Department of Chemical Engineering, Texas Tech University, Lubbock , Texas 79409, USA.
Biomicrofluidics. 2014 Jul 29;8(4):044111. doi: 10.1063/1.4891775. eCollection 2014 Jul.
Dilution of microfluidic droplets where the concentration of a reagent is incrementally varied is a key operation in drop-based biological analysis. Here, we present an electrocoalescence based dilution scheme for droplets based on merging between moving and parked drops. We study the effects of fluidic and electrical parameters on the dilution process. Highly consistent coalescence and fine resolution in dilution factor are achieved with an AC signal as low as 10 V even though the electrodes are separated from the fluidic channel by insulator. We find that the amount of material exchange between the droplets per coalescence event is high for low capillary number. We also observe different types of coalescence depending on the flow and electrical parameters and discuss their influence on the rate of dilution. Overall, we find the key parameter governing the rate of dilution is the duration of coalescence between the moving and parked drop. The proposed design is simple incorporating the channel electrodes in the same layer as that of the fluidic channels. Our approach allows on-demand and controlled dilution of droplets and is simple enough to be useful for assays that require serial dilutions. The approach can also be useful for applications where there is a need to replace or wash fluid from stored drops.
在基于液滴的生物分析中,逐渐改变试剂浓度的微流控液滴的稀释是一项关键操作。在这里,我们提出了一种基于电聚并的基于液滴的稀释方案,该方案基于移动和停泊液滴之间的合并。我们研究了流体和电气参数对稀释过程的影响。即使电极通过绝缘体与流体通道隔开,使用低至 10 V 的交流信号也可以实现高度一致的聚并和精细的稀释因子分辨率。我们发现,对于低毛细数,每一次聚并事件中液滴之间的物质交换量很大。我们还观察到不同类型的聚并取决于流动和电气参数,并讨论了它们对稀释速率的影响。总的来说,我们发现控制稀释速率的关键参数是移动和停泊液滴之间聚并的持续时间。所提出的设计很简单,将通道电极集成在与流体通道相同的层中。我们的方法允许按需和控制液滴的稀释,并且足够简单,可用于需要连续稀释的测定。该方法在需要从存储的液滴中替换或清洗流体的应用中也很有用。