Sabhachandani P, Motwani V, Cohen N, Sarkar S, Torchilin V, Konry T
Department of Pharmaceutical Sciences, Northeastern University, 360 Huntington Avenue, 140 The Fenway, Boston, MA 02115, USA.
Lab Chip. 2016 Feb 7;16(3):497-505. doi: 10.1039/c5lc01139f.
Here we describe a robust, microfluidic technique to generate and analyze 3D tumor spheroids, which resembles tumor microenvironment and can be used as a more effective preclinical drug testing and screening model. Monodisperse cell-laden alginate droplets were generated in polydimethylsiloxane (PDMS) microfluidic devices that combine T-junction droplet generation and external gelation for spheroid formation. The proposed approach has the capability to incorporate multiple cell types. For the purposes of our study, we generated spheroids with breast cancer cell lines (MCF-7 drug sensitive and resistant) and co-culture spheroids of MCF-7 together with a fibroblast cell line (HS-5). The device has the capability to house 1000 spheroids on chip for drug screening and other functional analysis. Cellular viability of spheroids in the array part of the device was maintained for two weeks by continuous perfusion of complete media into the device. The functional performance of our 3D tumor models and a dose dependent response of standard chemotherapeutic drug, doxorubicin (Dox) and standard drug combination Dox and paclitaxel (PCT) was analyzed on our chip-based platform. Altogether, our work provides a simple and novel, in vitro platform to generate, image and analyze uniform, 3D monodisperse alginate hydrogel tumors for various omic studies and therapeutic efficiency screening, an important translational step before in vivo studies.
在此,我们描述了一种强大的微流控技术,用于生成和分析三维肿瘤球体,该技术类似于肿瘤微环境,可作为一种更有效的临床前药物测试和筛选模型。在聚二甲基硅氧烷(PDMS)微流控装置中生成了单分散的载细胞藻酸盐液滴,该装置结合了T型结液滴生成和外部凝胶化以形成球体。所提出的方法能够整合多种细胞类型。为了我们的研究目的,我们用乳腺癌细胞系(MCF-7药物敏感型和耐药型)生成了球体,并将MCF-7与成纤维细胞系(HS-5)共同培养生成了球体。该装置能够在芯片上容纳1000个球体用于药物筛选和其他功能分析。通过向装置中持续灌注完全培养基,装置阵列部分球体的细胞活力维持了两周。我们在基于芯片的平台上分析了我们的三维肿瘤模型的功能性能以及标准化疗药物阿霉素(Dox)和标准药物组合Dox与紫杉醇(PCT)的剂量依赖性反应。总之,我们的工作提供了一个简单而新颖的体外平台,用于生成、成像和分析均匀的三维单分散藻酸盐水凝胶肿瘤,以进行各种组学研究和治疗效率筛选,这是体内研究之前的一个重要转化步骤。