Rapid detection and quantification of Enterovirus 71 by a portable surface plasmon resonance biosensor

被引:45
|
作者
Prabowo, Briliant Adhi [1 ,6 ]
Wang, Robert Y. L. [2 ,4 ]
Secario, Muhammad Khari [1 ]
Ou, Po-Ting [2 ]
Alom, Azharul [1 ]
Liu, Jia-Jung [1 ]
Liu, Kou-Chen [1 ,3 ,4 ,5 ]
机构
[1] Chang Gung Univ, Dept Elect Engn, 259 Wenhua 1st Rd, Taoyuan 33002, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Biomed Sci, Taoyuan 33302, Taiwan
[3] Chang Gung Univ, Ctr Biomed Engn, Taoyuan 33302, Taiwan
[4] Chang Gung Mem Hosp, Dept Pediat, Div Pediat Infect Dis, Linkou 33305, Taiwan
[5] Ming Chi Univ Technol, Dept Mat Engn, New Taipei 24301, Taiwan
[6] Indonesian Inst Sci, Res Ctr Informat, Bandung 40135, Indonesia
来源
BIOSENSORS & BIOELECTRONICS | 2017年 / 92卷
关键词
EV71; SPR; Sensor; VP1; Virus; Quantification method; SERS-ACTIVE SUBSTRATE; DROPLET DIGITAL PCR; VIRUS-LIKE PARTICLE; QUANTITATIVE DETECTION; JAPANESE ENCEPHALITIS; COXSACKIEVIRUS A16; CRYSTAL-STRUCTURE; EXPRESSION; AMPLIFICATION; ANTIGEN;
D O I
10.1016/j.bios.2017.01.043
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This study presents the first report on a label-free detection and rapid quantification method for human enterovirus 71 (EV71) using a portable surface plasmon resonance (SPR) system. The SPR sensor instrument was configured to run on low power in a miniaturized platform to improve the device portability for a wider application both in laboratories and in the field. A color tunable organic light emitting diode in red spectrum was attached on a trapezoidal prism for the disposable light source module. The SPR signal processing using integration area under the reflectivity curve is applied for optimum signal to noise ratio (SNR) enhancement. The major capsid protein VP1 of EV71 was selected as the biomarker target in the detection study. The experimental time required for the EV71 quantification was reduced from 6 days using the conventional viral plaque assay to several minutes using the proposed method. The study results establish a detection limit of approximately 67 virus particles per milliliter (vp/ml) of EV71 in a Dulbecco's modified Eagle's medium. The VP1 detection in the portable SPR biosensor had a detection limit of approximately 4.8 pg/ml in the PBS buffer. Therefore, the proposed direct EV71 viral particle quantification method can be rapidly performed in real time, with high sensitivity and less labor and without assays or fluorescence.
引用
收藏
页码:186 / 191
页数:6
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