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首页> 外文期刊>Advanced Functional Materials >Precisely Encoded Barcodes Using Tetrapod CdSe/CdS Quantum Dots with a Large Stokes Shift for Multiplexed Detection
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Precisely Encoded Barcodes Using Tetrapod CdSe/CdS Quantum Dots with a Large Stokes Shift for Multiplexed Detection

机译:使用具有大斯托克斯位移的四脚架CdSe / CdS量子点进行精确编码的条形码以进行多重检测

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摘要

A serious obstacle to the construction of high-capacity optical barcodes in suspension array technology is energy transfer, which can prompt unpredictable barcode signals, limited barcode numbers, and the need for an unfeasible number of experimental iterations. This work reports an effective and simple way to eliminate energy transfer in multicolor quantum dots (QDs)-encoded microbeads by incorporating tetrapod CdSe/CdS QDs with a large Stokes shift (about 180 nm). Exploiting this unique feature enables the facile realization of a theoretical 7 x 7-1 barcoding matrix combining two colors and seven intensity levels. As such, microbeads containing tetrapod CdSe/CdS QDs are demonstrated to possess a powerful encoding capacity which allows for precise barcode design. The ability of the Shirasu porous glass membrane emulsification method to easily control microbead size facilitates the establishment of a 3D barcode library of 144 distinguishable barcodes, indicating the enormous potential to enable large-scale multiplexed detection. Moreover, when applied for the multiplexed detection of five common allergens, these barcodes exhibit superior detection performance (limit of detection: 0.01-0.02 IU mL(-1)) for both spiked and patient serum samples. Therefore, this new coding strategy helps to expand barcoding capacity while simultaneously reducing the technical and economic barriers to the optical encoding of microbeads for high-throughput multiplexed detection.
机译:悬浮阵列技术中构建高容量光学条形码的一个严重障碍是能量转移,它可能会导致无法预测的条形码信号,有限的条形码数量以及需要进行不可行的实验迭代次数。这项工作报告了一种有效且简单的方法,通过结合具有大斯托克斯位移(约180 nm)的四脚CdSe / CdS QD来消除多色量子点(QDs)编码的微珠中的能量转移。利用此独特功能,可以轻松实现将两种颜色和七个强度级别结合在一起的理论7 x 7-1条形码矩阵。这样,包含四足体CdSe / CdS QD的微珠被证明具有强大的编码能力,可实现精确的条形码设计。 Shirasu多孔玻璃膜乳化方法易于控制微珠尺寸的能力有助于建立包含144个可区分条形码的3D条形码库,这表明实现大规模多重检测的巨大潜力。此外,当用于五种常见变应原的多重检测时,这些条形码对加标和患者血清样品均显示出卓越的检测性能(检测极限:0.01-0.02 IU mL(-1))。因此,这种新的编码策略有助于扩展条形码的容量,同时减少用于高通量多路复用检测的微珠光学编码的技术和经济障碍。

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