School of Nano-Bioscience and Chemical Engineering, Ulsan National Institute of Science & Technology, 100 Banyeon-ri, Eonyang-eup, Ulju-gun, Ulsan 689-798, Republic of Korea.
Anal Chem. 2012 Mar 6;84(5):2133-40. doi: 10.1021/ac203163u. Epub 2012 Feb 13.
This paper presents a cost-effective, rapid, and fully automated lab-on-a-disc for simultaneous detection of multiple protein biomarkers in raw samples such as whole blood or whole saliva. For the diagnosis of cardiovascular disease, here, a novel centrifugal microfluidic layout was designed to conduct the simultaneous detection of high sensitivity C-reactive protein, cardiac troponin I, and N-terminal pro-B type natriuretic peptide based on a bead-based sandwich type enzyme-linked immunosorbent assay (ELISA). Three reaction chambers are initially interconnected for the common processes such as sample injection, incubation, and washing and then isolated on-demand for the independent processes such as substrate incubation and final detection. The assay performances such as the limit of detection and the dynamic range were comparable with those of the conventional ELISA despite the significant reduction of the minimum sample volume (200 μL), the amount of washing buffer (700 μL), and the total process time (20 min).
本文提出了一种经济高效、快速且完全自动化的碟式实验室,可用于在原始样本(如全血或全唾液)中同时检测多种蛋白质生物标志物。在这里,为了心血管疾病的诊断,设计了一种新颖的离心微流控布局,用于基于基于珠的夹心型酶联免疫吸附测定(ELISA)同时检测高灵敏度 C 反应蛋白、心肌肌钙蛋白 I 和 N 末端 pro-B 型利钠肽。三个反应室最初相互连接,用于共同的过程,如样品注入、孵育和洗涤,然后按需隔离,用于独立的过程,如底物孵育和最终检测。尽管最小样品体积(200μL)、洗涤缓冲液量(700μL)和总过程时间(20min)显著减少,但检测限和动态范围等分析性能与传统 ELISA 相当。