Khademhosseini Ali, Yeh Judy, Eng George, Karp Jeffrey, Kaji Hirokazu, Borenstein Jeffrey, Farokhzad Omid C, Langer Robert
Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Lab Chip. 2005 Dec;5(12):1380-6. doi: 10.1039/b508096g. Epub 2005 Oct 13.
We present a soft lithographic method to fabricate multiphenotype cell arrays by capturing cells within an array of reversibly sealed microfluidic channels. The technique uses reversible sealing of elastomeric polydimethylsiloxane (PDMS) molds on surfaces to sequentially deliver various fluids or cells onto specific locations on a substrate. Microwells on the substrate were used to capture and immobilize cells within low shear stress regions inside channels. By using an array of channels it was possible to deposit multiple cell types, such as hepatocytes, fibroblasts, and embryonic stem cells, on the substrates. Upon formation of the cell arrays on the substrate, the PDMS mold could be removed, generating a multiphenotype array of cells. In addition, the orthogonal alignment and subsequent attachment of a secondary array of channels on the patterned substrates could be used to deliver fluids to the patterned cells. The ability to position many cell types on particular regions within a two dimensional substrate could potentially lead to improved high-throughput methods applicable to drug screening and tissue engineering.
我们提出了一种软光刻方法,通过将细胞捕获在可逆密封的微流体通道阵列中来制造多表型细胞阵列。该技术利用弹性聚二甲基硅氧烷(PDMS)模具在表面上的可逆密封,将各种流体或细胞依次输送到基板上的特定位置。基板上的微孔用于在通道内的低剪切应力区域捕获和固定细胞。通过使用一系列通道,可以在基板上沉积多种细胞类型,如肝细胞、成纤维细胞和胚胎干细胞。在基板上形成细胞阵列后,可以去除PDMS模具,生成多表型细胞阵列。此外,在图案化基板上二次通道阵列的正交排列和随后的附着可用于将流体输送到图案化细胞。在二维基板的特定区域上定位多种细胞类型的能力可能会导致适用于药物筛选和组织工程的改进的高通量方法。