Department of Bioelectronics, Ecole Nationale Supérieure des Mines, CMP-EMSE, MOC, 880 Avenue de Mimet, Gardanne 13541, France.
Lab Chip. 2018 Mar 13;18(6):933-943. doi: 10.1039/c8lc00067k.
Three dimensional cell culture systems have witnessed rapid expansion in the fields of tissue engineering and drug testing owing to their inherent ability to mimic native tissue microenvironments. High throughput technologies have also facilitated rapid and reproducible generation of spheroids and subsequently their use as in vitro tissue models in drug screening platforms. However, drug screening technologies are in need of monitoring platforms to study these 3D culture models. In this work we present a novel platform to measure the electrical impedance of 3D spheroids, through the use of a planar organic electrochemical transistor (OECT) and a novel circular-shaped microtrap. A new strategy was generated to overcome incompatibility of the integration of polydimethylsiloxane (PDMS) microdevices with OECT fabrication. The impedance platform for 3D spheroids was tested by using spheroids formed from mono-cultures of fibroblast and epithelial cells, as well as co-culture of the two cell types. We validated the platform by showing its ability to measure the spheroid resistance (R) of the 3D spheroids and differences in R were found to be related to the ion permeability of the spheroid. Additionally, we showed the potential use of the platform for the on-line R monitoring when a co-culture spheroid was exposed to a porogenic agent affecting the integrity of the cell membrane.
由于其内在的模拟天然组织微环境的能力,三维细胞培养系统在组织工程和药物测试领域得到了快速发展。高通量技术也促进了球体的快速和可重复生成,随后将其用作药物筛选平台中的体外组织模型。然而,药物筛选技术需要监测平台来研究这些 3D 培养模型。在这项工作中,我们通过使用平面有机电化学晶体管 (OECT) 和新型圆形微阱,提出了一种测量 3D 球体的电阻抗的新平台。我们生成了一种新策略来克服聚二甲基硅氧烷 (PDMS) 微器件与 OECT 制造集成的不兼容性。通过使用成纤维细胞和上皮细胞的单培养物以及两种细胞类型的共培养物形成的球体来测试用于 3D 球体的阻抗平台。我们通过证明其测量 3D 球体的球体电阻 (R) 的能力验证了该平台,并且发现 R 的差异与球体的离子渗透性有关。此外,当共培养球体暴露于影响细胞膜完整性的成孔剂时,我们展示了该平台用于在线 R 监测的潜力。