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Ultrasensitive on-chip immunoassays with a nanoparticle-assembled photonic crystal

机译:纳米组装光子晶体的超灵敏芯片免疫测定

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Electrophoretic particle entrapment system (EPES) is employed to generate 2D array of nanoparticles coated with biological molecules (i.e., antibodies). Phase matching of the excitation and the emission in the 2D arrays with particles produces a highly enhanced fluorescence signal that was shown to improve the limit of detection in immunoassays. The phase matching is achieved when the particle are in the sub-100 nm range. A comparison between different size particles shows that the sensitivity of an immunoassay is extended to a range that is difficult to achieve with standard technology (e.g., enzyme-linked immunosorbent assay-ELISA). The effectiveness of this novel configuration of particle-in-a-well was demonstrated with an assay for human epidermal growth factor receptor 2 (HER2; breast cancer biomarker), with a detection limit as low as 10 attomolar (aM) in less than 10 μL of serum-based sample. The limit of detection of HER2 indicated far superior assay performance compared to the corresponding standard 96-well plate-based ELISA. The particle-based photonic platform reduces the reagent volume and the time for performing an assay in comparison to competing methods. The simplicity of operation and the level of sensitivity demonstrated here can be used for rapid and early stage detection of biomarkers.
机译:电泳粒子捕获系统(EPES)用于生成包覆有生物分子(即抗体)的纳米粒子的二维阵列。二维阵列中激发和发射与粒子的相位匹配产生了高度增强的荧光信号,该信号显示出可以改善免疫测定中的检测极限。当颗粒在低于100 nm的范围内时,可以实现相位匹配。不同大小颗粒之间的比较表明,免疫测定的灵敏度扩展到了标准技术难以实现的范围(例如,酶联免疫吸附测定-ELISA)。通过对人类表皮生长因子受体2(HER2;乳腺癌生物标志物)的测定,证明了这种新颖构型的孔中粒子的有效性,其检出限低至10 attomolar(aM)在不到10 μL基于血清的样品。与相应的基于96孔板的标准ELISA试剂盒相比,HER2的检测限表明其卓越的检测性能。与竞争方法相比,基于粒子的光子平台减少了试剂体积和执行测定的时间。此处展示的操作简单性和灵敏度水平可用于生物标志物的快速和早期检测。

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