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A Microfluidic Localized Multiple Cell Culture Array using Vacuum Actuated Cell Seeding: Integrated Anticancer Drug Testing

机译:使用真空驱动的细胞播种的微流局部多细胞培养阵列:综合抗癌药物测试。

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摘要

In this study, we introduced a novel and convenient approach to culture multiple cells in localized arrays of microfluidic chambers using one-step vacuum actuation. In one device, we integrated 8 individually addressable regions of culture chambers, each only requiring one simple vacuum operation to seed cells lines. Four cell lines were seeded in designated regions in one device via sequential injection with high purity (99.9%-100%) and cultured for long-term. The on-chip simultaneous culture of HuT 78, Ramos, PC-3 and C166-GFP cells for 48 h was demonstrated with viabilities of 92%+/−2%, 94%+/−4%, 96%+/−2% and 97%+/−2%, respectively. The longest culture period for C166-GFP cells in this study was 168 h with a viability of 96%+/−10%. Cell proliferation in each individual side channel can be tracked. Mass transport between the main channel and side channels was achieved through diffusion and studied using fluorescein solution. The main advantage of this device is the capability to perform multiple cell-based assays on the same device for better comparative studies. After treating cells with staurosporine or anti-human CD95 for 16 h, the apoptotic cell percentage of HuT 78, CCRF-CEM, PC-3 and Ramos cells were 36%+/−3%, 24%+/−4%, 12%+/−2%, 18%+/−4% for staurosporine, and 63%+/−2%, 45%+/−1%, 3%+/−3%, 27%+/−12% for anti-human CD95, respectively. With the advantages of enhanced integration, ease of use and fabrication, and flexibility, this device will be suitable for long-term multiple cell monitoring and cell based assays.
机译:在这项研究中,我们介绍了一种新颖便捷的方法,可使用一步真空致动在微流控室的局部阵列中培养多个细胞。在一个设备中,我们集成了8个可单独寻址的培养室区域,每个区域仅需要一个简单的真空操作即可接种细胞系。通过顺序注射以高纯度(99.9%-100%)将四种细胞系接种到一台设备的指定区域中,并进行长期培养。证明了HuT 78,Ramos,PC-3和C166-GFP细胞在芯片上同时培养48小时的存活率分别为92%+ /-2%,94%+ /-4%,96%+ /-2分别为%和97%+ /-2%。在这项研究中,C166-GFP细胞的最长培养期为168小时,生存力为96%+ /-10%。可以追踪每个单独的侧通道中的细胞增殖。主通道和侧通道之间的质量传输是通过扩散实现的,并使用荧光素溶液进行了研究。该设备的主要优点是能够在同一设备上执行多个基于细胞的测定,以进行更好的比较研究。用星形孢菌素或抗人CD95处理细胞16小时后,HuT 78,CCRF-CEM,PC-3和Ramos细胞的凋亡细胞百分比分别为36%+ /-3%,24%+ /-4%,12对于星形孢菌素,为%+ /-2%,18%+ /-4%,对于星形孢菌素为63%+ /-2%,45%+ /-1%,3%+ /-3%,27%+ /-12%分别是抗人类CD95。具有增强的集成度,易于使用和制造以及灵活性的优点,该设备将适用于长期的多细胞监测和基于细胞的测定。

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