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基于上转换与金纳米粒子之间 FRET 的一步式固相基底全血免疫分析。

One-step in situ solid-substrate-based whole blood immunoassay based on FRET between upconversion and gold nanoparticles.

机构信息

State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, China; Graduate University of the Chinese Academy of Sciences, Beijing 100049, China.

State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, China; Graduate University of the Chinese Academy of Sciences, Beijing 100049, China; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

出版信息

Biosens Bioelectron. 2017 Jun 15;92:335-341. doi: 10.1016/j.bios.2016.11.003. Epub 2016 Nov 4.

Abstract

Despite their general clinical applications, current fluorescence-based immunoassays are confronted with serious challenges, e.g. the advance serum/ plasma separation and the tedious washing process in current heterogeneous approaches, and aggregation of particles, low sensitivity and the narrow linear range in homogeneous approaches. In this paper, these urgent problems were solved in a novel one-step in situ immunoassay of whole blood samples by combining the traditional fluorescence resonance energy transfer (FRET) technology (between upconversion nanoparticles (UCNPs) and gold nanoparticles (GNPs)) and the solid-substrate based immunoassay technology. The low detection limits of goat IgG (gIgG) as 0.042μg/mL in buffers, 0.51μg/mL in 20-fold diluted whole blood samples and a wide linear range from 0.75μg/mL to 60μg/mL in blood samples were achieved. To the best of our knowledge, it is the first one-step in situ solid-substrate-based immunoassay of whole blood samples with large linear detection range. This development provides a promising platform for a rapid and sensitive immunoassay of various bio-molecules directly in whole blood without tedious separation, washing steps and aggregation problems.

摘要

尽管当前的荧光免疫分析方法具有广泛的临床应用,但仍面临着一些严重的挑战,例如当前异质方法中需要先进的血清/血浆分离和繁琐的洗涤过程,以及同质方法中存在的颗粒聚集、低灵敏度和线性范围窄等问题。在本文中,通过将传统的荧光共振能量转移(FRET)技术(上转换纳米粒子(UCNPs)和金纳米粒子(GNPs)之间)与基于固相的免疫分析技术相结合,解决了全血样本一步法原位免疫分析中这些紧迫的问题。在缓冲液中,羊 IgG(gIgG)的检测限低至 0.042μg/mL,在 20 倍稀释的全血样本中的检测限为 0.51μg/mL,在血液样本中的线性范围从 0.75μg/mL 到 60μg/mL。据我们所知,这是首例具有大线性检测范围的一步法原位固相免疫分析全血样本的方法。这项研究为直接在全血中快速灵敏地分析各种生物分子提供了一个有前途的平台,无需繁琐的分离、洗涤步骤和颗粒聚集问题。

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