Department of Biomedical Engineering, The Ohio State University , Columbus, Ohio 43210, United States.
Department of Veterinary Biosciences, The Ohio State University , Columbus, Ohio 43210, United States.
ACS Sens. 2018 Feb 23;3(2):410-417. doi: 10.1021/acssensors.7b00834. Epub 2018 Jan 24.
Microfluidic encapsulation of cells or tissues in biocompatible solidlike hydrogels has wide biomedical applications. However, the microfluidically encapsulated cells/tissues are usually suspended in oil and need to be extracted into aqueous solution for further culture or use. Current extracting techniques are either nonselective for the cell/tissue-laden hydrogel microcapsules or rely on fluorescence labeling of the cells/tissues, which may be undesired for their further culture or use. Here we developed a microelectromechanical system (MEMS) to achieve label-free on-chip selective extraction of cell-aggregate-laden hydrogel microcapsules from oil into aqueous solution. The system includes a microfluidic device, an optical sensor, a dielectrophoretic (DEP) actuator, and microcontrollers. The microfluidic device is for encapsulating cell aggregates in hydrogel microcapsules using the flow-focusing function with microchannels for extracting microcapsules. The optical sensor is to detect the cell aggregates, based on the difference of the optical properties between the cell aggregates and surrounding solution before their encapsulation in hydrogel microcapsules. This strategy is used because the difference in optical property between the cell-aggregate-laden hydrogel microcapsules and empty microcapsules is too small to tell them apart with a commonly used optical sensor. The DEP actuator, which is controlled by the sensor and microcontrollers, is for selectively extracting the targeted hydrogel microcapsules by DEP force. The results indicate this system can achieve selective extraction of cell-aggregate-laden hydrogel microcapsules with ∼100% efficiency without compromising the cell viability, and can improve the purity of the cell-aggregate-laden microcapsules by more than 75 times compared with nonselective extraction.
微流控技术将细胞或组织包封在生物相容性的固态水凝胶中,在生物医学领域有广泛的应用。然而,微流控包封的细胞/组织通常悬浮在油中,需要提取到水溶液中进行进一步的培养或使用。目前的提取技术要么对负载细胞/组织的水凝胶微胶囊是非选择性的,要么依赖于细胞/组织的荧光标记,这对于它们的进一步培养或使用可能是不理想的。在这里,我们开发了一种微机电系统(MEMS),用于实现无标记的、芯片级的、从油相中选择性地提取负载细胞的水凝胶微胶囊到水溶液中。该系统包括微流控装置、光学传感器、介电泳(DEP)驱动器和微控制器。微流控装置用于使用微通道的流聚焦功能将细胞聚集体包封在水凝胶微胶囊中,以提取微胶囊。光学传感器用于在细胞聚集体被包封在水凝胶微胶囊之前,基于细胞聚集体和周围溶液之间的光学性质差异来检测细胞聚集体。之所以采用这种策略,是因为负载细胞的水凝胶微胶囊和空微胶囊之间的光学性质差异太小,用常用的光学传感器无法将它们区分开来。DEP 驱动器由传感器和微控制器控制,用于通过 DEP 力选择性地提取目标水凝胶微胶囊。结果表明,该系统可以以约 100%的效率实现负载细胞的水凝胶微胶囊的选择性提取,而不会影响细胞活力,与非选择性提取相比,还可以将负载细胞的微胶囊的纯度提高 75 倍以上。