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Universal quantum dot-based sandwich-like immunoassay strategy for rapid and ultrasensitive detection of small molecules using portable and reusable optofluidic nano-biosensing platform

机译:基于通用量子点的三明治样免疫测定策略,使用便携式和可重复使用的光流纳米生物传感平台,可以快速,超灵敏地检测小分子

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A universal sandwich-like immunoassay strategy based on quantum-dots immunoprobe (QD-labeled anti-mouse IgG antibody) was developed for rapid and ultrasensitive detection of small molecules. A portable and reusable optofluidic nano-biosensing platform was applied to investigate the sandwich-like immunoassay mechanism and format of small molecules, as well as the binding kinetics between QD immunoprobe and anti-small molecule antibody. A two-step immunoassay method that involves pre-incubation mixture of different concentration of small molecule and anti-small molecule antibody, and subsequent introduction of QD immunoprobe into the optofluidic cell was conducted for small molecule determination. Compared with the one-step immunoassay method, the two-step immunoassay method can obtain higher fluorescence signal and higher sensitivity index, thus improving the nano-biosensing performance. Based on the proposed strategy, two mode targets, namely, microcystin-LR (MC-LR) and Bisphenol A (BPA) were tested with high sensitivity, rapidity, and ease of use. A higher concentration of small molecules in the sample led to less anti-small molecule antibody bound with antigen-carrier protein conjugate immobilized onto the sensor surface, and less QD immunoprobes bound with anti-small molecule antibody. This phenomenon lowered the fluorescence signal detected by nano-biosensing platform. Under optimal operating conditions, MC-LR and BPA exhibited a limit of detection of 0.003 and 0.04 mu g/L, respectively. The LODs were better than those of the indirect competitive immunoassay method for small molecules via Cy5.5-labeled anti-small molecule antibody. The proposed QD-based sandwich-like immunoassay strategy was evaluated in spiked water samples, and showed good recovery, precision and accuracy without complicated sample pretreatments. All these results demonstrate that the new detection strategy could be readily applied to the other trace small molecules in real water samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:开发了一种基于量子点免疫探针(QD标记的抗小鼠IgG抗体)的通用三明治样免疫测定策略,用于快速,超灵敏地检测小分子。应用便携式和可重复使用的光流纳米生物传感平台来研究小分子的三明治样免疫测定机制和形式,以及QD免疫探针和抗小分子抗体之间的结合动力学。进行两步免疫测定法,包括预孵育不同浓度的小分子和抗小分子抗体的混合物,然后将QD免疫探针引入光流体细胞中以进行小分子测定。与一步免疫法相比,两步免疫法可以获得更高的荧光信号和更高的灵敏度指标,从而提高了纳米生物传感性能。基于提出的策略,以高灵敏度,快速和易于使用的方式测试了两种模式目标,即微囊藻毒素-LR(MC-LR)和双酚A(BPA)。样品中较高的小分子浓度导致较少的与固定在传感器表面的抗原-载体蛋白偶联物结合的抗小分子抗体,以及较少的与抗小分子抗体结合的QD免疫探针。这种现象降低了纳米生物传感平台检测到的荧光信号。在最佳操作条件下,MC-LR和BPA的检出限分别为0.003和0.04μg / L。通过Cy5.5标记的抗小分子抗体对小分子的检测限优于间接竞争免疫检测法。拟议的基于QD的三明治样免疫测定策略在加标水样品中进行了评估,显示了良好的回收率,精密度和准确性,无需进行复杂的样品预处理。所有这些结果表明,新的检测策略可以很容易地应用于实际水样中的其他痕量小分子。 (C)2015 Elsevier B.V.保留所有权利。

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