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基于捕获-嵌入-电化学(3C)策略的急性心肌梗死相关 microRNA 的快速检测。

Rapid detection of acute myocardial infarction-related miRNA based on a Capture-interCalation-electroCatalysis (3C) strategy.

机构信息

Laboratory of Biosensing Technology, School of Life Sciences, Shanghai University, Shanghai 200444, PR China.

Regeneration and Ageing Lab and Experimental Center of Life Sciences, School of Life Science, Shanghai University, Shanghai 200444, PR China.

出版信息

Biosens Bioelectron. 2016 Mar 15;77:1020-5. doi: 10.1016/j.bios.2015.08.067. Epub 2015 Aug 30.

Abstract

Acute myocardial infarction (AMI) is one of the most urgent and serious diseases that may cause cardiac death in a few hours. Rapid diagnosis of AMI is the pre-requisite for timely interventions. Recently, several specific circulating miRNAs have been proven to have high correlation with AMI. To adopt miRNA as a biomarker may improve the diagnostic accuracy. However, it is a pity that the current available methods for the detection of miRNA usually require a few hours, which is too long for the diagnosis of AMI. In this paper, by adopting a capture DNA, an electrochemical active intercalator and an unimmobilized enzyme, we develop a Capture-interCalation-electroCatalysis (3C) strategy for the rapid detection of AMI-related miRNA. The whole detection process can be completed in 35 min, which is much shorter than most current methods and is acceptable for the diagnosis of AMI. This strategy also shows favorable sensitivity and selectivity, thus provides an alternative for the detection of miRNA. Most importantly, this effort may promote miRNA to work as an effective biomarker in the diagnosis of AMI.

摘要

急性心肌梗死(AMI)是一种可能在数小时内导致心脏死亡的最紧急和最严重的疾病之一。AMI 的快速诊断是及时干预的前提。最近,已经证明几种特定的循环 miRNA 与 AMI 高度相关。采用 miRNA 作为生物标志物可能会提高诊断的准确性。然而,遗憾的是,目前检测 miRNA 的方法通常需要几个小时,对于 AMI 的诊断来说时间太长。在本文中,通过采用捕获 DNA、电化学活性嵌入剂和未固定的酶,我们开发了一种用于快速检测与 AMI 相关 miRNA 的捕获-嵌入-电化学催化(3C)策略。整个检测过程可以在 35 分钟内完成,比大多数当前方法都要短得多,可用于 AMI 的诊断。该策略还表现出良好的灵敏度和选择性,因此为 miRNA 的检测提供了一种替代方法。最重要的是,这项工作可能会促进 miRNA 在 AMI 的诊断中作为一种有效的生物标志物。

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