Zheng Wanli, Yao Li, Teng Jun, Yan Chao, Qin Panzhu, Liu Guodong, Chen Wei
School of Food Science & Engineering, Hefei University of Technology, 230009, Anhui, PR China.
Department of Chemistry & Biochemistry, North Dakota State University, Fargo, ND 58105, USA.
Sens Actuators B Chem. 2018 Jul 1;264:320-326. doi: 10.1016/j.snb.2018.02.159. Epub 2018 Mar 20.
The authors describe a rapid and low-cost approach for multiplex microRNA(miRNA) assay on lateral flow nucleic acid biosensor (LFNAB). The principle of assay is based on sandwich-type nucleic acid hybridization reactions to produce gold nanoparticle (GNP)-attached complexes (ssDNA-microRNA-ssDNA/GNPs), which are captured and visualized on the test zone of LFNAB. By designing three different test zones on LFNAB, simultaneous detection of microRNA-21, microRNA-155 and microRNA-210 was achieved with an adding-measuring model by using GNP as visual tag. The method was challenged by testing the microRNAs in spiked serum samples with satisfied results. In our perception, the test is a particularly valuable tool for clinical application and biomedical diagnosis, particularly in limited resource settings.
作者描述了一种用于在侧向流动核酸生物传感器(LFNAB)上进行多重微小RNA(miRNA)检测的快速且低成本的方法。该检测原理基于夹心型核酸杂交反应,以产生附着有金纳米颗粒(GNP)的复合物(单链DNA-微小RNA-单链DNA/GNPs),这些复合物在LFNAB的测试区被捕获并可视化。通过在LFNAB上设计三个不同的测试区,以GNP作为可视化标签,采用添加-测量模型实现了对微小RNA-21、微小RNA-155和微小RNA-210的同时检测。通过在加标的血清样本中检测这些微小RNA对该方法进行了验证,结果令人满意。在我们看来,该检测对于临床应用和生物医学诊断是一种特别有价值的工具,尤其是在资源有限的环境中。