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基于核酸适配体功能化金纳米十二面体阵列的表面增强拉曼散射检测平台,用于高效同步检测结直肠癌相关微小核糖核酸。

SERS detection platform based on a nucleic acid aptamer-functionalized Au nano-dodecahedron array for efficient simultaneous testing of colorectal cancer-associated microRNAs.

作者信息

Zhang Shuofeng, Chen Fengsong, Zhang Yanqing, Xu Yemin, Wang Lu, Wang Xiya, Jia Long, Chen Yong, Xu Yongcheng, Zhang Zhengrong, Deng Bin

机构信息

Clinical Medical College, Yangzhou University, Yangzhou 225001, China.

Gastroenterology Department, Nantong Haimen People's Hospital, Nantong 226600, China.

出版信息

Biomed Opt Express. 2024 Apr 26;15(5):3366-3381. doi: 10.1364/BOE.520161. eCollection 2024 May 1.

Abstract

A surface-enhanced Raman scattering (SERS) detection platform was constructed based on Au nano-dodecahedrons (AuNDs) functionalized with nucleic acid aptamer-specific binding and self-assembly techniques. SERS labels were prepared by modifying Raman signaling molecules and complementary aptamer chains and were bound on the aptamer-functionalized AuNDs array. Using this protocol, the limits of detection (LODs) of miR-21 and miR-18a in the serum were 6.8 pM and 7.6 pM, respectively, and the detection time was 5 min. Additionally, miR-21 and miR-18a were detected in the serum of a mouse model of colorectal cancer. The results of this protocol were consistent with quantitative real-time polymerase chain reaction (qRT-PCR). This method provides an efficient and rapid method for the simultaneous testing of miRNAs, which has great potential clinical value for the early detection of colorectal cancer (CRC).

摘要

基于用核酸适配体特异性结合和自组装技术功能化的金纳米十二面体(AuNDs)构建了一种表面增强拉曼散射(SERS)检测平台。通过修饰拉曼信号分子和互补适配体链制备SERS标记物,并将其结合在适配体功能化的AuNDs阵列上。使用该方案,血清中miR-21和miR-18a的检测限(LOD)分别为6.8 pM和7.6 pM,检测时间为5分钟。此外,在结直肠癌小鼠模型的血清中检测到了miR-21和miR-18a。该方案的结果与定量实时聚合酶链反应(qRT-PCR)一致。该方法为miRNAs的同时检测提供了一种高效、快速的方法,对结直肠癌(CRC)的早期检测具有巨大的潜在临床价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b86/11161369/fd4723a0084f/boe-15-5-3366-g001.jpg

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