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纳米颗粒增强型自驱动微流控生物传感器

Nanoparticles Enhanced Self-driven Microfludic Biosensor.

作者信息

Liu Chunxiu, Xue Ning, Cai Haoyuan, Sun Jianhai, Qi Zhimei, Zhao Peiyue, Xiong Fei, Geng Zhaoxin, Jiang Liying, Li Li

机构信息

State Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing 100190, China.

University of Chinese Academy of Sciences (UCAS), Beijing 100049, China.

出版信息

Micromachines (Basel). 2020 Mar 27;11(4):350. doi: 10.3390/mi11040350.

Abstract

C-reactive protein (CRP) plays an important role in inflammation detection and disease monitoring. The optical biosensor is a highly sensitive and easy detection tool. The microfluidic self-driving optical sensors were fabricated with transparent glass material and used for the enhanced surface plasmon resonance (SPR) optical detection of the model protein CRP using Au nanoparticles (AuNPs) and a sandwich immune reaction. The 3D design of the chip was devised to improve the optical coupling efficiency and enable integration with a microfluidic control and rapid detection. The array of pre-fixed antibody modified by Au nanoparticles was used to achieve rapid antigen capture and improve the optical sensitivity. The Au nanoparticle amplification approach was introduced for the SPR detection of a target protein. CRP was used as a model target protein as part of a sandwich assay. The use of Au NP measurements to detect the target signal is a threefold improvement compared to single SPR detection methods.

摘要

C反应蛋白(CRP)在炎症检测和疾病监测中发挥着重要作用。光学生物传感器是一种高度灵敏且易于使用的检测工具。采用透明玻璃材料制作了微流控自驱动光传感器,并利用金纳米颗粒(AuNPs)和夹心免疫反应,对模型蛋白CRP进行增强表面等离子体共振(SPR)光学检测。芯片的三维设计旨在提高光耦合效率,并实现与微流控控制及快速检测的集成。通过金纳米颗粒修饰的预固定抗体阵列实现了快速抗原捕获,并提高了光学灵敏度。引入金纳米颗粒放大方法用于目标蛋白的SPR检测。作为夹心测定的一部分,CRP被用作模型目标蛋白。与单一SPR检测方法相比,利用金纳米颗粒测量来检测目标信号有三倍的提升。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1750/7231021/85f1de8ab76f/micromachines-11-00350-g001.jpg

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