Chang Chunqi, Yang Haoyi, Bi Wenchuan, Huang Cuier, Xu Zhen
School of Biomedical Engineering Health Science Center, Shenzhen University, Shenzhen 518060, China.
Guangdong Provincial Key Laboratory of Biomedical Measurements and Ultrasound Imaging, Shenzhen University, Shenzhen 518060, China.
ACS Sens. 2023 Feb 24;8(2):543-554. doi: 10.1021/acssensors.2c01564. Epub 2023 Jan 27.
assays are an important platform for cancer research as they allow high-throughput experimentation that is not possible using animals. Although various assays are developed to study cell viability or migration, many of these assays are often limited to two dimensions, involving complex procedures or relying specialized equipment, etc. Here, we designed a simple colorimetric assay that accommodates automatic liquid samples loading, high-throughput generation of chemical concentration gradient, three-dimensional (3D) cell culture establishment, and smartphone-based colorimetric readouts. This assay is based on through-hole arrays in the poly(methyl methacrylate) (PMMA) layers. Liquid samples can be automatically loaded into through-hole arrays in PMMA layers by capillary force. Different drug concentrations can be generated by aligning and stacking to mix the contents of the corresponding through-holes with different volumes. 3D culture of cancer cells can be established by the rapid absorption of cell suspensions into the macroporous gels. After exposing the 3D cultured cells to different drug concentrations, the number of viable cells and migrated cells was reflected by the color change of Alamar blue, which enable on-site readout by a smartphone. This assay can study cell viability as well as cell migration, the two main characteristics of cancer cells, using one device. Interestingly, HeLa cells remained with high viability after cryopreservation at -80 °C, which allows for storage and distribution using dry ice. The simple protocol, along with the cryopreservability at -80 °C facilitates its ease of use to study cell viability together with cell migration in common laboratories or clinical settings.
分析方法是癌症研究的重要平台,因为它们允许进行高通量实验,而这是使用动物无法实现的。尽管已经开发了各种分析方法来研究细胞活力或迁移,但其中许多方法通常仅限于二维,涉及复杂的程序或依赖专门的设备等。在这里,我们设计了一种简单的比色分析方法,该方法可实现自动液体样品加载、化学浓度梯度的高通量生成、三维(3D)细胞培养的建立以及基于智能手机的比色读数。该分析方法基于聚甲基丙烯酸甲酯(PMMA)层中的通孔阵列。液体样品可以通过毛细作用力自动加载到PMMA层的通孔阵列中。通过对齐和堆叠以混合具有不同体积的相应通孔的内容物,可以产生不同的药物浓度。癌细胞的3D培养可以通过将细胞悬液快速吸收到大孔凝胶中来建立。在将3D培养的细胞暴露于不同药物浓度后,活细胞和迁移细胞的数量通过alamar蓝的颜色变化反映出来,这使得可以通过智能手机进行现场读数。该分析方法可以使用一个设备研究癌细胞的两个主要特征——细胞活力和细胞迁移。有趣的是,HeLa细胞在-80°C冷冻保存后仍具有很高的活力,这使得可以使用干冰进行储存和分发。简单的方案以及在-80°C下的冷冻保存能力便于在普通实验室或临床环境中轻松用于研究细胞活力和细胞迁移。