Wu Hongkai, Wheeler Aaron, Zare Richard N
Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.
Proc Natl Acad Sci U S A. 2004 Aug 31;101(35):12809-13. doi: 10.1073/pnas.0405299101. Epub 2004 Aug 24.
An integrated microfluidic device has been fabricated for analyzing the chemical contents of a single cell (chemical cytometry). The device is designed to accomplish four different functions: (i) cell handling, (ii) metering and delivering of chemical reagents, (iii) cell lysis and chemical derivatization, and (iv) separating derivatized compounds and detecting them by laser-induced fluorescence. These functions are accomplished with only two valves, formed by multilayer soft lithography. A new kind of three-state valve and a picopipette are described; these elements are crucial for minimizing the reaction volume and ensuring optimal shape of the channel for electrophoresis injection. By using these valves, a reaction volume of approximately 70 pl is achieved for the lysis and derivitization of the contents of a single Jurkat T cell (approximately 10 microm diameter). As a demonstration of the use of this integrated microfluidic device, electropherograms of amino acids from individual Jurkat T cells are recorded and compared with those collected from a multiple-cell homogenate.
一种用于分析单细胞化学组成(化学细胞计数法)的集成微流控装置已被制造出来。该装置旨在实现四种不同功能:(i)细胞处理,(ii)化学试剂的计量与输送,(iii)细胞裂解和化学衍生化,以及(iv)分离衍生化化合物并通过激光诱导荧光进行检测。仅通过多层软光刻形成的两个阀就能实现这些功能。文中描述了一种新型三态阀和一种皮升移液器;这些元件对于最小化反应体积以及确保用于电泳进样的通道具有最佳形状至关重要。通过使用这些阀,对于单个直径约为10微米的Jurkat T细胞内容物的裂解和衍生化,实现了约70皮升的反应体积。作为该集成微流控装置应用的演示,记录了来自单个Jurkat T细胞的氨基酸电泳图,并与从多个细胞匀浆中收集的电泳图进行了比较。