Guo,Peng He,Weiling Song,Hong Zhou,Xuemei Li
标识
DOI:10.1021/acs.analchem.5c05888
摘要
The development of nanodevices for simultaneous imaging, accurate diagnosis, and efficient therapy with high spatiotemporal precision remains highly challenging. Herein, we proposed an intelligent strategy that employed the light-controlled DNAzyme probe for dual-target imaging and integrated it with upconversion nanoparticle (UCNPs)-based synergistic therapy in mitochondria. This nanosystem was composed of silica-shelled UCNPs surrounded by DNA probes and mitochondria-targeting triphenylphosphonium. The core/shell-structured UCNPs were capable of codelivering photosensitizer molecules (Ce6) and DOX. Following controlled localization and photoactivation, the engineered DNAzyme probes first visualized miRNA-21 and subsequently allowed for the imaging of human uracil/pyrimidine-free nucleic acid endonuclease 1 (APE1). Once the target was recognized, the treatment was also performed with released DOX and near-infrared (NIR) light-mediated photodynamic therapy. As a result, the all-in-one nanodevice enabled specific imaging of tumors and enhanced synergistic therapy efficacy in live biosystems with high precision both spatially and temporally. These findings are expected to drive forward research on the utilization of intelligent nanodevices in the converging realms of diagnostic and therapeutic applications.
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