3B's Research Group-Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine , AvePark, 4806-909 Taipas, Guimarães, Portugal.
ACS Appl Mater Interfaces. 2014 Jun 25;6(12):9488-95. doi: 10.1021/am5018607. Epub 2014 Jun 10.
We suggest the use of biomimetic superhydrophobic patterned chips produced by a benchtop methodology as low-cost and waste-free platforms for the production of arrays of cell spheroids/microtissues by the hanging drop methodology. Cell spheroids have a wide range of applications in biotechnology fields. For drug screening, they allow studying 3D models in structures resembling real living tissues/tumors. In tissue engineering, they are suggested as building blocks of bottom-up fabricated tissues. We used the wettability contrast of the chips to fix cell suspension droplets in the wettable regions and evaluated on-chip drug screening in 3D environment. Cell suspensions were patterned in the wettable spots by three distinct methods: (1) by pipetting the cell suspension directly in each individual spot, (2) by the continuous dragging of a cell suspension on the chip, and (3) by dipping the whole chip in a cell suspension. These methods allowed working with distinct throughputs and degrees of precision. The platforms were robust, and we were able to have static or dynamic environments in each droplet. The access to cell culture media for exchange or addition/removal of components was versatile and opened the possibility of using each spot of the chip as a mini-bioreactor. The platforms' design allowed for samples visualization and high-content image-based analysis on-chip. The combinatorial analysis capability of this technology was validated by following the effect of doxorubicin at different concentrations on spheroids formed using L929 and SaOs-2 cells.
我们建议使用台式方法生产的仿生超疏水图案芯片作为低成本、无废物的平台,通过悬滴方法生产细胞球体/微组织阵列。细胞球体在生物技术领域有广泛的应用。对于药物筛选,它们允许在类似于真实组织/肿瘤的 3D 结构中研究 3D 模型。在组织工程中,它们被建议作为自下而上制造的组织的构建块。我们利用芯片的润湿性对比将细胞悬浮液滴固定在可润湿区域,并在 3D 环境中评估芯片上的药物筛选。通过三种不同的方法在可润湿点对细胞悬浮液进行图案化:(1)直接将细胞悬浮液逐滴滴入每个单独的点,(2)通过在芯片上连续拖动细胞悬浮液,以及(3)将整个芯片浸入细胞悬浮液中。这些方法允许以不同的通量和精度级别进行操作。该平台坚固耐用,我们能够在每个液滴中实现静态或动态环境。用于交换或添加/去除成分的细胞培养基的获取具有多样性,并为将芯片的每个点用作微型生物反应器提供了可能性。该平台的设计允许对样品进行可视化和基于高内涵图像的分析。通过在不同浓度下观察阿霉素对 L929 和 SaOs-2 细胞形成的球体的影响,验证了该技术的组合分析能力。