Sandia National Laboratories , Livermore, California 94550, USA.
Biomicrofluidics. 2014 Jun 12;8(3):034112. doi: 10.1063/1.4874715. eCollection 2014 May.
We present a droplet-based microfluidic system for performing bioassays requiring controlled analyte encapsulation by employing highly flexible on-demand droplet generation. On-demand droplet generation and encapsulation are achieved pneumatically using a microdispensing pump connected to a constant pressure source. The system generates single droplets to the collection route only when the pump is actuated with a designated pressure level and produces two-phase parallel flow to the waste route during the stand-by state. We analyzed the effect of actuation pressure on the stability and size of droplets and optimized conditions for generation of stable droplets over a wide pressure range. By increasing the duration of pump actuation, we could either trigger a short train of identical size droplets or generate a single larger droplet. We also investigated the methodology to control droplet contents by fine-tuning flow rates or implementing a resistance bridge between the pump and main channels. We demonstrated the integrated chip for on-demand mixing between two aqueous phases in droplets and on-demand encapsulation of Escherichia coli cells. Our unique on-demand feature for selective encapsulation is particularly appropriate for bioassays with extremely dilute samples, such as pathogens in a clinical sample, since it can significantly reduce the number of empty droplets that impede droplet collection and subsequent data analysis.
我们提出了一种基于液滴的微流控系统,该系统可通过采用高度灵活的按需液滴生成来执行需要控制分析物包封的生物测定。使用连接到恒压源的微分配泵气动实现按需液滴生成和封装。当泵以指定的压力水平致动时,系统仅将单个液滴输送到收集路径,而在待机状态下将两相平行流输送到废物路径。我们分析了致动压力对液滴稳定性和大小的影响,并优化了在较宽压力范围内生成稳定液滴的条件。通过增加泵致动的持续时间,我们可以触发相同大小的短液滴序列,或者生成单个较大的液滴。我们还研究了通过微调流速或在泵和主通道之间实施电阻桥来控制液滴含量的方法。我们演示了在液滴中按需混合两种水相以及按需包封大肠杆菌细胞的集成芯片。我们用于选择性封装的独特按需功能特别适用于非常稀释的样品的生物测定,例如临床样品中的病原体,因为它可以显著减少阻碍液滴收集和后续数据分析的空液滴的数量。