A photoacoustic immunoassay for biomarker detection

被引:37
|
作者
Zhao, Yunfei [1 ]
Cao, Mingfeng [2 ]
McClelland, John F. [3 ]
Shao, Zengyi [2 ]
Lu, Meng [1 ,4 ]
机构
[1] Iowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Biomol & Chem Engn, Ames, IA 50011 USA
[3] MTEC Photoacoust Inc, 3507 Oakland St, Ames, IA 50014 USA
[4] Iowa State Univ, Dept Mech Engn, Ames, IA 50011 USA
来源
BIOSENSORS & BIOELECTRONICS | 2016年 / 85卷
关键词
Biomarker; Photoacoustics; Immunoassay; Surface plasmon resonance; ELISA; Nanoparticle; Human interleukin-8; PLASMON RESONANCE SPECTROSCOPY; NANOPARTICLES;
D O I
10.1016/j.bios.2016.05.028
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Challenges in protein biomarker analysis include insufficient sensitivity for detecting low-abundance biomarkers, poor measurement reproducibility, and the high costs and large footprints of detection systems. To address these issues, a new detection modality was developed for analyzing protein biomarkers based on the plasmon-enhanced photoacoustic (PA) effect. The detection modality employed a heterogeneous immunoassay scheme and used gold nanoparticles (AuNPs) as the signal reporter. Due to their localized plasmon resonance, AuNPs can strongly interact with intensity-modulated laser excitation and generate strong PA signals, which are subsequently sensed and quantified using a microphone. As an example, the performance of the PA immunoassay was evaluated by detecting the human interleukin 8 chemokine. The PA immunoassay provided approximately 143 x lower limit of detection (LOD) than observed with the gold standard enzyme-linked immunosorbent assay - a decrease from 23 pg/mL to 0.16 pg/mL. In addition to the significant performance improvement in terms of the LOD, the PA immunoassay also offers advantages in terms of compatibility with low-cost instruments and the long-term stability of assay results. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:261 / 266
页数:6
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