Laboratory of Microsystems, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.
Anal Chem. 2009 Aug 1;81(15):6509-15. doi: 10.1021/ac9009319.
We propose an original concept for a sandwich immunoassay that is completely performed on-chip using streptavidin-coated beads as substrate. The latter are electrostatically self-assembled on aminosilane micropatterns at the bottom of a microfluidic channel. We use mouse IgG diluted in phosphate buffered saline (PBS) with 1% bovine serum albumin (BSA) solution as target antigen. The fluorescent sandwich immunocomplex is formed on the beads during the operation of the chip both in stop-flow and continuous-flow modes. Target mouse IgG antigen is detected down to a concentration of 15 ng/mL in stop-flow mode and 250 pg/mL in continuous-flow mode, using only 1300 nL of sample volume. We also demonstrate the possibility of simultaneous detection of two different antigens in a PBS-BSA solution using a dual microfluidic channel structure.
我们提出了一种基于夹心免疫分析的全新概念,该分析完全在芯片上进行,使用链霉亲和素包被的珠作为基底。这些珠通过静电自组装在微流道底部的氨基硅烷微图案上。我们使用磷酸盐缓冲盐水(PBS)中稀释的小鼠 IgG 与 1%牛血清白蛋白(BSA)溶液作为目标抗原。在芯片运行过程中,无论是在停流模式还是连续流模式下,荧光夹心免疫复合物都在珠上形成。在停流模式下,目标小鼠 IgG 抗原的检测下限低至 15ng/mL,在连续流模式下,检测下限低至 250pg/mL,仅需 1300nL 的样品量。我们还展示了使用双通道微流道结构同时检测 PBS-BSA 溶液中两种不同抗原的可能性。