Institute of Nanoengineering and Microsystems, National Tsing Hua University, Hsinchu, Taiwan.
Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
Biosens Bioelectron. 2018 Dec 30;122:104-112. doi: 10.1016/j.bios.2018.09.040. Epub 2018 Sep 13.
As cardiovascular diseases (CVD) are responsible for millions of deaths annually, there is a need for rapid and sensitive diagnosis of CVD at earlier stages. Aptamers generated by systematic evolution of ligands by exponential enrichment (SELEX) processes have been shown to be superior to conventional antibody-based cardiac biomarker detection. However, SELEX is a complicated, lengthy procedure requiring multiple rounds of extraction/amplification and well-trained personnel. To circumvent such issue, we designed an automated, miniaturized SELEX platform for the screening of aptamers towards three protein biomarkers associated with CVDs: N-terminal pro-peptide of B-type natriuretic peptide, human cardiac troponin I, and fibrinogen. The developed microfluidic platform was equipped with microfluidic devices capable of sample transport and mixing along with an on-chip nucleic acid amplification module such that the entire screening process (5 rounds of selection in 8 h.) could be performed consecutively on a single chip while consuming only 35 µL of reagents in each cycle. This system may therefore serve as a promising, sensitive, cost-effective platform for the selection of aptamers specific for CVD biomarkers.
由于心血管疾病(CVD)每年导致数百万人死亡,因此需要在早期阶段快速、灵敏地诊断 CVD。通过指数富集的配体系统进化(SELEX)过程产生的适体已被证明优于传统的基于抗体的心脏生物标志物检测。然而,SELEX 是一个复杂的、冗长的过程,需要多次提取/扩增和经过良好培训的人员。为了解决这个问题,我们设计了一种自动化、微型化的 SELEX 平台,用于筛选与 CVD 相关的三种蛋白质生物标志物的适体:B 型利钠肽前体 N 端肽、人心肌肌钙蛋白 I 和纤维蛋白原。开发的微流控平台配备了能够进行样品输送和混合的微流控器件,以及片上核酸扩增模块,使得整个筛选过程(在 8 小时内进行 5 轮选择)可以在单个芯片上连续进行,每个循环仅消耗 35µL 的试剂。因此,该系统可以作为一种有前途的、灵敏的、具有成本效益的平台,用于选择针对 CVD 生物标志物的适体。