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铕(III)螯合物染色纳米颗粒标记物在基于ITO波导的阿特拉津竞争性荧光免疫分析中的应用

Application of europium(III) chelate-dyed nanoparticle labels in a competitive atrazine fluoroimmunoassay on an ITO waveguide.

作者信息

Cummins C M, Koivunen M E, Stephanian A, Gee S J, Hammock B D, Kennedy I M

机构信息

Department of Biomedical Engineering, University of California Davis, Davis, CA 95616, USA.

出版信息

Biosens Bioelectron. 2006 Jan 15;21(7):1077-85. doi: 10.1016/j.bios.2005.04.003.

Abstract

We have demonstrated the use of an optical indium tin oxide (ITO) (quartz) waveguide as a new platform for immunosensors with fluorescent europium(III) chelate nanoparticle labels (Seradyn) in a competitive atrazine immunoassay. ITO as a solid surface facilitated the successful use of particulate labels in a competitive assay format. The limit of detection in the new nanoparticle assay was similar to a conventional ELISA. The effect of particle size on bioconjugate binding kinetics was studied using three sizes of bioconjugated particle labels (107, 304, and 396nm) and a rabbit IgG/anti-IgG system in a 96-well plate. A decrease in particle size resulted in faster binding but did not increase the assay sensitivity. Flux calculations based on the particle diffusivity prove that faster binding of the small particles in this study was primarily due to diffusion kinetics and not necessarily to a higher density of antibodies on the particle surface. The results suggest that ITO could make a good platform for an optical immunosensor using fluorescent nanoparticle labels in a competitive assay format for small molecule detection. However, when used in combination with fluorescent particulate labels, a highly sensitive excitation/detection system needs to be developed to fully utilize the kinetic advantage from small particle size. Different regeneration methods tested in this study showed that repeated washings with 0.1 M glycine-HCl facilitated the reuse of the ITO waveguide.

摘要

我们已经证明,在竞争性莠去津免疫分析中,使用光学铟锡氧化物(ITO)(石英)波导作为带有荧光铕(III)螯合物纳米颗粒标记物(Seradyn)的免疫传感器的新平台。ITO作为固体表面有助于在竞争性分析形式中成功使用颗粒标记物。新的纳米颗粒分析中的检测限与传统酶联免疫吸附测定(ELISA)相似。使用三种尺寸的生物共轭颗粒标记物(107、304和396nm)以及兔免疫球蛋白G/抗免疫球蛋白G系统在96孔板中研究了颗粒大小对生物共轭结合动力学的影响。颗粒尺寸减小导致结合更快,但并未提高分析灵敏度。基于颗粒扩散率的通量计算证明,本研究中小颗粒更快的结合主要是由于扩散动力学,而不一定是由于颗粒表面抗体密度更高。结果表明,在用于小分子检测的竞争性分析形式中,ITO可以成为使用荧光纳米颗粒标记物的光学免疫传感器的良好平台。然而,当与荧光颗粒标记物结合使用时,需要开发一种高灵敏度的激发/检测系统,以充分利用小颗粒尺寸带来的动力学优势。本研究中测试的不同再生方法表明,用0.1M甘氨酸 - 盐酸反复洗涤有助于ITO波导的重复使用。

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