Gao Xu, Li Jinze, Li Chuanyu, Zhang Zhiqi, Zhang Wei, Yao Jia, Guan Ming, Guo Zhen, Li Chao, Zhou Lianqun
CAS Key Laboratory of Bio-medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, Jiangsu 215163, People's Republic of China.
Huashan Hospital, Fudan University, Shanghai 200040, People's Republic of China.
Biomicrofluidics. 2020 Jun 1;14(3):034109. doi: 10.1063/5.0006374. eCollection 2020 May.
Sample digital technology is a powerful method for absolute quantification of target molecules such as nucleic acids and proteins. The excellent sample stability and mass production capability has enabled the development of microwell array-based sample digitizing methods. However, in current microwell array chips, samples are loaded by the liquid scraping method, which requires complex manual operation and results in a low filling rate and limited hole filling uniformity. Here, we perform sample loading of a through-hole array chip by a microfluidics-driven method and design a double independent S-shaped flow channels sandwiched through-hole array chip. Because of the capillary force and capillary burst pressure, the sample flowing in the channel can be trapped into through-holes, but cannot flow through the other side. Via air flow and displacement of the remaining sample in the channel, the sample can be partitioned consistently, with zero surplus sample residue in the channel. We evaluated the actual performance of the sample-loading process: the chip enables 99.10% filling rate of 18 500 through-holes, with a grayscale coefficient of variation value of 6.03% determined from fluorescence images. In performing digital polymerase chain reaction on chip, the chip demonstrates good performance for the absolute quantification of target DNA. The simple and robust design of our chip, with excellent filling rate and microsample uniformity, indicates potential for use in a variety of sample digitization applications.
样本数字化技术是对核酸和蛋白质等目标分子进行绝对定量的有力方法。其出色的样本稳定性和大规模生产能力推动了基于微孔阵列的样本数字化方法的发展。然而,在当前的微孔阵列芯片中,样本通过液体刮涂法加载,这需要复杂的手动操作,且填充率低,孔填充均匀性有限。在此,我们通过微流控驱动方法对通孔阵列芯片进行样本加载,并设计了一种夹有通孔阵列的双独立S形流道芯片。由于毛细作用力和毛细破裂压力,通道中流动的样本可被困在通孔中,但不会流到另一侧。通过气流和通道中剩余样本的置换,样本可被均匀分配,通道中无多余样本残留。我们评估了样本加载过程的实际性能:该芯片可实现18500个通孔99.10%的填充率,根据荧光图像确定的灰度变异系数值为6.03%。在芯片上进行数字聚合酶链反应时,该芯片在目标DNA的绝对定量方面表现良好。我们芯片简单而稳健的设计,具有出色的填充率和微量样本均匀性,表明其在各种样本数字化应用中具有应用潜力。