Huang Lei, Tian Shulin, Zhao Wenhao, Liu Ke, Ma Xing, Guo Jinhong
School of Automation Engineering, University of Electronic Science and Technology of China, Chengdu 611731, P. R. China.
Analyst. 2020 Apr 21;145(8):2828-2840. doi: 10.1039/c9an02485a. Epub 2020 Mar 27.
Multiplexed detection of biomarkers, i.e., simultaneous detection of multiple biomarkers in a single assay, is a process of great advantages including enhanced diagnostic precision, improved diagnostic efficiency, reduced diagnostic cost, and alleviated pain of patients. A typical lateral-flow immunoassay (LFIA) is a widely used paper-based immunochromatographic test strip designed to detect a target biomarker through two common formats: sandwich assay and competitive assay. In order to obtain qualitative or quantitative results, a probe with unique optical or magnetic properties is usually employed to characterize the concentration of the target biomarker. The typical LFIA is suitable for point-of-care testing due to its simplicity, portability, cost-effectiveness, and rapid detection of a target biomarker. However, detection of a single biomarker in the typical LFIA is not favorable for high throughput analysis. Therefore, multiplexed detection of biomarkers in LFIAs has been extensively studied in recent years for high throughput analysis. To accomplish multiplexed detection of biomarkers in LFIAs, the most frequently used structure is a test strip with multiple test lines (TLs), where each TL can detect a specific biomarker. An alternative structure, i.e., a multi-channel structure with multiple test strips, where each test strip has one TL for detecting a specific biomarker, is employed for multiplexed detection of biomarkers. Sometimes, a single test strip with only one TL containing different receptors, where each detection receptor corresponds to a specific biomarker, is another structure applied for multiplexed detection of biomarkers. This paper reviews three common structures for multiplexed detection of biomarkers in LFIAs, i.e., a test strip with multiple TLs, a multi-channel structure with multiple test strips, and a test strip with a single TL. Based on the three common structures, different signal detection strategies that include colorimetric detection, fluorescence detection, surface-enhanced Raman scattering detection, and magnetic detection, along with performance and perspectives are discussed.
生物标志物的多重检测,即在单一检测中同时检测多种生物标志物,是一个具有诸多优势的过程,包括提高诊断精度、提升诊断效率、降低诊断成本以及减轻患者痛苦。典型的侧向流动免疫分析(LFIA)是一种广泛使用的基于纸质的免疫层析试纸条,旨在通过两种常见形式检测目标生物标志物:夹心分析和竞争分析。为了获得定性或定量结果,通常采用具有独特光学或磁性特性的探针来表征目标生物标志物的浓度。典型的LFIA因其简单性、便携性、成本效益以及能够快速检测目标生物标志物,适用于即时检测。然而,典型LFIA中对单一生物标志物的检测不利于高通量分析。因此,近年来对LFIA中生物标志物的多重检测进行了广泛研究以用于高通量分析。为了实现LFIA中生物标志物的多重检测,最常用的结构是具有多个检测线(TL)的试纸条,其中每个TL可以检测特定的生物标志物。另一种结构,即具有多个试纸条的多通道结构,其中每个试纸条有一个TL用于检测特定的生物标志物,用于生物标志物的多重检测。有时,仅具有一个包含不同受体的TL的单个试纸条,其中每个检测受体对应于特定的生物标志物,是另一种用于生物标志物多重检测的结构。本文综述了LFIA中生物标志物多重检测的三种常见结构,即具有多个TL的试纸条、具有多个试纸条的多通道结构以及具有单个TL的试纸条。基于这三种常见结构,讨论了不同的信号检测策略,包括比色检测、荧光检测、表面增强拉曼散射检测和磁性检测,以及性能和前景。