Department of Chemistry, City University of Hong Kong, Kowloon 999077, Hong Kong, China.
Department of Chemistry, Seoul National University, Seoul 08826, Korea.
Nano Lett. 2023 May 10;23(9):3897-3903. doi: 10.1021/acs.nanolett.3c00533. Epub 2023 Apr 21.
Simple, low-cost, and accurate nucleic acid assay platforms hold great promise for point-of-care (POC) pathogen detection, disease surveillance, and control. Plasmonic photothermal polymerase chain reaction (PPT-PCR) is a powerful and efficient nucleic acid amplification technique, but it lacks a simple and convenient analysis method for POC applications. Herein, we propose a novel plasmonic cross-linking colorimetric PCR (PPT-ccPCR) assay by integrating plasmonic magnetic nanoparticle (PMN)-based PPT-PCR with gold nanoparticle (AuNP)-based cross-linking colorimetry. AuNPs form assembled structures with the PMNs in the presence of amplicons and collect in a magnetic field, resulting in color changes to the supernatant. Target DNA with concentrations as low as 5 copies/μL can be visually detected within 40 min. The achieved limit of detection was 1.8 copies/μL based on the absorption signals. This simple and sensitive strategy needs no expensive instrumentation and demonstrates high potential for POC detection while enabling further applications in clinical diagnostics.
简单、廉价且准确的核酸检测平台在即时检测(POC)病原体检测、疾病监测和控制方面具有巨大的应用前景。等离子体光热聚合酶链反应(PPT-PCR)是一种强大且高效的核酸扩增技术,但它缺乏用于 POC 应用的简单便捷的分析方法。在此,我们通过整合基于等离子体磁性纳米颗粒(PMN)的 PPT-PCR 与基于金纳米颗粒(AuNP)的交联比色法,提出了一种新颖的等离子体交联比色 PCR(PPT-ccPCR)检测方法。在存在扩增子的情况下,AuNPs 与 PMNs 形成组装结构,并在磁场中聚集,导致上清液发生颜色变化。目标 DNA 的浓度低至 5 拷贝/μL 时,在 40 分钟内即可进行可视化检测。基于吸收信号,检测限达到 1.8 拷贝/μL。这种简单灵敏的策略不需要昂贵的仪器,在 POC 检测方面具有很大的应用潜力,同时也能够在临床诊断中得到进一步的应用。