微泡
多路复用
化学
外体
小RNA
计算生物学
纳米技术
原位
癌细胞
DNA
癌症研究
癌症
基因
生物化学
生物信息学
生物
材料科学
遗传学
有机化学
作者
Bojun Liu,Di Zhao,Juan Chen,Mingqing Shi,Kun Yuan,Hongzhi Sun,Hong‐Min Meng,Zhaohui Li
标识
DOI:10.1021/acs.analchem.3c04883
摘要
Exosomal miRNAs are considered promising biomarkers for cancer diagnosis, but their accuracy is severely compromised by the low content of miRNAs and the large amount of exosomal miRNAs released from normal cells. Here, we presented a dual-specific miRNA's logical recognition triggered by an entropy-driven catalysis (EDC)-enhanced system in exosomes for accurate detection of liver cancer-cell-derived exosomal miR-21 and miR-122. Taking advantage of the accurate analytical performance of the logic device, the excellent membrane penetration of gold nanoparticles, and the outstanding amplification ability of the EDC reaction, this method exhibits high sensitivity and selectivity for the detection of tumor-derived exosomal miRNAs in situ. Moreover, due to its excellent performance, this logic device can effectively distinguish liver cancer patients from healthy donors by determining the amount of cancer-cell-derived exosomal miRNAs. Overall, this strategy has great potential for analyzing various types of exosomes and provides a viable tool to improve the accuracy of cancer diagnosis.
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