Institute for Materials Research IMO, Hasselt University, Wetenschapspark 1, 3590 Diepenbeek, Belgium.
Sensors (Basel). 2013 Oct 29;13(11):14650-61. doi: 10.3390/s131114650.
In this article we describe the integration of impedance spectroscopy (EIS) and surface plasmon resonance (SPR) into one surface analytic device. A polydimethylsiloxane (PDMS) flow cell is created, matching the dimensions of a commercially available sensor chip used for SPR measurements. This flow cell allowed simultaneous measurements between an EIS and a SPR setup. After a successful integration, a proof of principle study was conducted to investigate any signs of interference between the two systems during a measurement. The flow cell was rinsed with 10 mM Tris-HCl and 1× PBS buffer in an alternating manner, while impedance and shifts of the resonance angle were monitored. After achieving a successful proof of principle, a usability test was conducted. It was assessed whether simultaneous detection occurred when: (i) Protein A is adsorbed to the gold surface of the chip; (ii) The non-occupied zone is blocked with BSA molecules and (iii) IgG1 is bound to the Protein A. The results indicate a successful merge between SPR and EIS.
本文将阻抗谱(EIS)和表面等离子体共振(SPR)集成到一个表面分析设备中。制作了一个符合用于 SPR 测量的商业传感器芯片尺寸的聚二甲基硅氧烷(PDMS)流动池。该流动池允许在 EIS 和 SPR 设置之间进行同时测量。成功集成后,进行了原理验证研究,以研究在测量过程中两个系统之间是否存在任何干扰迹象。流动池采用 10mM Tris-HCl 和 1×PBS 缓冲液交替冲洗,同时监测阻抗和共振角的偏移。成功完成原理验证后,进行了可用性测试。评估了当同时发生以下情况时是否会同时检测到:(i)蛋白 A 被吸附到芯片的金表面;(ii)非占据区被 BSA 分子阻塞;(iii)IgG1 与蛋白 A 结合。结果表明 SPR 和 EIS 成功融合。