Active droplet-array microfluidics-based chemiluminescence immunoassay for point-of-care detection of procalcitonin

微流控 检出限 化学发光 注意事项 免疫分析 分析物 微流控芯片 频谱分析仪 纳米技术 计算机科学 色谱法 材料科学 化学 电信 生物 医学 护理部 抗体 免疫学
作者
Enqi Huang,Dezhi Huang,Yu Wang,Dongyang Cai,Yanzhang Luo,Zhong Zhimin,Dayu Liu
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:195: 113684-113684 被引量:24
标识
DOI:10.1016/j.bios.2021.113684
摘要

The application of conventional chemiluminescence immunoassay (CLIA) in resource-limited settings is limited due to the large apparatus footprint, cumbersome operation and maintenance process, and high consumption of reagents. To address this issue, we developed an active droplet-array (ADA) microfluidics-based CLIA system, which consists of a compact microchip analyzer and microfluidic chips with preloaded reagents. The microfluidic chip contains microslit-connected microchambers, in which all the required reagents were preloaded in water-in-oil droplets. The microfluidic chip analyzer can manipulate five microfluidic chips in parallel in a single run. By interacting the microchip with magnetic, thermal, optical mechanisms programmatically, the entire workflow of CLIA can be accomplished in an automated manner. With the proposed CLIA, the detection of procalcitonin (PCT) can be completed in 12 min, with a limit of detection (LOD) of 0.044 ng mL-1 and a detection range from 0.044 to 100 ng mL-1. We found a good linear correlation between the microfluidic CLIA and the conventional electrochemiluminescence immunoassay (R2=0.98).The microfluidic CLIA has significant advantages over the conventional ELISA in detection sensitivity, dynamic range, instrument size and turnaround time, and can provide more consistent and reliable results than the lateral flow immunoassays. The compact microfluidic system can perform automated and parallelized CLIA in a short turnaround time, and thus well suited to Point-of-Care detection of disease biomarkers.
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