纳米探针
适体
生物相容性
荧光团
共轭体系
荧光
化学
DNA
癌症治疗
共价键
纳米技术
前药
纳米载体
荧光寿命成像显微镜
生物物理学
组合化学
药物输送
癌症
生物化学
材料科学
纳米颗粒
分子生物学
生物
有机化学
物理
聚合物
量子力学
遗传学
作者
Chonghua Zhang,Ke Cai,Pengge Zhang,Zhan Wu,Ming Ma,Bo Chen
标识
DOI:10.1016/j.bios.2021.113654
摘要
We have developed a novel cancer theragnostic nanoassembly with high biocompatibility, stability and low toxicity which are activated rapidly by tumor microenvironment to realize selective fluorescence imaging, chemotherapy as well as chemoenzymatic therapy. The nanoprobes are synthesized by hybridization of fluorophore labeled hairpin DNAs containing a 5-aza-dC at hemimethylated CpG sites and pH-sensitive DNA sequence covalently conjugated with PEGylated GO. The aptamer, which is also covalently conjugated on PEGylated GO, enables to target the tumor site and the weak acid environment of tumor triggers the release of drug loaded by nanoprobes including functionalized DNA and DOXs, effectively activating fluorescence signals and selectively killing the tumor cells. The results revealed that the nanoprobe enables sensitive detection of pH changes within subcellular environment, selectively imaging and great synergy of multicombination therapeutic including chemotherapy and chemoenzymatic therapy, implying that developed pH activatable probe has considerable potential for diagnosis and efficient therapy of cancer.
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