Department of Chemistry, University of Washington, Box 351700, Seattle, WA 98195, USA.
Lab Chip. 2018 Jan 30;18(3):496-504. doi: 10.1039/c7lc01052d.
Microscale cell-based assays have demonstrated unique capabilities in reproducing important cellular behaviors for diagnostics and basic biological research. As these assays move beyond the prototyping stage and into biological and clinical research environments, there is a need to produce microscale culture platforms more rapidly, cost-effectively, and reproducibly. 'Rapid' injection molding is poised to meet this need as it enables some of the benefits of traditional high volume injection molding at a fraction of the cost. However, rapid injection molding has limitations due to the material and methods used for mold fabrication. Here, we characterize advantages and limitations of rapid injection molding for microfluidic device fabrication through measurement of key features for cell culture applications including channel geometry, feature consistency, floor thickness, and surface polishing. We demonstrate phase contrast and fluorescence imaging of cells grown in rapid injection molded devices and provide design recommendations to successfully utilize rapid injection molding methods for microscale cell-based assay development in academic laboratory settings.
微尺度细胞检测在为诊断和基础生物学研究重现重要细胞行为方面表现出了独特的能力。随着这些检测方法从原型阶段发展到生物和临床研究环境中,需要更快速、更具成本效益和可重复地生产微尺度培养平台。快速注塑成型有望满足这一需求,因为它在成本的一小部分上实现了传统大规模注塑成型的一些优势。然而,由于模具制造中使用的材料和方法,快速注塑成型存在局限性。在这里,我们通过测量细胞培养应用的关键特征(包括通道几何形状、特征一致性、底板厚度和表面抛光)来描述快速注塑成型在微流控器件制造中的优缺点。我们展示了在快速注塑成型器件中生长的细胞的相差和荧光成像,并提供了设计建议,以成功地将快速注塑成型方法用于学术实验室环境中的基于微尺度细胞的检测开发。