A PMMA microcapillary quantum dot linked immunosorbent assay (QLISA)

被引:12
作者
Babu, Sundar [1 ]
Mohapatra, Sakya [1 ]
Zubkov, Leonid [1 ]
Murthy, Sreekant [2 ]
Papazoglou, Elisabeth [1 ]
机构
[1] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[2] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
关键词
Quantum dots; ELISA; MPO; Inflammation; IBD; Microfluidic; Biosensor; QLISA; PMMA capillary; CAPILLARY IMMUNOSENSOR; MICROANALYTICAL DEVICES; FLOW IMMUNOSENSOR; WAVE-GUIDE; COLITIS; NANOPARTICLES; FLUORESCENCE; IMMUNOASSAYS; INFLAMMATION; ANTIBODIES;
D O I
10.1016/j.bios.2009.04.043
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The development of a simple and inexpensive quantum dot based immunoassay for detecting myeloperoxidase (MPO) in stool samples is reported (QLISA). The method developed utilizes readily available polymethylmethacrylate (PMMA) microcapillaries as substrates for performing the sandwich assay. High power (80 mW) and low power (10 mW) UV-LEDs were tested for their efficiency in maximizing detection sensitivity in a waveguide illumination or a side illumination mode. The results obtained indicate that both waveguide and side illumination modes can be employed for detecting MPO down to 15 ng/mL, however the high power LED in a side illumination mode improves sensitivity and simplifies the data acquisition process. The protocol and sensor robustness was evaluated with animal stool samples spiked with MPO and the results indicate that the sensitivity of detection is not compromised when used in stool samples. The effect of the ionic strength of the environment on the fluorescence stability of quantum dots was evaluated and found to affect the assay only if long imaging times are employed. Replacing the buffer with glycerol during imaging increased the fluorescence intensity of quantum dots while significantly minimized the loss in intensity even after 2 h. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3467 / 3474
页数:8
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