MOF-Powered MicroRNA Catch for Ultrasensitive Breast-Cancer Screening

适体 化学 生物传感器 小RNA 检出限 计算生物学 复矩阵 基质(化学分析) 纳米技术 电极 临床诊断 生物流体 色谱法 细胞生物学 分子生物学 信号转导 生物途径
作者
Qingping Sun,Zhi-Chao Lu,Rui-Cheng Li,Zhengxian Zhang,Jing-Lian Su,Cheng Wang,Hao Wang,Xing‐Hua Xia,Ya Ding
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:98 (5): 3803-3811
标识
DOI:10.1021/acs.analchem.5c05884
摘要

MicroRNAs (miRNAs) are key regulators of disease-associated signaling pathways and serve as critical biomarkers for cancer. However, their accurate and reliable quantification in complex biofluids such as serum remains challenging because of their ultralow abundance and matrix interference, which severely limit their clinical and point-of-care testing (POCT) utility. To overcome this hurdle, we developed an electrochemical biosensor that integrates a UiO-66-NH2 enrichment strategy for the specific and rapid detection of miRNAs and validated it in clinical serum samples. UiO-66-NH2 was used to adsorb Texas Red-labeled miRNA aptamers, generating a high-density capture material (Apt-UiO-66-NH2) that selectively enriched target miRNAs. After enrichment, sodium tripolyphosphate (STPP) was employed to release aptamers─both those bound to miRNAs and those remaining unbound─from the MOF. The released single-stranded aptamers were then quantified with an electrochemical biosensor fabricated on a screen-printed electrode (SPE), allowing the determination of the target miRNA. The assay accomplishes rapid (<45 min) and sensitive detection of miR-21, miR-155, and miR-96 and can distinguish breast-cancer patients from postoperative recovery subjects. These results demonstrate the potential of this biosensor for real-time health monitoring and POCT miRNA analysis, particularly for breast-cancer diagnosis.
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