Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Anal Chem. 2010 Mar 15;82(6):2505-11. doi: 10.1021/ac9029345.
This manuscript describes a straightforward fabrication process for embedding Ag/AgCl electrodes within a two-layer poly(dimethylsiloxane) (PDMS) microfluidic chip where an upper and a lower channel are separated by a semiporous membrane. This system allows for the reliable real-time measurement of transendothelial and transepithelial electrical resistance (TEER), an accepted quantification of cell monolayer integrity, across cells cultured on membranes inside the microchannels using impedance spectroscopy. The technique eliminates the need for costly or specialized microelectrode fabrication, enabling commercially available wire electrodes to easily be incorporated into PDMS microsystems for measuring TEER under microfluidic environments. The capability of measuring impedance across a confluent cell monolayer is confirmed using (i) brain-derived endothelial cells (bEND.3), (ii) Madin Darby Canine Kidney Cells (MDCK-2), and mouse myoblast (C2C12) (all from ATCC, Manassas, VA). TEER values as a function of cell type and cell culture time were measured and both agree with previously published values from macroscale culture techniques. This system opens new opportunities for conveniently resolving both transendothelial and transepithelial electrical resistance to monitor cell function in real-time in microfluidic cell cultures.
本文描述了一种简单的制造工艺,可将 Ag/AgCl 电极嵌入双层聚二甲基硅氧烷(PDMS)微流控芯片中,其中上通道和下通道由半渗透膜隔开。该系统允许使用阻抗谱法在微通道内的膜上培养的细胞可靠地实时测量跨内皮和跨上皮电阻(TEER),这是细胞单层完整性的公认量化指标。该技术消除了对昂贵或专用微电极制造的需求,使得商业上可用的金属丝电极可以轻松地被整合到 PDMS 微系统中,以便在微流控环境下测量 TEER。使用(i)脑源内皮细胞(bEND.3)、(ii)Madin Darby 犬肾细胞(MDCK-2)和小鼠成肌细胞(C2C12)(均来自 ATCC,弗吉尼亚州马纳萨斯)证实了测量融合细胞单层跨导的能力。测量了作为细胞类型和细胞培养时间函数的 TEER 值,两者都与来自宏观培养技术的先前发表的值一致。该系统为方便地解析跨内皮和跨上皮电阻以实时监测微流控细胞培养中的细胞功能提供了新的机会。