荧光
费斯特共振能量转移
检出限
材料科学
斯托克斯位移
生物传感器
纳米颗粒
分析化学(期刊)
免疫分析
吸收(声学)
接受者
化学
发光
纳米技术
色谱法
光电子学
光学
物理
凝聚态物理
抗体
复合材料
生物
免疫学
作者
Francesca Salis,Ana B. Descalzo,Elena Benito‐Peña,María C. Moreno‐Bondi,Guillermo Orellana
出处
期刊:Small
[Wiley]
日期:2018-04-17
卷期号:14 (20)
被引量:35
标识
DOI:10.1002/smll.201703810
摘要
Abstract Fluorescence immunoassays are popular for achieving high sensitivity, but they display limitations in biological samples due to strong absorption of light, background fluorescence from matrix components, or light scattering by the biomacromolecules. A powerful strategy to overcome these problems is introduced here by using fluorescent magnetic nanobeads doped with two boron‐dipyrromethane dyes displaying intense emission in the visible and near‐infrared regions, respectively. Careful matching of the emission and absorption features of the dopants leads to a virtual Stokes shift larger than 150 nm achieved by an intraparticle Förster resonance energy transfer (FRET) process between the donor and the acceptor dyes. Additionally, the magnetic properties of the fluorescent beads allow preconcentration of the sample. To illustrate the usefulness of this approach to increase the sensitivity of fluorescence immunoassays, the novel nanoparticles are employed as labels for quantification of the widely used Tacrolimus (FK506) immunosuppressive drug. The FRET‐based competitive inhibition immunoassay yields a limit of detection (LOD) of 0.08 ng mL −1 , with a dynamic range (DR) of 0.15–2.0 ng mL −1 , compared to a LOD of 2.7 ng mL −1 and a DR between 4.1 and 130 ng mL −1 for the immunoassay carried out with direct excitation of the acceptor dye.
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