Ultrasensitive On-Chip Immunoassays with a Nanoparticle-Assembled Photonic Crystal

被引:17
作者
Han, Jin-Hee [1 ]
Sudheendra, L. [1 ]
Kim, Hee-Joo [2 ]
Gee, Shirley J. [2 ]
Hammock, Bruce D. [2 ]
Kennedy, Ian M. [1 ]
机构
[1] Univ Calif Davis, Dept Mech & Aerosp Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
关键词
electrophoretic particle entrapment system (EPES); nanoparticles; nanoarray; immunoassay; human epidermal growth factor receptor 2 (HER2); ENHANCED-FLUORESCENCE; LABEL-FREE; PROTEIN; ASSAY; NANOARRAY; SYSTEM; SERUM; BEADS;
D O I
10.1021/nn301656c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrophoretic particle entrapment system (EPES) is employed to generate 2D array of nanoparticles coated with biological molecules (le., antibodies). Phase matching of the excitation and the emission in the 2D arrays with particles produces a highly enhanced fluorescence signal that was shown to improve the limit of detection in immunoassays. The phase matching is achieved when the particle are in the sub-100 nm range. A comparison between different size particles shows that the sensitivity of an immunoassay is extended to a range that is difficult to achieve: with standard technology (e.g., enzyme-linked immunosorbent assay-ELISA). The effectiveness 14 this novel configuration of particle-in-a-well was demonstrated with an assay for human epidermal growth factor receptor 2 (HER2; breast cancer biomarker), with a detection limit as low as 10 attomolar (aM) in less than 10 mu L of serum-based sample. The limit of detection of HER2 indicated far superior assay performance compared to the corresponding standard 96-well plate-based ELISA. The particle-based photonic platform reduces the reagent volume and the time for performing an assay in comparison to competing methods. The simplicity of operation and the level of sensitivity demonstrated here can be used for rapid and early stage detection of biomarkers.
引用
收藏
页码:8570 / 8582
页数:13
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