University of Illinois at Urbana Champaign - Department of Electrical and Computer Engineering, 1406 West Green Street, Urbana, Illinois, USA.
J Biophotonics. 2014 Apr;7(3-4):266-75. doi: 10.1002/jbio.201300158. Epub 2013 Dec 23.
We demonstrate the enhancement of a liquid-based homogenous fluorescence assay using the resonant electric fields from a photonic crystal (PC) surface. Because evanescent fields are confined to the liquid volume nearest to the photonic crystal, we developed a simple approach for integrating a PC fabricated on a silicon substrate within a fluid channel with submicron height, using electrohydrodynamic jet (e-jet) printing of a light-curable epoxy adhesive to define the fluid channel pattern. The PC is excited by a custom-designed compact instrument that illuminates the PC with collimated light that precisely matches the resonant coupling condition when the PC is covered with aqueous media. Using a molecular beacon nucleic acid fluorescence resonant energy transfer (FRET) probe for a specific miRNA sequence, we demonstrate an 8× enhancement of the fluorescence emission signal, compared to performing the same assay without exciting resonance in the PC detecting a miRNA sequence at a concentration of 62 nM from a liquid volume of only ∼20 nL. The approach may be utilized for any liquid-based fluorescence assay for applications in point-of-care diagnostics, environmental monitoring, or pathogen detection.
我们展示了一种基于液体的均相荧光分析方法的增强,该方法利用了光子晶体(PC)表面的共振电场。由于倏逝场被限制在最接近光子晶体的液体体积内,我们开发了一种简单的方法,将在硅衬底上制造的 PC 集成到具有亚微米高度的流体通道内,使用电光喷射(e-jet)打印光固化环氧树脂胶来定义流体通道图案。PC 由定制的紧凑型仪器激发,该仪器用准直光照射 PC,当 PC 被水介质覆盖时,该准直光精确匹配共振耦合条件。使用针对特定 miRNA 序列的分子信标核酸荧光共振能量转移(FRET)探针,我们展示了荧光发射信号的 8 倍增强,与在没有激发 PC 共振的情况下进行相同的测定相比,从仅约 20 nL 的液体体积中检测到浓度为 62 nM 的 miRNA 序列。该方法可用于任何基于液体的荧光分析方法,适用于即时诊断、环境监测或病原体检测等应用。