Product catalysis dual entropy-driven amplification reaction strategy for miRNA-21 detection in glioblastoma

IF 4.9 2区 化学 Q1 CHEMISTRY, ANALYTICAL Microchemical Journal Pub Date : 2024-09-01 DOI:10.1016/j.microc.2024.111515
Linbo Zou, Xiaojun Liu, Lizhu Yang, Wen Yun
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Abstract

MicroRNA is taken as diagnostic tumor markers in clinical diagnosis of various cancers. However, the complexity system and low utilization rate of entropy-driven amplification reaction (EDAR) limit its application. In this work, a product catalysis dual EDAR amplification strategy is developed for miRNA-21 detection. This strategy allows miRNA-21 to simultaneously catalyze two EDARs, greatly increasing the limit of detection to 0.40 pM and enhancing amplification efficiency. The amplification efficiency was also significantly enhanced with a much shorter reaction time by increasing concentration of the catalyzer (EDAR product). The approach was successfully applied in clinical samples, showing potential for early screening and diagnosis.
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用于胶质母细胞瘤 miRNA-21 检测的产物催化双熵驱动扩增反应策略
在各种癌症的临床诊断中,MicroRNA 被当作诊断肿瘤的标志物。然而,熵驱动扩增反应(EDAR)系统复杂、利用率低,限制了其应用。本研究开发了一种用于 miRNA-21 检测的产物催化双 EDAR 扩增策略。该策略可使 miRNA-21 同时催化两个 EDAR,大大提高了检测限至 0.40 pM,并提高了扩增效率。通过提高催化剂(EDAR 产物)的浓度,扩增效率也显著提高,反应时间大大缩短。该方法已成功应用于临床样本,显示出早期筛查和诊断的潜力。
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来源期刊
Microchemical Journal
Microchemical Journal 化学-分析化学
CiteScore
8.70
自引率
8.30%
发文量
1131
审稿时长
1.9 months
期刊介绍: The Microchemical Journal is a peer reviewed journal devoted to all aspects and phases of analytical chemistry and chemical analysis. The Microchemical Journal publishes articles which are at the forefront of modern analytical chemistry and cover innovations in the techniques to the finest possible limits. This includes fundamental aspects, instrumentation, new developments, innovative and novel methods and applications including environmental and clinical field. Traditional classical analytical methods such as spectrophotometry and titrimetry as well as established instrumentation methods such as flame and graphite furnace atomic absorption spectrometry, gas chromatography, and modified glassy or carbon electrode electrochemical methods will be considered, provided they show significant improvements and novelty compared to the established methods.
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