Cell Bench Research Center, KAIST, 373-1 Guseong-dong, Yuseong-gu, Daejeon, Republic of Korea 305-701.
Lab Chip. 2011 May 21;11(10):1825-30. doi: 10.1039/c1lc20234k. Epub 2011 Apr 12.
This paper presents a pumpless cell culture chip, where a constant-rate medium perfusion is achieved by balanced droplet dispensing. Previous pumpless cell culture chips, where the gravity-driven flow is induced by gradually decreasing the hydraulic-head difference, Δh, between source and drain reservoirs, result in a decreasing perfusion-rate. However, the present pumpless cell culture chip, where autonomous droplet dispensers are integrated on the source reservoirs, results in a constant perfusion-rate using a constant Δh maintained by balanced droplet dispensing between the source-inlet and the drain-outlet. In the experimental study, constant perfusion-rates of 0.1, 0.2, and 0.3 μl min(-1) are obtained by Δh of 38, 76, and 114 mm, respectively. At the constant perfusion-rate (Q=0.2 μl min(-1)), H358 lung cancer cells show the maximum growth-rate of 57.8 ± 21.1% d(-1), which is 1.9 times higher than the 30.2 ± 10.3% d(-1) of the static culture. At a perfusion-rate varying between 0.1-0.3 μl min(-1) (average=0.2 μl min(-1)), however, the H358 cells show a growth-rate of 46.9 ± 8.3% d(-1), which is lower than that of the constant Q of 0.2 μl min(-1). The constant-rate perfusion culture (Q=0.1, 0.2, and 0.3 μl min(-1)) also results in an average cell viability of 89.2%, which is higher than 75.9% of the static culture. This pumpless cell culture chip offers a favorable environment to cells with a high growth-rate and viability, thus having potential for use in cell-based bio-assays.
本文提出了一种无泵细胞培养芯片,通过平衡液滴分配实现恒速介质灌注。先前的无泵细胞培养芯片,通过逐渐减小源和汇储液器之间的水力头差 Δh 来诱导重力驱动的流动,导致灌注率降低。然而,本无泵细胞培养芯片通过在源储液器上集成自主液滴分配器,通过源入口和汇出口之间平衡的液滴分配来维持恒定的 Δh,从而实现恒定的灌注率。在实验研究中,通过 Δh 分别为 38、76 和 114 mm,获得了 0.1、0.2 和 0.3 μl min(-1) 的恒定灌注率。在恒定灌注率(Q=0.2 μl min(-1))下,H358 肺癌细胞的最大增长率为 57.8 ± 21.1% d(-1),比静态培养的 30.2 ± 10.3% d(-1)高 1.9 倍。然而,在 0.1-0.3 μl min(-1) 的灌注率变化范围内(平均=0.2 μl min(-1)),H358 细胞的增长率为 46.9 ± 8.3% d(-1),低于恒定 Q 值 0.2 μl min(-1)。恒定速率灌注培养(Q=0.1、0.2 和 0.3 μl min(-1))也导致细胞平均存活率为 89.2%,高于静态培养的 75.9%。这种无泵细胞培养芯片为具有高增长率和活力的细胞提供了有利的环境,因此具有在基于细胞的生物测定中应用的潜力。