基于负电介质电泳微粒子积累的快速免疫传感

T. Yasukawa, H. J. Lee, J. Ramón‐Azcón, Yusuke Yoshida, H. Shiku, T. Matsue, F. Mizutani
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引用次数: 0

摘要

本研究开发了一种基于微粒子介电电泳(DEP)操作技术的快速、无分离的微流控装置,该装置由交错微阵列(IDA)电极组成。将具有微流控通道的聚二甲基硅氧烷(PDMS)衬底放置在IDA板上,以便制造该装置。在负DEP (n-DEP)频率区对IDA施加交流电压,山羊抗小鼠免疫球蛋白(抗小鼠IgG)固定微粒通过n-DEP力移动到放置在IDA上方的PDMS底物表面,在PDMS表面的指定区域积累,并在该区域预涂覆抗小鼠免疫球蛋白。将携带抗小鼠IgG的荧光微粒子悬浮在分析物(小鼠IgG)溶液中,微粒子捕获分析物形成微粒子偶联物。偶联物通过抗体-抗原-抗体(三明治)反应在PDMS表面的指定区域积累和捕获。无论悬浮溶液中是否存在未捕获的微颗粒,通过荧光测量在聚焦的指定区域选择性地检测捕获的微颗粒。因此,常规免疫测定通常需要的分离和冲洗步骤在本方法中被消除。由于n-DEP明显加速了三明治结构的形成,因此只需30秒就足以检测到表面的免疫反应。在0.01 ~ 10 ng/mL范围内,在指定区域捕获的微粒的荧光强度随分析物的增加而增加。本程序在一个简单的装置中实现了快速、灵敏和无分离的免疫分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid immunosensing based on accumulation of microparticles by negative dielectrophoresis
In the work, microfluidic device consisting of an interdigitated microarray (IDA) electrode was developed for a rapid, and separation-free immuno-sensors based on a manipulation technique of microparticles by dielectrophoresis (DEP). A poly-dimethylsiloxane (PDMS) substrate with microfluidic channel was placed on the IDA plate to allow to fabricating the device. On applying AC voltage to the IDA in a negative DEP (n-DEP) frequency region, goat anti-mouse immunoglobulin (anti-mouse IgG)-immobilized microparticles moved to the surface of PDMS substrate placed above the IDA by n-DEP force to accumulate at the designated areas of the PDMS surface, where anti-mouse IgG was precoated. When the fluorescence microparticles bearing anti-mouse IgG were suspended in an analyte (mouse IgG) solution, the microparticles trapped the analyte to form microparticle-conjugates. The conjugates were accumulated and captured at the designated areas of the PDMS surface via antibody-antigen-antibody (sandwich) reaction. The captured microparticles were detected selectively by fluorescence measurements at the focused, designated areas regardless of the presence of uncaptured microparticles in the suspended solution. Thus, the separation and washing-out steps, usually required for conventional immunoassay, are eliminated in the presented procedure. Since the formation of the sandwich structures was accelerated significantly by n-DEP, as short as 30 sec was enough to detect the immunoreaction at the surface. The fluorescence intensity of the captured microparticles at the designated area increased with the analyte in the range, 0.01 ~ 10 ng/mL. The present procedure realizes a rapid, sensitive and separation-free immunoassay in a simple device.
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