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基于脂质体的集成微流控策略用于快速比色分析:以 microRNA-21 检测为例。

An integrated liposome-based microfluidic strategy for rapid colorimetric analysis: A case study of microRNA-21 detection.

机构信息

School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang, 212003, Jiangsu Province, PR China.

School of Grain Science and Technology, Jiangsu University of Science and Technology, Zhenjiang, 212003, Jiangsu Province, PR China.

出版信息

Talanta. 2024 May 15;272:125838. doi: 10.1016/j.talanta.2024.125838. Epub 2024 Feb 27.

DOI:10.1016/j.talanta.2024.125838
PMID:38430866
Abstract

In this study, a novel integrated liposome-based microfluidic platform combined with a smartphone was designed for the rapid colorimetric detection of microRNA-21 (miRNA-21) in real samples. The flowing surface-functionalized liposomes were first captured by nucleic acid-functionalized Au nanoparticles in the microfluidic chip. In the presence of miRNA-21, the DNA strand modified on the surface of Au nanoparticles hybridized with the target to form double-stranded products and was cleaved by duplex-specific nuclease (DSN) enzyme, causing the liposomes to be re-released. Then, as the liposomes in the colorimetric module were lysed and the "cellular" contents were released, a step-by-step "glucose-glucose oxidase-3,3',5,5'-tetramethylbenzidine (TMB)" colorimetric reaction process catalyzed by the G-quadruplex/hemin was triggered. The grayscale values were recorded and recognized by the smartphone camera for miRNA-21 analysis. The advantages of the present strategy included the portability of smartphone-based colorimetric assay, the encapsulation and transport of reactants by liposomes and the low solvent usage of microfluidic chip. Under optimal conditions, this assay exhibited a wide linear range from 1 pM to 1 nM (r = 0.9981), and the limit of detection of miRNA-21 was as low as 0.27 pM. Moreover, the high specificity of this strategy allowed its successful application to the rapid analysis of miRNA-21 in real blood serum samples of people with type 2 diabetes.

摘要

在这项研究中,设计了一种新型的基于脂质体的集成微流控平台,与智能手机结合,用于快速比色检测实际样本中的 microRNA-21 (miRNA-21)。首先,在微流控芯片中,流动的表面功能化脂质体被核酸功能化的 Au 纳米粒子捕获。在存在 miRNA-21 的情况下,表面修饰的 DNA 链与靶标杂交形成双链产物,并被双链特异性核酸酶 (DSN) 酶切割,导致脂质体重新释放。然后,作为比色模块中的脂质体被裂解,并且“细胞”内容物被释放,由 G-四链体/血红素催化的逐步“葡萄糖-葡萄糖氧化酶-3,3',5,5'-四甲基联苯胺(TMB)”比色反应过程被触发。灰度值通过智能手机摄像头记录和识别,用于 miRNA-21 分析。本策略的优点包括基于智能手机的比色测定的便携性、脂质体封装和反应物的运输以及微流控芯片的低溶剂使用量。在最佳条件下,该测定法显示出从 1 pM 到 1 nM 的宽线性范围(r=0.9981),miRNA-21 的检测限低至 0.27 pM。此外,该策略的高特异性允许其成功应用于 2 型糖尿病患者实际血清样本中 miRNA-21 的快速分析。

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