Pharmacy Academy of Xinjiang Medical University, Urumqi 830054, People's Republic of China.
Xinjiang Xingyi Bio-Science Co., Ltd, Urumqi 830011, People's Republic of China.
Nanotechnology. 2024 Oct 4;35(50). doi: 10.1088/1361-6528/ad7f61.
A simple and rapid system based on Raman nanosphere (R-Sphere) immunochromatography was developed in this study for the simultaneous detection of Influenza A, B virus antigens on a single test line (T-line). Two types of R-Sphere with different characteristic Raman spectrum were used as the signal source, which were labeled with monoclonal antibodies against FluA, FluB (tracer antibodies), respectively. A mixture of antibodies containing anti-FluA monoclonal antibody and anti-FluB monoclonal antibody (capture antibody) was sprayed on a single T-line and goat anti-chicken IgY antibody was coated as a C-line, and the antigen solution with known concentration was detected by the strip of lateral flow immunochromatography based on surface-enhanced Raman spectroscopy (SERS). The T-line was scanned with a Raman spectrometer and SERS signals were collected. Simultaneous specific recognition and detection of FluA and FluB were achieved on a single T-line by analyzing the SERS signals. The findings indicated that the test system could identify FluA and FluB in a qualitative manner in just 15 minutes, with a minimum detection threshold of 0.25 ng ml, excellent consistency, and specificity. There was no interference with the other four respiratory pathogens, and it exhibited 8 times greater sensitivity compared to the colloidal gold test strip method. The assay system is rapid, sensitive, and does not require repetitive sample pretreatment steps and two viruses can be detected simultaneously on a single T-line by titrating one sample, which improves detection efficiency, and provide a reference for developing multiplexed detection techniques for other respiratory viruses.
本研究建立了一种基于拉曼纳米球(R-Sphere)免疫层析的简单快速检测方法,可在单条测试线上(T 线)同时检测流感 A、B 病毒抗原。两种具有不同特征拉曼光谱的 R-Sphere 分别作为信号源,标记针对 FluA、FluB 的单克隆抗体(示踪抗体)。将含有抗 FluA 单克隆抗体和抗 FluB 单克隆抗体的混合抗体(捕获抗体)喷涂在单条 T 线上,并用鸡抗羊 IgG 抗体包被作为 C 线,然后用基于表面增强拉曼散射(SERS)的侧向流动免疫层析条检测已知浓度的抗原溶液。用拉曼光谱仪扫描 T 线并收集 SERS 信号。通过分析 SERS 信号,在单条 T 线上实现了 FluA 和 FluB 的同时特异性识别和检测。研究结果表明,该检测系统可在 15 分钟内定性识别 FluA 和 FluB,最低检测阈值为 0.25ng/ml,具有良好的一致性和特异性。与其他四种呼吸道病原体无干扰,与胶体金测试条法相比,灵敏度提高了 8 倍。该检测系统快速、灵敏,不需要重复的样本预处理步骤,通过滴定一个样本即可在单条 T 线上同时检测两种病毒,提高了检测效率,为开发其他呼吸道病毒的多重检测技术提供了参考。