Takano Atsushi, Ogawa Tomohisa, Tanaka Masato, Futai Nobuyuki
School of Science and Engineering, Tokyo Denki University, Saitama 350-0394, Japan.
Annu Int Conf IEEE Eng Med Biol Soc. 2011;2011:8404-7. doi: 10.1109/IEMBS.2011.6092073.
We demonstrate the use of a microfluidic cell culture chip with Braille pin-driven pumping, capable of on-chip CO2 incubation that does not require an external chamber or gas supply. The proposed chip consists of a poly(dimethylsiloxane)(PDMS)-made microfluidic chip, flip-mounted on a glass slide, that contains a nested pair of cell culture media reservoirs and water-jacket, insulated by a permeable PDMS wall. By using 0.8 M sodium bicarbonate with 65 mM sodium carbonate as the water-jacket and placing on a 37 °C surface, the chip maintained osmolality shift and the pCO2 in the media reservoir stabilized within < 3 mmol/kg and 5.0% ± 0.2% over at least 24 hours. The incubation capabilities were demonstrated through microfluidic culture of CV-1 epithelial cells under an inverted microscope for at least 12 days.
我们展示了一种具有盲文针驱动泵的微流控细胞培养芯片的应用,该芯片能够在芯片上进行二氧化碳孵育,无需外部腔室或气体供应。所提出的芯片由一个聚二甲基硅氧烷(PDMS)制成的微流控芯片组成,倒装在载玻片上,其中包含一对嵌套的细胞培养基储液器和水套,由可渗透的PDMS壁绝缘。通过使用含有65 mM碳酸钠的0.8 M碳酸氢钠作为水套并放置在37°C的表面上,芯片在至少24小时内保持渗透压变化,培养基储液器中的pCO2稳定在<3 mmol/kg且变化幅度为5.0%±0.2%。通过在倒置显微镜下对CV-1上皮细胞进行微流控培养至少12天,展示了其孵育能力。