Enhancing sensitivity towards electrochemical miRNA detection using an affordable paper-based strategy.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Analytical and Bioanalytical Chemistry Pub Date : 2024-08-01 Epub Date: 2024-06-20 DOI:10.1007/s00216-024-05406-6
Wanda Cimmino, Ada Raucci, Sara Pia Grosso, Nicola Normanno, Stefano Cinti
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引用次数: 0

Abstract

In the era of liquid biopsy, microRNAs emerge as promising candidates for the early diagnosis and prognosis of cancer, offering valuable insights into the disease's development. Among all the existing analytical approaches, even if traditional approaches such as the nucleic acid amplification ones have the advantages to be highly sensitive, they cannot be used at the point-of-care, while sensors might be poorly sensitive despite their portability. In order to improve the analytical performance of existing electroanalytical systems, we demonstrate how a simple chromatographic paper-based disk might be useful to rationally improve the sensitivity, depending on the number of preconcentration cycles. A paper-based electrochemical platform for miRNA detection has been developed by modifying a paper-based electrode with a methylene blue (MB)-modified single-stranded sequence (ssDNA) complementary to the chosen miRNA, namely miR-224 that is associated with lung cancer. A detection limit of ca. 0.6 nM has been obtained in spiked human serum samples. To further enhance the sensitivity, an external chromatographic wax-patterned paper-based disk has been adopted to preconcentrate the sample, and this has been demonstrated both in standard and in serum solutions. For each solution, three miR-224 levels have been preconcentrated, obtaining a satisfactory lowering detection limit of ca. 50 pM using a simple and sustainable procedure. This approach opens wide possibilities in the field of analytical and bioanalytical chemistry, being useful not only for electrochemistry but also for other architectures of detection and transduction.

Abstract Image

利用经济实惠的纸质方法提高电化学 miRNA 检测的灵敏度。
在液体活检时代,microRNAs 成为癌症早期诊断和预后的有希望的候选者,为疾病的发展提供了宝贵的见解。在现有的各种分析方法中,即使核酸扩增等传统方法具有灵敏度高的优点,但它们无法在医疗点使用,而传感器虽然便于携带,但灵敏度可能较低。为了提高现有电分析系统的分析性能,我们展示了一个简单的色谱纸基圆盘是如何根据预浓缩循环的次数合理提高灵敏度的。通过用亚甲蓝(MB)修饰的与所选 miRNA(即与肺癌相关的 miR-224)互补的单链序列(ssDNA)修饰纸基电极,开发出了一种用于检测 miRNA 的纸基电化学平台。在加标人体血清样品中的检测限约为 0.6 nM。为了进一步提高灵敏度,我们采用了一个外部色谱蜡型纸盘来预浓缩样品,并在标准溶液和血清溶液中进行了验证。在每种溶液中,都预先浓缩了三个浓度水平的 miR-224,通过一个简单而可持续的程序,达到了令人满意的约 50 pM 的检测下限。这种方法为分析和生物分析化学领域开辟了广阔的前景,不仅适用于电化学,也适用于其他检测和转导结构。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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