Pollema C H, Ruzicka J
Department of Chemistry BG-10, University of Washington, Seattle 98195.
Anal Chem. 1994 Jun 1;66(11):1825-31. doi: 10.1021/ac00083a008.
This paper introduces a new methodology of carrying out heterogeneous immunoassays automatically, using a flow injection technique on a renewable surface. Flow injection renewable surface immunoassay (FIRSI) relies on the use of a minute amount of beads to form a reactive surface, which is interrogated by fluorescence spectrometry. Following the assay, on-line regeneration normally used in flow based immunoassays is avoided by fluidically removing the spent reactive surface and replacing it with a new layer of beads. This allows the monitoring of antibody-antigen binding at its early stages, dramatically increases the sampling frequency of a serial assay, and eliminates the problems associated with a decrease in surface reactivity caused by repetitive use. A model system utilizing anti-mouse IgG1-coated beads and mouse IgG1 protein is used to characterize the method with respect to reproducibility, flow rate, contact time, and amount of beads.
本文介绍了一种在可再生表面上使用流动注射技术自动进行异质免疫测定的新方法。流动注射可再生表面免疫测定(FIRSI)依赖于使用微量珠子形成反应表面,通过荧光光谱法对其进行检测。在测定之后,通过流体方式去除用过的反应表面并用新的珠子层替换它,从而避免了基于流动的免疫测定中通常使用的在线再生。这允许在抗体 - 抗原结合的早期阶段进行监测,极大地提高了连续测定的采样频率,并消除了与重复使用导致的表面反应性降低相关的问题。使用抗小鼠IgG1包被的珠子和小鼠IgG1蛋白的模型系统来表征该方法在重现性、流速、接触时间和珠子量方面的特性。