Lin Chie-Chieh, Ko Fu-Hsiang, Chen Chun-Chi, Yang Yuh-Shyong, Chang Feng-Chi, Wu Chung-Shu
Department of Materials Science and Engineering, Institute of Nanotechnology, National Chiao Tung University, Hsinchu, Taiwan.
Electrophoresis. 2009 Sep;30(18):3189-97. doi: 10.1002/elps.200900120.
A miniaturized metal semiconductor metal photodetector was developed as the core detector for chemiluminescence biosensor. The biosensor utilized the semiconductor manufacturing to fabricate the 83 interdigitated patterns of 250-nm metal line and 278-nm space in 100 microm x 100 microm active region. The established real-time detector was operated at 0.4 V to ensure the maximal signal to background ratio of 3600 under illumination intensity of 1.46 mW/cm(2). A chemiluminescence in the miniaturized chamber was successfully proposed to determine the model protein concentration in real-time analysis. Before the emission of light from the catalytic reaction of substrate, the model protein of streptavidin bound to horseradish peroxidase was successfully immobilized onto the sensor surface through the high-affinity conjugate with biotin. The detection limit of 4.76 nM for streptavidin analysis was obtained under the calibration curve of linear range over 5-100 nM with correlation coefficient of 0.9999.
一种小型化的金属-半导体-金属光电探测器被开发出来作为化学发光生物传感器的核心探测器。该生物传感器利用半导体制造工艺在100微米×100微米的有源区域内制造了83个指状图案,金属线宽250纳米,间距278纳米。所建立的实时探测器在0.4伏电压下工作,以确保在1.46毫瓦/平方厘米的光照强度下最大信号与背景比为3600。成功提出在小型化腔室内进行化学发光以实时分析模型蛋白浓度。在底物催化反应发光之前,通过与生物素的高亲和力共轭,成功地将与辣根过氧化物酶结合的链霉亲和素模型蛋白固定在传感器表面。在5-100纳摩尔的线性范围内校准曲线下,链霉亲和素分析的检测限为4.76纳摩尔,相关系数为0.9999。