MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, the Key Laboratory of Chemical Biology of Fujian Province, State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemical Engineering, Department of Chemical Biology, College of Chemistry and Chemical Engineering , Xiamen University , Xiamen 361005 , China.
Institute of Molecular Medicine, Renji Hospital, Shanghai Jiao Tong University , School of Medicine , Shanghai , 200240 , China.
Anal Chem. 2018 Apr 17;90(8):5224-5231. doi: 10.1021/acs.analchem.8b00002. Epub 2018 Apr 2.
Digital microfluidics (DMF) is a powerful platform for a broad range of applications, especially immunoassays having multiple steps, due to the advantages of low reagent consumption and high automatization. Surface enhanced Raman scattering (SERS) has been proven as an attractive method for highly sensitive and multiplex detection, because of its remarkable signal amplification and excellent spatial resolution. Here we propose a SERS-based immunoassay with DMF for rapid, automated, and sensitive detection of disease biomarkers. SERS tags labeled with Raman reporter 4-mercaptobenzoic acid (4-MBA) were synthesized with a core@shell nanostructure and showed strong signals, good uniformity, and high stability. A sandwich immunoassay was designed, in which magnetic beads coated with antibodies were used as solid support to capture antigens from samples to form a beads-antibody-antigen immunocomplex. By labeling the immunocomplex with a detection antibody-functionalized SERS tag, antigen can be sensitively detected through the strong SERS signal. The automation capability of DMF can greatly simplify the assay procedure while reducing the risk of exposure to hazardous samples. Quantitative detection of avian influenza virus H5N1 in buffer and human serum was implemented to demonstrate the utility of the DMF-SERS method. The DMF-SERS method shows excellent sensitivity (LOD of 74 pg/mL) and selectivity for H5N1 detection with less assay time (<1 h) and lower reagent consumption (∼30 μL) compared to the standard ELISA method. Therefore, this DMF-SERS method holds great potentials for automated and sensitive detection of a variety of infectious diseases.
数字微流控(DMF)是一个强大的平台,适用于广泛的应用,特别是具有多个步骤的免疫分析,因为其具有低试剂消耗和高自动化的优点。表面增强拉曼散射(SERS)已被证明是一种用于高灵敏度和多重检测的有吸引力的方法,因为它具有显著的信号放大和优异的空间分辨率。在这里,我们提出了一种基于 DMF 的 SERS 免疫分析方法,用于快速、自动、灵敏地检测疾病生物标志物。用核壳纳米结构合成了标记有拉曼报告分子 4-巯基苯甲酸(4-MBA)的 SERS 标签,具有强信号、良好的均匀性和高稳定性。设计了一种夹心免疫分析方法,其中用抗体包被的磁性珠用作固体支撑物,从样品中捕获抗原以形成珠-抗体-抗原免疫复合物。通过用检测抗体功能化的 SERS 标签标记免疫复合物,可以通过强 SERS 信号灵敏地检测抗原。DMF 的自动化能力可以大大简化分析过程,同时降低接触危险样品的风险。通过缓冲液和人血清中的禽流感病毒 H5N1 的定量检测,证明了 DMF-SERS 方法的实用性。与标准 ELISA 方法相比,DMF-SERS 方法具有优异的灵敏度(LOD 为 74 pg/mL)和对 H5N1 的选择性,检测时间更短(<1 h),试剂消耗更少(约 30 μL)。因此,这种 DMF-SERS 方法在自动化和灵敏检测各种传染病方面具有很大的潜力。