An integrated enzyme-linked immunosorbent assay system with an organic light-emitting diode and a charge-coupled device for fluorescence detection

被引:16
|
作者
Nakajima, Hizuru [1 ]
Okuma, Yukiko [2 ]
Morioka, Kazuhiro [1 ]
Miyake, Mayo [2 ]
Hemmi, Akihide [2 ,3 ]
Tobita, Tatsuya [2 ,4 ]
Yahiro, Masayuki [5 ]
Yokoyama, Daisuke [5 ]
Adachi, Chihaya [5 ]
Soh, Nobuaki [2 ]
Nakano, Koji [2 ]
Xue, Shuhua [1 ]
Zeng, Hulie [1 ]
Uchiyama, Katsumi [1 ]
Imato, Toshihiko [2 ]
机构
[1] Tokyo Metropolitan Univ, Dept Appl Chem, Grad Sch Urban Environm Sci, Tokyo 1920397, Japan
[2] Kyushu Univ, Dept Appl Chem, Grad Sch Engn, Nishi Ku, Fukuoka 812, Japan
[3] Mebius Adv Technol Ltd, Suginami Ku, Tokyo, Japan
[4] NTT Adv Technol Corp, Kanagawa, Japan
[5] Kyushu Univ, Ctr Future Chem, Nishi Ku, Fukuoka 812, Japan
关键词
CCD; Fluorescence detection; Immunoassay; Microfluidics; Organic light-emitting diode; THERMAL LENS MICROSCOPE; MICROCHIP ELECTROPHORESIS; NONFLUORESCENT MOLECULES; MICROFLUIDIC DEVICE; RAPID-DETERMINATION; IMMUNOGLOBULIN-A; AMINO-ACIDS; CHIP; PLATFORM; FLOW;
D O I
10.1002/jssc.201100429
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fluorescence detection system for a microfluidic device using an organic light-emitting diode (OLED) as the excitation light source and a charge-coupled device (CCD) as the photo detector was developed. The OLED was fabricated on a glass plate by photolithography and a vacuum deposition technique. The OLED produced a green luminescence with a peak emission at 512 nm and a half bandwidth of 55 nm. The maximum external quantum efficiency of the OLED was 7.2%. The emission intensity of the OLED at 10 mA/cm(2) was 13 mu W (1.7 mW/cm(2)). The fluorescence detection system consisted of the OLED device, two band-pass filters, a five microchannel poly(dimethylsiloxane) (PDMS) microfluidic device and a linear CCD. The fluorescence detection system was successfully used in a flow-based enzyme-linked immunosorbent assay on a PDMS microfluidic device for the rapid determination of immunoglobulin A (IgA), a marker for human stress. The detection limit (S/N = 3) for IgA was 16.5 ng/mL, and the sensitivity was sufficient for evaluating stress. Compared with the conventional 96-well microtiter plate assay, the analysis time and the amounts of reagent and sample solutions could all be reduced.
引用
收藏
页码:2906 / 2912
页数:7
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