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Nano-plasmonics and electronics co-integration in CMOS enabling a pill-sized multiplexed fluorescence microarray system

机译:CMOS中的纳米等离子和电子共集成可实现丸状的多重荧光微阵列系统

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摘要

The ultra-miniaturization of massively multiplexed fluorescence-based bio-molecular sensing systems for proteins and nucleic acids into a chip-scale form, small enough to fit inside a pill (∼ 0.1cm3), can revolutionize sensing modalities in-vitro and in-vivo. Prior miniaturization techniques have been limited to focusing on traditional optical components (multiple filter sets, lenses, photo-detectors, etc.) arranged in new packaging systems. Here, we report a method that eliminates all external optics and miniaturizes an entire multiplexed fluorescence system into a 2 × 1 mm2 chip through co-integration for the first time of massively scalable nano-plasmonic multi-functional optical elements and electronic processing circuitry realized in an industry standard complementary-metal-oxide semiconductor (CMOS) foundry process with absolutely ‘no change’ in fabrication or processing. The implemented nano-waveguide based filters operating in the visible and near-IR realized with the embedded sub-wavelength multi-layer copper-based electronic interconnects inside the chip show for the first time a sub-wavelength surface plasmon polariton mode inside CMOS. This is the principle behind the angle-insensitive nature of the filtering that operates in the presence of uncollimated and scattering environments, enabling the first optics-free 96-sensor CMOS fluorescence sensing system. The chip demonstrates the surface sensitivity of zeptomoles of quantum dot-based labels, and volume sensitivities of ∼ 100 fM for nucleic acids and ∼ 5 pM for proteins that are comparable to, if not better, than commercial fluorescence readers. The ability to integrate multi-functional nano-optical structures in a commercial CMOS process, along with all the complex electronics, can have a transformative impact and enable a new class of miniaturized and scalable chip-sized optical sensors.
机译:用于蛋白质和核酸的大规模多路复用的基于荧光的生物分子传感系统的超小型化,使其变成芯片尺寸的形式,足够小以适合药丸(〜0.1cm 3 )的大小。体外和体内传感方式。先前的小型化技术仅限于集中于布置在新包装系统中的传统光学组件(多个滤光器,透镜,光电探测器等)。在这里,我们报告了一种方法,该方法首次通过大规模集成的纳米可扩展等离激元多功能技术消除了所有外部光学器件,并将整个多路复用荧光系统小型化为2×1 mm 2 芯片在工业标准的互补金属氧化物半导体(CMOS)铸造工艺中实现的光学元件和电子处理电路,其制造或加工过程绝对“不变”。在芯片内部通过嵌入的亚波长多层铜基电子互连实现的,在可见光和近红外中运行的已实现的基于纳米波导的滤波器,首次显示了CMOS内部的亚波长表面等离子体激元模式。这是在无准直和散射环境下运行的滤光片的角度不敏感特性背后的原理,从而实现了第一个无光学器件的96传感器CMOS荧光传感系统。该芯片展示了基于量子点的标记的分子结构的表面敏感性,以及对核酸的约100 fM的体积敏感性和对蛋白质的约5 pM的体积敏感性,与商业荧光读取器相比具有相当的优势。在商用CMOS工艺中集成多功能纳米光学结构的能力以及所有复杂的电子器件,可以产生变革性的影响,并可以实现新型的微型化和可扩展芯片尺寸光学传感器。

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