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基于微流控珠的免疫传感器,使用多酶-纳米粒子扩增和量子点标记物,用于灵敏检测癌症生物标志物蛋白。

Microfluidic beads-based immunosensor for sensitive detection of cancer biomarker proteins using multienzyme-nanoparticle amplification and quantum dots labels.

机构信息

School of Chemistry and Chemical Engineering, Hunan Institute of Engineering, Xiangtan 411104, People's Republic of China.

出版信息

Biosens Bioelectron. 2013 Apr 15;42:23-30. doi: 10.1016/j.bios.2012.10.076. Epub 2012 Nov 1.

Abstract

This study reports the development of a microfluidic beads-based immunosensor for sensitive detection of cancer biomarker α-fetoprotein (AFP) that uses multienzyme-nanoparticle amplification and quantum dots labels. This method utilizes microbeads functionalized with the capture antibodies (Ab₁) and modified electron rich proteins as sensing platform that was fabricated within a microfluidic channel, and uses gold nanoparticles (AuNPs) functionalized with the horseradish peroxidase (HRP) and the detection antibodies (Ab₂) as label. Greatly enhanced sensitivity for the cancer biomarker is based on a dual signal amplification strategy: first, the large surface area of Au nanoparticle carrier allows several binding events of HRP on each nanosphere. Enhanced sensitivity was achieved by introducing the multi-HRP-antibody functionalized AuNPs onto the surface of microbeads through "sandwich" immunoreactions and subsequently multiple biotin moieties could be deposited onto the surface of beads resulted from the oxidation of biotin-tyramine by hydrogen peroxide. Streptavidin-labeled quantum dots were then allowed to bind to the deposited biotin moieties and displayed the signal. Secondly, enhanced mass transport capability inherent from microfluidics leads to higher capture efficiency of targets because continuous flow within micro-channel delivers fresh analyte solution to the reaction site which maintains a high concentration gradient differential to enhance mass transport. Based on the dual signal amplification strategy, the developed microfluidic bead-based immunosensor could discriminate as low as 0.2 pg mL⁻¹ AFP in 10 μL of undiluted calf serum (0.2 fg/chip), and showed a 500-fold increase in detection limit compared to the off-chip test and 50-fold increase in detection limit compared to microfluidic beads-based immunoassay using single label HRP-Ab₂. The immunosensor showed acceptable repeatability and reproducibility. This microfluidic beads-based immunosensor is a promising platform for disease-related biomolecules at the lowest level at their earliest incidence.

摘要

本研究报告了一种基于微流控珠的免疫传感器的开发,用于灵敏检测癌症生物标志物甲胎蛋白(AFP),该传感器使用多酶-纳米粒子扩增和量子点标记。该方法利用微珠作为传感平台,微珠表面功能化有捕获抗体(Ab₁)和修饰的富电子蛋白,该微珠在微流道内制造,并使用金纳米粒子(AuNPs)作为标记,AuNPs 表面功能化有辣根过氧化物酶(HRP)和检测抗体(Ab₂)。基于双信号放大策略,大大提高了癌症生物标志物的灵敏度:首先,Au 纳米粒子载体的大表面积允许每个纳米球上发生几次 HRP 的结合事件。通过“三明治”免疫反应将多 HRP-抗体功能化的 AuNPs 引入微珠表面,并随后通过过氧化物酶将多个生物素部分沉积在珠表面上,生物素-酪胺通过过氧化氢氧化。然后,链霉亲和素标记的量子点被允许与沉积的生物素部分结合并显示信号。其次,微流控固有的增强质量传输能力导致更高的目标捕获效率,因为微通道内的连续流动将新鲜的分析物溶液输送到反应位点,从而保持高浓度梯度差,以增强质量传输。基于双信号放大策略,开发的基于微流控珠的免疫传感器可以在未稀释的小牛血清(0.2 fg/chip)中低至 0.2 pg mL⁻¹ AFP 进行区分,并与片外测试相比,检测限提高了 500 倍,与使用单标记 HRP-Ab₂的微流控珠免疫分析相比,检测限提高了 50 倍。该免疫传感器表现出可接受的重复性和再现性。这种基于微流控珠的免疫传感器是一种有前途的平台,可用于在疾病相关生物分子的最低水平和最早发病时进行检测。

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