Department of Life Science, University of Seoul, Seoul, 02504, South Korea.
Analyst. 2019 Apr 8;144(8):2820-2826. doi: 10.1039/c8an02489h.
Developing a sensitive and selective detection platform of disease-related biomarkers is important for the diagnosis and treatment of diseases at an early stage. Among clinically meaningful biomarkers, proteins are the most commonly used indicators, and they are generally detected via immunoassays. However, the use of conventional immunoassays in early diagnosis is hindered by the time required, complex steps, high-cost, and insufficient sensitivity and selectivity. Herein, we developed a novel on-chip immunoassay with degassing-driven microfluidic devices and gold nanoplasmonic particles (GNPs). To recognize target proteins, antibody-conjugated GNPs as probes were used in the assay owing to their excellent scattering properties. Using the proposed nonenzymatic immunoassay, we detected amyloid β (Aβ) and Tau proteins, representative biomarkers of Alzheimer's disease, in femtomolar levels. Selective and quantitative detection of Aβ spiked in blood plasma was also achieved for further clinical application of the proposed immunoassay. The proposed plasmonic immunoassay integrated with degassing-driven microfluidic chips provides a new platform for biological assays and diagnosis.
开发敏感和选择性的疾病相关生物标志物检测平台对于疾病的早期诊断和治疗非常重要。在有临床意义的生物标志物中,蛋白质是最常用的指标,通常通过免疫测定法进行检测。然而,传统免疫测定法在早期诊断中的应用受到时间、复杂步骤、高成本以及灵敏度和选择性不足的限制。在此,我们开发了一种基于脱气驱动微流控器件和金纳米等离子体颗粒(GNPs)的新型片上免疫分析方法。为了识别靶蛋白,我们在测定中使用了抗体偶联的 GNPs 作为探针,因为它们具有优异的散射性质。使用所提出的非酶免疫分析方法,我们在飞摩尔水平检测到了阿尔茨海默病的代表性生物标志物淀粉样β(Aβ)和 Tau 蛋白。还实现了对血液中 Aβ 的选择性和定量检测,为该免疫分析方法的进一步临床应用提供了依据。该研究将脱气驱动微流控芯片与等离子体免疫分析相结合,为生物分析和诊断提供了一个新的平台。