Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, United States.
Department of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Anal Chem. 2021 Jun 22;93(24):8622-8630. doi: 10.1021/acs.analchem.1c01558. Epub 2021 Jun 10.
Water-in-oil emulsion droplet microfluidic systems have been extensively developed, and currently, almost all cell handling steps can be conducted in this format. An exception is the cell washing and solution exchange step, which is commonly utilized in many conventional cell assays. This paper presents an in-droplet cell washing and solution exchange technology that utilizes dielectrophoretic (DEP) force to move all cells to one side of a droplet, followed by asymmetrical splitting of the droplet to obtain a small daughter droplet that contains all or most of the cells, and then finally merges this cell-concentrated droplet with a new droplet that contains the desired solution. These sequential droplet manipulation steps were integrated into a single platform, where up to 88% of the original solution in the droplet could be exchanged with the new solution while keeping cell loss to less than 5%. Two application examples were demonstrated using the developed technology. In the first example, green microalga cells were manipulated using negative DEP force to exchange the regular culture medium with a nitrogen-limited medium to induce lipid production. In the second example, cells were manipulated using positive DEP force to replace fluorescent dye that models fluorescent cell stains that contribute to high background noise in fluorescence-based droplet content detection with fresh buffer solution, significantly improving the droplet content detection sensitivity. Since the cell washing step is one of the most frequently utilized steps in many cell biology assays, we expect that the developed technology can significantly broaden the type of assay that can be conducted in droplet microfluidic format.
油包水乳滴微流控系统得到了广泛的发展,目前几乎所有的细胞操作步骤都可以在这种形式下进行。一个例外是细胞洗涤和溶液交换步骤,这在许多常规细胞检测中经常被使用。本文提出了一种在液滴内进行细胞洗涤和溶液交换的技术,该技术利用介电泳(DEP)力将所有细胞移动到液滴的一侧,然后不对称地分裂液滴,得到一个含有几乎所有或大部分细胞的小液滴,最后将这个浓缩细胞的液滴与含有所需溶液的新液滴合并。这些连续的液滴操作步骤被集成到一个单一的平台中,其中高达 88%的原始液滴中的溶液可以被新溶液交换,而细胞损失小于 5%。使用所开发的技术演示了两个应用示例。在第一个示例中,使用负介电泳力操纵绿色微藻细胞,用氮限制培养基代替常规培养基,以诱导脂质产生。在第二个示例中,使用正介电泳力替换荧光染料,该染料模拟荧光细胞染色剂,这些染色剂会导致基于荧光的液滴内容物检测中的背景噪声过高,用新鲜缓冲溶液代替后,显著提高了液滴内容物检测的灵敏度。由于细胞洗涤步骤是许多细胞生物学检测中最常用的步骤之一,我们预计所开发的技术可以显著拓宽可以在液滴微流控形式下进行的检测类型。