Department of Electrical and Computer Engineering, 1406 West Green Street, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Anal Chem. 2012 Jan 17;84(2):1126-33. doi: 10.1021/ac202817q. Epub 2011 Dec 29.
A photonic crystal (PC) surface is demonstrated as a high-sensitivity platform for detection of a panel of 21 cancer biomarker antigens using a sandwich enzyme-linked immunosorbent assay (ELISA) microarray format. A quartz-based PC structure fabricated by nanoimprint lithography, selected for its low autofluorescence, supports two independent optical resonances that simultaneously enable enhancement of fluorescence detection of biomarkers and label-free quantification of the density of antibody capture spots. A detection instrument is demonstrated that supports fluorescence and label-free imaging modalities, with the ability to optimize the fluorescence enhancement factor on a pixel-by-pixel basis throughout the microarray using an angle-scanning approach for the excitation laser that automatically compensates for variability in surface chemistry density and capture spot density. Measurements show that the angle-scanning illumination approach reduces the coefficient of variation of replicate assays by 20-99% compared to ordinary fluorescence microscopy, thus supporting reduction in limits of detectable biomarker concentration. Using the PC resonance, biomarkers in mixed samples were detectable at the lowest concentrations tested (2.1-41 pg/mL), resulting in a three-log range of quantitative detection.
一种光子晶体(PC)表面被证明是一种高灵敏度的平台,可用于使用夹心酶联免疫吸附测定(ELISA)微阵列格式检测 21 种癌症生物标志物抗原。采用纳米压印光刻技术制造的基于石英的 PC 结构,因其低自发荧光而被选中,支持两个独立的光学共振,同时能够增强生物标志物的荧光检测,并对抗体捕获点的密度进行无标记定量。演示了一种检测仪器,该仪器支持荧光和无标记成像模式,具有通过角度扫描方法为激发激光优化微阵列中每个像素的荧光增强因子的能力,该方法自动补偿表面化学密度和捕获点密度的变化。测量结果表明,与普通荧光显微镜相比,角度扫描照明方法将重复测定的变异系数降低了 20-99%,从而支持降低可检测生物标志物浓度的下限。利用 PC 共振,在最低测试浓度(2.1-41 pg/mL)下即可检测到混合样品中的生物标志物,从而实现了三个数量级的定量检测。