Xie Xin, Maharjan Sushila, Liu Sanwei, Zhang Yu Shrike, Livermore Carol
Department of Mechanical and Industrial Engineering, Northeastern University, Boston, MA 02115, USA.
Division of Engineering in Medicine, Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Cambridge, MA 02139, USA.
Micromachines (Basel). 2019 Dec 18;11(1):2. doi: 10.3390/mi11010002.
Modular microfluidics offer the opportunity to combine the precise fluid control, rapid sample processing, low sample and reagent volumes, and relatively lower cost of conventional microfluidics with the flexible reconfigurability needed to accommodate the requirements of target applications such as drug toxicity studies. However, combining the capabilities of fully adaptable modular microelectromechanical systems (MEMS) assembly with the simplicity of conventional microfluidic fabrication remains a challenge. A hybrid polydimethylsiloxane (PDMS)-molding/photolithographic process is demonstrated to rapidly fabricate LEGO-like modular blocks. The blocks are created with different sizes that interlock via tongue-and-groove joints in the plane and stack via interference fits out of the plane. These miniature strong but reversible connections have a measured resistance to in-plane and out-of-plane forces of up to >6000× and >1000× the weight of the block itself, respectively. The LEGO-like interference fits enable O-ring-free microfluidic connections that withstand internal fluid pressures of >120 kPa. A single layer of blocks is assembled into LEGO-like cell culture plates, where the in vitro biocompatibility and drug toxicity to lung epithelial adenocarcinoma cells and hepatocellular carcinoma cells cultured in the modular microwells are measured. A double-layer block structure is then assembled so that a microchannel formed at the interface between layers connects two microwells. Breast tumor cells and hepatocytes cultured in the coupled wells demonstrate interwell migration as well as the simultaneous effects of a single drug on the two cell types.
模块化微流控技术提供了一个机会,可将传统微流控技术的精确流体控制、快速样品处理、低样品和试剂用量以及相对较低的成本,与适应药物毒性研究等目标应用需求所需的灵活可重构性相结合。然而,将完全可适应的模块化微机电系统(MEMS)组件的功能与传统微流控制造的简单性相结合仍然是一个挑战。本文展示了一种混合聚二甲基硅氧烷(PDMS)模塑/光刻工艺,可快速制造类似乐高积木的模块化部件。这些部件具有不同尺寸,通过平面内的榫槽接头相互锁定,并通过平面外的过盈配合堆叠在一起。这些微型但可逆的连接在平面内和平面外的力作用下,其测量阻力分别高达部件自身重量的6000倍和1000倍以上。类似乐高积木的过盈配合实现了无O形环的微流控连接,能够承受大于120 kPa的内部流体压力。将单层部件组装成类似乐高积木的细胞培养板,并测量在模块化微孔中培养的肺上皮腺癌细胞和肝癌细胞的体外生物相容性和药物毒性。然后组装双层部件结构,使层间界面处形成的微通道连接两个微孔。在耦合孔中培养的乳腺肿瘤细胞和肝细胞表现出孔间迁移以及单一药物对两种细胞类型的同时作用。