化学
纳米技术
兴奋剂
荧光
猝灭(荧光)
活性氧
纳米颗粒
DNA
生物物理学
卟啉
共价键
光热治疗
量子点
癌症治疗
荧光寿命成像显微镜
核糖核酸
对偶(语法数字)
双重角色
癌细胞
小RNA
吸附
内吞作用
生物传感器
癌症治疗
癌症
作者
Peng Gao,Mengyao Yu,Ruyue Wei,Kaiye Wang,Xiaohan Liu,Wei Pan,Na Li,Bo Tang
标识
DOI:10.1021/acs.analchem.5c03774
摘要
DNA-engineered covalent organic frameworks (COFs) hold great promise for cancer theranostics. However, regulating the interaction between COFs and functional DNAs remains a significant challenge, despite its crucial role in ensuring the theranostic performance. In this study, we present a framework doping strategy that simultaneously optimizes the diagnostic imaging and phototherapeutic effects of the COF-DNA nanosystems. In situ doping of porphyrin allows the photocatalytic generation of reactive oxygen species (ROS) by COF nanoparticles and facilitates the adsorption and quenching of fluorescent single-stranded DNA (ssDNA). This enabled the construction of a high-performance COF-DNA nanosystem for RNA-imaging guided phototherapy: the system restored intense fluorescence signals in response to cancer-associated mRNA and miRNA and generated abundant ROS upon laser irradiation, thereby simultaneously lighting up and killing cancer cells. The developed framework doping strategy provides valuable insights into regulating COF-DNA interactions and constructing high-performance theranostic nanosystems.
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