用于点对点激发生物荧光信号的超高集成氮化硅荧光激发芯片

zejun yan, Qing Shi, Bo Wang, Shilun Feng, Jijun Feng, Chang Chen, Jianglong zhao
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引用次数: 0

摘要

目前的研究重点是生物目标检测设备的微型化和集成化,以适应户外和应急现场环境,并提高检测的灵活性和实用性。本研究提出了一种超高集成氮化硅荧光激发芯片,用于点对点激发生物荧光信号。采用有限差分时域(FDTD)方法,以氮化硅为功能材料,设计并制作了波长为 645nm 的可见光荧光激发芯片。该芯片由一个输入光栅耦合器、多个多模干涉仪和输出光栅耦合器组成。通过级联多个多模干涉分光器并在终端连接激发光栅,构建了包含 2016 个激发点的光栅阵列。芯片的单光栅耦合效率为 30%,总激发光面积为 4×4mm²,发射光角度约为 80 度。通过调整不同输出光栅耦合器的位置,芯片可以适应不同位置的激发要求,使其适用于荧光定量聚合酶链反应(PCR)和数字 PCR 等多种应用。在微流控芯片和光电探测器的帮助下,该芯片成功达到了 0.5 µmol/L 荧光试剂溶液的检测限,足以直接检测 PCR 荧光信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultra-high integrated silicon nitride fluorescence excitation chip for point-to-point excitation of biofluorescence signals
Current research is focused on the miniaturization and integration of detection devices for biological targets in order to adapt to outdoor and emergency field settings, as well as to enhance the flexibility and practicality of detection. This study proposes an ultra-high integrated silicon nitride fluorescence excitation chip for point-to-point excitation of biological fluorescence signals. By employing the finite-difference time-domain(FDTD) method and utilizing silicon nitride as the functional material, a visible light fluorescence excitation chip operating at the wavelength of 645nm was designed and fabricated. The chip is composed of an input grating coupler, multiple multimode interferometers, and output grating couplers. A grating array containing 2016 excitation points is constructed cascading multiple multimode interference splitters and connecting excitation gratings at the terminals. The single grating coupling efficiency of the chip is 30% with a total excitation light area of 4×4mm² and an emitted light angle of around 80 degrees. By adjusting the positions of different output grating couplers, the chip can adapt to excitation requirements at different locations, making it suitable for various applications such as fluorescence quantitative polymerase chain reaction(PCR) and digital PCR. With the help of microfluidic chambers and a photodetector, the chip successfully achieved the detection limit of 0.5 µmol/L Cyanine 5(Cy5) fluorescent reagent solution, which is sufficient for direct detection of PCR fluorescence signals.
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