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基于靶标识别和 HCR 扩增诱导的原位电化学信号探针合成策略用于痕量 ctDNA 分析。

Target Recognition- and HCR Amplification-Induced In Situ Electrochemical Signal Probe Synthesis Strategy for Trace ctDNA Analysis.

机构信息

School of Public Health, Nantong University, No.9 Seyuan Road, Nantong 226019, China.

Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong 226001, China.

出版信息

Biosensors (Basel). 2022 Nov 8;12(11):989. doi: 10.3390/bios12110989.

Abstract

An electrochemical-DNA (E-DNA) sensor was constructed by using DNA metallization to produce an electrochemical signal reporter in situ and hybridization chain reaction (HCR) as signal amplification strategy. The cyclic voltammetry (CV) technique was used to characterize the electrochemical solid-state Ag/AgCl process. Moreover, the enzyme cleavage technique was introduced to reduce background signals and further improve recognition accuracy. On the basis of these techniques, the as-prepared E-DNA sensor exhibited superior sensing performance for trace ctDNA analysis with a detection range of 0.5 fM to 10 pM and a detection limit of 7 aM. The proposed E-DNA sensor also displayed excellent selectivity, satisfied repeatability and stability, and had good recovery, all of which supports its potential applications for future clinical sample analysis.

摘要

电化学-DNA(E-DNA)传感器通过 DNA 金属化原位产生电化学信号报告子,并采用杂交链式反应(HCR)作为信号放大策略来构建。循环伏安法(CV)技术用于表征电化学固态 Ag/AgCl 过程。此外,还引入了酶切技术来降低背景信号,进一步提高识别准确性。在此基础上,所制备的 E-DNA 传感器在痕量 ctDNA 分析中表现出优异的传感性能,检测范围为 0.5 fM 至 10 pM,检测限为 7 aM。所提出的 E-DNA 传感器还表现出优异的选择性、令人满意的重复性和稳定性,以及良好的回收率,所有这些都支持其在未来临床样本分析中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7de/9688549/d0b5f9ca232f/biosensors-12-00989-sch001.jpg

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