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A pumpless cell culture chip with the constant medium perfusion-rate maintained by balanced droplet dispensing

机译:通过平衡的液滴分配保持恒定的培养基灌注速率的无泵细胞培养芯片

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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 sourceinlet 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.
机译:本文介绍了一种无泵细胞培养芯片,其中通过平衡液滴分配实现了恒定速率的培养基灌注。以前的无泵细胞培养芯片,其中通过逐渐减小源水库和排水库之间的水头差Δh来诱导重力流,导致灌注速率降低。但是,本发明的无泵细胞培养芯片将自主的液滴分配器集成在源容器上,利用在源入口和出口之间的平衡液滴分配所保持的恒定Δh来产生恒定的灌注速率。在实验研究中,通过38、76和114 mm的Δh分别获得0.1、0.2和0.3μlmin〜(-1)的恒定灌注速率。在恒定的灌注速率(Q = 0.2μlmin〜(-1))下,H358肺癌细胞的最大生长速率为57.8±21.1%d〜(-1),是30.2±的1.9倍。静态培养的d〜(-1)的10.3%。但是,在灌注速率介于0.1-0.3μlmin〜(-1)(平均= 0.2μlmin〜(-1))之间时,H358细胞的生长速率为46.9±8.3%d〜(-1) ),这低于0.2μlmin〜(-1)的常数Q的值。恒速灌流培养(Q = 0.1、0.2和0.3μlmin〜(-1))还导致平均细胞活力为89.2%,高于静态培养的75.9%。该无泵细胞培养芯片为具有高生长速率和活力的细胞提供了良好的环境,因此具有用于基于细胞的生物测定的潜力。

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