Department of Biomedical Engineering, Wisconsin Institutes for Medical Research, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Anal Chem. 2011 Feb 15;83(4):1408-17. doi: 10.1021/ac102897h. Epub 2011 Jan 24.
Microfluidic cell-based systems have enabled the study of cellular phenomena with improved spatiotemporal control of the microenvironment and at increased throughput. While poly(dimethylsiloxane) (PDMS) has emerged as the most popular material in microfluidics research, it has specific limitations that prevent microfluidic platforms from achieving their full potential. We present here a complete process, ranging from mold design to embossing and bonding, that describes the fabrication of polystyrene (PS) microfluidic devices with similar cost and time expenditures as PDMS-based devices. Emphasis was placed on creating methods that can compete with PDMS fabrication methods in terms of robustness, complexity, and time requirements. To achieve this goal, several improvements were made to remove critical bottlenecks in existing PS embossing methods. First, traditional lithographic techniques were adapted to fabricate bulk epoxy molds capable of resisting high temperatures and pressures. Second, a method was developed to emboss through-holes in a PS layer, enabling creation of large arrays of independent microfluidic systems on a single device without need to manually create access ports. Third, thermal bonding of PS layers was optimized in order to achieve quality bonding over large arrays of microsystems. The choice of materials and methods was validated for biological function in two different cell-based applications to demonstrate the versatility of our streamlined fabrication process.
微流控细胞系统通过改进微环境的时空控制,提高了高通量,从而能够研究细胞现象。虽然聚二甲基硅氧烷(PDMS)已成为微流控研究中最受欢迎的材料,但它具有特定的限制,阻碍了微流控平台充分发挥其潜力。我们在这里提出了一个完整的流程,从模具设计到压印和键合,描述了具有相似成本和时间支出的聚苯乙烯(PS)微流控器件的制造。重点是创建能够在稳健性、复杂性和时间要求方面与 PDMS 制造方法竞争的方法。为了实现这一目标,对现有的 PS 压印方法进行了一些改进,以消除关键的瓶颈。首先,采用传统的光刻技术来制造能够承受高温和高压的块状环氧树脂模具。其次,开发了一种在 PS 层中压印通孔的方法,能够在单个器件上创建大量独立的微流控系统阵列,而无需手动创建访问端口。第三,优化了 PS 层的热键合工艺,以实现大面积微系统的高质量键合。材料和方法的选择在两种不同的基于细胞的应用中得到了生物学功能的验证,证明了我们简化制造工艺的多功能性。