化学
纳米载体
同种类的
小RNA
生物传感器
DNA
纳米技术
生物物理学
基因
生物化学
材料科学
药物输送
生物
热力学
物理
有机化学
作者
Limin Yang,Heng Guo,Qian Gao,Ting Hou,George Zhang,Xiaojuan Liu,Feng Li
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-11-21
卷期号:95 (48): 17834-17842
被引量:23
标识
DOI:10.1021/acs.analchem.3c03914
摘要
Precise and sensitive analysis of exosomal microRNA (miRNA) is of great importance for noninvasive early disease diagnosis, but it remains a great challenge to detect exosomal miRNA in human blood samples because of their small size, high sequence homology, and low abundance. Herein, we integrated reliable Pt–S bond-mediated three-dimensional (3D) DNA nanomachine and magnetic separation in a homogeneous electrochemical strategy for the detection of exosomal miRNA with low background and high sensitivity. The 3D DNA nanomachine was easily prepared via a facile and rapid freezing method, and it was capable of resisting the influence of biothiols, thus endowing it with high stability. Notably, the as-developed magnetic 3D DNA nanomachine not only enabled the detection system to have a low background but also coupled with liposome nanocarriers to synergistically amplify the current signal. Consequently, by ingeniously combining the low background and multiple signal-amplification strategies in homogeneous electrochemical biosensing, highly sensitive detection of exosomal miRNA was successfully achieved. More significantly, with good anti-interference ability, the as-proposed method could effectively discriminate plasma samples from cancer patients and healthy subjects, thus showing a high potential for application in the nondestructive early clinical diagnosis of disease.
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