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用于同步多组分分析的磁性编码荧光多功能纳米球

Magnetic-encoded fluorescent multifunctional nanospheres for simultaneous multicomponent analysis.

作者信息

Song Erqun, Han Weiye, Li Jingrong, Jiang Yunfei, Cheng Dan, Song Yang, Zhang Pu, Tan Weihong

机构信息

Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University) Ministry of Education, College of Pharmaceutical Sciences, Southwest University , Chongqing, 400715, People's Republic of China.

出版信息

Anal Chem. 2014 Oct 7;86(19):9434-42. doi: 10.1021/ac5031286. Epub 2014 Sep 19.

Abstract

In this study, magnetic-encoded fluorescent (CdTe/Fe3O4)@SiO2 multifunctional nanospheres were constructed by adjusting the initial concentration of Fe3O4 in a fabrication process based on reverse microemulsion. The resultant multifunctional nanospheres were characterized by transmission electron microscopy, X-ray diffraction measurements, fluorescence spectrophotometry, and vibrating sample magnetometry. They showed good fluorescence properties, gradient magnetic susceptibility (weak, moderate, and strong), and easy biofunctionalization for biomolecules, such as immunoglobulin G (IgG), protein, and antibody. Then the capture efficiency of the (CdTe/Fe3O4)@SiO2 nanospheres were investigated by using the fluorophore-labeled IgG-conjugated nanospheres as a model. Further studies demonstrated the ability of these (CdTe/Fe3O4)@SiO2 multifunctional nanospheres to accomplish sequentially magnetic separation, capture, and fluorescent detection for each corresponding antigen of CA125, AFP, and CEA with a detection limit of 20 KU/L, 10 ng/mL, and 5 ng/mL, respectively, from a mixed sample under a certain external magnetic field within a few minutes. The strategy of combining magnetic-encoding-based separation and fluorescence-based detection proposed in this study shows great potential to achieve easy, rapid, economical, and near-simultaneous multicomponent separation and analysis for a variety of targets such as drugs, biomarkers, pathogens, and so on.

摘要

在本研究中,基于反向微乳液的制备过程,通过调节Fe3O4的初始浓度构建了磁性编码荧光(CdTe/Fe3O4)@SiO2多功能纳米球。通过透射电子显微镜、X射线衍射测量、荧光分光光度法和振动样品磁强计对所得多功能纳米球进行了表征。它们表现出良好的荧光特性、梯度磁化率(弱、中、强),并且易于对生物分子如免疫球蛋白G(IgG)、蛋白质和抗体进行生物功能化。然后,以荧光团标记的IgG偶联纳米球为模型,研究了(CdTe/Fe3O4)@SiO2纳米球的捕获效率。进一步的研究表明,这些(CdTe/Fe3O4)@SiO2多功能纳米球能够在几分钟内在一定外部磁场下对混合样品中的CA125、AFP和CEA的每种相应抗原依次进行磁性分离、捕获和荧光检测,检测限分别为20 KU/L、10 ng/mL和5 ng/mL。本研究中提出的基于磁性编码的分离和基于荧光的检测相结合的策略,在实现对药物、生物标志物、病原体等多种目标的简单、快速、经济且近乎同时的多组分分离和分析方面显示出巨大潜力。

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