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Enhancing the Sensitivity of Slow Light MZI Biosensors through Multi-Hole Defects

机译:通过多孔缺陷增强慢光MZI生物传感器的敏感性

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We demonstrate enhanced detection sensitivity of a slow light Mach-Zehnder interferometer (MZI) sensor by incorporating multi-hole defects (MHDs). Slow light MZI biosensors with a one-dimensional photonic crystal in one arm have been previously shown to improve the performance of traditional MZI sensors based on the increased light-matter interaction that takes place in the photonic crystal region of the structure. Introducing MHDs in the photonic crystal region increases the available surface area for molecular attachment and further increases the enhanced light-matter interaction capability of slow light MZIs. The MHDs allow analyte to interact with a greater fraction of the guided wave in the MZI. For a slow light MHD MZI sensor with a 16 μm long sensing arm, a bulk sensitivity of 151,000 rad/RIU-cm is demonstrated experimentally, which is approximately two-fold higher than our previously reported slow light MZI sensors and thirteen-fold higher than traditional MZI biosensors with millimeter length sensing regions. For the label-free detection of nucleic acids, the slow light MZI with MHDs also exhibits a two-fold sensitivity improvement in experiment compared to the slow light MZI without MHDs. Because the detection sensitivity of slow light MHD MZIs scales with the length of the sensing arm, the tradeoff between detection limit and device size can be appropriately mitigated for different applications. All experimental results presented in this work are in good agreement with finite difference-time domain-calculations. Overall, the slow light MZI biosensors with MHDs are a promising platform for highly sensitive and multiplexed lab-on-chip systems.
机译:我们证明增强的检测灵敏度的慢光Mach-Zehnder干涉仪(MZI)通过将多孔缺陷(MHDS)传感器。在一个臂的一维光子晶体慢光MZI生物传感器先前已经显示出改善的基础上增加光 - 物质相互作用,发生在该结构的光子晶体区域传统MZI传感器的性能。在光子晶体区引入MHDS增加了分子附着和进一步增加慢光的MZI的增强的光 - 物质相互作用的能力的可用表面积。所述MHDS允许分析物与所述MZI的导波的一个较大部分交互。对于慢光MHD MZI传感器具有16微米长传感臂,是通过实验证实151,000弧度/ RIU厘米的体的敏感性,这是大约两倍高于我们以前报道慢光MZI传感器和13倍高于传统的生物传感器MZI用毫米长度的感测区域。用于核酸的无标记检测,与MHDS慢光MZI也表现出比不含MHDS慢光MZI在实验两倍灵敏度的改善。因为慢光MHD的MZI尺度与感测臂的长度的检测灵敏度,检测极限和设备大小之间的折衷可以适当地减轻用于不同的应用。在这项工作中提出的所有实验结果与有限差分时域计算吻合。总体而言,慢光MZI生物传感器与MHDS是高度敏感和复用的实验室芯片系统有前途的平台。

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